Deskripsi Pekerjaan
Join Am-Europharma Corporation as a Quality Assurance Associate and become part of a dynamic team dedicated to delivering excellence in the pharmaceutical manufacturing industry. Located in Calamba City, Laguna, this full-time position offers an exciting opportunity for professionals who are passionate about ensuring product quality and regulatory compliance.
At Am-Europharma Corporation, we are committed to maintaining the highest standards of Good Manufacturing Practice (GMP) and regulatory compliance. As a Quality Assurance Associate, you will play a critical role in conducting comprehensive audits, managing documentation systems, and ensuring that all operational processes adhere to stringent quality and regulatory requirements.
This role is ideal for detail-oriented professionals who thrive in fast-paced manufacturing environments. You will collaborate closely with cross-functional teams to handle deviations, resolve complaints, and support internal and external audit activities. Your expertise will contribute to our mission of producing safe, effective, and high-quality pharmaceutical products that make a difference in people's lives.
We offer competitive compensation, professional development opportunities, and a supportive work environment where your contributions are valued and recognized. If you are looking to advance your career in quality assurance within a reputable pharmaceutical organization, we encourage you to apply today.
Tanggung Jawab
- Conduct regular audits and inspections to ensure compliance with GMP standards and regulatory requirements
- Maintain and manage comprehensive quality documentation, including standard operating procedures (SOPs) and batch records
- Handle product deviations and complaints by investigating root causes and implementing corrective actions
- Support internal and external audits, including preparation of documentation and coordination with auditors
- Monitor and ensure adherence to regulatory guidelines set by governing authorities
- Collaborate with production and quality control teams to resolve quality-related issues
- Participate in the development and implementation of CAPA (Corrective and Preventive Action) plans
Kualifikasi
- Bachelor's degree in Pharmacy, Chemistry, Chemical Engineering, or a related scientific field
- Minimum of 1-2 years of experience in quality assurance within pharmaceutical or manufacturing industries
- Strong knowledge of GMP regulations and regulatory compliance requirements
- Proficient in documentation management and record-keeping practices
- Excellent attention to detail and analytical problem-solving skills
- Effective communication and interpersonal abilities for cross-departmental collaboration
- Experience with audits and regulatory inspections is highly advantageous
- Ability to work independently and manage multiple priorities in a deadline-driven environment