About the Position

In the role of inspector within Bulk Production, you will have a central and quality-critical role in Rechon’s pharmaceutical production. Your main responsibility is to ensure that filled pharmaceutical units meet high quality standards through careful inspection, documentation, and follow-up according to GMP.

The work takes place in Rechon’s Bulk department where inspections are conducted both mechanically, semi-mechanically, and manually. You will work with several different unit formats such as syringes, cartridges, vials, and ampoules, as well as bulk packaging. The role requires high concentration, accuracy, and a good understanding of quality systems, as each step is crucial for patient safety and product quality.

The position is full-time and operates on a rotating 3-shift schedule, where you will work morning, day, and evening shifts according to a schedule. You will become part of Bulk Production, which is a growing department in the company’s continued expansion.

Examples of Responsibilities:

Inspection of filled units from Bulk Production (syringes, cartridges, vials, and ampoules) using fully and semi-automatic machines as well as manual inspection at light tables
Performing AQL controls on inspected batches
Conducting IPC analyses and sampling during inspection
Documentation in manufacturing orders and correction of balances in Jeeves after completed inspections
Conducting bulk packaging
Preparation of materials before inspection and packing after inspection
Reporting deviations and participating in investigations of production deviations
Assisting in updating and improving documentation such as TO and SOPs
Working in class C/D cleanrooms
Training new operators
Participating in upgrading production facilities in connection with installations and renovations
Contributing to continuous improvements of both working methods and documentation within Bulk Production

The position is full-time and operates on a rotating 3-shift schedule Monday to Friday with varied working hours between 06:00 and 00:00. You will start with a thorough introduction during the first two months during daytime (07:00-15:30), where you will shadow an experienced operator.

About You

We are looking for someone who is very meticulous, quality-conscious, and has an easy time following written instructions and established routines. You thrive in a regulated environment where documentation, structure, and discipline are a natural part of everyday life.

You have good collaboration skills and contribute to positive teamwork, while also taking great personal responsibility for your work. The role requires that you can work focused for long periods and handle tasks that place high demands on attention and endurance.

You are fluent in Swedish, both spoken and written, and have a good ability to read and understand English.

Requirements for the Position

Completed high school diploma
Fluent Swedish in speech and writing
Good understanding of English

Preferred Experience

Experience in pharmaceutical production
Experience with GMP and documentation requirements
Experience in inspection, quality control, or similar tasks
Experience in cleanrooms or other controlled environments
Experience in industrial work

About Rechon Life Science

Rechon Life Science AB is a privately owned pharmaceutical company with about 350 employees, operating in Malmö and Arlöv. For over 60 years, they have delivered aseptic products according to international pharmaceutical standards. Today, the focus is on contract manufacturing and contract packaging of both registered pharmaceuticals and materials for clinical trials.

Clients are located worldwide and include both smaller start-up companies and large international pharmaceutical companies. Rechon Life Science is in an expansive phase with new projects and clients, which means great development opportunities for you as a future employee.

Would you like to learn more about Rechon Life Science? Please visit their website here: Rechon Life Science (https://Rechon%20Life%20Science%20-%20%20A%20Passion%20for%20People%C2%B4s%20Health)

Other Information

Start date according to agreement
The position is a consultancy assignment with a probationary period of 6 months via Adecco, with the possibility of extension by the client company
A background check will be conducted as part of the recruitment process
A police record extract must be presented at the interview if applicable

Contact Information

If you have questions about the position or the recruitment process, you are warmly welcome to contact the responsible recruiter: Sarah Hallberg via [email protected] (mailto:[email protected])

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

Welcome with your application!