Scientist - The Staffing Resource Group, Inc

Scientist
SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

• Title: Scientist
• Location: Somerset, NJ
• Industry: Pharmaceutical
• Shift: Monday-Friday: 8:30AM-5:00PM
• Salary: $39.42/ hour paid weekly with benefits options
• Employment Type: Contract 3-6 months

Environment: This client is a worldwide leading generic pharmaceutical company and one of the top 15 companies in the industry. With over 45,000 employees in 60 countries worldwide, they are proud to say that our employees are the reason for our success . They believe in empowering employees, presenting them with new challenges and letting them grow and develop professionally.

Overview:
The Scientist reports to the Quality Control & Analytical Product Development, Manager/Senior Scientist/Principal Scientist. The Scientist will be performing routine analysis of Finish products using laboratory techniques and instrumentation such as HPLC, Dissolution, Karl Fisher, pH meter. Analyst will perform Assay, Content Uniformity, Blend Uniformity, Moisture testing, related substances, dissolution on finish product.
Analyst will test In Process and FP samples and test stability samples at different ICH conditions.

Job Scope:

Performing tests and reporting data according to approved procedures.
Following internal methods, SOPs, procedures, and monographs for testing.
Conducting data review, data trending, and laboratory investigations as assigned.
Assisting other scientists to ensure timely project completion and supporting other lab personnel as needed.
Adhering to regulatory guidelines, SOPs, cGMPs, and laboratory procedures.
Perform Finish product Testing (Stability, development), QC release and data review.
Perform, Assay, related substances, KF, Dissolution, disintegration, Hardness.
Work on lab instruments (HPLC/GC/UPLC, KF, Dissolution, Hardness, disintegration).
Perform test and report data as per the Catalent approved procedures.
Analyst will follow the internal methods, SOPs, procedures, monographs to perform the testing.
Work on DEA controlled substance.
Conduct Laboratory investigation using the TrackWise system following SOPs and Procedures.
Perform Opex activities, data trending, SOPs revisions, as assigned.
Job Requirements:
Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience
Master of Science in Analytical Chemistry/Pharmaceutics preferred
3 or more years of applicable industry experience in support of pharmaceutical product development
Expertise in Instrumentation techniques: HPLC, GC, FTIR, UV, KF, and other wet chemistry testing.
Experience with GMP and ICH regulations
Requires excellent written and verbal communication
Candidate must be comfortable in a fast-paced work environment
Mathematical and reasoning ability
Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
Ability to work effectively under pressure to meet deadlines.
Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.

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