Company Description
AbbVie’s mission is to discover and deliver innovative medicines and solutions 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, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
The Associate Scientist II - Biologics Drug Product Development will support the formulation development of protein biologics from early development (pre-clinical/First-In-Human candidates) through commercialization, with a specific focus on neurotoxins for therapeutics and aesthetic use.
This position requires laboratory work in areas requiring select agents and Toxins access (i.e., Biosafety level 2 laboratories). Access to and use of select agents is regulated by federal policies. Therefore, the candidate must conduct all work activities in compliance with AbbVie internal and applicable regulatory requirements. AbbVie internal requirements include compliance with ethics, environmental health and safety, financial, human resources, and general business policies, requirements, and objectives.

Responsibilities

• Execute formulation composition and drug product process development studies for sterile liquids, lyophilized, and pre-filled dosage forms.
• Manufacture drug product formulation batches for evaluating formulation stability and/or to support animal studies.
• Conduct clinical in-use studies to guide dose solution administration.
• Interpret results and draw conclusions from multistage experiments; note significant deviations and propose relevant new experiments.
• Generate high-quality data based on sound scientific principles and prepare formulation data summaries, technical reports, and scientific presentations.
• Support functional technical initiatives by investigating and developing novel experimental approaches and/or technologies in the field of drug product development.
• Maintain oversight of day-to-day laboratory activities; manage inventory of raw materials and drug product packaging and manufacturing supplies; coordinate ordering, shipping, and receiving.

Qualifications

MINIMUM QUALIFICATIONS

• Bachelors with a minimum of 3-5 years OR Masters with a minimum of 0-2 years of experience in pharmaceutics, pharmaceutical sciences, chemical engineering, analytical sciences, or equivalent field in the biotechnology industry
• Experience in a formulation development lab OR process development lab
• Hands-on experience with analytical techniques used for protein characterization and stability studies are required (e.g HPLC, spectroscopy, SEC, HIAC, MFI, DLS, ELISA, Karl Fisher).

PREFERRED QUALIFICATIONS:

• CMC development experience in protein formulation, drug delivery, or analytical functions is preferred.
• Prior experience with drug product manufacture processes and lyophilization is a plus

OTHER REQUIRED SKILLS:

• Excellent communication skills required.
• Candidates must exhibit the technical ability to execute and troubleshoot experiments through rational and critical thinking.
• Candidates must be highly organized and detail oriented.
  Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. Salary: $94,750 - $107,500
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company’s sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.htm

• Execute formulation composition and drug product process development studies for sterile liquids, lyophilized, and pre-filled dosage forms.
• Manufacture drug product formulation batches for evaluating formulation stability and/or to support animal studies.
• Conduct clinical in-use studies to guide dose solution administration.
• Interpret results and draw conclusions from multistage experiments; note significant deviations and propose relevant new experiments.
• Generate high-quality data based on sound scientific principles and prepare formulation data summaries, technical reports, and scientific presentations.
• Support functional technical initiatives by investigating and developing novel experimental approaches and/or technologies in the field of drug product development.
• Maintain oversight of day-to-day laboratory activities; manage inventory of raw materials and drug product packaging and manufacturing supplies; coordinate ordering, shipping, and receiving