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

Working with Pfizer’s dynamic engineering team, you will play a critical part in managing the maintenance and reliability engineering activities involving the redesign, maintenance, and repair of utilities systems, buildings, and production/non-production equipment.

As a Senior Associate, your knowledge and skills will contribute towards the goals and objectives of the team.  Your ability to meet team targets will help in completing critical deliverables. Your innovative use of communication tools and techniques will facilitate in managing difficult issues and establishing consensus between teams.

It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

• Contribute to completion of projects, manage own time to meet agreed targets, develop plans for short-term work activities on own projects.
• Provide engineering support to develop scope of work, project execution plans, and associated engineering studies for equipment and component installation, modification etc.
• Provide necessary operational support as needed.
• Review preventive and corrective work order activities, and provide equipment maintenance history review.
• Manage technical writing and document review.
• Ensure calibration compliance with (Current) Good Manufacturing Practices (part of GxP) contemporary technologies and best aseptic practices.
• Participate in equipment/system-based Root Cause Failure Analysis (RCFA) investigations and update equipment reliability plans.
• Partner with Production and Quality Team Leads on troubleshooting and scheduling.
• Promote safety within the workplace by following site safety procedures and perform proactive safety assessments, foster a safe work culture.
• Actively participate in site & corporate initiatives such as Communities of Practice, Limited Duration Teams.
• Facilitate and participate in the investigation teams created to determine root cause of exemption reports, QARs and laboratory investigation reports. Serve as a liaison between quality, Operations and regulatory/Compliance to facilitate timely closure of investigations.

Qualifications

Must-Have

• Must have a High School Diploma (or Equivalent) and 8 years of relevant experience.
• OR an associate degree with 6 years of experience OR a bachelors with at least 3 years of experience OR Masters with more than 1 year of experience.
• Experience with Root Cause Failure Analysis, Equipment Criticality Ranking, PM/PdM optimization, and/or Failure Modes and Effects Analysis
• Understanding and experience with process automation systems
• Strong knowledge and understanding of Current Good Manufacturing Practices {part of GxP}
• Excellent oral and written communication skills
• Working knowledge of MS Excel

Nice-to-Have

• Relevant pharmaceutical experience

PHYSICAL/MENTAL REQUIREMENTS

Lifting, sitting, standing, walking, bending, ability to perform mathematical calculations and ability to perform complex data analysis.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Ability to work particular hours (shift, overtime), travel or adhere to safe work practices and procedures such as aseptic gowning].

Work Location Assignment: On Premise

Relocation assistance may be available based on business needs and/or eligibility.