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Associate Director, Planning & Scheduling(m/w/x)
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
- English – Business Fluent
Tools & Technologies
- SAP
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Associate Director, Planning & Scheduling(m/w/x)
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
- English – Business Fluent
Tools & Technologies
- SAP
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA
Industry
Pharmaceuticals
Description
The company's Marketing team is passionate about bringing medicines and vaccines to customers worldwide, using digital listening and patient analytics to understand and meet customer needs.
Not a perfect match?
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