Skip to main content

This job has expired

You will need to login before you can apply for a job.

Senior Scientist II, CMC Strategy & Portfolio Leadership Scientific Affairs

Employer
AbbVie
Location
North Chicago, Illinois
Start date
Feb 5, 2023

View more

Discipline
Marketing, Science/R&D, Biotechnology, CMC
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
BioMidwest, Best Places to Work

Job Details

AbbVie’s CMC Strategy & Portfolio Leadership group is seeking an experienced and dynamic Senior Scientist II to join its Scientific Affairs group. As a member of drug substance development teams, Scientific Affairs collaborates closely with team members to advance AbbVie’s small molecule and antibody drug conjugate pipelines through the development of manufacturing control strategies, CMC strategy, and preparation of related regulatory submissions.

This is a non-laboratory position where scientists with experience in drug substance process development will contribute their broad knowledge to AbbVie drug substance teams while gaining subject matter expertise in a new field. Strong candidates are those with experience in late-stage drug substance development with an emphasis in process chemistry, process engineering, or process analytical.

Key Responsibilities

Drug Substance Development:

  • Integrated into API and CMC teams at all stages of development with increased involvement during late-stage development
  • Contribute to the development of control strategies and justification of controls for late-stage small molecule and antibody drug conjugate development programs
  • Consult with drug substance development teams on ICH guidelines and global regulatory expectations.
  • Provide perspectives based on prior experience, feedback from Health Authorities, and benchmarking.

Regulatory Submissions:

  • Author Module 3 (Quality) documents relevant to drug substance manufacturing and controls for investigational new drug applications and marketing applications and ensure consistency and scientific thoroughness of content
  • Author responses to informational requests from Health Authorities
  • Contribute to identifying submission-related risks and developing mitigation strategies with CMC team
  • Author briefing documents for meeting or advice requests with Health Authorities
  • Represent CMC in relevant meetings with Health Authorities

Strategic Influence and Process Improvements:

  • Drive continuous improvements to Module 3 content
  • Represent AbbVie in industry working groups
  • Maintain knowledge of current industry and regulatory trends in CMC development and controls
  • Participate in CMC process improvement initiatives

Basic: 

*Level and compensation will be commensurate with experience*

  • Bachelors, Masters, or Ph.D. in Chemistry or Chemical Engineering with a minimum of 12+ years (BS), 10+ years (MS), or 4+ years (Ph.D.) of relevant pharmaceutical development experience.
  • In-depth knowledge of drug substance manufacturing process development, control strategies, and regulatory/ICH guidelines
  • Experience with late-stage drug substance development
  • Demonstrated strong technical writing skills
  • Strong negotiation skills, oral and written communication skills, and influencing skills
  • Demonstrated ability to collaborate with allied areas

Key Leadership Competencies:

  • Builds strong relationships with peers and cross functionally with partners outside of team to enable higher performance
  • Learns fast, grasps the 'essence' and can change the course quickly when indicated
  • Raises the bar and is never satisfied with the status quo
  • Creates a learning environment, open to suggestions and experimentation for improvement
  • Embraces the ideas of others, nurtures innovation and manages innovation to reality

AbbVie is an equal opportunity employer including disability/vets. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a disabled veteran, recently separated veteran, Armed Forces service medal veteran or active duty wartime or campaign badge veteran or a person’s relationship or association with a protected veteran, including spouses and other family members, or any other protected group status. We will take affirmative action to employ and advance in employment qualified minorities, women, individuals with a disability, disabled veterans, recently separated veterans, Armed Forces service medal veterans or active-duty wartime or campaign badge veterans. The Affirmative Action Plan is available for viewing in the Human Resources office during regular business hours.


Company

AbbVie’s mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, and YouTube.

Stock Symbol: ABBV

Stock Exchange: NYSE

Company info
Website
Phone
1-800-255-5162
Location
1 North Waukegan Road
North Chicago
Illinois
60064
US

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert