534,639open jobs
19,018companies
74,061added this week
Browse all
Location
In office
Seniority
Middle · 2+ years exp
Overview
Company
Impact
Profile match
CooperVision is a medical device enterprise specializing in the design, manufacture, and distribution of soft contact lenses and advanced vision care solutions. Headquartered in San Ramon, California, United States, and operating locally through CooperVision Singapore, the firm functions as a core business unit of The Cooper Companies, Inc. (NYSE: COO). It produces a broad portfolio of spherical, toric, multifocal, and childhood myopia control lenses, leveraging proprietary optical technologies to serve eye care professionals and consumers across more than 130 countries.

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.

Essential Functions & Accountabilities:

  • Execute SOPs and perform assigned 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
  • Perform basic molecular biology laboratory procedures with accuracy and attention to detail
  • Maintain proficiency in applicable procedures and contamination-controlled processing techniques
  • 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 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 issues
  • Follow all applicable SOPs, quality, safety, regulatory, and corporate requirements
  • Perform additional duties as assigned by management

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, 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 manufacturing environments preferred

Education:

  • Bachelor’s degree in the sciences required

Travel:

• Limited travel may be required afterward (<10>

Free account
Stop reading job ads. Get the ones that fit.
One free account turns this page into a shortlist built around your stack, your level and your pay.
Match on every job. Stack, seniority, pay and location, scored against your profile.
534,639 open roles. Read straight off company career pages, refreshed every day.
Unlimited applications. Every one you send is tracked in one place, on-site or on a company board.
3 tailored CVs a month. Rewritten for the exact job you are applying to. Included free.
Create a free account Continue with Google
Free forever. No card. Under a minute.

Recommended for you based on this role

Similar stack
Same company
In your city
In office • 3+ years exp • Bachelor's Degree
Apply
In office • 5+ years exp • Bachelor's Degree
Analytics
Microsoft Excel
Apply
In office • 10+ years exp • Bachelor's Degree • Kuala Lumpur
Analytics
Power BI
Apply
In office
Apply
In office
Management
Outlook
Apply
See all jobs
This is one of many
534,639 more open roles from verified company boards, updated every day.