Quality Associate, Quality Processes (GCP training coordinator)

Ergomed Group

Pune District

On-site

INR 900,000 - 1,400,000

Full time

2 days ago
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Job summary

Ergomed Group seeks a Quality Associate in Quality Processes (GCP training coordinator) to support quality operations and training across the group. The role involves developing, managing, and implementing controlled procedures and ensuring alignment with regulatory standards.

With a university degree in biomedical or health sciences, you will assist in CAPA and deviation handling, participate in audits, and help maintain the quality management system.

Qualifications

  • GxP knowledge and regulatory awareness for Quality Operations.
  • Experience in training and development within quality processes.
  • Ability to support CAPA and deviation management.
  • Assist audits and inspections with GMP/GxP context.
  • Interpret and report quality metrics to leadership.

Responsibilities

  • Support development and implementation of Controlled Procedures.
  • Ensure GxP activities comply with ICH, CIOMS and ISO.
  • Provide guidance on quality systems within Ergomed Team.
  • Assist in Business Continuity planning and audits.
  • Prepare and analyze quality-related metrics for management.
  • Coach and develop team capability across global regions.

Skills

GxP knowledge
Training
CAPA management
Audit support
Quality metrics

Education

Biomedical sciences / Health Sciences degree

Job description

Quality Associate, Quality Processes (GCP training coordinator)
  • Full-time
  • Department: Quality Operations - Quality Process

Medicine moves forward here. So willyou.

Ergomed is a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most complextrials,the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.

We choose complex work on purpose. Rare disease and oncology trials carry real operational risk, and our people are experts at reducing it, protecting timelines, dataqualityand the experience of sites and patients at the same time. It is demanding, meaningful work, and no one here forgets that patients cannot wait.

That is why culture matters to us as much as capability. We have built a collaborative, international team where people share ideas, grow theircareersand are trusted to take ownership early. With colleagues across North America, South America, Europe,Asiaand Australia, we value teamwork,flexibilityand a real commitment to work-life balance, because good science comes from people who feel supported.

If you wantworkwith purpose, the agility to make an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you.

Leadership and Compliance:

  • Provide support to Ergomed colleagues and functional teams in developing, managing, and implementing Controlled Procedures.
  • Support GxP activities to ensure they are conducted in compliance with applicable legislation,guidelines, and standards, including ICH, CIOMS, and ISO.
  • May provide guidance to Ergomend group staff over procedures and requirements related toGxP Quality Operations and Training as required.

Training and Development:

  • Support GxP training activities across the Ergomed group, helping to ensure employees areadequately trained to meet global GxP requirements and client expectations, with supportfrom the Learning and Development team.
  • Support GxP training to ensure it is efficient and effective and that training activities aretracked to completion
  • Partner with Learning and Development to assist in the development of effective training

Quality Management System Oversight:

  • May assist in the triage and management of processes controlling access to Ergomed GroupQuality Management System.
  • Participate in efficiency projects to enhance the use and management of the Ergomed GroupQuality Management System.
  • Ensure access requests to Controlled Systems for employees and clients are correctlymanaged.

Business Continuity and Audit Support:

  • Assist in Business Continuity activities across the Ergomed Group.
  • Provide support to functional and Quality teams for audits and inspections by supplyingreports or procedures from the Ergomed Group Quality Management System.

Metrics and Reporting:

  • Aid the preparation and analysis of Quality Operations and Training related metrics, providingdata and periodic reports to management as required.
  • Assist in preparing any required CAPA or Deviation records resulting from issues in theControlled Document, GxP Training or BCP process.

Team Leadership and Development

  • Aid in fostering a collaborative, high‑performing quality culture across global teams andregions.
  • Provide coaching and professional development opportunities to enhance team capabilityand succession planning.

University degree in Biomedical sciences, Natural sciences or Health
Sciences is required: Nursing, Pharmacy or BS/Master’s degree in a
scientific discipline, or suitable experience

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