Senior Scientist, Pharmacy I

Responsibilities

• Act as the Drug Product lead for pipeline and marketed products.
• Lead or support process development for eye care and gene therapy products, including solution, suspension, lyophilized, and other injectable dosage forms.
• Drive development of drug product strategies aligned with target product profiles, quality attributes, and clinical/commercial requirements.
• Provide technical oversight for process development, process characterization, scale-up, validation, and tech transfer activities.
• Support manufacturing issue resolution, deviation investigations, root cause analysis, and implementation of corrective and preventive actions.
• Partner with internal and external manufacturing sites, CMOs, and vendors to ensure product robustness and supply reliability.
• Contribute to CMC documentation for regulatory submissions, technical reports, responses to agency questions, and lifecycle changes.
• Evaluate and implement innovative drug product solutions for novel therapies.
• Assess product stability, compatibility, container closure systems, and storage/shipping considerations.
• Collaborate with Quality, Regulatory, Analytical, and Clinical teams to ensure alignment on development strategy and execution.
• Mentor junior scientists and contribute to scientific capability building within the organization.
• Represent drug product expertise in cross-functional governance forums and project teams.
• PhD, PharmD, or MS in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biotechnology, or related scientific discipline.
• Typically 6+ years of relevant industry experience for a Grade 17 level, or equivalent combination of education and experience.
• Experience with process development and/or commercial product support, aseptic processing, sterile manufacturing, process Validation.
• Demonstrated understanding of CMC principles, GMP requirements, and technical transfer.
• Proven ability to work effectively in cross-functional and matrixed environments.
• Strong scientific judgment, problem-solving skills, and communication skills.

Requirements

• Experience supporting ophthalmic or eye care products.
• Experience with novel modalities or advanced therapeutic platforms.
• Knowledge of container closure systems, extractables/leachables, and stability programs.
• Experience with global regulatory filings and product lifecycle management.
• Prior experience with external partners or contract manufacturing organizations.
• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
• 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.
• 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.html

Benefits

Additional Information

The Senior Scientist, Drug Product/Parenteral Expert serves as the technical subject matter expert for drug product and parenteral development across pipeline and commercial products within Eye Care and Novel Therapies. This role provides scientific leadership in process development, manufacturing support, tech transfer, scale-up, and lifecycle management of sterile and parenteral product. The candidate will partners cross-functionally with Research, Development, Manufacturing, Quality, Regulatory, Supply Chain, and external partners to ensure robust product development and reliable commercial supply.

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