Abdera Therapeutics
Associate Director, Radiopharmaceutical Process Development
Abdera Therapeutics, South San Francisco, California, us, 94083
Who we areAbdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy cells. Abdera is using this platform to enable the rapid development of a broad range of safe and efficacious therapies serving cancer patients with limited treatment options.Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. Come join us and be a part of the ground-breaking team set to unlock the power of targeted radiotherapy!What we look forAt Abdera Therapeutics, we are looking for curious and committed individuals who are ready for the opportunity to transform the way people living with cancer can be treated. We are relentless in our focus to offer new hope to families facing devastating diagnoses. We are in search of team members who work collaboratively with a diverse group of colleagues, respectfully engaging one another while collectively and inclusively tackling any challenges we may face. We are building an exciting and fast paced company passionate about discovering and developing tomorrow's most innovative cancer therapies.Abdera is seeking an
Associate Director of Radiopharmaceutical Process Development
to drive the CMC radiopharmaceutical process development for Abdera's novel clinical programs. The Associate Director of Radiopharmaceutical Process Development will be executing the CMC development plan and IND enabling activities, leading to the clinical manufacturing of the Drug Product. In this function, the candidate will be translating pre-clinical /research methods and data to develop cGMP compliant processes and clinical drug product specifications, manage the execution of CMC studies and author drug substance/product IND sections. In addition, this role will provide technical support / technical assessment to clinical manufacturing including root cause analysis, change control, and process optimization. This role will be the main liaison between Tech Ops and research as well as the CDMO development team.
Salary Range - 150 - 185k - SF Bay Area, USA
Principal Responsibilities
Process Development of Radiopharmaceutical DP
Working with a multidisciplinary team, this role will lead Abdera's process development of radiopharmaceuticals for phase 1 clinical trialsFor each new program, be part of the selection team to review RFP, assess technical fit and select the appropriate CDMO for development and manufacturing of Abdera's novel productLead the process development of DP from DC selection to IND submission, including:
Create technology transfer package for CDMO's by translating pre-clinical analytical methods and drug product synthesis to processes suitable for clinical developmentDefine and manage DP development program timeline and activities from DC to IND submissionDesign study / experiments to determine suitable process flow, process conditions, materials selection, acceptable range, etc. to enable process lockClosely partner with antibody and conjugation process development lead to ensure materials readinessPartner with external/internal development lab to define IND enabling study protocols, review study run data, provide feedback throughout the development processLead the execution (with CDMO) of the process qualification and validation campaign and prepare the relevant reports and data for the relevant IND sections.Write relevant CMC sections and supporting reports for submission to regulatory agencies (IND to the FDA)Execute clinical readiness activities (such as compatibility and transportation studies, aseptic process qualification) to enable clinical manufacturing.
Drive delivery and execution of CMC program plans for DP Process Development via tracking/reporting key milestones and decision points to meet IND and clinical readiness timelineTechnical Support of Clinical Manufacturing
Partner with internal CMC team, provide technical direction to external CDMO to draft manufacturing documentation including specification, analytical method, batch records, protocols, etc.Partner with Quality to provide periodic technical review of manufacturing data, including analysis of trendsPartner with Quality, Supply Chain, and manufacturing, identify opportunities for risk reduction and continuous improvement within the cGMP manufacturing processProvide technical impact assessment to support Quality/Regulatory assessments including but not limited to batch release, change control, deviations, OOs, CAPAs.Liaison between Research/pre-clinical and CMC
Support the set-up and on-going function of Abdera's radiochemistry laboratory to support translational development from pre-clinical and clinical activitiesRepresent CMC, act as the liaison to partner with research radiochemistry and in-vivo team to share best practices and facilitate knowledge exchangeQualifications, Education & Experience
MSc or PhD in scientific fields with 10+ years of experience in the pharmaceutical industry, including radiopharmaceuticals. Priority given to candidates with experience with therapeutic radiopharmaceuticals.Knowledge of cGMP requirements, aseptic process, and equipment qualification.Experience in writing CMC sections of regulatory submissions (IND, NDA, andequivalent) and clinical development and manufacturing in the biotechnology or pharmaceutical industry
Experience working with antibodies and a working knowledge of bioconjugation of antibodies are a plus.Good understanding of the radiation regulations and guidelines preferredSkills and Abilities
Good understanding of cGMP and FDA regulations and guidelines relating to CMC-related areasExcellent written and verbal communication skills; strong communicator and influencer within all levels of the organization, including executive leadershipStrong analytical capabilities, including quantitative and qualitative assessment skills and demonstrated critical thinking skillsAbility to critically evaluate and troubleshoot complex problemsStrong problem-solving skillsAbility to build rapport with all levels of organizationTeam-oriented, progressive thinker who enjoys participating in an innovative and creative work environmentAbility to operate in a fast-paced, multi-disciplinary industrial environment.
