Jobs

Description

100% onsite

Top 3 – 5 Skills Needed for each role

• Candidates must exhibit the technical ability to execute and troubleshoot experiments through rational and critical thinking. Candidates must be highly organized and detail oriented.
• Hands-on laboratory experience in biologics formulation development, drug delivery, drug product manufacturing processes, lyophilization or analytical functions is preferred.
• Strong organizational and documentation skills; ability to maintain accurate experimental records and reports.
• Effective verbal and written communication skills with the ability to work collaboratively in cross-functional teams 

Purpose:

• The incumbent in this role will support the formulation and process 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 involves designing, executing, and reporting of laboratory experiments to advance the development of stable and effective biologic formulations.
• The incumbent will collaborate across multidisciplinary teams and contribute to solving technical challenges in both formulation and process optimization, to enable successful clinical and commercial progression of therapeutic biologics.
• 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 for animal studies.
• Conduct clinical in-use studies to guide dose solution administration.
• Perform analytical testing and characterization of biologic samples, assessing critical quality attributes to support formulation and process decisions.
• Interpret results and draw conclusions from multistage experiments; note significant deviations and propose relevant new experiments
• Thoroughly document experimental procedures, results, and interpretations in laboratory notebooks and reports, ensuring compliance with company and regulatory standards.
• Generate high-quality data based on sound scientific principles and prepare formulation data summaries, technical reports, and scientific presentations
• Participate in the evaluation, implementation, and ongoing improvement of new and existing technologies, techniques, and equipment to continuously enhance formulation and process development.

Qualifications:

• BS with a minimum of 3 years or MS with a minimum of 2 years of experience in pharmaceutics, pharmaceutical sciences, chemical engineering, analytical sciences, or equivalent field in the biotechnology industry.
• Candidates must exhibit the technical ability to execute and troubleshoot experiments through rational and critical thinking. Candidates must be highly organized and detail oriented.
• Hands-on laboratory experience in biologics formulation development, drug delivery, drug product manufacturing processes, lyophilization or analytical functions is preferred.
• Prior hands-on experience working with neurotoxins or highly potent compounds within a Biosafety Level 2 (BSL-2) laboratory environment is strongly desired.
• Strong organizational and documentation skills; ability to maintain accurate experimental records and reports.
• Effective verbal and written communication skills with the ability to work collaboratively in cross-functional teams.