12 Compliance Training jobs in India

Job Title: Senior Microbiology Trainer – Medical Devices

Location: Remote

Job Type: Part-time

Job Summary:

We are seeking an experienced Microbiologist with over 10 years of hands-on expertise in microbiology, sterilization, and quality assurance in the medical devices industry. The ideal candidate will design, develop, and deliver training programs to enhance the knowledge and technical capabilities of staff across R&D, quality control, manufacturing, and regulatory teams. The trainer will ensure compliance with global standards, including ISO 13485, FDA, and GMP requirements.

Key Responsibilities:

• Design and deliver training programs on microbiology concepts, testing methods, and aseptic processing techniques relevant to medical devices.
• Develop curriculum covering sterility testing, bioburden testing, microbial limit testing, endotoxin testing, and cleanroom practices.
• Conduct hands-on workshops, practical demonstrations, and assessments for lab personnel and manufacturing teams.
• Stay updated on latest industry trends, regulatory requirements, and technological advancements in microbiology.
• Collaborate with cross-functional teams (QA/QC, Production, R&D) to identify training needs.
• Ensure all training programs meet compliance standards and are documented properly.
• Mentor junior microbiologists and support their professional development.
• Review and update training materials, SOPs, and protocols as per regulatory changes.

Qualifications & Experience:

• Master’s or Ph.D. in Microbiology, Biotechnology, or related field.
• Minimum 10 years of experience in microbiology within the medical devices or pharmaceutical industry.
• Hands-on experience with sterility testing, microbial limit tests, endotoxin testing, environmental monitoring, and aseptic techniques.
• Strong knowledge of regulatory standards: ISO 13485, ISO 14698, USP <
  71>
  , FDA, and GMP.
• Proven experience in delivering technical training and preparing training materials.
• Excellent communication, presentation, and mentoring skills.
• Experience with cleanroom operations and GMP documentation preferred.

Key Competencies:

• Deep understanding of microbiological principles and testing methods.
• Ability to translate complex technical concepts into effective training modules.
• Strong analytical and problem-solving skills.
• Attention to detail and commitment to quality and compliance.

Job Title: Clinical Quality Assurance Compliance & training

Experience : 5 plus years

Location: Mumbai

Type: Full-time

Experience Level: (Senior) Manager/Senior Manager

Department: Clinical Research Department

Purpose of this Role:

This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness. This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.

Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices.  Identify and decide team member’s job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required. Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team. uality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement. uality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring – site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement.

Required & Preferred Skills : • .

5 years’ experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department.  Stro eye for detail and ability to spot inconsistencies a must and good conflict management skills. ust have experience in handling audits & inspections of DCGI, US FDA. horough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials. xperience of working in matrix business environments preferred. trong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

We are seeking an experienced professional to deliver training sessions on workplace safety and compliance, empowering organizations to create a culture of respect and inclusivity.

This is an excellent opportunity for those passionate about making a positive impact in the workplace. As a safety and compliance expert, you will:

• Develop and deliver comprehensive training programs on the Prevention of Sexual Harassment Act and workplace conduct.
• Train employees, HR professionals, and management on legal duties, responsibilities, and reporting procedures.
• Collaborate with organizations to establish and maintain Internal Committees (ICCs).
• Represent our organization in corporate CSR programs and awareness campaigns.

You will receive attractive per-session remuneration, flexible scheduling, exposure to top corporates, national recognition as a certified safety and compliance trainer, networking opportunities within HR, legal, and corporate training communities, and long-term engagement opportunities with our CSR initiatives.

A free Train-the-Trainer & Orientation Program will be provided to shortlisted candidates, equipping them with expert knowledge on the POSH Act 2013 and workplace compliance, ready-to-use PPTs, scripts, and activity tools, and a national-level trainer code under our organization.

To succeed in this role, you should have:

• Proven experience in delivering training sessions on workplace safety and compliance.
• Strong knowledge of the Prevention of Sexual Harassment Act and related laws.
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively as part of a team.

Join us in shaping a safer and more respectful workplace culture. Apply now to take your career to the next level!

