Vacant job

Do you want to help ensure quality in Life Science alongside the sharpest minds in the industry? Then this is where you should be. With us, you will find assignments that require curiosity, solution-driven thinking, and sharp competence, 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.

We are looking for a senior validation leader or validation expert who wants to take a central role in our most challenging and business-critical projects within Life Science. With your extensive experience, technical expertise, and ability to build strong relationships, you will be a key person in ensuring quality, regulatory compliance, and success for our clients.

With us, you will be part of our Compliance business area, the Quality & Validation unit – an environment where specialist knowledge, business development, and team spirit go hand in hand. You will lead and drive validation assignments from planning to execution while contributing with solution-oriented advice and business-minded thinking.

As a senior consultant, you will also have the opportunity to act as a mentor and source of inspiration for more junior colleagues. You are eager to share your experience, guide in complex issues, and help develop both our offerings and our clients' operations. Here, you will have the chance to combine your technical depth with your ability to create long-term collaborations and drive business forward.

This is a role for you who want to help our clients with various projects where each day presents new challenges – and where your competence truly makes a difference.

The role includes:

• Ensuring that regulatory requirements and standards according to GMP/GxP are met, thereby contributing to successful, safe, and sustainable projects.

• Developing validation strategies and preparing and ensuring the quality of validation documentation.

• Qualifying and validating computerized systems in complex environments.

• Driving cross-functional work with requirements management, risk management, and quality assurance, as well as coordinating validation activities and leading resources in larger projects where close collaboration between client and colleagues is crucial for the outcome.

• Managing deviations, CAPA, and change requests in a structured and solution-oriented manner.

• Establishing and developing collaborations with suppliers.

• Acting as an advisor and knowledge bearer in client projects and serving as a mentor and educator 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 Uppsala.

With your ability to build long-term relationships, communicate personally, and always put the client's needs at the center, you will play a key role with us. You are a confident role model who is eager to share your experience and serve as a mentor for more junior colleagues. You are driven by identifying new business opportunities, developing collaborations, and contributing to our growth through a business-minded and solution-oriented approach.

Your technical competence is combined with a strong problem-solving ability and the capacity to plan and prioritize in a structured way. You have the persistence to see things through and are eager to take initiatives that create value for both the client and the team. We value your ability to combine high quality with a business development focus – and that you thrive in an environment where collaboration, knowledge sharing, and engagement are integral parts of everyday life.

To succeed in this role, you have:

• A university degree or equivalent in a relevant field.

• At least 5 years of experience in Pharma/Biotech and working according to GMP.

• At least 3 years of experience in validating various types of computerized systems (CSV) and knowledge of GAMP, including systems related to production and processes, lab systems, IT systems such as eQMS/ERP/LIMS, FMS, Historian, and data migration.

• Experience working according to various quality management systems and in electronic systems for document and issue management.

• Fluent in Swedish and English, both spoken and written.

• Experience with other regulations and guidelines beyond those mentioned above is highly meritorious.

We are a consulting company passionate about Life Science, from MedTech startups to global pharmaceutical companies. With us, you will follow the entire chain, from manufacturing to care, and work with regulations, audits, project management, and evaluations. What drives us is helping clients achieve their goals and making a real difference for patients and society.

With us, you will get something different. We stand out from traditional consulting firms through our unique culture, which permeates everything we do, and we are extremely proud to be a Great Place To Work, year after year. Some say that a culture is in the walls. If ours were, we would have soft walls. Welcome to us at Plantvision!

We welcome you to submit your application as soon as possible. Selection and interviews are conducted on an ongoing basis.

If you have questions about this position, please contact Ida Holmberg at 076 108 84 87 or [email protected]