Company Introduction
Tiefenbacher Laboratories is a pharmaceutical organization engaged in the development and quality evaluation of regulated drug products for domestic and international markets.
Core Responsibilities
- Perform laboratory testing on oncology drug samples using high performance liquid chromatography systems and dissolution apparatus.
- Handle gas chromatography instruments for quantitative analysis of raw materials and finished formulations.
- Prepare sample solutions from raw materials, packaging components, and cleaning verification samples using calibrated glassware.
- Record analytical observations in laboratory notebooks and approved quality control documentation formats.
- Verify calibration status of laboratory instruments before analytical testing and document equipment usage logs.
- Conduct stability sample testing under defined storage conditions within the quality control laboratory.
Skills and Technical Exposure
- High performance liquid chromatography systems for assay and impurity testing.
- Dissolution testing equipment for solid oral dosage forms.
- Gas chromatography instruments for residual solvent analysis.
- Particle size distribution instruments used in material characterization.
- Approved analytical test methods and laboratory control documents.
- Good laboratory practice documentation systems.
Experience Context
- Work is carried out in a pharmaceutical quality control laboratory supporting commercial and development batches.
- Daily testing involves multiple samples across raw materials, in process materials, and finished drug products.
- Laboratory data supports batch release decisions and regulatory compliance for oncology products.
- Absence of this role results in delayed sample evaluation and halted product disposition.
How to Apply
Send your CV to k.surendra@tiefenbacher.com