If you are a current Jazz employee please apply via the Internal Career site.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life‑changing medicines for people with serious diseases — often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient‑focused and science‑driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.
The Biologics Drug Substance Senior Quality Assurance Specialist is responsible for performing key quality tasks in respect of Company Biologics products. This role is within the External Manufacturing Quality Group in the Technical Operations department, which oversees contract manufacturing operations and internal quality systems. The position reports directly to the Drug Substance Lead, External Manufacturing QA.
Essential Functions/Responsibilities
- Monitoring the daily operations at the Contract Manufacturer, performing batch review and disposition, reviewing and approving product complaints, deviations, validation protocols, change controls and leading product‑related investigations.
- CMO batch file and product testing record review and approval. Associated lot disposition activity.
- Ensuring compliance of all respective contract manufacturers to both internal Jazz requirements and country‑specific regulations.
- Collaboration with all contract manufacturers, packagers and testing laboratories to resolve any quality issues.
- Contributing to the successful outcome of all regulatory inspections associated with company business, both internally and at contract manufacturers, as required.
- Highlighting any risks associated with maintaining supply of commercial drug products to all markets.
- Conducting vendor audits and vendor site visits as required.
- Assisting in internal audits and regulatory agency inspections.
- Summarizing CMO annual product quality reviews and supporting regulatory submissions.
- Assisting with the generation of Jazz APQR (annual product quality review).
- Maintaining product‑related quality technical agreements (QTAs).
- Understanding new regulations and guidelines, as they apply to the company business and implementing systems and procedures to incorporate these new regulations as appropriate.
- Reviewing and approving moderate‑complexity deviations and associated corrective actions.
- Supporting the generation of new, as well as improvement of, existing department SOPs.
- Supporting delivery of projects.
- Working with management to resolve project issues and resource constraints within the team.
- Liaising with internal and external stakeholders to resolve and clarify any point of issue.
- Reviewing and approving less complex validation documents.
- Partnering with other departments/groups to problem‑solve and address moderately complex issues.
- Collaborating in the continuous improvement of the QA processes, identifying opportunities and leading them up to the implementation.
- Representing QA in cross‑functional project teams for moderately difficult projects.
- Participating in and facilitating regulatory inspection readiness.
- Coordinating and collaborating with other teams to meet organizational goals and work requirements.
- Receiving assignments in the form of objectives and determining how to use resources to meet schedules and goals.
- Following processes and operational policies in selecting methods and techniques for obtaining solutions; solving moderately complex problems and can identify viable and often innovative options.
- Using analytical skills and judgment to recommend best solution.
- Demonstrating success using compliance knowledge, creativity, and regulatory perspectives to solve problems, especially those associated with major and critical deviations.
- Maintaining quality from cell banking through to production and post‑release events (e.g., stability, product complaints).
Required Knowledge, Skills, And Abilities
- Strong knowledge of GMP and regulatory compliance as applicable to the pharmaceutical/biotechnology industry.
- Ability to understand and apply GMP regulations as they relate to manufacturing, QC analytical testing, and facility operations, with deep knowledge of biologics manufacturing.
- Substantial experience working in or directly supporting manufacturing within a biologics drug‑substance manufacturing site.
- Experience with contract manufacturing is desirable.
- Significant experience (>5 years) of commercial and/or late‑state clinical‑phase GMP manufacturing of biologics.
- Highly organized, with exceptional time management and prioritization.
- Excellent verbal and written communication skills.
- Experience in drug product manufacture in addition to drug substance an advantage.
- QP eligibility or progress toward QP certification is highly desirable.
Required/Preferred Education And Licenses
- Bachelor’s degree in pharmacy, chemistry, biotechnology, biochemistry, microbiology or a related discipline.
Jazz Pharmaceuticals is an equal‑opportunity/affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any characteristic protected by law.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, retirement savings plan, and flexible paid vacation. For more information on our benefits offerings please visit https://careers.jazzpharma.com/benefits.html.
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