BeiGene, Ltd.

Senior Manager, Analytical Manufacturing Science and Technology

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

Qualifications

  • Bachelor's degree in analytical chemistry, biochemistry, pharmaceutical sciences, or related discipline; Master's preferred.
  • 7+ years of experience in biopharmaceuticals required; 5+ years with Master's preferred.
  • Expertise in biologics analytical methods and protein quality attributes.
  • 5 years of leadership experience managing analytical teams, projects, or programs.
  • Preferred experience in regulatory submissions and laboratory capability expansion.

Responsibilities

  • Provide strategic oversight for analytical capabilities in monoclonal and bispecific antibody manufacturing.
  • Lead method transfers for physicochemical, potency, and structural characterization methods.
  • Support analytical readiness for new products by defining deliverables and project timelines.
  • Perform laboratory testing using HPLC, UHPLC, and capillary electrophoresis technologies.
  • Guide method qualification, validation, and complex investigations.
  • Author and approve GMP documentation including analytical transfer plans and protocols.
  • Establish metrics for transfer progress and escalate risks as needed.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401(k) retirement plan options.
  • Flexible spending accounts (FSA/HSA).
  • Life insurance policies available.
  • Generous paid time off.
  • Wellness programs to support employee health.
  • Eligibility for company stock options and participation in an Employee Stock Purchase Plan.
Full Job Description
General Description:
  • The Senior Manager, Analytical Manufacturing Science and Technology (MST), provides technical leadership and project management for analytical method transfers to Hopewell QC laboratories. The role is also accountable for overseeing the MST Analytical Laboratory and its personnel, and instruments.


Essential Functions of the Job:
  • Provide strategic and technical oversight for MST Analytical Laboratory capabilities supporting monoclonal and bispecific antibody drug substance and drug product manufacturing.
  • Lead analytical method transfers of physicochemical, potency, and structural characterization methods to Hopewell Quality Control laboratories, including gap assessments, transfer strategy, protocol execution, acceptance criteria, and final reports.
  • Support analytical readiness for new product introductions and lifecycle projects by defining deliverables, risks, resources, dependencies, and completion criteria aligned with approved project timelines.
  • Perform or direct laboratory testing, as needed, using technologies including high-performance and ultra-high-performance liquid chromatography (HPLC/UHPLC) and capillary electrophoresis (CE).
  • Provide scientific leadership for method qualification and validation, analytical comparability, method performance trending, and complex OOS, OOT, and investigations.
  • Author, review, and approve GMP documentation, including analytical transfer plans, protocols, reports, study plans, deviations, corrective and preventive actions, change controls, and standard operating procedures.
  • Support analytical content for global regulatory submissions, supplements, health authority responses, commitments, and inspection-readiness activities.
  • Establish metrics and governance for transfer progress, laboratory readiness, method performance, investigation closure, and on-time delivery; escalate risks and implement mitigation plans.


Supervisory Responsibilities:
  • Manage and develop direct report(s), including workforce planning, hiring, onboarding, objective setting, coaching, performance management, succession planning, and technical capability development.
  • Build an analytical team capable of supporting technology transfer, process development and small scale studies.
  • Lead cross-functional collaboration with Manufacturing Operations, Quality Assurance, Quality Control, CMC, Regulatory Affairs, Process Development, and external partners.

Computer Skills:
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
  • Statistical software application experience preferred (JMP, minitab, etc)
  • Experience with LIMS (Laboratory Information Management System ) preferred.


Education:
  • Bachelor's degree in analytical chemistry, biochemistry, pharmaceutical sciences, or a related scientific discipline with 7+ years of relevant biopharmaceutical experience required.
  • Master's degree in a related discipline with 5+ years of relevant biopharmaceutical experience preferred.


Other Qualifications:
  • Required: Demonstrated expertise in biologics analytical methods and protein product quality attributes; analytical method transfer.
  • 5 years of direct people-management or substantial leadership of analytical teams, projects, or programs.
  • Preferred: Experience with regulatory submissions, laboratory start-up or capability expansion.

Travel: Up to 10%

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