Quality Control Analyst III

About the Company

Viatris is a global healthcare organization that brings together the strengths of both generic and branded medicines to better support healthcare needs around the world. Its purpose is to help people live healthier lives at every stage, and it supplies high-quality medicines to around 1 billion patients each year.

The company has appeared on a number of award lists reflecting its impact and reputation. Its portfolio includes established brand-name products, key global brands, generics, branded generics, and complex generics across many therapeutic areas. Viatris also supports healthier communities through education, outreach, and improved access to treatment.

People who want to work with purpose can find a collaborative environment at Viatris, where the culture is designed to encourage courage, resilience, and personal growth. The company positions itself as a place to contribute to meaningful global impact.

Role Overview

The Quality Control Analyst III is responsible for advanced chromatographic and wet chemistry testing of raw materials, in-process samples, finished products, and stability samples, along with the preparation and maintenance of the required GMP records and documentation.

Key Responsibilities

• Perform routine chromatographic testing, mainly HPLC and also GC, as well as wet chemistry analysis on raw materials, in-process samples, finished goods, and stability samples, while following GLP and cGMP requirements.
• Support the implementation and troubleshooting of analytical method transfers into the QC laboratory when needed.
• Lead or assist laboratory investigations, ensuring issues are documented, tracked, and resolved promptly; escalate out-of-specification results and initiate FARs within the required timeframe where applicable.
• Provide training support to other QC analysts in chromatography and wet chemistry techniques.
• Evaluate and approve chromatographic and non-chromatographic data.
• Act as a technical expert during third-party inspections when required.
• Contribute to laboratory improvement initiatives such as 6S and lean projects.
• Handle QC SOPs, change controls, deviations, and IRFs.
• Carry out calibration and maintenance tasks for wet chemistry and chromatography equipment.
• Take part in departmental projects assigned by the QC Team Leader or QC Manager.

Requirements

• A bachelor's degree, or an equivalent qualification, in a science-related field such as Chemistry, Biochemistry, or Analytical Science.
• At least 5 years of relevant industrial experience.
• Hands-on experience with HPLC, GC, and peptide analysis, including method validation and transfer; experience using Empower is essential.
• Strong understanding of chemistry and biochemistry techniques, especially chromatographic, wet chemistry, and peptide analysis methods.
• Well-developed technical writing skills.
• Working knowledge of Empower and other laboratory systems.
• Familiarity with cGMP environments and requirements.
• Good computer skills, including MS Office, TrackWise, Minitab, and LIMS.
• College-level mathematics ability.
• Ability to solve routine issues using established procedures and practical solutions, with limited need for judgment.

Benefits

• Competitive salary package.
• Opportunities for career progression.
• Support for work-life balance.
• Bonus scheme.
• Health insurance.
• Pension coverage.

Diversity and Inclusion

Viatris emphasizes an inclusive and authentic workplace and encourages candidates to apply even if their background does not match every listed requirement. The company states that diversity, equity, and inclusion are central to its mission.

Sustainability

Corporate social responsibility and sustainable operations are described as core parts of the company’s mission. Viatris also highlights its commitment to using its expertise to help people live healthier lives while considering the impact of its actions on stakeholders and communities.

Equal Opportunity

Viatris states that it is an equal opportunity employer.