Requirement for QC Analyst:
The resources, placed within the Quality Unit, will report to the Quality Control Laboratory Manager.

Specifically, they will be responsible for:

• Perform analyses, define procedures and validations related to QC.
• Perform analytical tests on chemicals and raw materials.
• Accurately document the work process and test results in accordance with GMP requirements.
• Write and review analytical procedures, SOPs, protocols and reports
• Request materials and equipment needed for work activities and train staff to maintain them Using HPLC in accordance with GMP and internal guidelines
• Plan work to ensure correct project steps.
• File and maintain appropriate documentation for the laboratory
• Maintain up-to-date safety and environmental regulations in the laboratory
• Write and review protocols, procedures and reports

The ideal candidate possesses:

• Masters Degree in pharmaceutical chemistry and technology, chemistry, pharmacy
• Knowledge of and compliance with regulations related to Environment, Health and Safety (HSE).
• Basic knowledge of GMP / GDP rules, rules related to Environment Health and Safety (HSE) and proper use of Personal Protective Equipment (PPE)
• Ability to work in full compliance with Data Integrity in order to ensure that data is attributable, understandable, up-to-date, original and accurate (ALCOA)
• Ability to implement the rules of good behavior while maintaining the cleanliness of one’s workplace
• Prior experience in Laboratory environment, knowledge of basic laboratory SOPs, quality Knowledge of analytical techniques, knowledge of GC Chromatographic instruments, HPLC.
• Good knowledge of Office package
• Willingness to work on deadlines with good energy level, self-motivation and high organizational skills

Requirement for Production Workers:
Production workers with the following characteristics:

• Meets production objectives.
• Applies regulations on safety, health environment in the production department, major accident hazard prevention.
  Complies with GMP (good manufacturing practice) regulations.
• Independently operates equipment assigned to him/her.
• Specializes in the control and supervision of production equipment and machinery in the solvent-using synthesis, finishing, and micronization departments.
• Responsibility in monitoring production processes, operating parameters of machines and equipment by reporting any anomalies.
• Verifies the setup and operation of tools equipment or machinery.
• Checks product status during processing.
• Fills out all production batch and plant documentation according to current standards and procedures.
• Is responsible for cleaning and keeping work areas and department equipment tidy.
• Is responsible for reclaiming production equipment and related transfer lines

The ideal candidate possesses:

• Possesses a chemical technician diploma.
• Has previous experience of at least 3 years in a similar role in departments of synthesis of active pharmaceutical ingredients
• Willingness to work 3 shifts