What are the responsibilities and job description for the Quality Assurance Supervisor position at Catalent?
QA Supervisor
Position Summary
The Quality Assurance department is responsible for ensuring compliance with quality system and product quality requirements defined by international regulations and corporate, network, and local standard operating procedures. The Quality Operations department supports this by providing oversight and guidance on matters affecting the quality system or product quality in daily operations.
The Role
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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.
Position Summary
- Work schedule: M-F 8am-5pm
- 100% based on-site in Philadelphia, PA
The Quality Assurance department is responsible for ensuring compliance with quality system and product quality requirements defined by international regulations and corporate, network, and local standard operating procedures. The Quality Operations department supports this by providing oversight and guidance on matters affecting the quality system or product quality in daily operations.
The Role
- Responsible for all QA activities related to incoming, distribution and destruction and process auditing
- Assist In ensuring the quality and identity of pharmaceutical products during all aspects of the incoming, distribution, or packaging processes
- Act as the Quality partner to support the Supply Chain and Operations department
- Enforce Catalent policy and regulatory requirements
- Act as site subject matter expert for "Good Manufacturing Practices" and "Good Distribution Practices"
- Work to schedule a daily resource plan to support Supply Chain/Operations activities
- Act as lead investigator for all compliance issues regarding incoming, distribution, returns, destruction, or packaging/production
- Develop process excellence and efficiencies prior to the beginning of a project
- Track and report metrics and identify trends and predictive models
- All other duties as assigned
- HS Diploma/GED and 5 years of Production QA experience required.
- College degree preferred (BA, BS)
- Proven track record of monitoring/auditing quality and identifying potential efficiencies in a production environment.
- Previous supervisory experience of 5 years or more preferred.
- Experience in a regulated field – pharma, food, automotive, etc.
- Experience working on continuous improvement activities in partnership with other functions (e.g. Production, Validation, etc.)
- Good Computer Skills. Knowledge of MS Office and Inventory Management system are a plus.
- Basic knowledge of Lean Six Sigma methodologies an advantage
- Good knowledge of the application of FDA cGMP’s.
- Ability to be on feet and move easily throughout the Operations facilities.
- Ability to quickly learn and implement QA Auditing techniques.
- Knowledge reading engineering drawings/material specifications, a plus.
- Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.
- Be accessible to production floor, supply chain and office staff and to use required office equipment.
- Specific vision requirements include reading of written documents and use of computer monitor screen frequently.
- Defined career path and annual performance review and feedback process
- Diverse, inclusive culture
- Positive working environment focusing on continually improving processes to remain innovative
- Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
- 152 hours of PTO 8 paid holidays
- Several Employee Resource Groups focusing on D&I
- Dynamic, fast-paced work environment
- Community engagement and green initiatives
- Generous 401K match
- Medical, dental and vision benefits
- Tuition Reimbursement - Let us help you finish your degree or start a new degree!
- WellHub- program to promote overall physical wellness
- Perkspot - offers exclusive or private discounts from approximately 900 merchants in a wide array of categories
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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.