Quality Assurance Executive

Synokem Pharmaceuticals Limited is inviting applications for the position of Quality Assurance Executive at its manufacturing facility located in Haridwar, Uttarakhand. This opportunity is ideal for B.Pharm professionals with 3 to 6 years of relevant experience in the pharmaceutical industry. The selected candidate will play an important role in maintaining quality systems, ensuring compliance with GMP guidelines, supporting documentation activities, and contributing to continuous quality improvement initiatives. Candidates should possess strong knowledge of quality assurance processes, regulatory requirements, documentation practices, deviation management, and audit readiness. Working with a well-established pharmaceutical company like Synokem offers exposure to modern manufacturing practices, regulatory compliance frameworks, and opportunities for long-term professional growth in quality management. Professionals seeking to advance their career in pharmaceutical quality assurance are encouraged to apply for this rewarding opportunity.

Location

Haridwar, Uttarakhand, India

Employment Type

Full-time

Experience Required

3 to 6 years

Educational Qualification

B.Pharm

Key Responsibilities

• Review and approve batch manufacturing records and batch packaging records for compliance.
• Ensure implementation and adherence to GMP, GDP, and company quality standards.
• Handle deviations, investigations, CAPA activities, and change control documentation.
• Support internal audits, self-inspections, and regulatory audit preparedness activities.
• Review SOPs, protocols, specifications, and validation documents.
• Monitor documentation practices across manufacturing and quality departments.
• Coordinate with production, QC, and warehouse teams to resolve quality-related issues.
• Participate in qualification and validation activities as per regulatory requirements.
• Ensure timely closure of quality events and maintain compliance records.
• Assist in training employees on quality systems and compliance procedures.

Required Skills & Competencies

• Strong understanding of pharmaceutical quality assurance systems.
• Knowledge of GMP, GDP, and regulatory compliance requirements.
• Experience in deviation investigation and CAPA management.
• Excellent documentation review and approval skills.
• Ability to manage quality records and compliance documentation.
• Good communication and cross-functional coordination abilities.
• Familiarity with audit preparation and regulatory inspections.
• Strong analytical and problem-solving capabilities.
• Attention to detail and commitment to quality standards.
• Proficiency in MS Office and quality documentation systems.

Why Join Synokem Pharmaceuticals Limited?

Synokem Pharmaceuticals Limited offers employees a professional work environment focused on quality, innovation, and regulatory excellence. The company provides opportunities to work with experienced pharmaceutical professionals, gain exposure to advanced manufacturing operations, strengthen regulatory knowledge, and build a successful long-term career within a growing pharmaceutical organization.