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Senior Specialist QC Investigations - 1st Shift

Viatris
United States, Vermont, St. Albans
Aug 11, 2025
Mylan Technologies, Inc.

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

  • Access - Providing high quality trusted medicines regardless of geography or circumstance;

  • Leadership - Advancing sustainable operations and innovative solutions to improve patient health; and

  • Partnership - Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here's how the Senior Specialist QC Investigations - 1st Shift role will make an impact:

Key responsibilities for this role include:

  • Leads investigations of incidents, aberrant results, and trends. Propose associated CAPA actions and prepare associated investigation reports.

  • Interacts with QC department personnel and cross functional teams in support of investigations.

  • Prepare periodic reports as assigned.

  • Compile and analyze investigation information. Present to local and vertical leadership as required.

  • Supports and executes department CAPA as assigned.

  • Leads periodic and special cause trending assessments to determine corrective actions to address trends.

  • Supports continuous improvement project teams and help propose strategies and tactics for accomplishing objectives.

  • Authors quality documentation including SOPs, specifications, STMs, and change controls.

  • Assists in preparing documentation supporting regulatory submission of post approval changes.

  • Participate on project teams as assigned.

  • Prepares and provides training related to investigations, site procedures, and cGMP as assigned. Provides training of laboratory personnel in aspects of the laboratory quality system.

The minimum qualifications for this role are:

  • Minimum of a bachelor's degree (or equivalent), 4+ years of relevant experience, and a fundamental understanding of Quality Systems, Quality Control laboratory, and cGMP. A combination of experience and/or education will be taken into consideration.

  • Must possess a working knowledge of Pharmaceutical cGMP, Quality Systems, and analytical chemistry. Must understand the cGMP standards for the investigation of aberrant results and the contents of investigation reports.

Exact compensation may vary based on skills, experience, and location. The salary range for this position is $55,000 - $105,000.

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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