Manufacturing Quality Assurance Specialist

Novartis

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profile Job Location:

Durham, NC - USA

profile Monthly Salary: $ 81200 - 150800
Posted on: 5 hours ago
Vacancies: 1 Vacancy

Job Summary

Job Description Summary

Help ensure every dose we produce reaches patients safely. As our onsite Manufacturing Quality Assurance Specialist in Durham youll be the quality partner from material release through aseptic filling and final product releaseproviding shop floor oversight reviewing batch records and alarms guiding investigations and corrective and preventive actions and championing data driven continuous improvement. Youll 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

  • Bachelors degree preferably in microbiology chemistry or biochemistry with 5 years experience in health authority GMP regulated industry or Associates 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 CFRs and cGMPs 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 productrelated 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 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 or call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$81200.00 - $150800.00


Skills Desired

Continued Learning Dealing With Ambiguity Gmp Procedures Qa (Quality Assurance) Quality Control (Qc) Testing Quality Standards Self-Awareness Technological Expertise Technological Intelligence

Required Experience:

IC

Job Description SummaryHelp ensure every dose we produce reaches patients safely. As our onsite Manufacturing Quality Assurance Specialist in Durham youll be the quality partner from material release through aseptic filling and final product releaseproviding shop floor oversight reviewing batch reco...
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About Company

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Novartis is a global healthcare company based in Switzerland that provides solutions to the evolving needs of patients worldwide.

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