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
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A university degree in analytical chemistry or a related field.
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At least 5 years of practical laboratory experience in a pharmaceutical environment.
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Knowledge of wet chemistry and modern analytical techniques.
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Orientation in GMP/GLP and the European Pharmacopoeia.
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Knowledge of APIs, excipients and bio-pharmaceutical raw materials.
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Fluent Czech
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Communicative English for everyday cooperation.
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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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