Viatis is a global healthcare company dedicated to delivering high-quality generic and branded medicines worldwide.
We strive to empower people to live healthier lives at every stage by offering innovative treatments at scale.
Role & What You Will Be Doing
The Quality Control (QC) Analyst I is responsible for wet chemistry analysis of raw materials, in-process, finished product and stability samples, and completing relevant GMP documentation.
This role will:
Perform routine wet chemistry testing of raw materials, in-process, finished product, and stability samples in compliance with GLP and cGMP procedures.
Sample raw materials, excipients, and water samples as required to assist the QC Sampling Technician.
Support validation programmes, including process and method validations.
Participate in department projects assigned by the QC Team Leader/QC Manager.
Contribute to continuous improvement initiatives such as 6S and lean processes for the laboratory.
Perform other duties as assigned.
About Your Skills & Experience
Bachelor's degree (or equivalent) in a science-related discipline, preferably chemistry, with 0-2 years relevant industrial experience (a combination of education and experience may be considered).
Strong analytical skills and excellent attention to detail.
Effective verbal and written communication skills with good time management.
A demonstrated ability to work as part of a team and communicate basic concepts.
Knowledge of basic/intermediate chemistry and proficiency with MS Office.
Ability to read and interpret general business documents and write routine reports.
Benefits
Competitive salary and bonus scheme.
Health insurance and pension plans.
Work-life balance initiatives and career progression opportunities.
Diversity and inclusion culture.
Viatis is an Equal Opportunity Employer.
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