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Role Summary

We are looking for an Analytical Development Project Manager as part of a permanent contract.

You ensure the analytical monitoring of projects and the Customer interface for the entire technical part of the project:

Carry out physicochemical analyzes of pharmaceutical, cosmetic and veterinary samples (raw materials, finished products, etc.) in accordance with regulatory standards as well as internal procedures and operating methods according to the defined schedule.

Establish validation or analytical transfer protocols.

• Carry out the contract review (and possibly manage the sending of subcontracted samples, etc.)
• Transmit the deadline for delivering results and the project to the client under the responsibility of the R&D Project Manager
• Prepare working documents (framework, feasibility/development protocols)
• Prepare projects by ordering the necessary equipment and consumables in collaboration with the R&D Project Manager
• Plan analyzes relating to projects with the R&D team and in conjunction with laboratory managers
• Supervise the analyzes carried out and be proactive in the event of a technical problem
• Review the data after analysis
• Interpret the results obtained
• Process out-of-specification or out-of-trend results related to projects
• Manage quality files (Deviation, Customer Complaints, etc.) linked to the projects for which he is responsible
• Carry out and verify the drafting of project-related methods
• Carry out the writing of study reports or project analysis bulletins
• Send all information necessary for invoicing to the Billing Department
• Ensure the archiving of project files

Establish an end-of-project report.

Participate in laboratory quality actions as part of your activity:

Participate in audits,

Participate in the drafting of Qualities documents related to your activity.

You ensure the replacement of other Project Managers in their absence.

Requirements

• With a bac+5 background in the field of analytical chemistry, you have acquired at least two years of experience in the pharmaceutical industry, and you have a pharmacist profile.
• Technical English is required.
• Knowledge of pharmaceutical regulations.

About the Company

SGS is the world leader in inspection, control, analysis and certification.

We employ more than 97,000 people and operate a network of more than 2,600 offices and laboratories around the world.

The Villeneuve La Garenne site is the SGS site in France specializing in quality control for the pharmaceutical, veterinary and cosmetics industries. As such, the site is a pharmaceutical establishment subject to Good Manufacturing Practices (GMP) rules.