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Sr Lab Tech Ops

Job in Branchburg Township, Somerset County, New Jersey, USA
Listing for: 247Hire
Full Time position
Listed on 2026-05-21
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Pharmaceutical Manufacturing, Manufacturing Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 50000 - 70000 USD Yearly USD 50000.00 70000.00 YEAR
Job Description & How to Apply Below
Location: Branchburg Township

Responsibilities

  • Work in a dynamic team dedicated to developing purification methods for oligonucleotides.
  • Performing and documenting purification, downstream processing, characterization, and final formulation of various oligonucleotides using lab instruments such as HPLC, UV-VIS, etc. Assist in new platform development, scale ‐ up activities, and troubleshooting issues in the Oligonucleotide Manufacturing group.
  • Perform and oversee production and production support duties for Operations; ensure quality of production and lab testing.
  • Follow departmental work instructions, SOPs, OSHA safety regulations, and cGMPs.
  • Monitor lab supply inventory, generate expense purchase requisitions, input production data into SAP/LIMS, and maintain documentation.
  • Interface with internal groups to ensure lab equipment maintenance, calibration, and documents conform to established practices.
  • Attend required training and participate in on ‐ the ‐ job training.
  • Participate in design and organization of experiments with supervisor; provide input for experimental protocols, investigations, and reports.
  • Provide input for improving lab procedures; assist with new procedure development and evaluation of products/equipment; help generate SOPs.
  • Perform other duties as assigned.
Required Skills
  • 2-4 years experience
  • Associate Degree
  • Basic proficiency with MS Word and Excel
  • Excellent written and verbal communication skills
  • Able to follow SOPs, safety regulations, and cGMPs
  • Detail ‐ oriented with ability to maintain accurate documentation
  • Comfortable interfacing with internal groups for equipment compliance
  • Willing to participate in training and assist in experiment design
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