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BeOne

Global oncology therapeutics discovery, development, manufacturing

Manager – Quality Control Chemistry

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeHopewell, NJ, USA

About the Job

Requirements

  • Bachelor’s degree in Chemistry, Biochemistry, or a Biotechnology-related scientific discipline and 5+ years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology or pharmaceutical company.
  • At least 2 years of managerial experience directly managing people.
  • Leadership experience leading teams, projects, or programs, or directing the allocation of resources.
  • Expertise in Quality Control within a Good Manufacturing Practice environment, with hands-on laboratory experience ensuring compliance with industry standards and regulations.
  • Working knowledge and experience with capillary electrophoretic analytical methods such as reduced and non-reduced CGE, CZE, and cIEF/icIEF.
  • Knowledge of USP/EP and cGMP/EU GMP regulations.
  • Familiarity with instrument and equipment validation.
  • Expert knowledge of quality control principles, practices, and standards for the biopharmaceutical industry.
  • A demonstrable track record and skills or experience gained in similar positions at a similar level.
  • Strong leadership and team-management skills and experience.
  • Strong written and verbal communication skills to interact at all levels.
  • Strong analytical and problem-solving ability, attention to detail, and ability to work accurately in a busy and demanding environment.
  • Excellent project-management skills.
  • Ability to prioritize and demonstrate good time-management skills.
  • Self-motivation and ability to work proactively using own initiative.
  • Strong PC literacy and skills in Outlook, Word, Excel, and PowerPoint.
  • Ability to work on a computer for extended periods.
  • Willingness to travel approximately 10%.

Responsibilities

  • Lead the daily workflow of the QC Chemistry capillary electrophoresis laboratory.
  • Establish and maintain QC Chemistry laboratory quality systems to ensure conformance with regulations and global quality standards.
  • Manage routine laboratory operations, including validation, SOPs, specifications, testing records, personnel training and assessment, and scheduling.
  • Ensure the laboratory complies with Environmental Health and Safety standards.
  • Ensure timely completion of in-process control, drug substance release, drug product release, and stability testing, and timely reporting of results to support manufacturing operations.
  • Review laboratory test results and ensure adherence to Good Documentation Practices.
  • Ensure appropriate investigation of out-of-specification events, discrepancies, laboratory errors, and equipment failures.
  • Implement effective corrective and preventive actions.
  • Participate in internal and external Good Manufacturing Practice audits where possible.
  • Ensure the laboratory meets or improves upon budget, cost, volume, and efficiency targets in line with business objectives.
  • Manage direct reports in the QC Chemistry laboratory.
  • Manage, motivate, coach, and mentor direct reports.
  • Interact with employees at all levels of the company.
  • Undertake other duties as required.

Desired Qualifications

  • A bachelor’s degree in Chemistry, Biology, Molecular Biology, Biotechnology, Biochemistry, or a related scientific discipline.
  • A master’s degree and 4+ years of relevant experience.
  • Strong analytical thinking and data analysis.
  • Ability to foster teamwork, provide and solicit actionable feedback, demonstrate self-awareness, act inclusively, take initiative, maintain an entrepreneurial mindset, pursue continuous learning, embrace change, and demonstrate results orientation and financial excellence.

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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