Associate, Quality & Technical Support

Ferring Com Ar

Parsippany, New Jersey, US
Base: $95,000 to $110,000; bonus/equity: competiti...
Hybrid (based on company culture and flexibility described)
Gmp quality assurance
Validation documentation review
Quality systems support
Ferring Com Ar is seeking an Associate for Quality & Technical Support in Parsippany, New Jersey. The role involves providing Quality Assurance oversight for manufacturing processes and ensuring compliance with regulatory standards within a biopharmaceutical company that values innovation and a people-first culture

Job Summary

  • The Associate, Quality & Technical Support will provide Quality Assurance (QA) oversight for commissioning, qualification, and validation activities at the manufacturing site, including review and approval of all associated documentation.
  • The position supports quality systems, investigations, change controls, aseptic operations, and regulatory compliance across multiple functional areas.
  • Ferring offers competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities.

Matching Summary

Match Score: 85

Ferring Com Ar is seeking an Associate for Quality & Technical Support in Parsippany, New Jersey. The role involves providing Quality Assurance oversight for manufacturing processes and ensuring compliance with regulatory standards within a biopharmaceutical company that values innovation and a people-first culture.

Salary

Base: $95,000 to $110,000; Bonus/Equity: Competitive annual incentive compensation targets in the form of an annual bonus; Benefits: Comprehensive healthcare, 401k plan and company match, disability coverage, life insurance, wellness benefits, tuition reimbursement, sick time, vacation time, paid holidays, paid parental leave

Skills & Requirements

Must-have

  • GMP Quality Assurance
  • Validation documentation review
  • Quality systems support
  • cGMP compliance
  • Regulatory compliance

Nice-to-have

  • Entrepreneurial spirit
  • People first philosophy
  • Innovative companies
  • Agile and scalable

Key Requirements

  • Bachelor of Science in Natural Sciences or Engineering
  • Minimum 5 years of experience in GMP Quality Assurance
  • Minimum 3 years of experience with aseptic techniques
  • Experience reviewing Process Validation, Cleaning Validation, Computer Validation
  • Strong understanding of cGMP, 21 CFR 210/211
  • Proficiency with Microsoft Office Suite

Work Rights

Not specified

Tailored Resume

Cover Letter