QA Engineer

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  "last_changed_at": "2026-06-05T01:11:29.626Z",
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  "language": "en",
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    "raw": "At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?\n There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.\n We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.\n Job Summary \r This role provides quality oversight of plant operation and laboratory processes to ensure adherence to cGMP requirements, regulatory requirements, corporate policies and established procedures. This position is responsible for promoting and maintaining regulatory standards compliance, supporting continuous improvement initiatives, and driving data integrity programs to strengthen quality systems and operational excellence.\n Essential Duties and Responsibilities\n Support in maintaining compliance with cGMP standards within the laboratories.\n Provide GMP support for activities such as method validation, method transfer, instrument qualification, and verification of compendial test methods.\n Provide technical guidance on calibration of analytical instruments, validation of Excel spreadsheets, and implementation of computerized systems.\n Perform data audits and periodic reviews of laboratory test results, electronic raw data, laboratory notebooks, computerized systems, and Excel spreadsheets to ensure compliance and data integrity.\n Oversee proper administration and timely completion of cGMP processes, including\n On-time review of procedures\n Guide internal and external audits, including audit CAPA tracking and on-time completion\n Oversight of OOS and Deviations to ensure compliant and timely closure\n Provide training on GMP-related topics\n Provide GMP support to ensure proper completion of instrument qualifications, change control, method transfers, etc.\n Support and drive data integrity initiatives in collaboration with global teams.\n Perform annual product review.\n Involve in A3 investigations, root cause analysis, CAPA management and CAPA effectiveness. Ensure CAPA",
    "city": "At West",
    "region": null,
    "country": "United States",
    "is_remote": false,
    "confidence": 0.95
  },
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  "inferred_at": "2026-06-06T13:46:55.062Z",
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    "language": "en",
    "location": {
      "raw": "At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?\n There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.\n We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.\n Job Summary \r This role provides quality oversight of plant operation and laboratory processes to ensure adherence to cGMP requirements, regulatory requirements, corporate policies and established procedures. This position is responsible for promoting and maintaining regulatory standards compliance, supporting continuous improvement initiatives, and driving data integrity programs to strengthen quality systems and operational excellence.\n Essential Duties and Responsibilities\n Support in maintaining compliance with cGMP standards within the laboratories.\n Provide GMP support for activities such as method validation, method transfer, instrument qualification, and verification of compendial test methods.\n Provide technical guidance on calibration of analytical instruments, validation of Excel spreadsheets, and implementation of computerized systems.\n Perform data audits and periodic reviews of laboratory test results, electronic raw data, laboratory notebooks, computerized systems, and Excel spreadsheets to ensure compliance and data integrity.\n Oversee proper administration and timely completion of cGMP processes, including\n On-time review of procedures\n Guide internal and external audits, including audit CAPA tracking and on-time completion\n Oversight of OOS and Deviations to ensure compliant and timely closure\n Provide training on GMP-related topics\n Provide GMP support to ensure proper completion of instrument qualifications, change control, method transfers, etc.\n Support and drive data integrity initiatives in collaboration with global teams.\n Perform annual product review.\n Involve in A3 investigations, root cause analysis, CAPA management and CAPA effectiveness. Ensure CAPA",
      "city": "At West",
      "region": null,
      "country": "United States",
      "is_remote": false,
      "confidence": 0.95
    },
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      "United States"
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  "salary_period": "day",
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}

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