BeOne Medicines
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Principal Scientist, Drug Product
role at
BeOne Medicines 2 days ago Be among the first 25 applicants Join to apply for the
Principal Scientist, Drug Product
role at
BeOne Medicines Get AI-powered advice on this job and more exclusive features. 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
This role in the Manufacturing Science and Technology (MST) department supports BeOne’s Drug Product Manufacturing Technology Transfer and support. based in New Jersey (Hopewell), this role will be to lead the Hopewell drug product MST function to support technology transfer, validation, continued process verification, investigations, change management and site startup of Hopewell internal drug product manufacturing activities. Reporting to the MST leadership, this role is responsible for managing the technical operations supporting both clinical and commercial manufacturing activities.
Leadership
Serve as MST DP SME and process lead for drug product, ensuring the materials, strategy and documentation are in place. Collaborate with DP/SC/QC/QA to develop testing strategy for DP raw materials and in-process samples. Author and maintain process control strategy documents throughout the lifecycle of a program and maintain process risk assessment documents. Author PPQ protocols and reports. Oversee execution of PPQ and PPQ related activities Support engineering teams on equipment selection, qualification, and start up activities. Monitor and CPV trend process performance, including input and output parameters. Responsible for technical transfer, validation, investigation, and technical support of aseptic manufacturing operations in Hopewell and CMOs. Collaborate with Drug Product Operations to establish robust and compliant manufacturing performance. Collaborate with Global DP MS&T and Technical Development to enable new DP filling capability at Hopewell Location. Provide technical support for Drug Product Operations. Provide input into operational metrics, budgeting, and planning. Establish a data and metrics driven culture. Relentlessly maintain alignment with other global manufacturing sites through shared knowledge, shared manufacturing data, shared manufacturing issues, and common solutions. Partner with GZ Technical Development to successfully transfer and validate HPW DP processes. Product scope includes parenteral vials and lyophilized products. Collaborate with Technical Development in investigating and resolving complex manufacturing issues at CMOs. Manage and coordinate global change ensuring stakeholders alignment. Assist in Regulatory filings and Health Authority site inspections to license and maintain BeOne’s pipeline and product portfolio.
Essential Functions
Lead technology transfer for cGMP manufacturing focused drug product fill/finish. Ensure effective information flow, risk assessment, timeline execution, issue resolution and documentation for cross-functional teams. Includes leading tech transfer, detailed process definition and facility fit assessment exercises. Execute scale down model of manufacturing processes. Maintains a good laboratory practice. Author and maintain process control strategy documents throughout the lifecycle of a program and maintain process risk assessment documents Author PPQ protocols and reports. Oversee execution of PPQ and PPQ related activities Support engineering teams on equipment selection, qualification, and start up activities. Monitor and trend process performance, including input and output parameters. Investigate root causes of major deviations for cGMP manufacturing, and implement CAPA for major deviations Identifying opportunities to improve systems and practices Work with counterparts in Process Development, Process Sciences, Manufacturing, Quality, Project Management teams etc. to facilitate technology transfer and project success.
Preferred Skills/Experience
Facility Start-Up Commissioning, Qualification & Validation Equipment and/or Process Design Quality Risk Assessments Health Authority Interaction/Audits OE and/or LEAN Methodologies Distributed Control system / Control Systems Deviation Assessments / Investigations SAP, LIMS, CMMS, Veeva Expert level knowledge in all Drug Product aseptic filling operation Expert level knowledge of Isolator, packaging and automated inspection machines. Expert level knowledge in IQ/OQ/PQ and process engineering Expertise in late stage/commercial Drug Product technology transfer, process characterization and process validation biopharmaceutical/gene transfer vector manufacturing preferred. Working knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing. Ability to work both independently and as part of a team. Ability to function in a fast-paced dynamic team environment and balance prioritize multiple projects Excellent troubleshooting skills and ability to solve complex technical issues. Ability to compile, analyze and interpret data; Ability to write routine reports and correspondence. Strong interpersonal and communication skills, verbal and written. Ability to speak effectively before groups of customers. Ability to communicate in a dynamic environment.
