Manufacturing Planner

6 days ago


Grand Island, United States Tekwissen Full time
Overview:

TekWissen Group is a workforce management provider throughout the USA and many other countries worldwide. The job opportunity is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory equipment, chemicals, supplies, and services essential in healthcare, scientific research, safety, and education. As the global leader in serving the field of science, our client boasts an annual revenue of around $40 billion with a mission to empower customers to make the world healthier, cleaner, and safer. Our client's global team is committed to delivering an unparalleled blend of cutting-edge technologies, convenient procurement options, and pharmaceutical services under their industry-leading brands.

Position: ManufacturingPlanner

Location: Grand Island, NY 14072

Duration: 12 Months

Job Type: Contract

Work Type: Onsite

Shift Timings: Monday-Friday - 08:00 AM to 04:30 PM

Summary:
  • The Manufacturing Planner/Scheduler II will be responsible for planning and scheduling all aspect of production.
  • The position will require to lead planning assignment and analysis of data to resolve most cost effective and optimal production schedule that Manufacturing can successfully execute.
  • Planners at this level can lead projects and make decision with minimum supervision. Individual will drive continuously process improvement to improve key metrics such as OTIF, Backorder, Schedule Attainment, & Utilization.
  • Strong analytical, interpersonal, and communication skills are a must.
Key responsibilities include, but are not exclusively:
  • Responsible for key performance indicators such as on-time delivery, maintaining Safety Stock levels of products and internal raw material shortages levels.
  • Excellent oral and written communication skills for preparing and presenting planning reports and projects.
  • Assists with timely and accurate planning of material requirements to support MPS (Master Production Schedule).
  • Plans, schedules, and monitors movement of materials through production cycle for on time delivery.
  • Assists with the coordination of new product introductions as assigned.
  • Provide input to management to reschedule in case of design changes, labor and material shortages, backlogs, and other potential schedule interruptions
  • Ability to work on several projects or issues simultaneously by either facilitate or lead with minimum supervision.
  • Creative problem-solving skills to collect relevant information to solve less well- defined planning problems.
  • Be able to identify goals, review and update Supervisor throughout the year and complete the PMD.
  • Implement material master changes, product structures, BOMs and Router into production process as the need arises.
  • Recalculate orders and requirements as needed by analyzing trends in demand, changes in lead time, minimum order quantities, standard batch sizes and safety stock levels.
  • Follow up on open orders and partial shipments, expedite as required.
  • Partner effectively with external departments to resolve issues.
  • Identify and proactively communicate inventory stock level risks to Marketing and present during SIOP meeting.
  • Analyze root causes of stock outs and work with cross-functional teams to implement corrective and preventive measures.
  • Proven knowledge of ISO/FDA, GMP, ISO Regulations and other regulatory requirements for diagnostics manufacturing.
  • Control all documentation relative to the operations planning function.
  • Such documentation includes but is not limited to, backlog reports, lead-time analysis, shop floor orders (including rework orders), delivery performance, daily production status, pull from stock sheet, lead-time maintenance, shortage reports, and close production order reports.
  • Handle replenishment levels for applicable safety stocking programs.
  • Key areas also include capacity requirements evaluation, constant monitoring of production readiness and materials availability, continuous improvement of responsible areas and support activities related to PR1 system maintenance to ensure MRP update.
  • Responsible for understanding and implementing relevant company/department policies and procedures.
Minimum Requirements:
  • Bachelor's degree in a business, supply chain, data scientists or equivalent relevant experience can be considered.
  • At least 2 years of experience in planning and scheduling experience is required.
  • Prior experience with SAP systems is required.
  • Proficiency in Microsoft Office and ERP systems is required
  • Expertise in problem solving and data analysis
  • Recognize problems, analyze, recommend solutions, and drives continuous improvements to completion.
  • Excellent knowledge of production planning. Detail oriented, creative, robust analytical skills, strong organization and time management skills.
  • Ensure compliance with corporate, site, and regulatory policies, practices, and guidelines.
  • Project management, interpersonal, and communication skills.
  • Ability to react appropriately to changing priorities and impending deadlines.
  • Demonstrated knowledge of ISO/FDA, GMP, ISO Regulations and other regulatory requirements for diagnostics manufacturing.
  • OSHA safety compliance required
  • Demonstrates the clients values - Integrity, Intensity, Involvement and Innovation (The Four I's)
  • Highly responsive to internal and external customers.
  • High degree of experience and capability in working with all levels of the organization to achieve requirements.
  • Ability to write reports, business correspondence and standard operating procedures.
  • Collaborate to implement improvements/cost savings on time.
Preferred Qualifications:
  • APICS certified in Planning & Inventory Management preferable with medical device manufacturer experience a plus.
  • Six Sigma Certification a plus.


TekWissen® Group is an equal-opportunity employer supporting workforce diversity.
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