Manufacturing Quality Assurance Specialist at Novartis

Durham, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

08 Mar, 26

Salary

72.5

Posted On

08 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Gmp Procedures, Quality Assurance, Quality Control Testing, Quality Standards, Technical Writing, Data Synthesis, Regulatory Compliance, Continuous Improvement, Problem Solving, Collaboration, Deviation Management, Training, Investigation, Documentation, Communication, Project Management

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary Help ensure every dose we produce reaches patients safely. As our onsite Manufacturing Quality Assurance Specialist in Durham, you’ll be the quality partner from material release through aseptic filling and final product release—providing shop floor oversight, reviewing batch records and alarms, guiding investigations and corrective and preventive actions, and championing data driven continuous improvement. You’ll collaborate across Production, Quality, and Technical Operations to uphold current Good Manufacturing Practice standards, support health authority and internal inspections, and turn complex regulations into clear, confident decisions. If you love solving problems at the source and empowering teams to deliver consistently, this role lets you make a measurable impact on therapies that can change lives. #LI-Onsite Location: Durham, NC Multiple positions available. Various shifts available. Relocation Support: This role is based in Durham, NC. Novartis is unable to offer relocation support: please only apply if accessible. Job Description Key Responsibilities Provide quality oversight for all manufacturing processes from material release to final product release. Conduct area walkthroughs, shop floor support, and batch record reviews to ensure compliance. Review and approve master and issued batch records, SOPs, and specifications for clinical and commercial manufacturing. Collaborate with manufacturing and quality teams to maintain cGMP standards and regulatory adherence. Lead projects to address quality gaps and drive continuous improvement in Operations or Quality Systems. Manage deviations and CAPA, ensuring thorough documentation and investigation of all incidents. Support internal, board of health, and self-inspections, providing guidance and training to team members. Essential Requirements Bachelor’s degree preferably in microbiology, chemistry, or biochemistry with 5 years’ experience in health authority GMP regulated industry or Associate’s degree with 7 years’ experience health authority GMP regulated industry; preferably in pharma/biotech/med device. Experience with viral gene therapies and/or orphan disease indications is a plus. Knowledge and application of the CFR’s and cGMP’s and have been involved in regulatory inspections. Knowledge of FDA and EU regulations and experience in US and international regulatory agency inspections. Direct experience reviewing and/or authoring standard operating procedures and partnering with operations on product‑related investigations and deviations. Excellent oral and written communication skills with strong technical writing experience. Ability to synthesize data and summarize outcomes to provide recommendations on compliant path forward. Novartis Compensation and Benefit Summary: The salary for this position is expected to range between $39.03 and $72.50/hour. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range $81,200.00 - $150,800.00 Skills Desired Continued Learning, Dealing With Ambiguity, Gmp Procedures, Qa (Quality Assurance), Quality Control (Qc) Testing, Quality Standards, Self-Awareness, Technological Expertise, Technological Intelligence Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

Provide quality oversight for all manufacturing processes from material release to final product release. Collaborate with manufacturing and quality teams to maintain cGMP standards and regulatory adherence.