Senior Associate Director, Clinical Supply Quality — Hybrid

Regulatory Jobs; Pennsylvania; Hybrid; USD 129,000 - 203,000; Full time

Benefits offered by this job

Medical insurance

Dental and Vision

401(k) retirement plan

Paid holidays and vacation

Job summary

Merck & Co., Inc. in Rahway, NJ, invites applications for Associate Director, Clinical Supplies Quality, Global Development Quality.

You will provide strategic quality leadership for Clinical Supply Chain activities across the company’s development portfolio, ensuring materials are compliant, available, and fit for use. The role requires collaboration with Global Clinical Supplies, Regulatory Affairs, Device Development & Technology, External Development & Manufacturing, and QA functions to

Qualifications

• Bachelor’s degree in Scientific Discipline with 8+ years in pharma GMP or related field; advanced degree with 6+ years acceptable.
• Experience with Medical Device/Combination Products preferred.
• Strong leadership and cross-functional collaboration capabilities.

Responsibilities

• Provide quality oversight for clinical supply operations and disposition.
• Lead quality initiatives and investigations across the clinical supply chain.
• Engage with external partners and internal stakeholders to ensure compliance and continuous improvement.
• Identify risks and drive resolution of significant quality events.

Skills

Deviation Management

Process Implementations

Product Compliance

Project Leadership

Project Risk Assessments

Quality Oversight

Quality Risk Management

Regulatory Compliance

Stakeholder Management

Standards Compliance

Strategic Leadership

Strategy Development

Education

Bachelor’s Degree in Scientific Discipline

Job description

Merck & Co., Inc. in Rahway, NJ, invites applications for Associate Director, Clinical Supplies Quality, Global Development Quality.

You will provide strategic quality leadership for Clinical Supply Chain activities across the company’s development portfolio, ensuring materials are compliant, available, and fit for use. The role requires collaboration with Global Clinical Supplies, Regulatory Affairs, Device Development & Technology, External Development & Manufacturing, and QA functions to