Compliance Officer
Location: Onitsha, Anambra
Employment Type: Full-time
Responsibilities
- Coordinate and perform batch record disposition of development, finished products, and raw materials.
- Review and approve manufacturing and QC related documents for batch record disposition.
- Provide risk-assessment tracking and other established mechanisms for risk assessment.
- Initiate, Review, and approve deviations, change controls, facility Work Orders, and any other site/product-related documents ensuring adequate levels of documentation are adequate and compliant to existing procedures.
- Drive continuous improvement and enhancement efforts to the Disposition process to ensure an efficient yet Compliant process is maintained.
- Develop reports and analyses to expose potential risks and gaps that need corrective action or preventative action.
- Compose and disseminate standardized internal communications to pharmaceutical personnel on important compliance developments, company policies, and procedures.
- Support quality manual implementation teams in area of technical expertise as required.
- Support regulatory agency inspections, by way of auditing, training, and preparation, and tracking commitments.
- Write, review, and approve Policies, Standard Operating Procedures (SOPs) and associated processes/guidelines.
Requirements
- Bachelor’s Degree in relevant field.
- A minimum of 2 years of experience
- Familiarity with industry practices and professional standards
- Exposure and hands-on experience in handling different roles at different manufacturing disciplines is a plus.
- Outstanding communication and interpersonal abilities.
Application Closing Date
Not Specified.
How to Apply
Interested and qualified candidates should forward their CV and Cover Letter to: pharmarecruitment2online@gmail.com using the position applied for as the subject of the email.
Note: Only shortlisted candidates will be reached.