Associate Manager, Supply Chain Planning
US–NJ–Plainsboro, Vacancy ID JR-4401

Integra LifeSciences is a global medical technology leader in neurosurgery and regenerative medicine driven by our purpose of restoring patients’ lives. The company offers a broad portfolio of products and innovative solutions for dural access and repair, cerebral spinal fluid management and neuro-critical care. Its regenerative tissue technologies include products that address soft tissue, peripheral nerve and tendon repairs and for the treatment of acute and chronic wounds, burns, as well as for plastic and reconstructive surgery.
Founded in 1989 by Richard E. Caruso, the company is headquartered in Princeton, New Jersey. Today, Integra LifeSciences has grown immensely, with more than 4200 employees worldwide as well as offices, manufacturing and research facilities in Asia, Australia, Europe, Middle East, and the Americas.
Changing lives. Building Careers.
Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
SUMMARY
The Associate Manager, Supply Chain Planning plays a key role in the success of our supply chain and operations by overseeing and coordinating all scheduling activities for the manufacturing, testing, release, and shipping of new product introductions (NPIs), sub-assemblies, and finished goods to fulfill our customer commitments. This individual is responsible for developing the production schedule and tracking progress, identifying and mitigating schedule risks, while coordinating cross-functional support activities / constraints. The Master Scheduler ensures proper supply related data maintenance and reporting among internal and external SCM teams.
ESSENTIAL DUTIES AND RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities:
Plan, prepare, issue and control the production schedule to support the manufacturing of skin, medical, and private label NPIs, sub-assemblies (SAs), and finished goods (FGs) to meet customer demand, delivery commitments, and production requirements.
Foresees and escalates scheduling interruptions, constraints, or capacity issues and works cross-functionally with manufacturing, planning, procurement, project management, quality systems (QS), quality control (QC), quality assurance (QA), analytical and micro labs, warehouse, engineering, maintenance / calibration, product development (PD), and facilities to resolve and minimize impact to the production schedule.
Issue / reconcile daily task sheets by department / function based on the production schedule.
Tracks progress against the production schedule and work-in-process (WIP), optimizing and rescheduling when needed – considering constraints, capacity issues, and NCs, interfacing with cross-functional teams to align on the production schedule.
Chair daily cross-functional operations meetings to monitor progress against the production schedule and escalate issues to appropriate groups to resolve / mitigate.
Work with engineering, PD, facilities, and maintenance / calibration to coordinate engineering, validation, re-qualification, equipment and building utility preventative maintenance (PM) and corrective maintenance (CM), instrumentation calibration, shutdown, continuous improvement (CI), and production suite breach activities.
Track Non-Conformances (NCs), monitoring impact on product availability, working closely with planning and QA to prioritize NCs.
Coordinate with analytical, micro, and QC to schedule product testing and track results including outside laboratories.
Expedite manufacturing work orders (WOs) that are needed in less than the normal lead time to improve the shortfall between the current plan and the requirements to meet or exceed our customer expectations.
Acts on signals from ASCP, planned order recommendations, order release actions, and exception messages from Oracle, rescheduling WOs in the case of capacity / supply constraints, material / labor shortages, backlogs or schedule interruptions.
Develop, implement, and support planning continuous improvements, providing input and recommendations on improving supply chain strategies, policies and practices, to achieve cost reductions, quality improvements, productivity increases, inventory integrity, and overall best-in-class SCM.
Be a Subject Matter Expert (SME) for line capacity, capacity models, lot genealogy, and the manufacturing / material process flow, serving as a partner to manufacturing.
Develop and maintain positive working relationships with internal and external customers to support manufacturing operations.
Support and participate in cross-functional teams.
Performs other related duties as assigned.
DESIRED MINIMUM QUALIFICATIONS
The requirements listed below are representative of the knowledge, skill and/or ability required for his position.
Minimum required education and experience: Bachelor's degree or equivalent with 3+ years of experience leading a team,
Education: Bachelor’s degree: SCM, business, economics, or sciences background (relevant work experience may be considered in lieu of degree).
Experience:
Experience using Oracle is highly desirable.
Extensive knowledge in analyzing and solving problems in a disciplined fashion, ensuring clear understanding of the root cause(s) and efficient recommendations for resolution.
Possess team-focused attitude and work in team-oriented environment.
Creative / innovative mindset, with demonstrated ability to “think outside the box”.
Demonstrated computer skills. Advanced MS Excel user.
Ability to work on multiple projects with limited direction.
Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.
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EEO Is the Law | EOE including Disability/Protected Veterans
Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.
Integra – Employer Branding from Integra LifeSciences on Vimeo
We are proud of our 25 year heritage as a leader in regenerative medicine. Today, our scientific innovation and diverse product portfolio continue to help patients and surgeons around the world.
We have an entrepreneurial, small company feel, yet deliver big company results. Your ideas – big and small – are welcome here. We embrace change and reward our people who are committed to making Integra a stronger company.
We believe how we do things is as important as what we do. Our Values guide how we work and how we act towards our customers, patients and each other every day. We value Our People, Integrity, Excellence, Embracing Change, Decisiveness and Teamwork.