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Principle Roles & Responsibilities / Accountabilities
Engineering Project Support and Operation Readiness:
Collaborate with cross-functional teams to implement GMP-related systems processes and workflows for the production department.
Develop and implement GMP training programs tailored to production staff aligned with corporate quality policies and regulatory requirements.
Establish the deviation management and CAPA processes in manufacturing for handling non- conformances effectively and ensuring timely resolutions.
Implement a robust change control process ensuring GMP compliance and proper documentation of changes in the production environment.
Participate in the preparation for facility qualification audits and regulatory inspections ensuring that all systems and practices meet GMP standards.
Lead consumable materials/service introduction and track the status to ensure to meet the manufacturing requirement.
Support the development of GMP documentation including SOPs validation protocols and project-specific documentation for compliance.
Perform other duties as assigned.
Routine Operation:
Ensure routine operation in compliance with Roches GMP/SHE and regulation requirements.
Serve as the primary interface between the production department and QA/Compliance teams for GMP-related matters.
Manage ongoing GMP training programs ensuring production personnel are regularly updated on GMP and compliance requirements.
Oversee the timely identification investigation and resolution of deviations ensuring proper execution of CAPAs to avoid recurrence.
Evaluate and coordinate changes within the production department ensuring proper implementation and documentation in line with regulatory requirements.
Act as the production departments primary liaison during internal and external audits ensuring inspection readiness and addressing observations.
Monitor GMP compliance in daily operations identifying gaps and implementing corrective actions.
Proactively identify areas for improvement in GMP operations driving initiatives to enhance quality and productivity while maintaining compliance.
Perform other duties as assigned.
Qualification and Experience
Education/Qualifications
Bachelors Degree (Pharmaceutical / Biological is preferred) and above.
Job Required Competencies
5 or more years operation experience in GMP compliance roles in the injection pharmaceutical industry MNC Bio-pharma preferred.
Experienced in strategic projects of facility including design commissioning & qualification is preferred.
Strong knowledge of cGMP and regulations relevant to the pharmaceutical industry especially in the biological industry.
Hands-on experience in deviation handling CAPA management change control and audit preparation is required.
Familiarity with compliance tools and systems for managing training deviations and CAPAs.
Fluent communications skills in English is preferred and the ability to effectively communicate collaborate and foster positive interactions with team members and stakeholders.
A healthier future drives us to innovate. Together more than 100000 employees across the globe are dedicated to advance science ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities foster creativity and keep our ambitions high so we can deliver life-changing healthcare solutions that make a global impact.
Lets build a healthier future together.
Roche is an Equal Opportunity Employer.
Required Experience:
IC
F. Hoffmann-La Roche AG is a Swiss multinational healthcare company that operates worldwide under two divisions: Pharmaceuticals and Diagnostics. Its holding company, Roche Holding AG, has bearer shares listed on the SIX Swiss Exchange. The company headquarters are located in Basel.