Soothe Operatormembuka lowonganAnalytical Scientist

Soothe Operator is a consumer health startup focused on creating science-backed products that help people relieve everyday pains and discomforts. We’re a small, hands-on team based in West Jakarta, building innovative solutions that genuinely improve daily life.

📩 Contact us: [email protected]

Ringkasan

  • Perusahaan :
  • Soothe Operator
  • Situs :
  • https://sootheoperator.com/
  • Industri :
  • Pharmaceutical
  • Kategori :
  • Perbankan
  • Status Pekerjaan :
  • Kontrak
  • Pola Kerja :
  • OnSite
  • Jam Kerja :
  • Sesuai kontrak
  • Perolehan Gaji :
  • Rp 5.500.000 s/d Rp 10.000.000
  • Pengalaman :
  • 1 Tahun Pengalaman
  • Lokasi Kerja :
  • Jakarta
  • Tanggal Berakhir :
  • 11 May 2026

Deskripsi Pekerjaan

  • 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.
  • Bachelor’s Degree in Chemistry or Pharmacy.
  • Minimum 1 year 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.

1 Benefit Pekerjaan

💵 Gaji Kompetitif

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Butuh Cepat Full Time OnSite 1 Tahun Pengalaman 6 Benefit Apply Via URL Perbankan 26 Pelamar
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