Associate Director, Planning & Scheduling Onsite

Job Description

Job Description:

The Global Clinical Supply (GCS) organization manages the end-to-end clinical supply for the companys portfolio. GCS is accountable for the planning sourcing labeling packaging and delivery of clinical supplies to clinical sites across more than 60 countries in compliance with worldwide regulations company policies and standard operating procedures.

The Print Team Lead is responsible for overseeing daily label production operations ensuring compliance with GMP and quality standards driving process improvements supporting team development and coordinating both local and global labeling activities to meet operational goals efficiently and effectively.

Role requires full

Primary activities:

• Ensure each component or bulk material used in label production is properly identified not expired and verified throughout processing and that it corresponds to the written information on the work order before proceeding to the next step.

• Print inspect proof and maintain accountability for clinical product labels.

• Maintain label inventory including the disposal of expired materials.

• Serve as a Qualified Trainer.

• Conduct periodic quality inspections during the printing process to ensure product integrity.

• Prepare shipments of labels to external packaging sites.

• Receive bulk labels from booklet manufacturing vendors.

• Participate in equipment-related testing and upgrades.

• Ensure team members perform tasks in accordance with GMP and batch record instructions.

• Initiate and implement process improvements aimed at increasing quality customer satisfaction and efficiency.

• Monitor the production schedule on a weekly monthly and quarterly basis while managing group headcount and employee utilization.

• Advance operational capabilities by identifying new opportunities seeking input from key stakeholders and implementing ideas.

• Lead promote and support the use of innovation and technology in Label Production.

• Regularly evaluate employee performance conduct development discussions and complete year-end performance reviews.

• Manage the team including problem-solving and proactive escalation to next-level management when needed.

• Lead local and global label projects including organizing meetings and delegating tasks.

• Author review and approve standard operating procedures and job aids for packaging and labeling activities.

• Participate in and support internal and external audits.

• Recommend process improvements to enhance team efficiency.

• Coordinate and train new employees.

Education:

• Bachelors degree or equivalent with four (4) years of relevant experience or

• High School Diploma or equivalent with six (6) years of relevant experience in Pharmaceutical Operations preferably in a clinical supply-related area.

Preferred Experience and Skills

• At least two (2) years of experience in management or leadership positions required.

• Minimum of six (6) years of relevant experience in supply chain or operations preferred.

• Ability to collaborate effectively across functional boundaries in multicultural environments to align stakeholders and drive tech transfer strategies and solutions.

• Demonstrated problem-solving ability strong verbal and written communication skills and excellent interpersonal skills.

• Strong understanding of clinical supplies and supply chain processes with relevant regulatory and GMP requirements.

• Ability to establish clear goals delegate effectively and hold self and others accountable.

• Ability to succeed in a dynamic environment and adapt to changing priorities.

• Well-developed team facilitation and leadership skills with the ability to build inclusive team environments.

• Proven project and team management skills.

• Prior experience with SAP is beneficial.

#MSJR

Required Skills:

Preferred Skills:

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The salary range for this role is

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employees position within the salary range will be based on several factors including but not limited to relevant education qualifications certifications experience skills geographic location government requirements and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive if applicable.

We offer a comprehensive package of benefits. Available benefits include medical dental vision healthcare and other insurance benefits (for employee and family) retirement benefits including 401(k) paid holidays vacation and compassionate and sick days. More information about benefits is available at can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:We will consider for employment all qualified applicants including those with criminal histories in a manner consistent with the requirements of applicable state and local laws including the City of Los Angeles Fair Chance Initiative for Hiring Ordinance

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Merck & Co. Inc. Rahway NJ USA also known as Merck Sharp & Dohme LLC Rahway NJ USA does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place introductions are position specific. Please no phone calls or emails.

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