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Sr. Scientist, Radiopharmaceutical Development

Bristol-Myers Squibb

Healthcare Jobs

Sr. Scientist, Radiopharmaceutical Development

full-timePosted: Oct 1, 2025

Job Description

Process Development & Scale-Up: Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition, ensuring scalability and compliance with regulatory standards. Technology Transfer: Lead the transfer of advanced radiopharmaceutical processes and technologies to internal and external manufacturing sites, including the Indianapolis facility and CDMO partners. Laboratory Oversight: Oversee the development, operation, and maintenance of radiochemistry laboratory infrastructure, ensuring readiness for translational activities from preclinical through clinical phases. Collaboration: Foster collaborative relationships with discovery scientists, external academic partners, and CDMOs to address complex scientific questions and pursue joint research efforts. Lead Research Initiatives: Independently design and execute advanced radiochemistry and radiolabeling experiments, with a special focus on novel radioisotope and chelator development to enable new classes of radiopharmaceuticals. Technical Leadership: Serve as a subject matter expert in radiopharmaceutical production processes, quality control, and advanced analytical methodologies. Provide scientific leadership across multidisciplinary teams. Innovation in Isotope and Chelator Chemistry: Direct research into the identification, synthesis, and characterization of novel isotopes and chelators to enhance therapeutic and diagnostic radiopharmaceutical properties. Safety & Compliance: Ensure strict adherence to radiation safety protocols, federal and state regulations, and internal guidelines for handling radioactive materials; promote a culture of safety-first and regulatory compliance. Data Analysis & Reporting: Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings in technical reports, regulatory documentation, and presentations for internal and external stakeholders. Project Management & Mentorship: Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates. Documentation: Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports. Travel: Less than 10% travel required, including external research sites and manufacturing facilities. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. BSc +7 years, MSc + 5 years or PhD +3 years in Chemistry, Radiochemistry, Pharmaceutical Sciences, or related field with relevant industry experience, including significant work with radioactive materials, novel isotopes, and chelator chemistry. Demonstrated expertise in radiochemical synthesis, purification, formulation, and analytical techniques. Proven track record of innovation in radiopharmaceutical development, including novel isotope and chelator research. Deep familiarity with federal and state regulatory requirements and safety protocols for radioactive materials. Advanced experience developing stable radiopharmaceutical formulations with targeted attributes such as extended shelf-life, radiochemical purity, and enhanced bio-distribution. Hands-on expertise with commercial and custom radiopharmaceutical manufacturing and analytical equipment systems, including automation platforms, radioHPLC, radioTLC, gamma counters, dose calibrators, hot cell manipulators, and advanced gamma spectroscopy. Extensive experience with a broad spectrum of radioactive materials for both diagnostic and therapeutic applications. Strong professional ethics, integrity, and ability to maintain confidential information. Outstanding written and verbal communication skills, with the ability to influence and communicate effectively across all levels, including executive leadership. Proactive, innovative thinker who thrives in a fast-paced, multi-disciplinary industrial environment. Demonstrated ability to manage complex research projects and mentor junior staff.

Key Responsibilities

  • Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition
  • Ensure scalability and compliance with regulatory standards
  • Lead the transfer of advanced radiopharmaceutical processes and technologies to internal and external manufacturing sites
  • Oversee the development, operation, and maintenance of radiochemistry laboratory infrastructure
  • Ensure readiness for translational activities from preclinical through clinical phases
  • Foster collaborative relationships with discovery scientists, external academic partners, and CDMOs
  • Independently design and execute advanced radiochemistry and radiolabeling experiments
  • Focus on novel radioisotope and chelator development to enable new classes of radiopharmaceuticals
  • Serve as a subject matter expert in radiopharmaceutical production processes, quality control, and advanced analytical methodologies
  • Provide scientific leadership across multidisciplinary teams
  • Direct research into the identification, synthesis, and characterization of novel isotopes and chelators
  • Ensure strict adherence to radiation safety protocols, federal and state regulations, and internal guidelines for handling radioactive materials
  • Promote a culture of safety-first and regulatory compliance
  • Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings
  • Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates
  • Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports

