Principal Scientist, In Vitro Safety Pharmacology (Willimantic)

Compensation

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

Employment Type

: Full-Time

Industry

: Scientific Research



principal biological scientist Jobs in Ridgefield, CT

Principal Scientist, In Vitro Safety Pharmacology

3.8 Boehringer Ingelheim ? Ridgefield, CT 15 days ago
$78k-$132k(Glassdoor Est.)

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  • Job
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 boehringer-ingelheim.com 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

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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 boehringer-ingelheim.com 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


Associated topics: drug discovery, histologist, histology, immunoassay, immunology, kinesiology, microbiological, nutrition, physiology, protein * 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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