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BeOne

Global oncology therapeutics discovery, development, manufacturing

Senior Manager of Process Engineering - Drug Substance and Drug Product

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeHopewell, NJ, USA$138.8k - $183.8k /yr

About the Job

Requirements

  • A minimum of 7 years of experience supporting GMP pharmaceutical operations in biopharmaceutical manufacturing, engineering, and/or project management, including at least 5 years of project management experience in biologics or GMP.
  • Effective leadership of technical teams.
  • Expertise in developing a team of engineers.
  • Ability to give and receive feedback effectively.
  • Ability to identify, share, and implement site improvement opportunities proactively.
  • Ability to manage multiple complex priorities simultaneously under tight timelines.
  • Analytical problem-solving and proactive decision-making skills.
  • Ability to work in an office environment, construction site, laboratory, or manufacturing area.
  • Ability to sit, stand, and use standard office equipment for extended periods.
  • Proficiency in Microsoft Office Suite, including Excel, PowerPoint, Word, and Outlook.
  • Experience with project management tools such as Microsoft Project, AutoCAD, and Smartsheet.
  • Familiarity with data management and visualization tools such as SharePoint, Teams, and Power BI.
  • Ability to create and maintain Gantt charts, dashboards, and tracking templates.
  • Comfort working within document management systems such as Veeva Vault, eQMS, or similar.
  • BS or higher in engineering and/or a related discipline.

Responsibilities

  • Lead hands-on subject matter experts supporting technology transfers and new equipment selections, day-to-day manufacturing troubleshooting and support, deviation and investigation root cause analysis, regulatory inspections, and continuous improvement.
  • Provide technical direction and project management support while working independently with minimal supervision and direction.
  • Lead technical teams effectively, with a focus on right-first-time quality.
  • Apply hands-on experience designing, selecting, and troubleshooting systems and equipment used in commercial drug substance and drug product manufacturing.
  • Support technology transfer and qualification studies associated with developing and implementing processes, systems, and facilities related to drug product manufacturing.
  • Partner with Operations, Quality, and Automation functional areas.
  • Develop and review technical documentation.
  • Participate in and lead controls fault analysis and remediation.
  • Directly support operations with troubleshooting and issue resolution.
  • Work in an industrial manufacturing environment, including gowning.
  • Support operations and ensure compliance with regulatory, corporate, and site requirements.
  • Travel domestically up to 5%, including possible visits to partner or manufacturing sites.

Desired Qualifications

  • Experience with Operational Excellence and/or Lean methodologies.

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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