BeiGene, Ltd.

Senior Manager, Process Engineering Drug Substance and Drug Product

BeiGene, Ltd.$138K — $183K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 7+ years in GMP pharmaceutical operations, engineering, or project management
  • 5+ years managing projects in biologics or GMP
  • Expertise in team leadership and development
  • Strong feedback communication skills
  • Ability to identify and implement improvement opportunities
  • Proven problem-solving and decision-making skills
  • Capability to manage multiple priorities under tight deadlines

Responsibilities

  • Lead technical teams to ensure quality standards are met
  • Design, select, and troubleshoot manufacturing systems and equipment
  • Oversee technology transfer and qualification studies
  • Collaborate with Operations, Quality, and Automation teams
  • Develop and review relevant technical documentation
  • Conduct controls fault analysis and drive remediation efforts
  • Support manufacturing operations with troubleshooting

Benefits

  • Medical, Dental, Vision coverage
  • 401(k) plan with employer match
  • Flexible Spending Account (FSA) / Health Savings Account (HSA)
  • Life Insurance policy
  • Generous Paid Time Off
  • Wellness programs
  • Equity awards and Employee Stock Purchase Plan
Full Job Description

BeOne Medicines is seeking a highly motivated and organized Senior Manager of Process Engineering for Dug Substance and Drug Product to join our team at the Hopewell, NJ site. The successful candidate will be responsible for leading a hands-on team of subject matter experts focused on supporting technology transfers and new equipment selections, troubleshooting and supporting day-to-day manufacturing, supporting deviation/investigation root cause analysis, regulatory inspections, and continuous improvement. This role works independently, with minimal supervision and direction and will provide technical direction, Project Management support.

Responsibilities

  • Effective leadership of technical teams with focus on right-first time Quality.

  • Prior hands-on experience in the design, selection, and troubleshooting of systems and equipment used in commercial Drug Substance and Drug Product manufacturing.

  • Support of technology transfer and qualification studies associated with the development and implementation of processes, systems, and facilities related to drug product manufacturing.

  • Partner with Operations, Quality, and Automation functional areas.

  • Develop and review technical documentation

  • Participate and lead in controls fault analysis and remediation

  • Directly support operations with troubleshooting and issue resolution

  • Requires working in an industrial manufacturing environment including gowning

  • Support operations and ensure compliance with regulatory, corporate and site requirements

Required Skills/Experience

  • Minimum 7 years of experience GMP pharmaceutical operations support. in biopharmaceutical manufacturing, engineering, and/or project management and at least 5 years of project management experience in biologics or GMP.

  • Effective leadership of technical teams.

  • Passion and expertise developing a team of Engineers

  • Effectively gives and receives feedback.

  • Proactively identifies, shares, and implements improvement opportunities that supports the site.

  • Proven ability to manage multiple complex priorities simultaneously under tight timelines.

  • Analytical problem-solving skills and proactive decision-making.

Preferred Skills/Experience

  • OE and/or LEAN Methodologies

Physical Requirements:

  • Ability to work in an office environment, construction site, and laboratory or manufacturing areas.

  • May require up to 5% travel, including visits to partner or manufacturing sites.

  • Must be able to sit, stand, and use standard office equipment for extended periods.

Computer Skills: 

  • Proficiency in Microsoft Office Suite (Excel, PowerPoint, Word, Outlook).

  • Experience with project management tools such as Microsoft Project, Autocad, Smartsheet.

  • Familiarity with data management and visualization tools (e.g., SharePoint, Teams, Power BI).

  • Ability to create and maintain Gantt charts, dashboards, and tracking templates.

  • Comfortable working within document management systems (e.g., Veeva Vault, eQMS, or similar).

Education Required:

  • BS or higher in engineering and/or related discipline.

Travel:

  • May require domestic travel up to 5% travel

    Salary Range: $138,800.00 - $183,800.00 annually

    BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process.  Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.

    About BeiGene, Ltd.

    BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
    Learn more about BeiGene, Ltd.
    Size
    8,300 employees
    Market Cap
    $22.2 billion
    Industry
    Net Income
    -$1.5 billion
    Founded
    2010
    5 Year Trend
    +305.7%
    Revenue
    $308.8 million
    NASDAQ

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