Base: $95,000 to $110,000; bonus/equity: competiti...
Not specified (assumed to be on-site based on job responsibilities)
Quality assurance oversight
Cgmp compliance
Validation documentation review
Ferring is seeking an Associate for Quality & Technical Support in Parsippany, New Jersey, to provide Quality Assurance oversight for various validation and commissioning activities. The ideal candidate will have a strong background in GMP Quality Assurance and relevant experience in the pharmaceutical industry
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, flexible benefits, personal support, and tailored learning and development opportunities, embodying their 'People First' philosophy.
Matching Summary
Match Score: 85
Ferring is seeking an Associate for Quality & Technical Support in Parsippany, New Jersey, to provide Quality Assurance oversight for various validation and commissioning activities. The ideal candidate will have a strong background in GMP Quality Assurance and relevant experience in the pharmaceutical industry.
Salary
Base: $95,000 to $110,000; Bonus/Equity: Competitive annual incentive compensation targets; Benefits: Comprehensive healthcare, 401k, disability, life insurance, wellness, tuition reimbursement, sick/vacation time, paid holidays, parental leave
Skills & Requirements
Must-have
Quality Assurance oversight
cGMP compliance
Validation documentation review
Aseptic operations support
Regulatory compliance
Nice-to-have
Entrepreneurial spirit
People first philosophy
Innovative company culture
Agile and scalable operations
Key Requirements
Bachelor of Science in Natural Sciences or Engineering
Minimum 5 years GMP QA/Manufacturing/Validation experience
Minimum 3 years aseptic techniques/cell manufacturing experience