INVESTIGATION & QUALITY SPECIALIST

30 set - Ferentino
Grafton Recruitment

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

Investigation & Client Quality Specialist The main function of an Investigation & Client Quality Specialist is to manage quality investigations, deviations, and CAPAs related to clinical and commercial batch production. This role supports customer interactions, audits, SOP reviews, and quality reporting, ensuring compliance with GMP standards and alignment with corporate and client expectations.

Job Responsibilities:

- Manage deviations and investigations related to quality issues impacting clinical and commercial batches, ensuring timely completion.
- Manage CAPAs resulting from quality investigations.
- Support the preparation of periodic quality trend reports for Management and Corporate visits.




- Manage non-conformities in receiving raw materials, active ingredients, and GMP materials.
- Participate in Operational Excellence initiatives and projects.
- Attend meetings for new and ongoing projects, addressing quality topics.
- Collaborate with cross-functional teams to define root causes and implement corrective actions within agreed timelines.
- Coordinate technical and management meetings with DPS (Commercial division) colleagues and Clients

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 Assurance/Quality Control, preferably, familiarity with Root Cause Analysis tools.

Contract Offer: Fixed-term agency contract until 31/12/2026 with the possibility of renewal. CCNL Chimico-Farmaceutico, livello D1.

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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