Analytical Chemist 319

Largo, FL

Posted: 03/29/2019 Industry: Chemist Job Number: JN -032019-10581
ANALYTICAL (Validation) CHEMIST- PHARMACEUTICAL:

2nd shift-3PM to 11PM


SRG Life Sciences offers the industry flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services in the clinical, manufacturing, medical and scientific fields. Through our innovative approach and proprietary database of over one million professionals, SRG Life Sciences offers ready access to the talents that drive today's rapid paced and competitive landscape. Additionally, SRG Life Sciences has a proven track record of placing cross-functional roles such as Information Technology, Accounting and Finance, Engineering, Professional and Government Services for our Life Sciences clients.

KEY WORDS: Analytical, Compendia, USP, Validation, transfer, method validation, cleaning, OOS (out of spec) and CAPA, GMP, GLP, HPLC and GC

Title: ANALYTICAL CHEMIST
Location: Tampa Bay Area, FL
Industry: Pharmaceutical
Department: Quality

Job Summary / Overview:

Analytical Validation Chemist will support the Quality department to ensure continuity in the laboratory utilizing HPLC, GC, and AA.

Key Duties & Responsibilities:
  • Perform all of the activities for transferring and validating analytical methods.
  • Revise and write Test Methods and SOP s.
  • Testing of incoming materials, in process samples and finished product testing.
  • Accurately records raw data and analyzes, as well as calculates and interprets the results.
  • Responsible for out of specification test results, investigation and implementation of corrective actions.
  • Ensure testing is performed accurately and in compliance with GLP, GMP, USP, SOP and other approved test methods
  • Maintain analytical reagents in laboratory including but not limited to: inventory, current MSDS, PPE required for handling, waste generation and disposal.
  • Assist Validation teams in cleaning validation activities.
  • Promote GMP and safety throughout the facility.
  • Promote continuous improvement and customer satisfaction.
  • Follow-up on OOS s and CAPAs to verify compliance
  • Potential exists for exposure to potentially harmful chemicals
MUST HAVES:
  • Bachelor s degree with 2 years of relevant experience
  • Must have experience within FDA regulated industry
  • Must have HPLC, GC experience
  • Experience with USP/Compendia
  • Experience with Method Transfer & Validation
  • May require lifting up to 50lbs
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