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Pharming Group NL0010391025

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Vacatures bij Pharming

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  1. forum rang 8 Janssen&Janssen 2 november 2023 21:49
    Sr. Director Corporate & Healthcare Compliance

    The role:
    The Sr Director Corporate & Healthcare Compliance EU/RoW (hereafter: the “EU/RoW Senior Compliance Director”) leads the healthcare compliance operations for Pharming in Europe and the rest of the world. In that capacity, the EU/RoW Senior Compliance Director builds and manages a team of senior compliance officers and strategically partners with and advises senior management to promote and ensure that Pharming acts in an ethical manner and is compliant with all applicable healthcare-related rules and regulations.

    The EU/RoW Senior Compliance Director also has a leading role in (i) ensuring compliance with applicable rules and regulations in the field of data protection/privacy and (ii) developing, implementing and maintaining corporate law-related policies and controls to ensure that Pharming is compliant with all rules, codes, and regulations applicable to it as a company listed in both the Netherlands and the US.

    In doing so, the EU/RoW Senior Compliance Director, as a senior executive, plays a pivotal role in fostering and promoting a culture of ethics and integrity across the global Pharming organization.



    Areas of responsibility:



    Leads and oversees the healthcare compliance operations for Pharming in Europe and the rest of the world (“RoW”), building and managing a team of (initially, three) senior compliance officers. Also leads the activities across Pharming aimed at ensuring that Pharming is compliant with all applicable rules and regulations in the field of data protection/privacy, including the GDPR. The Privacy Officer also reports to the Sr. Director Corporate & Healthcare Compliance EU/RoW.
    Together with the Sr Director Healthcare Compliance US, responsible for the design, maintenance, implementation and monitoring of an effective Global Business Integrity program for Pharming, to be adopted by the Executive Committee, (i) to enhance an ethics and compliance-oriented culture across the organization, and (ii) to prevent, identify, mitigate and manage ethics and compliance risks. This program includes the development of global compliance policies, procedures and practices and the design, implementation and monitoring of compliance-related systems and processes.
    Leads and manages for the EU and the RoW the implementation, maintenance and monitoring of the Global Business Integrity program, as adopted by the Executive Committee, including, inter alia the design, development and implementation, to the extent required, of specific, tailor-made policies and procedures for the Pharming operations in the EU and RoW in accordance with the global policies and procedures, the execution of monitoring activities and the execution of the related training programs for management and staff.
    Strategically partners with and advises senior management of Pharming, and oversees effective advice and other support activities by team members regarding specific files and projects, to promote and ensure that Pharming acts in an ethical manner and is compliant with all applicable healthcare-related rules and regulations governing its operations in Europe and the RoW, including, inter alia, sales, marketing and medical activities.
    Strategically partners with and advises senior management of Pharming to ensure compliance by Pharming with all Dutch and US corporate-law related rules, codes, and regulations applicable to it as a listed company.
    Executes the tasks, responsibilities, and powers as attributed to the Compliance Officer by and under the prevailing Internal Code on Inside Information and Reporting Obligations (hereafter the “Insider Code”) and other applicable policies.
    Monitors and executes the notification responsibilities to regulatory authorities (including the AFM and the SEC, as the case may be) applicable to Pharming, as listed company, and members of the Board of Directors and the Executive Committee.
    Contributes to effective compliance risk assessment and management, trend analysis and root cause analysis for the EU and RoW, by:
    - implementing and testing internal controls in accordance with Pharming’s global business integrity program;
    - designing, implementing and testing adequate internal control (including those required for SOX compliance);
    - driving and overseeing the monitoring plan, including following-up on monitoring results, analyzing trends and root causes, contributing to remediation plans, and updating policies and processes, if necessary;
    - supporting process reviews and implementing improvements through system integration and data analytics in alignment with Pharming’s Global Compliance strategies; and
    - conducting compliance-related investigations, including those as identified in the Alert Reporting Procedure, the Insider Code and other applicable internal policies.
    Reports on a regular basis, and without undue delay in case of incidents, to the Chief Ethics & Compliance Officer and senior management on the existing and emerging business integrity risks.
    Monitors developments in healthcare and corporate rules and regulations and compliance practices relevant to Pharming. Regularly educates and informs senior management and other staff members, together with team members, on matters related to the compliance program as well as relevant healthcare industry legal and compliance developments.
    Manages budget resources assigned to Business Integrity for the EU and RoW.
    Member of the Pharming Disclosure Committee.

    Qualifications:



    EU Master’s Degree. Advanced EU Healthcare Compliance certification.
    A senior compliance executive with 12+ years of experience in healthcare compliance gained in the EU Pharma/Biotech industry/life sciences sector, including 5+ years of management experience. At least, executive experience in the following areas: bribery and anti-corruption regulations, HCO/HCP/HCC regulations and practices, transfer of value/transparency reporting/FMV processes, Due Diligence processes, promotional activities, speaker programs, advisory boards, HCO sponsorships and grants and donations.

    Both healthcare compliance experience gained in the rare disease segment and experience regarding pharmaceutical product launches will be a plus.

    Expert knowledge of prevailing EU healthcare compliance standards and practices, including EFPIA code requirements and standards.
    5+ experience of international healthcare compliance in Pharma/Biotech healthcare compliance practices outside of EU and the US, preferably including the APAC region.
    3+ experience with listing requirements gained at a European (preferably Dutch) listed company, including expert knowledge of the EU market abuse regulations. Expert knowledge and experience of US (SEC and Nasdaq) listing requirements is a plus.
    Flexibility as well the ability to work effectively in a senior compliance role in global cross-cultural and cross-functional teams.
    High risk awareness and risk management skills
    Proficient in Microsoft Office
    Languages: English: fluent; Dutch: a plus.
  2. forum rang 8 Janssen&Janssen 22 november 2023 20:13
    Procurement
    Category Manager Leiden Full time 685

    Manufacturing, Science, Technology
    Office Facility Manager Leiden Full time 1038

    Sales
    Ruconest Account Manager - Pacific Northwest US Full time 1057

    Information Technology
    SAP Application Manager Leiden 1000

    Regulatory Affairs
    Director, Advertising and Promotion Warren Full Time 920

    Human Resources
    Sr. Manufacturing Officer- Solid dosage forms Leiden Full time 1004

    Legal & Compliance
    Corporate Counsel Warren Full Time 1039

    Information Technology
    SAP Application Manager Supply Chain Leiden Full time 1043

    Finance
    ESG Reporting Manager Leiden Full time 1050

    Human Resources
    HR Business Partner Leiden Full time 1002

    Marketing
    Director of Marketing Warren, Full time 918

    Commercial Operations
    Commercial Trade Relations Manager Leiden Full time 940

