Biotechnologist - Night Shift (Cell Therapy)

Lonza

Portsmouth (NH)

Presencial

USD 65.000 - 90.000

Jornada completa

Hace 9 días

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

Medical, dental, and vision insurance
Career growth and development
Exposure to advanced Cell Therapy tech
Collaborative and supportive team

Descripción de la vacante

Lonza in Portsmouth, NH is expanding our operations and seeking biotechnologists across multiple experience levels for on-site night shifts. You'll work in a regulated production environment, supporting manufacturing activities and ensuring adherence to cGMP, quality, and safety standards.

You will collaborate with Manufacturing, Quality, MSAT and cross-functional teams, participate in training and process transfers, and help maintain documentation.

Formación

  • Experience in biotechnology, pharmaceutical, manufacturing, or related industries preferred.
  • Roles across multiple levels are welcome, with nights shift experience beneficial.

Responsabilidades

  • Support manufacturing operations while ensuring safety, quality, and cGMP compliance.
  • Perform manufacturing activities in controlled cleanroom environments.
  • Participate in training, process implementation, and operational readiness activities.
  • Support technical transfers and manufacturing projects.
  • Create, review, and maintain manufacturing documentation.
  • Collaborate with Manufacturing, Quality, MSAT, and cross-functional teams.
  • Contribute to continuous improvement initiatives for safety, quality, and efficiency.

Conocimientos

Communication skills
Teamwork
Problem solving
Adaptability
Attention to detail

Educación

Associate's degree or equivalent
Bachelor's degree or equivalent

Descripción del empleo

Lonza in Portsmouth, NH is expanding our operations and seeking biotechnologists across multiple experience levels for on-site night shifts. You'll work in a regulated production environment, supporting manufacturing activities and ensuring adherence to cGMP, quality, and safety standards.

You will collaborate with Manufacturing, Quality, MSAT and cross-functional teams, participate in training and process transfers, and help maintain documentation.

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