Quality Control Analyst - Novato - R&D Partners

    R&D Partners
    R&D Partners Novato

    1 day ago

    $48,000 - $82,000 (USD) per year *
    Description

    The QC Analytical Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. The Analyst works independently on assays they have mastered and performs advanced assays for multiple products. Work assignments will encompass performing and documenting activities and requires the ability to recognize deviations from approved procedures. Good record keeping, organizational, and written and verbal communication skills are essential. The Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide training and educational development of other staff.

    This is a 12-month contract based in Novato, California. Monday to Friday onsite schedule.

    Responsibilities

    • Performs, under minimal supervision, biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. General cGMP lab experience at the Analyst level.
    • Works independently on assays they have mastered.
    • Develops and maintains proficiency in a broad range of test methods.
    • Develops a technical understanding of each assay and assists with trouble shooting and laboratory investigations.
    • Evaluates data against defined criteria/specifications.
    • Actively applies knowledge in non-routine situations using a thorough understanding of the work processes and practices.
    • Identifies key issues in complex situations, analyzes problems, and makes sound decisions.
    • Assists in the revision of written procedures, method/equipment validation, and/or method transfers as assigned.
    • Mentors and trains other analysts, including new hires and more junior analysts, in areas of expertise.
    • Holds self and others accountable for adherence to department and company policies and practices.
    • Maintains a safety and quality focused culture.

    Qualifications

    • B.S./B.A. in Science in Chemistry, Biology, or Biochemistry.
    • 1-2+ years of Quality Control laboratory experience.
    • 1-2+ years of hands-on experience in separation sciences (HPLC, UPLC, CE).
    • 1-2 + years of experience in a cGMP/GLP laboratory.
    • Ability to follow written instructions and to perform tasks with direct or minimal supervision.
    • Strong leadership skills demonstrated through past work history.
    • Use of a computer: e.g., Proficient in Windows, Microsoft Word, Excel.
    • Good written and verbal communication skill.
    • Attention to detail and strong documentation skills.
    • Ability to contribute effectively in team environments and independently.
    • Equipment: Waters HPLC, Waters UPLC, Dionex HPLC, Sciex PA800, ProteinSimple iCE3, UV/VIS Spectrophotometer, pH Meter.

    Salary

    • $64,771-$80,974

    Why Choose R&D Partners?

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

    • Medical insurance – PPO, HMO & HSA
    • Dental & Vision insurance
    • 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.

    * This salary range is an estimation made by beBee
  • Work in company

    Quality Control Analyst

    Only for registered members

    The Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. · The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen, become a subject matter expert for regulatory inspections, and provide traini ...

    Novato

    2 weeks ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Analyst is responsible for the timely completion of lot release, · stability, · and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · Performs biochemical/physical/chemical analyses of tes ...

    Novato, CA

    6 days ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    ++ The QC Analytical Analyst is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in accordance with cGMP guidelines. · +Perform biochemical, physical, and chemical analyses of test samples ...

    Novato

    1 week ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Analyst is responsible for timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products under cGMP guidelines. · Performs biochemical/physical/chemical analyses of test samples. · Develops proficiency i ...

    Novato

    1 week ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Analyst performs biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. · Performs biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines. · Works independently on assays they have ma ...

    Novato

    6 days ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Analyst is responsible for timely completion of lot release, stability, · and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines.Performs biochemical/physical/chemical analyses of test samples under cGMP to ...

    Novato

    1 week ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Senior Analyst works independently on assays they have mastered and performs advanced assays for multiple products. The Senior Analyst is expected to demonstrate strong cGMP and compliance acumen and provide training and educational development of other staff. · ...

    Novato, CA

    2 weeks ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Analyst is responsible for the timely execution of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products in accordance with cGMP guidelines. · This role operates with minimal supervision and requires strong technica ...

    Novato, CA

    1 week ago

  • Work in company

    Quality Control Analyst

    Only for registered members

    The QC Analytical Analyst is responsible for the timely completion of lot release and stability testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.Performs biochemical/physical/chemical analyses of test samples under cGMP ...

    Novato, CA

    1 week ago

  • Work in company

    Senior Quality Control Analyst

    TalentBurst, an Inc 5000 company

    Title: Senior Analyst, Quality Control Analytical · Location: Novato, CA · Duration: 12+ Months · Summary: · The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical ...

    Novato

    1 day ago

  • Work in company

    Senior Quality Control Analyst

    Only for registered members

    The QC Analytical Senior Analyst under minimal supervision responsible timely completion lot release stability non routine testing pharmaceutical drug substances drug products adhering cGMP guidelines procedures. · Performs biochemical physical chemical analyses test samples unde ...

    Novato

    2 weeks ago

  • Work in company

    Senior Quality Control Analyst

    Only for registered members

    The Senior Quality Control (QC) Analytical Analyst is responsible for the timely execution of lot release, · stability, and non-routine testing of pharmaceutical drug substances and drug products in compliance with cGMP guidelines.Perform biochemical, physical, and chemical analy ...

    Novato

    2 weeks ago

  • Work in company

    Senior Quality Control Analyst

    Only for registered members

    The Senior Analyst, Quality Control Analytical is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · ...

    Novato

    2 weeks ago

  • Work in company

    Senior Quality Control Analyst

    R&D Partners

    The Senior Analyst, Quality Control Analytical is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. The Senior Analyst works independently ...

    Novato

    1 day ago

  • Work in company

    Senior Quality Control Analyst

    Only for registered members

    The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures.The Senior Analyst works i ...

    Novato

    2 weeks ago

  • Work in company

    Senior Quality Control Analyst

    Only for registered members

    The Senior Analyst, Quality Control Analytical is responsible for the rigorous execution of lot release, · stability and non-routine testing of pharmaceutical drug substances · and products under strict cGMP guidelines. ...

    Novato

    2 weeks ago

  • Work in company

    Senior Quality Control Analyst

    Only for registered members

    The QC Analytical Senior Analyst is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines and procedures. · Performs biochemical/physical/chemical analyses of ...

    Novato

    6 days ago

  • Work in company

    Senior Analyst, Quality Control Analytical

    Only for registered members

    The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, · stability,and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guidelines · and procedures. · Performs biochemical ...

    Novato

    2 weeks ago

  • Work in company

    Senior Analyst, Quality Control Analytical

    Planet Pharma

    -12 month contract · -Pay: $ /hr · SUMMARY · The QC Analytical Senior Analyst, under minimal supervision, is responsible for the timely completion of lot release, stability, and non-routine testing of pharmaceutical drug substances and drug products while adhering to cGMP guideli ...

    Novato

    1 day ago

  • Work in company

    Senior Analyst, Quality Control Analytical

    Only for registered members

    The QC Analytical Senior Analyst is responsible for the timely completion of lot release and testing of pharmaceutical drug substances and drug products under cGMP guidelines. The job involves working independently on advanced assays for multiple products with minimal supervision ...

    Novato

    2 weeks ago

Jobs
>
Quality control analyst
>
Jobs for Quality control analyst in Novato