52 applicants

Company

Original Job Post

Pfizer · 3 days ago

Scientist

United States - New York - Pearl River

Full-time

Onsite

Mid, Senior Level

$75K/yr - $125K/yr

5+ years exp

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Responsibilities

Perform chemical, in-vitro, or in-vivo biological assays of various samples in compliance with regulatory requirements.

Write, review, and approve protocols, reports, and investigations associated with the laboratory.

Provide time-sensitive in-process testing support for Operations.

Compile validation data into reports and work on analytical methods for new and existing products.

Conduct assays, analyze results, train analysts, and provide lab support.

Contribute to the development of new technologies, revise methods, and ensure compliance with regulations.

Make sound decisions under pressure and work collaboratively within Quality Control and across network channels.

Qualification

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Quality ControlAnalytical ExperienceLab EquipmentEquipment TroubleshootingRegulatory InspectionsNetwork ChannelsICH StandardsData IntegrityMathematical CalculationsData AnalysisProblem-SolvingDecision-MakingCollaborationLaboratory InvestigationsChange ControlTest Methods RevisionProtocol WritingAnalytical Methods SupportNew Product LaunchesMeasurement Technologies ImplementationValidation Data CompilationAssay AnalysisTraining & MentoringSOPsPlanning & ExecutionDevelopment of New TechnologiesMethod DevelopmentRegulatory ComplianceTechnical Duties

Required

High School Diploma (or Equivalent) and 8 years of relevant experience

OR an associates degree with 6 years of experience

OR a bachelors with at least 3 years of experience

OR Masters with more than 1 year of experience

A minimum of a BS/BA in Chemistry or Biochemistry or Advanced degree preferred

5 years experience within Quality Control or other relevant analytical experience in the pharmaceutical industry

General lab equipment

Equipment troubleshooting

Making sound and effective decisions under pressure

Working with other manufacturing sites to understand a broader perspective

Exposure to Regulatory inspections including direct interactions

Ability to effectively work within Quality Control, and across network channels, to accomplish goals

Knowledge of ICH and other applicable industry standards

Understanding the principles of Data Integrity

Ability to perform mathematical calculations

Ability to perform complex data analysis

Preferred

Prior experience in most, if not all, of the following areas: Laboratory investigations, Change Control, test methods revision, protocol writing and approvals, analytical methods support for new product launches and existing marketed products, new measurement technologies implementation, and validation data compilation into reports

Experience in conducting assays, analyzing results, training & mentoring, lab support, SOPs and Admin

Experience in planning and execution of tasks to achieve routine goals, coordinating testing activities of the group, and making independent contributions to the development of new technologies and methods

Experience in developing and revising methods and procedures to assure compliance with applicable regulations, and carrying out technical and administrative duties as assigned