What are the responsibilities and job description for the Quality Specialist position at Recruits Lab?
Quality Specialist (Contract – 18–24 Months)
📍 Phillipsburg, NJ | 💼 Full-Time | 100% Onsite
Compensation: $33.65 – $43.27/hour ($70K–$90K annually equivalent)
Schedule: Monday – Friday, 8:00 AM – 5:00 PM
🚀 About the Opportunity
We are seeking a Quality Specialist to join a leading global manufacturer’s operations team in Phillipsburg, NJ. This is a long-term contract role (18–24 months) with the potential to convert to a permanent hire. You’ll be part of a collaborative 15-person Quality team, supporting key initiatives that strengthen compliance, digitize batch records, and improve processes within a GMP-regulated environment.
📝 What You’ll Do
As a Quality Specialist, you’ll play a critical role in ensuring quality standards, regulatory compliance, and process improvements. Key responsibilities include:
✅ What We’re Looking For
Education: Bachelor’s degree in Biology, Chemistry, or a related scientific field.
🎯 Why This Role?
📌 Interview Process
🔒 Requirements
👉 If you’re a Quality professional with manufacturing experience who thrives in GMP environments and enjoys both hands-on work and process improvement, we’d love to hear from you!
📍 Phillipsburg, NJ | 💼 Full-Time | 100% Onsite
Compensation: $33.65 – $43.27/hour ($70K–$90K annually equivalent)
Schedule: Monday – Friday, 8:00 AM – 5:00 PM
🚀 About the Opportunity
We are seeking a Quality Specialist to join a leading global manufacturer’s operations team in Phillipsburg, NJ. This is a long-term contract role (18–24 months) with the potential to convert to a permanent hire. You’ll be part of a collaborative 15-person Quality team, supporting key initiatives that strengthen compliance, digitize batch records, and improve processes within a GMP-regulated environment.
📝 What You’ll Do
As a Quality Specialist, you’ll play a critical role in ensuring quality standards, regulatory compliance, and process improvements. Key responsibilities include:
- Supporting the digitization of the batch records project and overall Quality Management System improvements.
- Assisting Quality Engineers in updating procedures, SOPs, and work instructions.
- Investigating quality events, CAPAs, complaints, and discrepancies, ensuring timely resolution and documentation.
- Conducting process reviews, quality control evaluations, and statistical analysis of data.
- Serving as a document owner for SOPs, training materials, and compliance documentation.
- Providing hands-on training for quality processes.
- Collaborating with cross-functional teams, supervisors, and engineers to implement corrective actions.
- Participating in audits, quality meetings, and trending reports.
✅ What We’re Looking For
- 5 years of Quality experience in a manufacturing environment.
- Experience with CAPA initiation, event investigations, and complaint handling.
- Strong knowledge of GMP compliance and SOP development/updates.
- Background in Quality Control/Assurance/Technician work (warehouse or production environment).
- Comfort working around chemicals or medical devices on the production floor.
- Hands-on experience supporting process digitization or database-driven systems (a plus).
Education: Bachelor’s degree in Biology, Chemistry, or a related scientific field.
🎯 Why This Role?
- Long-term stability: 18–24 month contract with potential to convert to permanent.
- Be at the forefront of a major digitization project in manufacturing quality.
- Work with an established and collaborative 15-person Quality team.
- Competitive pay range with full-time, consistent hours.
📌 Interview Process
- 15-minute virtual prescreen with hiring manager.
- On-site panel interview (45–60 min) with 2–3 team members and facility tour.
🔒 Requirements
- Must pass background check and drug screen.
- 100% onsite in Phillipsburg, NJ.
👉 If you’re a Quality professional with manufacturing experience who thrives in GMP environments and enjoys both hands-on work and process improvement, we’d love to hear from you!
Salary : $70,000 - $90,000