Interim Analytical Development Project Manager

JR France; Grand Est; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading pharmaceutical organization in the Grand Est region seeks an experienced Freelance Analytical Development Project Manager for a 6-month interim assignment. This role involves leading analytical development projects and managing a team within a GMP-regulated environment, ensuring compliance with industry standards and collaborating with various departments.

Prestations

Competitive daily rate for freelance professionals

Opportunity to work with a global leader in the pharmaceutical industry

6-month contract with potential for extension

Qualifications

• Extensive experience in analytical development & quality control.
• Strong knowledge of ICH guidelines, GMP, ISO 17025 & 13485.
• Proven leadership in project & team management.

Responsabilités

• Lead analytical development projects within a GMP-regulated environment.
• Oversee method development, validation, and transfer.
• Manage a team of analytical scientists and drive technical problem-solving.
• Ensure compliance with regulatory standards (ICH, GMP).
• Collaborate cross-functionally with R&D, Quality, and Production teams.

Connaissances

HPLC

GC

ICP

MS

Elemental analysis

Project management

Team management

Regulatory compliance

Problem-solving

Fluency in French

Fluency in English

Description du poste

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Interim Analytical Development Project Manager, grand est

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Client:

Amoria Bond

Location:

grand est, France

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

25170090191015116832760

Job Views:

2

Posted:

29.05.2025

Expiry Date:

13.07.2025

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Job Description:

A leading pharmaceutical organisation, specializing in the production of sterile and non-sterile pharmaceutical products, currently has a number of projects and is urgently seeking an experienced Freelance Analytical Development Project Manager for a 6-month interim assignment in the Grand Est region.

Key Responsibilities:

• Lead analytical development projects within a GMP-regulated environment
• Oversee method development, validation, and transfer
• Manage a team of analytical scientists and drive technical problem-solving
• Ensure compliance with regulatory standards (ICH, pharmacopoeias, GMP)
• Collaborate cross-functionally with R&D, Quality, and Production teams

Ideal Profile:

• Extensive experience in analytical development & quality control
• Expertise in HPLC, GC, ICP, MS, and elemental analysis
• Strong knowledge of ICH guidelines, GMP, ISO 17025 & 13485
• Proven leadership in project & team management
• Fluent in French & English

What We Offer

• Competitive daily rate for freelance professionals.
• Opportunity to work with a global leader in the pharmaceutical industry.
• 6-month contract with potential for extension.

For more details or to express interest, please apply and get in touch via direct message. Due to the urgent need, we hope to screen and shortlist by Friday 14th for interviews the coming week.

Disclaimer:

Amoria Bond is an independent recruitment consultant specializing in sustainable recruitment. None of the terms used in this advert are (in)directly intended to exclude candidates on the basis of age and experience. We hereby confirm that we are accepting applications from suitable candidates regardless of age and experience.