Process Engineer at Clairo

Tampa, Florida, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

ManufacturingIndustries

Requirements

Bachelor’s degree in Engineering or other technical discipline
5+ years of applicable work experience in manufacturing
Solid understanding and experience with the statistics related to manufacturing process, understanding of common cause and special cause, Ishikawa and team problem solving
Six Sigma (preferred)
Willing and able to work in a matrix organization (preferred)
Excellent team building and communication skills (preferred)
Ability to set priorities, work independently, and coordinate multiple projects utilizing available resources (preferred)

Responsibilities

Drive process stability through reduction of nonstandard conditions
Support and encourage teams in operator training, visual factory, 5S, Kaizen events, Value Stream Mapping, etc
Identify Special and Common Cause Variation leading to top scrap and rework issues or adding risk to downstream operations
Deploy a team approach, engaging operators and other experts
Deploy proven tools to identify root causes and implement lasting corrective actions, such as Pareto, Ishikawa, 5-why, KT, DMAIC process, SPC analysis, distribution analysis, etc
Ensure operator instructions clearly guide the operator and are visual when needed
Coordinate the PFMEA based product quality risk reduction activities (reducing the probability of an occurrence and the chance of detection)
Drive Risk reduction and conformance to IATF and customer requirements
For new product/equipment launches, work with the launch, QE, ME and production team to ensure measurement systems are both proven and understood, that operator training is adequate to ensure process stability, and to sign off on process capability for significant and critical characteristics
Responsible for process signoff of the DV/PV/prototype production runs (DBDS signoff)

Skills

Pareto

Ishikawa

5-Why

DMAIC

SPC

PFMEA

Kaizen

Value Stream Mapping

Six Sigma

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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