    Market Access
    Associate Director, Reimbursement and Access - West Warren, Full time 1055

    Ethics & Compliance
    Sr. Director Corporate & Healthcare Compliance Leiden Full time 1023

    Transgenic Platform
    Dierverzorger- Biotechnicus (omgeving Eindhoven) 632

    Procurement
    Procurement Officer Leiden Full time 1047

    Continuous Improvement
    Project Manager CoE Full time Leiden 979

    Ethics & Compliance
    Executive Secretary Full time Leiden 1013

    Finance
    Teamlead BPE Global R2R Full time Leiden 1052

    Finance
    Teamlead Global O2C Full time Leiden 1051

    Finance
    Teamlead and BPE Global Purchase-to-Pay Full time Leiden 1053

    Regulatory Affairs
    Manager, Medical Writing Full time Warren 1046

    Commercial Operations
    Commercial Trade Relations Manager Location GB 1001

    Finance
    Financial Accountant Leiden Full time 901

    Transgenic Platform
    Veterinarian Eindhoven Full time 1009

    Quality Assurance
    QA officer Oss Full time 1003

    Human Resources
    Payroll Specialist Leiden Full time 1040

    Finance
    Financial Reporting Analyst / Specialist Leiden Full time 904

    Bijgekomen;

    Manufacturing, Science, Technology
    Office Facility Manager Leiden Full time 1038

    Sales
    Ruconest Account Manager - Pacific Northwest US Full time 1057

    Information Technology
    SAP Application Manager Supply Chain Leiden Full time 1043

    Finance
    ESG Reporting Manager Leiden Full time 1050

    Market Access
    Associate Director, Reimbursement and Access - West Warren, Full time 1055

    Procurement
    Procurement Officer Leiden Full time 1047

    Afgenomen:
    Business Integrity
    Healthcare Compliance Officer Full time Leiden 1045

    Business Integrity
    Healthcare Compliance Officer Full time Leiden 1044

    Human Resources
    HR Officer Leiden Full time 1005

    Legal & Compliance
    Sr Director of Compliance Warren, Fulltime 656

    Quality Assurance
    Quality Systems Specialist (CSV) Full time Leiden 744

    Legal & Compliance
    Manager, IT Risk & Control Leiden Full time 964

    Information Technology
    Manager SAP Leiden Full time 906

    Aantal openstaand: 28

    Totaal vacatures toe of afname vanaf 29 sept 2020
    Bijgekomen: 295
    Vervuld: 279

    2023
    Bijgekomen: 111
    Afgenomen: 101
  3. forum rang 8 Janssen&Janssen 22 november 2023 20:13
    Manufacturing, Science, Technology
    Office Facility Manager Leiden Full time 1038

    Doel van de functie
    Als Office Facility Manager zorg je ervoor dat onze faciliteiten en apparatuur altijd in topconditie verkeren. Jij plant preventief onderhoud met externe dienstverleners volgens een strak schema. Als eerste aanspreekpunt voor alles met betrekking tot faciliteiten, apparatuur en technische installaties in ons hoofdkantoor in Leiden, speel je een cruciale rol.



    Leidinggeven aan het plannen en toezicht houden op preventief onderhoud van apparatuur en gebouwen in Leiden.
    Fungeren als back-up voor de labcoördinator in Leiden.
    Zorgen dat het gebouw, de apparatuur en het meubilair in optimale staat blijven.
    Opstellen, bekijken en uitvoeren van werkvoorschriften, SOP's, protocollen en rapporten met betrekking tot gebouw- en apparatuurgerelateerde activiteiten.
    Regelmatig contact onderhouden met externe leveranciers, onderhoudsproviders, verhuurders, eigenaren en medehuurders.
    Vernieuwing en aanpassingen van het pand coördineren op het gebied van duurzaamheid, nutsvoorzieningen en meer.
    Onderhandelen en coördineren van alle facilitaire contracten (gebouwen, groenvoorziening, beveiliging, schoonmaak, afvalverwerking, parkeren, enz.).
    Verkrijgen en controleren van contracten voor facilitaire dienstverleners (groenvoorziening, afvalverwerking, beveiliging, schoonmaak, koffiemachines) die nodig zijn voor Pharming in Leiden.
    Actieve betrokkenheid bij veiligheids- en duurzaamheidscommissies, en het initiëren van verbeteringen op deze gebieden (gerelateerd aan ESG).
    Eerste aanspreekpunt voor alle Leidse medewerkers met betrekking tot facilitaire vragen (airconditioning, ventilatie, deuren, vloeren, gedeelde ruimtes, parkeren, meubilairreparaties, expeditieruimte, koffiemachines, badkamers, verlichting).

    In deze rol draag je bij aan de algehele efficiëntie, veiligheid en duurzaamheid van het kantoor in Leiden, en zorg je ervoor dat het een omgeving is waarin alle medewerkers optimaal kunnen werken. Het vereist effectieve communicatie, onderhandelingsvaardigheden en een proactieve aanpak van facilitair management.



    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.

    Apply for the job
    Does this sound like you and do you want to join our team? Then we'd love to hear from you!

    We’re an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
  4. forum rang 8 Janssen&Janssen 22 november 2023 20:14
    Sales
    Ruconest Account Manager - Pacific Northwest US Full time 1057

    Pharming is committed to our core values: “We Care, We Collaborate, We Walk the Talk”, which is complementary to our focus on self-development of our people, teamwork, leadership and being results orientated. In our growing organization, it is important that employees feel connected and engaged. Our core values enable our mission of bringing the unserved rare disease patients the solutions they need and create a clear pathway forward to meet our strategic goals and objectives.

    Overview



    Pharming is seeking to hire a Ruconest Account Manager (RAM) - Pacific Northwest who will be responsible for all sales and marketing activities for Ruconest therapy. Our goal is for the RAM to be accountable for all business-related activities within the Pacific Northwest, including achievement of sales goals, business planning, and expense control. Successful execution will involve implementation of sales strategic initiatives and development of strong working relationships with all physicians and accounts who treat patients appropriate for Ruconest therapy in the Pacific Northwest. The position reports to the Regional Business Director- West Region and is an individual contributor role. Territory includes the areas around San Francisco Bay, San Jose, Sacramento, and Oakland.



    Key Responsibilities



    The Ruconest Account Manager (RAM) – Pacific Northwest will be responsible for a wide variety of matters in support of Pharming’s growth as we increase the number of both pipeline and marketed products.



