Validation Specialist Associate - Mirandola Area Italy

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7fb0gh

About Us
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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.

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 seeking a Validation Specialist Associate 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 Mirandola in Italy with a hybrid working policy.

About The Job





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

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- 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 analysisdrafting SOPs

Required Skills And Experience

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

- 1-2 years relevant professional experience

- Exp riences in qualification and commissioning

- Writing Skills (Sentence Structure and Construction, Clarity and Effectiveness,)

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

- Good understanding of GMP requirements and validation principles. xysqume

Additional Skills

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- Attention to detail

- Team working

- Problem solving

- Good Interpersonal skills

- Flexibility and willingness to travel to client sites as required.

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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7fb0gh