Becoming a Safety and Compliance Trainer with Us:

We offer a unique opportunity to gain expertise in workplace safety and compliance, develop valuable skills, and make a positive impact in the lives of others. Our trainers are equipped with the latest knowledge, tools, and resources to deliver high-quality training programs that drive real results.

Your Benefits:

• Attractive per-session remuneration.
• Flexible scheduling.
• National recognition as a certified safety and compliance trainer.
• Networking opportunities within HR, legal, and corporate training communities.
• Long-term engagement opportunities with our CSR initiatives.

Job Title: Clinical Quality Assurance Compliance & training

Experience : 5 plus years

Location: Mumbai

Type: Full-time

Experience Level: (Senior) Manager/Senior Manager

Department: Clinical Research Department

Purpose of this Role:

This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness. This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.

Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices. Identify and decide team member’s job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required. Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team. Quality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement. Quality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring – site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement.

Required & Preferred Skills : • .

5 years’ experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department. Strong eye for detail and ability to spot inconsistencies a must and good conflict management skills. Must have experience in handling audits & inspections of DCGI, US FDA. Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials. Experience of working in matrix business environments preferred. Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

Job Title: Clinical Quality Assurance Compliance & training

Experience : 5 plus years

Location: Mumbai

Type: Full-time

Experience Level: (Senior) Manager/Senior Manager

Department: Clinical Research Department

Purpose of this Role:

This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be accountable for Quality Compliance (QC) activities of Clinical Trial Medical Science team and Operations team, Clinical Trial Supply Management (CTSM) team, and Clinical Data Management team by way of Review of all study related activities, processes, procedures and adherence to applicable regulations and guidelines to ensure 24x7 Inspection/audit readiness. This role will be responsible for establishing the procedures and trainings of teams which ensure protection of human subjects from research risk, reliability/Integrity of the data, and thereby assures internal consistency and Quality Compliance measures.

Develop and implement a risk-based and flexible approach to Quality Compliance (QC) within the function, which will ensure that trial participants and data are safeguarded in compliance with applicable regulatory requirements and best practices. Identify and decide team member’s job specific SOP training requirements in view of their role and maintain oversight of training to ensure all team members are trained on each SOP as required. Preparation of SOPs related to QC function and support in review of SOPs specific to Medical science, Clinical team and Data Management team. Quality review of the clinical trial medical science related activities like Synopsis, Protocol, Clinical Study Report (CSR) and appendices, and SOPs in line with ICH GCP requirement, Indian and global regulatory requirement. Quality review of the clinical trial operation related activities, related tools, plans and documentation like site feasibility, site selection visit, site initiation, Ethic committee documentation, monitoring – site specific reports, Site Documents, logs and close out activities in line with ICH GCP requirement, Indian and global regulatory requirement.

Required & Preferred Skills : - .

5 years’ experience in a CRO/Pharma/Biotech organization in Quality department with experience of Quality activities in Clinical Research department. Strong eye for detail and ability to spot inconsistencies a must and good conflict management skills. Must have experience in handling audits & inspections of DCGI, US FDA. Thorough knowledge of recent GCP guidelines, ICMR guidelines, Drugs and Cosmetic Act regulations and other applicable regulations pertaining to clinical trials. Experience of working in matrix business environments preferred. Strong track record of success as demonstrated through annual performance ratings and/or professional accomplishments and awards.

• Conduct training needs analysis in collaboration with business stakeholders.
• Develop training modules on banking operations, financial products, KYC/AML, and customer service.
• Deliver classroom, virtual, and on-the-job training sessions.
• Evaluate training effectiveness through assessments and feedback.
• Maintain training records and generate performance reports.
• Continuously update content based on regulatory changes and business needs.
• Improved process accuracy and compliance scores.
• Enhanced employee confidence and customer satisfaction.
• Reduced onboarding time for new hires.
• Increased productivity and reduced rework.
• Equip new hires and existing employees with in-depth knowledge of BFSI processes.
• Ensure compliance with industry regulations and internal policies.
• Improve customer handling skills and operational efficiency.
• Reduce process errors and enhance quality metrics.
• Support digital transformation through upskilling in fintech tools and platforms.