Officer Regulatory Affairs

Tyropharma; Mumbai; On-site; INR 600,000 - 800,000; Full time

Job summary

Tyropharma is seeking an Officer Regulatory Affairs to manage pharmaceutical product life cycles and ensure regulatory compliance. Ideal candidates will have a Bachelor’s degree in science and 2-3 years of experience in the regulated industry.

The role involves maintaining regulatory documentation, coordinating with teams, and supporting submission activities. Strong organizational and communication skills, along with knowledge of EU regulations, are essential for success in this position.

Qualifications

• Preferably 2–3 years of experience within the regulated industry.
• Experience in Pharmaceutical Regulatory Affairs is an added advantage.
• Ability to work effectively in a team environment.

Responsibilities

• Responsible for the life cycle management of assigned pharmaceutical products.
• Ensure compliance with regulatory requirements and international guidelines.
• Maintain and update regulatory documentation for product registrations.
• Coordinate with internal regulatory teams and external stakeholders.

Skills

Knowledge of EU regulations

Strong organizational skills

Strong English communication skills

Experience with eCTD submissions

Proficiency in MS Office

Education

Bachelor’s degree in science

Tools

Adobe Acrobat

Job description

Orion Pharma Hiring Officer Regulatory Affairs 2026

Orion Pharma is hiring an Officer Regulatory Affairs professional with experience in life‑cycle management, regulatory documentation, and compliance activities. Candidates with strong knowledge of regulatory guidelines and submission processes are encouraged to apply for this full‑time role.

About Orion Pharma

Orion Pharma is a pharmaceutical organization focused on regulatory compliance, quality standards, and efficient life‑cycle management of pharmaceutical products. The company collaborates closely with international regulatory guidelines to ensure global compliance.

Job Responsibilities

• Responsible for the life cycle management of assigned pharmaceutical products.
• Ensure compliance with regulatory requirements and international guidelines.
• Maintain and update regulatory documentation for product registrations.
• Coordinate with internal regulatory teams and external stakeholders for regulatory activities.
• Assist with submission activities related to regulatory filings.
• Support regulatory strategy planning and submission preparation.
• Manage documentation activities and regulatory records.
• Perform other regulatory responsibilities as assigned by supervisors.

Required Qualifications and Skills

• Bachelor’s degree in science from a reputed college or university.
• Preferably 2–3 years of experience within the regulated industry.
• Experience in Pharmaceutical Regulatory Affairs is an added advantage.
• Knowledge of EU regulations and ICH guidelines is an advantage.
• Ability to work effectively in a team environment.
• Strong organizational and documentation skills.
• Proficiency in MS Office Software Package (Word, Excel, PowerPoint).
• Knowledge of Adobe Acrobat and internet resources.
• Strong English communication skills.

Preferred or Bonus Skills

• Experience with eCTD submissions.
• Experience in lifecycle management and regulatory submissions.
• Ability to coordinate with cross‑functional teams.
• Knowledge of international regulatory requirements.

Salary and Benefits

The salary for this role is as per company norms, with compensation aligned to industry standards and opportunities for professional growth within regulatory affairs.

Job Position Details

Post: Officer Regulatory Affairs
Department: Regulatory Affairs
Qualification and Experience: Bachelor’s degree in science with preferably 2–3 years of regulated industry experience.
Key Responsibilities: Lifecycle management, regulatory compliance, documentation management, regulatory submissions, coordination with stakeholders.

Conclusion

The Officer Regulatory Affairs position at Orion Pharma offers a clear career path for professionals skilled in regulatory strategy, documentation, and life‑cycle management. Candidates with regulatory knowledge and industry experience should consider applying to advance their career in pharmaceutical regulatory affairs.