Solomon Page
Sr. Pharmaceutical Quality Assurance Associate - Second Shift
Solomon Page, Fairfield, New Jersey, us, 07004
Our client is seeking a Senior QA Associate to maintain Quality compliance for GMP production in North Caldwell, NJ! The second shift will need to oversee 2nd shift production. The hours for this role are 3:30pm-12am Monday-Friday.Salary: $90-$100kResponsibilities:
Maintain the quality management system to meet cGMP and regulatory requirements.Maintain all quality system documentation in accordance with cGMP guidelines.Responsible for leading FDA inspections and any vendor audits.Continuous review of QMS for evaluation and to drive process efficiency.Assist with executing development projects to define Quality strategy.Work closely with laboratory, development and operations teams to ensure Quality compliance.Assist with Annual Product Reviews.Manage complaint investigation procedures as required.
Required Qualifications:
Bachelor's Degree requiredPrior Pharma industry experience required3-5 years relevant experience in a Quality organizationSound knowledge of cGMP guidelinesMS Office proficiencyClinical Resource Network DistinctionCRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
Opportunity Awaits.
Maintain the quality management system to meet cGMP and regulatory requirements.Maintain all quality system documentation in accordance with cGMP guidelines.Responsible for leading FDA inspections and any vendor audits.Continuous review of QMS for evaluation and to drive process efficiency.Assist with executing development projects to define Quality strategy.Work closely with laboratory, development and operations teams to ensure Quality compliance.Assist with Annual Product Reviews.Manage complaint investigation procedures as required.
Required Qualifications:
Bachelor's Degree requiredPrior Pharma industry experience required3-5 years relevant experience in a Quality organizationSound knowledge of cGMP guidelinesMS Office proficiencyClinical Resource Network DistinctionCRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
About CRN
Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
Opportunity Awaits.