Position

Manager, Quality Assurance (Lynchburg, VA)


Department:

Quality

For over 150 years, Fleet Laboratories’ success has come from adapting to a changing world with creative thinking and innovative product development. We've grown into a global leader of over 100 personal health and beauty products. As the world keeps evolving, so do we-- with unique new technologies and products that help customers like you look and feel their best.

At Fleet Laboratories, the future is bright and our commitment to quality and innovation has never been stronger. You'll enjoy working here at our Lynchburg, VA location where you will be part of a diverse team that works collaboratively sharing thoughts and ideas to meet our consumer needs.

We seek a new  Manager, Quality Assurance to be responsible for overseeing and coordinating the activities engaged in release of in-house manufactured finished cosmetic products and OTC drugs, both monograph and NDA.  This role assures cGMP compliance with vendors through effective management of the Supplier Quality Program. This person manages and maintains various quality programs, such as change control, cGMP training, auditing, stability, product reviews, quality incident and quality incident investigation systems. 

WHAT YOU’LL DO

  • Manage the activities engaged in final product release of in-house manufactured drug and cosmetic products.
  • Approval of various documents for cGMP compliance.
  • Indirect responsibility of approximately $430,000 (QA portion of Quality budget, including salaries). 
  • Provide product quality through quality initiatives, accurate release of finished products, and quality maintenance of approximately 100 vendors.  
  • Interface with corporate Quality Assurance team and continuously identify opportunities for quality systems improvements and synergies
  • Manage programs for qualifying new or alternate cGMP compliant sources for finished drug and cosmetic products and for new components, packaging, and chemical starting materials. 
  • Manage the Supplier Quality Program for assuring the continued quality performance of existing vendors.
  • Develop, manage and maintain various quality programs, such as change control, deviation system, cGMP training, internal drug cGMP audits and Annual Product Reviews.
  • Manage the stability program for in-house and contract manufactured products.
  • Interact with various regulatory agencies such as FDA as needed and lead FDA inspections.
  • Responsible for managing the program for investigation of product quality incidents, including follow-up CAPA activities.
  • Manage batch record, deviation and incident issuance.
  • Provide technical support for a variety of corporate programs.
  • Analyze training needs, develop training programs, mentor or discipline Quality Assurance employees as necessary. 

EDUCATION AND EXPERIENCE YOU WILL BRING

  • BS in Math, Science, Engineering, or related technical field.
  • Minimum of seven years of directly related work experience in the pharmaceutical industry including supervisory experience in quality assurance.

WHAT WE OFFER

  • The start of a great career working with a diverse group of great people
  • The health and safety of every employee... our top priority
  • A clean, air-conditioned cGMP environment
  • Top notch benefits – paid time off, 401(K) retirement savings with company match, medical, dental and vision, pay annual targeted bonus, competitive pay, life insurance, Flexible spending account, and tuition reimbursement
  • Stability – a record of strong financial performance and a growing company, a business in the community for over 150 years.

Connect with us at: www.prestigebrands.com


Prestige is an Equal Opportunity Employer

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