Why Patients Need You

Our breakthroughs would not make it to the hands of patients without our pharmaceutical manufacturing team. We rely on a team of dedicated and agile members, who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always look to improve outcomes. You will help to ensure that patients and physicians have the medicines they need, when they need them.

What You Will Achieve

Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring that customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you will play a key role in accelerating the delivery of medicines to the world. Your innovative ideas and proactive actions will help us imagine new possibilities and bring them to life, ensuring that our solutions are both timely and effective. Your contributions will be essential in ensuring that our manufacturing processes are efficient, reliable, and of the highest quality, ultimately helping us deliver life-saving medicines to those who need them most.

How You Will Achieve It

In this role, you will:

• Develop and refine process formulations, methods, and controls to meet high-quality standards.
• Recommend and implement enhancements to solve complex problems and improve processes.
• Evaluate product requirements for compatibility and assist in determining optimal production costs and schedules.
• Contribute to project tasks and milestones, organizing work to meet deadlines.
• Learn and apply basic team effectiveness skills within the immediate work team.
• Make decisions within limited options to resolve basic problems under the supervisor's direction.
• Work in a structured environment using established procedures and seek guidance from colleagues.
• Ensure data integrity and compliance with Standard Operating Procedures and regulatory requirements.
• Coordinate all work on scheduled projects, including personnel activities, documentation, and outside resources.
• Support site compliance with regulatory requirements, including performing equipment cleaning, swabbing, visual inspections, and assisting in document preparation and training.

Qualifications

Must-Have

• Applicant must have a High School Diploma (or Equivalent) and 6 years of relevant experience OR an associates degree with 4 years of experience OR a bachelors degree with 0+years of experience.
• Demonstrated ability to provide technical solutions for complex problems through equipment and process understanding
• Working knowledge of Food and Drug Administration Regulations and Good Manufacturing Practices
• Proactive, with experience in high-performance teams, strong interpersonal and project management skills
• Strong written and verbal communication skills
• Proficiency in Microsoft Applications
• Ability to work effectively in a team environment and collaborate with cross-functional teams

Nice-to-Have

• Demonstrated experience in a relevant manufacturing environment
• Knowledge and experience with Drug Product processing and equipment
• Experience with process validation and equipment qualification
• Familiarity with Lean Manufacturing principles and Six Sigma methodologies
• Excellent organizational skills and attention to detail
• Strong leadership and mentoring abilities
• Ability to adapt to changing priorities and work effectively under pressure

  
 

PHYSICAL/MENTAL REQUIREMENTS

• No unique physical requirements
• Remains organized & positive in ambiguous and fast-paced, rapidly changing situations
• Ability to analyze data from detailed schedule and risk management tools
• Interface effectively with multiple stakeholder groups

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Schedule is on 2nd shift, 12-Hour Night Shift (6pm - 6am). Limited travel required.  Non-standard work hour support of global conference calls, 24/7 manufacturing, etc. required when needed, though not typical of weekly requirements.

Work Location Assignment: On Premise

OTHER JOB DETAILS

• Last Date to Apply for Job: January 16th, 2025
• Referral Bonus Eligibility: YES
• Eligible for Relocation Package: NO

The annual base salary for this position ranges from $64,600.00 to $107,600.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% 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

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