Senior Validation Consultant Stockholm

Do you want to help ensure quality within Life Science alongside some of the sharpest minds in the industry? Then this is the place for you. Exciting assignments that thrill await you here—assignments that require curiosity, sharp intellect, and a willingness to find solutions where others see challenges. The variety in our projects means you will constantly develop and put your skills to the test in new contexts. At the same time, you will contribute to something greater. Through our work, we shape tomorrow's solutions—we make a difference for people, society, and the future. We do all this together, in teams filled with some of the industry's most skilled and experienced colleagues. Here, we inspire each other, share knowledge generously, and drive development forward—with quality, curiosity, and sharpness as our common foundation. This will be your role 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. You will become part of our Compliance business area, within the Quality & Validation unit—a setting where specialist knowledge, business development, and team spirit go hand in hand. You will lead and drive validation assignments, from planning to execution, while also providing solution-oriented advice and a business-minded approach. As a senior consultant, you will also have the opportunity to act as a mentor and source of inspiration for more junior colleagues. You will gladly share your experience, guide in complex matters, and contribute to developing 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 brings new challenges—and where your expertise 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 producing and quality-assuring validation documentation. • Qualifying and validating computerized systems in complex environments. • Driving cross-functional work with requirements management, risk management, and quality assurance while coordinating validation activities and leading resources in larger projects where close collaboration between clients 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, as well as serving 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 Kista. Here’s how you will excel 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 willingly shares your experience and acts as a mentor for more junior colleagues. You are driven to identify new business opportunities, develop collaborations, and contribute to our growth through a business-oriented and solution-focused approach. You combine your technical expertise with strong problem-solving skills and the ability to plan and prioritize in a structured manner. You have the perseverance to see things through to completion 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 higher education 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 the validation of various types of computerized systems (CSV) and knowledge of GAMP, including systems related to production and processes, laboratory systems, IT systems such as eQMS/ERP/LIMS, FMS, Historian, and data migration. • Experience working with various quality management systems and in electronic document and case management systems. • Fluent in Swedish and English, both spoken and written. • Experience with other regulations and guidelines beyond those mentioned above is highly meritorious. Being part of Team PV We are a consulting company passionate about being part of Life Science in Sweden. From small startups in MedTech to global pharmaceutical giants and everything in between. This means an opportunity to follow the entire chain—from manufacturing to use in healthcare—and work with everything from regulations and audits to project management, standards, and evaluations. Helping our clients achieve their goals is what drives us. So, if you want to be part of something bigger, something that makes a real difference and can ultimately save lives and secure patients—then you have come to the right place. Here, some of