QA Specialist II

Quality Talent Group

  • Penryn, Pennsylvania
  • 7 days ago

    Highlights

    This is a global organization in the consumer health and personal care industry , with 135+ years of heritage , 22,000+ employees , and a presence across 100+ countries . A minimum of 2 years of GMP experience in either Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production.

    Numbers & Facts

    LocationPenryn, Pennsylvania

    Description

    Overview:

    Recognized in 2024 by Seramount as one of the 100 Best Companies for Working Parents and Caregivers, the company also earned a place on the 2024 US Inclusion Index and Global Inclusion Index across 7 countries - Brazil, Canada, China, Germany, India, Japan, and the UK.

    This is a global organization in the consumer health and personal care industry, with 135+ years of heritage, 22,000+ employees, and a presence across 100+ countries. Its portfolio includes iconic consumer health and personal care brands used by millions of people worldwide.

    Benefits:

    • Competitive benefits package.
    • Paid time off.
    • Health insurance benefits, including coverage for doctor visits and mental health care.
    • Retirement program.
    • Employee Assistance Program (EAP) and mental well-being resources.
    • Global exercise/well-being reimbursement.
    • Adoption, fertility, and surrogacy benefits.
    • Global parental leave.
    • Paid company holidays and volunteer time.
    • Learning and development opportunities.

    Qualifications

    • A minimum of a Bachelors Degree
    • A minimum of 2 years of GMP experience in either Pharmaceutical, Medical Device, OTC Drug, Cosmetic and/or Food and Dietary Supplements Production.
    • Basic working knowledge of cGMP requirements and current FDA enforcement issues.
    • Ability to communicate thoughts and ideas effectively – verbal and written.
    • Demonstrated ability to accomplish work goals

    Responsibilities

    • Perform quality review of production records including manufacturing, packaging, and laboratory documents.
    • Responsible for releases of finished product based on conformance to established standards.
    • Apply quality assurance processes, procedures, and activities.
    • Conduct walkthroughs and assessments of GMP areas.
    • Partner with Operations to address quality/compliance issues and improvements.

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