Qualifications
BA/BS or higher in science, biochemistry, biotechnology, biology, chemical engineering and/or related discipline. Minimum of 7 years of experience working in Biopharmaceutical DP process development or manufacturing experience.
Physical Requirements
Must be able to stand for long periods, up to 8 to 10 hours/day. Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently. Must be able to work scheduled at least 40 hours/week (on-site). Must be comfortable in working in varying temperatures. Frequent lifting, pushing, pulling, and carrying. Ability to lift up to 40 lbs. Regular reaching, bending, stooping, and twisting. Repetitive motion and substantial movement of the wrists, hands, and/or fingers. Environment requires dedicated gowns, depending on area. Work with hazardous materials and chemicals.
Computer Skills:
Familiarity with computer-based systems. Word, Excel, and PowerPoint a must.
Travel:
International and domestic – periodically.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity
Salary Range: $132,200.00 - $177,200.00 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.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
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Principal Scientist, Drug Product
role at
BeOne Medicines 2 days ago Be among the first 25 applicants Join to apply for the
Principal Scientist, Drug Product
role at
BeOne Medicines Get AI-powered advice on this job and more exclusive features. 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
This role in the Manufacturing Science and Technology (MST) department supports BeOne’s Drug Product Manufacturing Technology Transfer and support. based in New Jersey (Hopewell), this role will be to lead the Hopewell drug product MST function to support technology transfer, validation, continued process verification, investigations, change management and site startup of Hopewell internal drug product manufacturing activities. Reporting to the MST leadership, this role is responsible for managing the technical operations supporting both clinical and commercial manufacturing activities.
Leadership
Serve as MST DP SME and process lead for drug product, ensuring the materials, strategy and documentation are in place. Collaborate with DP/SC/QC/QA to develop testing strategy for DP raw materials and in-process samples. Author and maintain process control strategy documents throughout the lifecycle of a program and maintain process risk assessment documents. Author PPQ protocols and reports. Oversee execution of PPQ and PPQ related activities Support engineering teams on equipment selection, qualification, and start up activities. Monitor and CPV trend process performance, including input and output parameters. Responsible for technical transfer, validation, investigation, and technical support of aseptic manufacturing operations in Hopewell and CMOs. Collaborate with Drug Product Operations to establish robust and compliant manufacturing performance. Collaborate with Global DP MS&T and Technical Development to enable new DP filling capability at Hopewell Location. Provide technical support for Drug Product Operations. Provide input into operational metrics, budgeting, and planning. Establish a data and metrics driven culture. Relentlessly maintain alignment with other global manufacturing sites through shared knowledge, shared manufacturing data, shared manufacturing issues, and common solutions. Partner with GZ Technical Development to successfully transfer and validate HPW DP processes. Product scope includes parenteral vials and lyophilized products. Collaborate with Technical Development in investigating and resolving complex manufacturing issues at CMOs. Manage and coordinate global change ensuring stakeholders alignment. Assist in Regulatory filings and Health Authority site inspections to license and maintain BeOne’s pipeline and product portfolio.
Essential Functions
Lead technology transfer for cGMP manufacturing focused drug product fill/finish. Ensure effective information flow, risk assessment, timeline execution, issue resolution and documentation for cross-functional teams. Includes leading tech transfer, detailed process definition and facility fit assessment exercises. Execute scale down model of manufacturing processes. Maintains a good laboratory practice. Author and maintain process control strategy documents throughout the lifecycle of a program and maintain process risk assessment documents Author PPQ protocols and reports. Oversee execution of PPQ and PPQ related activities Support engineering teams on equipment selection, qualification, and start up activities. Monitor and trend process performance, including input and output parameters. Investigate root causes of major deviations for cGMP manufacturing, and implement CAPA for major deviations Identifying opportunities to improve systems and practices Work with counterparts in Process Development, Process Sciences, Manufacturing, Quality, Project Management teams etc. to facilitate technology transfer and project success.
