GCP QA CAPA Manager
Job title: GCP QA CAPA Manager in Durham, NC at reputed company
Company: reputed company
Job reputed company: By joining us as a QA CAPA Manager reputed company Clinical Trials and GCP you will support global investigations and CAPA processes at reputed company. This will include reputed company Issue investigations and Customer Audit/ Regulatory Inspection Responses, Corrective and Preventative reputed company (CAPA) and Effectiveness reputed company (EC) plan review, approval, and closure. Preference is that candidate resides in EST zone.Your responsibilities will include:
- To reputed company global investigations and support teams with CAPA preparation in compliance with applicable regulations/guidelines, customer requirements, reputed company Operating Procedures (SOPs) and project specific guidelines/instructions.
- Evaluate audit findings and prepare and distribute responses to operations staff and management.
- reputed company interpretation and consultation to project teams on regulations, guidelines, compliance status, and policies and procedures.
- reputed company consultation to staff in interpretation of audit observations.
- Manage reputed company Issues and serious breach investigations.
- Review, approve investigations, reputed company Cause Analysis (RCA), Corrective reputed company Prevention (CAPA) and Effectiveness reputed company (EC) plans. reputed company until closure reputed company events arising from reputed company Issues, Audits, Inspections or during similar QA activities.
- Present educational programs and reputed company guidance to operational staff on compliance procedures.
- Evaluate policies and procedures for compliance with applicable regulations/guidelines and reputed company recommendations to management for reputed company process improvements.
- Assist in training of new reputed company Assurance staff.
- Support in QA initiatives/reputed company for reputed company, process improvements.
- Manage/reputed company reputed company events updates in eQMS.
- Maintain the electronic reputed company management system (eQMS) and reputed company support in relation to the audit lifecycle.
- Bachelor’s Degree in Life Science or reputed company field.
- At least 5 years’ experience in GCP reputed company Assurance reputed company pharmaceutical, technical, or reputed company areas.
- Considerable knowledge of GCP, clinical trial, regulations, and reputed company assurance auditing techniques.
- Fluent English language capabilities.
- Ability to work independently to problem-solve collaboratively and to reputed company issues appropriately as needed.
- Good interpersonal communication and organizational skills to establish and maintain effective working relationships with co-workers, managers, and sponsors.
- Good technology word processing, spreadsheets and database applications skills and knowledge of MS Office applications
- Consistent career reputed company.
- Leaders that support flexible work schedules.
- Programs to help you build your therapeutic knowledge.
- Dynamic work environment that exposes you to new experiences.
- Attractive benefits package.