• 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 stability & method validation testing and the corresponding documentation to support the timely disposition of product.
• 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.
• Write technical reports or prepare graphs or charts to document experimental results.
• Participate in out-of-specification and failure investigations and recommend corrective actions.
• Supply quality control data necessary for regulatory submissions.
• Investigate or report questionable test results.
• Manage stability chambers.
• Perform Data loggers monitoring, downloading, and reviewing.
• Work on improving his/her process by implementing lean and 6 projects.
• Ensure that all results generated follow data integrity requirements and following ALCOA principles all over operations.
• Comply with all Viatris Quality Standards and procedures.
• Knowledgeable with basic Laboratory instruments such as pH, Spectrophotometry, HPLC and reagent preparation.
• Raise Notification of critical quality events to Management whenever condition in Viatris policies applies.
• Support Supply department by sending stability samples on time, evaluation of stability results and taking any immediate actions required in addition to archive of these results for toll manufacturing products.
• Create/review of stability schedule, protocols, reports, and trends.
• Follow up stability equipment calibration & maintenance and ensure appropriate documentation and archiving.
• Maintain laboratory supplies inventory required for Stability analysis.
• Handle the global changes affecting stability and methodology.
• Support QA with all CCRs and Deviations related to Stability & Methodology.
• Perform all method validation activities required.
• Create/review of method validation protocols and reports.

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, interact with various priorities and meet deadlines.
• Active, organized and planner with high attention to details.
• High observation skills.
• Self-motivated and able to consistently meet timelines.

At Viatris, we offer competitive salar ies , 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.