What are the responsibilities and job description for the Quality Assurance (QA) Lead – FDA/ISO Manufacturing (3rd shift) position at VRS Recruitment (US)?
VRS has an exciting opportunity for a supervisor of QA staff looking for a fast-paced role in a dynamic manufacturing environment. The ideal candidate will have worked under regulations for FDA and ISO manufacturing, ideally for pharmaceutical, nutraceutical, dietary supplement, or food-related products.
Primary Responsibilities
- Candidates must be able to work on a THIRD SHIFT
- Oversee and manage quality assurance staff; liaise directly with manufacturing teams on large scale production lines
- Ensure regulatory compliance (primarily FDA and ISO); review and implement quality processes
- Focus on continuous improvement for new and existing processes
- Host and coordinate audits and prepare reports for final release
Primary Qualifications
- Minimum of a BS degree, ideally in a scientific field
- Expertise with regulations for Pharma, Dietary Supplements, or Food-related products (FDA, GMP, and/or ISO experience is preferred)
- Minimum of 4 years of QA experience in a manufacturing environment
- Prior direct management of 2 or more staff is required
- Team player who can think on their feet and enjoys collaboration and creative problem solving
Salary / Benefits
- $80-85k base salary commensurate with experience
- Annual discretionary bonus
- Health, vision, dental, and life insurance
- 401k with company match
- Childcare and tuition assistance
- Excellent relocation assistance!
Salary : $80,000 - $85,000
