Duties & Responsibilities:

• Conducting experiments and analyzing data using various scientific techniques and instruments

• Identifying out-of-specification (OOS), deviations and quality problems of products, materials, packaging and utilities

• Inspecting laboratory equipment and utilities.

• Monitor laboratory testing processes according to validation plans and schedules.

• Prepare SOPs and other related documents required for the equipment and laboratory processes

• Collect data required for validation activities aligned with the standard operating procedures (SOPs).

• Interpreting data and making recommendations based on findings

• Document and report sampling conditions, testing activities and results. 

• Inspect in-coming and out-going samples/products.

• Prepare samples, standards and solutions.

• Maintaining accurate records of experiments and results

• Perform routine calibration and maintenance of laboratory equipment.

• Record results of audits and gather information for product and process quality metric management reports.

• Review and verify supplier raw material records and results.

• Working collaboratively with other scientists and researchers to advance the organization's research goals

• Staying up-to-date with industry advancements and incorporating new techniques and technologies into your work

• Maintaining laboratory equipment and ensuring a safe work environment

Job Requirements

• MSc or BSc degree in chemistry, biochemistry or related field from a recognized and qualified higher education institute 

• A minimum of three years relevant experience as a laboratory chemist in bioanalytical lab, research institutes/pharmaceutical industries/Food industries

• Demonstrated knowledge of Good Laboratory Practice (GLP) 

• Hands on experience in a pharmaceutical, biotech or research laboratory setting

• Hands on experience with mass spectrometry, HPLC, FTIR, and other advanced scientific instruments and techniques

• Knowledge in use of pharmaceutical and/or research laboratory equipment 

• Ability to work with hazardous materials and in a regulated environments

• Strong background in quantitative analysis and pharmacokinetic sample handling

• Ability to understand statistical analysis (PK/PD data interpretation)

• Ability to work independently and as part of a team

• Record-keeping abilities

• Self-initiated, high ethical standard and willing to comply with Droga Group culture

• Fast learner to apply and identify areas of improvement in the work processes, and be able to analyze to identify possible issues and solve routine problems effectively.

• Willingness to travel (both locally and internationally).

How To Apply

Interested Applicants can apply using our email hr@drogapharma.com