Pharma QMS Job Openings at VINS Bioproduct Ltd
Professionals aiming to build a career in pharmaceutical quality systems can explore Pharma QMS Job Openings at VINS Bioproduct Ltd, a strong opportunity for science and pharmacy graduates with experience in quality management systems. These openings are ideal for candidates seeking hands-on exposure to GMP, GDP compliance, audit readiness, and documentation control within a regulated biopharmaceutical manufacturing environment.
VINS Bioproduct Ltd – QMS (Quality Management System) Role
Company: VINS Bioproduct Ltd
Role: QMS (Quality Management System)
Department: Quality Assurance (QA)
Location: Hyderabad, Karnataka
Employment Type: Full-time
Mode of Interview: Online
VINS Bioproduct Ltd is looking for a knowledgeable and experienced QMS professional to manage and strengthen the Quality Management System in compliance with regulatory and company quality standards. The role is critical in maintaining documentation control, audit readiness, and continuous quality improvement across the organization.
Key Responsibilities
· Implement, maintain, and continuously improve the Quality Management System (QMS)
· Prepare, review, issue, revise, and control SOPs, policies, manuals, formats, and records
· Manage document control systems, including document numbering, version control, archival, and retrieval
· Handle deviations, change controls, incidents, OOS, OOT, and CAPA processes
· Track and ensure timely closure of CAPA and quality events
· Coordinate and support internal audits, external audits, and regulatory inspections
· Prepare audit responses, follow-ups, and compliance reports
· Manage training systems, including training matrices, training schedules, and training records
· Monitor quality metrics, KPIs, and compliance indicators
· Ensure compliance with GMP, GDP, and regulatory guidelines
· Support continuous improvement and risk management initiatives
· Coordinate with cross-functional teams to ensure quality system effectiveness
Requirements
· Proven hands-on experience in Quality Management System (QMS) activities
· Strong knowledge of GMP, GDP, SOPs, and pharmaceutical quality systems
· Experience in handling documentation, audits, and regulatory compliance
· Familiarity with CAPA, change management, deviation management, and risk assessment
· Ability to work independently and manage multiple quality activities
· Strong analytical, organizational, and problem-solving skills
· Good communication and interdepartmental coordination skills
· Ability to work in a regulated pharmaceutical or life sciences environment
Qualification
· Any Science discipline (B.Sc / M.Sc)
· Pharmacy qualification (B.Pharm / M.Pharm)
· Proven experience in QMS is mandatory
Salary
· Salary will be based on previous CTC and interview performance
