Quality Assurance Pharmaceutical Industries

Pengiklan Anonim; Jakarta Timur; On-site; IDR 144,000,000 - 216,000,000; Full time

Benefits offered by this job

Competitive compensation package

Career development opportunities

Job summary

PT Nellco Indopharma seeks a dedicated Quality Assurance Specialist to join our East Jakarta quality management team. You will ensure all pharmaceutical products and processes meet stringent quality standards, regulatory requirements, and industry best practices, safeguarding product integrity and patient safety.

Responsibilities include implementing QC procedures, analyzing test results, and supporting regulatory inspections.

Qualifications

• 3–5 years of QA/QC experience in pharmaceutical manufacturing or related industry.
• Solid knowledge of pharmaceutical regulations, GMP, and quality management systems.
• Laboratory testing techniques and analytical methods for pharmaceutical products.

Responsibilities

• Conduct quality inspections and testing of pharmaceutical products across production stages to ensure compliance with standards.
• Develop, implement, and maintain QC procedures and documentation for pharmaceutical manufacturing.
• Analyze test results, identify deviations, and initiate corrective actions as needed.
• Monitor production processes to identify quality risks and implement preventative measures.
• Collaborate with production, R&D, and regulatory teams to ensure GMP adherence.

Skills

Quality assurance

GMP knowledge

ISO 9001

Laboratory testing

Statistical analysis

Bilingual Indonesian/English

Independent collaboration

Education

Apothecary degree

Tools

Quality management software

Job description

Quality Assurance Pharmaceutical Industries

About the role

PT Nellco is seeking a dedicated and detail-oriented Quality Assurance Specialist for Pharmaceutical Industries to join our quality management team. This is a full-time position based in East Jakarta, Jakarta. In this role, you will be responsible for ensuring that all pharmaceutical products and processes meet stringent quality standards, regulatory requirements, and industry best practices. You will play a critical part in safeguarding product integrity, patient safety, and compliance with pharmaceutical regulations, making this position strategically important to our operations and reputation.

Key responsibilities

• Conduct comprehensive quality inspections and testing of pharmaceutical products at various stages of production to ensure compliance with established quality standards
• Develop, implement, and maintain quality control procedures and documentation systems specific to pharmaceutical manufacturing
• Perform analysis of test results and identify any deviations or non-conformances, initiating corrective actions as necessary
• Monitor and evaluate production processes to identify potential quality risks and implement preventative measures
• Collaborate with production, research, and regulatory teams to ensure adherence to Good Manufacturing Practice (GMP) guidelines
• Prepare and maintain detailed quality assurance reports, batch records, and regulatory documentation
• Conduct internal audits and inspections to verify compliance with company policies and pharmaceutical regulations
• Support regulatory inspections and audits by external authorities, providing necessary documentation and explanations
• Investigate product complaints and quality issues, documenting findings and recommending corrective actions
• Contribute to continuous improvement initiatives to enhance quality systems and manufacturing processes

What we're looking for

• Apothecary Degree.
• Minimum of 3-5 years of professional experience in quality assurance or quality control within pharmaceutical manufacturing or a closely related industry
• Strong knowledge of pharmaceutical regulations, GMP standards, and quality management systems (ISO 9001 or equivalent)
• Proficiency in laboratory testing techniques and analytical methods relevant to pharmaceutical products
• Excellent attention to detail with the ability to identify deviations and non-conformances in products and processes
• Competence in statistical analysis and data interpretation for quality control purposes
• Strong written and verbal communication skills in Indonesian and English, with the ability to document findings clearly and concisely
• Ability to work independently whilst collaborating effectively with cross-functional teams
• Familiarity with quality management software and documentation systems
• Professional certification in quality assurance, such as certified quality auditor (CQA) or similar, is preferred but not essential

About us

PT Nellco Indopharma is a leading pharmaceutical manufacturing company committed to delivering high-quality medicines and healthcare solutions. We operate with a strong emphasis on innovation, safety, and regulatory compliance. Our mission is to improve patient outcomes through rigorous quality standards and continuous improvement. We pride ourselves on maintaining the highest ethical standards whilst fostering a collaborative and supportive work environment. Our team is composed of dedicated professionals who are passionate about advancing pharmaceutical excellence and contributing positively to the healthcare industry.

What we offer

PT Nellco Indopharma provides a competitive compensation package tailored to your qualifications and experience. We are committed to professional development and offer opportunities for skills enhancement through training programmes and career advancement pathways. We foster a collaborative workplace culture where your contributions are valued and recognised.