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Supervisor, Manufacturing

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: Novartis Farmacéutica
Full Time position
Listed on 2026-07-18
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Pharmaceutical Manufacturing, Production Manager, Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 41 - 76 USD Hourly USD 41.00 76.00 HOUR
Job Description & How to Apply Below

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.

Shift

This position follows a 2‑2‑3 night shift schedule, with working hours from 5:45 PM to 6:15 AM.

Key Responsibilities
  • Lead shift manufacturing operations to meet production targets aligned with site strategy and quality standards.
  • Assign tasks and coordinate team activities to ensure efficient and compliant operations each shift.
  • Act as primary contact during shift for troubleshooting and emergency response coordination.
  • Lead and document investigations, including deviations, non‑conformances, and corrective and preventive actions.
  • Partner with Quality to resolve issues compliantly and drive timely closure of investigations.
  • Ensure batch records and standard operating procedures are accurate, complete, and up to date.
  • Maintain safe, environmentally responsible, and compliant manufacturing processes at all times.
  • Monitor operations and identify continuous improvement opportunities to enhance performance and efficiency.
  • Communicate shift performance and key updates clearly through end‑of‑shift summaries.
  • Mentor, coach, and develop team members, managing performance, goals, and employee relations.
Essential Requirements
  • One of the following experience pathways is required:
    • Bachelor of Science degree with at least five years of biopharmaceutical GMP manufacturing experience.
    • Bachelor of Science degree with three years of experience manufacturing Novartis Gene Therapies products.
    • Seven years of experience in biologics, pharmaceutical, or vaccine manufacturing within a GMP environment.
  • Hands‑on experience in cell culture, recovery, purification, and aseptic fill‑finish operations.
  • Solid knowledge of FDA regulations and GMP systems.
  • Demonstrated leadership skills with ability to manage, mentor, and motivate teams.
  • Strong written and verbal communication skills, including technical writing.
  • Ability to meet physical requirements, including lifting over thirty‑five pounds and approximately ten percent travel.
Compensation and Benefits

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 such as relevant skills and experience and will be reviewed periodically. Your compensation will include a performance‑based cash incentive and may be eligible 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. Employees are also eligible for a generous time‑off package including vacation, personal days, holidays and other leaves.

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