VALIDATION OFFICER - VIE CONTRACT (W/M)

Job description

ROYAUME-UNI(Haverhill)
du01 novembre 2020au01 novembre 2022(pour24mois)
ETABLISSEMENT :SANOFI-AVENTIS GROUPE
REMUNERATION MENSUELLE :1681€ (indemnité non contractuelle fixée par décret et arrêté, dont le montant peut varier notamment en
fonction de l’évolution du barème de référence, de la localisation de la mission et des cas d’abattements prévus par les textes)

Sanofi is a global life sciences company committed to improving access to healthcare and supporting the people we serve throughout the continuum of care. From prevention to treatment, Sanofi transforms scientific innovation into healthcare solutions, in human vaccines, rare diseases, multiple sclerosis, oncology, immunology, infectious diseases, diabetes and cardiovascular solutions and consumer healthcare. More than 110,000 people at Sanofi are dedicated to make a difference in patients’ daily life, wherever they live and enable them to enjoy a healthier life.

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

We are looking for a candidate for a VIE mission of:

Validation Officer - VIE Contract (W/M)
The position will be based in Haverhill, United Kingdom.
Your responsibilities as a Validation Officer VIE:

-To undertake validation duties assigned by the Validation Team Leader

-Provide support and guidance to Haverhill site projects and operations to meet the quality and compliance requirements of the site.

-To prepare validation documentation, plans, reports and protocols.

-To execute and report validation protocols in accordance with appropriate regulations for quality, health and safety.

-To drive continuous improvement.

-To keep up to date on regulations and legislation.

-To provide support during internal and third-party audits.

-Ensure all corrective and preventative actions in their value stream are completed within the agreed timelines.

-Maintain core training and prior to conducting any activity ensure you are trained in the current version.

-Work in close collaboration with primary customers such as Engineering, MTS (Manufacturing Technical Support, Development Sciences, Warehouse, Labelling and QC (Quality Control)

-Work under relatively close supervision and follows established practices and processes. -Project work is closely supervised.

-Use existing clearly defined procedures to solve routine tasks and issues.

-Support the successful completion of departmental objectives and projects on time.

-Prioritizing and organizing own daily work to meet agreed deadlines is important.

Candidate's profile:

Education:

Master’s degree in science, engineering pharmaceutical or any related degree

Professional experience:

Demonstrated knowledge of working within a Quality Management System and understanding of current industry requirements of current Good Manufacturing Practice (cGMP)

Validation experience would be a big plus

Demonstrated ability to successfully facilitate quality project work

Soft skills:

Good communicator

Attentive to detail, autonomous

Good organisational skills with ability to prioritize workload

Language:

Fluent English