Job Description Summary

What if your leadership could directly impact the delivery of life-changing therapies to patients worldwide? As a Supervisor, Manufacturing, you will lead frontline operations in a dynamic GMP environment, driving performance, quality, and continuous improvement. You’ll empower a team, ensure operational excellence, and play a critical role in producing high-quality clinical and commercial products safely and efficiently.

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.

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

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

 

Salary Range

$85,400.00 - $158,600.00

 

Skills Desired

Data Analytics