Director, CMC Product Development (Onsite, Irvine CA)

Further develop your expertise and join our team as Director CMC Product Development. Must have Medical Device experience. 

The Product Development Director (PDD) will be a member of the Operations Strategy & Pipeline Leadership (OSPL) team within the Product Development Science & Technology (PDS&T) organization. Reporting to one of the Therapeutic Area Leads the PDD will be responsible for pipeline programs from a Chemistry Manufacturing and Controls (CMC) perspective. They will lead the Product Presentation and Device Strategy Team (PPDST) and build the CMC development strategy for the late-stage assets aligning with the clinical and regulatory development strategy from the Asset Strategy Team (AST). The programs can span modalities and presentations. Modalities can include small molecules biologics (protein gene therapy toxin etc) and antibody drug conjugates.  Product presentations can include oral dose parentals and devices (therapeutics and aesthetic).  

The PDD is accountable for creating a CMC development plan in collaboration with line functions and ensures strategic alignment with the enterprise functions (Clinical Regulatory and Commercial) cross-functionally at the AST. The PDD is the spokesperson for CMC-related aspects at asset-level governances and represents the assets within Operations to ensure support of late-stage development activities and readiness for launch. They are responsible for communicating development and regulatory risks and seeking feedback from CMC leadership. 

Key Responsibilities:

• Represents all CMC areas on the AST serving as spokesperson for the CMC project team and ensures information flow among the AST and all line functions. Ensures high quality science technology deliverables and collaborates to ensure compliance with global regulatory and quality requirements. Participates in interactions with Regulatory and Health Authorities.
• Critically evaluates and integrates drug substance drug product and device inputs to CMC team strategies and plans that align with corporate business objectives. Decision-making will often require assessment and integration of physical chemical properties formulation science engineering analytical and device technical information in conjunction with the project strategy with full consideration of current regulatory and compliance requirements.
• Manages multiple projects and contributes to project prioritization. Negotiates for additional resources when required influences project timelines to ensure proper completion of required activities. Implements creative approaches to conserve resources and achieve efficiency with respect to time and budget. Provides feedback to CMC management on resource and talent opportunities.
• Reviews contracts with external partners and consultants. Develops a budget in collaboration with AST and obtains resources from functional areas. Accountable for the success and overall CMC quality of a given project. Ensures timely execution of project plan to deliver high quality with respect to science technology compliance and cost effectiveness.
• Represents AbbVie on high profile partnerships and collaborations with other pharma/biotech companies and at the Joint Development Committee level driving decisions for the development programs.
• Promotes scientific and entrepreneurial thinking encourage creativity and manage quality and results with respect to science time budget and resources.
• Ensures compliance with regulatory health safety and environmental requirements. Stay abreast of developments in global technical regulatory and compliance arena and industry practice.
• Apprises CMC Management of plans and risks through regular communications and periodic reviews throughout development and in support of global filings approvals and launches.
• Ensures high level of morale in the CMC team.

Qualifications :

• Bachelors Degree with at least 15 years of experience in CMC functions required; Masters Degree with at least 10 years of relevant CMC experience required; or PhD with at least 8 years of relevant CMC experience required to effectively manage global teams and all CMC activities with respect to science technology quality regulatory/compliance requirements budget and resources.
• Multiple product development experiences of leading a CMC team through regulatory submissions (NDA/BLA/PMA/510K preferred).
• Must possess good scientific writing skills and good verbal skills.
• Must have a good working knowledge of regulatory requirements and familiarity with relevant CMC development approaches. (Device regulatory requirements)
• Knowledge of pharmaceutical sciences and the drug/device development process.
• Must have CMC interdisciplinary experience and expertise.
• Possess negotiating influencing and leadership skills. Creative in implementing entrepreneurial thinking and capable of making smart business decisions.

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.

• 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. 

• This job is eligible to participate in our long-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 Companys sole and absolute discretion unless and until paid and may be modified at the Companys 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. 

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