    Core functions include:

    Promoting Ruconest within approved labeling, to all targeted physicians and patient candidates.
    Identifying and educating providers managing patients with Hereditary Angioedema (HAE) on the benefits of using Ruconest therapy with appropriate patients.
    Assisting the clinical staff with the steps necessary to get the patient access to Ruconest including areas such as reimbursement, proper testing, and site of care determination.
    Achieving and exceeding targeted sales forecasts and other key performance objectives.
    Establish a leadership role and acts as a trusted advisor to customers.
    Collaborating cross-functionally to assess and influence change to improve business processes.
    Independently build comprehensive strategic and tactical business plan.
    This is a field/remote role: must have the ability to travel within mentioned territory.




    Minimum Qualifications



    Bachelor’s degree in business or science related field (or equivalent).
    8+ years selling specialty biologics, preferably infused products.
    Demonstration of clinical, technical, and scientific knowledge in complex disease states.




    Preferred Qualifications



    5+ years of complex sales model experience Biotech, biologics, and specialty pharmacy experience.
    Demonstrated track record of success (Top 20% performance), President’s Club or other top tier awards.
    Strong knowledge and understanding of reimbursement, distribution, and managed care processes as well as previous experience in the facilitation of in-office billing processes for reimbursement.




    Travel Requirements



    This position requires extensive travel (50-75%).
    Compensation & Benefits:



    Flexible hybrid work schedule to promote a health work-life balance.
    Competitive compensation package including annual target bonus.
    Long-Term Incentive Program.
    401(k) plan with company match.
    Paid-Time Off Days.
    16 Company Holidays per year (typically last week of December up until New Year’s Day)


    Other Benefits:



    Excellent Healthcare Plans including Medical, Dental and Vision.
    Flexible Spending Accounts for Medical and Dependent Care.
    Company-provided Life Insurance, Short-Term and Long-Term Disability Plans.
    Accident, Hospital Indemnity and Critical Illness Plans.
    Pet Insurance Plan.
    On Premise Fitness Center.
    Health & Wellness Program.
    Choice of Mobile Phone for Work Use or Cell Phone Stipend.
    Pharming Academy – Continuing Learning & Development Program.
  5. forum rang 8 Janssen&Janssen 22 november 2023 20:16
    Information Technology
    SAP Application Manager Supply Chain Leiden Full time 1043

    Purpose of the role:
    The Application Manager advises and supports the business on application requirements and collaborates with them to ensure best fit of application and optimal use by the organization. He/she is responsible for the life cycle management of a set of allocated applications, from operational functionality to maintenance, version control and upgrades of these applications.



    Responsibilities:

    Maintains knowledge of one or more functional modules in SAP S/4HANA to enable the effective delivery of support and improvement for those modules.
    Collaborates with internal stakeholders to analyze business requirements, translating them into clear functional specifications and proactively evaluate and challenge solution design proposals from external partners.
    Maintain the application to ensure availability, reliability, and continuity.
    Contribute to the integration in the business processes and links with other applications and translate the needs of your business partners into new or improved solutions.
    Develops test scenarios, take the lead in planning, executing, and guiding the various testing activities, ensuring meticulous documentation of all testing results.
    Maintains strong presentation skills needed to deliver training and application demonstrations.
    Handles incidents, issues, service requests and changes from business.
    Coordinates and follow-up open tickets from business with our SAP support partner.
    Participate as ICT representative in system implementation and integration projects.
    Ad hoc execution of SAP support activities.


    Your profile:

    Bachelor’s degree in a Business, Finance, or ICT related field
    5+ years’ hands-on experience with MM, SD, modules in SAP.
    Experience with PP, QM, PM modules in SAP is an advantage.
    Proven user requirements gathering and documenting skills.
    Experience with SAP S/4HANA is an advantage.
    Experience in the Pharmaceutical industry is an advantage.
    Good knowledge of Supply Chain business processes and their integration with Finance.
    SAP certification and/ or SAP training preferred.
    Fluency in English


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  6. forum rang 8 Janssen&Janssen 22 november 2023 20:16
    Finance
    ESG Reporting Manager Leiden Full time 1050

    urpose of the role:

    The ESG Reporting Manager, will be responsible for developing, managing, and enhancing our Environmental, Social, and Governance (ESG) reporting initiatives. He / she will collaborate with various departments to collect and analyze ESG data, prepare comprehensive reports, and drive transparency and accountability in our ESG performance. As the ESG Reporting Manager, he / she will play a pivotal role in helping the company meet its reporting requirements on its sustainability goals and communicate its efforts to stakeholders effectively. He / She will also act as a back-up for the financial accountant.



    Responsibilities:

    ESG Data Collection and Analysis:

    Oversee the collection of ESG data from different departments and external sources.
    Analyze ESG data to identify trends, performance indicators, and areas for improvement.
    Develop methodologies for data verification and validation.
    Reporting Frameworks:

    Stay up-to-date with evolving ESG reporting standards and frameworks (e.g., GRI, ESRS, CSRD).
    Ensure compliance with industry-specific regulations and guidelines.
    Develop and maintain a reporting framework tailored to the organization's needs.
    Sustainability Reporting:

    Lead the preparation of periodic ESG reports, including annual sustainability reports and other ad-hoc reports as required.
    Coordinate with internal and external stakeholders to gather relevant information and insights for reporting purposes.
    Ensure the reports are accurate, clear, and transparent in their presentation of ESG performance.
    Data Management:

    Develop and maintain a robust ESG data management system.
    Ensure data accuracy, consistency, and accessibility for reporting purposes.
    ESG Strategy and Goal Alignment:

    Collaborate with cross-functional teams to align ESG strategies with the organization's mission, values, and long-term goals.\Support the development and monitoring of ESG performance targets and objectives.
    Training and Awareness:

    Occasionally provide ESG training and awareness programs for employees, enabling them to contribute to the company's sustainability goals.
    Promote a culture of ESG awareness and responsibility within the organization.
    Back-up for Financial Accountant:

    Periodic consolidating the financial reports of Pharming Group N.V. and its subsidiaries.
    Contribute to the preparation of the Annual Report, IFRS Financial Statements and other related matters such as press releases.
    Contribute to the preparation of position papers for accounting matters and valuation.


