Job Description

Reference # : 18-03594Title : Director, Global Manufacturing
Location : New Brunswick, NJ
Position Type : Contract
Experience Level : Start Date / End Date : 04/30/2018 / 09/29/2018
Assignment Detail
Industry:Biotech/PharmaJob Category:Manufacturing / Supply Chain
Description
Director, Global Manufacturing

Eclaro is looking for a Director for an opportunity with our client in New Brunswick, NJ

Job Title: Director, Global Manufacturing
Location: One Squibb Drive New Brunswick, NJ 08903
Schedule: 40 hours/week

Qualifications:
  • Minimum 15 years’ experience in the Pharmaceutical Industry with 5 years in a Quality Function/Role
  • Supply Chain, distribution, Product Transportation, Pedigree/Traceability, Anti-counterfeiting technology, returns and recalls
  • Leading and supporting projects of a Global nature and management of Quality related issues.
  • Project Manager/ Program Manager
  • Development and Implementation of Policies, Directives, SOPs and Best Practices.
  • Contract / Vendor Management
  • Technical expertise; SAP, Business Planning and Control Systems, Inventory management Systems, Quality software/tools.
  • Current Industry knowledge on anti-counterfeiting and supply chain security strategies, technologies and practices.
  • Leadership skills
  • Influencing and negotiation skills
  • Critical thinking, a decisive manner and ability to remain calm under adverse events.

Responsibilities:
  • Lead the Authentication / Track & Trace Work Stream of the Serialization PMO for successful implementation of appropriate processes and systems.
  • Participate in the Serialization PMO and Country meetings.
  • Formulate and interpret policy and laws/regulations for authentication and Track & Trace efforts.
  • Develop sustainability strategy for serialization in support of authentication and track & trace including:
    • Product Authentication
    • Track & Trace Plan
    • Alignment with U.S. Trade Sales on ATPs relative to serialization / Track & Trace technology, Business-to-Business process, contractual agreements and authentication / Track & Trace pilots.
    • Management of Health Authority access to authentication and Track & Trace data/ information.
  • Support the Product Surety/Illegitimate and/or Falsified Medicinal Product Strategy in various assigned activities/projects.
  • Participate in external industry organizations, identifying and communicating to management key points/issues.
  • Identifies and recommends appropriate actions, activities and projects for continuous improvements.
  • Perform other duties as assigned.
If interested, you may contact:
Froilyn Jane Bautista

Froilyn.Bautista@eclaro.com
(201) 285-8622

ECLARO is a company that delivers talent. We provide fully customizable, comprehensive talent acquisition and management of seasoned professionals through a number of business models, including: Consulting, Professional Hire, Global Integrated Delivery™ and Managed Services. ECLARO recruits and manages a staff of highly skilled individuals in an array of specialized disciplines. This approach enables our clients to leverage new opportunities, respond to increased and changing demands and increase their profitability. Please visit www.eclaroIT.com to see why the Right People are The Answer™.

Specialties: Customized solutions for Human Capital and Talent Acquisition, Permanent placement and retained search, Recruiting, Staff Augmentation, Contract Labor, Managed Services, RPO, MSP, VMS, IT solutions, management and support, offshore business process outsourcing.

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Website: http://www.eclaro.com
Industry: Staffing and Recruiting
Type: Privately Held
Company Size: 501-1000 employees
Founded: 1999

Application Instructions

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