Pfizer-posted 14 days ago
$23 - $38/Yr
Full-time • Mid Level
Onsite
5,001-10,000 employees

Use Your Power for Purpose Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need. What You Will Achieve In this role, you will: Supports manufacturing operations on the production floor for Vaccines Buffer/Media/Process Support with varying levels of automation. Follow SOPs and batch records for unit operations. Supports operation of manufacturing equipment associated with process equipment commissioning, qualification and validation. Assists troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor. Strives for Right first time execution and continuous improvement, the timely review of daily documentation and completes data entry; Identify and/or Communicate process and compliance concerns in real time. Participate in audits, as required. Assists the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations. Responsible for remaining current on assigned training. Supports Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas. Assists in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk. Escalates the need for work requests when issues arise with facility/manufacturing equipment. Utilizes enterprise systems to support manufacturing operations including but not limited to DeltaV, SAP, LIMS, AMPS, PDOCS and/or QTS. Assists in performance of cleaning, inventory, and maintaining facility in a safe and GMP compliant manner.

  • Supports manufacturing operations on the production floor for Vaccines Buffer/Media/Process Support with varying levels of automation.
  • Follow SOPs and batch records for unit operations.
  • Supports operation of manufacturing equipment associated with process equipment commissioning, qualification and validation.
  • Assists troubleshooting, technical support/analysis and resolution of equipment, automation, and process issues on the manufacturing floor.
  • Strives for Right first time execution and continuous improvement, the timely review of daily documentation and completes data entry
  • Identify and/or Communicate process and compliance concerns in real time.
  • Participate in audits, as required.
  • Assists the Subject Matter Expert for manufacturing operations in support of QTS investigations and CAPA implementations.
  • Responsible for remaining current on assigned training.
  • Supports Lean Manufacturing, Sustainability, Operational Excellence initiatives; facilitate the drive towards continuous improvement in all manufacturing areas.
  • Assists in the escalation process through various levels of management when operations, personnel safety, equipment functionality, product supply and/or quality compliance are at risk.
  • Escalates the need for work requests when issues arise with facility/manufacturing equipment.
  • Utilizes enterprise systems to support manufacturing operations including but not limited to DeltaV, SAP, LIMS, AMPS, PDOCS and/or QTS.
  • Assists in performance of cleaning, inventory, and maintaining facility in a safe and GMP compliant manner.
  • High School Diploma or GED with 2+ years of relevant experience, Associate 0 years of experience
  • Strong verbal and written communication skills
  • Proficiency in using standard manufacturing equipment and tools
  • Basic understanding of Good Manufacturing Practices (GMP)
  • Ability to follow detailed instructions and standard operating procedures
  • Strong problem-solving skills in a structured environment
  • Capability to work effectively in a team setting
  • Basic computer skills, including familiarity with data entry and reporting systems
  • Experience in a pharmaceutical or biotechnology manufacturing environment
  • Knowledge of regulatory requirements and quality systems
  • Strong organizational skills and attention to detail
  • Ability to adapt to changing priorities and manage multiple tasks
  • Demonstrated ability to take initiative and drive continuous improvement
  • Strong analytical skills and the ability to interpret technical data
  • 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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