QC Analyst I

Novato, CA 94949

Posted: 06/25/2019 Employment Type: Contract Industry: Clinical & Scientific Job Number: 15965

Bayside Solutions is seeking a QC Analyst I to be part of our client’ s team in Novato. This is an opportunity to work with the largest privately held pharmaceutical corporation in the world and ranks among the world' s 20 leading pharmaceutical corporations.

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 Analyst I

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:
  • Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with department procedures.
  • Organize, maintain, track and archive department documents and records while adhering to the document lifecycle procedures and in accordance with the records retention schedule.
  • Execute select microbiological and/or analytical methods to facilitate in-process testing under applicable cGMP guidelines, as well as contribute to the prompt reporting of results to meet the required timetables of internal customers.
  • Evaluate completed assay validity, calculate and summarize results, analyze data per expected or specification ranges. Assist with the compilation and verification of trend analysis reports.
  • Perform and collaborate with co-workers to appropriately share general housekeeping activity assignments, and ensure systems for laboratory maintenance are adequate for creating a consistent state of inspection readiness.
  • Assist with monitoring and the control of laboratory supply and critical reagent inventories.
  • Provide on call coverage for action level conditions to support oversight of QC laboratory equipment functionality.
  • Exhibit proactive communication upon occurrence of compliance risks and deviations from laboratory procedures, perform initiation of investigation records within required timeframes.
  • Perform other responsibilities as deemed necessary.

Summary of Qualifications:
  • Bachelor of Science in a Biological or Biochemical Science with at least 0-2 years of relevant laboratory experience
  • The QC analyst should have the ability to prioritize, manage time well, multitask and troubleshoot. Strong interpersonal, communication and customer service skills are also essential because the QC analyst will regularly communicate with internal and external business partners.
  • Must have excellent record keeping, written and verbal skills.
  • Ability to perform most tasks without supervision.
  • Experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices is a plus.
  • Able to lift up to 25lbs
  • Computer literacy is required, proficiency with Microsoft Word and Excel is essential.
  • Must have excellent record keeping, written and verbal skills.
  • Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or laboratory process requirements.

Allison Glogovac

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