BeOne
Biotechnology
Biotechnician
“Biotechnician at BeOne. Skills: cGMP Manufacturing, Equipment troubleshooting, Sterile Filtration / Integrity testing, drug product formulation, filling vials inside a Grade A isolator. Equipment start-up, troubleshoot, and perform acceptance testing. Execute on the floor operations during clinical and GMP campaigns”
What You'll Achieve.
Driving Excellence; Results-Oriented; Financial Excellence
Industry & Context.
Problem Solving; Analytical Thinking/Data Analysis
Must be flexible to work 1st or 2nd shift with holidays, weekends and overtime as per business needs, Must be able to stand for long periods, up to 8 to 12 hours/day, Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently, Must be able to work scheduled 40 hours with the ability to work overtime as needed, Must be comfortable in working in varying temperatures, Frequent lifting, pushing, pulling, and carrying, Ability to lift to 40 lbs, Regular reaching, bending, stooping, and twisting, Repetitive motion and substantial movement of the wrists, hands, and/or fingers, Environment requires dedicated gowns, depending on area, Work with hazardous materials and chemicals, Willing to work any shift and must be flexible to support all business needs, cleanroom environment, International and domestic travel – periodically
What They're Looking For.
Must Have
Demonstrated ability to successfully gown into aseptic manufacturing areas, Must be able to manage heavy workload and aggressive timelines in a timely manner, prioritize and work under pressure, Ability to work in a fast-paced environment while demonstrating excellent time management and organization skills, Must be dependable and punctual, Must be flexible to work 1st or 2nd shift with holidays, weekends and overtime as per business needs, Must be able to stand for long periods, up to 8 to 12 hours/day, Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently, Must be able to work scheduled 40 hours with the ability to work overtime as needed, Must be comfortable in working in varying temperatures, Frequent lifting, pushing, pulling, and carrying, Ability to lift to 40 lbs, Regular reaching, bending, stooping, and twisting, Repetitive motion and substantial movement of the wrists, hands, and/or fingers, Work with hazardous materials and chemicals, Willing to work any shift and must be flexible to support all business needs, follow cGMP batch records and SOPs to manufacture drug products, prepare suites for manufacturing operation and operate in a safe and compliant manner
What You'll Do.
and perform acceptance testing
Execute on the floor operations during clinical and GMP campaigns
Equipment cleaning and sterilization
Solution preparation and transfer
Room and Equipment Cleaning
Equipment and process troubleshooting
Sterile Filtration / Integrity testing
Good Documentation Practices
Environmental Monitoring
Autoclaves and parts washers (equipment prep
cleaning and sterilization)
Reports any accidents
incidents and injuries or illnesses immediately and notifies manager of any hazards
unsafe acts or conditions in the workplace
ISO5 area and CNC with a variety of manufacturing production equipment and technologies
work in a cleanroom environment and follow cGMP batch records and SOPs to manufacture drug products
support projects in conjunction with other GMP Manufacturing personnel (Leads
prepare suites for manufacturing operation and operate in a safe and compliant manner
participate in the execution of all phases and facets of drug product formulation
filling vials inside a Grade A isolator with an automated filling machine
How You'll Work.
Team & Collaboration
collaborative; Fosters Teamwork; support projects in conjunction with other GMP Manufacturing personnel (Leads, Supervisors, Managers); Collaborative Spirit
Communication Scope
Communicates with Clarity
Process & Methodology
aggressive timelines, prioritize, organizational skills with the proven ability to prioritize
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