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

The Quality Control (QC) Data Load Specialist is responsible for supporting laboratory operations through effective sample management, data handling, and analytical testing in a regulated life sciences environment. This role involves working with Laboratory Information Management Systems (LIMS), operating analytical instruments, and preparing and maintaining Standard Operating Procedures (SOPs) to ensure data integrity and compliance with cGMP, GLP, GDP, and internal quality standards. The QC Specialistwill collaborate with cross-functional teams while maintaining a high level of accuracy, attention to detail, and commitment to continuous learning and quality excellence.

Key Responsibilities

Manage sample workflows and data handling using LIMS, including setting up templates and ensuring accurate data entry.
Prepare and maintain SOPs for site-specific data load processes and QC operations.
Ensure compliance with cGMP, GLP, GDP, and company quality standards.
Attention to detail, problem-solving skills, and ability to work independently or in a team environment

Required Qualifications

Degree in a relevant Science field or Equivalent
Relevant work experience in Lab experience in a lifescience field would be advantage
1-3 years experience in QC
Demonstrates an ability and desire to learn from experience
Uses knowledge of his/her business area to make accurate and timelydecisions
Ensures quality standards are maintained while delivering results
Experience in QC analytical techniques, method development, and validation.
Hands-on experience with LIMS for sample management and data handling.
Proficiency in operating analytical instruments.
Experience in creating SOP and supporting documentation processes.

Why join us

Generous Leave Policy.
Comprehensive Health & Wellness Coverage: Receive robust medical and dental coverage to support your health needs.
Professional Development Opportunities: Access continuous learning programs and resources for career growth within the company.
Inclusive Culture: Work in an environment where innovation, collaboration, and diverse perspectives are encouraged and celebrated.
Shape the Future: Make a real difference in the pharmaceutical industry while advancing your career.

How To Apply

Are you ready to play a key role in shaping the future of pharmaceutical solutions If you're passionate about making an impact, we want you on our team!

Please submit your resume, outlining your qualifications and experience relevant to the role, here.

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