Senior Process Engineer | Freelance | Paris

il y a 3 semaines


Paris, Ile-de-France Optimus Search Temps plein

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


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