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Sterile Manufacturing Operator B (1st shift)

|  Posted On: Jan 23, 2026

location:Rochester, MI 48307

Duration:Direct Hire (Full Time)

mode of work:On-site

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Job Summary

Job Title:  
Sterile Manufacturing Operator B (1st shift)

Posted Date:  
Jan 23, 2026

Duration:  
Direct Hire (Full Time)

Shift(s):  

08:00 - 16:00


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Talk to our Recruiter

Name:
 
Mariah Marsh

Email:
 
mariah@rangam.com

Phone:
 
908-704-8843

Description

Rangam is seeking candidates for a Direct Hire role as a Sterile Manufacturing Operator B (1st shift) with our client Pfizer, one of the world’s largest pharmaceutical companies. Seeking candidates in Rochester, MI or willing to relocate.

Applicants cannot be allergic to penicillin or amoxicillin
 

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.

 

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

Essential Duties and 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 sort 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.

 

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 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

N/A

Hourly Rate: $26.57

Work Location Assignment: On Premise

Last Day to Apply: January 28th, 2026.

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.

 

Sunshine Act

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations.  These laws and regulations require Pfizer to provide government agencies with information such as a health care provider’s name, address and the type of payments or other value received, generally for public disclosure.  Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act.  Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.  If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

 

EEO & Employment Eligibility

 

It is the policy of Rangam Consultants, Inc. to provide equal employment opportunities to all applicants and employees without regard to any legally protected status such as race, color, religion, gender, national origin, age, disability or veteran status. 

 

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