    Your profile:

    Master’s degree in a relevant field (Finance, Accounting, or Similar);
    5-10+ years of proven experience in Finance / Accounting and Reporting;
    3+ years of proven experience in a similar (ESG related) role;
    Working experience in a multinational, multicultural, stock-listed company;
    Strong communication skills;
    Fluent in English both in word and writing, and preferably one other language;
    Basic knowledge of IFRS and consolidation requirements;
    Familiar with SOx and the administrative documentation of the work performed;
    Project management experience is a plus;
    Professional certifications in ESG reporting or sustainability are a plus.
    Proficiency in ESG reporting standards and frameworks;


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  7. forum rang 8 Janssen&Janssen 22 november 2023 20:17
    Market Access
    Associate Director, Reimbursement and Access - West Warren, Full time 1055

    verview



    Pharming is seeking to hire an Associate Director, Reimbursement and Access - West (RAD) to support patient and healthcare providers (HCPs) across sites of care in gaining access for patients to Ruconest. Our goal is to ensure that HCPs have the most up to date information when prescribing and working through the approval and logistics processes for Ruconest. Successful execution will involve the RAD being a regional expert in patient access, reimbursement, prior authorization appeal, obtaining financial assistance, and navigation through any complex access related issues. RADs are regionally split across the U.S., supporting Ruconest Account Manager (RAM) territories in their assigned regions. This role will support the US West Coast territory to include Colorado, California, Washington, Utah, and Arizona.





    Key Responsibilities



    The Associate Director, Reimbursement and Access (RAD) will be responsible for a wide variety of matters in support of Pharming’s growth as we increase the number of both pipeline and marketed products.



    Core functions include:

    Handling all coverage, reimbursement and access needs across their territories/regions and work directly with their respective RAM’s, Ruconest Patient Advocates (RPAs), Hub Case Managers, National Account Directors (NADs) and customers (HCP facing).
    Work directly with Hub vendor to understand payer coverage issues and assist with prior-authorization (PA) denials and appeals by working with physicians and staff, helping prepare HCPs for Peer-to-Peer needs.
    Proactively track patients from submission of enrollment form through to shipment in order to identify potential issues and work to enable timely resolutions.
    Provide training and education to HCPs on payor specific coverage policies and authorization documentation requirements, appeals processes and patient financial assistance support programs.
    Develop and maintain positive working relationships with both internal team members (e.g., RAMs, NADs, Case Managers and RPAs) and external stakeholders (e.g., physicians, office staff, Specialty Pharmacy partners).
    Work with HCPs and specialty pharmacy to overcome quantity limits or high dollar overrides.
    Escalate and engage the NAD when payer coverage or payment issues are identified, providing detailed specifics on issues, steps attempted to resolve, and identify key items that need addressing with the payer.
    Communicate issues and status with internal stakeholders and leaders (NADs, RBDs, VP of Sales).
    Communicate opportunities and challenges related to patient access issues to internal stakeholders.
    Work collaboratively to improve access and reimbursement tools and processes.
    This is a field-based role; candidate should live within the mentioned territory, ideally local to a major airport.




    Minimum Qualifications:



    Bachelor’s Degree from an accredited university.
    3+ years’ experience as a Field Reimbursement Manager.
    5+ years cross-functional experience in the pharmaceutical/biotech industry.
    2+ Years' experience with prior authorization and multi-level appeals.




    Preferred Qualifications:



    3+ years’ experience as a Field Reimbursement Manager for a biologic / buy & bill (physician-administered, IM/SC injectable, IV injection, infusion) drug experience highly preferred.
    Immunology background and rare or ultra-rare disease industry experience highly preferred.
    Excellent working knowledge of reimbursement and access challenges in the current healthcare environment.
    Ability to communicate payer coverage criteria and prior authorization/appeals processes to HCPs and staff including prepping HCPs for Peer-to-Peer discussions.
    Experience working with Specialty Pharmacies to resolve access issues.
    Experience working with a Hub to obtain necessary payer information and facilitating next steps.
    Experience working with multiple internal stakeholders (sales, managed markets, patient advocacy, government affairs, etc.)
    Demonstrated ability to apply reimbursement knowledge to address/resolve patient access barriers.
    Possess interpersonal skills including managing and resolving conflict and building strong working relationships.
    Proven track record for consistently meeting or exceeding goals and objectives.
    Proficient in working in a cross functional environment while handling multiple tasks.




    Travel Requirements

    Travel as needed to HCP offices, with or without RAMs, to work with appropriate level stakeholders to respond to coverage or payment issues (i.e., 2 to 3 days in the field).






    Compensation & Benefits:



    Flexible hybrid work schedule to promote a health work-life balance.
    Competitive compensation package including annual target bonus.
    Long-Term Incentive Program
    401(k) plan with company match
    Paid-Time Off Days
    16 Company Holidays per year (typically last week of December up until New Year’s Day)






    Other Benefits:



    Excellent Healthcare Plans including Medical, Dental and Vision.
    Flexible Spending Accounts for Medical and Dependent Care.
    Company-provided Life Insurance, Short-Term and Long-Term Disability Plans.
    Accident, Hospital Indemnity and Critical Illness Plans.
    Pet Insurance Plan.
    On Premise Fitness Center.
    Health & Wellness Program.
    Choice of Mobile Phone for Work Use or Cell Phone Stipend.
    Pharming Academy – Continuing Learning & Development Program.
  8. forum rang 8 Janssen&Janssen 22 november 2023 20:18
    Procurement
    Procurement Officer Leiden Full time 1047

    Purpose of the role:
    The Procurement Officer partners with the business on Purchase to Pay processes, together translates their needs into the systems and procedures and ensures process optimization. The Procurement Officer analyses spend of goods and services, ensures contract compliance and controls the Purchase to Pay process in SAP and connected systems.



    Responsibilities:

    Advice end users and contract owners on Procurement procedures and ensure proper Procurement process is followed
    Spend analysis and ensure contract compliancy with Procurement policy
    Purchase goods, materials, and services to ensure that the company can meet their operational needs, taking into account price, quality, service and delivery levels and to ensure continuity of supply
    Controls and checks purchase requisitions, purchase orders, outline agreements, services/goods confirmations in SAP and tracks full order process
    In collaboration with the Procurement team members and internal stake holders develop and improve Procurement procedures and processes
    Play a key role in ensuring Supplier (and Material) data are correct in the system and take pro-actively action when required.
    Executes periodic reports to the departments and management
    In collaboration with departments conduct research to find the best product and supplier within the company’s budget
    Meet with other departments to ensure problem resolution associated with the Procure to Pay process
    Participate in cross departmental Projects.


