QA Vacancy At Gypto Pharma
Join our team as a Validation Professional Specialist
Responsibilities:
- Analyze essential data and prepare comprehensive reports for quality assurance.
- Develop plans for revalidation activities and assist in qualification processes during execution.
- Collaborate with relevant departments to prepare validation plans/protocols for various production processes, including:
- Process Validation
- Cleaning Validation
- CIP Validation
- Hold Time Validation
- Media Fill
- Filtration Validation
- Conduct activities required by regulatory authorities.
- Prepare the Validation Master Plan (VMP) for the facility in accordance with the latest guidelines.
- Draft all necessary documents and SOPs for different validation activities.
- Review supportive documentation needed during validation processes.
- Ensure facility, utilities, equipment, and machines conform to validation requirements.
- Supervise the investigation team on validation-related items.
- Develop and implement action plans.
- Participate in the CAPA system and monitor implementation.
- Adhere to safety instructions and requirements, ensuring compliance with GLP, GMP, and GDP rules.
**Qualifications:**
- Bachelor's degree in Pharmaceutical Sciences.
- 4 to 5 years of experience in the pharmaceutical industry and operations.
- Strong understanding of quality assurance methodologies and practices.
- Skilled in documentation review and requirements analysis.
- Problem-solving skills with the ability to troubleshoot complex issues.
- Capable of working collaboratively with others and meeting project deadlines.
- Excellent verbal and written communication in English.
- Proficient computer skills.
Don’t miss this opportunity, Apply today!!