PDS Analytical Development & GMP Technician a Ferentino, Frosinone
Grafton LifeScience* is a dedicated team focused on enhancing the experiences, skills, and potential of candidates in Sales & Marketing, Clinical Research, Regulatory, and Operations within the Pharmaceutical and Medical sectors. We also specialize in roles related to customer support in the health-impacting distribution field (Pharmacies and Parapharmacies).We are a team of passionate professionals working to guide our candidates towards roles and corporate environments that best match their skills and expectations.
In partnership with an integrated CDMO with around 60 locations worldwide, specializing in integrated sterile liquid and lyophilized product development and commercial manufacturing, we offer an opportunity for
PDS Analytical Development & GMP Technician
The main function of a PDS Analytical Development & GMP Technician is to perform chemical analyses and support laboratory operations within the QC PDS Laboratory. This role ensures compliance with GMP standards, SOPs, and safety regulations while contributing to documentation, equipment maintenance, and continuous improvement initiatives.
Job Responsibilities:
• Use and control analytical equipment in the laboratory.
• Execute chemical analysis of semi-finished products, finished products, stability samples, and products under transfer or validation studies.
• Monitor the progress of analyses according to priorities defined by the Team Leader and company quality standards.
• Contribute to the correct management and calibration of laboratory equipment in compliance with GMP and regulatory standards.
• Support laboratory investigations for out-of-specification (OOS) results or deviations
Do you have these skills and requirements?
MSc in a scientific/pharmaceutical area, knowledge of GMP regulations and pharmaceutical manufacturing processes, Experience 0/6 months in Quality Control; HPLC knowledge is mandatory.
Contract Offer: Fixed-term agency contract 11/08/2026 - 10/03/2027. CCNL Chimico-Farmaceutico, livello D2.
Working time weekly: 5x2 – mattina /pomeriggio + ciclo continuo (6x4)
Place of work: Ferentino (FR)
Grafton LifeScience is a specialization of Gi Group Spa authorized to operate by the Ministry of Labor and Social Policies (Authorization No. 26/11/2004 PROT. 1101 - SG).
The offer is intended for candidates in compliance with Legislative Decree No. 198/2006 and subsequent amendments, as well as Legislative Decrees No. 215 and No. 216 of 2003 on equal treatment.
Candidates are invited to read the privacy notice pursuant to Articles 13 and 14 of EU Regulation 679/2016 at the following address: www.gigroup.it/privacy-candidati"
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Grafton LifeScience* is a dedicated team focused on enhancing the experiences, skills, and potential of candidates in Sales & Marketing, Clinical Research, Regulatory, and Operations within the Pharmaceutical and Medical sectors. We also specialize in roles related to customer support in the health-impacting distribution field (Pharmacies and Parapharmacies).We are a team of passionate professionals working to guide our candidates towards roles and corporate environments that best match their skills and expectations.
In partnership with an integrated CDMO with around 60 locations worldwide, specializing in integrated sterile liquid and lyophilized product development and commercial manufacturing, we offer an opportunity for
PDS Analytical Development & GMP Technician
The main function of a PDS Analytical Development & GMP Technician is to perform chemical analyses and support laboratory operations within the QC PDS Laboratory. This role ensures compliance with GMP standards, SOPs, and safety regulations while contributing to documentation, equipment maintenance, and continuous improvement initiatives.
Job Responsibilities:
• Use and control analytical equipment in the laboratory.
• Execute chemical analysis of semi-finished products, finished products, stability samples, and products under transfer or validation studies.
• Monitor the progress of analyses according to priorities defined by the Team Leader and company quality standards.
• Contribute to the correct management and calibration of laboratory equipment in compliance with GMP and regulatory standards.
• Support laboratory investigations for out-of-specification (OOS) results or deviations
Do you have these skills and requirements?
MSc in a scientific/pharmaceutical area, knowledge of GMP regulations and pharmaceutical manufacturing processes, Experience 0/6 months in Quality Control; HPLC knowledge is mandatory.
Contract Offer: Fixed-term agency contract 11/08/2026 - 10/03/2027. CCNL Chimico-Farmaceutico, livello D2.
Working time weekly: 5x2 – mattina /pomeriggio + ciclo continuo (6x4)
Place of work: Ferentino (FR)
Grafton LifeScience is a specialization of Gi Group Spa authorized to operate by the Ministry of Labor and Social Policies (Authorization No. 26/11/2004 PROT. 1101 - SG).
The offer is intended for candidates in compliance with Legislative Decree No. 198/2006 and subsequent amendments, as well as Legislative Decrees No. 215 and No. 216 of 2003 on equal treatment.
Candidates are invited to read the privacy notice pursuant to Articles 13 and 14 of EU Regulation 679/2016 at the following address: www.gigroup.it/privacy-candidati"
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