Our client is looking for a QC Analyst to join their team.
The selected candidate will be responsible for carrying out analysis of raw materials, Active Pharmaceutical Ingredients (APIs), and Finished Dosage Forms in accordance with GMP standards and company procedures. The role also includes supporting various Quality Control functions as required by the organisation.
Responsibilities
Sample, analyse, and report on the quality of raw materials, APIs, and Finished Dosage Form products.
Compile, review, and interpret laboratory test results.
Perform equipment calibration and confirmatory testing.
Maintain accurate documentation and review standard operating procedures.
Support additional Quality Control activities in line with company and regulatory requirements.
Requirements
Diploma or Degree in Chemistry or a related scientific field.
Previous experience within a pharmaceutical environment is considered an asset.
Strong organisational and communication skills.
Excellent analytical thinking and problem-solving abilities.
Ability to work both independently and collaboratively within a team.
High level of attention to detail and self-motivation.
Results-oriented with a professional attitude aligned with company values.
Benefits
Continuous professional training and development opportunities
