Sr Manager, Quality Assurance

Breckenridge Pharmaceutical, Inc.

$120K — $145K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor of Science required (technical focus preferred)
  • At least 10 years' experience in the pharmaceutical industry, with 5 in a QA-management role
  • Willingness to travel domestically 3-4 times annually, potential for international travel
  • Strong understanding of cGMP regulations and quality compliance
  • Demonstrated leadership skills and attention to detail

Responsibilities

  • Perform and evaluate third-party audits for cGMP compliance at vendors
  • Manage and maintain the Standard Operating Procedures (SOP) system
  • Support the market distribution of production batches
  • Review and resolve deviations and Out-of-Specification reports
  • Manage product quality complaints and related investigations
  • Assist during FDA inspections and audits of the company and manufacturers
  • Conduct product quality reviews, including annual assessments from manufacturers
  • Oversee change control processes for products in the Dietary Supplements and Medical Foods categories

Benefits

  • Flexible work approach
  • Health benefits and time-off programs
  • Comprehensive benefits package for all employees
  • Emphasis on total well-being investment
Full Job Description
About the Role

This position reports to the Vice President, Quality Assurance and will manage or support: cGMP compliance assessment of contract manufacturers, the company SOP and Training systems, QA/QC Testing /Audit program, and Quality/Compliance decisions related to the Company's ANDA products, as well as its products subject to OTC Monographs and FDA or other industry-accepted standards for Dietary Supplements, Medical Foods or Foods for special dietary use.

Responsibilities

  • Perform, support and evaluate third party audits of current and proposed vendors for cGMP compliance
  • Manage the SOP system, including writing/ revising and maintaining SOPs, SOP Tracking and SOP Training
  • Support market distribution of batches
  • Manage the review and resolve batch deviations / Out-of-Specification (OOS) reports and proposed Corrective and Preventative Actions (CAPAs) from manufacturers for Dietary Supplements and Medical Foods
  • Manage product quality complaints
  • Support FDA audits/inspections of the company or its manufacturing partners, as needed
  • Product Quality Reviews, including review of manufacturers' reports of annual product reviews
  • Manage change control review of Dietary Supplements and Medical Foods products
  • Batch record reviews, as required


Qualifications

  • Bachelor of Science required (preferably technical / science-biology, chemistry, pharmacy or other suitable science/technology)
  • Minimum 10 years' experience in the pharmaceutical industry with focus in Quality Assurance / Quality Systems (preferably at least 5 years in a QA-management role)
  • Ability to travel domestically 3-4 times per year to perform audits on facilities, potential international travel


Required Skills

  • Strong knowledge of quality and compliance for drug production
  • Strong knowledge of cGMP regulations (21 CFR 210 and 211 and 21 CFR 110 and 111)
  • Strong leadership skills
  • Excellent attention to detail and organizational skills
  • Effective communication and interpersonal skills


Pay range and compensation package

At Breckenridge Pharmaceutical Inc, we're committed to investing in every team member's total well-being, now and in the future. Our benefits programs vary but we offer the following to all BPI team members, regardless of geographic location:
  • Flexible approach to how we work
  • Health benefits and time-off programs
  • Competitive compensation packages
  • The anticipated annual salary for this role is $120,000 - 145,000


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