Senior Manager, Depot and Production

Join Parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do.Job TitleSenior Manager, Depot and ProductionIntroductionAt Parexel, we are a leading Clinical Research Organization (CRO) company specializing in delivering life- changing medicines to patients. We are seeking a Senior Manager, Depot and Production to join our team. In this role, you’ll be joining a fast-paced, driven environment that’s helping to make life-changing difference to patients by providing leadership to a team of skilled depot staff, implementing process improvements and driving business growth and productivity. Through the collaboration, and diversity, of teams the Senior Manager, Depot and Production is provided with multiple opportunities to excel and discover where your skills can take you.Who we’re looking for:• Driven team leader with experience in a high growth global service environment.• Detail-oriented individual who can ensure the facility is maintained according to cGMP requirements.• System knowledge in supply chain enterprise solutions.• Relevant direct pharmaceutical industry experience in Clinical Trial Supply, Ancillary Supply or Central Laboratory Service.• Prior management experience that enables a high-performance culture through a positive, results-oriented work environment.• Educated to B.A. / B.S. degree in logistics, pharmacy, biological science or other related discipline.What you’ll do:• Support and improve levels of productivity through effective task-allocation and staff assignment.• Ensure direct reports meet and aim to exceed their personal goals and objectives through orientation, performance review, and ongoing development.• Complete the formal performance and salary review process to corporate standards.• Drive business and project growth with the goal of increasing revenues and profits.• Analyze and implement lean management approach and process improvement in line with corporate, quality, client and team feedback.• Monitor and support the current Good Manufacturing Practices (cGMPs) and current Good Distribution Practices (cGDPs).• Ensure that appropriate documents are in place for distribution of clinical materials.• Review TIME entries and TIME reports and provide accurate input into monthly reports.• Contribute to projects, committees and task force groups as needed.Why join us:Be part of groundbreaking projects that are pushing the boundaries of the industry.Experience a collaborative and inclusive work environment that highly appreciates your expertise. Unlock your full potential with professional growth and development opportunities.Enjoy work life balance and flexible working hours.Parexel US Benefits:Health, Vision & Dental InsuranceTuition ReimbursementVacation/Holiday/Sick TimeFlexible Spending & Health Savings AccountsWork/Life Balance401(k) with Company matchPet InsuranceFull list of benefits available here: https://www.parexel.com/us-benefitsIf this job doesn’t sound like the next step in your career, but perhaps you know of someone who’d be a perfect fit, send them the link to apply!At Parexel we embrace flexibility and understand that in today’s fast-paced world, employees need to balance their careers with their personal lives. Come join us where learning is constant, and you’re exposed to a world of experiences and open doors.