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  • Sr Quality Control Chemist

    Actalent (Eugene, OR)



    Apply Now

    Sr QC Chemist

    * Relocation offered - Shift: 8-5/8:30-5:30 M-F *

    Occasionally weekend work required (delay in production, in-process sample coming – rare)

    2 facilities, 10 minutes apart

    MUST HAVE:

    + Bachelor’s degree in Chemistry, Biochemistry, or related scientific discipline (Master’s or Ph.D. preferred).

    + Minimum of 7 years of experience with a bachelor’s degree, 5 years with a master’s degree or 1 year with a PhD in a QC laboratory within the pharmaceutical, biotechnology, or chemical industry, with at least 3 years in a leadership role.

    + Strong knowledge of analytical techniques such as GC, HPLC, KF, FTIR, water content, UV-Vis, titration, wet chemistry, analytical balances, and pH meters,

    + Know how to validate or qualify pharmaceutical test measures (Med device) – test or chemical radiance (small molecules)

    + Expedience from large molecules and validation

    + Tested drug products for API

    + Experience writing reports & SOPs

    + Testing and validating at the same time

    + GMP experience

    Description

    We are seeking a highly skilled and experienced Quality Control Chemistry Manager to lead and oversee the QC Chemistry team. This role is responsible for ensuring the integrity, accuracy, and compliance of all chemical testing activities in support of manufacturing and product release. The ideal candidate will bring strong leadership, technical expertise, and a deep understanding of cGMP regulations within a pharmaceutical or life sciences environment.

     

    Independent execution of various standard laboratory techniques, including but not limited to HPLC, LC/MS, GC, GC/MS, FTIR, KF, LOD, and appearance assessment

     

    Independent preparation of samples, solutions, instrument set-up and breakdown

     

    Lead the transfer of analytical methods to QC from internal and external sources

     

    Analysis of various sample types with approved prescribed test methods

     

    Provide guidance and support on day-to-day tasks to QC personnel

     

    Represent the Quality Control Department on internal and external matters as requested by QC Manager

     

    Independent authoring, reviewing, and execution of analytical method validation protocols

     

    Lead internal meetings as requested

     

    Independent authoring, reviewing, and execution of stability study protocols

     

    Independent preparation of data packets, stability reports, and certificates of analysis to summarize analytical testing

     

    Participation in, or lead, Out of Specification investigations and the documentation of analytical deviations along with qualified investigators and management

     

    A working knowledge of QC laboratory operating under US FDA/EU GMPs

     

    Provide mentorship to co-workers as needed.

     

    Skills

     

    Quality control, Hplc, Gmp, pharmaceutical, gc-ms, gcms, lc-ms

    Experience Level

    Intermediate Level

    Pay and Benefits

    The pay range for this position is $43.00 - $60.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

    • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Eugene,OR.

     

    Application Deadline

     

    This position is anticipated to close on Aug 7, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.

     


    Apply Now



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