Gerencia de Ingeniería at Clairo

Ciénega de Flores, Nuevo Leon, Mexico

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Battery, Automotive, ChemicalIndustries

Requirements

Bachelor’s degree in Mechanical, Chemical, or Industrial Engineering
8+ years of experience in manufacturing or process engineering, preferably within the automotive, chemical, or battery industries
Previous experience as a Process Engineer, Manufacturing Engineer, or Process SME
Proven leadership in improvement projects, automation, and new product launches
Strong understanding of battery manufacturing processes
Design for Manufacturing and process standardization
Process FMEA, Statistical Process Control (SPC), 8D, Six Sigma
CMS, PowerD3, 1PLUS, or equivalent methodologies
Engineering drawings interpretation
Change management and technical documentation
Technical leadership, decision-making, effective communication, results orientation, analytical thinking, teamwork, and problem-solving
Advanced English

Responsibilities

Lead the plant engineering function for battery manufacturing processes, ensuring adherence to process specifications
Drive continuous improvement and automation projects, and standardize best practices
Manage process changes, support new product introductions, and lead technological enhancements to achieve production, quality, and safety targets
General administration of maintenance systems
Manage the creation and maintenance of process documentation for battery manufacturing
Evaluate compliance with process specifications and identify improvement opportunities
Lead implementation of process improvement, standardization, and automation initiatives
Administer process changes resulting from projects, best-practice replications, and improvement ideas, ensuring proper documentation
Coordinate the launch of new products and/or processes at the plant level
Collaborate with Production, Maintenance, Quality, and Project teams for problem-solving and process optimization
Ensure compliance with Quality, Environmental, Health & Safety, and CMS management systems
Participate in audits, root cause analyses, and support High-Performance Teams (HPT) initiatives

Skills

Battery Manufacturing

Process Engineering

Manufacturing Engineering

Process FMEA

Statistical Process Control

SPC

Six Sigma

Design for Manufacturing

Process Standardization

Change Management

Engineering Drawings

Automation

Root Cause Analysis

CMS

PowerD3

1PLUS

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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