Process Engineer - France

Barrington James Limited; Occitanie; Sur place; EUR 40 000 - 80 000; Plein temps

Résumé du poste

An innovative pharmaceutical company is seeking a talented Process Development Engineer to join their dynamic team in the beautiful South of France. This exciting role focuses on developing and optimizing manufacturing processes for cutting-edge injectable products in a GMP environment. You will lead process scale-up and technology transfer, ensuring compliance with regulatory standards while collaborating with cross-functional teams. If you are passionate about advancing pharmaceutical development and thrive in a fast-paced environment, this opportunity offers career growth and the chance to work with a highly skilled team on groundbreaking products.

Prestations

Competitive salary

Benefits package

Career growth opportunities

Qualifications

• Proven experience in process development and scale-up for pharmaceuticals.
• Strong understanding of GMP regulations and sterile manufacturing.

Responsabilités

• Develop and optimize manufacturing processes for injectable products.
• Lead process scale-up and technology transfer to commercial manufacturing.

Connaissances

Process Development

Scale-Up

Technology Transfer

GMP Regulations

Problem-Solving

Project Management

Formation

Degree in Engineering

Degree in Pharmaceutical Sciences

Outils

Quality by Design (QbD)

Description du poste

Job Opportunity: Process Development Engineer
Location: South of France

Are you an experienced Process Development Engineer looking to join an innovative pharmaceutical company at the forefront of injectable product development? We are seeking a talented professional to contribute to the advancement of our proprietary sterile injectable product. This is an exciting opportunity to work in a cutting-edge GMP environment, focusing on process development and scale-up.

Key Responsibilities:

• Develop and optimize manufacturing processes for injectable pharmaceutical products.
• Ensure compliance with GMP, aseptic, and sterile manufacturing requirements.
• Lead process scale-up and technology transfer from development to commercial manufacturing.
• Collaborate with cross-functional teams including CDMO partners to ensure seamless process execution.
• Apply Quality by Design (QbD) principles to improve process efficiency and robustness.
• Support engineering and process validation activities to meet regulatory standards.
• Troubleshoot manufacturing challenges and implement continuous improvements.

Key Requirements:

• Degree in Engineering, Pharmaceutical Sciences, or a related field.
• Proven experience in process development, scale-up, and technology transfer.
• Strong understanding of GMP regulations, sterile and aseptic manufacturing.
• Expertise in process engineering for injectable pharmaceutical products.
• Experience working with CDMOs and external manufacturing partners.
• Knowledge of Quality by Design (QbD) principles.
• Excellent problem-solving and project management skills.

Why Join Us?

• Be part of a dynamic and innovative pharmaceutical company in the beautiful South of France.
• Work on cutting-edge injectable products with a highly skilled team.
• Competitive salary and benefits package.
• Career growth opportunities in a rapidly expanding organization.

If you are passionate about pharmaceutical process development and looking for a challenging yet rewarding role, we would love to hear from you!