ISO 9001:2015, GMP and GLP and assist with internal audits. To develop, review and update Quality Control 9001:2015 Internal Audits Conduct ISO 9001:2015 Internal audits & Supplier Quality Audits. Educational
before project commencement.
assigned portfolio of products: Assisting with internal product queries from relevant departments Assisting regulatory authorities Work in collaboration with internal and external stakeholders to assess regulator's Guidelines pertaining to the pharmaceutical industry. Internal training and mentoring Establish and maintain effective relationships with Regulatory Authorities, internal and external stakeholders Formulate or implement maintained or enhanced. Support activities such as internal audits or regulatory agency inspections Ensure alignment
QMS etc. are QA-compliant. Assist with 3rd party audits when required. B.Pharm degree required (non-negotiable)
QMS etc. are QA-compliant. Assist with 3rd party audits when required. B.Pharm degree required (non-negotiable)
DUTIES
sources and ensuring data quality through regular audits and assessments Designing and implementing database required Ensure all customer interaction (Both internal and external customers) is of the highest professional conferences, policy setting workshops etc. Manage internal and external stakeholder expectations and communicate
sources and ensuring data quality through regular audits and assessments Designing and implementing database required Ensure all customer interaction (Both internal and external customers) is of the highest professional conferences, policy setting workshops etc. Manage internal and external stakeholder expectations and communicate
sources and ensuring data quality through regular audits and assessments
Preparing and dispatching samples to local and international customers. Coordinating projects between the new NPD briefs, spec sheets etc. Assisting with internal factory trials when required to do so. Salary