Process Excellence Specialist

buscojobs España; Almería; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

Join UBC as a Process Excellence Specialist to enhance patient outcomes in the pharmaceutical sector. Responsibilities involve managing Pharmacovigilance System Master Files and supporting quality management systems. Ideal candidates will possess strong skills in management and metrics production, contributing to a culture of respect and inclusivity.

Formación

• Experience managing Pharmacovigilance System Master Files.
• Support quality management systems.
• Experience managing deviations and CAPAs.

Responsabilidades

• Manage Pharmacovigilance System Master Files for clients.
• Support PV Management in procedural documents.
• Produce standardized quality metrics for clients.

Conocimientos

Management of deviations

Production of standardized quality metrics

Ability to prioritize PV Safety Regulatory Intelligence

Descripción del empleo

Join us to apply for the Process Excellence Specialist role at UBC.

As a leader in the pharmaceutical support industry, UBC is dedicated to empowering health solutions for a better tomorrow. We pride ourselves on improving patient outcomes and advancing healthcare. UBC provides services that enhance the entire drug development process and commercialization lifecycle—from clinical trial support to real-world evidence generation.

Embark on a rewarding career journey with UBC as a Process Excellence Specialist! Grow your career while making a meaningful impact on the world around you. Our culture is built on our Core Values of Collaboration, Conscientiousness, Curiosity, Compassion, and Consultation. We foster an inclusive workplace that encourages creativity.

If you're seeking a career that challenges, inspires, and rewards you, join us at UBC!

Role Overview: As a Process Excellence Specialist, you will manage Pharmacovigilance System Master Files for clients and support quality management system aspects.

Key Responsibilities:

• Management of deviations and CAPAs.
• Production of standardized quality metrics for the UBC Global PV Department and PV projects contracted by UBC clients.
• Support PV Management in developing and maintaining UBC PV procedural documents and serve as the lead global PV trainer.
• Prioritize and disseminate information related to global PV Safety Regulatory Intelligence.
• Manage Pharmacovigilance System Master Files for European clients and support quality management system activities.

Supervisory Responsibility: N/A

Skills and Qualifications:

• Experience managing Pharmacovigilance System Master Files (writing and updating).
• Support for quality management systems.
• Experience managing deviations and CAPAs.
• Ability to produce standardized quality metrics.
• Experience supporting PV Management with procedural documents.
• Ability to prioritize and disseminate PV Safety Regulatory Intelligence.

UBC is proud to be an equal opportunity employer and values diversity. We do not discriminate based on race, color, sex, age, national origin, religion, sexual orientation, gender identity/expression, veteran status, disability, or other protected classes. We are committed to a culture of respect, diversity, and inclusion.

Additional Details:

• Seniority level: Entry level
• Employment type: Full-time
• Job function: Management and Manufacturing
• Industry: Pharmaceutical Manufacturing

Note: This job posting is active and not expired.