BeOne

biotechnology, pharmaceutical

Manager,QualityControlChemistry

$111–151k Hopewell, New Jersey, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Manager, Quality Control Chemistry at BeOne. Skills: Quality Control (QC) Chemistry Laboratory Management, Capillary Electrophoresis (CE) expertise, GMP Compliance, Regulatory Affairs (FDA/EU). Manages all Quality Control (QC) Chemistry Laboratory – Capillary Electrophoresis (CE) activities to support GMP manufacturing, testing and release of materials, intermediates, and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures.. Establishe”

What You'll Achieve.

Ensure timely completion of testing; Ensure that the QC Chemistry (CE) laboratory meets or improves on budget, cost, volume, and efficiency targets (KPIs) in line with business objectives.

Industry & Context.

biotechnology, pharmaceutical
Problems you'll solve

analytical, problem-solving ability; Analytical Thinking/Data Analysis

Eligibility Requirements

Must be willing to travel approximately 10%

What They're Looking For.

Must Have

Bachelor’s Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with 5+ years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology, pharmaceutical company is required., 2+ years of managerial experience directly managing people required, Leadership experience leading teams, projects, programs or directing the allocation of resources., PC literacy MS Office skills (Outlook, Word, Excel, PowerPoint)., Ability to work on a computer for extended periods of time, Must be willing to travel approximately 10%

Nice to Have

Bachelor's degree in Chemistry, Biology, Molecular Biology, Biotechnology, Biochemistry, or related scientific discipline preferred., Master's degree and 4+ years of relative experience preferred.

What You'll Do.

Manages all Quality Control (QC) Chemistry Laboratory – Capillary Electrophoresis (CE) activities to support GMP manufacturing

testing and release of materials

and finished products under FDA/EU regulations

applicable International Regulations

BeOne processes and procedures.

Establishes and implements QC Chemistry procedures including but not limited to capillary electrophoresis and supports regulatory compliance inspections.

Ensures efficient and effective day-to-day operations of the CE laboratory.

Lead the QC Chemistry (CE) laboratory daily workflow.

Establish and maintain QC Chemistry (CE) laboratory related quality systems to ensure conformance with regulations and BeOne Global quality standards.

Manage QC Chemistry (CE) laboratory routine operations

including but not limited to validation

personnel training and assessment

Ensure QC Chemistry (CE) laboratory compliance with Environmental Health and Safety (EHS) standards.

Ensure timely completion of testing (e. g.

and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations.

Review of laboratory test results

ensuring adherence to Good Documentation Practices.

Ensure appropriate investigation of OOS events

and equipment failures.

Implementation of effective corrective actions and preventive actions (CAPAs).

Participate in internal and external GMP audits where possible.

Ensure that the QC Chemistry (CE) laboratory meets or improves on budget

and efficiency targets (KPIs) in line with business objectives.

Manage direct reports from QC Chemistry (CE) laboratory

How You'll Work.

Team & Collaboration

collaborative; Fosters Teamwork; Interacts with all levels of BeOne employees

Communication Scope

Credible and confident communicator (written and verbal) at all levels; Communicates with Clarity

Process & Methodology

Excellent project management skills.

Full Job Description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. **General Description:** Manages all Quality Control (QC) Chemistry Laboratory – Capillary Electrophoresis (CE) activities to support GMP manufacturing, testing and release of materials, intermediates, and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures. Establishes and implements QC Chemistry procedures including but not limited to capillary electrophoresis and supports regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports to the Senior Manager QC and is located full-time at the Hopewell, NJ site. **Essential Functions of the Job:** * Lead the QC Chemistry (CE) laboratory daily workflow. * Establish and maintain QC Chemistry (CE) laboratory related quality systems to ensure conformance with regulations and BeOne Global quality standards. * Manage QC Chemistry (CE) laboratory routine operations, including but not limited to validation, SOPs, specifications, testing records, personnel training and assessment, scheduling, etc. * Ensure QC Chemistry (CE) laboratory compliance with Environmental Health and Safety (EHS) standards. * Ensure timely completion of testing (e.g., In-process control, DS release, DP release, and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations. * Review of laboratory test results, ensuring adherence to Good Documentation Practices. * Ensure appropriate investigation of OOS events, discrepancies, lab errors, and equipment failures. * Implementation of effective corrective actions and preventive actions (CAPAs). * Participate in internal

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