Principal Scientist, In Vitro Safety Pharmacology (East Hampton)

Compensation

: $101,200.00 - $151,450.00 /year *

Employment Type

: Full-Time

Industry

: Scientific Research



principal biological scientist Jobs in Connecticut

Principal Scientist, In Vitro Safety Pharmacology

3.7 Boehringer Ingelheim ? Connecticut 4 days ago

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Principal Scientist, In Vitro Safety Pharmacology

Boehringer Ingelheim is currently seeking a driven and innovative Principal Scientist to join our Non-clinical Drug Safety (NDS) Department at our Ridgefield, CT facility.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Integrative Toxicology Group is currently recruiting a Laboratory Head to develop advanced in vitro models to support toxicology species selection and de-risking of new therapeutic products (small molecules, biologics novel modalities) across several therapeutic areas. The candidate will collaborate with our Modeling, Molecular Pathology, PK/PD, Immunopharmacology, Toxicodynamics, and Omics groups.

Main tasks:
  • Demonstrates an expertise in a specific project-relevant area or technology ( i.e. microphysiological systems, 3D cultures and development of complex in vitro system)
  • Directs and oversees the experimental design and results of technical scientists; has full accountability for direct reports, including but not limited to goal setting and definition of personal development plans
  • Supervises and reviews preparation of clear technical reports, publications and oral presentations. Independently communicates team results in the form of reports and or presentations; delivers updates to senior level management in context of overall project/lab goals
  • Proposes new technologies and concepts in support of multiple projects; develops broad knowledge in field of expertise, including the ability to interpret current literature relevant to R & D projects, and visibility outside of functional area
  • Assumes departmental responsibility for projects in the Discovery phase and/or supports multiple project teams as subject matter expert
  • Complies with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintains proper records in accordance with SOPs, appropriate guidance and policies
  • Contributes to departmental administration; demonstrates fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel
Required Education & Experience:
  • PhD degree or equivalent with 5+ years' experience in the field(s) of Molecular & Cellular Biology, Toxicology or similar area of study
  • Demonstrates broad knowledge in the field of expertize i.e. microphysiological systems, 3D cultures and development of complex in vitro systems
  • Appropriate level of understanding of applicable regulations
  • Ability to communicate effectively both orally and in writing in an interdisciplinary environment
  • Previous supervisory and matrix working experience highly preferred
Eligibility Requirements:
  • Must be legally authorized to work in the United States
  • Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background
  • Must be willing to take a drug test and post-offer physical (if required)
  • Must be 18 years of age or older
Desired Experience, Skills and Abilities:
  • Experience with mammalian cell culture techniques (primary cells and cell lines). Experience with stable cell line development or integration of reporter gene constructs. Experience with ex vivo cell isolation from large animals a plus
  • General knowledge of molecular and cell biology, genomics and principles of virology required
  • Familiarity with the use of data display platforms (e.g. GraphPad Prism, TIBCO Spotfire)
  • Basic experience with SPR analysis (instrumentation, experimental setup, execution) of advantage
  • Familiarity with genomic database and data mining, and statistical analysis of biological data a plus
  • Familiarity with the drug development process and/or toxicology and/or immune-oncology and/or anti-inflammatory therapies of advantage
  • Evidence of publication records a plus
Boehringer Ingelheim is currently seeking a driven and innovative Principal Scientist to join our Non-clinical Drug Safety (NDS) Department at our Ridgefield, CT facility.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Integrative Toxicology Group is currently recruiting a Laboratory Head to develop advanced in vitro models to support toxicology species selection and de-risking of new therapeutic products (small molecules, biologics novel modalities) across several therapeutic areas. The candidate will collaborate with our Modeling, Molecular Pathology, PK/PD, Immunopharmacology, Toxicodynamics, and Omics groups.

