Anbarlarda keyfiyyət və qida təhlükəsizliyi sistemlərinin tətbiqini idarə edir, minimum 3-4 il təcrübə tələb olunur
Vakansiya haqqında
Key Responsibilities
- Plan, organize, and monitor the daily operations of the Quality Control laboratory.
- Manage the analysis of raw materials, packaging materials, intermediates, finished products, and stability samples.
- Ensure that analytical results comply with GMP requirements and relevant quality standards.
- Plan laboratory staff activities, allocate responsibilities, and manage the team.
- Coordinate investigations into OOS (Out of Specification), OOT (Out of Trend), and laboratory-related deviations.
- Contribute to CAPA, change control, deviation management, and other quality-related processes.
- Monitor analytical method validation, verification, and transfer activities.
- Oversee the commissioning of laboratory equipment and monitor calibration, maintenance, and qualification activities.
- Ensure that laboratory documentation complies with GMP requirements and data integrity principles.
- Represent the Quality Control department during internal and external audits.
- Monitor laboratory performance indicators and lead continuous improvement initiatives.
Qualifications
- Bachelor’s degree in Chemistry or Chemical Engineering.
- At least 7 years of experience in Quality Control within the pharmaceutical industry, preferably including 3 years of team management experience.
- Knowledge of GMP, GLP, and relevant quality management systems.
- Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, and FTIR.
- In-depth knowledge of analytical method validation, verification, and transfer processes.
- Experience in managing OOS (Out of Specification), OOT (Out of Trend), deviation, CAPA, and change control processes.
- Proficiency in Microsoft Office applications.
- Experience with laboratory information management systems, SAP, and QMEX documentation systems is preferred.
- Good command of English.
- Strong analytical thinking, problem-solving, and decision-making skills.
- Excellent team management and communication skills.
- Strong planning and organizational abilities.
Key Responsibilities
- Plan, organize, and monitor the daily operations of the Quality Control laboratory.
- Manage the analysis of raw materials, packaging materials, intermediates, finished products, and stability samples.
- Ensure that analytical results comply with GMP requirements and relevant quality standards.
- Plan laboratory staff activities, allocate responsibilities, and manage the team.
- Coordinate investigations into OOS (Out of Specification), OOT (Out of Trend), and laboratory-related deviations.
- Contribute to CAPA, change control, deviation management, and other quality-related processes.
- Monitor analytical method validation, verification, and transfer activities.
- Oversee the commissioning of laboratory equipment and monitor calibration, maintenance, and qualification activities.
- Ensure that laboratory documentation complies with GMP requirements and data integrity principles.
- Represent the Quality Control department during internal and external audits.
- Monitor laboratory performance indicators and lead continuous improvement initiatives.
Qualifications
- Bachelor’s degree in Chemistry or Chemical Engineering.
- At least 7 years of experience in Quality Control within the pharmaceutical industry, preferably including 3 years of team management experience.
- Knowledge of GMP, GLP, and relevant quality management systems.
- Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, and FTIR.
- In-depth knowledge of analytical method validation, verification, and transfer processes.
- Experience in managing OOS (Out of Specification), OOT (Out of Trend), deviation, CAPA, and change control processes.
- Proficiency in Microsoft Office applications.
- Experience with laboratory information management systems, SAP, and QMEX documentation systems is preferred.
- Good command of English.
- Strong analytical thinking, problem-solving, and decision-making skills.
- Excellent team management and communication skills.
- Strong planning and organizational abilities.
Bu vakansiyaya uyğunsan?
CV‑ni yüklə — 10 saniyəyə uyğunluq faizini, bazar dəyərini və CV‑də çatışmayanı gör.
Maaş bazarla müqayisədə
İşəgötürən məbləği göstərməyib. Keyfiyyətə nəzarət üzrə mühəndis üzrə bazar adətən 700–1 400 ₼ ödəyir, median — 1 160 ₼.
53 açıq vakansiya, 38 maaş rəqəmi: elanlar, anketlər, «Maaşını yoxla».
Keyfiyyətə nəzarət üzrə mühəndis kimi öz maaşını yoxlaŞirkət haqqında
Müraciətin
Bu vakansiya haqqında suallar
İş Pirallahı, Bakı İqtisadi Zonasında yerləşir.
Ən azı 7 il keyfiyyətə nəzarət sahəsində təcrübə tələb olunur, 3 il isə komanda idarəetməsi üzrə.
Müraciət bu səhifədəki formadan göndərilir: məktub birbaşa işəgötürənin poçtuna gedir, qeydiyyat lazım deyil.
Müraciət formasına keçOxşar vakansiyalar
Bütün oxşar vakansiyalarKeyfiyyətə nəzarət üzrə mühəndis üzrə Bakıda digər açıq elanlar.
İstehsalat prosesində keyfiyyətə nəzarət edir və HACCP sertifikatına malikdir.
İstehsalat proseslərinin keyfiyyətinə nəzarət edir və keyfiyyət standartları üzrə təcrübəyə malikdir.
Tikinti işlərinin keyfiyyətinə nəzarət edir və ISO standartları üzrə təcrübə tələb olunur





