Kindeva Drug Delivery
Supervisor, Quality Assurance -2nd Shift
Kindeva Drug Delivery, Des Moines, Iowa, United States
Supervisor, Quality Assurance - 2nd Shift
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Supervisor, Quality Assurance - 2nd Shift
role at
Kindeva Drug Delivery .
Location & Salary Bridgeton, MO | Salary: $113,740.00 - $153,549.00
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
Role Overview The Supervisor‑Quality Assurance plans and coordinates the activities of the Quality Assurance colleagues to support P&I production activities. The responsibilities include ensuring quality inspections are consistent with established standards and batch record requirements, adherence to SOPs and GMP regulations. The incumbent supervises QA employees and supports P&I on identification and resolution of issues.
Responsibilities
Supervision/coordination of duties such as AQL sampling, line clearances, label printing, product/component segregation, labeling, and batch record issuance on shift.
Assist P&I Supervisors in the resolution/identification of issues and escalation of critical issues to P&I and QA management.
Coordinate and approve changes to SOPs, specifications, and batch records (BRs).
Initiate ERs/QARs and Change Management as required.
Coordinate shift personnel activities—training, vacations, sick time—to ensure appropriate coverage in the QA department.
Handle personnel issues as they arise.
Ensure QA inspectors’ curriculum and training are up‑to‑date.
Maintain quality assurance objectives complementary to departmental and corporate procedures.
Maintain a working knowledge of government and industrial quality assurance codes and standards, including PQS, cGMPs, combination product regulations, and ANSI sampling plans.
Review and approve Packaging Batch Records and recognize product statuses such as Approved Hold, Rejected, etc.
Qualifications
Bachelor’s degree or Associate’s degree in a technical or science discipline and at least two years of experience and/or training; or equivalent combination of education and experience.
Supervisory experience in a pharmaceutical/combination product/medical devices manufacturing industry preferred.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Quality Assurance
Industries Pharmaceutical Manufacturing
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Supervisor, Quality Assurance - 2nd Shift
role at
Kindeva Drug Delivery .
Location & Salary Bridgeton, MO | Salary: $113,740.00 - $153,549.00
Our Work Matters At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.
Role Overview The Supervisor‑Quality Assurance plans and coordinates the activities of the Quality Assurance colleagues to support P&I production activities. The responsibilities include ensuring quality inspections are consistent with established standards and batch record requirements, adherence to SOPs and GMP regulations. The incumbent supervises QA employees and supports P&I on identification and resolution of issues.
Responsibilities
Supervision/coordination of duties such as AQL sampling, line clearances, label printing, product/component segregation, labeling, and batch record issuance on shift.
Assist P&I Supervisors in the resolution/identification of issues and escalation of critical issues to P&I and QA management.
Coordinate and approve changes to SOPs, specifications, and batch records (BRs).
Initiate ERs/QARs and Change Management as required.
Coordinate shift personnel activities—training, vacations, sick time—to ensure appropriate coverage in the QA department.
Handle personnel issues as they arise.
Ensure QA inspectors’ curriculum and training are up‑to‑date.
Maintain quality assurance objectives complementary to departmental and corporate procedures.
Maintain a working knowledge of government and industrial quality assurance codes and standards, including PQS, cGMPs, combination product regulations, and ANSI sampling plans.
Review and approve Packaging Batch Records and recognize product statuses such as Approved Hold, Rejected, etc.
Qualifications
Bachelor’s degree or Associate’s degree in a technical or science discipline and at least two years of experience and/or training; or equivalent combination of education and experience.
Supervisory experience in a pharmaceutical/combination product/medical devices manufacturing industry preferred.
Seniority Level Mid‑Senior level
Employment Type Full‑time
Job Function Quality Assurance
Industries Pharmaceutical Manufacturing
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