Viatris

Plant QA Verifier I - 3rd Shift

Viatris San Antonio, Texas, United States

Pharmaceutical Manufacturing · 10,001+ employees

19 h ago
qa Junior (0-2 yrs) Full-time United States
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About the role

The Plant QA Verifier is responsible for performing quality reviews of manufacturing documentation and ensuring compliance with procedural requirements. They also monitor clean and use logbooks and manage QA holds for production equipment as necessary.

What they look for

Quality assurance Manufacturing documentation Compounding Cleaning verification Packaging verification Validation activities Equipment hold procedures Logbook monitoring Documentation review Safety compliance Environmental compliance SOP adherence Regulatory compliance

Requirements

Candidates must have a high school diploma or GED, with a preference for technical school certification. A minimum of 0-2 years of related experience in a pharmaceutical or regulated industry is required.

Benefits

Competitive salaries

Full description

DPT Laboratories, Ltd.

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of award lists that demonstrate the impact we are making.

Every day, we rise to the challenge to make a difference and here’s how the Plant QA Verifier I role will make an impact:

Key responsibilities for this role include:

  • Understand and execute procedural requirements for the QA verification of processes.
  • Issue and perform quality review of manufacturing documentation for Compounding, Cleaning and Packaging verification processes or validation activities.
  • Release and determine the need to place production equipment and/or utensils on QA hold as directed by procedure.
  • Issue and monitor the Clean and Use Logbooks for Manufacturing across all facilities.
  • Responsible for notifying QA Supervisor/Manager of any documentation discrepancies and/or requirements for QA Holds.
  • Within area of responsibility, understand and comply with all safety, environmental and quality practices and procedures as outlined in organizational/departmental guidelines and SOPs as well as applicable federal, state, and local regulations.
  • Perform other duties as assigned.

The minimum qualifications for this role are:

  • High school diploma or general degree (GED).
  • 1 year from college or technical school certification preferred.
  • Minimum 0 -2 years of related experience is required.
  • Pharmaceutical-Quality or other regulated industry experience preferred.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.

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