Process Engineer at Clairo

Tampa, Florida, United States

Clairo Logo
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

Key technologies and capabilities for this role

ParetoIshikawa5-WhyDMAICSPCPFMEAKaizen5SValue Stream MappingSix Sigma

Questions & Answers

Common questions about this position

What benefits are offered for this Process Engineer position?

Benefits include medical, dental and vision care coverage, a 401(k) savings plan with company matching starting on date of hire, tuition reimbursement, perks and discounts, parental and caregiver leave programs, paid time off, flexible spending, short- and long-term disability, basic life insurance, business travel insurance, Employee Assistance Program, and domestic partner benefits.

Where is this Process Engineer role located?

The role is based at the fully integrated plant in Tampa, Florida.

What are the required qualifications for the Process Engineer position?

Candidates need a Bachelor’s degree in Engineering or other technical discipline, 5+ years of applicable work experience in manufacturing, and solid understanding and experience with statistics related to manufacturing processes, including common cause and special cause variation, Ishikawa, and team problem solving.

What is the work environment like at Clarios in Tampa?

The Tampa plant is fully integrated, manufactures batteries for vehicles, employs over 280 people, operates six days per week, and is actively involved in the local community through organizations like Metropolitan Ministries, The United Way, and Adopt-A-Road Tampa.

What makes a strong candidate for this Process Engineer role?

Strong candidates have a Bachelor’s degree in Engineering, 5+ years in manufacturing, experience with manufacturing statistics and tools like Ishikawa and team problem solving, plus preferred skills in working in a matrix organization, team building, communication, setting priorities, working independently, and coordinating multiple projects.

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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