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Senior Process Engineer | Freelance | Paris
Il y a 4 mois
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
rcatchpole@optimussearch.com