Required Qualifications

  • BSc with 7+ years of experience, MSc with 5+ years of experience, or PhD with 3+ years of experience in Chemistry, Radiochemistry, Pharmaceutical Sciences, or related field
  • Significant work experience with radioactive materials, novel isotopes, and chelator chemistry
  • Demonstrated expertise in radiochemical synthesis, purification, formulation, and analytical techniques
  • Proven track record of innovation in radiopharmaceutical development, including novel isotope and chelator research
  • Deep familiarity with federal and state regulatory requirements and safety protocols for radioactive materials
  • Advanced experience developing stable radiopharmaceutical formulations with targeted attributes such as extended shelf-life, radiochemical purity, and enhanced bio-distribution
  • Hands-on expertise with commercial and custom radiopharmaceutical manufacturing and analytical equipment systems, including automation platforms, radioHPLC, radioTLC, gamma counters, dose calibrators, hot cell manipulators, and advanced gamma spectroscopy
  • Extensive experience with a broad spectrum of radioactive materials for both diagnostic and therapeutic applications

Skills Required

  • Strong professional ethics and integrity
  • Ability to maintain confidential information
  • Outstanding written and verbal communication skills
  • Ability to influence and communicate effectively across all levels, including executive leadership
  • Proactive and innovative thinking
  • Ability to thrive in a fast-paced, multi-disciplinary industrial environment
  • Demonstrated ability to manage complex research projects and mentor junior staff

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Additional Requirements

  • Less than 10% travel required, including external research sites and manufacturing facilities

Locations

  • San Diego RayzeBio, Canada

Salary

Estimated Salary Rangemedium confidence

100,000 - 150,000 CAD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong professional ethics and integrityintermediate
  • Ability to maintain confidential informationintermediate
  • Outstanding written and verbal communication skillsintermediate
  • Ability to influence and communicate effectively across all levels, including executive leadershipintermediate
  • Proactive and innovative thinkingintermediate
  • Ability to thrive in a fast-paced, multi-disciplinary industrial environmentintermediate
  • Demonstrated ability to manage complex research projects and mentor junior staffintermediate

Required Qualifications

  • BSc with 7+ years of experience, MSc with 5+ years of experience, or PhD with 3+ years of experience in Chemistry, Radiochemistry, Pharmaceutical Sciences, or related field (experience)
  • Significant work experience with radioactive materials, novel isotopes, and chelator chemistry (experience)
  • Demonstrated expertise in radiochemical synthesis, purification, formulation, and analytical techniques (experience)
  • Proven track record of innovation in radiopharmaceutical development, including novel isotope and chelator research (experience)
  • Deep familiarity with federal and state regulatory requirements and safety protocols for radioactive materials (experience)
  • Advanced experience developing stable radiopharmaceutical formulations with targeted attributes such as extended shelf-life, radiochemical purity, and enhanced bio-distribution (experience)
  • Hands-on expertise with commercial and custom radiopharmaceutical manufacturing and analytical equipment systems, including automation platforms, radioHPLC, radioTLC, gamma counters, dose calibrators, hot cell manipulators, and advanced gamma spectroscopy (experience)
  • Extensive experience with a broad spectrum of radioactive materials for both diagnostic and therapeutic applications (experience)

Responsibilities

  • Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition
  • Ensure scalability and compliance with regulatory standards
  • Lead the transfer of advanced radiopharmaceutical processes and technologies to internal and external manufacturing sites
  • Oversee the development, operation, and maintenance of radiochemistry laboratory infrastructure
  • Ensure readiness for translational activities from preclinical through clinical phases
  • Foster collaborative relationships with discovery scientists, external academic partners, and CDMOs
  • Independently design and execute advanced radiochemistry and radiolabeling experiments
  • Focus on novel radioisotope and chelator development to enable new classes of radiopharmaceuticals
  • Serve as a subject matter expert in radiopharmaceutical production processes, quality control, and advanced analytical methodologies
  • Provide scientific leadership across multidisciplinary teams
  • Direct research into the identification, synthesis, and characterization of novel isotopes and chelators
  • Ensure strict adherence to radiation safety protocols, federal and state regulations, and internal guidelines for handling radioactive materials
  • Promote a culture of safety-first and regulatory compliance
  • Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings
  • Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates
  • Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

