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BeOne

Global oncology therapeutics discovery, development, manufacturing

Biotechnician 1

Bioprocess & BiomanufacturingPosted on Nov 13
Full-timeHopewell, VA, USA$25.48 - $33.48 /hr

About the Job

Requirements

  • High school education or GED is required.
  • Familiarity with computer-based systems, including Word, Excel, and PowerPoint, is required.
  • Must be able to stand for up to 8 to 10 hours per day and frequently reach above shoulder level, bend or stoop, push or pull, and handle or grip.
  • Must be able to work a scheduled 40-hour week with overtime as needed and be willing to work any shift.
  • Must be comfortable working in varying temperatures, wearing dedicated gowns depending on the area, and handling hazardous materials and chemicals.
  • Must be able to lift, push, pull, and carry up to 40 pounds, and perform repetitive motions and substantial movement of the wrists, hands, or fingers.
  • Must be able to communicate verbally and in writing and collaborate within and between diverse groups.
  • Must be able to learn moderately complex technical systems and work in a fast-paced environment with competing priorities.
  • Must travel internationally and domestically as required.

Responsibilities

  • Support the startup phase of the Hopewell manufacturing facility, then perform hands-on support and execution of current good manufacturing practice (cGMP) manufacturing operations.
  • Support activities to design, build, commission, and license the biopharmaceutical plant, including design review, equipment selection, procurement and testing, protocol development and execution, acceptance testing, equipment and automation debugging, and technical training.
  • Follow cGMP procedures to support manufacturing execution and automated recipes.
  • Prepare and transfer media and buffers, and perform filtration.
  • Sample, monitor, and transfer cell cultures, and perform harvest operations.
  • Operate and clean chromatography and filtration systems; troubleshoot equipment and processes.
  • Identify and report deviations, draft and investigate them through closure, and assist with deviation investigations and corrective and preventive action (CAPA) implementation as needed.
  • Draft, present, and close change controls; develop and optimize cGMP procedures.
  • Request, stage, and verify materials for production activities.
  • Set up and prepare equipment for formulation and filling; perform final filtration and drug product formulation.
  • Aseptically fill vials inside a Grade A isolator using automated filling equipment.
  • Perform in-process visual inspection for quality assurance; label and package finished drug product in compliance with cGMP.
  • Complete batch documentation and review records for accuracy.
  • Support routine cleanroom operations, equipment sanitization, and environmental monitoring, including collecting environmental monitoring samples.
  • Operate the Distributed Control System (DCS), Clean-in-Place (CIP) and Steam-in-Place (SIP) skids, caustic skid, autoclave, parts washer, filter integrity tester, biowelders, and other equipment.
  • Operate the SoloVPE protein concentration analyzer.
  • Clean the facility and remove process waste.
  • Support the supervisor in managing day-to-day activities, including staff availability and task load.
  • Escalate issues and concerns in a timely manner as appropriate.
  • Identify and implement continuous improvement opportunities.

Desired Qualifications

  • An associate's or bachelor's degree in a science-related or biopharmaceutical field, or equivalent technical experience, is preferred.
  • Evidence of collaboration across diverse groups and an ability to work effectively in a fast-paced environment with competing priorities.
  • Ability to receive and incorporate feedback, with ongoing professional development as a plus.

About the Company

BeOne

Global oncology therapeutics discovery, development, manufacturing

BeOne Medicines discovers, develops, and commercializes oncology therapies worldwide, focusing on hematologic cancers and solid tumors. Its products work by leveraging internal R&D and clinical development to bring therapies to market quickly, with Brukinsa serving as a leading backbone in the US and European markets. It differentiates itself through a large-scale global clinical network and cost-efficient development and manufacturing that support high margins and a focus on large-market cancer indications. Its goal is to expand access to high-impact, affordable cancer treatments across more than 45 countries while growing its pipeline into immunology and solid tumors.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Dongcheng District, China
Founded
2010

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