Manufacturing Operator

Rangam is seeking candidates for a Direct Hire role as a Sterile Manufacturing Operator with our client Pfizer, one of the world’s largest pharmaceutical companies.

Applicants cannot be allergic to penicillin or amoxicillin

Seeking candidates on-site in Rochester, MI 48307

First shift | Full Time | Hourly Rate: $26.57

* This position is being offered as part of a disability/neurodiversity hiring program which is designed to provide a more inclusive and supportive hiring process and work environment for job seekers with physical and cognitive disabilities, which includes, but is not limited to autism, ADD/ADHD, PTSD, OCD, Anxiety Disorder, Dyslexia, Bipolar, and Tourette's Syndrome*

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
• 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…