Main Responsibilities: 

• Develop and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols for new and existing analytical instruments.

• Generate comprehensive and audit-ready documentation for all qualification activities, ensuring compliance.

• Conduct tests to verify that instruments function according to manufacturer specifications and user requirements, analyzing the resulting data to confirm accuracy, precision, and linearity.

• Collaborate with field service engineers and lab personnel to troubleshoot equipment issues and ensure instruments remain in a qualified state after repairs, software updates, or relocation.

• Train laboratory staff on the proper use of qualified equipment and associated standard operating procedures (SOPs).

• Support internal and external audits by providing documentation and technical expertise related to instrument qualification.

About You:

• Bachelor degree in a relevant scientific field (e.g., Chemistry, Biology, Biomedical Engineering, or related discipline). 

• Min 1 - 2 years of relevant experience in pharma or biotech facilities. 

• Knowledge of current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) in a pharma or biotech facility 

• Good interpersonal, communication and presentation skills. 

• Must be a self-starter, fast learner, curious with strong analytical and organizational skills

• Self-motivated and willingness to learn 

• Reliable and Responsible

  Duration: 06 months, renewable based on performance