Production Planner

Overview: We are seeking a detailed-oriented and proactive Production Planner to join our new manufacturing location in Alpharetta, Georgia. This role is responsible for planning, scheduling and coordinating production activities to meet our customer demand, quality standards and regulatory compliance. The ideal candidate will have experience in an ISO 13485 regulated environment as well as being well-versed in supply chain planning, inventory control and production workflows/ value chain mapping. This is a full time, onsite position working out of our Alpharetta location.

Key Responsibilities:

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• Develop and maintain detailed production schedules based on sales forecasts, customer orders, and inventory levels.

• Work closely with the Production Team/ Manager and S&OP manager to ensure an efficient production planning.

• Coordinate with cross-functional teams (Manufacturing, Warehousing/ Logistics, Quality Control, Quality Assurance, Procurement, Finance (regarding impact or financial analysis) and Engineering) to ensure production plans are aligned with operational capacity, maintenance schedules, material and component availability, and quality standards.

• Monitor work orders and production progress, proactively identifying and resolving any delays or bottlenecks.

• Adjust schedules as needed due to material shortages, equipment failures, or changes in demand. Proactively align/ escalate in case a decision needs to be made regarding prioritization in the schedule.

• Collaborate with the Quality Assurance team to ensure compliance with ISO 13485, FDA 21 CFR Part 820, and other applicable regulatory standards.

• Support ERP/MRP system data integrity, including BOMs, routings, and inventory parameters.

• Track key performance indicators (KPIs) related to production planning, including on-time delivery, schedule adherence, and inventory turns.

• Support new product introductions (NPI), New markets/ country introductions by coordinating ERP/MRP readiness and materials planning.

• Participate in audits, inspections, and continuous improvement initiatives related to manufacturing and supply chain processes.

Qualifications:

• Education:

• Bachelor’s degree in Engineering, Biology, or Operational Management required. A Master’s degree in related fields or an MBA, preferred.

• Lean Six Sigma Green Belt or Black Belt Certification

• Experience:

• 3-5+ years in Operations management in an ISO13485 regulated industry

• Experience with regulatory environments such as GMP, FDA, or ISO standards

• Skills:

• Strong analytical and problem-solving skills

• Excellent communication and interpersonal abilities

• Proven leadership and team management expertise

• Proficiency in lean methodologies and Six Sigma tools

• Experience in the identification of the 8 wastes, line balancing and performing theory of constraints.

• Experience in developing and sustaining a 6S program

• Experience in developing and sustaining morning markets and value stream structure organization.

• Proficiency in data analysis tools and software such as minitab, powerBI, Tableau.

• Proficiency in ERP and Master data, preferably in Microsoft Dynamics 365

• Experience in developing and continuously improving upon operations KPI's such as manufacturing efficiency, Capacity utilizations, Process Cycle times, Reject/Scrap rates, Inventory Accuracy, First Pass Yield, and Monitoring budget to fiscal year plan.

Pay Range
$67,200—$77,200 USD

Physical Requirements and Work Conditions

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform these functions.

• Mobility & Posture: May require occasional sitting, standing, walking, climbing, reaching, bending, or stooping.

• Lifting/Carrying: May require lifting and carrying items 50 pounds or more, depending on the role.

• Manual Dexterity: Frequent use of hands and fingers for typing, writing, grasping, and operating office or job-specific equipment.

• Driving: Some roles may require the ability to operate a motor vehicle for extended periods and maintain a valid driver’s license.

Specific requirements may vary by role. Contact an HR representative for details related to the position.

Our credentials

Kuros is a Swiss-headquartered biotech company, listed on the SIX Swiss Stock Exchange since 2016 (under symbol KURN). With additional operations in the Netherlands and the USA, we continue to grow our global team.

To deliver the ideal bone graft, you need the highest quality and quantity of scientific evidence behind it. We believe that this is a key differentiator for Kuros, given the urgent need to advance bone healing.

• Listing on the SIX Swiss Exchange under the symbol KURN since 2016

• A commercial & research footprint that spans >20 markets

• Dozens of clinical and scientific expert Advisers

• >25 orthobiologics-related patents

• >400 patients evaluated in Level I, randomized controlled clinical trials

• >20 well-controlled Level I-IV clinical trials initiated, including 6 that are complete1

• Published Level I evidence published in Spine

Kuros Biosciences is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Kuros Biosciences complies with GDPR and the California Consumer Privacy Act (CCPA). View our CCPA Notice here.