Since our current Quality Specialist is moving on within the organization, we are now seeking her successor. As our new Quality Specialist, you will become part of a well-functioning QC organization with 25 helpful, skilled, and dedicated colleagues on the team!
About the Position
You will become an important part of the QC department, a well-functioning group that supports each other, enjoys working together, and supports one another in meeting quality requirements and deadlines from authorities and customers. We are responsive and offer a work environment where our employees are given the opportunity to speak up and influence their work situation. For us, well-being, a good work environment, and personal development are very important. Because we deeply care about the well-being of our personnel, great emphasis will be placed on your personality.
As a Quality Specialist, you will primarily work with quality assurance activities, such as investigations of deviations and abnormal analysis results. You will also participate in inspections from authorities and customers and ensure that appropriate measures are taken based on these. The position involves a lot of cross-functional work where you work closely with both the development department, production specialists, and the QA department. It also includes quality improvement work to ensure that our processes continuously meet current requirements and regulations.
Your areas of responsibility include:
Handling inspection observations from authorities and customers
Lab investigations, OOS investigations, and deviation management
CCs, CAPAs, risk assessments, and quality improvement work
Who We Are Looking For
The most important thing to succeed in this role is that you are quality-conscious and have experience with quality work within GMP. You need to be responsible, service-oriented, thorough, and flexible in both your working methods and how you interact with your colleagues. You have a positive mindset and thrive in an environment with varied work tasks. You may currently work in QA and have previous experience from QC, which would be a suitable background for the role.
In addition to this, you have:
Academic education as a chemical engineer or equivalent.
Very good knowledge of Swedish and English (fluent in speech and writing).
Experience working according to GMP.
Meritorious Experience and Knowledge
Experience with FDA
Quality Assurance
HPLC/GC, Ph Eur/USP analyses of raw materials
Qualification and validation of laboratory equipment and computerized systems
What We Offer
With us, you will work with outstanding products in an operation characterized by quality and commitment. For us, well-being, a good work environment, and personal development are central parts of the business.
Good location at Malmö Harbor with parking
Benefits package including wellness allowance, breakfast and fruit daily, and the opportunity for a benefits bicycle
Shortened work week, ATF hours, and flexible working time
Public holidays off, shorter workday the day before a public holiday, and time off between Christmas and New Year
Continuous professional development
Practical Information
The position is a full-time permanent employment with immediate start
The employment is covered by a collective agreement
Application
We process applications on a rolling basis as we intend to fill the position as soon as possible, so do not delay in applying. You apply with your CV and a personal letter by clicking "Apply for Position".
If you have any questions, you are warmly welcome to call Ylva Andersson (Head of QC) at 040–28 75 09 from August 17.
· The deadline for applications is 2026-08-31
· Please note that we do not have the ability to accept applications via email.
About Us
Bioglan AB develops, manufactures, and markets pharmaceuticals, medical devices, dietary supplements, and cosmetics that help people around the world every day. In Malmö, products are manufactured for topical use in the form of creams, ointments, and gels. Bioglan AB is part of the Spanish pharmaceutical company Reig Jofré Group. The quality system follows GMP and ISO 13485. At Bioglan, we value courageous and curious employees who strive to develop themselves and our organization with high quality. We appreciate a positive and curious attitude and a professional and competence-based approach.
Bioglan AB has just over 140 employees characterized by great diversity, with regard to age, nationality, and education, at the facility in Malmö. The organization is affiliated with the IKEM union.Since our current Quality Specialist is moving on within the organization, we are now seeking her successor. As our new Quality Specialist, you will become part of a well-functioning QC organization with 25 helpful, skilled, and dedicated colleagues on the team!
About the Position
You will become an important part of the QC department, a well-functioning group that supports each other, enjoys working together, and supports one another in meeting quality requirements and deadlines from authorities and customers. We are responsive and offer a work environment where our employees are given the…