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 (QC Finished Products Analyst) role will make an impact:
Position summary:Conduct routine and non-routine analysis and relevant documentation and reporting.Performance of lab-related tasks.Job Specific technical/Functional/Professional Competencies:
Conduct routine and non-routine analysis of in-process materials, finished goods, or stability samples in a timely manner.Conduct chemical or physical laboratory tests in making qualitative or quantitative analysis.Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release.Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms.Calibrate, validate, and maintain laboratory equipment.Report and investigate questionable test results.Participate in out-of-specification and failure investigations and recommend corrective actions.Supply quality control data necessary for regulatory submissions.Perform data entry and trend analysis.Prepare and execute SOPs, calibration, and validation documents (IQ, OQ & PQ) related to chemical laboratory tasks.Implement Viatris Policies’ requirements regarding the chemical laboratory.Use, monitor, and control Reference standards inventory and expiry.Use, monitor, and control expiry and inventory of laboratory stock items including reagents, glassware, filters, etc.Perform Data loggers monitoring, downloading, and reviewing.Write and review Quality Control SOP’sWork to improve process by implementing lean and 6σ projects.Responsible to implement Data integrity principals in relevant work area and insure following up ALCOA+ principles all over operations.Responsible to comply with Viatris Quality Standards.cGMP & cGLP knowledge is preferred with particular emphasis on Quality Control.Knowledgeable with basic Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.Responsible to ensure that all results generated follow data integrity requirements.Responsible to raise “NTM” Notification to Management whenever condition in Viatris policies applies.Experience and Knowledge
Good command of English in both written and spoken.Excellent in Microsoft office (word, excel & PowerPoint)Knowledgeable with interpersonal, good communication and presentation skills.cGMP & cGLP knowledge is preferred with particular emphasis on Quality Control.Knowledgeable with Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.Essential Personal Qualifications
Bachelor’s degree in pharmacy or science.1-3 years’ experience in a related area.Demonstrated ability to work independently.Excellent documentation and technical writing skills.Able to work in a team with an effective manner, interact with various priorities and meet deadlines.Active, organized and planner with high attention to details.High observation skills.Self-motivated.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.