Job Description

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 3 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
Job Type: Contract
Contract length: 6 months

Pay: $5,000.00 - $7,500.00 per month