Deskripsi Pekerjaan
Informasi lengkap tentang posisi dan persyaratan
Ringkasan Yukerja
Lowongan Analytical Scientist Lead di Soothe Operator kami kurasi dari JobStreet (kategori Teknologi & IT). Perhatikan lokasi kerja (West Jakarta, Jakarta) sebelum melamar. Yukerja.com bukan pemberi kerja — lamaran diproses di situs sumber resmi.
Job Summary
We are looking for a detail-oriented and knowledgeable Analytical Scientist to support our laboratory operations, method validation activities, and compliance with regulatory and compendial standards. This role focuses on analytical method development/validation, laboratory documentation, and ensuring that all testing activities meet GMP requirements and internal quality standards.
Key Responsibilities
Manage and maintain laboratory documentation, including SOPs, STPs, protocols and reports.
Assist in writing, reviewing, and updating Standard Operating Procedures and Standard Test Procedures in alignment with GMP, PQS, and compendial requirements (FI, USP, BP, etc.).
Perform analytical and trials, verification activities, prepare protocols and reports, and ensure timely execution of project deliverables.
Support the implementation and monitoring of compendial compliance within the laboratory.
Support QC/R&D teams in laboratory investigations, including handling out-of-specification (OOS) cases.
Ensure reagents, reference standards, and laboratory equipment are properly maintained and ready for testing.
Provide necessary training to laboratory personnel regarding analytical procedures, documentation, and compliance.
Qualifications
Bachelor’s Degree in Chemistry or Pharmacy.
Minimum 3 years of experience in analytical method development, validation, or laboratory compliance in the pharmaceutical industry.
Strong knowledge of analytical instruments and test procedures (HPLC, UV-Vis, FTIR, dissolution tester, etc.) and familiarity with compendial requirements (USP, FI, BP, etc.).
Understanding of GMP, GLP, and regulatory compliance requirements in pharmaceutical manufacturing.
Strong analytical thinking, attention to detail, and high integrity.
Ability to work independently and collaboratively within cross-functional teams.
Good communication and interpersonal skills.
Experience in laboratory investigation and documentation for OOS or deviations.