Cell Therapy Manufacturing Associate I

Bristol-Myers Squibb Company; Bothell (WA); Presencial; USD 43.000 - 51.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible Time Off

11 paid company holidays

Paid vacation (160 hours annually)

Descripción de la vacante

Bristol Myers Squibb is seeking candidates to support routine Cell Therapy manufacturing operations in a cleanroom environment. You will contribute to GMP-compliant processes, batch records, and SOPs while collaborating with a multi-disciplinary team to ensure safety and quality.

The role emphasizes training, documentation, and adherence to ALCOA+ principles, with shifts covering various schedules. Prior cGMP exposure and detail-oriented mindset are valued.

Formación

• 0-1 years of cGMP cell therapy manufacturing or related experience.
• Proven teamwork experience with collaborative results.
• Proficiency in common computer tools (word processing, spreadsheets, browser apps).
• Meticulous attention to detail and personal accountability.

Responsabilidades

• Learn and execute Cell Therapy Manufacturing operations in a compliant manner.
• Execute operations per SOPs, batch records, and work instructions.
• Maintain safety and quality systems, document contemporaneously.
• Train for proficiency in process systems and business tools.
• Support daily unit operations across multiple shifts and cleanroom environments.

Conocimientos

GMP knowledge

Team collaboration

Attention to detail

Safety awareness

Educación

Associate or bachelor's degree preferred

High school diploma or equivalent required

Herramientas

Word processing

Spreadsheets

Web-based applications

Descripción del empleo

Bristol Myers Squibb is seeking candidates to support routine Cell Therapy manufacturing operations in a cleanroom environment. You will contribute to GMP-compliant processes, batch records, and SOPs while collaborating with a multi-disciplinary team to ensure safety and quality.

The role emphasizes training, documentation, and adherence to ALCOA+ principles, with shifts covering various schedules. Prior cGMP exposure and detail-oriented mindset are valued.