Senior Quality Compliance Specialist - Pharmaceutical Manufacturing

Takeda · 📍 Badung, Bali, Indonesia · Diposting 2026-10-09
FULL_TIME⭐ TERVERIFIKASI
IDR 500,000,000 - 800,000,000
Takeda is seeking a highly skilled and experienced Senior Quality Compliance Specialist to join our team in Badung, Bali. In this role, you will be responsible for ensuring that our pharmaceutical manufacturing processes comply with all relevant regulations and standards. You will play a key role in maintaining the highest standards of quality and safety in our operations.

📋 Tanggung Jawab Pekerjaan

Develop and implement quality assurance and control systems to ensure compliance with regulatory requirements.,Monitor and evaluate manufacturing processes to identify areas for improvement and implement corrective actions.,Conduct audits and inspections to verify compliance with quality standards and regulatory requirements.,Prepare and maintain documentation for quality control procedures and records.,Provide training and guidance to staff on quality control procedures and best practices.,Collaborate with cross-functional teams to ensure that quality standards are met throughout the manufacturing process.,Stay up-to-date with industry trends, regulations, and best practices in pharmaceutical quality assurance.

🎓 Kualifikasi & Syarat

Bachelor's degree in Pharmacy, Chemistry, or a related field.,Minimum of 5 years of experience in quality assurance and control in the pharmaceutical industry.,Knowledge of Good Manufacturing Practices (GMP) and regulatory requirements (e.g., ICH, FDA, PIC/S).,Experience with quality management systems (e.g., ISO 9001, ISO 13485).,Strong analytical and problem-solving skills.,Excellent communication and interpersonal skills.,Ability to work in a fast-paced, dynamic environment.

🛠️ Keahlian

Quality assurance and controlRegulatory complianceProcess improvementDocumentation and record-keepingTraining and developmentTeam collaboration
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