Main tasks:
  • Demonstrates an expertise in a specific project-relevant area or technology ( i.e. microphysiological systems, 3D cultures and development of complex in vitro system)
  • Directs and oversees the experimental design and results of technical scientists; has full accountability for direct reports, including but not limited to goal setting and definition of personal development plans
  • Supervises and reviews preparation of clear technical reports, publications and oral presentations. Independently communicates team results in the form of reports and or presentations; delivers updates to senior level management in context of overall project/lab goals
  • Proposes new technologies and concepts in support of multiple projects; develops broad knowledge in field of expertise, including the ability to interpret current literature relevant to R & D projects, and visibility outside of functional area
  • Assumes departmental responsibility for projects in the Discovery phase and/or supports multiple project teams as subject matter expert
  • Complies with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintains proper records in accordance with SOPs, appropriate guidance and policies
  • Contributes to departmental administration; demonstrates fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel
Required Education & Experience:
  • PhD degree or equivalent with 5+ years' experience in the field(s) of Molecular & Cellular Biology, Toxicology or similar area of study
  • Demonstrates broad knowledge in the field of expertize i.e. microphysiological systems, 3D cultures and development of complex in vitro systems
  • Appropriate level of understanding of applicable regulations
  • Ability to communicate effectively both orally and in writing in an interdisciplinary environment
  • Previous supervisory and matrix working experience highly preferred
Desired Experience, Skills and Abilities:
  • Experience with mammalian cell culture techniques (primary cells and cell lines). Experience with stable cell line development or integration of reporter gene constructs. Experience with ex vivo cell isolation from large animals a plus
  • General knowledge of molecular and cell biology, genomics and principles of virology required
  • Familiarity with the use of data display platforms (e.g. GraphPad Prism, TIBCO Spotfire)
  • Basic experience with SPR analysis (instrumentation, experimental setup, execution) of advantage
  • Familiarity with genomic database and data mining, and statistical analysis of biological data a plus
  • Familiarity with the drug development process and/or toxicology and/or immune-oncology and/or anti-inflammatory therapies of advantage
  • Evidence of publication records a plus
Eligibility Requirements:

Must be legally authorized to work in the United States without restriction.

Must be willing to take a drug test and post-offer physical (if required)

Must be 18 years of age or older

Who We Are:

At Boehringer Ingelheim we create value through innovation with one clear goal: to improve the lives of patients. We develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company we focus on long term performance. We are powered by 50.000 employees globally who nurture a diverse, collaborative and inclusive culture. Learning and development for all employees is key because your growth is our growth.

Want to learn more? Visit ************************ and join us in our effort to make more health.

Boehringer Ingelheim, including Boehringer Ingelheim Pharmaceuticals, Inc., Boehringer Ingelheim USA, Boehringer Ingelheim Animal Health USA Inc., Boehringer Ingelheim Animal Health Puerto Rico LLC and Boehringer Ingelheim Fremont, Inc. is an equal opportunity and affirmative action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; citizenship status, marital, domestic partnership or civil union status; gender, gender identity or expression; affectional or sexual orientation; pregnancy, childbirth or related medical condition; physical or psychiatric disability; veteran or military status; domestic violence victim status; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by applicable federal, state or local law.

#LI-SS1

Research & Development

Americas-US-Connecticut

US-BI Pharma/BI USA

Full-time

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Principal Scientist, In Vitro Safety Pharmacology

Boehringer Ingelheim is currently seeking a driven and innovative Principal Scientist to join our Non-clinical Drug Safety (NDS) Department at our Ridgefield, CT facility.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Integrative Toxicology Group is currently recruiting a Laboratory Head to develop advanced in vitro models to support toxicology species selection and de-risking of new therapeutic products (small molecules, biologics novel modalities) across several therapeutic areas. The candidate will collaborate with our Modeling, Molecular Pathology, PK/PD, Immunopharmacology, Toxicodynamics, and Omics groups.

