Senior Validation Consultant

Description:

Do you want to help ensure quality within Life Science alongside the sharpest minds in the industry? Then this is the place for you. We offer assignments that require curiosity, problem-solving drive, and sharp expertise – giving you the chance to develop in new contexts. Together, we contribute to a better tomorrow and shape future solutions that make a difference for people and society. Your Role We're looking for a senior validation leader or expert who wants to take a central role in our most business-critical projects within Life Science. You'll be responsible for ensuring quality, regulatory compliance, and success in customer assignments – from strategy to implementation. You'll be part of Quality & Validation within our Compliance business area – a team with a strong mix of expertise and curiosity. Here you work closely with colleagues at a similar experience level, while sharing your knowledge and mentoring more junior consultants in their development. The role involves: • Ensuring that regulatory requirements and standards according to GMP/GxP are met and thereby contributing to successful, safe, and sustainable projects. • Developing validation strategies and preparing and quality-assuring validation documentation. • Qualifying and validating computerized systems in complex environments. • Driving cross-functional work with requirements definition, risk management, and quality assurance, as well as coordinating validation activities and leading resources in larger projects where close collaboration between customer and colleagues is crucial for results. • Managing deviations, CAPAs, and change requests in a structured and solution-oriented manner. • Acting as an advisor in customer projects and serving as mentor and trainer to share your experience and contribute to the team's development. We have offices in several locations in Sweden; this position is based at our office in Kista. How You'll Excel You're a confident and business-minded consultant who builds trust in customer relationships and drives work forward with structure and quality. You thrive in complex environments, take responsibility all the way to the goal, and enjoy sharing your knowledge. Combining technical depth with a solution-oriented approach comes naturally to you – as does contributing to both team and business development. To succeed in this role, you have: • University degree or equivalent in a relevant field. • At least 5 years of experience in Pharma/Biotech and working according to GMP. • Solid experience validating computerized systems (CSV). • Knowledge of GAMP and experience with systems such as eQMS/ERP/LIMS, FMS, or Historian. • Experience working according to different quality management systems and in electronic systems for document and issue management. • Very good knowledge of Swedish and English. • Experience with additional regulations and guidelines is a merit. Being Part of Team PV We're different here. We don't recruit for a specific assignment – we recruit to build our team long-term. This means we look at you, your expertise, and your development over time, and create the right conditions for you to continue growing. We work as advisory partners to our customers and value long-term relationships – both externally and internally. In the team, there's a strong culture of knowledge sharing, where senior consultants learn from each other and contribute to the whole. Our culture is something we're genuinely proud of. We're a Great Place to Work, year after year – and we see it as a testament to the environment we build together every day. And yes – if our culture were in the walls, they'd be soft. Application Welcome to submit your application as soon as possible. Selection and interviews are ongoing. If you have questions about this position, feel free to contact Ida Holmberg at 076 108 84 87 or [email protected] Do you have your own company and are interested in collaborating with us as a subcontractor? Instead of applying for a specific position, feel free to connect with us via our career page and indicate that you're interested in working as a subcontractor – we'll get back to you when something suitable comes up.

Overview

Type

job

Status

active

Visibility

public

City

Kista

Address

Färögatan 33

GPS

59.401685711652, 17.946437208993copyopen in

Email

[email protected]

Phone

076 108 84 87

Views

4

Published

11. 3. 2026

Edited

21. 6. 2026

Specifications