Media Fill - Aseptic Engineer

Pfizer • Rocky Mount, NC

1d • Onsite

About The Position

USE YOUR POWER FOR PURPOSE 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. WHAT YOU WILL ACHIEVE 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.

Requirements

• Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with 0+ years of experience; OR an associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant 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 Haves

• 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.
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance.

Responsibilities

• 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.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees