OBS! Ansökningsperioden för denna annonsen har
About Johnson & Johnson
For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.
We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences.
That is why we in the Nordics are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feel that they belong and can reach their potential. No matter who they are.
Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”! Johnson & Johnson is a company committed to doing good for the world. We blend Heart, Science and Ingenuity to profoundly change the trajectory of health for humanity.
The Johnson & Johnson Medical Devices Companies’ purpose is to reach more patients and restore more lives. Having advanced patient care for more than a century, these companies represent an unparalleled breadth of products, services, programs and research and development capabilities in surgical technology, orthopedics, cardiovascular and specialty solutions with an offering directed at delivering clinical and economic value to health care systems worldwide.
Introduction And Overview
We are looking for a new Manager for the Quality control Microbiology laboratory, for our Medical Devices business segment in.
The team is responsible for the Microbiology Quality control of Healon Finished products and raw materials/components and consists of seven (7) employees located in J&J Uppsala site at Fyrislund Business park. You will together with Manager QA/QS and Manager QC be part of the Quality leadership team. This role reports directly to the Quality Director. The position is located at Uppsala, Sweden. Some travel may be required depending on your home location.
Objectives of the Position
Lead and develop the business so that J&J Uppsala and UQ's goals regarding quality & compliance, delivery reliability and cost efficiency are reached.
Resource and cost dimension QM Microbiology
Run the work environment work within QM Microbiology in accordance with applicable laws and regulations.
Personnel responsibility for QM Microbiology, work environment responsibility
Ensure that the necessary microbiological tests and checks are carried out for product, raw materials/inputs, media and manufacturing processes in requirements of pharmacopoeia and other regulations.
Ensure validated and qualified processes in the microbiological laboratory and maintenance and calibration according to applicable requirements according to delegation
Member of the Quality Function Management Team and Quality Management Team.
Ensure that monitoring and detection controls are in place.
Handle deviations in critical processes, premises and equipment that may affect the hygienic status in production and in the laboratory.
Approve documents for microbiological tests and sterilization processes, hygiene and microbiology
Replace Chief UQ in his shorter absence, according to the delegate in particular.
Review and approve documentation, test method, process for QM Mikorbiology
Review and approve laboratory investigation and non-conformity investigations for QM microbiology.
Five-year academic higher education with a microbiological, pharmaceutical, natural sciences or technical focus (or equivalent).
Relevant leadership training for the position.
Basic knowledge of financial accounting and budgeting
At least three to five years of work experience from quality work in the quality certified laboratory or manufacturing industry
At least three years of experience in the pharmaceutical industry or other process industry.
Experience and understanding of sterilization and sterilization processes and techniques.
Experience in project management and human resources management.
Good GMP/ ISO knowledge, as well as knowledge of regulations and guidances (e.g. CFR, pharmacopoeia).
Good IT skills
Good knowledge of both Swedish and English in both speech and writing.
What You Will Need To Succeed
Efficient working methods
Ability to plan and prioritize the department's goals and work
Ability to cross-functional collaboration between departments – and have a holistic approach