QC Associate Scientist

West Chester, PA

Posted: 01/27/2020 Job Number: JN -012020-11354

Job Description

QC Associate 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: QC Associate Scientist
  • Location: West Chester, PA
  • Industry: Pharmaceutical
  • Salary: $23.00 hour-$26.00 hour based on experience
  • Shifts Available: Monday- Friday: 8am-5pm
  • Employment Type: Contract, up to one year contract
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. Isn t this the type of company you want to work for?

Overview
This position contributes to the successful timely sampling, inspection and releasing testing of raw materials and components, intermediates, in-process and drug substance of GMP clinical pharmaceutical manufacturing. Individual functions with supervision as an Associate Scientist and is actively engaged in analytical activities within a dynamic QC project team.
Responsibilities
  • Perform compendial testing (appearance, pH, osmolality, protein concentration, etc.) in support of release samples and in process testing.
  • Record data per GxP requirements. Provide peer review of documentation as needed.
  • Perform environmental monitoring and raw materials testing as requested.
  • Assist with sample maintenance as requested.
  • Participate in the writing/editing of standard operational procedures, forms and reports and data archiving as requested.
  • Maintain compliance with applicable ICH, GLP, GMP and safety regulations. Notify management of unexpected results, procedural deviations and equipment problems.
  • May participate in laboratory investigations.
  • May perform non-compendial analytical testing (e.g., chromatography HPLC, UPLC).
  • Maintain a collaborative working relationship with QC staff and other departments (Quality Assurance, Analytical Development).
  • Actively contribute to the maintenance of a clean, safe working environment in the laboratories
Requirements
  • B.S. in Chemistry, Biology, Microbiology, or related sciences with 1-3 years of related experience with raw materials, in-process and finished product testing
  • Pharmaceutical experience is highly preferred or closely related industry along with HPLC experience
  • Accurately and completely records experimental procedures, test results, and observations to meet corporate and cGMP requirements
  • Good understanding and application of scientific principles and techniques.
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
  • Ability to work effectively and diligently to meet deadlines.
  • Highly organized and motivated, have strong communication and presentation skills and the ability to multi-task, collaborate and work within a team environment.
  • Preparation of reagents/standards/medias as needed for analysis according to established methods
EOE/ADA
Search words: Scientist, Chemist, QC, Quality Control, raw materials, in-process, finished products, pharmaceuticals
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