MQA Supervisor

Bachelor of Science degree preferred, or equivalent combination of education and relevant work experience.

Four to six years of relevant experience in the pharmaceutical industry.

Experience with cGMP and FDA regulations.

Experience supporting regulatory audits preferred.

Frequent sitting, standing, walking, reading written documents, using a computer monitor, reaching, talking, writing, and listening.

Occasional bending, grasping, carrying, stooping, kneeling, and crouching.

Frequent lifting and/or moving up to 10 pounds, with occasional lifting and/or moving up to 30 pounds.

Fast-paced, performance-driven, customer-focused, collaborative, and inclusive work environment.

Join a team with more than 50 years of BFS technology leadership and a strong commitment to sterility excellence, client partnership, operational flexibility, and continuous innovation. In this role, you will directly influence quality performance and help advance reliable aseptic manufacturing for sterile pharmaceutical products.

Notice to Agency and Search Firm Representatives: Woodstock Sterile Solutions is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Woodstock Sterile Solutions employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Woodstock Sterile Solutions. 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.