Production Planner at Clairo

García, Nuevo Leon, Mexico

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

ManufacturingIndustries

Requirements

Education in Industrial Engineering, Business Administration, Mechanical Engineering, Manufacturing Engineering, or Logistics Engineering
+3 years of experience developing and executing weekly production schedules for assembly and pasting areas, aligning customer requirements, sales forecasts, inventory targets, and resource optimization according to Clarios Manufacturing System (CMS) standards
Experience managing material planning and capacity requirements (MRP & CRP) to ensure timely availability of raw materials, components, and in-process inventory for production, while identifying and mitigating bottlenecks
Experience monitoring production performance against schedules, implementing corrective actions for deviations, and ensuring compliance with CMS principles, quality standards, and safety regulations
Experience leading implementation and continuous improvement of CMS practices, including material control assessments, high-performance team guidance, and environmental and safety compliance initiatives
Proficient in Manufacturing Systems (MFG), Material Requirements Planning (MRP), and inventory control processes for large-scale production environments
Skilled in capacity planning, resource optimization, and constraint management to achieve production targets and maintain balanced inventory levels
Experienced in Six Sigma methodologies for process improvement and quality assurance within battery manufacturing operations
Knowledgeable in ISO 14001 environmental management standards and safety systems for occupational health and risk prevention
Expertise in Production Planning & Scheduling, creating weekly and long-term production programs aligned with customer demand, inventory targets, and resource optimization
Skilled in Material Requirements Planning (MRP), determining raw material, component, and in-process material needs for current and future production cycles
Skilled in Capacity Resource Planning (CRP)

Responsibilities

Analyze customer requirements and sales forecasts to develop the production schedule, managing resources for manufacturing in Pasting and Assembly areas to meet production goals, inventory levels, inventory mix quality, and customer service
Implement and mature the Clarios Manufacturing System (CMS) within operations
Implement CMS principles, including material control and continuous improvement initiatives
Develop weekly and long-term production programs for assembly and pasting areas, optimizing resources and meeting inventory and quality targets
Apply expertise in MRP and CRP to ensure timely availability of raw materials and identify bottlenecks
Monitor inventory levels, prevent obsolescence, and ensure quality mix of components according to CMS standards
Manage Manufacturing Systems (MFG and MFG-PRO) for accurate planning, order management, and long-term material reliability
Apply Six Sigma methodologies for efficiency and quality improvements in manufacturing processes
Ensure compliance with ISO 14001 standards, occupational health and safety procedures, and halt activities posing risks to personnel or the environment
Guide High-Performance Teams (HPTs), provide training, feedback, and performance measurement through scorecards

Skills

Production Planning

Scheduling

MRP

CRP

Inventory Control

CMS

MFG

MFG-PRO

Six Sigma

ISO 14001

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters

1972Year Founded

$29.9MTotal Funding

GROWTH_EQUITY_VCCompany Stage

Biotechnology, HealthcareIndustries

5,001-10,000Employees

Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.

The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.

AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.

The company has nearly 50 years of experience in clinical trial technology solutions.

Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.

The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.

Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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