Quality Control Coordinator - Process Control

Full Time

    Job Description

    Job#: 1317988

    Job Description:

    Rapidly growing pharmaceutical company in Phoenix is looking to hire a Quality Control Coordinator in our Process Control department. We are expanding our workforce to keep up with production needs and are looking for quality, talented team members to join our team!

    This position will be working during the day on first shift and start as soon as a qualified candidate is identified. Join our team now and expand with our company as we grow!

    Position Summary:

    Ensure and assist with site-specific quality compliance according to Standard Operating Procedures (SOPs) & specifications, quality review of documents, label control, assist with raw material and final product release, batch record review, and product inspections.

    We value attention to detail as well as a strong efficiency and will teach you ways to accomplish both!

    Essential Duties/Responsibilities:

    Manufacturing area:
    • Perform product inspection for defects, leaks and particulates.
    • Perform environmental monitoring of personnel (as needed) and complete documentation.
    • Assist in the manufacturing validations
    • Perform document review of activities such as cleaning records, line clearance forms and inventory sheets:
      • Verify that raw materials meet specification
      • Verify and account for labeling
      • Review temperature and BMS alarms
      • Verify that product test results meet specification limits
      • Verify that all documentation is complete
      • Document non-compliance and work with supervisor/lead if further investigation is needed
    • Submit samples to the appropriate lab for particulate identification or microbial analysis.
    • Assist with equipment calibration program and maintenance record files.
    • Assist with raw material release and movement.
    • Under the direction of supervisor/lead, document and initiate quality events for deviation and complaint investigations.
    • Support internal & external audits.
    • Maintain quality records (equipment calibration and maintenance, training, deviation and complaint investigation, environmental monitoring, Certificate of Analysis, clean room certification etc.).
    • Participate in Quality Manager's staff meetings

    Qualifications - Experience/Training/Education/Certification/Etc:

    • Minimum of BS degree with work experience.
    • Minimum of 2 years' experience in a quality or manufacturing department of a pharmaceutical, Medical Device or related industry

    • Experienced in laboratory or aseptic operations.
    • Experience within a regulated environment
    • Progressive experience and responsibilities in a regulated industry

    Pay rate is $25.75/hour, eligible for OT pay

    Apply today for immediate consideration to phoenix@apexlifesciences.com

    EEO Employer

    Apex Systems is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at employeeservices@apexsystems.com or 844-463-6178.