Senior Process Engineer | Freelance | Paris > Joboolo FR :
Société : Optimus Search Lieu : 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 SeniorProcessEngineer to join the team on a contract basis for a minimum of 12 months.
As a SeniorProcessEngineer, 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:
SeniorProcessEngineer 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 processengineering 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 rcatchpoleoptimussearch.com OptimusSearch Paris Expérience souhaitée