Main tasks:
  • Demonstrates an expertise in a specific project-relevant area or technology ( i.e. microphysiological systems, 3D cultures and development of complex in vitro system)
  • Directs and oversees the experimental design and results of technical scientists; has full accountability for direct reports, including but not limited to goal setting and definition of personal development plans
  • Supervises and reviews preparation of clear technical reports, publications and oral presentations. Independently communicates team results in the form of reports and or presentations; delivers updates to senior level management in context of overall project/lab goals
  • Proposes new technologies and concepts in support of multiple projects; develops broad knowledge in field of expertise, including the ability to interpret current literature relevant to R & D projects, and visibility outside of functional area
  • Assumes departmental responsibility for projects in the Discovery phase and/or supports multiple project teams as subject matter expert
  • Complies with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintains proper records in accordance with SOPs, appropriate guidance and policies
  • Contributes to departmental administration; demonstrates fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel
Required Education & Experience:
  • PhD degree or equivalent with 5+ years' experience in the field(s) of Molecular & Cellular Biology, Toxicology or similar area of study
  • Demonstrates broad knowledge in the field of expertize i.e. microphysiological systems, 3D cultures and development of complex in vitro systems
  • Appropriate level of understanding of applicable regulations
  • Ability to communicate effectively both orally and in writing in an interdisciplinary environment
  • Previous supervisory and matrix working experience highly preferred
Eligibility Requirements:
  • Must be legally authorized to work in the United States
  • Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background
  • Must be willing to take a drug test and post-offer physical (if required)
  • Must be 18 years of age or older
Desired Experience, Skills and Abilities:
  • Experience with mammalian cell culture techniques (primary cells and cell lines). Experience with stable cell line development or integration of reporter gene constructs. Experience with ex vivo cell isolation from large animals a plus
  • General knowledge of molecular and cell biology, genomics and principles of virology required
  • Familiarity with the use of data display platforms (e.g. GraphPad Prism, TIBCO Spotfire)
  • Basic experience with SPR analysis (instrumentation, experimental setup, execution) of advantage
  • Familiarity with genomic database and data mining, and statistical analysis of biological data a plus
  • Familiarity with the drug development process and/or toxicology and/or immune-oncology and/or anti-inflammatory therapies of advantage
  • Evidence of publication records a plus
Boehringer Ingelheim is currently seeking a driven and innovative Principal Scientist to join our Non-clinical Drug Safety (NDS) Department at our Ridgefield, CT facility.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Integrative Toxicology Group is currently recruiting a Laboratory Head to develop advanced in vitro models to support toxicology species selection and de-risking of new therapeutic products (small molecules, biologics novel modalities) across several therapeutic areas. The candidate will collaborate with our Modeling, Molecular Pathology, PK/PD, Immunopharmacology, Toxicodynamics, and Omics groups.

Main tasks:
  • Demonstrates an expertise in a specific project-relevant area or technology ( i.e. microphysiological systems, 3D cultures and development of complex in vitro system)
  • Directs and oversees the experimental design and results of technical scientists; has full accountability for direct reports, including but not limited to goal setting and definition of personal development plans
  • Supervises and reviews preparation of clear technical reports, publications and oral presentations. Independently communicates team results in the form of reports and or presentations; delivers updates to senior level management in context of overall project/lab goals
  • Proposes new technologies and concepts in support of multiple projects; develops broad knowledge in field of expertise, including the ability to interpret current literature relevant to R & D projects, and visibility outside of functional area
  • Assumes departmental responsibility for projects in the Discovery phase and/or supports multiple project teams as subject matter expert
  • Complies with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintains proper records in accordance with SOPs, appropriate guidance and policies
  • Contributes to departmental administration; demonstrates fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel
Required Education & Experience:
  • PhD degree or equivalent with 5+ years' experience in the field(s) of Molecular & Cellular Biology, Toxicology or similar area of study
  • Demonstrates broad knowledge in the field of expertize i.e. microphysiological systems, 3D cultures and development of complex in vitro systems
  • Appropriate level of understanding of applicable regulations
  • Ability to communicate effectively both orally and in writing in an interdisciplinary environment
  • Previous supervisory and matrix working experience highly preferred
Desired Experience, Skills and Abilities:
  • Experience with mammalian cell culture techniques (primary cells and cell lines). Experience with stable cell line development or integration of reporter gene constructs. Experience with ex vivo cell isolation from large animals a plus
  • General knowledge of molecular and cell biology, genomics and principles of virology required
  • Familiarity with the use of data display platforms (e.g. GraphPad Prism, TIBCO Spotfire)
  • Basic experience with SPR analysis (instrumentation, experimental setup, execution) of advantage
  • Familiarity with genomic database and data mining, and statistical analysis of biological data a plus
  • Familiarity with the drug development process and/or toxicology and/or immune-oncology and/or anti-inflammatory therapies of advantage
  • Evidence of publication records a plus
Eligibility Requirements:

