Principal Quality Associate, Supplier Audits

7 hours ago

Greenville, United States Disability Solutions Full time

Principal Quality Associate, Supplier Audits

Position Summary

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Catalent’s Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

The Principal Quality Associate, Supplier Audits requires the ability to perform and facilitate system-based audits and risk assessments for Supplies Audits and Internal Quality Systems. The Principal Quality Associate, Supplier Audits will support non-commercial and commercial audits as well as the Inspection Readiness Program.

The Role

  • Conduct external supplier audits (Desktop, Virtual or On-Site) per schedule, communicate findings and ensure CAPA plan is appropriate to address the findings.

  • Ensure the Supplier Audit Team members are properly qualified and assign their roles and responsibilities; train staff to conduct or assist with audits and risk assessments.

  • Participate in Regulatory Inspections and assist Inspection Readiness Team with inspection preparation, including walkthroughs and gathering of documentation, per inspection agenda as required.

  • Assist with the generation of the Internal Audit Schedule, preparation and execution of Internal Quality Audits of Catalent systems / subsystems.

  • Participate in process improvement projects and investigations, as required.

  • Ensure all work is performed and documented according to approved standard operating procedures (SOPs), in general compliance with cGMPs, and in a timely manner consistent with agreed upon schedules.

  • All other duties as assigned.

The Candidate

  • Bachelor’s degree in a technical field with at least 6 years of professional experience in the pharmaceutical

  • industry, 3 of which must have been in a Quality Auditing function or;

  • Associate degree in a technical field with at least 7 years of professional experience in the pharmaceutical industry, 4 of which must have been in a Quality Auditing function or;

  • In lieu of a technical field degree, at least 8 years of years of professional experience in the pharmaceutical industry, 5 of which must have been in a Quality Auditing function and completion of formal auditing training may be substituted.

  • At least 5 years of experience in a direct Quality role required.

  • Demonstrated knowledge of regulations and guidelines associated with cGMPs for pharmaceutical industry.

  • Knowledge of manufacturing and/or laboratory processes required.

  • ASQ CQA or equivalent certification preferred.

  • Some exposure to hazardous chemicals and other active chemical ingredients.

  • Position requires the capacity to handle and manipulate objects using hands and arm.

Why You Should Join Catalent 

  • Competitive medical benefits and 401K 

  • 152 hours of PTO + 8 Paid Holidays 

  • Dynamic, fast-paced work environment 

  • Opportunity to work on Continuous Improvement Processes 

Catalent offers rewarding opportunities to further your career  Join the global drug development and delivery leader and help us bring over 7,000 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 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.

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