Senior Scientist II / Principal Scientist I, Biologics Drug Product Development

External

Abbvie · North Chicago, IL

Full-timeOn-site4w ago

LessRisk Management

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About the role

Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie's R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy). AbbVie is seeking a highly motivated candidate for the position of Senior Scientist II / Principal Scientist I, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics drug product formulation and process development, scale-up and tech transfer. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, combination products development, product development science and technology, pilot plants and third-party manufacturers.

Requirements

BS, MS, or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Chemical Engineering, or related disciplines with Senior Scientist II: 12+ (Bachelors), 10+ (Masters), or 4+ (PhD) years of relevant industry experience.

Principal Scientist I: 14+ (Bachelors), 12+ (Masters), or 6+ (PhD) years of relevant industry experience.

Proven ability to solve critical scientific problems.

Experience with biologics (proteins, conjugates, peptides and/or neurotoxins), parenteral synthetic molecules and/or genetic medicine (AAV, LNPs, cell therapy) drug product process development.

Experience with sterile manufacturing unit operations (freeze-thaw, compounding, mixing, filtration and filling, lyophilization), characterization, scale-down models, simulation, scale-up, technology transfer, and batch record authoring.

Experience leading drug product development as the functional lead within cross-functional teams

Hand-on experience with authoring regulatory filings for biologics and sterile parenteral products

Understanding of relevant cGMP and regulatory guidance for biologics and sterile parenteral products

Experience in managing third party manufacturers of sterile parenteral products

Experience with quality risk management and control strategies for biologics and sterile parenteral products

Key Competencies:

Deep scientific knowledge and significant hands-on experience with drug product process development and tech transfer

Effectively communicates to influence without authority, drives technical excellence, and inspires continuous improvement.

Builds strong relationships with peers and cross-functional partners to enable higher performance.

Connects ideas from disparate fields, integrates data and information quickly, and takes risks to achieve the highest performance.

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.

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.

Senior Scientist II / Principal Scientist I, Biologics Drug Product Development

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