    Your profile:

    Bachelor level Purchasing/Supply Chain certification or similar level
    2+ years in a similar Corporate Procurement position
    Experience in spend analysis and contract management is preferred
    Experience in executing Request for Proposals is a plus
    ERP (SAP) working knowledge is a must
    Good working knowledge of Word and Excel
    Proficiency in verbal and written English AND Dutch


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  9. forum rang 8 Janssen&Janssen 6 december 2023 14:51
    Transgenic Platform
    Dierverzorger- Biotechnicus (omgeving Eindhoven) 632

    Ethics & Compliance
    Executive Secretary Full time Leiden 1013

    Finance
    Teamlead BPE Global R2R Full time Leiden 1052

    Finance
    Teamlead and BPE Global Purchase-to-Pay Full time Leiden 1053

    Finance
    Teamlead Global O2C Full time Leiden 1051

    Regulatory Affairs
    Manager, Medical Writing Full time Warren 1046

    Commercial Operations
    Commercial Trade Relations Manager Location GB 1001

    Operations
    Dierverzorger- Biotechnicus (omgeving Oss) 620

    Procurement
    Category Manager Leiden Full time 685

    Manufacturing, Science, Technology
    Office Facility Manager Leiden Full time 1038

    Sales
    Ruconest Account Manager - Pacific Northwest US Full time 1057

    Regulatory Affairs
    Director, Advertising and Promotion Warren Full Time 920

    Human Resources
    Sr. Manufacturing Officer- Solid dosage forms Leiden Full time 1004

    Legal & Compliance
    Corporate Counsel Warren Full Time 1039

    Information Technology
    SAP Application Manager Supply Chain Leiden Full time 1043

    Human Resources
    HR Business Partner Leiden Full time 1002

    Commercial Operations
    Commercial Trade Relations Manager Leiden Full time 940

    Market Access
    Associate Director, Reimbursement and Access - West Warren, Full time 1055

    Ethics & Compliance
    Sr. Director Corporate & Healthcare Compliance Leiden Full time 1023

    Bijgekomen;
    Operations
    Dierverzorger- Biotechnicus (omgeving Oss) 620

    Afgenomen:
    Information Technology
    SAP Application Manager Leiden 1000

    Finance
    ESG Reporting Manager Leiden Full time 1050

    Marketing
    Director of Marketing Warren, Full time 918

    Procurement
    Procurement Officer Leiden Full time 1047

    Continuous Improvement
    Project Manager CoE Full time Leiden 979

    Finance
    Financial Accountant Leiden Full time 901

    Transgenic Platform
    Veterinarian Eindhoven Full time 1009

    Quality Assurance
    QA officer Oss Full time 1003

    Human Resources
    Payroll Specialist Leiden Full time 1040

    Finance
    Financial Reporting Analyst / Specialist Leiden Full time 904

    Aantal openstaand: 20

    Totaal vacatures toe of afname vanaf 29 sept 2020
    Bijgekomen: 296
    Vervuld: 289

    2023
    Bijgekomen: 112
    Afgenomen: 111
  10. forum rang 8 Janssen&Janssen 6 december 2023 14:52
    Operations
    Dierverzorger- Biotechnicus (omgeving Oss) 620

    Our Culture

    We zijn een open organisatie met ambitieuze en gepassioneerde mensen die zich inzetten voor het bedrijf, de collega's en de patiënten die we bedienen. Teamwork, leiderschap en respect is voor ons de basis. Zo komen wij tot goede prestaties en creeëren we een prettige werkomgeving.

    Together to get ther(e)!

    “We hire for attitude and train for skills” is ons simpele mantra, maar één die invloed heeft op de manier waarop wij nieuwe medewerkers selecteren.

    Pharming is een wereldwijd actieve biofarmaceutische onderneming in de commerciële fase die innovatieve eiwitvervangende therapieën en precisiegeneesmiddelen ontwikkelt voor de behandeling van zeldzame ziekten en onvervulde medische behoeften.



    Cultuur:
    Wij zijn een dynamisch bedrijf en onze cultuur wordt gekenmerkt door een prettige sfeer, gericht op samenwerking.
    Het transformeren van de toekomst van onze patiënten en het ontwikkelen van medicijnen voor de behandeling van zeldzame ziekten en onvervulde medische behoeften is altijd onze topprioriteit!
    Deze combinatie is de basis voor een uitdagende omgeving met volop ruimte voor persoonlijke en professionele ontwikkeling.

    Pharming is internationaal gevestigd en groeit snel. Door deze groei zijn wij op zoek naar een Dierverzorger/Animal Caretaker (omgeving Oss).

    Wil je graag een belangrijke rol spelen in het transformeren van de toekomst van onze patienten? Wil je bijdragen aan het ontwikkelen en het op de markt brengen van medicijnen? Heb je een goed oog voor dierenwelzijn?

    Dan is Pharming wellicht interessant voor jou!


    Over de rol:
    Binnen Pharming zoeken wij een proactieve en enthousiaste Dierverzorger- Biotechnicus (omgeving Oss) ter aanvulling van ons team. De dierverzorger/ Biotechnicus voert onder supervisie van de teamleider en coordinating Biotechnician (biotechnische) werkzaamheden uit. Samen met het team ben je verantwoordelijk voor het melken en de juiste verzorging, voeding en observatie van de dieren. Je begeleidt de dieren in de gehele levenscyclus.

    Nieuwsgierig naar hoe een gemiddelde werkdag eruit ziet? Klik hier


    Taken en verantwoordelijkheden:

    Produceren van konijnenmelk
    Registratie/invoer van productie data
    Opfokken van konijnen
    Gezondheidscontroles en dierenwelzijnsbewaking
    Werkzaamheden t.b.v. een hoogwaardige hygiëne
    Uitvoeren van alle voorkomende werkzaamheden rondom productie
    Werkzaamheden uitvoeren volgens werkinstructies en procedures
    Uitvoeren van biotechnische handelingen en laboratorium werkzaamheden

    Functie-eisen:

    Afgeronde MBO-Dieropleiding (minimaal niveau 3)
    Basiskennis van de Nederlandse (en Engelse) taal
    In het bezit van een kwalificatie conform art.12 WOD of Art 13F WOD is een pre maar niet noodzakelijk

    Competenties en vaardigheden:

    Kwaliteitsgericht
    Resultaatgericht
    Een teamplayer die ook goed zelfstandig kan werken
    Effectieve communicatie


    Wat kun je van ons verwachten

    Wij bieden je een vaste aanstelling (te beginnen met een jaarcontract), met een uitstekende verloningsregeling, waaronder:

    Een zeer competitief salaris
    8,33% vakantiegeld
    Minimaal 30 vakantiedagen
    Een uitstekende pensioenregeling
    Reiskostenvergoeding
  11. forum rang 4 Japaho 6 december 2023 15:27
    quote:

    Drieklezoor schreef op 6 december 2023 15:08:

    Dankjewel voor deze publicatie; Er zijn genoeg veeboeren die stoppen .
    Of werven onder personeel van kinderboerderijen
  12. forum rang 4 Drieklezoor 6 december 2023 15:31
    Maar dit is geen kinderachtig gedoe, in het brabantseland. Zou je ook rode konijnen hebben. Een vlaamse reus misschien.
  13. forum rang 8 Janssen&Janssen 1 januari 2024 12:05
    Ethics & Compliance
    Executive Secretary Full time Leiden 1013

