Quality Engineer

Rhian_Convatec; Reynosa; Presencial; MXN 735,000 - 1,104,000; Jornada completa

Descripción de la vacante

A global medical solutions provider in Reynosa is seeking a Quality Specialist to ensure compliance with internal and external requirements. Responsible for validation protocols, supporting audits, and implementing process improvements using Lean and Six Sigma methodologies. Ideal candidates have a degree in engineering, relevant experience, and strong regulatory knowledge. This role offers opportunities to participate closely with cross-functional teams in a dynamic environment.

Formación

• Minimum 2+ years in a similar role, preferably within the medical device industry.
• Intermediate - Advanced English proficiency required.
• Proficiency in Microsoft Office required.

Responsabilidades

• Contribute to the development and execution of validation protocols for products.
• Support test method validation for in-process checks.
• Support external and internal audits.
• Apply structured problem-solving tools such as Lean and Six Sigma.

Conocimientos

Regulatory and compliance knowledge of validation

Knowledge and experience of working with a Quality Management System within Medical Device manufacturing

English proficiency

Microsoft Office proficiency

Educación

Bachelor’s degree in engineering or related careers

Descripción del empleo

About Convatec

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in Advanced Wound Care, Ostomy Care, Continence Care, and Infusion Care. With more than 10,000 colleagues, we provide our products and services in around 90 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2024 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more please visit http://www.convatecgroup.com

About the role

Participate in changes within the project portfolio in Convatec ensuring compliance with internal and external requirements according to standards, customer, and authorities; ensuring quality system is developed, maintained, and improved; assuring Process Validation and CCR system is followed accordingly and supporting as leader on quality issues or non-conformities raised from the project-change

Key responsibilities

• Contribute to the development and execution of validation protocols (e.g. IQ/OQ/PQ) for new and existing
  products and processes.
• Support test method validation for in process checks and NPD development method to ensure critical‑to‑quality (CTQ) attributes are defined and controlled.
• Supporting business unit in assuring compliance with internal and external requirements according to
  standards, customers and authorities.
• Support external and internal audits as applicable.
• Support, participate and perform statistical analysis, sampling plans, quality control plans and capability
  studies to support product development and manufacturing.
• Act as a support for process FMEAs and validation strategies, ensuring robust design and smooth transfer to
  manufacturing.
• Work closely with key stakeholders like R&D, Manufacturing, Regulatory, and Supply Chain teams to ensure
  quality is embedded in all phases of product development and lifecycle management.
• Support, participate, lead cross‑functional teams in implementing process improvements and resolving quality
  issues.
• Apply structured problem‑solving tools such as Lean and Six Sigma, to drive continuous improvement and
  process development

Requirements

• Bachelor’s degree in engineering or related careers.
• Minimum 2+ years in a similar role, preferably within the medical device industry but not essential.
• Regulatory and compliance knowledge of validation.
• Knowledge and experience of working with a Quality Management System within Medical Device manufacturing.
• English proficiency: Intermediate - Advanced.
• Microsoft Office proficiency: Intermediate - Advanced.

Beware of scams online or from individuals claiming to represent Convatec

A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.

If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at [e-mail].

Equal opportunities

Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.

Notice to Agency and Search Firm Representatives

Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Already a Convatec employee?

If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!