Quality Control Research Associate - III

Quality Control Research Associate - III
  • $34.50 per Hour
  • Temporary
  • Santa Monica CA, US Santa Monica LOS ANGELES US 90404
Job Ref: JO000130179
Sector: Science
Sub-sector: Science- Bio
Date Added: 11 April 2022

Job Title: Quality Control Research Associate Senior

1 year - Renewable Contract or potential for conversion

Onsite training and excellent benefits.


Location: Santa Monica, CA


Responsibilities include, but are not limited to:


• Under some guidance and supervision perform routine Raw Materials release testing by following established procedures as written.
• Participates as needed in the testing of raw materials by following analytical methods compendial methods and/or analytical procedures such as, pH, Osmolality, Conductivity, LAL, Identity, ELISA, Gel/Western Blot, FT-IR, HPLC, LC-MS, PCR, UV and Fluorescence spectroscopy, enzyme assays, microbiological assays and other applicable methods for the testing of Raw Materials and Reagents.
• Maintains instruments, by ensuring calibration and routine maintenance is performed in a timely manner.
• Leads laboratory OOS investigations, deviations, CAPAs and change controls, as assigned.
• Authors and revises Standard Operating Procedures.
• Compile data for trending or investigation purposes or conduct research in regulatory guidance and peer-reviewed journals.
• Performs GMP documentation with attention to detail.
• Gathering of documentation and data entry.
• Documentation and test record review.
• Keeps laboratory area clean and ensures waste is properly disposed.
• Keeps laboratory reagent and supply inventory.
• Supports the department with other duties as assigned.
Basic Qualifications
• Master’s Degree and 2+ years’ experience in biopharmaceutical or pharmaceutical industry OR
• Bachelor’s Degree and 3+ years’ experience in biopharmaceutical or pharmaceutical industry
Preferred Qualifications
• Strong understanding and experience operating within an GMP environment.
• Working knowledge and understanding of analytical techniques to include HPLC, LC-MS, FACS, ELISAs, PCR, FTIR, UV and Fluorescence spectroscopy, Gel/ Western Blot, enzyme assays, microbiological assays, and other applicable methods to the testing of Raw Materials and Reagents within an GMP environment.
• Preferred, experience leading OOS’s, CAPAs, change controls, deviations and laboratory investigations.
• Preferred, knowledge of current Good Manufacturing Practices (cGMPs), GxP, pharmacopoeia, and regulatory requirements for testing pertaining to the pharmaceutical industry.
• Preferred, Knowledge of aseptic technique and previous experience with cell culture.
• Exceptional attention to detail and ability to keep track of multiple ongoing projects
• Experience writing, reviewing, or executing standard operating procedures, protocols, and reports.
• Ability to perform duties with minimal supervision and be adaptable to a dynamic and fast-paced environment
• Excellent interpersonal and organizational skills
• Strong project and time management skills.
• Excellent oral and written communication skills
• Proficiency in MS Word, Excel, Power Point and other applications

SRG is an Equal Opportunity Employer - All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.


SRGTalent https://www.srgtalent.com https://www.srgtalent.com/-/media/srg/1---new-website/logos/website-logo-all-padding-removed.png
26/05/2022 12:00:00
USD 34.50 34.50 Hour
Contact Consultant:
Sam Royall

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