QA/QP Specialist

Meribel Pharma Solutions

Sweden - South of Sweden/Denmark

Apply now Meribel Pharma Solutions in Höganäs is looking for an experienced QP/QA Specialist
Do you want to join a quality team at a manufacturing site with great opportunities for developing the site’s quality processes, deliver quality to patients and customers, and make an impact? In collaboration with Meribel Pharma Solutions in Höganäs, PharmaRelations are now seeking an experienced QP/QA specialist.

Location: Höganäs

Employment: Full-time Hybrid position (3 days/week on-site)

About Meribel Pharma Solutions
Founded in 2024, Meribel Pharma Solutions (MPS) is a niche player, mid-sized CDMO specializing in providing tailored solutions to pharmaceutical companies. Headquartered in London, UK and with 11 sites across France, Spain and Sweden, the company provides specialist expertise in sterile multidose, lyophilization, sachets and stick packs, and services to support product development from concept through to commercialization. MPS is dedicated to elevating pharmaceutical services to new heights, delivering comprehensive support through every step of a product’s journey, whether it is an oral solid dose, liquid or semi-solid.

The facility in Höganäs is specialized in the manufacturing and packaging of pharmaceutical products of powder mixture and granules. MPS are specialized in sachet and stick filling and offer a wide range of technologies including primary and secondary packaging, serialization and aggregation. The position provides a stimulating variety of different tasks as well as great opportunity for personal responsibility and development.

The role
As QP/QA specialist, you will entail responsibility as an expert (QP) according to the company's manufacturing permit. You find it exciting to take on different types of tasks within the QA department and enjoy a dynamic work environment collaborating both with people from different parts of the company, customers and external partners. It comes naturally for you to interact with production personnel, gaining knowledge about the site’s manufacturing processes and conduct valuable exchange of experiences.

Key Responsibilities

• Provide QP-expertise and ensure the appropriate documents have been approved.
• Make appropriate decisions on dispositions of finished goods.
• Participate in authority inspection and inspections from customers.
• Participate in the development of the company's quality system. Acting as a process owner for selected quality processes.
• Participate in various projects as a QA representative.
• Approve change requests, deviations and CAPA.

Requirements

• Meet the expert (QP) profile according to the requirements of the Swedish Medical Product Agency.
• Has a minimum of 5 years’ experience from a quality organization within pharmaceutical manufacturing.
• Has in depth knowledge in one or more areas of pharmaceutical QMS.

As a person, you are meticulous, structured, and have the ability to make decisions independently. In order to create valuable collaborations internally and externally with customers and suppliers, we believe that you are service-oriented, has an interest in developing good and long-term relationships and is skilled in communication. As the company language in Meribel Pharma Solutions is English and you will work with customers and suppliers from different parts of the world, it is expected that you are fluent in written and spoken Swedish and English.

The position is a permanent position. The working hours are daytime with flextime.

The Process - Your Application
PharmaRelations is managing this recruitment on behalf of Meribel Pharma Solutions. If you believe your background and expertise align with the requirements, we encourage you to submit your application through the “Apply” button. We will review all applications with great care in our search for the right candidate. A kind reminder is that the application documents should not be sent via email. If you would like to know more and/or have questions, please contact Stefan Lind for a confidential conversation. Tel: 070/165 22 45; mail: [email protected].