Catalent Pharma Solutions Inc

Quality Assurance Supervisor

Catalent Pharma Solutions Inc • $75K — $95K *
Philadelphia, PA 19120In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
2 weeks ago
Job Overview by Ladders

Qualifications

  • HS Diploma/GED with 5+ years of Production QA experience required
  • College degree preferred (BA, BS)
  • Proven track record in monitoring and auditing quality
  • Supervisory experience of 5 years or more preferred
  • Regulatory field experience (pharma, food, automotive, etc.) required
  • Experience in continuous improvement initiatives
  • Basic knowledge of Lean Six Sigma methodologies is an advantage

Responsibilities

  • Oversee all QA activities related to incoming, distribution, destruction, and auditing
  • Ensure quality and identity during pharmaceutical product processes
  • Act as Quality partner for Supply Chain and Operations
  • Enforce Catalent policy and regulatory compliance
  • Serve as site expert in Good Manufacturing and Distribution Practices
  • Develop resource plans to support operational activities
  • Lead investigations on compliance issues regarding QA processes

Benefits

  • Defined career path with annual performance reviews
  • Diverse, inclusive culture
  • Positive, innovative work environment
  • Generous PTO policy (152 hours + 8 holidays)
  • Employee Resource Groups promoting diversity and inclusion
  • Community engagement and sustainability initiatives
  • Generous 401K match
  • Comprehensive medical, dental, and vision coverage
  • Tuition reimbursement for degree completion
  • Wellness program promoting physical health
  • Exclusive discounts through Perkspot from 900+ merchants
Full Job Description
QA Supervisor

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


The Candidate
  • 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.


Why you should join Catalent
  • 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

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Pharmaceuticals & Biotech
Founded
2007
* Ladders Estimates

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