Senior Process Engineer | Freelance | Paris

Overview : My client is an innovative pharmaceutical company located in the monumental city of Paris dedicated to advancing healthcare through cutting-edge research, development, and manufacturing of pharmaceutical products.

They are seeking a talented Senior Process Engineer to join the team on a contract basis for a minimum of 12 months. As a Senior Process Engineer, you will play a crucial role in the development, optimization, and implementation of pharmaceutical manufacturing processes.

You will work closely with cross-functional teams to ensure the efficiency, quality, and compliance of the production processes in accordance with regulatory standards.

Title : Senior Process Engineer

Location : Paris, France

Positions Available : 1

Type : Contract (12+ months)

Salary : 130+ Euros an hour

This role is available immediately, contact us now!

Responsibilities :

• Lead process development and optimization initiatives to enhance efficiency, scalability, and robustness of pharmaceutical manufacturing processes.
• Design and implement innovative solutions to improve process yields, reduce cycle times, and minimize waste generation.
• Conduct thorough analysis and troubleshooting of process deviations, identifying root causes and implementing corrective actions.
• Collaborate with R&D, Quality Assurance, and Regulatory Affairs teams to ensure compliance with cGMP guidelines, regulatory requirements, and industry standards.
• Provide technical expertise and guidance to junior engineers and production staff, fostering a culture of continuous learning and improvement.
• Participate in cross-functional teams to support technology transfer, scale-up activities, and new product introductions.
• Drive continuous improvement initiatives through data-driven decision-making and utilization of process analytical technologies (PAT).

Requirements :

• Bachelor’s or Master’s degree in Chemical Engineering, Pharmaceutical Engineering, or related field.
• Minimum of 5 years of experience in process engineering within the pharmaceutical or biotechnology industry.
• In-depth knowledge of pharmaceutical manufacturing processes, including solid dosage forms, liquid formulations, or sterile products.
• Strong understanding of cGMP guidelines, regulatory requirements (e.g., FDA, EMA), and industry best practices.
• Proficiency in process simulation software (e.g., Aspen Plus, SuperPro Designer) and statistical analysis tools (e.g., Minitab, JMP).
• Excellent problem-solving skills with a systematic approach to troubleshooting and root cause analysis.
• Effective communication and interpersonal skills, with the ability to collaborate effectively across multidisciplinary teams.
• Proven track record of leading process improvement projects and driving results in a fast-paced environment.
• Demonstrated commitment to safety, quality, and compliance in all aspects of work.
• Fluency in French, English is a plus

If you are interested in this role, please do not hesitate to send me your CV today for an immediate response!

[email protected]