Candoo Pharmatech is seeking a dedicated and detail-oriented
Quality Control Chemist
to join our dynamic team. In this role, you will provide analytical support for the development of new drug products across various dosage forms. The ideal candidate will perform analytical testing, maintain accurate documentation, ensure compliance with GMP standards, and contribute to the continued success of our R&D and manufacturing operations.
Key Responsibilities
Perform
release, in-process, and stability testing
using analytical techniques such as FTIR, KF titration, dissolution, and HPLC assay, in accordance with established methods and SOPs.
Conduct
purified water monitoring
and
cleaning validation
analyses using a TOC analyzer.
Perform
daily verification and calibration
of laboratory instruments and assist with annual calibrations per SOP requirements.
Load and pull
stability samples
as assigned, following approved procedures.
Coordinate with equipment service vendors for
preventive maintenance and calibration
, maintaining proper documentation for audit purposes.
Document all experimental data in compliance with
Good Documentation Practices (GDP)
.
Report
unexpected or Out of Specification (OOS)
results immediately to the Manager, assist in laboratory investigations, and complete CAPA as required.
Prepare
raw data packages
and
OpenLab reports
for clients as needed.
Summarize analytical results and prepare
technical reports
as assigned.
Properly
collect and dispose of laboratory waste
according to company policy.
Maintain a
clean, organized, and audit-ready
laboratory environment, ensuring compliance with applicable SOPs, regulations, and safety standards.
Support