Laboratory Technician III

CooperSurgical; Livingston (NJ); On-site; USD 65,000 - 90,000; Full time

Job summary

CooperSurgical in Livingston, New Jersey is seeking a Laboratory Technician III to support reagent manufacturing, validation and production transfer activities in a regulated laboratory environment.

You will perform routine lab and manufacturing tasks, execute SOPs, maintain accurate documentation, assist with validation, transfer projects, and collaborate with Manufacturing, Quality, Engineering and cross‑functional teams; a BS in the sciences and 3–5 years of relevant experience are required.

Qualifications

• Bachelor’s degree in the sciences.
• Minimum 3–5 years of relevant laboratory and/or manufacturing experience.
• Experience supporting validation, qualification, startup, or manufacturing transfer activities preferred.
• Experience with molecular biology techniques (PCR, qPCR, DNA extraction, next-generation sequencing workflows) preferred.
• Experience working in GMP or regulated manufacturing environments preferred.
• Strong documentation and GDP practices.
• Ability to communicate and collaborate across cross-functional teams.

Responsibilities

• Support daily manufacturing activities and production priorities according to the production schedule.
• Serve as a technical resource to other laboratory technicians during routine manufacturing activities.
• Execute SOPs and perform complex manufacturing tasks independently and in a timely manner.
• Perform reagent formulation, filling, labeling, packaging, and related manufacturing activities according to procedure.
• Perform routine quality control inspections according to procedure.
• Maintain proficiency in contamination-controlled processing techniques and laboratory workflows.
• Support contamination prevention and good laboratory practices during manufacturing operations.
• Assist with onboarding and hands-on training of new technicians as needed.
• Accurately complete production and test records according to GDP.
• Report deviations, nonconformances, and operational issues in a timely manner.
• Participate in troubleshooting, root cause investigations, and continuous improvement activities.
• Support equipment qualification, process validation, and manufacturing transfer activities.
• Receive, inspect, stock, and organize production materials and laboratory supplies.
• Perform routine laboratory cleaning and equipment maintenance.
• Participate in reviews and updates of SOPs, forms, and work instructions.
• Support manufacturing documentation and technical records.
• Collaborate with QA, R&D, Engineering, and Operations to support manufacturing and resolve process or product issues.
• Follow all applicable SOPs, quality, safety, regulatory, and corporate requirements.
• Perform additional duties as assigned by management.

Skills

Biochemical concepts

Molecular biology concepts

Contamination control

GDP/documentation

Communication

Team collaboration

Attention to detail

Pipetting tasks

MS Office

Education

Bachelor’s degree in the sciences

Tools

Laboratory equipment

qPCR

DNA extraction

Job description

Job Description

This position will execute standard operating procedures (SOPs) supporting reagent manufacturing, validation, and production transfer activities at the CooperSurgical laboratory in Livingston, New Jersey.

The Laboratory Technician III will support reagent manufacturing activities at the CooperSurgical laboratory in Livingston, NJ. This role will perform routine laboratory and manufacturing activities, follow established procedures, maintain accurate documentation, and support validation and production readiness. The technician will work closely with Manufacturing, Quality, Engineering, and other cross-functional teams.

Responsibilities

Essential Functions & Accountabilities:

• Support daily manufacturing activities and production priorities according to the production schedule
• Serve as a technical resource to other laboratory technicians during routine manufacturing activities
• Execute SOPs and perform complex manufacturing tasks independently and in a timely manner
• Perform reagent formulation, filling, labeling, packaging, and related manufacturing activities according to procedure
• Perform routine quality control inspections according to procedure
• Maintain proficiency in contamination-controlled processing techniques and laboratory workflows
• Support contamination prevention and good laboratory practices during manufacturing operations
• Assist with onboarding and hands-on training of new technicians as needed
• Accurately complete production and test records according to good documentation practices (GDP)
• Report deviations, nonconformances, and operational issues in a timely manner
• Participate in troubleshooting, root cause investigations, and continuous improvement activities
• Support equipment qualification, process validation, and manufacturing transfer activities
• Receive, inspect, stock, and organize production materials and laboratory supplies
• Perform routine laboratory cleaning and equipment maintenance
• Participate in reviews and updates of SOPs, forms, and work instructions
• Support manufacturing documentation and technical records
• Collaborate with QA, R&D, Engineering, and Operations to support manufacturing and resolve process or product issues
• Follow all applicable SOPs, quality, safety, regulatory, and corporate requirements
• Perform additional duties as assigned by management

Qualifications

Qualifications, Knowledge, Skills and Abilities:

• Understanding of fundamental biochemical and molecular biology concepts (e.g., nucleic acid structure, PCR, pH, contamination control, etc.)
• Ability to work effectively within a contamination-controlled processing environment
• Strong understanding of contamination prevention practices, gowning procedures, and controlled workflow behaviors
• Ability to follow procedures and protocols with a high degree of consistency and accuracy
• Ability to identify operational issues and support troubleshooting activities in a manufacturing environment
• Ability to communicate and collaborate effectively across cross-functional teams
• Strong attention to detail, organization, and documentation accuracy
• Ability to support training and coordination of junior laboratory personnel
• Ability to perform repetitive pipetting and laboratory tasks for extended periods of time
• Proficiency with Microsoft Office programs including Excel, Word, and PowerPoint
• Ability to maintain confidentiality as required

Work Environment

• Frequent reaching, grasping, repetitive motions, and eye/hand coordination
• Ability to work in office and laboratory/manufacturing environments
• Ability to wear contamination-controlled processing garments, gloves, eye protection, and masks for extended periods
• Ability to sit or stand for extended periods of time
• Ability to lift up to 50 lbs

Experience

• Minimum 3–5 years of relevant laboratory and/or manufacturing experience required
• Hands‑on experience in a laboratory, manufacturing, or contamination‑controlled environment is required
• Prior experience supporting production execution, floor coordination, or technician training activities preferred
• Experience supporting validation, qualification, startup, or manufacturing transfer activities preferred
• Experience with molecular biology laboratory techniques preferred, including PCR, qPCR, DNA extraction, next‑generation sequencing workflows, or related methods
• Experience working with electronic quality systems, manufacturing systems, or laboratory information systems is preferred
• Experience working in GMP or regulated manufacturing environments preferred

Education

• Bachelor’s degree in the sciences required

Travel

Limited travel may be required afterward (