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Quality Control Analyst (Entry Level)

R&D Partners
Novato, CA Temporary
POSTED ON 2/25/2025
AVAILABLE BEFORE 5/23/2025

Pharmaceuticals company is hiring a Quality Control Analyst to assist with testing of incoming samples and in-process testing under GMP guidelines. This is a 12-month contract.

Schedule :

  • Wednesday-Saturday 1 : 00pm-midnight
  • Seeking a candidate who is open to being flexible to switching shifts if necessary.
  • Early notice would be provided in the event a switch becomes needed.

Responsibilities

  • Timely facilitation of incoming sample receipt and accessioning flow, decipher batch assignments across all assay types in accordance with agreed upon best practices.
  • Execute microbiological and 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.
  • Perform environmental monitoring sampling and testing of facilities, equipment, and utilities.
  • 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.
  • Perform growth promotion of media and microbial identification testing.
  • Qualify as trainer for specified methods, provide training to less experienced staff.
  • Provide on call coverage 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.
  • Provide input or assay support to the progression of test method validation, investigations, technical studies, and method transfer protocols.
  • Attend team huddles and department meetings, generate ideas for laboratory infrastructure improvements and method optimization.
  • Qualifications

  • Bachelor of Science degree
  • 0-3 years of relevant laboratory experience; QC specific experience is preferred.
  • Experience with quality management systems, current Good Manufacturing Practices, and QC principles.
  • Demonstrated working knowledge with respect to certified functional activities.
  • Good documentation, written and verbal communication skills are essential.
  • Must possess the ability to perform most tasks with minimal supervision.
  • Computer literacy is required, proficiency with Microsoft Word and Excel is essential, experience with Microsoft PowerPoint, Access, or Visio is desired.
  • Must have a quality service attitude and focus, exhibit flexibility and willingness to work additional hours to meet production or laboratory process requirements.
  • Salary

  • 46,592-$58,240
  • Why Choose R&D Partners?

    As an employee, you have access to a comprehensive benefits package including :

  • Medical insurance, Dental and Vision insurance
  • Sick Pay
  • 401k plan
  • Employee Assistance Program
  • Long-term disability
  • Weekly payroll
  • Expense reimbursement
  • Online timecard approval
  • R&D Partners is a global functional service provider and strategic staffing resource specializing in scientific, clinical research & engineering. We provide job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

    R&D Partners is an equal-opportunity employer.

    Salary : $46,592 - $58,240

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