Skip to main content
Back to jobs

Junior Consultant for Pharma Industry

External
Syntegon logoSyntegon · Lisboa, Portugal
Full-timeOn-site3w ago
ComplianceDocumentation
Cover LetterConnect

Prepare for this interview

Elite

AI-generated questions, company research, and talking points tailored to this role


Requirements

  • University Degree such as Engineering, IT, Chemical, Biotechnology, Pharmaceutical Sciences or similar.
  • Fluent in Portuguese and English (written and spoken).
  • Strong analytical skills, proactive approach, and dynamic attitude.
  • Excellent communication and interpersonal skills.
  • Availability to travel.
  • Applications :
  • At Syntegon Telstar, we don't just hire talent - we build success stories . If you are passionate about making a difference in the Life Sciences industry and want to grow in an environment that values excellence, collaboration, and innovation , we would love to hear from you!

Benefits

Health insurance

Additional Information

Scope: Junior CSV Consultant - Life Sciences Industry We're looking for curious and driven minds to join our consultancy team in Barcarena . No experience? No problem. We value talent, a passion for learning, and a desire to make an impact in healthcare and life sciences. As a Junior CSV Consultant , you'll work alongside a dynamic team supporting pharmaceutical companies in Portugal, contributing to exciting projects that truly matter. You'll be involved in projects focused on GMP compliance, CSV (Computer System Validation), and specialized consultancy. You will provide technical support to ensure our clients meet the highest standards in regulated environments. It's a hands-on role where you'll learn fast, grow your expertise, and make a meaningful impact from day one. Functions: Participate in and develop Computer System Validation (CSV) projects for pharmaceutical industry clients. Manage projects in compliance with client requirements, regulatory frameworks (GxP, FDA 21 CFR Part 11, EU Annex 11), and industry best practices. Write and review validation documentation, including Validation Plans, Protocols (IQ, OQ, PQ), and Validation Reports. Perform validation activities such as risk assessments, qualification testing, and regulatory impact analysis. Present and discuss project solutions to clients and within internal team.


Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Syntegon? Share your experience

Interested in this role?

Apply on the company's website.

Cover LetterConnect