Analytical Chemist; Analytical Testing, Raw Materials Testing

Job Title: Associate Quality Control

Duration: 12 months with possibility of extension

Terms: Contract W2

Description:

The Associate Quality Control (QC) position will provide general support to Quality Control laboratories at Rhode Island. The role will be based out of Rhode Island and will work under the guidance of the hiring manager. It is an administrative 100% onsite shift, Monday through Friday 8:00AM – 5:00PM. Occasional need to start 7:00 AM.

The Quality Control team provides analytical expertise in testing of drug substance and raw materials to meet specifications and ensure a constant supply of raw materials for products.

Quality Control is searching for an analyst to support routine testing of Raw Materials in the Wet Chemistry laboratory. This person will be responsible for working in the Quality analytical laboratory, using GMPs and GDPs to execute analytical testing.

Ideal Candidate: B.S. and 1-3+ years of experience.

Key Responsibilities:

• Strong Analytical Skills: Ideal candidate will have experience 1-3 years performing analytical testing.
• Attention to Detail: Ideal candidate will be thorough and deliver polished work product.
• Can Do Attitude: Ideal Candidate will have a positive attitude and be willing to participate in lean initiatives on site.

Preferred Qualifications:

• 1-3 years of experience in GMP analytical laboratory.
• Experience with bench chemistry.
• Experience with Compendial testing.
• Self-motivated, strong organizational skills and ability to manage multiple tasks at one time with minimal supervision.
• Strong communication skills (both written and oral), facilitation and presentation skills.
• Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories.
• Understanding of biopharmaceuticals process and related unit operations.
• Strong analytical skills with the ability to collect, organize, analyze, and disseminate significant amounts of information with attention to detail and accuracy.
• Independent, self-motivated, organized, able to multi-task in time-sensitive environments.
• Demonstrated experience in investigations and QC processes.

Entry level

Contract

Quality Assurance

Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research