Quality Control LIMS Specialist

Why This Role Matters
This role plays a vital part in maintaining quality systems and regulatory compliance within pharmaceutical manufacturing. By managing LIMS and driving QC training initiatives, you ensure data integrity, audit readiness, and adherence to global standards like USFDA and GMP—directly contributing to product quality and patient safety.

Job Description
Oxalis Labs is hiring for the position of Quality Control Officer/Senior Officer in the Training/LIMS section. This role focuses on managing laboratory systems, conducting training programs, and ensuring compliance with global regulatory standards in a USFDA-approved manufacturing environment.

Key Features of the Role:
• Opportunity to work in a USFDA-approved pharmaceutical facility
• Hands-on experience with LIMS (Laboratory Information Management System)
• Involvement in QC training and capability development
• Exposure to audits and global regulatory standards
• Strong career growth in Quality Control and compliance functions

Responsibilities
• Manage and maintain Laboratory Information Management System (LIMS)
• Conduct training programs for QC team members and track training effectiveness
• Ensure compliance with USFDA, GMP, and other regulatory guidelines
• Handle documentation related to QC processes and training records
• Support internal and external audits, including regulatory inspections
• Maintain data integrity and accuracy within QC systems
• Coordinate with cross-functional teams for continuous quality improvement
• Monitor adherence to SOPs and quality standards

Required Qualifications
• Strong understanding of QC processes and regulatory compliance
• Knowledge of LIMS and training systems preferred
• Familiarity with GMP and data integrity principles

Educational Requirements:
• B.Pharm
• M.Pharm
• M.Sc (relevant specialization)

Experience and Skills:
• 3–6 years of experience in Quality Control
• Hands-on experience in LIMS and/or QC training activities preferred
• Strong documentation and audit handling skills
• Good communication and training delivery capability
• Attention to detail and problem-solving mindset
• Ability to work in cross-functional teams
• Understanding of regulatory inspections and compliance frameworks

Salary Insights
• Estimated salary range: ₹3.5 LPA – ₹6.5 LPA (based on experience)

Company Overview
Oxalis Labs is a USFDA-approved pharmaceutical manufacturing organization known for its adherence to global quality standards. The company offers a strong platform for professionals to gain exposure to regulatory environments, advanced quality systems, and continuous learning opportunities in the pharma industry.

FAQs
• Is LIMS experience mandatory?
It is preferred, especially for candidates applying for senior roles.

• What kind of audits will I be exposed to?
You may work on USFDA audits and other regulatory inspections.

• Is this a pure QC role?
It is a specialized QC role focusing on LIMS management and training functions.

• What is the career growth path?
QC Officer → Senior Officer → QC Manager → Quality Systems/Compliance Lead

Application Tips
• Highlight your experience with LIMS and QC documentation
• Mention any involvement in audits or regulatory inspections
• Showcase training or mentoring experience if applicable
• Emphasize knowledge of GMP and data integrity
• Prepare examples of process improvements or quality initiatives