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Plant QA Verifier I - 3rd Shift

Viatris
Posted 2 days ago, valid for 13 days
Location

San Antonio, TX, US

Salary

Competitive

Contract type

Full Time

By applying, a Viatris account will be created for you. Viatris's Privacy Policy and Terms & Conditions will apply.

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Sonic Summary

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  • DPT Laboratories, Ltd. is seeking a Plant QA Verifier I to ensure quality assurance processes in manufacturing.
  • Candidates should have a high school diploma or GED, with 0-2 years of related experience, preferably in pharmaceutical quality or a regulated industry.
  • The role involves executing QA verification procedures, reviewing manufacturing documentation, and monitoring compliance with safety and quality guidelines.
  • Viatris offers competitive salaries and benefits in an inclusive environment aimed at making a global healthcare impact.
  • The position emphasizes the importance of quality assurance in providing access to high-quality medicines for approximately 1 billion patients annually.
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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By applying, a Viatris account will be created for you. Viatris's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.