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The Senior Specialist is responsible for leading technical reviews, ensuring compliance, mentoring junior staff, and supporting quality investigations related to assays and technologies in a life sciences environment.

As an Intern, you'll gain hands-on experience in pharmaceutical manufacturing, adhering to cGMP, and supporting daily operations while developing problem-solving skills.

The Senior Analyst QC will execute and interpret analytical methods, ensure compliance with cGMP, support investigations, and mentor team members in a biochemistry QC lab setting.

The Associate Manager in Process Development leads a team in downstream purification activities, ensuring compliance, coaching members, and handling projects and lab work.

Lead technology transfer of manufacturing processes for cell & gene therapy while providing technical oversight during GMP runs and continuous improvements.

In this role, you will perform GMP manufacturing operations, handle equipment, maintain lab standards, and apply aseptic techniques in a team-oriented environment.

As a Biotechnologist, you will perform GMP manufacturing operations, maintain facility standards, handle bioreactors, and utilize process control systems.

The AnT1 Trainee will undergo a 15-month training program involving analysis, documentation, lab support, and adherence to cGMP, aimed at building competencies in quality control within biopharmaceuticals.

Lead and supervise electrical engineers and technicians to perform maintenance, troubleshooting, repairs, and preventive maintenance in a cGMP manufacturing environment. Manage electrical and fire alarm systems, supervise vendors, ensure GMP/EHS compliance, train staff, and lead root cause analyses to minimize production disruption.

The QA Specialist will perform QA activities including batch record review, product release documentation, deviation investigations, CAPA monitoring, and supporting regulatory inspections in a GMP facility.