Operations and Quality Systems Manager

Full Time Position

DUTIES & RESPONSIBILITIES

  • To analyze data, to inform operational decisions or activities, develop operating strategies, plans, or procedures, direct organizational operations, projects, or services and evaluate quality of materials or products.
  • Review of BMRs and BPRs. Creation and review of Protocols, SPS, GLP and GMP.
  • Ensure regulatory compliance – FDA, State, Federal and International.
  • Responsible for Material and Equipment procurement and GLP/GMP training of staff.
  • Provide QA oversight for entire manufacturing site.
  • Must have a Master’s Degree in Pharmacy or Pharmaceutical Science and 2+ years’ experience in Formulation research & development (Product development), Process design, Scale-up and validation of Oral dosage forms.

CLICK HERE  to submit resume, statement of interest and salary requirements

NO PHONE CALLS PLEASE

Marlex Pharmaceuticals, Inc. is an Equal Opportunity Employer