Pds Quality Operations Analyst
Pubblicato il 23-10-2026 - GiGroup H-7241 in Monza
pbLuogo di lavoro: /b Monza /p pbGrafton LifeScience* /bis 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. /p pbIn 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 /b /p h3QC PDS Quality Operations Analyst /h3 h3Summary: /h3 pAs a QC PDS Quality Operations Analyst, you will join our collaborative PDS team, working cross-functionally in a GMP/GLP-regulated environment and contributing to the development and delivery of advanced products and technologies that help address global challenges in healthcare and environmental protection. /p h3Job Responsibilities: /h3 ul liThe primary focus of this role will be the review and verification of analytical activities and documentation generated by the QC PDS laboratory, ensuring accuracy, completeness, data integrity, and compliance with applicable procedures and GMP/GLP requirements. /li liReview of analytical testing and documentation related to product release, stability studies, analytical method validation and transfer activities, and Active Pharmaceutical Ingredients (APIs), using standard analytical techniques and instrumentation such as HPLC, UV-Vis, FT-IR, and Pharmacopoeial methods.
/li liYou will also receive appropriate laboratory training to maintain the capability to operate as a QC PDS Laboratory Analyst. /li liWhen required, you may provide hands-on support to routine laboratory activities and analytical testing. /li /ul pWe offer an environment that values performance, quality, and innovation, providing the resources and opportunities to develop your expertise and grow your career while contributing to our mission of enabling our customers to make the world healthier, cleaner and safer. /p h3Skills: /h3 ul liExperience in a GMP Quality Control lab. /li liFamiliarity with techniques including HPLC, UV-Vis, FT-IR, and compendial tests (pH, osmolality, container content, appearance). /li liAbility to work to critical timelines. /li liEffective interpersonal skills and attention to detail. /li liStrong documentation and analytical review capabilities. /li /ul h3Education/Experience: /h3 ul liDegree in Biotechnology, Pharmaceutical Chemistry (CTF) or a related scientific field preferred. /li liExperience in reviewing QC data and documentation in a GMP-regulated environment. /li /ul pbContract Offer: 12 months Fixed-term agency contract. CCNL Chimico-Farmaceutico, livello D1. /b /p pbWorking time weekly: /b Monday to Friday /p pbPlace of work /b: bMonza /b /p pGrafton 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). /p pThe 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. /p pCandidates are invited to read the privacy notice pursuant to Articles 13 and 14 of EU Regulation 679/2016 at the following address: /p #J-18808-Ljbffr