Analytical Scientist

Pfizer; Austin (TX); Vor Ort; USD 140.000 - 190.000; Vollzeit

Zusammenfassung

Pfizer leads analytical testing in a quality-controlled laboratory, featuring technical leadership across investigations, method development, and validation. The role emphasizes troubleshooting and ensuring regulatory and safety compliance.

The successful candidate will hold a Bachelor’s or Master’s degree in chemistry or related life sciences with 10+ years of experience, with strong writing and communication skills and familiarity with ISO 9001/17025/17034 requirements.

Qualifikationen

• Bachelor’s or Master’s degree in chemistry or a related life science field with 10+ years of related experience.
• Strong knowledge of analytical methods and interpretation of results.
• Knowledge of ISO 9001, ISO 17025, and ISO 17034 requirements.
• Excellent verbal communication and technical writing skills, including the ability to write procedures and reports.

Aufgaben

• Perform analytical testing of finished products, raw materials, custom projects, and in-process samples.
• Develop investigation strategies, participate in out-of-specification investigations, and write reports.
• Lead or participate in method development, validation, and technical studies.
• Qualify, maintain, and troubleshoot analytical instruments.
• Document work and maintain laboratory readiness in accordance with quality, regulatory, and safety requirements.

Kenntnisse

Analytical testing

Troubleshooting

Investigations

Technical writing

Communication

Ausbildung

Bachelor’s or Master’s degree in chemistry or related life sciences

Tools

Analytical instruments

Jobbeschreibung

Role overview

Our client is seeking a Lead Scientist to perform analytical testing and provide technical leadership in a quality-controlled laboratory. The role includes troubleshooting, investigations, and development and validation of analytical methods.

Key responsibilities

• Perform analytical testing of finished products, raw materials, custom projects, and in-process samples.
• Develop investigation strategies, participate in out-of-specification investigations, and write reports.
• Lead or participate in method development, validation, and technical studies.
• Qualify, maintain, and troubleshoot analytical instruments.
• Document work and maintain laboratory readiness in accordance with quality, regulatory, and safety requirements.
• Bachelor’s or master’s degree in chemistry or a related life science field with 10+ years of related experience
• Knowledge of ISO 9001, ISO 17025, and ISO 17034 requirements.
• Demonstrated knowledge and experience in analytical methods and interpretation of results.
• Strong verbal communication and technical writing skills, including the ability to write procedures and reports.

Preferred qualifications

• Experience in a GLP, GMP, or ISO environment.
• Knowledge of quality system requirements in medical device, pharmaceutical, or clinical industries.