Quality Auditor - Scientific - II (Associate)

Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies. Minimum of 3 years related experience in the pharmaceutical, biotech, or regulated industry, focusing on batch disposition, quality assurance, or GMP environments.

JSG is recruiting a Quality Auditor for our client in Rahway NJ. This is a 2 year contract assignment that will have raining onsite and after training period a hybrid schedule will be allowed.

Pay $35/hour to $39/hour

Overview:
As a Quality Auditor, you will play a vital role in maintaining regulatory compliance and supporting the integrity of clinical-stage drug products.
What You’ll Do:

• Review post-executed batch records, Certificates of Analysis, investigations, and supporting quality documents to ensure compliance.
• Make independent decisions on batch release or rejection based on your thorough review.
• Support quality system activities such as audits, deviations, CAPAs, and risk management.
• Prepare, analyze, and document data to support continuous quality improvement initiatives.
• Collaborate daily with cross-functional teams including quality, laboratory, manufacturing, and warehouse staff.
• Assist in preparing materials for audits and participating in site readiness activities.
• Develop, review, or update GMP procedures and standards to uphold regulatory compliance.
• Maintain accurate electronic documentation using systems like SAP and Veeva, supporting overall project and document management.

Must-Have Qualifications:

• Bachelor’s degree in a scientific or engineering discipline (e.g., engineering, chemistry, biology, biochemistry, microbiology).
• Minimum of 3 years related experience in the pharmaceutical, biotech, or regulated industry, focusing on batch disposition, quality assurance, or GMP environments.
• Experience reviewing batch records, Certificates of Analysis, investigations, and regulated documents.
• Familiarity with GMP regulations, regulatory compliance, and quality systems.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint, Teams) and SAP.
• Ability to work onsite 3 days/week (Wednesday required) with adaptability to a hybrid model.
• Strong attention to detail, problem-solving skills, and the ability to manage multiple tasks accurately.

Nice-to-Have Skills:

• Experience with Veeva systems and other electronic record systems.
• Prior exposure to manufacturing or QA on the production floor.
• Background in biologics, sterile manufacturing, or related fields.
• Advanced degrees (Masters) or previous quality auditing experience preferred.

Johnson Service Group, Inc. (JSG) is a North American leader in the staffing and consulting services industry, with over 35 years of experience investing in people and companies.

Johnson Service Group (JSG) is an Equal Opportunity Employer. JSG provides equal employment opportunities to all applicants and employees without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, marital status, protected veteran status, or any other characteristic protected by law.

JSG offers medical, dental, vision, life insurance options, short-term disability, 401(k), weekly pay, and more. Johnson Service Group (JSG) is an Equal Opportunity Employer.

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