About this role
Maribel Pharma in Höganäs, formerly Recipharm AB, is an established CDMO partner that develops and delivers tailored pharmaceutical solutions to pharmaceutical companies worldwide.
Are you analytical, solution-oriented, and skilled at combining attention to detail with a clear overall perspective?
Maribel Pharma is currently seeking a Validation Engineer for its site in Höganäs.
In this role, you will be responsible for leading and executing validation assignments of varying nature, from the introduction of new products and qualification of equipment to validation of computerized systems. You will develop validation strategies and documentation, and work collaboratively with cross-functional teams to ensure professional execution. The role also involves contributing to the development and improvement of the validation process as well as preparing the annual plan for periodic reviews for all GMP-classified objects.
Does this sound like an exciting challenge? Then you might be the right person for us!
Your Responsibilities
• Responsible for validation assignments including the development and execution of validation strategies, as well as planning, leading, and following up on validation activities.
• Perform various types of qualifications/validations (equipment, processes, facilities, cleaning, and computerized systems) in close collaboration with production, engineering, and quality departments.
• Develop validation plans, protocols, and reports. Responsible for documenting and evaluating validation results.
• Manage deviations and improvement actions within the framework of validation assignments.
• Contribute to the development and improvement of the validation process and validation documentation.
• Responsible for preparing the annual plan for the periodic review and ensuring the execution of the plan.
• Lead and participate in projects, both customer projects and internal projects.
What We Believe You Will Contribute
We believe you will contribute your extensive experience in validation and qualification within the pharmaceutical industry, as well as your knowledge of manufacturing processes. With your strong quality mindset, analytical ability, and solution-oriented approach, you can see both the details and the big picture, contributing to improved processes and methods.
You are structured, communicative, and thrive in cross-functional work, where you take initiatives that drive development forward. Your engineering education in chemistry, biotechnology, or equivalent, along with experience in process and product validation, product formulation, or validation of computerized systems, prepares you well for the role. Experience in project management and LEAN is also advantageous.
As we operate internationally, it is important that you are fluent in both Swedish and English, in both spoken and written forms. To thrive with us, we value that you share our core values: respect, trust, and transparency.
What We Offer
The company is characterized by a passion for making a real difference, creating a supportive and developing work environment where every employee has the opportunity to grow. Maribel invests in employee development and ensures they have the tools and support to reach their full potential.
Maribel offers exciting career paths in science, technology, business development, and operations, where employees can contribute their unique talents and make a meaningful impact on the future of medicine.
• Collective agreement and occupational pension
• Wellness allowance
• Opportunity for hybrid work
• Fruit and coffee in the office
• Professional development
• An inclusive culture and engaged colleagues.
The position is a permanent employment with daytime hours and flexible working hours, based at Maribel's office in Höganäs.
More About Maribel
Meribel Pharma Solutions is a rapidly growing, specialized CDMO partner founded in 2024. The company offers tailored pharmaceutical solutions to pharmaceutical companies worldwide. With headquarters in the UK and 11 modern facilities in France, Spain, and Sweden, Meribel is at the forefront of sterile multi-doses, freeze-drying, pouch filling, and stick packaging – delivering support throughout the entire chain, from concept to commercialization.
The facility in Höganäs is one of Meribel's centers of expertise and specializes in the manufacturing and packaging of powdered medicines and granules. Approximately 95 dedicated employees work here with state-of-the-art equipment and a wide range of technologies – from filling pouches and stick packs to primary and secondary packaging, serialization, and aggregation.
Working at Meribel means becoming part of an ambitious organization with a strong forward momentum, where innovation, quality, and collaboration are the focus every day.
Recruitment Process
In this process, we use ongoing selection, which means we continuously review incoming applications to see how well the profiles match the requirements for the position. If we see you as one of our potential candidates, we will contact you for an interview. At that time, you will receive information about the interview format and other steps in the process. If you do not proceed in the process, you will be informed of this no later than when the position has been filled.
Start: By agreement.
Location: Höganäs
Application
We welcome you to apply with your CV and a cover letter explaining why you are the right person for this position.
For more information about the position and the recruitment process, please contact Maria Gren, Recruitment Manager at Skånestor, phone 072 451 58 72 or