Preferred Skills/Experience
Facility Start-Up Commissioning, Qualification & Validation Equipment and/or Process Design Quality Risk Assessments Health Authority Interaction/Audits OE and/or LEAN Methodologies Distributed Control system / Control Systems Deviation Assessments / Investigations SAP, LIMS, CMMS, Veeva Expert level knowledge in all Drug Product aseptic filling operation Expert level knowledge of Isolator, packaging and automated inspection machines. Expert level knowledge in IQ/OQ/PQ and process engineering Expertise in late stage/commercial Drug Product technology transfer, process characterization and process validation biopharmaceutical/gene transfer vector manufacturing preferred. Working knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing. Ability to work both independently and as part of a team. Ability to function in a fast-paced dynamic team environment and balance prioritize multiple projects Excellent troubleshooting skills and ability to solve complex technical issues. Ability to compile, analyze and interpret data; Ability to write routine reports and correspondence. Strong interpersonal and communication skills, verbal and written. Ability to speak effectively before groups of customers. Ability to communicate in a dynamic environment.
Qualifications
BA/BS or higher in science, biochemistry, biotechnology, biology, chemical engineering and/or related discipline. Minimum of 7 years of experience working in Biopharmaceutical DP process development or manufacturing experience.
Physical Requirements
Must be able to stand for long periods, up to 8 to 10 hours/day. Must be able to reach above shoulder level, bend/stoop, push/pull, and handle/grip frequently. Must be able to work scheduled at least 40 hours/week (on-site). Must be comfortable in working in varying temperatures. Frequent lifting, pushing, pulling, and carrying. Ability to lift up to 40 lbs. Regular reaching, bending, stooping, and twisting. Repetitive motion and substantial movement of the wrists, hands, and/or fingers. Environment requires dedicated gowns, depending on area. Work with hazardous materials and chemicals.
Computer Skills:
Familiarity with computer-based systems. Word, Excel, and PowerPoint a must.
Travel:
International and domestic – periodically.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters Teamwork Provides and Solicits Honest and Actionable Feedback Self-Awareness Acts Inclusively Demonstrates Initiative Entrepreneurial Mindset Continuous Learning Embraces Change Results-Oriented Analytical Thinking/Data Analysis Financial Excellence Communicates with Clarity
Salary Range: $132,200.00 - $177,200.00 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.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com. Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Research, Analyst, and Information Technology Referrals increase your chances of interviewing at BeOne Medicines by 2x Get notified about new Principal Scientist jobs in
Hopewell, NJ . Senior Scientist/Principal Scientist, Oncology Translational Development
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Piscataway, NJ $120,000.00-$168,000.00 2 days ago Bridgewater, NJ $112,400.00-$187,400.00 3 days ago Warrington, PA $80,000.00-$120,000.00 2 weeks ago Bristol, PA $85,000.00-$130,000.00 17 hours ago Research Scientist – Bayesian Optimization & Experimental Design
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Robbinsville, NJ $105,000.00-$140,000.00 2 weeks ago Warrington, PA $80,000.00-$110,000.00 2 weeks ago Trenton, NJ $77,143.55-$113,263.75 2 weeks ago Sr. Manager, Clinical Research Scientist
Princeton, NJ $165,000.00-$195,000.00 2 days ago Analytical Research and Development Scientist 503B
Princeton, NJ $134,720.00-$202,080.00 2 weeks ago Bridgewater, NJ $115,000.00-$161,867.00 3 weeks ago Senior Principal Scientist, Development DMPK
Associate Principal Scientist, Gene Editing and Biologics Research
Bridgewater, NJ $135,000.00-$189,667.00 6 days ago Senior Food Scientist, Master Beverage Formulation
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Bridgewater, NJ $83,000.00-$154,500.00 2 weeks ago Bridgewater, NJ $90,000.00-$210,000.00 6 days ago Principal Scientist, Cleaning Verification, Analytical Testing
Senior Scientist, Quality Control Technical Services
Branchburg, NJ $80,000.00-$120,000.00 2 weeks ago Assistant Professor Physician Scientist translational research in neurodegenerative disorders
Philadelphia, PA $75,000.00-$95,000.00 2 days ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr