Vacant job

Do you have experience in quality work within pharmaceuticals, medical technology, or manufacturing? Do you thrive in an administrative role where you get to work with documentation, systems, and process improvements? Then this might be the position for you!

About the company

Rechon Life Science AB is a privately owned pharmaceutical company with approximately 260 employees based in Malmö. For more than 60 years, they have delivered aseptic products according to international requirements for pharmaceuticals. Today, the focus is on contract manufacturing of both registered drugs and materials for clinical trials. Their customers are located around the world and include both smaller start-up companies and big pharma.

About the role

As a QA Administrator, you will be responsible for supporting the quality department in managing various quality documents and systems. You will work with administration, coordination, and archiving of documentation as well as support within the company's quality system.

Your tasks will include:

- Coordination, review, and administration of quality documents, quality agreements, and other documents within QA

- Support and training within the quality systems

- Review training modules regarding content and design

- Archiving of quality documents and agreements

- Review and ensure that daily work is performed in accordance with cGMP

- Propose changes and improvements for safer or more efficient routines

- Translation of documents to/from English

- Work with change requests (CR), deviations (DEV), and complaints (PQC)

- Coordination and participation in audits and inspections

- Development of routines within the quality area

The position is a consulting assignment where you will be employed by EMPLOID and work as a hired consultant for our client. EMPLOID is a member of the Competence Companies, which is an industry and employer organization within Almega. Almega is part of the Swedish Business Association. For more information, see www.kompetensforetagen.se (http://www.kompetensforetagen.se/) and www.almega.se (http://www.almega.se/).

About you

To succeed in this role, we believe you are meticulous, structured, and have a good understanding of quality work within the Life Science industry. You are a solution-oriented person with the ability to prioritize and make decisions based on the needs of the business.

We are looking for someone who has:

- Experience in quality work within pharmaceuticals, medical technology, or manufacturing

- Good knowledge of Swedish and English, both spoken and written

- Good computer and system skills, preferably experience with eQMS

- Experience in improvement and simplification work, such as LEAN

- Relevant education or equivalent experience from the Life Science industry

Other information

Start: By agreement

Location: Malmö

Extent: Full-time, consulting assignment

Working hours: Daytime

Salary: By agreement

A background check will be conducted on candidates who proceed in the process.

If you have questions about the position, please email the responsible recruiter Lina Johansson at lina.johansson@emploid.se. Please specify which position you are referring to.

We recommend that you submit your application promptly as we are conducting ongoing selection.

Welcome with your application!

Keywords: QA, quality, eQMS, pharmaceuticals, medical technology, documentation, deviation management, LEAN, GMP, Life Science, Malmö, Lund, Helsingborg