Pfizer-posted 15 days ago
Full-time • Entry Level
Onsite • Sanford, NC
5,001-10,000 employees

Use Your Power for Purpose Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is flexible, innovative, and customer-oriented. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that we consistently meet the needs of those we serve. By being part of our team, you play a crucial role in maintaining this high standard and making a difference in the lives of patients. What You Will Achieve In this role, you will: Conduct and support laboratory operations, including sample preparation, data collection, and analysis Apply technical skills to assignments, ensuring high-quality results and solving moderately complex problems with sound judgment Follow procedures with general instructions, maintaining compliance with regulatory standards and working under moderate supervision Identify activities to support team goals, contributing to overall project success and ensuring adherence to project timelines Perform testing on clinical and commercial products, raw materials, and validation samples, maintaining a neat and orderly work area Independently write Standard Operating Procedures, technical reports, project plans, and other documents Train junior colleagues, develop training plans, oversee training activities, and handle laboratory investigations for events and Out of Stock results Create, review, and approve compliant test method transfer and validation protocols, reports, and equipment qualification/computer validation records

  • Conduct and support laboratory operations, including sample preparation, data collection, and analysis
  • Apply technical skills to assignments, ensuring high-quality results and solving moderately complex problems with sound judgment
  • Follow procedures with general instructions, maintaining compliance with regulatory standards and working under moderate supervision
  • Identify activities to support team goals, contributing to overall project success and ensuring adherence to project timelines
  • Perform testing on clinical and commercial products, raw materials, and validation samples, maintaining a neat and orderly work area
  • Independently write Standard Operating Procedures, technical reports, project plans, and other documents
  • Train junior colleagues, develop training plans, oversee training activities, and handle laboratory investigations for events and Out of Stock results
  • Create, review, and approve compliant test method transfer and validation protocols, reports, and equipment qualification/computer validation records
  • Applicant must have a Bachelor’s degree with 0 years of experience OR Associate’s degree with 4 years of experience OR High School Diploma (or Equivalent) and 6 years of relevant experience.
  • Demonstrated experience in manufacturing, quality, or engineering within the biotech or pharmaceutical industry
  • Solid understanding of aseptic laboratory techniques and quality systems
  • Ability to establish strong relationships within business lines
  • Excellent written and verbal communication and interpersonal skills
  • Proficiency in laboratory information management systems and data analysis software
  • Strong problem-solving skills and attention to detail
  • Ability to stand for several hours.
  • Ability to lift up to 50 pounds.
  • Non-Standard work schedule, travel or environment requirements Regular schedule: 2nd shift M-F (12md-8:30pm)
  • Ability to work recurring weekend shifts or flexible hours when business needs require it.
  • Experience in Quality Operations
  • Laboratory experience including Cell Culture, Bioassay, Aseptic Technique, and ELISA
  • Familiarity with regulatory requirements and compliance standards
  • Ability to work independently and as part of a team
  • Strong organizational and time management skills
  • Ability to adapt to changing priorities and work in a fast-paced environment
  • 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
  • health benefits to include medical, prescription drug, dental and vision coverage
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