    Finance
    Teamlead BPE Global R2R Full time Leiden 1052

    Information Technology
    IT Data Architect Full time Leiden 1102

    Information Technology
    Chief Information Security Officer (CISO) Full time Leiden 1103

    Finance
    Group Accounting & Reporting Specialist Full time Leiden 901

    Operations
    Dierverzorger- Biotechnicus (omgeving Oss) 620

    Pharmacovigilance
    Pharmacovigilance (PV) Associate Full time Warren 1104

    Manufacturing, Science, Technology
    Office Facility Manager Full time Leiden 1038

    Sales
    Ruconest Account Manager - Pacific Northwest US Full time 1057

    Quality Assurance
    Manager Clinical QA Full time Leiden 1099

    Legal & Compliance
    Legal Officer Full time Leiden 1056

    Quality Assurance
    Senior QA Officer Full time Leiden 1098

    Regulatory Affairs
    Director, Advertising and Promotion Full time Warren 920

    Human Resources
    Sr. Manufacturing Officer- Solid dosage forms Full time Leiden 1004

    Information Technology
    SAP Application Manager Supply Chain Leiden Full time 1043

    Finance
    ESG Reporting Manager Leiden Full time 1050

    Human Resources
    Global HRIS Project Manager US (Consultant) Full time Warren 1101

    Human Resources
    HR Business Partner Leiden Full time 1002

    Market Access
    Associate Director, Reimbursement and Access - West Warren, Full time 1055

    Medical Affairs
    Medical Science Liaison Germany - North East Full time DE 1080

    Program Management Office
    Global HRIS Project Manager (consultant) Leiden Full time 1079

    Transgenic Platform
    Dierverzorger- Biotechnicus (omgeving Eindhoven) 632

    Bijgekomen;

    Information Technology
    IT Data Architect Full time Leiden 1102

    Information Technology
    Chief Information Security Officer (CISO) Full time Leiden 1103

    Finance
    Group Accounting & Reporting Specialist Full time Leiden 901

    Pharmacovigilance
    Pharmacovigilance (PV) Associate Full time Warren 1104

    Quality Assurance
    Manager Clinical QA Full time Leiden 1099

    Legal & Compliance
    Legal Officer Full time Leiden 1056

    Quality Assurance
    Senior QA Officer Full time Leiden 1098

    Finance
    ESG Reporting Manager Leiden Full time 1050

    Human Resources
    Global HRIS Project Manager US (Consultant) Full time Warren 1101

    Medical Affairs
    Medical Science Liaison Germany - North East Full time DE 1080

    Program Management Office
    Global HRIS Project Manager (consultant) Leiden Full time 1079

    Afgenomen:

    Finance
    Teamlead and BPE Global Purchase-to-Pay Full time Leiden 1053

    Finance
    Teamlead Global O2C Full time Leiden 1051

    Regulatory Affairs
    Manager, Medical Writing Full time Warren 1046

    Commercial Operations
    Commercial Trade Relations Manager Location GB 1001

    Procurement
    Category Manager Leiden Full time 685

    Legal & Compliance
    Corporate Counsel Warren Full Time 1039

    Commercial Operations
    Commercial Trade Relations Manager Leiden Full time 940

    Ethics & Compliance
    Sr. Director Corporate & Healthcare Compliance Leiden Full time 1023

    Aantal openstaand: 22

    Totaal vacatures toe of afname vanaf 29 sept 2020
    Bijgekomen: 307
    Vervuld: 298

    2023
    Bijgekomen: 123
    Afgenomen: 119
  14. forum rang 8 Janssen&Janssen 1 januari 2024 12:05
    Information Technology
    IT Data Architect Full time Leiden 1102

    Our Culture
    Pharming is committed to our core values: “We Care, We Collaborate, We Walk the Talk”, which is complementary to our focus on self-development of our people, teamwork, leadership and being results orientated. In our growing organization, it is important that employees feel connected and engaged. Our core values enable our mission of bringing the unserved rare disease patients the solutions they need and create a clear pathway forward to meet our strategic goals and objectives.

    Purpose of the role:
    The IT Data Architest designs, implements, and maintains our organization's data architecture. He/she works closely with cross-functional teams to define data requirements, create blueprints, and oversees the development of robust data solutions that align with business objectives.He/she advises management regarding our IT architecture and data policies.



    Responsibilities:

    Data Architecture Design:

    Develop and maintain the organization's data architecture strategy in alignment with business goals.
    Design scalable and efficient data models, ensuring optimal performance and reliability.
    Data Governance and Compliance:

    Establish and enforce data governance policies and procedures. Ensure compliance with industry standards, regulations, and best practices related to data security, privacy, and integrity.
    Data Lifecycle Management:

    Oversee the entire data lifecycle, including data acquisition, storage, transformation, and retrieval.
    Implement strategies for data quality assurance and metadata management.
    Data Classification and Leak Prevention:

    Develop and implement robust data classification policies, ensuring sensitive information is appropriately identified and secured. Design and oversee leak prevention strategies to safeguard data integrity.
    Data Lake / Warehouse:

    Oversee the design, development, and maintenance of our data warehouse infrastructure.
    Optimize data storage and retrieval processes to facilitate efficient analytics and reporting.
    Asset Management in CMDB:

    Lead the management and maintenance of the Configuration Management Database (CMDB), ensuring accurate and up-to-date information on all IT assets.
    Implement best practices for asset tracking and utilization.
    Recovery:

    Design and maintain recovery plans for data systems, ensuring minimal disruption and quick recovery in case of unforeseen events.
    Conduct regular assessments and simulations to test the effectiveness of these plans.
    Collaboration and Communication:

    Collaborate with stakeholders across departments to understand data needs and requirements.
    Communicate complex technical concepts to non-technical stakeholders effectively.
    Technology Evaluation and Implementation:

    Evaluate emerging technologies and tools in the data management space.
    Recommend and implement solutions that enhance data storage, analytics, and visualization capabilities.