Must be legally authorized to work in the United States without restriction.

Must be willing to take a drug test and post-offer physical (if required)

Must be 18 years of age or older

Who We Are:

At Boehringer Ingelheim we create value through innovation with one clear goal: to improve the lives of patients. We develop breakthrough therapies and innovative healthcare solutions in areas of unmet medical need for both humans and animals. As a family owned company we focus on long term performance. We are powered by 50.000 employees globally who nurture a diverse, collaborative and inclusive culture. Learning and development for all employees is key because your growth is our growth.

Want to learn more? Visit ************************ and join us in our effort to make more health.

Boehringer Ingelheim, including Boehringer Ingelheim Pharmaceuticals, Inc., Boehringer Ingelheim USA, Boehringer Ingelheim Animal Health USA Inc., Boehringer Ingelheim Animal Health Puerto Rico LLC and Boehringer Ingelheim Fremont, Inc. is an equal opportunity and affirmative action employer committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; citizenship status, marital, domestic partnership or civil union status; gender, gender identity or expression; affectional or sexual orientation; pregnancy, childbirth or related medical condition; physical or psychiatric disability; veteran or military status; domestic violence victim status; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by applicable federal, state or local law.

#LI-SS1

Research & Development

Americas-US-Connecticut

US-BI Pharma/BI USA

Full-time

Principal Scientist, In Vitro Safety Pharmacology

Boehringer Ingelheim is currently seeking a driven and innovative Principal Scientist to join our Non-clinical Drug Safety (NDS) Department at our Ridgefield, CT facility.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Integrative Toxicology Group is currently recruiting a Laboratory Head to develop advanced in vitro models to support toxicology species selection and de-risking of new therapeutic products (small molecules, biologics novel modalities) across several therapeutic areas. The candidate will collaborate with our Modeling, Molecular Pathology, PK/PD, Immunopharmacology, Toxicodynamics, and Omics groups.

Main tasks:
  • Demonstrates an expertise in a specific project-relevant area or technology ( i.e. microphysiological systems, 3D cultures and development of complex in vitro system)
  • Directs and oversees the experimental design and results of technical scientists; has full accountability for direct reports, including but not limited to goal setting and definition of personal development plans
  • Supervises and reviews preparation of clear technical reports, publications and oral presentations. Independently communicates team results in the form of reports and or presentations; delivers updates to senior level management in context of overall project/lab goals
  • Proposes new technologies and concepts in support of multiple projects; develops broad knowledge in field of expertise, including the ability to interpret current literature relevant to R & D projects, and visibility outside of functional area
  • Assumes departmental responsibility for projects in the Discovery phase and/or supports multiple project teams as subject matter expert
  • Complies with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintains proper records in accordance with SOPs, appropriate guidance and policies
  • Contributes to departmental administration; demonstrates fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel
Required Education & Experience:
  • PhD degree or equivalent with 5+ years' experience in the field(s) of Molecular & Cellular Biology, Toxicology or similar area of study
  • Demonstrates broad knowledge in the field of expertize i.e. microphysiological systems, 3D cultures and development of complex in vitro systems
  • Appropriate level of understanding of applicable regulations
  • Ability to communicate effectively both orally and in writing in an interdisciplinary environment
  • Previous supervisory and matrix working experience highly preferred
Eligibility Requirements:
  • Must be legally authorized to work in the United States
  • Must be willing to submit to a background investigation, including verification of your past employment, criminal history, and educational background
  • Must be willing to take a drug test and post-offer physical (if required)
  • Must be 18 years of age or older
Desired Experience, Skills and Abilities:
  • Experience with mammalian cell culture techniques (primary cells and cell lines). Experience with stable cell line development or integration of reporter gene constructs. Experience with ex vivo cell isolation from large animals a plus
  • General knowledge of molecular and cell biology, genomics and principles of virology required
  • Familiarity with the use of data display platforms (e.g. GraphPad Prism, TIBCO Spotfire)
  • Basic experience with SPR analysis (instrumentation, experimental setup, execution) of advantage
  • Familiarity with genomic database and data mining, and statistical analysis of biological data a plus
  • Familiarity with the drug development process and/or toxicology and/or immune-oncology and/or anti-inflammatory therapies of advantage
  • Evidence of publication records a plus
Boehringer Ingelheim is currently seeking a driven and innovative Principal Scientist to join our Non-clinical Drug Safety (NDS) Department at our Ridgefield, CT facility.

