Sterile Manufacturing Operator

What You Will Achieve

In this role, you will:

• Provide technical and business support to engineers on various tasks.

• Prepare detailed engineering documentation, reports, and drawings.

• Conduct preliminary analyses of trajectory adequacy data and ensure model dimensional consistency.

• Make quantitative judgments on technical data and conduct tests to assist in engineering evaluations.

• Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others.

• Manage personal time and professional development, being accountable for results.

• Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe.

• Identify and solve moderately routine problems.

• Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor.

• Ensure work is reviewed for accuracy, quality, and adherence to standards.

Role Responsibilities

The essential duties for this position include but are not limited to:

• Performs all tasks as outlined in the Batch Card, SOPs, and/or Job Aids.
• Effectively demonstrates and understands the SOPs and Job Aids pertinent to all assigned tasks.
• Inspects filled syringes to established criteria and sorts defects into the appropriate receptacle for reconciliation.
• Performs manual packaging operations as assigned by the supervisor according to the appropriate SOP or Job Aid.
• Observes all SOPs and Safety and Health Regulations.
• Re-stocks packaging supplies from line stock as required to maintain packaging operation.
• Notifies supervisor, PMO and/or Quality Specialist of unusual or recurring defects in syringe products or packaging materials.
• Maintains work area in a clean and orderly manner.
• Assists in training new colleagues as required.
• If required, verifies packaging supplies and product against product board or Batch Card to assure correctness.
• Signs pertinent forms as required.
• Participates in all required training programs to maintain required level of cGMP compliance.
• Performs off-line inspection of product, such as media reading, as required.
• Performs other miscellaneous duties as assigned by supervisor.

Here Is What You Need (Minimum Requirements)

• High School Diploma or GED with 2+ years of experience

• Understanding basic problem-solving methods, mathematics, and reading skills

• Good Manufacturing Practices (also cGMP) and Batch Record comprehension

• Strong communication and leadership skills

• Ability to contribute to department success in a team environment

• Performing tasks at a productive level under demanding conditions

• Solid understanding of procedures, techniques, tools, materials, and equipment

Bonus Points If You Have (Preferred Requirements)

• Experience in a pharmaceutical or manufacturing environment

• Proficiency in engineering software and tools

• Knowledge of regulatory requirements and quality standards

• Strong analytical and problem-solving skills

• Excellent organizational and time management skills

• Demonstrated ability to prioritize tasks and manage multiple projects simultaneously

• Familiarity and basic understanding of common AI tools and a curiosity for learning how they can be used to enhance productivity

PHYSICAL/MENTAL REQUIREMENTS

• This position is in a Penicillin Facility. The candidate cannot be allergic to Penicillin, and will be required to undergo Penicillin allergy testing.
• This department requires the SMO to bend, reach, lift and stand for extended periods of time.
• The SMO must be able to grasp from 4 – 5 filled syringes at a time in one hand while manipulating them with the other hand for overall evaluation for defects.
• All SMOs must have corrected 20/20 vision including color and must be able to pass a routine inspection test using seeded syringes. The Penicillin Inspection/Packaging department is currently operating on a one-shift basis, five days per week. However, SMOs must be available for extended hours and six to seven day operations, if required. In order to maintain the required delivery schedule, overtime may be required.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

This is a Collective Barging Agreement (Union) position. The work schedule is 3pm to 11:30pm with overtime as needed.

OTHER JOB DETAILS

 

Last Date to Apply for Job: 9/17/26

Work Location Assignment: On Premise

Union Hourly Rate: $27.36

 

 

The salary for this position ranges from $0.00 to $0.00 per hour. In addition, this position offers eligibility for overtime, weekend, holiday and other pay premiums depending on the work schedule and the Company’s policies. 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 applies only to the United States - Michigan - Rochester location.

 

 

 

 

 

 

 

 

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

 

 

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

 

 

 

 

 

 

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

 

 

Engineering