job summary: Looking to expand your quality career with a top-tier global life sciences leader? We are seeking a detail-oriented Compliance Specialist to lead non-conformance investigations and quality resolution for production operations in Ridgefield, NJ. If you bring strong investigative instincts and cGMP experience within a reasonable commute, this is an excellent opportunity to make a direct impact on operational quality.

location:

Ridgefield, New Jersey job type: Contract salary: $20 - 25 per hour work hours: 9 to 5 education: Bachelors responsibilities: Investigate, author, and manage non-conformance reports (NCRs) for production and environmental monitoring (EM) events. Perform root cause analysis to identify underlying issues and document comprehensive investigation findings. Collaborate with cross-functional teams to design, implement, and track actionable CAPAs. Conduct effectiveness checks (ECs) to verify CAPA outcomes and prevent recurring quality issues. Ensure continuous compliance with c

GMP, ISO

9001, and FDA guidelines across all manufacturing activities.

qualifications:

2+ years of hands-on experience authoring, investigating, and managing NCRs and deviations in a cGMP manufacturing environment. Working knowledge of CAPA management, effectiveness checks, and document control systems. Strong familiarity with regulatory standards including c

GMP, ISO

9001, and FDA guidelines. Proven tenure and stability in previous quality assurance or manufacturing roles. Local to Ridgefield, NJ (within a 45-minute commute) to support potential overtime and weekend needs.

skills:

Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA), Food and Drug Administration (FDA)

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. job detailssummary$20 - $25 per hourcontractbachelor degreecategorylife, physical, and social science occupationsreference54208job details job summary: Looking to expand your quality career with a top-tier global life sciences leader? We are seeking a detail-oriented Compliance Specialist to lead non-conformance investigations and quality resolution for production operations in Ridgefield, NJ. If you bring strong investigative instincts and cGMP experience within a reasonable commute, this is an excellent opportunity to make a direct impact on operational quality.

location:

Ridgefield, New Jersey job type: Contract salary: $20 - 25 per hour work hours: 9 to 5 education: Bachelors responsibilities: Investigate, author, and manage non-conformance reports (NCRs) for production and environmental monitoring (EM) events. Perform root cause analysis to identify underlying issues and document comprehensive investigation findings. Collaborate with cross-functional teams to design, implement, and track actionable CAPAs. Conduct effectiveness checks (ECs) to verify CAPA outcomes and prevent recurring quality issues. Ensure continuous compliance with c

GMP, ISO

9001, and FDA guidelines across all manufacturing activities.

qualifications:

2+ years of hands-on experience authoring, investigating, and managing NCRs and deviations in a cGMP manufacturing environment. Working knowledge of CAPA management, effectiveness checks, and document control systems. Strong familiarity with regulatory standards including c

GMP, ISO

9001, and FDA guidelines. Proven tenure and stability in previous quality assurance or manufacturing roles. Local to Ridgefield, NJ (within a 45-minute commute) to support potential overtime and weekend needs.

skills:

Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA), Food and Drug Administration (FDA)

Equal Opportunity Employer:

Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.