BeiGene, Ltd.

Sr. Scientist, Drug Product, MST

BeiGene, Ltd.$103K — $138K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree with 4+ years of pharmaceutical Drug Product experience required
  • Master's degree and 2+ years of Drug Product experience preferred
  • Technical experience in sterile drug product manufacturing
  • Strong PC literacy with MS Office skills required
  • Experience with GMP systems for document management and batch records

Responsibilities

  • Support technology transfer for cGMP drug product fill/finish operations
  • Provide on-floor technical support for GMP practices and troubleshooting
  • Author and maintain process documentation for the product lifecycle
  • Monitor and analyze process performance data for continued verification
  • Support qualification and validation activities including IQ/OQ/PQ and PPQ
  • Develop and maintain Bills of Material and manufacturing support documentation
  • Lead investigations for deviations and assess technical impacts

Benefits

  • Comprehensive benefits including Medical, Dental, and Vision
  • 401(k) plan with company contributions
  • Paid Time Off and Wellness programs
  • Opportunities for discretionary equity awards
  • Employee Stock Purchase Plan
Full Job Description
General Description:
  • This role in Manufacturing Science and Technology (MST) provides technical support for BeOne's large molecule Drug Product manufacturing operations, with emphasis on lyophilization, liquid drug product processing, aseptic filling, visual inspection, technology transfer, process validation, continued process verification, continuous improvement, and quality investigations.

Essential Functions of the Job:
  • Support technology transfer and lifecycle management for cGMP drug product fill/finish operations, including liquid formulation/filling and lyophilization.
  • Provide on-floor and technical support to Drug Product Operations for aseptic processing, GMP practices, process troubleshooting, and manufacturing readiness.
  • Author and maintain process related documents, process risk assessments, and technical documentation throughout the product lifecycle.
  • Monitor, trend, and analyze process performance data to support continued process verification and identify improvement opportunities.
    Support qualification, process engineering, and validation activities, including IQ/OQ/PQ, PPQ, CPV, and related protocols and reports.
  • Support implementation and maintenance of key drug product controls, including PUPSIT, CCIT, sterile filtration, container closure, and aseptic process controls.
  • Develop and maintain Bills of Material (BOM), material specifications, and manufacturing support documentation as needed.
  • Lead or support investigations for deviations and process-related events, including root cause analysis, technical impact assessment, and CAPA implementation.
  • Collaborate with Manufacturing, Quality, Engineering, Validation, MSAT/MST, Supply Chain, and Document Management to support compliant and reliable operations.
  • Assist in regulatory filings, audits, and Health Authority inspections related to Hopewell drug product manufacturing operations.

Supervisory Responsibilities:
  • Individual Contributor (no direct reports)
  • May provide technical guidance, coaching, and review support to junior staff or cross-functional team members during manufacturing support, investigations, validation, and documentation activities.
  • Collaborate cross-functionally with Manufacturing, Facilities & Engineering, Validation, Quality Control/Assurance, Supply Chain, and Document Management.


Education:
  • Bachelor's degree and 4+ years of pharmaceutical Drug Product experience required
  • Master's degree and 2+ years of Drug Product experience preferred

Computer Skills:
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
  • Experience with GMP systems for document management, deviations, CAPA, change control, training, and batch record support.
  • Ability to analyze manufacturing and process performance data using Excel and statistical software such as JMP or Minitab preferred.
  • Experience with SAP, Veeva, electronic batch records, or other manufacturing/quality systems preferred.

Other Qualifications:
  • Technical experience in sterile drug product manufacturing, including aseptic technique, liquid drug product processing, filling, lyophilization, capping, visual inspection, and GMP documentation practices.
  • Ability to apply scientific and engineering judgment to troubleshooting, investigations, risk assessments, validation, and process improvement activities.


Travel: Up to 5%

Salary Range: $103,900.00 - $138,900.00 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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