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Quality Control Team Lead

Menej ako 2 týždne

Brenntag Specialties Czech a.s.

Stachovice 176, Fulnek

Vzdialenosť od teba uvidíš po zadaní adresy vo výpise ponúk.


Plat

50 000 - 60 000 Kč hrubého

Úväzok

Práca na plný úväzok

Zmluva

Pracovná zmluva

Benefity

Company catering, Cell phone, Holidays 5 weeks, Notebook

Vzdelanie

Vysokoškolské II. stupňa

Jazyky

Angličtina (Stredne pokročilá)

Zaradené

Pharmaceutical, Chemical industry, Regulatory Manager, Research worker, researcher, Chemist, Laboratory technician


O pozícii

Become part of a leading international company and help build a modern quality control laboratory in a new, state-of-the-art production facility focused on excipients and pharmaceutical raw materials. As a QC analyst team lead, you will be a key member of the newly emerging team and will have a unique opportunity to participate in setting up processes and the overall quality strategy on site.

Main responsibilities

  • Leading and managing small team of QC analysts
  • Design and optimization of procedures for testing raw materials, intermediate products and final products in cooperation with QA.
  • Developing methods and performing sample and laboratory analyses using HPLC, GC, UV-VIS, FT-IR, ICP-OES/MS methods.
  • Ensuring compliance with Good Laboratory Practice (GLP) principles
  • Preparation of Certificates of Analysis (CoA) and participation in the batch release/release process.
  • Handling non-routine analyses, including investigating customer/supplier complaints, internal deviations, and validation and qualification activities.
  • Calibration of laboratory equipment and maintenance of relevant documentation.
  • Laboratory inventory management, reagent and standard preparation.
  • Creation and updating of SOPs, implementation of stability studies according to regulatory requirements.
  • Collaborate with Production, QA, Maintenance and Purchasing on validation and verification plans.
  • Laboratory testing of new product formulations.

Required Qualifications

  • A university degree in analytical chemistry or a related field.

  • At least 5 years of practical laboratory experience in a pharmaceutical environment.

  • Knowledge of wet chemistry and modern analytical techniques.

  • Orientation in GMP/GLP and the European Pharmacopoeia.

  • Knowledge of APIs, excipients and bio-pharmaceutical raw materials.

  • Fluent Czech

  • Communicative English for everyday cooperation.

  • Demonstrated ability to supervise and develop a small team, including task coordination and performance management.

  • Ability to work independently and excellent communication skills.

Why join us

  • The opportunity to participate in building a new QC laboratory from scratch.
  • An active role in shaping the quality strategy of the entire plant.
  • Career growth in a dynamic international environment.

Sign up today and become part of a team that influences the quality of pharmaceutical products around the world.

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