    Your profile:

    Bachelor's or Master's degree in Computer Science, Information Technology, or related field
    At least 4-5 years experience as an IT Data Architect or in a similar role
    Experience with cloud-based data solutions and architectures
    Familiarity with data analytics, machine learning, and AI concepts
    In-depth knowledge of data architecture principles, methodologies, and best practices (e.g. ISA-88 and ISA-95)
    Proficiency in data modeling, database design, and optimization
    Strong understanding of data governance frameworks and regulatory requirements (e.g., GDPR, HIPAA)
    Experience with data management technologies, such as databases, ETL tools, and data warehousing solutions
    Excellent analytical, problem-solving, and decision-making skills
    Effective communication and collaboration abilities
    Certifications in relevant areas (e.g., Certified Data Management Professional, AWS Certified Big Data - Specialty)
    Fluency in the English (and ideally Dutch) language, both oral and written


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  15. forum rang 8 Janssen&Janssen 1 januari 2024 12:06
    Information Technology
    Chief Information Security Officer (CISO) Full time Leiden 1103

    Purpose of the role:
    The CISO professionalizes and implements the information security strategy, governance and policies in compliance with applicable laws and standard (ISMS with e.g. NIS2 and ISO 27001). He /she ensures the state of information security is at the desired (NIS2) level and that the behavior of employees is in line with the desired culture in the field of information security.



    Responsibilities:

    Develop and execute Pharming Group’s information security strategy in alignment with business objectives;
    Advice IT management and board w.r.t. information security;
    Initiate and execute our Cyber Security improvement program on organizational awareness, strategy and create and deploy all necessary security policies;
    Manage security operations, risk management, compliance, and incident response (ISO 27001 and NIS2);
    Oversee the implementation of security measures to protect the organization's computer systems and networks;
    Conduct regular security assessments and audits to identify vulnerabilities and recommend solutions;
    Coordinate and lead internal and external security and compliance audits;
    Collaborate with cross-functional teams to integrate security best practices into business processes and projects;
    Stay updated on emerging security threats, industry trends, and best practices to proactively address potential risks;


    Your profile:

    Bachelor's or Master’s degree in Computer Science, Information Technology, or a related field;
    At least 4 years of proven and relevant experience in Cyber Security and Senior IT management role;
    Strong understanding of security protocols, cryptography, authentication, and security standards and regulations (ISO 27001, NIS2, GDPR, SOX, etc.);
    Demonstrated experience in managing security incidents and implementing effective incident response plan;
    Relevant certifications such as CISSP, CISM, or CISA are highly desirable;
    Excellent leadership, communication, and interpersonal skills;
    Must be Fluent in the English (and ideally Dutch) language, both oral and written.




    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  16. forum rang 8 Janssen&Janssen 1 januari 2024 12:06
    Finance
    Group Accounting & Reporting Specialist Full time Leiden 901

    Purpose of the role:

    The Group Accounting & Reporting Specialist improves and maintains the financial consolidation, the global transfer pricing system, the periodic reporting to governmental agencies, and advises the internal organization on complex technical (IFRS) accounting and reporting. You will have exposure to lots of complex technical matters, including convertible bonds, Share Based Compensation, and the valuation of new commercial product across the global. You will partner with Financial Administration, Business Control and external Auditors and Advisors, and support HR and Manager Finance related to SBC.



    Responsibilities:

    Periodic consolidating the financial reports of Pharming Group N.V. and its subsidiaries.
    Preparation of periodic reporting to governmental bodies.
    Maintenance of transfer pricing system including yearly updates of master and local transfer pricing reports.
    Contribute to the preparation of the Annual Report, IFRS Financial Statements and other related matters such as press releases.
    Contribute to the preparation of position papers for accounting matters and valuation.
    Internal subject matter expert on IFRS
    Participates in projects, including Convertible Bonds, SBC, Commercial valuations, and SOX.


    Your profile

    At least 7-8+ years of proven experience in technical (IFRS) Financial Accounting and Reporting;
    In a stock-listed, international corporate environment;
    Ideally working experience with a Big Four Audit Firm;
    Master degree, preferably in Auditing, Accounting or in a comparable study. Ideally in combination with professional qualification (RA, CPA, ACCA or similar)
    Deep familiarity with consolidation, with eye for detail and first-time right mentality
    Fluent in English, both oral and written
    Strong knowledge of IFRS
    Strong data analysis skills
    Familiar with Sox and the administrative documentation of the work performed.


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  17. forum rang 8 Janssen&Janssen 1 januari 2024 12:07
    Pharmacovigilance
    Pharmacovigilance (PV) Associate Full time Warren 1104

    Our Culture



    Pharming is committed to our core values: “We Care, We Collaborate, We Walk the Talk”, which is complementary to our focus on self-development of our people, teamwork, leadership and being results orientated. In our growing organization, it is important that employees feel connected and engaged. Our core values enable our mission of bringing the unserved rare disease patients the solutions they need and create a clear pathway forward to meet our strategic goals and objectives.





    Overview



    Pharming is seeking to hire a Pharmacovigilance (PV) Associate to bring case processing of all (S)AE reports for Pharming product(s) in the ARGUS safety database including conduction of all follow-up queries, requests, and working with PV colleagues on assigned tasks. Our goal is for the PV Associate to work collaboratively among our Pharmacovigilance Department. Successful execution will involve a willingness to adjust to multiple demands and shifting priorities with confidence and professionalism. The position reports to our Senior PV Manager and will not have any direct reports.







    Key Responsibilities



    The Pharmacovigilance (PV) Associate will be responsible for a wide variety of matters in support of Pharming’s growth as we increase the number of both pipeline and marketed products.



    Core functions include:



    Review, triage, verify, book-in, and data enter reported (S)AEs associated with the use of Pharming’s product(s) both in development and authorized as per the compliance requirements of the competent authorities.
    Perform case assessment including determining case validity and seriousness.
    Determine and perform appropriate case follow-up activities including generation of follow-up requests via fax, phone, mail, or e-mail and product complaint notifications to consumers, HCPs, Specialty Pharmacies and/or vendors.
    Coordinate and schedule trainings for internal and external stakeholders as per PV managers’ requests.
    Collaborate with the PV team and ensure all assigned tasks (e.g., training) are completed within defined timelines.
    Other PV tasks as assigned or requested by the US PV Team and/or VP Pharmacovigilance.
    This is a hybrid role; 2 to 3 days at the US HQ in Warren, NJ.






    Minimum Qualifications:



    Bachelor of Science Degree in the life sciences, pharmacy, nursing or equivalent.
    Minimum of 1+ years of industry experience in pharmacovigilance and drug safety.






    Preferred Qualifications:



    Extensive knowledge of pharmacovigilance especially case processing including MedDRA coding.
    Extensive knowledge of the ARGUS safety database.
    In depth understanding of good pharmacovigilance practices and current drug safety regulations.
    Good knowledge of GCP/ICH guidelines.
    Computer proficiency.