Travel Requirements

0%

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Bristol-Myers Squibb logo

Sr. Scientist, Radiopharmaceutical Development

Bristol-Myers Squibb

Healthcare Jobs

Sr. Scientist, Radiopharmaceutical Development

full-timePosted: Oct 1, 2025

Job Description

Process Development & Scale-Up: Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition, ensuring scalability and compliance with regulatory standards. Technology Transfer: Lead the transfer of advanced radiopharmaceutical processes and technologies to internal and external manufacturing sites, including the Indianapolis facility and CDMO partners. Laboratory Oversight: Oversee the development, operation, and maintenance of radiochemistry laboratory infrastructure, ensuring readiness for translational activities from preclinical through clinical phases. Collaboration: Foster collaborative relationships with discovery scientists, external academic partners, and CDMOs to address complex scientific questions and pursue joint research efforts. Lead Research Initiatives: Independently design and execute advanced radiochemistry and radiolabeling experiments, with a special focus on novel radioisotope and chelator development to enable new classes of radiopharmaceuticals. Technical Leadership: Serve as a subject matter expert in radiopharmaceutical production processes, quality control, and advanced analytical methodologies. Provide scientific leadership across multidisciplinary teams. Innovation in Isotope and Chelator Chemistry: Direct research into the identification, synthesis, and characterization of novel isotopes and chelators to enhance therapeutic and diagnostic radiopharmaceutical properties. Safety & Compliance: Ensure strict adherence to radiation safety protocols, federal and state regulations, and internal guidelines for handling radioactive materials; promote a culture of safety-first and regulatory compliance. Data Analysis & Reporting: Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings in technical reports, regulatory documentation, and presentations for internal and external stakeholders. Project Management & Mentorship: Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates. Documentation: Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports. Travel: Less than 10% travel required, including external research sites and manufacturing facilities. Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday, up to 120 hours of paid vacation, up to two (2) paid days to volunteer, sick time off, and summer hours flexibility. BSc +7 years, MSc + 5 years or PhD +3 years in Chemistry, Radiochemistry, Pharmaceutical Sciences, or related field with relevant industry experience, including significant work with radioactive materials, novel isotopes, and chelator chemistry. Demonstrated expertise in radiochemical synthesis, purification, formulation, and analytical techniques. Proven track record of innovation in radiopharmaceutical development, including novel isotope and chelator research. Deep familiarity with federal and state regulatory requirements and safety protocols for radioactive materials. Advanced experience developing stable radiopharmaceutical formulations with targeted attributes such as extended shelf-life, radiochemical purity, and enhanced bio-distribution. Hands-on expertise with commercial and custom radiopharmaceutical manufacturing and analytical equipment systems, including automation platforms, radioHPLC, radioTLC, gamma counters, dose calibrators, hot cell manipulators, and advanced gamma spectroscopy. Extensive experience with a broad spectrum of radioactive materials for both diagnostic and therapeutic applications. Strong professional ethics, integrity, and ability to maintain confidential information. Outstanding written and verbal communication skills, with the ability to influence and communicate effectively across all levels, including executive leadership. Proactive, innovative thinker who thrives in a fast-paced, multi-disciplinary industrial environment. Demonstrated ability to manage complex research projects and mentor junior staff.

Key Responsibilities

  • Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition
  • Ensure scalability and compliance with regulatory standards
  • Lead the transfer of advanced radiopharmaceutical processes and technologies to internal and external manufacturing sites
  • Oversee the development, operation, and maintenance of radiochemistry laboratory infrastructure
  • Ensure readiness for translational activities from preclinical through clinical phases
  • Foster collaborative relationships with discovery scientists, external academic partners, and CDMOs
  • Independently design and execute advanced radiochemistry and radiolabeling experiments
  • Focus on novel radioisotope and chelator development to enable new classes of radiopharmaceuticals
  • Serve as a subject matter expert in radiopharmaceutical production processes, quality control, and advanced analytical methodologies
  • Provide scientific leadership across multidisciplinary teams
  • Direct research into the identification, synthesis, and characterization of novel isotopes and chelators
  • Ensure strict adherence to radiation safety protocols, federal and state regulations, and internal guidelines for handling radioactive materials
  • Promote a culture of safety-first and regulatory compliance
  • Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings
  • Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates
  • Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports

Required Qualifications

  • BSc with 7+ years of experience, MSc with 5+ years of experience, or PhD with 3+ years of experience in Chemistry, Radiochemistry, Pharmaceutical Sciences, or related field
  • Significant work experience with radioactive materials, novel isotopes, and chelator chemistry
  • Demonstrated expertise in radiochemical synthesis, purification, formulation, and analytical techniques
  • Proven track record of innovation in radiopharmaceutical development, including novel isotope and chelator research
  • Deep familiarity with federal and state regulatory requirements and safety protocols for radioactive materials
  • Advanced experience developing stable radiopharmaceutical formulations with targeted attributes such as extended shelf-life, radiochemical purity, and enhanced bio-distribution
  • Hands-on expertise with commercial and custom radiopharmaceutical manufacturing and analytical equipment systems, including automation platforms, radioHPLC, radioTLC, gamma counters, dose calibrators, hot cell manipulators, and advanced gamma spectroscopy
  • Extensive experience with a broad spectrum of radioactive materials for both diagnostic and therapeutic applications

