QC Data Reviewer for Biochemical Methods

Posted 2 Days Ago
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Visp, Valais
In-Office
Mid level
Pharmaceutical
At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization.
The Role
The role involves reviewing data from QC analysis, ensuring compliance with GMP, investigating unexpected results, and evaluating quality parameters for pharmaceutical products.
Summary Generated by Built In

 

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Join our dynamic and international team in the scenic town of Visp as a Scientist / Data Reviewer (all genders). In this role, you will be responsible for reviewing data generated during routine Quality Control (QC) analysis in the QC Laboratory. Your expertise will ensure that all laboratory work aligns with GMP and SOPs, enabling the timely release of monoclonal antibody batches.

Do you thrive in a fast-paced environment where priorities can shift quickly? Are you meticulous and enjoy precision in your work? In this role, you will gain valuable insights into production and quality control processes for ground breaking biologic medicines.

What you’ll get: 

  • An agile career and a dynamic work culture.

  • An inclusive and ethical workplace.

  • Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.

Benefits in Visp: https://bit.ly/3wjkoFi 

What you’ll do:

  • Data review of ELISA and qPCR analyses

  • Checking correct execution of assays in the lab and correct result evaluation

  • Evaluation of quality parameters for stability studies and batch release

  • Investigation of unexpected results

  • Ensuring compliance with GMP and internal procedures

What we’re looking for :

  • BSc or MSc or equivalent experience in Chemistry, Biochemistry or similar field

  • Experience in a GMP environment within Quality Control is highly preferred

  • Hands-on experience with qPCR and/or ELISA (impurities or relative potency) is highly preferred

  • You are very detail-oriented and you can adapt flexibly to changing priorities. You enjoy to curiously question and investigate ambiguous results.

  • Knowledge of Quality Management Systems and LIMS is a plus

  • Fluency in English is a must, language skills in German are a plus

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now

Top Skills

Elisa
Gmp
Lims
Qpcr
Quality Management Systems
Sops
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The Company
HQ: Basel
0 Employees
Year Founded: 1897

What We Do

At Lonza, we enable A Healthier World by supporting our healthcare customers on the path to commercialization. Our community of 16,000 talented employees work across a global network of more than 30 sites to deliver for our customers across the pharma, biotech and nutrition markets.

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