Officer Regulatory Affairs Jobs Orion Pharma in Mumbai 2026
If you are searching for Regulatory Affairs jobs in pharmaceutical companies, this opportunity could be an excellent career move. Orion Pharma is hiring an Officer Regulatory Affairs professional with experience in lifecycle management, regulatory documentation, and compliance activities. Candidates with strong knowledge of regulatory guidelines and submission processes are encouraged to apply for this full-time pharmaceutical regulatory job.
This role offers a chance to work with regulatory experts, manage regulatory documentation, and support regulatory submissions across various pharmaceutical products. If you have relevant experience in regulatory affairs and want to advance your pharmaceutical career, this opportunity may be ideal for you.
About Orion Pharma
Orion Pharma is a pharmaceutical organization focused on regulatory compliance, quality standards, and efficient lifecycle management of pharmaceutical products. The company works closely with international regulatory guidelines and ensures that pharmaceutical products meet global compliance standards. Working at Orion Pharma provides professionals with exposure to regulatory documentation, submission processes, and collaboration with global regulatory stakeholders.
Orion Pharma Regulatory Affairs Job Overview
| Job Title | Officer Regulatory Affairs |
| Company Name | Orion Pharma |
| Location | Mumbai Metropolitan Region |
| Employment Type | Full Time |
| Application Deadline | Not Available |
| Category | Latest Pharma Walk-in Interview |
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 will be an added advantage.
- Knowledge of EU regulations and ICH guidelines will be an advantage.
- Strong English communication skills.
- Ability to work effectively in a team environment.
- Strong organizational and documentation skills.
- Teamwork skills.
- Proficiency in MS Office Software Package (Word, Excel, PowerPoint).
- Knowledge of Adobe Acrobat and Internet resources.
Preferred or Bonus Skills
- eCTD submission experience will be an added advantage.
- 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. Selected candidates may receive compensation according to industry standards along with professional growth opportunities within the regulatory affairs domain.
Job Position Details
| Post | Officer Regulatory Affairs |
| Department | Regulatory Affairs |
| Qualification and Experience | Bachelor’s degree in science from a reputed college or university with preferably 2–3 years of experience within the regulated industry. |
| Job Responsibility and Skill | Lifecycle management of products, regulatory compliance, documentation management, regulatory submissions, coordination with internal and external stakeholders. |
How to Apply
Interested candidates can apply by submitting their updated CV and required documents before the application deadline. Make sure to include your current CTC, expected CTC, and notice period details while applying.
- Prepare an updated resume.
- Attach relevant academic and professional documents.
- Mention current CTC, expected CTC and notice period.
- Submit the application before the deadline.
Interview Tips for Regulatory Affairs Jobs
- Revise regulatory guidelines such as ICH and EU regulations before the interview.
- Understand regulatory documentation and submission processes.
- Prepare examples of lifecycle management experience.
- Be ready to discuss teamwork and communication skills.
- Review MS Office and documentation tools used in regulatory affairs.
Career Growth and Related Opportunities
Regulatory Affairs professionals have strong career growth in the pharmaceutical industry. With experience, professionals may progress to roles such as Senior Regulatory Affairs Officer, Regulatory Affairs Manager, Global Regulatory Specialist, or Compliance Manager. These roles involve managing regulatory strategies, handling international product submissions, and ensuring regulatory compliance for pharmaceutical products worldwide.
Officer Regulatory Affairs Jobs Orion Pharma FAQs
What qualification is required for Officer Regulatory Affairs at orion Pharma?
A Bachelor’s degree in science from a reputed college or university is required.
How much experience is required for this job?
Preferably 2–3 years of experience within the regulated industry is required.
What skills are important for Regulatory Affairs jobs?
Knowledge of EU regulations, ICH guidelines, regulatory documentation, MS Office skills, and strong communication abilities are important.
Is eCTD experience required?
eCTD submission experience is not mandatory but will be considered an added advantage.
Conclusion
The Officer Regulatory Affairs job at Orion Pharma is a great opportunity for candidates who want to grow in the pharmaceutical regulatory field. The role involves lifecycle management, regulatory documentation, and regulatory submission activities. Candidates with regulatory knowledge and industry experience should consider applying for this role to advance their career in pharmaceutical regulatory affairs.
