We are currently searching for a QC professional to support our client’s manufacturing operations on an initital 12 months contracts. In this role, you will provide analytical services to manufacturing teams, contribute to continuous improvement initiatives, and ensure compliance with all regulatory and safety standards. This is a great opportunity to grow your career in a dynamic and innovative environment.
Main Responsibilities:
• Providing analytical expertise for any project, troubleshooting, investigation on analytical methods and lab technologies.
• Coordinate analytical testing on projects (validation/transfer), ensuring adherence to the committed scheduled plans
• Performing his/her tasks in accordance with cGMP and HSE requirements, and with the associated instructions, procedures, records related to these tasks
• Recording all expected raw data, calculations, information, related to his/her tasks, to comply with cGMP and Data integrity requirements
• Writing/reviewing protocols and reports related to analytical validation/transfers and qualification activities
• Writing/reviewing and maintaining accurate analytical methods procedures
• Informing his/her manager of any quality or HSE event (deviations or OOx) in a timely manner to ensure investigation and impact assessment are performed appropriately
• Participating actively to any investigation, where he/she is involved, to ensure investigations and impact assessment are performed appropriately
• Performing periodically trend analysis on method performance in order to determine the need to revalidate, optimize or replace the method
• Ensuring that his/her lab/facilities, lab instruments, are kept in a quality and safety status to ensure that they can be used appropriately
• Supporting QC teams during internal, external audits and inspections
Qualifications:
• Higher-level degree in a scientific or technical discipline (e.g., Chemistry, Biochemistry, or related field).
• Minimum of 3 years’ experience in Quality Control, Pharmaceutical Development, Analytical, or Manufacturing environments within the pharmaceutical industry.
• Strong knowledge of Good Manufacturing Practices (GMP) and regulatory requirements.
• Proven ability to analyse complex data and laboratory results to support decision-making and identify opportunities for improvement.
• High attention to detail to ensure accuracy in testing, reporting, and regulatory compliance.
• Skilled in problem-solving with a proactive approach to resolving quality control issues.
• Flexible and adaptable, with a positive attitude toward change and continuous improvement.