Process Engineer - France

Barrington James; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

An innovative pharmaceutical company in the beautiful South of France is seeking a skilled Process Development Engineer. This role offers the chance to work on cutting-edge injectable products in a dynamic GMP environment. You will be responsible for developing and optimizing manufacturing processes, ensuring compliance with industry regulations, and leading technology transfer initiatives. Join a talented team dedicated to advancing proprietary sterile injectable products and enjoy competitive salary and career growth opportunities in this rapidly expanding organization. If you're passionate about pharmaceutical process development, this is the perfect opportunity for you.

Benefits

Competitive salary

Benefits package

Career growth opportunities

Qualifications

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

Responsibilities

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

Skills

Process Development

GMP Regulations

Problem-Solving

Project Management

Education

Degree in Engineering

Degree in Pharmaceutical Sciences

Tools

Quality by Design (QbD)

Process Engineering

Job description

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:

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

Key Requirements:

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

Why Join Us?

1. Be part of a dynamic and innovative pharmaceutical company in the beautiful South of France.
2. Work on cutting-edge injectable products with a highly skilled team.
3. Competitive salary and benefits package.
4. 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!