QS Analyst // Johnson & Johnson
View: 117
Update day: 26-03-2024
Location: Neuchâtel Neuchâtel NE
Category: Sales
Industry: Staffing Recruiting Biotechnology Pharmaceuticals
Position: Entry level
Job type: Full-time
Job content
Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.Johnson & Johnson is looking for their futur : Quality System Analystfor Neuchâtel
Responsibilities
- The Quality Systems Analyst ensures the continuous education, implementation and improvement of Quality Systems and compliance with QS Regulation within the Medos Sarl (Mitek Division) facility.
- The Quality Systems Analyst ensures that the Medos Sarl (Mitek Division), Document Control and Change Control Processes and structure meet all business and regulatory requirements.
- Lead the implementation and administration of quality management systems in accordance with applicable standards.
- Ensures quality systems are effectively deployed. / Performs periodic checks to verify appropriate application.
- Maintain regular interface with Management:
- To assist in the development of Quality Metrics.
- To achieve company’s Quality goals.
- Uses statistical methods, quality tools and computer-generated reports to continuously improve process capability.
- Provide education/training as needed regarding Document Control and Change Control processes including MVI/Validation Documents.
- Leads and participates in quality system improvement initiatives. / Suggests process changes when appropriate.
- Determines root causes of quality issues and develops corrective actions and recommendations.
- Establishes, maintains and implements communications to increase awareness and promote improvement of quality issues across the business.
- Assists with external audits, generating reports with corrective action plans and ensuring implementation of corrective actions in a timely manner.
- Backup on other tasks within QS department to assure business continuity, if required.
- Responsible for communicating business related issues or opportunities to next management level.
- Follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
- Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
- Performs other duties assigned as needed.
- University/Bachelor’s Degree or Equivalent / Commercial CFC with experience in quality departement
- Requires up to a minimum of 2 years related experience. Medical device manufacturing experience preferred.
- Desirable Lean/Six Sigma Green Belt for this position and background in Statistics.
- Able to communicate and writing skills in English
- Mathematical and analytical thinking skills
Deadline: 10-05-2024
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