Manufacturing Process Engineer; Nights

Use Your Power for Purpose

Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need.

In this role, you will:

• Spends time on the production floor to proactively identify areas for improved efficiencies and ensure that product quality is maintained through all phases of production

• Serve as the areas technical SME and develops expertise in various manufacturing operations and processes including automation controls that operate and monitor the processes. Role will also support batch record and SOP revisions, electronic batch record design and deployment, commitment ownership, project management, and investigations as needed.

• Requires general knowledge of scientific principles, technical knowledge of production equipment, automation control systems, processing requirements and any related procedural requirements with emphasis on assigned production area.

• Capable of identifying technical problems and solving them with minimal guidance. Ability to analyze operational process issues and automation challenges and initiates appropriate corrective and preventative actions. Acts as a departmental liaison with primary support groups such as engineering, technical operations, quality control, quality assurance, development, and utilities.

• Primary point of contact for shift technical support and issue resolution

• Responsible for problem diagnosis / root cause(s) determination (automation, mechanical, documentation, training, etc.)

• Uses scientific and Operational Excellence tools/techniques to identify areas to optimize yield and/or and improve efficiencies

• Reviews and contributes to applicable documentation (i.e. MBRs, SOPs, etc.)

• Ensures equipment requirements can meet processing needs

• Participates in process operational improvements

• Focuses on Safety and GMP Compliance as operational priorities and as performance measures that should be included in metrics.

• Knows the processes and procedures, including the principles and practices of good data management (ALCOA), and be able to guide, advise, and coach their teams.

• High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience

• Strong leadership and teamwork skills.

• Ability to work independently and ability to apply problem-solving / troubleshooting skills in a fast-paced environment.

• Ability to work collaboratively with cross-functional teams

• Relevant pharmaceutical manufacturing experience and knowledge of current Good Manufacturing Practices (cGMP).

• Relevant automation, eM , and scheduling system experience.

• Experience in process improvement and innovation

• Strong analytical and decision-making skills

• Experience with managing projects.