56 Quality jobs in Köniz found

Essential duties

People management:

• Manage and organize the workload within the Product Quality sub-team
• Lead and develop the team members including target definition and performance review
• Initiate and support the hiring and on boarding process for new staff
• Ensure that the training of the team members is relevant and performed on time
• Ensure that the team members are competent for the activities to be performed
• Defines relevant and adequate objectives for the team members, and measures performance
• Manage the team performance regarding the defined objectives, and escalate to the NCPQ Manager as appropriate

• Design strategies to ensure that quality requirements and business needs are met
• Supporting Operations in ensuring that a product is ready for being manufactured under GMP conditions (GMP readiness)
• Ensuring the quality of manufactured products meets the applicable GMP requirements
• On time disposition / preparation for disposition of manufactured products – Planning of the relevant activities
• Supports GMP-compliant production of active ingredients and drugs for clinical trials and market launch
• Verification and support for the disposition for QP release of manufactured batches and related documentation
• Support QA Laboratory & Material Management (LMM) team in releasing materials for Production (MfPs)
• Support Quality Operations and QA LMM in ensuring GMP readiness for NPI projects
• Supports the collection of KPIs to measure Quality and Operations’ performance
• Review and approval of non-conformances, CAPAs, and Change Controls
• Ensure the relevancy and effectiveness of corrective and preventive actions
• Contact person for production, development and quality control for compliance related topics
• Review and approval of process documents (e.g. SOPs, work instructions, process descriptions, etc.) and risk assessments
• Support the material creation activities in SAP
• Support for processing complaints
• Support for product escalation activities
• Support for internal and external audits as Subject Matter Expert
• Support the execution for risk management activities for the site
• Ensures that batch records’ documentation is stored and archived at adequate location and according to applicable requirements

• Delivery on annual goals & objectives, guided by Our Credo and Leadership Imperatives
• Conformance to quality KPIs (QSMR, performance review)

• University degree in pharmacy, natural science, medicine, or equivalent
• At least 5 years of working experience in Quality department in pharmaceuticals, biotechnologies or chemistry industry

• Ability to design strategies to meet quality and business needs
• Good leadership capabilities – Able to manage a team of minimum 3 people
• Very good communication skills in both German and English language
• Excellent communication and teamwork skills
• Ability to work in a diverse and changing environment
• Flexibility, accuracy and reliability
• Ability to prioritize and to continuously review priorities

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.