Program Manager, MES

Purpose:

The Program Manager MES will organize and lead high-performing cross-functional teams in the planning and execution of programs associated with assembly labeling and packaging of drug delivery devices and combination products. This individual provides leadership and coordinated project management for all manufacturing and/or technical activities needed to ensure successful tech transfer and commercialization of the assigned products by integrating the efforts of R&D S&T Quality Supply Chain Regulatory. After product launch this individual is responsible for managing the capacity strategy for the product assurance of supply programs and cost reduction initiatives across the network.           

Responsibilities:

Assemble and lead matrixed cross-functional teams comprised of scientist and engineers responsible for all operational aspects of process development manufacturing quality assurance and quality control spanning multiple sites

Implement site transfers new indications new presentations and lifecycle projects for on market programs on time and within budget

Proactively identify and drive technical and project plan related issues to closure by working with all relevant functional lines and effectively troubleshooting and driving decisions

Manage multiple projects concurrently operating with minimal supervision

Understand project drivers requirements scenarios and options. Proactively drive development of contingency and/or risk mitigation plans.

Manage competing timelines and make difficult decisions regarding priorities among projects.

Effectively communicate and present project status to Operations senior management and stakeholders

Accountable for setting program and project plans including timelines and expenses that meet business and organizational objectives and ensuring those plans are achieved.

Define budget requirements and report monthly actuals LBE and Plan/LRP schedules per financial schedule

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Qualifications :

Bachelors Degree in Engineering science or closely related discipline or equivalent technical experience plus demonstrated competence

10 years of combined experience in positions related to process development project management engineering/process support and manufacturing

Must have strong knowledge of GMP Manufacturing Supply Chain Validation Engineering CMC technical development and pharmaceutical regulations

Must have demonstrated organizational and planning skills excellent verbal and written communication skills

Must have demonstrated strong project management skills with successful delivery of projects

Must be able to effectively facilitate the resolution of complex scientific technical analytical and business issues across functional lines

Plant experience a must

PMP certification a plus

Proficiency in multiple languages a plus

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 thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic locationand 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 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 commissionincentive 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 anduntil 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. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

No

Employment Type :

Full-time