Manager, Production Services

Job not on LinkedIn

🔥 0 minutes ago

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🍿 Producer

🦅 H1B Visa Sponsor

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👻 Ghost score 10%

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Parexel

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1983

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 Venture Round on 1990-01

Consulting • Healthcare • Logistics

Parexel is one of the world's largest clinical research organizations (CROs), providing comprehensive services for the clinical development process from Phase I to IV. The company specializes in portfolio management, clinical trial management, regulatory strategy, market access, and lifecycle management for biopharmaceuticals. Parexel aims to speed life-changing medicines to market by leveraging its clinical, regulatory, and therapeutic expertise. With a global team of over 21,000 professionals, Parexel works to integrate patient insights and innovative trial designs to develop treatments across therapeutic areas such as oncology, neuroscience, rare diseases, and more. It focuses on delivering patient-centric and efficient clinical trials.

📋 Description

• Lead, mentor, and develop Production Services team members • Oversee clinical trial supply production workflows and ensure projects remain on schedule • Monitor operational progress, manage priorities, and provide escalation support for complex supply chain challenges • Support packaging, labeling, manufacturing support, batch documentation, and production planning activities • Ensure compliance with GMP, GDP, regulatory requirements, and departmental procedures • Drive problem solving and mitigation planning for project risks and timeline challenges • Support supplier compliance, quality metrics, training compliance, audits, inspections, CAPA activities, and continuous improvement initiatives • Collaborate with cross-functional clinical supply chain stakeholders across global regions • Contribute to operational excellence, process improvement initiatives, and lean management practices • Support business growth through internal initiatives, client-facing activities, and strategic operational planning

🎯 Requirements

• Bachelor's degree in Life Sciences, Pharmaceutical Sciences, Logistics, Engineering, or a related discipline, or equivalent experience • Approximately 6 to 10+ years of experience in clinical trial supply chain, pharmaceutical production, clinical logistics, or a related regulated environment • Strong knowledge of Good Manufacturing Practices (GMP) requirements and clinical supply chain operations • Experience with production planning, packaging design, labeling operations, and supply chain execution • Ability to identify risks, resolve operational issues, and implement mitigation strategies • Strong project management, organizational, and stakeholder management skills • Fluent English communication skills • Strong leadership, problem-solving, and operational decision-making skills • Expertise in clinical trial supply chain operations and GMP-regulated environments • Experience supporting packaging, labeling, production planning, and clinical supply activities • Experience within a Contract Manufacturing Organization (CMO) supporting clinical trial supplies preferred • Previous people leadership or team management experience preferred • Experience leading global or geographically dispersed teams preferred • Financial, budgeting, profitability, KPI, and forecasting experience preferred

🏖️ Benefits

• Health, Vision & Dental Insurance • Tuition Reimbursement • Vacation/Holiday/Sick Time • Flexible Spending & Health Savings Accounts • Work/Life Balance • 401(k) with Company Match • Pet Insurance • Paid time off • Life insurance • Flexible work arrangements