Skills Required

  • Strong professional ethics and integrity
  • Ability to maintain confidential information
  • Outstanding written and verbal communication skills
  • Ability to influence and communicate effectively across all levels, including executive leadership
  • Proactive and innovative thinking
  • Ability to thrive in a fast-paced, multi-disciplinary industrial environment
  • Demonstrated ability to manage complex research projects and mentor junior staff

Benefits & Perks

  • Paid national holidays and optional holidays
  • Global Shutdown Days between Christmas and New Year's holiday
  • Up to 120 hours of paid vacation
  • Up to two (2) paid days to volunteer
  • Sick time off
  • Summer hours flexibility

Additional Requirements

  • Less than 10% travel required, including external research sites and manufacturing facilities

Locations

  • San Diego RayzeBio, Canada

Salary

Estimated Salary Rangemedium confidence

100,000 - 150,000 CAD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Strong professional ethics and integrityintermediate
  • Ability to maintain confidential informationintermediate
  • Outstanding written and verbal communication skillsintermediate
  • Ability to influence and communicate effectively across all levels, including executive leadershipintermediate
  • Proactive and innovative thinkingintermediate
  • Ability to thrive in a fast-paced, multi-disciplinary industrial environmentintermediate
  • Demonstrated ability to manage complex research projects and mentor junior staffintermediate

Required Qualifications

  • BSc with 7+ years of experience, MSc with 5+ years of experience, or PhD with 3+ years of experience in Chemistry, Radiochemistry, Pharmaceutical Sciences, or related field (experience)
  • Significant work experience with radioactive materials, novel isotopes, and chelator chemistry (experience)
  • Demonstrated expertise in radiochemical synthesis, purification, formulation, and analytical techniques (experience)
  • Proven track record of innovation in radiopharmaceutical development, including novel isotope and chelator research (experience)
  • Deep familiarity with federal and state regulatory requirements and safety protocols for radioactive materials (experience)
  • Advanced experience developing stable radiopharmaceutical formulations with targeted attributes such as extended shelf-life, radiochemical purity, and enhanced bio-distribution (experience)
  • Hands-on expertise with commercial and custom radiopharmaceutical manufacturing and analytical equipment systems, including automation platforms, radioHPLC, radioTLC, gamma counters, dose calibrators, hot cell manipulators, and advanced gamma spectroscopy (experience)
  • Extensive experience with a broad spectrum of radioactive materials for both diagnostic and therapeutic applications (experience)

Responsibilities

  • Drive CMC process development and optimization for clinical drug products, including formulation lock and robust process definition
  • Ensure scalability and compliance with regulatory standards
  • Lead the transfer of advanced radiopharmaceutical processes and technologies to internal and external manufacturing sites
  • Oversee the development, operation, and maintenance of radiochemistry laboratory infrastructure
  • Ensure readiness for translational activities from preclinical through clinical phases
  • Foster collaborative relationships with discovery scientists, external academic partners, and CDMOs
  • Independently design and execute advanced radiochemistry and radiolabeling experiments
  • Focus on novel radioisotope and chelator development to enable new classes of radiopharmaceuticals
  • Serve as a subject matter expert in radiopharmaceutical production processes, quality control, and advanced analytical methodologies
  • Provide scientific leadership across multidisciplinary teams
  • Direct research into the identification, synthesis, and characterization of novel isotopes and chelators
  • Ensure strict adherence to radiation safety protocols, federal and state regulations, and internal guidelines for handling radioactive materials
  • Promote a culture of safety-first and regulatory compliance
  • Interpret complex experimental data, draw scientifically rigorous conclusions, and communicate findings
  • Manage and prioritize research projects, oversee third-party vendors, and mentor junior scientists and associates
  • Draft and review CMC sections for regulatory submissions, SOPs, and comprehensive development reports

Benefits

  • general: Paid national holidays and optional holidays
  • general: Global Shutdown Days between Christmas and New Year's holiday
  • general: Up to 120 hours of paid vacation
  • general: Up to two (2) paid days to volunteer
  • general: Sick time off
  • general: Summer hours flexibility

Travel Requirements

0%

Target Your Resume for "Sr. Scientist, Radiopharmaceutical Development" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Sr. Scientist, Radiopharmaceutical Development. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr. Scientist, Radiopharmaceutical Development" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

Answer 10 quick questions to check your fit for Sr. Scientist, Radiopharmaceutical Development @ Bristol-Myers Squibb.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.