Operational Scientist (Pharmaceutical Manufacturing)

Job summary

The role involves supporting the Upstream microbial manufacturing line within a pharmaceutical manufacturing environment, focusing on Drug Bulk Intermediate (DBI) and Active Pharmaceutical Ingredient (API) production. The position requires collaboration with a team of technicians and supervisors to ensure compliance with cGMP standards and efficient production processes.

Qualifications

• Master's degree in chemical engineering or a related field.
• Minimum of 3 years of experience in a GMP environment within the pharmaceutical industry.
• Strong understanding of Upstream processes and LEAN principles.
• Professional fluency in English.

Responsibilities

• Ensure cGMP compliance and train manufacturing associates.
• Manage production activities according to the production plan and participate in execution as needed.
• Coordinate preparations for various projects.
• Support training on new equipment and secure short-term planning.
• Participate in daily reviews and board meetings.
• Act as a Subject Matter Expert (SME) on microbial equipment and processes.
• Update cGMP SOPs and TEQs.

Skills

• Strong analytical and structured approach to tasks.
• Ability to thrive in a dynamic, high-paced work environment.
• Excellent teamwork and collaboration skills.

Education

• Master's degree in chemical engineering or a similar field.

Tools

• Familiarity with cGMP standards and microbial manufacturing equipment.