Bioprocess Specialist | cGMP Biologics Manufacturing

CAMRIS International, LLC; Silver Spring (MD); Presencial; USD 90.000 - 130.000; Tempo integral

Resumo da vaga

CAMRIS International, LLC is seeking a Bioprocess Specialist to support the Pilot Bioproduction Facility at WRAIR in Silver Spring, MD. The role encompasses hands-on cGMP manufacturing, documentation, and cross-functional collaboration across QA, engineering, and supply chain.

The ideal candidate will bring a Bachelor’s in science with 4+ years in regulated manufacturing, and hands-on experience with purification, downstream processing, and multiple bioprocess platforms.

Qualificações

• Bachelor’s degree in science with at least four years in a regulated lab or manufacturing setting.
• Hands-on GMP/cGMP manufacturing experience in pharma/biotech, vaccine, or related field.
• Experience following SOPs, GDP, and contemporaneous documentation; ability to escalate issues.
• Proficiency in purification and downstream processing of biologics or vaccines.
• Ability to support multiple manufacturing areas as priorities evolve.

Responsabilidades

• Author, revise, and maintain SOPs, batch records, work instructions, and other controlled documentation.
• Operate, qualify, and support cGMP equipment and processes per site policies.
• Execute manufacturing operations in compliance with cGMP, GDP, and approved SOPs.
• Document deviations, equipment concerns, and process issues; elevate as needed.
• Train personnel in procedures, equipment operation, and manufacturing activities.
• Maintain safe workplace and proper PPE; support cross-functional teams.

Conhecimentos

GMP manufacturing

Documentation

Process monitoring

Cross-functional collaboration

Purification/downstream processing

Formação

Bachelor's degree in science

Ferramentas

BioCommand SCADA

KrosFlo KMPi TFF

UNICORN

Column packing

Descrição da vaga

CAMRIS International, LLC is seeking a Bioprocess Specialist to support the Pilot Bioproduction Facility at WRAIR in Silver Spring, MD. The role encompasses hands-on cGMP manufacturing, documentation, and cross-functional collaboration across QA, engineering, and supply chain.

The ideal candidate will bring a Bachelor’s in science with 4+ years in regulated manufacturing, and hands-on experience with purification, downstream processing, and multiple bioprocess platforms.