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Viatris

QC Analyst Biologics (12 month agency contract)

Posted 16 Days Ago
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In-Office
Baldoyle, Dublin
Mid level
In-Office
Baldoyle, Dublin
Mid level
The QC Analyst Biologics will test bioanalytical methods, participate in method transfers, troubleshoot issues, and ensure compliance with quality standards in a GMP lab setting.
The summary above was generated by AI
McDermott Laboratories Limited

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

Every day, we rise to the challenge to make a difference and here’s how the QC Analyst Biologics (12 month agency contract) role will make an impact:

  • Testing of Bioanalytical test methods for a range of biological pharmaceutical products (used for treatment of cancer, diabetes and ocular disease).

  • Participate in Analytical Method Transfer/Validation to the Bioanalytical laboratory from global transferring laboratories.

  • Knowledge and experience in some or all the following: different analytical methods, e.g. HPLC techniques (i.e. Ion Exchange Chromatography, Reverse phase HPLC, Size Exclusion Chromatography), UV Visible Spectrophotometry, Capillary Electrophoresis-SDS, ELISA and Western Blot.

  • Protocol and report generation and review for method transfer / validation studies.

  • Troubleshooting complex problems and presenting findings to various stakeholders.

  • Partake in cross functional training through creation of training material and providing training to other team members.

  • Perform laboratory investigations to determine root cause and implementation of appropriate corrective and preventative action (Trackwise).

  • Review of Bioanalytical data to a high-quality standard and adhering to ALCOA practices at all times.

  • Ensure that all laboratory operations are carried out in compliance with EHS, cGMP and regulatory commitments.

  • Participate in risk assessments, inspections, audits, incident investigations, etc. and implement and follow-up on corrective / preventative measures.

  • Maintain data integrity and ensure compliance with company SOPs, specifications, and cGMP regulations.

  • Demonstrate a proactive approach towards Continuous Improvement.

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:

  • BSc in Science or equivalent qualification.

  • Additional qualification in Biopharma Science an advantage.

  • Proven relevant experience working with a variety of analytical and bioanalytical techniques in a GMP laboratory within the biological and/or pharmaceutical industry.

  • Demonstrated knowledge and testing experience in an FDA/HPRA approved QC laboratory.

  • Good working knowledge of QC Systems (Empower, LIMS and Trackwise) is an advantage.

  • Previous experience in the transfer and qualification of analytical methods an advantage.

  • Excellent communication skills and strong teamwork credentials

  • Work with minimal supervision; able to perform under pressure to competing demands and stakeholders.

  • Continuous improvement mindset.

  • Positive, can-do attitude.

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.

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.

Top Skills

Capillary Electrophoresis-Sds
Elisa
Empower
Hplc
Lims
Trackwise
Uv Visible Spectrophotometry
Western Blot

Viatris Dublin, Dublin, IRL Office

Dublin, Dublin, Ireland

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