Skip to content
New Job?Nejo!

Your personal AI career agent

MEMerck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA

Associate Director, Planning & Scheduling(m/w/x)

Luzern
Full-timeOn-siteExperienced

Overseeing daily label production for clinical supplies in 60+ countries. GMP compliance and process improvement focus. Bachelor's degree with 4 years relevant experience required.

Requirements

  • Bachelor's degree or equivalent with four years relevant experience
  • High School Diploma or equivalent with six years relevant experience in Pharmaceutical Operations, preferably clinical supply-related
  • At least two years of management or leadership experience
  • Minimum six years relevant supply chain or operations experience preferred
  • Effective cross-functional collaboration in multicultural environments
  • Demonstrated problem-solving ability
  • Strong verbal and written communication skills
  • Excellent interpersonal skills
  • Strong understanding of clinical supplies and supply chain processes
  • Relevant regulatory and GMP requirements understanding
  • Ability to establish clear goals
  • Effective delegation ability
  • Accountability for self and others
  • Ability to succeed in dynamic environment
  • Adaptability to changing priorities
  • Well-developed team facilitation skills
  • Well-developed leadership skills
  • Ability to build inclusive team environments
  • Proven project management skills
  • Proven team management skills
  • Prior SAP experience beneficial

Tasks

  • Oversee daily label production operations
  • Ensure compliance with GMP and quality standards
  • Drive process improvements
  • Support team development
  • Coordinate local and global labelling activities
  • Identify and verify components and materials
  • Print, inspect, proof, and maintain clinical product labels
  • Manage label inventory and dispose of expired materials
  • Serve as a Qualified Trainer
  • Conduct periodic quality inspections
  • Prepare label shipments to external sites
  • Receive bulk labels from vendors
  • Participate in equipment testing and upgrades
  • Ensure tasks follow GMP and batch record instructions
  • Initiate and implement process improvements
  • Monitor production schedule and manage team resources
  • Advance operational capabilities
  • Lead innovation and technology use in Label Production
  • Evaluate and develop employee performance
  • Manage team and escalate issues
  • Lead and delegate label projects
  • Author, review, and approve SOPs and job aids
  • Support internal and external audits
  • Recommend efficiency-enhancing process improvements
  • Train new employees

Work Experience

  • 4 years

Education

  • Bachelor's degree

Languages

  • EnglishBusiness Fluent

Tools & Technologies

  • SAP
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

Like this job?

Beta

Your Career Agent finds similar jobs for you every day.


  • Merck & Co., Inc., Rahway, NJ, USA

    Associate Director Quality Assurance(m/w/x)

    Full-timeOn-siteSenior
    Luzern
  • 3568 MSD Int. Business GmbH

    Specialist, Supply Chain Management(m/w/x)

    Full-timeOn-siteExperienced
    Luzern
  • Neogen Europe Ltd

    Supply Planning Manager EMEA(m/w/x)

    Full-timeOn-siteSenior
    Luzern
  • Merck & Co., Inc.

    Sr Director Drug Substance Facility Lead(m/w/x)

    Full-timeOn-siteManagement
    Luzern
  • Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA

    Associate Director, Strategic Operations & Commercial Solutions(m/w/x)

    Full-timeOn-siteSenior
    Luzern
View all 100+ similar jobs