Quality Control Associate III, HPLC

Fremont, CA 94555

Posted: 10/19/2020 Employment Type: Contract Industry: Clinical & Scientific Job Number: 18060

Job Description

Bayside Solutions is seeking a Quality Control Associate III, HPLC to be part of our client’ s team in Fremont. This is an opportunity to work with one of the largest Biopharmaceutical companies in the world developing innovative medicine to improve the quality of patients’ lives.

Our Client’ s culture is highly collaborative, offers an environment that encourages employees to expand their knowledge in order to make a profound impact on patients’ lives. This could explain why their company has been recognized as one of the “ Top Twenty Employers” in biotechnology and pharmaceuticals by Science Careers.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

QC Associate, HPLC

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.  
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Under supervision, performs HPLC/CE testing, conducts lab investigations, problem solves and reports aberrant results to management.
  • Performs Titer, CEX, SEC, PS80, Peptide Map, Oligo, HIC, and CE assays.
  • Ensures IPC testing, stability and release timelines are met.
  • Follows well-defined and established procedures and best practices.
  • Reviews QC test results.
  • Generates, reviews, and/or maintains records or documents in a detailed and consistent manner.
  • Prepare, execute and complete all documentation in accordance to procedures.
  • Assists with QCs data management, including data review of control charting, retrieving documents.  
  • Assists in general laboratory activities including receiving and sorting of incoming chemicals/reagents required for testing.

Required Qualifications:
  • Bachelor' s or Master’ s Degree in Chemistry, Biology, or a related field.
  • Industry experience performing the assays mentioned, in biotech and/or pharmaceutical labs is required. 
  • Knowledge of SAP, Trackwise and LIMS desired.
  • Working knowledge of Microsoft Office systems, LIMS, lab instrumentation and other relevant systems
  • Highly productive, attention to detail, ability to manage time and prioritize tasks with input from manager to meet time lines.
  • Demonstrated problem-detection and problem-resolution skills required
  • Lifting, carrying, pushing or pulling up to 50 pounds occasionally
  • Frequent periods of sitting, walking, and standing
  • Occasionally must climb stairs or ladders, balance, bend or stoop, crouch or squat
  • Occasional low level work, fine finger dexterity/ including grasping or pinching required
  • Writing and use of a computer keyboard frequently
  • Occasional use of personal protective equipment
  • Visual / Hearing Demands: Color vision and depth perception required. May require extended hours at a computer screen. Hearing acuity required.

Meet Your Recruiter

Allison Glogovac

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