CNX Therapeutics is recruiting for two Quality department positions in Mumbai, Maharashtra, with fully remote work arrangements. The openings are for Executive, Quality Assurance and Executive, Quality Systems.

These opportunities are suitable for candidates with a life sciences background or equivalent practical pharmaceutical quality experience and exposure to GMP or GxP-regulated environments. The roles focus on pharmaceutical quality compliance, supplier management, Quality Management Systems (QMS), documentation, audits, and continuous improvement.

CNX Therapeutics Recruitment 2026: Job Details

Positions Available

1. Executive, Quality Assurance

The Executive, Quality Assurance will support GMP compliance, supplier assurance, and Marketing Authorisation Holder (MAH) oversight. The role involves coordinating supplier audits, managing quality documentation, supporting product quality reviews, and maintaining inspection readiness.

Key Responsibilities

• Support GMP compliance and MAH oversight activities.
• Coordinate supplier audits, track observations, and follow up on corrective and preventive actions (CAPAs).
• Support supplier onboarding, qualification, and lifecycle management.
• Maintain and periodically review Quality Technical Agreements.
• Coordinate Product Quality Reviews and stability programmes.
• Review and maintain validation documentation, manufacturing documentation, and pharmacopoeial compliance assessments.
• Support quality events, investigations, change controls, and supplier-related quality issues.
• Maintain quality trackers, schedules, metrics, and performance data.
• Support product launches, technology transfers, acquisitions, and improvement projects.

Eligibility and Qualifications

• Degree in a life science subject, such as pharmacy, chemistry, biology, or biochemistry, or equivalent practical experience in pharmaceutical quality assurance.
• Experience working in a GMP-regulated environment, ideally in quality assurance or a related function.
• Working knowledge of supplier assurance and GMP.
• Good Excel skills and the ability to maintain trackers, schedules, and metrics.

Desirable Skills

• Exposure to Quality Technical Agreements, Product Quality Reviews, and stability programmes.
• Knowledge of EU/UK GMP guidance, ICH quality guidelines, and pharmacopoeial standards.
• Experience with an electronic quality management system.
• Audit training or experience supporting audits.

2. Executive, Quality Systems

The Executive, Quality Systems will support the maintenance and continuous improvement of the company’s Quality Management System (QMS). The role covers electronic quality management system administration, document control, deviations, CAPAs, change controls, complaints, and audit preparation.

Key Responsibilities

• Maintain and improve the QMS to support compliance with GMP, GDP, and applicable regulatory requirements.
• Administer the electronic Quality Management System (eQMS), including document control, user administration, record management, and archiving.
• Review and coordinate controlled documents, including SOPs, policies, work instructions, and forms.
• Maintain training matrices and coordinate role-based training through the eQMS.
• Support deviations, CAPAs, change controls, complaints, and root cause investigations.
• Monitor overdue actions and support corrective and preventive action effectiveness reviews.
• Assist with internal audits, regulatory inspections, customer audits, and supplier audits.
• Manage incoming product quality complaints and customer quality communications.
• Conduct administrative batch documentation reviews.
• Track quality metrics and KPIs and prepare data for Quality Management Review.
• Maintain confidentiality and uphold GDPR requirements.

Eligibility and Qualifications

• Degree in a life science subject, such as pharmacy, chemistry, biology, or biochemistry, or equivalent practical experience in pharmaceutical quality.
• Experience in a GxP-regulated environment, ideally in quality assurance or quality systems.
• Working knowledge of document control, deviations, CAPA, and change control.
• Good Excel skills and confidence working with metrics and reports.
• Strong analytical, communication, and documentation skills.

Desirable Skills

• Experience administering an electronic quality management system.
• Knowledge of GMP and GDP requirements.
• Exposure to complaint handling, supplier qualification, or batch documentation review.
• Internal audit training or experience supporting audits and inspections.
• Experience delivering training to colleagues.
• Awareness of GDPR and data protection principles.

Common Skills Required

Candidates applying for either position should demonstrate relevant skills based on the specific role requirements.

• Regulatory compliance: Understanding of applicable GMP or GxP requirements.
• Documentation management: Maintaining accurate, complete, and controlled quality records.
• Analytical skills: Identifying discrepancies, investigating issues, and supporting corrective actions.
• Communication: Coordinating with internal teams, suppliers, service providers, and other stakeholders.
• Organisation: Managing multiple priorities, tracking actions, and meeting deadlines.
• Continuous improvement: Supporting quality initiatives and strengthening compliance processes.

Salary and Benefits

CNX Therapeutics offers a competitive salary and benefits package in line with local practices and statutory requirements. Further details will be shared during the recruitment process.

Application Details

Application Link For Executive, Quality Assurance

Application Link For Executive, Quality Systems