the ASSURANCE group
Contract manufacturer is seeking a Quality Assurance Supervisor to join their team. The QA Supervisor will provide management of Compliance activities for the site following company policies, standards, procedures, and cGMPs, including USA & Canadian regulatory compliance to the FDA and Health Canada regulations.
Base pay range $75,000.00 – $85,000.00 per year
Key Responsibilities
Lead and manage the Quality Compliance team to meet operational and regulatory objectives.
Oversee deviation investigations, CAPA development, and change control activities.
Ensure compliance with FDA, cGMP, and ISO requirements (21 CFR 210/211, ISO 22716).
Plan and execute internal audits and ensure timely closure of findings.
Develop, review, and maintain SOPs, GMP documentation, and validation activities.
Identify compliance risks, trends, and corrective actions; serve as an independent compliance authority.
Collaborate cross-functionally to resolve compliance issues and improve quality systems.
Provide compliance reporting, regulatory guidance, and strategic recommendations to senior leadership.
Requirements
Must have a Bachelor’s Degree in Chemistry, Biology, Environmental Sciences, or related field of study.
Minimum 5 years related Quality supervisory experience.
Must have GMP, Quality, and in-depth risk management knowledge.
Must be able to interpret problems and effectively prepare surrounding communication in a productive manner to management with clarity and accuracy.
Must be skilled in planning and organizing, conflict management, coaching others, talent selection, developing others, decision making and building relationships.
Bilingual in English & Spanish is preferred.
For immediate consideration please send resume outlining your related experience.
Seniority level Mid-Senior level
Employment type Full-time
Job function Quality Assurance and Manufacturing
Industries Manufacturing and Personal Care Product Manufacturing
Location Parsippany, NJ
#J-18808-Ljbffr
Base pay range $75,000.00 – $85,000.00 per year
Key Responsibilities
Lead and manage the Quality Compliance team to meet operational and regulatory objectives.
Oversee deviation investigations, CAPA development, and change control activities.
Ensure compliance with FDA, cGMP, and ISO requirements (21 CFR 210/211, ISO 22716).
Plan and execute internal audits and ensure timely closure of findings.
Develop, review, and maintain SOPs, GMP documentation, and validation activities.
Identify compliance risks, trends, and corrective actions; serve as an independent compliance authority.
Collaborate cross-functionally to resolve compliance issues and improve quality systems.
Provide compliance reporting, regulatory guidance, and strategic recommendations to senior leadership.
Requirements
Must have a Bachelor’s Degree in Chemistry, Biology, Environmental Sciences, or related field of study.
Minimum 5 years related Quality supervisory experience.
Must have GMP, Quality, and in-depth risk management knowledge.
Must be able to interpret problems and effectively prepare surrounding communication in a productive manner to management with clarity and accuracy.
Must be skilled in planning and organizing, conflict management, coaching others, talent selection, developing others, decision making and building relationships.
Bilingual in English & Spanish is preferred.
For immediate consideration please send resume outlining your related experience.
Seniority level Mid-Senior level
Employment type Full-time
Job function Quality Assurance and Manufacturing
Industries Manufacturing and Personal Care Product Manufacturing
Location Parsippany, NJ
#J-18808-Ljbffr