Supervisor, Quality Assurance

Catalent


Job Location:

Madison, OH - USA

Monthly Salary: Not Disclosed
Posted on: 5 days ago
Vacancies: 1 Vacancy

Job Summary

Supervisor Quality Assurance

Position Summary:

  • Work Schedule: 2nd shift Monday-Friday afternoons
  • 100% on-site

Catalent Madison is a pharmaceutical manufacturing site specializing in the development and production of high-quality drug products with a strong focus on biologics and sterile injectables. The site supports global clients by delivering compliant reliable and scalable manufacturing solutions.

The Quality Assurance Supervisor at Catalent Madison is responsible for ensuring full compliance with FDA regulations and internal quality systems to support the delivery of high-quality drug products. This position leads team performance oversees daily QA operations and drives continuous improvement across quality systems including deviations CAPAs document control materials management and training. The Quality Assurance Supervisor partners closely with cross-functional stakeholders to maintain efficient processes support manufacturing operations and ensure audit and inspection readiness. Additionally it is accountable for developing talent managing performance and reinforcing a compliant and high-performing quality culture.

The Role:

  • Lead coach and develop team members to strengthen performance and support career growth
  • Set clear goals monitor progress and address performance issues with timely feedback
  • Oversee daily QA operations to ensure quality standards and project timelines are met
  • Partner with stakeholders to maintain efficient processes and ensure compliant quality practices
  • Support and execute Quality Management Systems within CGMP manufacturing and QC environments
  • Track KPIs report performance and implement action plans to close gaps and meet objectives
  • Author review and approve procedures protocols deviations and investigation records
  • Drive continuous improvement initiatives across systems processes training and regulatory readiness
  • Manage document control processes ensuring integrity compliance and system enhancements
  • Oversee materials quality and training programs including compliance onboarding system management and cross-functional support
  • Other duties as assigned

The Candidate:

  • Doctorate Degree in STEM discipline with minimum of 2 years related experience
  • Masters Bachelors or Associates Degree in STEM discipline with minimum of 4 years related experience
  • Leadership experience 0-2 years
  • Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL GOLD LEAD Now GM Excellence and GROW) may be considered in place of external experience

Why you should join Catalent:

  • Potential for career growth on an expanding team
  • Abundance of cross-functional exposure to other areas within the organization
  • Opportunity to work globally
  • 152 hours of paid time off annually 8 paid holidays
  • Day one benefits! Medical dental vision and 401K benefits effective on your first day

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability you may submit your request by sending an email and confirming your request for an accommodation and include the job number title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment bank details photocopies of identification social security number or other highly sensitive personal information during the offer process and we NEVER do so via email or social media. If you receive any such request DO NOT respond it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


Required Experience:

Manager

Supervisor Quality AssurancePosition Summary:Work Schedule: 2nd shift Monday-Friday afternoons100% on-siteCatalent Madison is a pharmaceutical manufacturing site specializing in the development and production of high-quality drug products with a strong focus on biologics and sterile injectables. The...

About Company

Company Logo

Providing CDMO services, delivery technologies and manufacturing solutions to develop pharmaceuticals, biologics and consumer health products.

View Profile View Profile