QA Inspector
at Viatris
Inverin, County Galway, Ireland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 02 Jan, 2025 | Not Specified | 03 Oct, 2024 | 1 year(s) or above | Consideration,Interpersonal Skills,Perspectives,Business Correspondence,Pension,Microsoft Office,Computer Skills,Health Insurance | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Mylan Teoranta
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 Inverin site with primary responsibility for incoming inspection of primary packaging components and maintenance of the stability/retain rooms. The role also requires assistance in Casla when required in performing incoming inspection of printed matter and line clearance duties.
Every day, we rise to the challenge to make a difference and here’s how the QA Inspector role will make an impact:
- Sampling and inspection of primary packaging components as per defined company procedures, including sending samples to external laboratories for analysis.
- Maintenance of the stability/retain rooms and assistance with the site routine stability program.
- Organisation and participation in the annual retain inspection program.
- Daily review of FMS printouts for the appropriate stability rooms.
- Participate in the cleanroom personnel observation program.
- Assistance in handling customer complaints (performing retain inspection when required).
- Provide QA approval of material, component and finished product reject labels.
- Update relevant SOPs as required.
- Deputise for QA Inspectors in Casla as required.
- Deputise for Packaging Coordinator as required in coordinating artwork activities
About Your Skills & Experience
For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:
- 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
- Computer skills (Microsoft office, excel etc…)
- Ability to follow prescribed and detailed procedures to solve routine problems.
At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.
Benefits at Viatris
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. Some of our benefits include the following on top of a competitive salary:
- Excellent career progression opportunities
- Work-life balance initiatives
- Bonus scheme
- Health insurance
- Pension
Diversity & Inclusion at Viatris
At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be. If you would like to know more about what diversity, equity and inclusion means to us, please visit
https://www.viatris.com/en/Careers/Diversity-and-Inclusion
Sustainability at Viatris
Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve. To learn more about our efforts, please visit
https://www.viatris.com/en/about-us/corporate-responsibility
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.
Responsibilities:
Every day, we rise to the challenge to make a difference and here’s how the QA Inspector role will make an impact:
- Sampling and inspection of primary packaging components as per defined company procedures, including sending samples to external laboratories for analysis.
- Maintenance of the stability/retain rooms and assistance with the site routine stability program.
- Organisation and participation in the annual retain inspection program.
- Daily review of FMS printouts for the appropriate stability rooms.
- Participate in the cleanroom personnel observation program.
- Assistance in handling customer complaints (performing retain inspection when required).
- Provide QA approval of material, component and finished product reject labels.
- Update relevant SOPs as required.
- Deputise for QA Inspectors in Casla as required.
- Deputise for Packaging Coordinator as required in coordinating artwork activitie
For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:
- 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
- Computer skills (Microsoft office, excel etc…)
- Ability to follow prescribed and detailed procedures to solve routine problems
REQUIREMENT SUMMARY
Min:1.0Max:2.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Testing
Trade Certificate
A pharmaceutical company
Proficient
1
Inverin, County Galway, Ireland