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

• Applicant must have a HS Diploma (or Equivalent) and 8 years of
  relevant experience OR an associates 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.

Nice-to-Have

• Experience with maintenance best practices (TPM, RBN, CBN)

• Relevant pharmaceutical experience

  
 

PHYSICAL/MENTAL REQUIREMENTS

• The noise level in the work environment is usually moderate.  While performing the duties of this job the employee is occasionally required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear; and lift up to 25 lbs.  Specific vision abilities required by this job include ability to adjust focus.

• Collects and researches data; gathers and analyzes information skillfully; approaches problems objectively and systematically; draws accurate conclusions from complex information.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

• Job will require supporting the production schedule which includes certain level of availability on long days, weekends or alternative shifts.

• At different times of the year, this position will work long hours for scheduled manufacturing shutdown periods and throughout the year may be required to work late with little notice as need arises when equipment is unexpectedly down.  

• Limited travel may be required.

Relocation support available

Work Location Assignment: On Premise

The annual base salary for this position ranges from $78,000.00 to $130,000.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.

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

Engineering