About Us
ProductLife Group (PLG) is a dedicated life sciences and pharmaceutical outsourcing and consulting company providing expertise and services in areas such as: Product Development, Market & Patient Access, Regulatory Affairs and Safety & Vigilance as well as Engineering and Digital Transformation.The group has its HQ in Paris and affiliates around the globe with teams in all key regions: North America, Europe and APAC.

We are now on the look out for an experienced Validation Specialist Officer to enhance and join PLG Center of Expertise Engineering (previousl y C&P; Engineering). Our Center of Expertise, is a multidisciplinary engineering and consulting firm specializing in providing tailored solutions for the pharmaceutical, medical, nutraceutical, and cosmetics industries in areas such as Engineering, Construction, Qualification & Validation as well as Energy & Waste Management.

The job location is around Parma in Italy with a hybrid working policy.

About The Job
You will have ownership of the following activities supporting our clients' Qualification & Validation Opeeations:

Plan, execution, and documentation of qualification and validation activities (IQ/OQ/PQ) for facilities, utilities and equipment

Preparation and review of validation protocols, reports and related documentation

Coordinationn of qualification and validation activities, ensuring timely execution and documentation review

Ensure compliance with GMP requirements and internal quality standards





Support change controls, deviations, CAPAs, and risk assessments related to validation

Collaborate with clients cross-functional teams (QA, Production, Engineering, QC) to support validation projects

Maintain validation documentation and ensure the validated state of equipment and processes

drafting Validation Master Plan

risk analysis

drafting SOPs

Required Skills And Experience

Bachelor's/ Master's degree in Engineering, Life Sciences, Chemistry, Pharmacy, or a related discipline.

3+ years relevant professional experience

Experience in Facility, Utility, and Equipment Qualification and Commissioning within a GMP-regulated environment.

Strong technical writing skills, with the ability to prepare clear, accurate, and compliant qualification and validation documentation

Experience in drafting qualification protocols, reports, SOPs, and other GMP documentation

Good understanding of GMP requirements and validation principles.

Proficiency in Microsoft Office 365 (Word, Excel, PowerPoint, Outlook).

Additional Skills

Strong attention to detail and commitment to quality

Team coordination or leadership experience

Excellent teamwork and collaboration skills

Strong analytical and problem-solving abilities

Good interpersonal and communication skills

Client relationship and stakeholder management experience

Flexibility and willingness to travel to client sites as required

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📌 Validation Specialist Officer (Senior Role)- Parma area Italy
🏢 Altro
📍 Parma