Technical Operations

Nusantics Group; Jakarta Pusat; On-site; IDR 178,560,000 - 290,160,000; Full time

Job summary

Nusantics Group is seeking a QC Lead to supervise quality control across raw materials, packaging, and laboratory reagents, ensuring adherence to procedures. You will also oversee in-process QC, issuing CoA when results meet specifications, and perform library prep and sequencing using Illumina platforms.

Ideal candidates have a biology/chemistry background, NGS experience, and GMP/GLP familiarity, with strong pipetting skills and hands-on lab leadership.

Qualifications

• Bachelor of Science in Biology, Pharmaceuticals, Chemistry, or related major.
• Minimum of 3 years experience in QC and laboratory operations, with at least 2 years in a supervisory or lead role.
• At least 2 years hands-on experience in lab/research roles, including NGS workflows in academic or industry settings.
• Experience in PCR, qPCR, electrophoresis, nucleic acid extraction, and NGS library preparation.
• Excellent pipetting skills.
• Understanding of GMP, GLP, CPAKB, ISO 9001, ISO 13485, and ISO 17025 is an added value.

Responsibilities

• Lead QC inspections on raw materials, packaging, and consumables per established procedures.
• Lead in-process QC and issue CoA when results meet standards.
• Perform library preparation, QC, and sequencing runs on Illumina platforms.
• Troubleshoot issues arising during testing and inspection activities.

Skills

QC inspections

In-process QC

Troubleshooting

NGS workflows

PCR / qPCR

Pipetting skills

GMP/GLP knowledge

ISO 17025 understanding

Education

Bachelor of Science in Biology/Pharmacy/Chemistry

Tools

Illumina platforms

NGS library prep

PCR / qPCR

Electrophoresis

Nucleic acid extraction

Job description

• Lead and responsible for conducting Quality Control (QC) inspections on raw materials, packaging, and consumables used in production, as well as materials for research and laboratory use (chemicals, reagents, and consumables), following established procedures.
• Lead and responsible for conducting in-process Quality Control (QC) based on established procedures and production schedules, and issuing Certificates of Analysis (CoA) when test results meet defined standards/specifications.
• Perform library preparation, quality control, and sequencing runs using Illumina platforms (e.g., MiSeq, NextSeq, NovaSeq).
• Conduct troubleshooting for any issue/problem that might arise during the testing and inspection activity.

Ideally, You Would Have

• Bachelor of Science in Biology, Pharmaceuticals, Chemistry, or other related major.
• Minimum of 3 years of experience in QC and laboratory operations, with at least 2 years of experience in a supervisory or lead role.
• Having experience at least 2 years of hands-on experience in laboratory/research roles, including NGS workflows in academic or industry settings.
• Having experience in PCR, qPCR, electrophoresis, nucleic acid extraction, and NGS library preparation.
• Having excellent pipetting skills.
• Understanding of GMP, GLP, CPAKB, ISO 9001, ISO 13485, and ISO 17025 is an added value.