Roles & Responsibilities
Responsibilities
- Oversee and approve GMP documentation, conduct internal / external audits, and manage vendor qualification to ensure compliance with PQS and reduce quality risks.
- Maintain inspection readiness, support regulatory inspections, and ensure GMP standards are upheld through site walks and communication / training.
- Perform gap analyses of procedures against PQS, propose corrective actions, and support regulatory submissions and queries.
- Track quality metrics, identify trends / atypical observations, and support reporting through monthly and ad-hoc Quality Review Team meetings.
- Collaborate with cross-functional teams to resolve quality issues, uphold compliance standards, and support EHS-related investigations.
Requirements
Diploma or Degree with relevant QA experience, preferably in the pharmaceutical industry.Ability to work independently to resolve issues with appropriate escalation when needed.Strong verbal and written communication, presentation, and teamwork skills.Proven problem-solving capabilities and a proactive, positive work attitude.Adaptability and willingness to embrace digital tools to enhance efficiency.Ownership mentality with a drive to deliver high-quality outcomes.If you have what it takes, please send your resume to or click APPLY NOW. For more information, please visit Data provided is for recruitment purposes only. Regrettably, only shortlisted candidates will be notified. Business Reg No : D | Licence No : 10C5117 | EA Reg No : R
Tell employers what skills you have
Pharmaceutical Industry
Agile Testing
Verbal Communication
Ability To Work Independently
Quality Assurance
Release Management
GMP
Test Cases
Written Communication
Adaptability
Compliance
Audits
Teamwork Skills
Regulatory Submissions