QA Inspector
تفاصيل الوظيفة
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. Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment. For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world. The Role & What You Will Be Doing The QA Inspector is required to act as the QA representative on the Casla site with primary responsibility for ensuring the routine packaging operation on the site is conducted following GMP guidelines and according to site procedures. The role also requires performing incoming inspection of printed matter according to defined procedures. Every day, we rise to the challenge to make a difference and here’s how the QA Inspector role will make an impact:
- Perform line clearance and provide line approval to start the packaging operation for the vial and syringe lines according to defined procedures as required in a timely manner.
- Perform line clearance/line approval of other areas to defined procedures as required in a timely manner.
- Perform incoming inspection of printed/non-printed matter according to defined procedures.
- Perform inspection of packaged product (AQLs) as per defined procedures.
- Reporting any GMP issues to the QA Team Leader/ Senior QA Manager as observed and required in a timely manner.
- Obtaining samples for Inverin as requested/required.
- Act as QA representative for the pest prevention program in Casla.
- Minimum of a Leaving Certificate level with 1- 2 years’ experience within a Pharmaceutical Company. However, a combination of experience and/or education will be taken into consideration.
- Ability to solve practical problems through standardized solutions that require limited judgment.
- Excellent attention to detail
- Ability to read and interpret general business documents. Ability to write routine reports and general business correspondence. Ability to work with peers and communicate basic concepts.
- Excellent communication and interpersonal skills.
- Self-starter with demonstrated efficient work methods and excellent initiative.
- Team player
- Ability to follow prescribed and detailed procedures to solve routine problems.
- Excellent career progression opportunities
- Work-life balance initiatives
- Health insurance
- Pension
About Us
Viatris is a global healthcare company formed in 2020 through the combination of Mylan and Upjohn, a legacy division of Pfizer. By integrating the strengths of these two companies, including our global workforce of ~45,000, we aim to deliver increased access to affordable, quality medicines for patients worldwide, regardless of geography or circumstance. We believe in healthcare as it should be – empowering people worldwide to live healthier at every stage of life. Because of our unwavering belief that better access leads to better health, we leverage our best-in-class manufacturing and scientific expertise and proven commercial capabilities to bring quality medicines to patients when and where they need them. #J-18808-LjbffrApply safely
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