ABOUT NO DEVIATION

At No deviation, we are dedicated to delivering patient-centric solutions that revolutionize the pharmaceutical landscape. As a dynamic expert in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we are looking for individuals who are excited to contribute to impactful projects and drive innovation.
We believe that great things happen when Empathy, Integrity, and Transparency guide our actions. That’s why we foster a culture of collaboration, inclusion, and continuous development – empowering our team members to grow personally and professionally.

POSITION OVERVIEW

We are seeking a QC Equipment & System Qualification Specialist with expertise in laboratory equipment qualification, including Mass Spectrometry (MS), Fourier Transform Infrared Spectroscopy (FTIR), and other analytical instruments. The ideal candidate will also have a strong understanding of Computer System Validation (CSV) in a regulated environment.
This role is crucial in ensuring that all Quality Control (QC) instruments and computerized systems meet compliance standards and function efficiently within GMP/GxP frameworks.

REQUIRED QUALIFICATIONS

• Bachelors or masters degree in chemistry, Analytical Science, Pharmaceutical Science, Engineering, or a related field.
• Experience in laboratory equipment qualification, specifically Mass Spec, FTIR, and other QC analytical instruments.
• Strong knowledge of Computer System Validation (CSV), 21 CFR Part 11, Data Integrity, and GAMP 5 guidelines.
• Familiarity with GMP, GLP, and regulatory requirements for pharmaceutical laboratories.
• Hands-on experience with LIMS, chromatography data systems, and electronic documentation systems is a plus.
• Excellent documentation, communication, and troubleshooting skills.
• Ability to work collaboratively with cross-functional teams, vendors, and regulatory bodies.

• Perform Qualification for Mass Spectrometry, FTIR, and other analytical instruments.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and regulatory guidelines (FDA, EMA, ICH, USP, etc.).
• Develop and execute qualification protocols, risk assessments, and validation reports.
• Collaborate with vendors and internal teams for instrument commissioning, calibration, and maintenance.
• Conduct Computer System Validation (CSV) activities for laboratory instruments and software systems following GAMP 5 guidelines.
• Ensure compliance with 21 CFR Part 11 and data integrity (ALCOA+ principles).
• Assist in software verification and validation (IQ, OQ, PQ) for laboratory data systems (e.g., LIMS, chromatography data systems, electronic lab notebooks).
• Work with IT and Quality teams to implement and maintain validated computerized systems.
• Maintain accurate and complete documentation for all qualification and validation activities.
• Conduct periodic reviews, requalification, and risk assessments of laboratory systems.
• Support audits and regulatory inspections by providing necessary qualification and validation records.
• Investigate deviations and implement corrective and preventive actions (CAPA) related to QC systems.