Job Description
**Lead Specialist, Client QA**
**Position Summary:**
+ **Work Schedule: Monday – Friday, 8am – 5pm.**
+ **100% on-site**
Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD—just minutes from BWI Airport—features EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products.
The Lead Specialist, QA is responsible for providing QA lead support and oversight of Client Projects from start to finish for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product. You’ll play a key role in ensuring the quality and compliance of cutting-edge gene therapy products. Acting as the dedicated Cl...
**Position Summary:**
+ **Work Schedule: Monday – Friday, 8am – 5pm.**
+ **100% on-site**
Catalent is a leading global CDMO partnering with pharma and biotech innovators to accelerate development and delivery of life-changing therapies. Our FDA-licensed, state-of-the-art CGMP gene therapy campus in Harmans, MD—just minutes from BWI Airport—features EMA and FDA-approved manufacturing suites, fill/finish capabilities, labs, and warehousing to support Phase 3 through commercial production of advanced therapies, including AAV and other viral vector-based products.
The Lead Specialist, QA is responsible for providing QA lead support and oversight of Client Projects from start to finish for GMP Manufacturing of master/working cell banks, biological bulk drug substance and finished drug product. You’ll play a key role in ensuring the quality and compliance of cutting-edge gene therapy products. Acting as the dedicated Cl...
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