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.

The Integrative Toxicology Group is currently recruiting a Laboratory Head to develop advanced in vitro models to support toxicology species selection and de-risking of new therapeutic products (small molecules, biologics novel modalities) across several therapeutic areas. The candidate will collaborate with our Modeling, Molecular Pathology, PK/PD, Immunopharmacology, Toxicodynamics, and Omics groups.

Main tasks:
  • Demonstrates an expertise in a specific project-relevant area or technology ( i.e. microphysiological systems, 3D cultures and development of complex in vitro system)
  • Directs and oversees the experimental design and results of technical scientists; has full accountability for direct reports, including but not limited to goal setting and definition of personal development plans
  • Supervises and reviews preparation of clear technical reports, publications and oral presentations. Independently communicates team results in the form of reports and or presentations; delivers updates to senior level management in context of overall project/lab goals
  • Proposes new technologies and concepts in support of multiple projects; develops broad knowledge in field of expertise, including the ability to interpret current literature relevant to R & D projects, and visibility outside of functional area
  • Assumes departmental responsibility for projects in the Discovery phase and/or supports multiple project teams as subject matter expert
  • Complies with all applicable regulations; ensures that work performed in area of responsibility is conducted in a safe and compliant manner; maintains proper records in accordance with SOPs, appropriate guidance and policies
  • Contributes to departmental administration; demonstrates fiscal responsibility with respect to cost of experiments, technology, external collaborations, and travel
Required Education & Experience:
  • PhD degree or equivalent with 5+ years' experience in the field(s) of Molecular & Cellular Biology, Toxicology or similar area of study
  • Demonstrates broad knowledge in the field of expertize i.e. microphysiological systems, 3D cultures and development of complex in vitro systems
  • Appropriate level of understanding of applicable regulations
  • Ability to communicate effectively both orally and in writing in an interdisciplinary environment
  • Previous supervisory and matrix working experience highly preferred
Desired Experience, Skills and Abilities:
  • Experience with mammalian cell culture techniques (primary cells and cell lines). Experience with stable cell line development or integration of reporter gene constructs. Experience with ex vivo cell isolation from large animals a plus
  • General knowledge of molecular and cell biology, genomics and principles of virology required
  • Familiarity with the use of data display platforms (e.g. GraphPad Prism, TIBCO Spotfire)
  • Basic experience with SPR analysis (instrumentation, experimental setup, execution) of advantage
  • Familiarity with genomic database and data mining, and statistical analysis of biological data a plus
  • Familiarity with the drug development process and/or toxicology and/or immune-oncology and/or anti-inflammatory therapies of advantage
  • Evidence of publication records a plus
Eligibility Requirements:

Must be legally authorized to work in the United States without restriction.

Must be willing to take a drug test and post-offer physical (if required)

Must be 18 years of age or older

Who We Are:

At Boehringer Ingelheim we creat
Associated topics: antibody, bacteria, biomedical, biopharma, drug development, healthcare, immunoassay, microbiology, physiology, vaccine * The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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