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ANALYTICAL DEVELOPMENT AND QUALITY CONTROL LABORATORY MANAGER

Jobdetails

publiziert
15 October 2021
Gehalt
Négociable
Ort
Plan-les-Ouates
Jobtyp
Temporärstellen
Disziplin
Life Sciences
Referenz
BBBH485549_1633937518

Jobbeschreibung



For its pharmeutical partner, Kelly Scientific is looking for:
Analytical Development and Quality Control Laboratory Manager

(6 months temporary position)


Your responsabilities :

  • Responsible for managing the QC and analytical laboratory in accordance with cGMP and company requirements,
  • Responsible to resolve problems with instruments, test methods, lab chemicals, standards, and samples,
  • Overall responsibility for development and validation of innovative analytical methodologies, and support method transfers as needed
  • Responsible to assure that all raw materials and finished goods are tested in accordance with GMP,
  • Responsible to release raw material,
  • Organize and supervise the scientific activities carried out on the analytical techniques available in the laboratory (LC-MS, GC-MS, FTIR, …),
  • Manage stability study protocol development, execution, data analysis and reporting
  • Support continued business process improvement activities.
  • Cultivate and maintain relationships with key internal and external customers
  • Initiate Change Controls to support change of equipment, specification documents and test methods, Provide technical support to other QC activities as business needs arises.
  • Maintain training records current and GMP compliance.


Your profile:

  • Bachelor or Master degree in Chemistry, Pharmacy, or Biochemistry
  • Minimum of 5 years’ experience in QC and/or analytical development in biotech or pharmaceutical industry (GMP environment)
  • Experience in management; demonstrated leadership and organization skills
  • Deep knowledge of a variety of analytical techniques such as HPLC, GC, FTIR, and other analytical techniques.
  • Experience in analytical investigations, handling of OOS, OOT investigations
  • General knowledge of the ICH guidelines and of the major pharmacopoeias
  • Excellent team player with a strong ability to communicate within a multicultural environment, at all organizational levels
  • Strong communication and technical writing skills.
  • Fluency in English (both oral and written)
  • Extremely motivated, with rigorous work habits and problem-solving skills

Your contact at Kelly:
Mrs Karine Legerot
Consultant Professional Staffing Life Science
Kelly Scientific Geneva

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Deadline: 13-05-2024

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