(Junior) Head of Laboratory at BI Pharma GmbHCoKG
BADR, , Germany -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

0.0

Posted On

09 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Food Chemistry, Pharmaceutical Industry, Method Development, Know How, Working Experience, Ion, Project Management Skills, Icp Ms, Chromatography, Manufacturing, Industrial Experience, Gmp

Industry

Pharmaceuticals

Description

THE POSITION

We are looking for a Laboratory Head with an excellent background in the field of organic and inorganic trace analysis. Join our international team of experienced scientists and develop advanced analytical methods with your team for our innovative products within our Analytical Development department for new chemical entities in Biberach.

REQUIREMENTS

  • Ph.D in Chemistry, Food chemistry, Pharmacy or equivalent; alternatively Master’s degree with longtime, industrial experience
  • Expert knowledge in the development/validation of HPLC-HRMS, HPLC-MS/MS with several years of practical working experience
  • Knowledge of ICP-MS and Ion chromatography
  • Basic regulatory and GMP know-how in pharmaceutical chemistry, manufacturing, and controls
  • Excellent organizational and project management skills
  • Ability to respond to changing priorities and short lead times for multiple tasks as well as ability to identify problems and work towards solutions with the teamFluent in written and spoken German and English
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Additional requirements for Head of Laboratory

  • Long-term experience in independently leading of an analytical laboratory in the pharmaceutical industry with a focus on HPLC-HRMS and HPLC-MS/MS
  • Profound regulatory and GMP know-how in pharmaceutical chemistry, manufacturing, and controls and experience
  • Solid background in ICP-MS and Ion Chromatograph method development.

How To Apply:

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Responsibilities
  • In your new role you will lead the Organic and Inorganic Trace Analysis laboratory within Analytical Development for new chemical entities.
  • You will safeguard development and validation of accurate, precise, and robust trace analytical methods, especially HPLC-MS/MS and HPLC-HRMS, for the respective phase of clinical development and commercial.
  • Furthermore, you will ensure that all analytical testing are in compliance with internal and external requirements, e.g. GMP.
  • In addition, you will proactively collaborate within the department and project teams.Moreover, you will contribute to clinical and commercial submission dossiers
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Additional tasks for Head of Laboratory

  • You will manage a network of internal and external partners e.g. CROs.Additionally, you will independently write clinical and commercial submission dossiers documents in your field of expertise

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