Descrizione dell'offerta
Job title: Lab Specialist
Location: Parma
Employment type: Tempo Indeterminato, Full time
Orario su turni: 7-15 / 14-22 (una settimana mattina e una settimana pomeriggio). Turnazione 6 su 7 con sabato a rotazione.
Closing date for applications: 26 luglio 2026 COB
Overview
We manufacture and supply reliable, high‑quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 manufacturing sites delivered 1.7billion packs of medicines and 409million vaccine doses in 2024, helping to make a positive impact on the health of millions of people. Technology is transforming how we manufacture, enabling us to increase the speed, quality and scale of product supply. Responsibilities
Apply GSK values, GMP, Data Integrity, EHS policies and GSK Expectations in daily work. Complete required training on time. Perform analytical tests on release and stability samples accurately and independently, following current analytical methods or protocols. Record analytical data promptly and precisely using appropriate systems. Verify data compliance with specifications and acceptance criteria. Report out‑of‑limit or atypical data promptly to enable appropriate investigations. Support improvements to analytical workflows to ensure laboratory performance. Follow escalation rules, understand responsibilities, and make decisions within scope. Maintain up‑to‑date technical and analytical documentation in line with official and group regulations. Train junior staff, new hires or personnel assigned from other roles. Facilitate problem resolution and the improvement of procedures and methods. Participate in inspections, audits, and self‑inspections when required. Act as subject‑matter expert in executing laboratory anomalies and investigations. Use GSK information systems (SAP, SCADA, etc.) and area‑specific tools. Keep the work environment orderly, clean, and well stocked. Qualifications
Bachelor’s degree in Biology, Biotechnology, Chemistry, or a related field. Minimum of 2years’ experience as a quality control laboratory analyst. Good command of the English language (preferred). Strong problem‑solving and teamwork skills. Knowledge of major bio‑analytical techniques. Experience managing laboratory anomalies and investigations. Benefits
Permanent contract with an inclusive working environment. Flexible benefits package. Company healthcare plan. Integrative pension fund. Employee assistance programme. Company canteen. Annual gross base salary range: EUR30150 to EUR50250. Additional annual bonus and long‑term incentive options may be available.
#J-18808-Ljbffr
We manufacture and supply reliable, high‑quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 manufacturing sites delivered 1.7billion packs of medicines and 409million vaccine doses in 2024, helping to make a positive impact on the health of millions of people. Technology is transforming how we manufacture, enabling us to increase the speed, quality and scale of product supply. Responsibilities
Apply GSK values, GMP, Data Integrity, EHS policies and GSK Expectations in daily work. Complete required training on time. Perform analytical tests on release and stability samples accurately and independently, following current analytical methods or protocols. Record analytical data promptly and precisely using appropriate systems. Verify data compliance with specifications and acceptance criteria. Report out‑of‑limit or atypical data promptly to enable appropriate investigations. Support improvements to analytical workflows to ensure laboratory performance. Follow escalation rules, understand responsibilities, and make decisions within scope. Maintain up‑to‑date technical and analytical documentation in line with official and group regulations. Train junior staff, new hires or personnel assigned from other roles. Facilitate problem resolution and the improvement of procedures and methods. Participate in inspections, audits, and self‑inspections when required. Act as subject‑matter expert in executing laboratory anomalies and investigations. Use GSK information systems (SAP, SCADA, etc.) and area‑specific tools. Keep the work environment orderly, clean, and well stocked. Qualifications
Bachelor’s degree in Biology, Biotechnology, Chemistry, or a related field. Minimum of 2years’ experience as a quality control laboratory analyst. Good command of the English language (preferred). Strong problem‑solving and teamwork skills. Knowledge of major bio‑analytical techniques. Experience managing laboratory anomalies and investigations. Benefits
Permanent contract with an inclusive working environment. Flexible benefits package. Company healthcare plan. Integrative pension fund. Employee assistance programme. Company canteen. Annual gross base salary range: EUR30150 to EUR50250. Additional annual bonus and long‑term incentive options may be available.
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
Ricevi annunci simili
Inserisci la tua email: ti avvisiamo quando escono nuovi annunci corrispondenti.
✅ Controlla la tua email e clicca il link per confermare l'alert.
Nessun account necessario. Disiscrizione con un clic dall'email.