Laboratory Technician II CooperSurgical - 3.4 Livingston, NJ Job Details Full-time 9 hours ago Qualifications Contamination control Bachelor's degree Full 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.

Job Summary:

The Laboratory Technician II 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. CooperSurgical is a leading fertility and women's healthcare company dedicated to putting time on the side of women, babies, and families at the healthcare moments that matter most in life. As a business unit of CooperCompanies (

Nasdaq:

COO) , we're driven by a unified purpose of helping people experience life's beautiful moments. Guided by our shared values - dedicated, innovative, friendly, partners, and do the right thing - our offerings support patients throughout their lifetimes, from contraception to fertility and birth solutions, to women's and family care, and beyond. We currently offer over 600 clinically relevant medical devices to healthcare providers, including testing and treatment options, as well as an innovative suite of assisted reproductive technology and genomic testing solutions. Learn more at www.coopersurgical.com.

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 follow procedures and protocols with a high degree of consistency and accuracy
• Ability to work effectively within a contamination-controlled processing environment
• Ability to interpret procedures, identify minor process issues, and propose improvements when appropriate
• Knowledge of good documentation practices and laboratory safety standards
• Ability to communicate and collaborate effectively across cross-functional teams
• Strong attention to detail, organization, and documentation accuracy
• 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 2-4 years of relevant laboratory and/or manufacturing experience required
• Hands-on contamination-controlled processing experience in a laboratory, manufacturing, or controlled environment is required
• Experience supporting validation, qualification, or manufacturing transfer activities preferred
• Experience with molecular biology laboratory techniques preferred, including PCR, q

PCR, 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 manufacturing environments preferred

Education:

Bachelor's degree in the sciences required

Travel:

Limited travel may be required afterward (