    Compensation & Benefits:



    Flexible hybrid work schedule to promote a health work-life balance.
    Competitive compensation package including annual target bonus.
    Long-Term Incentive Program
    401(k) plan with company match
    Paid-Time Off Days
    16 Company Holidays per year (typically last week of December up until New Year’s Day)










    Other Benefits:



    Excellent Healthcare Plans including Medical, Dental and Vision.
    Flexible Spending Accounts for Medical and Dependent Care.
    Company-provided Life Insurance, Short-Term and Long-Term Disability Plans.
    Accident, Hospital Indemnity and Critical Illness Plans.
    Pet Insurance Plan.
    On Premise Fitness Center.
    Health & Wellness Program.
    Choice of Mobile Phone for Work Use or Cell Phone Stipend.
    Pharming Academy – Continuing Learning & Development Program.








    Additional Information



    Pharming is committed as an Equal Opportunity and Affirmative Action employer for all employees and qualified applicants without regard to race, color, sex, gender identity or expression, genetic information, sexual orientation, marital status, race, religion, color, national origin, disability, protected Veteran status, age, or any other characteristic protected under applicable law.



    An applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request via email to HR-US@pharming.com.



    Unsolicited resumes from agencies should not be forwarded to Pharming. Pharming will not be responsible for any fees arising from the use of resumes through this source. Pharming will only pay a fee to agencies if a formal agreement between Pharming and the agency has been established. The Human Resources/Talent Acquisition department is responsible for all recruitment activities; please contact us directly to be considered for a formal agreement.



    Please note that we review every submission, and we will keep submissions on file for six months.
  18. forum rang 8 Janssen&Janssen 1 januari 2024 12:08
    Quality Assurance
    Manager Clinical QA Full time Leiden 1099

    About Pharming
    Pharming Group N.V. (Nasdaq: PHAR/Euronext Amsterdam: PHARM) is a global biopharmaceutical company dedicated to transforming the lives of patients with rare, debilitating, and life-threatening diseases. Pharming is commercializing and developing an innovative portfolio of protein replacement therapies and precision medicines, including small molecules, biologics, and gene therapies that are in early to late-stage development. Pharming is headquartered in Leiden, Netherlands, and has employees around the globe who serve patients in over 30 markets in North America, Europe, the Middle East, Africa, and Asia Pacific.

    Our Culture
    Pharming is committed to our core values: “We Care, We Collaborate, We Walk the Talk”, which is complementary to our focus on self-development of our people, teamwork, leadership and being results orientated. In our growing organization, it is important that employees feel connected and engaged. Our core values enable our mission of bringing the unserved rare disease patients the solutions they need and create a clear pathway forward to meet our strategic goals and objectives.



    Purpose of the role
    The Manager of Clinical QA leads and supervises the Clinical QA team, being accountable for GCP and GVP oversight, inspection readiness, and ensuring the compliance of studies with Pharming SOPs and all applicable worldwide regulations and guidelines (e.g., FDA, EU, ICH, and national regulations).


    Areas of responsibility

    To lead and supervise a team, ensure that each team member is trained and qualified for their tasks
    Build and foster a team environment where employees know what is expected of them, can work well together and can flourish and further develop themselves. Share the workload in the team, ensuring that all feel noticed, heard and have a reasonable challenging workload. Ensure that due dates and KPI’s are met.
    Review all clinical and Pharmacovigilance QMS documents and ensure they comply with the relevant guidelines.
    Collaborate with and seek alignment with other departments (e.g. clinical, medical, PHV.) to ensure compliancy with GXP guidelines
    Ensure continuous inspection readiness (GCP and GVP) internally and for the clinical trials
    Identify risks, identify and communicate areas for improvement, provide subject matter expert reports as required. Identify documents which need to be created or updated and ensure this is organized.
    Resolve problems and conducts investigations associated with deviations, complaints, non-conformances, Change Controls, CAPA, Risk Assessments, protocols and reports in collaboration with other Pharming departments
    Act as trainer, coach and expert for Quality Assurance Officers and other departments, and ensure that everyone has suitable GCP/GVP training.
    Perform internal and external audits to determine compliance with GCP, GLP and GVP, communicates the results to relevant stakeholders and ensure that corrective and preventative actions are taken to close CQA observations.
    Perform e-TMF audits
    Participate in company projects as CQA subject matter expert
    Assess effects of changes to regulations and guidelines covering clinical trial activities and ensure timely implementation of these changes.
    Represent CQA as a single point of contact and provides CQA guidance


    Knowledge:

    MSc Biotechnology, chemistry, biopharmaceutics or equivalent field, or BSc Biotechnology, chemistry, biopharmaceutics or equivalent field

    Experience:

    Min. 8 years of experience in (bio)pharmaceutical environment
    Min. 6 year of experience in Quality Assurance
    Preferably 1-year managerial experience


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.
  19. forum rang 8 Janssen&Janssen 1 januari 2024 12:08
    Legal & Compliance
    Legal Officer Full time Leiden 1056

    Our Culture
    Pharming is committed to our core values: “We Care, We Collaborate, We Walk the Talk”, which is complementary to our focus on self-development of our people, teamwork, leadership and being results orientated. In our growing organization, it is important that employees feel connected and engaged. Our core values enable our mission of bringing the unserved rare disease patients the solutions they need and create a clear pathway forward to meet our strategic goals and objectives.

    Purpose of the role:
    As a Legal Officer at Pharming, you play a crucial role in advising on the general business operations of the company and its various entities, anticipating and guarding against legal risks. Your responsibilities include preparing, executing, reviewing, compiling, and filing all business contracts and other legal documentation.

    Areas of responsibility

    Provide general legal advice to different internal stakeholders on a variety of legal issues.
    Draft, review, track and monitor the status of agreements and contracts.
    Participate in projects from a legal perspective.
    Independently and in collaboration with outside legal professionals design and draft documents supporting the company’s entities, obtain the required approvals and handle the execution and subsequent notarization, apostil and or legalization of such documents.
    Keep the company updated on legislative and regulatory changes that may affect the company and its entities.
    Interface with outside legal counsel on matters related to contracts, litigation or specific legal topics.


    Knowledge

    Master of Laws (LL.M.) and Bachelor of Laws (LL.B.) degree from a European University.
    Excellent knowledge of (inter)national contracting law.
    Excellent communication skills in English

    Experience:

    Minimum three years of relevant experience
    Experience within a listed company is a plus
    Experience in the pharmaceutical industry is a plus


    What you'll get in return
    We offer you a permanent position (starting with a one-year contract), with an excellent remuneration scheme, including:

    A highly competitive salary
    8.33% holiday allowance (for NL)
    A minimum of 30 vacation days
    An excellent pension plan
    Commuting allowance

    You will also join our Learning & Development program, which can offer a tailor made development plan, based on your personal and professional needs. Learning opportunities are everywhere, in all forms imaginable and we want to create learning memories for all “Pharmers”.

    Also important! We truly value a healthy life-work balance with a lot of flexibility.

    Apply for the job
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