Why Patients Need You

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is vital to making sure customers and patients have the medicines they need, when they need them. Working with our innovative engineering team, you'll help bring medicines to the world even faster by imagining what’s possible and taking action.

What You Will Achieve

To lead several solvent recovery process campaigns from the start of production and track this material with respect to quality and EHS until completion and release of the material.

How You Will Achieve It

• Responsible for developing Solvent recovery /Operating Instructions and necessary Standard Operating Procedures.
• Process control system knowledge and troubleshooting.
• Investigate, troubleshoot and report findings of manufacturing/ solvent recovery issues.
• Develop, implement and monitor technical solutions for processing issues.
• Play a pro-active role in ensuring the site safety standards are adhered to.
• Ensure the process meets the agreed site quality standards.
• Proactively monitor, identify, develop and implement improvements in processes and equipment.
• Perform alarms trends review using DCS Delta V control system and effectively reduce.
• Focus on Safety and GMP Compliance as operational priorities and as performance measures.
• Know the processes and procedures, including the principles and practices of good data management (ALCOA), and be able to guide, advise and coach their teams.
• Be accountable for the Good Data Management and Data integrity understanding and performance of their team.
• Communicate on a regular basis to the plant personnel on process updates.
• Train the process technicians on the process and procedures as required.
• Ensure we adhere to our approved procedures and update these as required.
• Accountable for Documentation, Training, Process knowledge

Qualifications

Must-Have

• Degree in Science or Degree in Engineering, in Chemical Engineering
• 3+ years of demonstrated experience in {Current} Good Manufacturing Practices {part of GxP} industrial experience, ideally covering Operations, Engineering, Projects and equipment qualification within bioprocess manufacturing.
• Demonstrated ability to provide technical solutions for complex problems through equipment/process knowledge.
• Familiar with site Learning Management System and processes
• Proven ability leading and working in cross functional teams, excellent leadership, communication, and interpersonal skills.

Nice-to-Have

• Master's degree
• Relevant pharmaceutical experience
• Knowledge of site operations.

 
Work Location Assignment: On Premise

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.