Quality Control Research Associate - III

Quality Control Research Associate - III
  • $34.50 per Hour
    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.

DAY SHIFT AVAILABLE

Location: Santa Monica, CA

Description:

Responsibilities include, but are not limited to:

Description:

Description
Responsibilities
• 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.

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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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