Job Description

Title: Maintenance Manager

Location: Verna, Goa

Experience: 10+ years in the Pharma, Manufacturing or Chemical Industry

OVERVIEW

We are seeking an experienced and detail-oriented QMS Head to lead our Quality Management initiatives and ensure compliance with the highest manufacturing and regulatory standards. The ideal candidate will bring deep expertise in ISO, GMP, and API quality systems, with a proven ability to drive continuous improvement and uphold a culture of quality excellence across all departments.

Key responsibilities:

Develop, implement, and maintain the organization's Quality Management System (QMS) in compliance with ISO, GMP, and other relevant manufacturing standards. Ensure full compliance with regulatory, statutory, and customer-specific quality requirements. Lead, mentor, and develop the QA/QC teams, fostering a culture of accountability, precision, and continuous improvement. Monitor and report on quality performance metrics, identifying trends and executing corrective measures where necessary. Conduct and manage internal audits, and coordinate external audits by customers, certification bodies, and regulatory agencies. Plan, conduct, and oversee API audits, ensuring supplier and process compliance with cGMP and industry standards. Manage and oversee Corrective and Preventive Actions (CAPA) related to process deviations and audit findings. Oversee all quality documentation and record management as per QMS requirements. Collaborate cross-functionally with Production, R&D, Maintenance, Procurement, and Supply Chain to embed quality standards at every stage. Lead risk assessments, process validations, and equipment verification to ensure compliance and operational efficiency. Stay updated on industry regulations, ISO and GMP guidelines, and quality best practices to align the organization with global standards.

Qualifications:

Bachelor's or Master's degree in Engineering or a related technical field. 10-15 years of experience in Quality Management within a manufacturing environment, preferably in the pharmaceutical or API sector. Proven expertise in implementing and improving QMS frameworks aligned with ISO and GMP standards. Strong hands-on experience with API supplier audits and vendor compliance management. Comprehensive understanding of ISO 9001, GMP, FDA, and other regulatory frameworks. Lead Auditor Certification is mandatory. Strong leadership skills with the ability to manage cross-functional quality teams and influence strategic decision-making. Excellent analytical, communication, and problem-solving abilities.
Job Types: Full-time, Permanent

Ability to commute/relocate:

Verna, Goa: Reliably commute or planning to relocate before starting work (Required)
Application Question(s):

What is your current CTC? (in LPA) What is your expected CTC? (in LPA) What is your notice period? Do you have experience in the Chemical / Manufacturing / Machinery industry?
Experience:

API (American Petroleum Institute): 10 years (Required)
License/Certification:

Lead Auditor Certificate (Required)
Location:

Verna, Goa (Required)
Work Location: In person