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On behalf of our customer Prostatype Genomics – a company pioneering prediction and treatment choices for prostate cancer – we are looking for a Laboratory & R&D Associate.
WHAT PROSTATYPE GENOMICS CAN OFFER
The opportunity to work for a growing and innovative company in an accelerated growth phase:
o Having launched a groundbreaking prostate cancer prognostic solution in Europe.
o Proximity to and readiness for the US market.
-Being part of a company developing a highly attractive solution with the potential to truly improve the lives of countless prostate cancer patients
-An opportunity to join a dynamic, skilled and experienced team driven by a strong commitment to evolving both the company and its technology.
-A unique role spanning over lab work and product development, contributing to a product launch on the global stage.
THE COMPANY
Prostatype Genomic´s mission is to make a difference in prostate cancer patients’ lives through the discovery and commercialization of transformative tests to guide treatment decisions. In doing so, the company contributes to increasing patients’ quality of life and peace of mind, while also bringing significant health economic benefits to the community. Prostatype Genomics will achieve this by making Prostatype® the global test system of choice for newly diagnosed prostate cancer patients. The company's vision is to ensure that both doctors and patients facing a prostate cancer diagnosis can make treatment decisions with complete confidence. Prostatype Genomics AB is a public listed company in Stockholm, Sweden with an ISO 13485:2016 certified quality management system and already holds the necessary IVDR-certification.
THE ROLE
As the company moves toward entering the U.S. market and advances its product development this exciting phase calls for reinforcing the team with additional expertise in Sweden to support its continued growth also in the European market.
RESPONSIBILITIES
Laboratory Work
-Perform molecular biology analyses, including PCR and RNA workflows, according to established protocols.
-Ensure compliance with quality and safety standards in the laboratory, including regular equipment calibration and maintenance.
-Manage and document samples in line with regulatory requirements and internal procedures.
-Develop and optimize laboratory protocols to improve workflow efficiency and analytical performance.
Research and Development (R&D)
-Contribute to the development and validation of new methods and technologies relevant to the company’s applications.
-Analyze study data and support the preparation of scientific reports and publications.
-Collaborate with external research partners and academic institutions on ongoing and future studies.
-Explore and implement new technologies.
Quality and Regulatory Affairs (QMS, RA, QA)
-Support the maintenance and development of the company’s Quality Management System (QMS) in accordance with ISO 13485 and IVDR standards.
-Prepare and review documentation such as SOPs, risk assessments, and technical files.
-Coordinate and participate in both internal and external audits.
-Identify and implement improvements to QMS-related processes.
-Assist with regulatory submissions and follow-ups, including documentation required for market approval.
Additional Responsibilities
-Travel to hospitals and laboratories around the world—approximately twice a year initially—to train and support staff in the use of the company’s technology and related protocols.Plan and deliver training sessions, both in person and online, to ensure high-quality product implementation.
-Act as a technical and quality point of contact during the implementation phase at new customer sites.
COMPETENCE REQUIREMENTS
-University degree in biology, molecular biology, biotechnology, or a related discipline.
-A minimum of 2–3 years of laboratory experience, preferably with PCR and RNA methods.
-Experience working within a Quality Management System (ISO 13485 is a plus).
-Background in R&D related to molecular biology or medical devices is a strong advantage.
-Basic understanding of IVDR and regulatory requirements for medical devices is considered a merit.
WHO ARE YOU?
-Engaging and positive, with a genuine sense of curiosity and interest in learning.
-Ambitious with a personal drive to take on a broad responsibility and work independently.
-Structured, meticulous, and focused.
-Strong interpersonal and collaborative skills.
-Well-developed communications skills in English and Swedish.
-Hands-on mindset with an appreciation for routine and consistency in daily work.
-Dynamic, prestige less personality that adapts well to different people, situations and changing circumstances.
Interested? For more information, please contact us at Brice Group;
Anders Larsson, +46 73 203 46 91, anders.larsson@brice.se
Adina Lekberg Salamon, +46 73 974 43 34, adina.lekbergsalamon@brice.se