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PSG Global Solutions R&D Technician III in Bridgewater, New Jersey

The Opportunity

We're looking for a R&D Technician III , working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey .

Job description:

  • Precisely follow company tissue requests, study designs, protocols and SOPs for the complete processing of tissue based products with minimal supervision.

  • Perform routine lab testing to demonstrate the ability of the product/device to function as intended under study director/management supervision.

  • Contribute to the development of processes for manufacturing and commercial tissue products.

  • Work with in-house engineering groups to scale-up, validate, and transfer the commercial manufacturing process.

  • Monitor and analyze the performance of processes and equipment and make recommendations for continuous improvement with minimal guidance.

  • Serve as a subject matter expert, provide guidance to junior staff.

  • Train employees and staff on complex technical methods.

  • Independently operates a variety of laboratory and manufacturing equipment.

  • Follows Good Documentation Practices when recording information on batch records, equipment and cleaning logs, and other documents.

  • Maintains/manages inventory of processing supplies with little to no guidance.

Our Client

Our client is an award-winning clinical development company. Improving lives globally with 20+ years experience in clinical research and strategic resourcing. Elevating results with proven strategies, comprehensive solutions, and customized delivery models.

Serving pharmaceutical, biopharmaceutical, biotechnology, and medical device organizations.

Strong relationships provide you connections and access to great opportunities. Industry expertise sets you up for success with helpful insights, career coaching, and professional training. Grow and learn while you put your skills to work.

Experience Required for Your Success


  • High School Diploma or equivalent

  • 3 years related experience in R&D or Quality laboratory or an equivalent combination of education and experience

  • Ability to independently enter data and generate reports in data entry systems such as MS Office and SAP

Knowledge of:

  • Current Good Manufacturing Practices (cGMP) and other relevant regulatory requirements

  • Basic chemistry laboratory practices and techniques

  • Personal computer hardware and software applications

  • Business English usage, spelling, grammar and punctuation

  • Basic mathematical computations

  • Current Company policies, practices and procedures, including safety rules and regulations


The pay range we are offering is 20 to 23 per hour. This position may present an opportunity to go permanent.

What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here .

Not exactly? Join Our Talent Community ( , and we'll let you know of additional opportunities.

EOE Protected Veterans/Disability