Vacant job

Do you want to ensure quality in Life Science alongside the sharpest minds in the industry? Then this is where you belong. With us, you will find assignments that require curiosity, a solution-driven mindset, 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 Lead 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 become a key person in ensuring quality, regulatory compliance, and success for our customers.

At our company, you will become 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 solution-oriented advice and business acumen.

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 others through complex issues, and contribute to developing both our offerings and our customers' operations. Here, you have the opportunity to combine your technical depth with your ability to create long-term collaborations and drive business forward.

This is a role for you if you want to help our customers in various projects where every day brings new challenges – and where your competence truly makes a difference.

The role involves:

• Ensuring that regulatory requirements and standards according to GMP/GxP are met, thereby contributing to successful, safe, and sustainable projects.
• Developing validation strategies and creating and quality-assuring validation documentation.
• Qualifying and validating computerized systems in complex environments.
• Driving cross-functional work with requirement setting, 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 the result.
• Handling deviations, CAPA, and change requests in a structured and solution-oriented manner.
• Establishing and developing collaborations with suppliers.
• Acting as an advisor and knowledge holder in customer projects, as well as functioning as a 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 Uppsala.

With your ability to build long-term relationships, communicate personally, and always put the customer's needs at the center, you will play a key role with us. You are a reliable role model who is happy 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.

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

To succeed in the role, you have:

• A university degree or equivalent in a relevant field.
• At least 5 years of experience within Pharma/Biotech and work according to GMP.
• At least 3 years of experience in validating various types of computerized systems (CSV) as well as knowledge of GAMP, including systems such as production and process-related systems, lab systems, IT systems like eQMS/ERP/LIMS, FMS, Historian, and data migration.
• Experience working according to different quality management systems and in electronic systems for document and case management.
• Fluent proficiency 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 firm passionate about Life Science, from MedTech startups to global pharmaceutical companies. With us, you get to follow the entire chain, from manufacturing to care, and work with regulations, audits, project management, and evaluations. What drives us is helping customers reach their goals and make a real difference for patients and society.

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

Welcome 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 Bas Nord at 073 060 47 21 or [email protected].

Do you have your own company and are interested in collaborating with us as a subconsultant?

Instead of applying for a specific position, please connect with us via our career page and state that you are interested in working as a subconsultant – we will get in touch when something suitable arises.