Pfizer-posted 1 day ago
$21 - $35/Yr
Full-time • Entry Level
Onsite • Kalamazoo, MI
5,001-10,000 employees

Use Your Power for Purpose Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them. What You Will Achieve The Trainer position supports their assigned with training and support activities. Trainers develop and conduct training and qualification activities for all new and established Operators . Work is performed in strict compliance with manufacturing standards (SOPs) and following all regulatory requirements (i.e., GMPs & OSHA) . This job includes the following functions: Perform all tasks in strict compliance with operating procedures, best practices and regulatory requirements. Dependable – Follows unit / area / plant requirements and guidelines. Demonstrate leadership behaviors within the unit, taking ownership and accountability of the production schedule , product quality, and leading by example. Willing to assist other production units in order to meet unit / site goals. Demonstrating growth mindset to share best practices and utilize downtime effectively. Working safely and compliantly following all applicable SOPs and standards including recording of GMP documentation. Completing and maintaining all required training on time ; oversee all aspects of training documentation in PLS and update curricula . Update and maintain OJT training reports . Conduct new hire training per curricula. Conduct AQL, TAQL, and defect classifications Perform necessary process audits on operators including , but not limited to cartons, sleeves, trays, and procedure audits. These audits may have a direct impact on individual colleague performance. Utilize computer skills to interact with multiple systems, performing entries is systems such as but not limited to SAP, PEPs, WPM , VDIT, PLS, QTS, etc. Display robust communication between shifts as well as with colleagues in the area I nteract and possibly correct individual colleague behavior and practices Train and mentor new colleagues and TCWs Working safely and compliantly following all applicable SOPs and standards including recording of GMP documentation Completing and maintaining all required training on time Consistently displays Own-It behaviors in accordance with Pfizer Core Competencies: Seizes accountability; grows self; change agile; self-awareness; commits to one Pfizer; peer relationships. Utilize downtime effectively and learn production principles Other duties as assigned by the supervisor 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. Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run. Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations. Perform in-process quality inspections, and seek to implement process and safety improvements.

  • Perform all tasks in strict compliance with operating procedures, best practices and regulatory requirements.
  • Dependable – Follows unit / area / plant requirements and guidelines.
  • Demonstrate leadership behaviors within the unit, taking ownership and accountability of the production schedule , product quality, and leading by example.
  • Willing to assist other production units in order to meet unit / site goals.
  • Demonstrating growth mindset to share best practices and utilize downtime effectively.
  • Working safely and compliantly following all applicable SOPs and standards including recording of GMP documentation.
  • Completing and maintaining all required training on time ; oversee all aspects of training documentation in PLS and update curricula .
  • Update and maintain OJT training reports .
  • Conduct new hire training per curricula.
  • Conduct AQL, TAQL, and defect classifications
  • Perform necessary process audits on operators including , but not limited to cartons, sleeves, trays, and procedure audits. These audits may have a direct impact on individual colleague performance.
  • Utilize computer skills to interact with multiple systems, performing entries is systems such as but not limited to SAP, PEPs, WPM , VDIT, PLS, QTS, etc.
  • Display robust communication between shifts as well as with colleagues in the area I nteract and possibly correct individual colleague behavior and practices
  • Train and mentor new colleagues and TCWs
  • Working safely and compliantly following all applicable SOPs and standards including recording of GMP documentation
  • Completing and maintaining all required training on time
  • Consistently displays Own-It behaviors in accordance with Pfizer Core Competencies: Seizes accountability; grows self; change agile; self-awareness; commits to one Pfizer; peer relationships.
  • Utilize downtime effectively and learn production principles
  • Other duties as assigned by the supervisor
  • 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.
  • Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run.
  • Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations.
  • Perform in-process quality inspections, and seek to implement process and safety improvements.
  • High School Diploma or GED with 2+ years of relevant experience
  • Strong analytical and problem-solving skills
  • Excellent problem-solving and decision-making skills
  • Excellent communication and interpersonal skills
  • Ability to work independently and as part of a team
  • Detail-oriented with strong organizational skills
  • Previous experience in cGMPs (current Good Manufacturing Practices) environment
  • Previous Experience on Inspection is Highly preferred.
  • Proficiency in using manufacturing software and tools
  • Ability to adapt to changing priorities and work in a fast-paced environment
  • Demonstrated leadership skills and ability to mentor team members
  • 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.
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