PSG Global Solutions R&D Technician III in Bridgewater, New Jersey
We're looking for a R&D Technician III , working in the Pharmaceuticals & Medical Products industry in Bridgewater, New Jersey .
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 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
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 .
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EOE Protected Veterans/Disability