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Bio-Chemist / QC Analyst (Chantilly, VA) at Granules Pharmaceuticals

Chantilly, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Aug, 26

Salary

0.0

Posted On

07 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC, UV-Vis, GC, FTIR, Dissolution Testing, Malvern Mastersizer 2000, Karl Fisher, Next Generation Sequencing, cGMP, cGLP, Empower, Microbiological Testing, USP/USP-NF

Industry

Pharmaceutical Manufacturing

Description

Description As a Biochemist / QC Analyst for Granules Pharmaceuticals Inc, you would be responsible for: Analyze bio-availability and bioequivalency of pharmaceutical products using next generation sequencing, UV-Vis, GC, FTIR; Identify and develop analytical Methods to compare dissolution profiles using cGMP/cGLP, Empower, HPLC, pH meter, dissolution and Malvern Mastersizer 2000; Coordinate and execute microbiological testing as per USP/USP-NF; Compile and analyze laboratory test data for physical, biochemical, chemical, and analytical testing using Dissolution Apparatus, Karl Fisher; Interpret test results and established specifications and control limits to ensure appropriateness of data for release; Analyze biochemical results. Requirements Must have a Master’s degree in Biotechnology, Biochemistry, Chemistry, Chemical Engineering, or Pharmaceutical Science Skills and knowledge of HPLC, UV-Vis, GC, FTIR, dissolution and Malvern Mastersizer 2000, Karl Fisher. This position is eligible for employee referral program. Submit résumé referencing job code AKK002 to HR, Granules Pharmaceuticals, Inc., 3701 Concorde Parkway, Chantilly, VA 20151.

Responsibilities

Analyze the bio-availability and bioequivalency of pharmaceutical products using various analytical instruments. Develop analytical methods and execute microbiological testing to ensure data appropriateness for product release.