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Penicillin Sterile Manufacturing Operator; 2nd shift - Rochester, MI

Job in Rochester, Oakland County, Michigan, 48308, USA
Listing for: VetJobs
Full Time position
Listed on 2026-02-15
Job specializations:
  • Manufacturing / Production
    Operations Engineer, Manufacturing Production
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below
Position: Penicillin Sterile Manufacturing Operator(2nd shift) - Rochester, MI

Job Description

ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps.

Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.

SMO
- Penicillin Sterile Manufacturing Operator(2nd shift-3:00p.m-11:30p.m)

Use Your Power for Purpose

At Pfizer, we believe that every role contributes to our mission of improving patients' lives. Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a pivotal role in accelerating the delivery of medicines to the world.

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.
Essential Duties And Responsibilities
  • 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.
  • Restocks 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.
Additional Qualifications/Responsibilities

Minimum Requirements
  • High School Diploma or GED with 2+ years of experience.
  • Understanding basic problem‑solving methods, mathematics, and reading skills.
  • Good Manufacturing Practices (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…
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