Principal Manager, CMC External Manufacturing at ABBVIE BIORESEARCH CENTER

North Chicago, Illinois, United States -

Full Time

Start Date

Immediate

Expiry Date

29 Sep, 26

Salary

202500.0

Posted On

01 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

CMC External Manufacturing, cGMP Manufacturing, Technical Oversight, CRO/CDMO Management, Budget Management, Regulatory Compliance, Supplier Review Board, CMC Supply Chain Planning, Reaction Optimization, Scale-up Protocols, Research Project Management, Scientific Presentation

Industry

Pharmaceutical Manufacturing

Description

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 Principal Manager, CMC External Manufacturing, AbbVie Inc., North Chicago, IL: Onsite (onsite 5 days per week). Key Responsibilities Manage DS/ DP cGMP manufacturing and technical oversight at CRO/CDMO, & external budget. Manage & ensure CRO/CDMO compliance with quality, finance, ethics, & regulatory standards. Lead Supplier Review Board activities, & conduct site visits for diligence and audits. Stay updated on pipeline needs for CMC supply chain planning & support regulatory filings. Qualifications Education & Experience Must have a MS in chemistry, chemical engineering, analytical chemistry or related field & 3 years working in an academic or industry setting supporting development & synthesis of pre-clinical or clinical stage small molecule or natural products. Of experience required, must have 3 years of each of the following: preparing written & oral presentations of scientific material to peers, business stakeholders & senior management; supporting reaction optimization & developing protocols for scale-ups; supporting the preparation of research proposals & managing research projects; & authoring & delivering publications & presentations to the broader scientific community. Alternatively, would accept PHD in chemistry, chemical engineering, analytical chemistry or related field & 1 year working in an academic or industry setting supporting development & synthesis of pre-clinical or clinical stage small molecule or natural products. Of experience required, must have 1 year of each of the following: preparing written & oral presentations of scientific material to peers, business stakeholders & senior management; supporting reaction optimization & developing protocols for scale-ups; supporting the preparation of research proposals & managing research projects; & authoring & delivering publications & presentations to the broader scientific community. Work experience may be gained concurrently. Will accept combination of education, work experience & training. Additional Information Salary Range: $184,538 - $202,500 per year. Apply online at https://careers.abbvie.com/en or send resume to [email protected]. Refer to Req ID: REF49837Z ---------------------------------------------------------------------------- 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 and long-term incentive programs. AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. 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 protected veteran, or any other legally protected group status. 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 Salary Min: 0 Salary Max: 0 Workday Global Grade: 00 Compensation: USD 0 - USD 0 - yearly

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Responsibilities

Manage DS/DP cGMP manufacturing and technical oversight at CRO/CDMOs while overseeing external budgets. Lead supplier review activities and support regulatory filings through CMC supply chain planning.