Trimb Healthcare is a rapidly growing healthcare company based in Stockholm, Sweden.
Trimb Healthcare portfolio ranges across different classifications and include OTC, medical device and cosmetic products. The company is the Marketing Authorization Holder of the Pharmaceutical portfolio and Legal Manufacturer of the medical device portfolio. All manufacturing is outsourced to contracting manufacturing organizations.
The portfolio is constantly growing over time by product development and strategic acquisitions.

What we do
• We focus on the development, sales and marketing of OTC pharmaceuticals and consumer healthcare products
• We commercialize innovative products that provide consumers better alternatives to existing solutions.

For more information about Trimb Healthcare and our products please visit



Trimb is a rapidly growing OTC and consumer healthcare company based in Stockholm, Sweden. The company’s experience and competencies span across all regulatory classes and most therapy fields relevant to consumer healthcare. Trimb’s products are sold in more than 50 countries and the company has its own go-to-market organization in northern Europe. 

If you decide to work at Trimb it means that:
· Being part of an exciting journey at Trimb, an entrepreneurial fast-growing company with a clear commitment to future growth and development within the OTC and Consumer Healthcare market – this means a lot of opportunities for personal responsibility, influence and development over time
· Work together with a team of top skilled professionals in a company with an attractive culture and appealing working environment
· Work in a "flat" organization with short decision-making processes
· Be part of a competent team with a great atmosphere

The position
Regulatory and Quality Affairs is a scientific process-driven support function to the Trimb organization. We efficiently assure compliance to EU regulations and standards to support TRIMBs continuous growth and expansion. Since the portfolio of Trimb Healthcare consists of medical devices and pharmaceuticals the QA manager will participate in quality work of both ISO13485 and Good Distribution Practice and applicable Good Manufacturing Practice.
The focus when it comes to the QA manager main duties is to manage the quality assurance processes within the organization. The QA manager is together with the Director of RA/QA, responsible to implement the quality driven focus in the organization.

For more information about the position and inquiries please contact Jarl Molin, recruitment consultants at Peak Search.
Mobile: +46 70 560 20 56