Vacant job

About the role

We are now looking to strengthen the production department at our client Rechon Life Science and are seeking a Production Support.

The department is responsible for producing pharmaceutical solutions – from clinical material to finished product. The production includes, among other things, preparation, filtration, and aseptic filling of injectable preparations.

As a Production Support, you will work closely with production with a focus on documentation, quality, and improvement work. You will become an important part of the operation and serve as a support to operators and production in their daily work. The role involves frequent contact with production, and a large part of the work takes place on the shop floor together with the team.

At Rechon, we work according to GMP (Good Manufacturing Practice), and most of the work is performed in classified cleanroom facilities. High demands are placed on quality, documentation, production hygiene, and the application of current GMP regulations during all work tasks.

Your main responsibilities will include, among other things:

• Review and updating of batch records/protocols
• Handling, registration, and investigation of deviations
• Supporting production staff in process-related events
• Writing and updating MBRs, SOPs, CAPAs, CRs, and other quality documents
• Driving and participating in improvement and change management work
• Monitoring KPIs, CAPAs, and investigations
• Maintaining close contact with QA and Supply Chain regarding manufactured batches

The position is onsite, and working hours are daytime, Monday to Friday, 08:00–16:25. The start date is planned for August/September 2026. Initially, a 6-month probationary employment is offered with good opportunities for permanent placement with the client.

About you

We are looking for someone who is driven, structured, and has a strong focus on quality. You thrive in a role where you can combine administration and documentation with close collaboration on the production floor. You have a technical interest, are analytical, and enjoy working with improvements and problem-solving.

You are accustomed to handling multiple parallel tasks simultaneously and have the ability to prioritize in a changing daily routine. This role suits you if you appreciate structure, documentation, and working in an operation where quality and precision are crucial.

We believe you have:

• A high school education, preferably in technology, industry, or similar
• Previous experience from manufacturing industry or production environments
• Good knowledge of Swedish and English, both spoken and written
• Good computer skills and a technical interest

Meritorious if you also have:

• Previous experience in administrative work
• Experience with GMP and pharmaceutical production
• Experience with documentation and quality work

We will place great emphasis on personal suitability.

Contact information

If you have questions about the role or the recruitment process, you are warmly welcome to contact the responsible recruiter, Enna Dedagic, via [email protected] (mailto:[email protected]).

If you have questions regarding registration, please contact support via [email protected] (mailto:[email protected]).

Please note that we do not accept applications via email.

We look forward to receiving your application!