Abdera is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Abdera, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.This commitment is applicable to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship.
Associate Director of Radiopharmaceutical Process Development
to drive the CMC radiopharmaceutical process development for Abdera's novel clinical programs. The Associate Director of Radiopharmaceutical Process Development will be executing the CMC development plan and IND enabling activities, leading to the clinical manufacturing of the Drug Product. In this function, the candidate will be translating pre-clinical /research methods and data to develop cGMP compliant processes and clinical drug product specifications, manage the execution of CMC studies and author drug substance/product IND sections. In addition, this role will provide technical support / technical assessment to clinical manufacturing including root cause analysis, change control, and process optimization. This role will be the main liaison between Tech Ops and research as well as the CDMO development team.
Salary Range - 150 - 185k - SF Bay Area, USA
Principal Responsibilities
Process Development of Radiopharmaceutical DP
Working with a multidisciplinary team, this role will lead Abdera's process development of radiopharmaceuticals for phase 1 clinical trialsFor each new program, be part of the selection team to review RFP, assess technical fit and select the appropriate CDMO for development and manufacturing of Abdera's novel productLead the process development of DP from DC selection to IND submission, including:
Create technology transfer package for CDMO's by translating pre-clinical analytical methods and drug product synthesis to processes suitable for clinical developmentDefine and manage DP development program timeline and activities from DC to IND submissionDesign study / experiments to determine suitable process flow, process conditions, materials selection, acceptable range, etc. to enable process lockClosely partner with antibody and conjugation process development lead to ensure materials readinessPartner with external/internal development lab to define IND enabling study protocols, review study run data, provide feedback throughout the development processLead the execution (with CDMO) of the process qualification and validation campaign and prepare the relevant reports and data for the relevant IND sections.Write relevant CMC sections and supporting reports for submission to regulatory agencies (IND to the FDA)Execute clinical readiness activities (such as compatibility and transportation studies, aseptic process qualification) to enable clinical manufacturing.
Drive delivery and execution of CMC program plans for DP Process Development via tracking/reporting key milestones and decision points to meet IND and clinical readiness timelineTechnical Support of Clinical Manufacturing
Partner with internal CMC team, provide technical direction to external CDMO to draft manufacturing documentation including specification, analytical method, batch records, protocols, etc.Partner with Quality to provide periodic technical review of manufacturing data, including analysis of trendsPartner with Quality, Supply Chain, and manufacturing, identify opportunities for risk reduction and continuous improvement within the cGMP manufacturing processProvide technical impact assessment to support Quality/Regulatory assessments including but not limited to batch release, change control, deviations, OOs, CAPAs.Liaison between Research/pre-clinical and CMC
Support the set-up and on-going function of Abdera's radiochemistry laboratory to support translational development from pre-clinical and clinical activitiesRepresent CMC, act as the liaison to partner with research radiochemistry and in-vivo team to share best practices and facilitate knowledge exchangeQualifications, Education & Experience
MSc or PhD in scientific fields with 10+ years of experience in the pharmaceutical industry, including radiopharmaceuticals. Priority given to candidates with experience with therapeutic radiopharmaceuticals.Knowledge of cGMP requirements, aseptic process, and equipment qualification.Experience in writing CMC sections of regulatory submissions (IND, NDA, andequivalent) and clinical development and manufacturing in the biotechnology or pharmaceutical industry
Experience working with antibodies and a working knowledge of bioconjugation of antibodies are a plus.Good understanding of the radiation regulations and guidelines preferredSkills and Abilities
Good understanding of cGMP and FDA regulations and guidelines relating to CMC-related areasExcellent written and verbal communication skills; strong communicator and influencer within all levels of the organization, including executive leadershipStrong analytical capabilities, including quantitative and qualitative assessment skills and demonstrated critical thinking skillsAbility to critically evaluate and troubleshoot complex problemsStrong problem-solving skillsAbility to build rapport with all levels of organizationTeam-oriented, progressive thinker who enjoys participating in an innovative and creative work environmentAbility to operate in a fast-paced, multi-disciplinary industrial environment.
Abdera is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Abdera, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.This commitment is applicable to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship.