Group Lead Phys-Chem QC

Group Lead Phys-Chem QC

Lonza

Basel, Switzerland

Job Description Summary

For DPS (Drug Product Services) in Basel Switzerland, we have an open position for a Group Lead Phys-Chem QC in our growing Phys-Chem QC team. Working closely with Analytical and Formulation Development, this team offers specialized services solutions for customers.

Key Accountabilities and Duties

  • Establish DP analytical infrastructure and services for biologics, small molecule and peptide parenterals for clinical and commercial products;
  • Supervise the installation, qualification and maintenance of all instruments for DP phys-chem analytics in close alignment with current best practices and regulations;
  • Develop and establish analytical methods and technologies to support formulation development and DP QC (specifically including HPLC and CE purity methods, content by UV, identity, color, clarity and opalescence, pH, osmolality, extractable volume, CCI, visual inspection, etc.;
  • Build, lead and manage a small team of lab scientists within the Phys-Chem Analytics and QC group, also in a matrix organization across the entire group;
  • Liaise with partner units within the Lonza network to ensure the successful delivery of projects. Ensure effective use of resources (time, personnel, equipment, material, rooms), maintenance of equipment, order and safety and health protection and following lab and safety instructions and guidance and all cGMP regulations;
  • Ensure the proper maintenance and qualification of equipment, safety and health protection following lab and safety instructions and all cGMP regulations;
  • Enable innovation and technical strategy projects, generate IP and contribute to scientific publications and conference talks, evaluate and implement of new methods, as required;
  • Perform other duties as assigned.

Minimum Required Qualifications/Skills

  • PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences or related field;
  • > 4 years of industry, working experience in analytical development and quality control, preferably under cGMP regulations;
  • Very good working knowledge in all relevant analytical techniques;
  • Excellent communication, supervisory as well as reporting and scientific skills;
  • Outstanding ability to interpret complex analytical data;
  • Ability to work independently and in a team environment;
  • Detail oriented;
  • Good inter-personal skills;
  • Enthusiastic and open-minded;
  • Willingness to learn and carry out new and complex tasks;
  • Proactive attitude;
  • Excellent knowledge of written and spoken English.

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© EuroJobsites 2019

EuroJobsites is a registered company number: 4694396 VAT number: GB 880 9055 04

Registered address: EuroJobsites Ltd, Unit 8, Kingsmill Business Park, Kingston Upon Thames, London, KT1 3GZ, United Kingdom

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