Demo

Specialist, Quality Control - Raw Materials

U473 (FCRS = US473) Novartis Gene Therapies
Durham, NC Full Time
POSTED ON 4/2/2026
AVAILABLE BEFORE 5/31/2026
Job Description Summary The Specialist, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring conformance to established quality processes and standards for manufacturing and production. Job Description Location: This position will be located in Durham, NC and will be an On-Site role. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Key Responsibilities: Execute routine and non-routine analysis for cGMP release and characterization testing using techniques including but not limited to chromatography (HPLC, UPLC), AUC, SEC, compendial assays (pH, Conductivity, Osmolality), electrophoresis (CE, Western Blot) and assist with data review. Execute method verifications/transfers as required for various projects. Assist with enrollment of vendors, ordering reagents and consumables for new assays. Initiate all paperwork (LIMS, SOPs, assay forms) for testing and transfers of methods for projects. Assists in the evaluation of internal controls, communications, risk assessments and maintenance of documentation as related to compliance with internal and external safety, quality, and regulatory standards. Reviews data obtained for compliance with specifications and reports abnormalities. Performs trend analysis of methods /environmental data / assay controls & standards and draws conclusions. Capable of delivering to assigned work schedule with attention to detail and accuracy. Support department risk assessments and participate in audit walkthroughs. Participates in the preparation of investigations, summaries and reports. Reviews data obtained for compliance with specifications and reports. Investigates and resolves non-conforming test results by completing thorough Deviation, OOS/OOT/OOE and Investigation. Authors new/revise Standard Operating Procedures, Protocols / Summary Reports / Analytical Master Plans for QC. Oversee special projects on analytical and instrument problem solving. May develop testing and analysis methods and procedures in accordance with established guidelines. Supports training of departmental personnel in appropriate techniques and related topics. Other related job duties as assigned. Essential Requirements: Bachelor's degree in scientific disciplines such as Biochemistry, Biology, Microbiology or related field with 5 years’ experience in GMP environment or 4 years’ at GTx. Excellent interpersonal, verbal and written communication skills with strong technical writing experience required. Previous investigation experience a plus. Proven ability to work effectively in a team environment. Collaborates cross functionally with other departments to achieve site goals. Works on problems of moderate scope where analysis of situations or data requires a review of a variety of factors.  Exercises judgment within defined procedures and practices to determine appropriate action including critical thinking, troubleshooting and problem-solving skills. Normally receives general instructions on routine work, detailed instructions on new projects or assignments. Self-motivated, detail-oriented, and willing to accept temporary responsibilities outside of core duties. Novartis Compensation and Benefit Summary: The salary for this position is expected to range between $41.06 and $76.25 per 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. #LI-Onsite 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 $85,400.00 - $158,600.00 Skills Desired Business Partnering, Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge, Risk Management, Stakeholder Management 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. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. 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 .

Salary : $85,400 - $158,600

If your compensation planning software is too rigid to deploy winning incentive strategies, it’s time to find an adaptable solution. Compensation Planning
Enhance your organization's compensation strategy with salary data sets that HR and team managers can use to pay your staff right. Surveys & Data Sets

What is the career path for a Specialist, Quality Control - Raw Materials?

Sign up to receive alerts about other jobs on the Specialist, Quality Control - Raw Materials career path by checking the boxes next to the positions that interest you.
Income Estimation: 
$72,210 - $96,012
Income Estimation: 
$91,665 - $118,322
Income Estimation: 
$103,208 - $149,238
Income Estimation: 
$90,652 - $121,490
Income Estimation: 
$90,652 - $121,490
Income Estimation: 
$91,665 - $118,322
Income Estimation: 
$103,208 - $149,238
Income Estimation: 
$116,025 - $158,364
Employees: Get a Salary Increase
View Core, Job Family, and Industry Job Skills and Competency Data for more than 15,000 Job Titles Skills Library

Not the job you're looking for? Here are some other Specialist, Quality Control - Raw Materials jobs in the Durham, NC area that may be a better fit.

  • U473 (FCRS = US473) Novartis Gene Therapies Durham, NC
  • Job Description Summary The Analyst, Quality Control, assists and supports the organization with compliance and ongoing preparation, testing and monitoring... more
  • 19 Days Ago

  • OXB Durham, NC
  • Location: Durham, NC, US Company: oxfordbiom Join Us in Changing Lives Location: on-site role, Durham, NC At OXB , our people are at the heart of everythin... more
  • 3 Days Ago

AI Assistant is available now!

Feel free to start your new journey!