Job Description Summary
Imagine being the go-to expert who helps bring life-changing medicines to patients without interruption. As a Senior Specialist, Manufacturing Technical Support, you will play a critical role at the heart of our manufacturing operations, partnering closely with production teams to ensure every batch is delivered safely, efficiently, and in full compliance with quality standards. This is an opportunity to apply your technical expertise, drive continuous process improvements, solve complex manufacturing challenges, and influence the performance of innovative biopharmaceutical products in a highly regulated environment. Your work will directly contribute to operational excellence and our mission to reimagine medicine for patients around the world.
Job Description
Location:
- This position will be located in Durham, NC and will be an onsite role.
- Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.
Key Responsibilities:
- Provide frontline technical support to manufacturing teams to ensure safe, compliant, and on-time batch execution.
- Serve as the SME for assigned products and processes, driving technical excellence and process knowledge.
- Review and maintain master manufacturing documents, including MBRs, BOMs, and manufacturing recipes.
- Monitor critical process parameters and ensure compliance with approved manufacturing instructions and quality requirements.
- Lead and support manufacturing investigations, root cause analyses, and timely CAPA implementation.
- Assess technical changes and ensure execution through established change control procedures.
- Develop, review, and continuously improve manufacturing SOPs and electronic batch records.
- Support ongoing process verification through data analysis, product performance monitoring, and CAPA effectiveness tracking.
- Perform technical assessments and resolution of process-related issues, including deviations, complaints, OOS, and OOE events.
- Lead or support process validations, technology transfers, new technology implementation, and continuous improvement initiatives while maintaining GMP inspection readiness.
Essential Requirements:
- Bachelor's degree in Engineering or Life Sciences with 7+ years of experience in biopharmaceutical GMP manufacturing operations.
- Demonstrated experience developing, revising, and maintaining manufacturing documentation in a regulated environment.
- Proven experience investigating complex manufacturing deviations and driving timely CAPA implementation.
- Strong knowledge of FDA regulations, GMP requirements, and quality management systems.
- Experience providing technical process support within a pharmaceutical or biotechnology manufacturing facility.
- Working knowledge of Quality by Design (QbD) principles, Six Sigma methodologies, and operational excellence tools.
- Excellent written and verbal communication skills with strong technical writing capabilities.
- Ability to travel up to 20% to support activities at internal sites, vendor locations, and CMOs.
Novartis Compensation and Benefit Summary:
The salary for this position is expected to range between $108,500 and $201,500 annually
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.
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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 [email protected] 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
$108,500.00 - $201,500.00
Skills Desired
Data AnalyticsSkills Required
- Bachelor's degree in Engineering or Life Sciences with 7+ years of experience in biopharmaceutical GMP manufacturing operations
- Experience developing, revising, and maintaining manufacturing documentation in a regulated environment
- Proven experience investigating complex manufacturing deviations and driving timely CAPA implementation
- Strong knowledge of FDA regulations, GMP requirements, and quality management systems
- Experience providing technical process support within a pharmaceutical or biotechnology manufacturing facility
- Working knowledge of Quality by Design (QbD), Six Sigma methodologies, and operational excellence tools
- Excellent written and verbal communication skills with strong technical writing capabilities
- Ability to travel up to 20% to support activities at internal sites, vendor locations, and CMOs
- Onsite role in Durham, NC (Novartis unable to offer relocation support)
Novartis Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Novartis and has not been reviewed or approved by Novartis.
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Healthcare Strength — Pay and benefits are described as a strong overall package, supported by medical, dental, and vision insurance alongside FSAs/HSAs and disability and life coverage. Mental-health support is reinforced through an employee assistance program with psychological support and a network of mental health first aiders.
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Retirement Support — Retirement support is positioned as a standout element, with an automatic company contribution plus dollar-for-dollar matching in the 401(k). Additional retirement funding is described through an age-based defined contribution program and access to an employee share purchase plan discount.
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Parental & Family Support — Family-related benefits are framed as robust, including a global minimum of paid parental leave for new parents following birth or adoption. Added supports include domestic partner coverage, dependent-care resources, and benefits such as adoption assistance and child/elder care options.
Novartis Insights
What We Do
Novartis is an innovative medicines company. Every day, working to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide.
