Asst. QC Scientist – Contract – Princeton, NJ - $31.00-$41.00

The end client is unable to sponsor or transfer visas for this position; all parties authorized to work in the US without sponsorship are encouraged to apply.

A Pharmaceutical Company is seeking a Asst. QC Scientist in Princeton, NJ.

Role Description

The QC Clinical Associate is responsible for supporting Quality Control microbiology testing for release of clinical products and environmental monitoring. This includes the ability to interface with multiple groups, the ability to independently perform tasks, interpret results, and troubleshoot. Additionally, when needed, this position will be able to assist with training and assay transfer.

• Perform environmental monitoring and testing of final product samples.

• Utilize scientific principles to assist in microbiological testing methods and the proper use of laboratory equipment.

• Understanding of regulatory guidelines and can independently develop, write and execute methods, protocols, reports and other related documents.

• Complete all work in a timely manner.

• Work and communicate effectively within the team to ensure timelines are met.

• Review all data in accordance with applicable procedures and cGMP requirements.

corrections required.

• Document training per procedural and cGMP requirements.

• Perform assigned tasks within a CAPA, deviation, or project

• Draft and review technical documents, such as SOPs and protocols/reports.

• Communicate effectively with management regarding task completion, roadblocks, and needs.

• Demonstrate initiative, courage, and continuous improvement throughout investigation/corrective action lifecycles.

• Performs other tasks as assigned.

Skills & Requirements

• Bachelor’s degree required, preferable in Science.

• 0-3 years of relevant work experience, preferable in a regulated environment.

• An equivalent combination of education and experience may substitute.

• Experience working in clean room environments and with cell therapy products preferred.

• Hands on experience with various microbiology techniques and environmental monitoring.

• Ability to accurately and completely understand, follow, interpret and apply Global

Regulatory and cGMP requirements.

• Problem solving ability/mentality, technically adept and logical.

• Ability to set priorities of the group and manage timelines.

• Ability to work with management locally and globally.

• Ability to communicate effectively with peers, department management and cross- functional peers.

Why Hays?

You will be working with a professional recruiter who has intimate knowledge of the Information Technology industry and market trends . Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there’s a position you really want, you’re fully prepared to get it.

Additionally, this position is a contract role where Hays offers you the opportunity to enroll in full medical, dental or vision benefits.

• Medical

• Dental

• Vision

• 401K

• Life Insurance ($20,000 benefit)

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Hays is an Equal Opportunity Employer.

Drug testing may be required; please contact a recruiter for more information