Orion Pharma Hiring Officer – Regulatory Affairs (Assistant Role)

Orion Pharma Hiring Regulatory Affairs Officer in Mumbai – Life Science Graduates Can Apply

Orion Pharma has announced a new hiring opportunity for the position of Officer – Regulatory Affairs within its Regulatory Affairs department. The role is based in Mumbai, India with a hybrid work model, offering a strong career pathway for professionals interested in global pharmaceutical regulatory affairs and drug approval processes.

The company is looking for candidates with 2–3 years of experience in pharmaceutical or regulated healthcare environments who can support regulatory submissions, lifecycle management, and compliance documentation. For life science and pharmacy graduates aiming to build careers in regulatory affairs, drug registration, and pharmaceutical compliance, this position offers valuable exposure to global regulatory systems.

Professionals joining this role will work closely with regulatory specialists and cross‑functional teams to ensure pharmaceutical products meet international regulatory guidelines and quality standards before reaching patients.

Company Overview

Orion Pharma is a globally recognized Nordic pharmaceutical company headquartered in Finland with more than 100 years of experience in advancing healthcare innovation. The organization develops, manufactures, and markets human and veterinary medicines as well as active pharmaceutical ingredients.

The company operates across several international markets and employs over 4,000 professionals worldwide. Orion’s pharmaceutical portfolio includes proprietary medicines, generic formulations, and consumer health products used by patients across multiple therapeutic areas.

Job Role & Responsibilities

The Officer – Regulatory Affairs will support Orion Pharma’s regulatory team by ensuring pharmaceutical products comply with international regulatory guidelines and internal quality systems. The role involves managing documentation, supporting global submissions, and maintaining regulatory records.

Key responsibilities include:

• Managing lifecycle activities for assigned pharmaceutical products according to regulatory policies
• Ensuring product compliance with applicable regulatory guidelines and internal procedures
• Maintaining Orion’s internal regulatory systems with accurate and up‑to‑date information
• Managing regulatory archives and ensuring licenses and labeling documentation remain current
• Coordinating with internal departments and external stakeholders to manage regulatory changes
• Supporting electronic formatting and preparation of global regulatory submissions
• Assisting with documentation required for regulatory filings and compliance reviews
• Following defined internal policies and quality procedures while handling regulatory documentation
• Supporting administrative and regulatory tasks assigned by regulatory supervisors

This position plays an important role in maintaining compliance with international pharmaceutical regulations while ensuring smooth product lifecycle management.

Eligibility / Qualifications

Candidates applying for this regulatory affairs position should have strong attention to detail, regulatory knowledge, and the ability to coordinate with cross‑functional teams in a pharmaceutical environment.

Educational Qualification

Candidates must hold a Bachelor’s degree in science or life sciences from a recognized university.

Relevant educational backgrounds include:

B.Pharm, M.Pharm, Pharm.D, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Pharmaceutical Sciences, MSc Clinical Research.

Preferred Experience and Skills

Candidates should ideally possess the following experience and competencies:

• 2–3 years of experience in pharmaceutical, biotechnology, or regulated healthcare environments
• Knowledge of product lifecycle management within pharmaceutical regulatory systems
• Familiarity with international regulatory guidelines such as ICH standards
• Understanding of European Union regulatory requirements will be an advantage
• Experience with electronic regulatory submissions including eCTD formats is beneficial
• Strong written and verbal communication skills in English
• Ability to collaborate with cross‑functional teams across regulatory, quality, and clinical departments
• Proficiency in Microsoft Office tools such as Word, Excel, PowerPoint, and Outlook
• Experience working with documentation tools such as Adobe Acrobat and digital regulatory systems

Candidates should also demonstrate strong organizational ability, teamwork skills, and a proactive approach to learning regulatory processes.

Location & Salary

Location: Mumbai, India (Hybrid work model)

Office Location:
Smartworks Coworking – Times Square Building, C Wing, 9th Floor, Andheri Marol, Andheri East, Mumbai.

Application Process

Interested candidates can apply by sending their updated CV directly to Orion Pharma’s recruitment team via email.

Email Application: recruitmentindia@orion.fi

More information click here 

Applicants must include the following details while submitting their application:

• Updated CV / Resume
• Current CTC
• Expected CTC
• Notice Period

Application Deadline: 27 February 2026

Candidates are encouraged to apply early since regulatory affairs roles in multinational pharmaceutical companies often receive high numbers of applications from pharmacy and life science professionals.

Frequently Asked Questions (FAQs)

Who can apply for the Orion Pharma Regulatory Affairs Officer role?

Candidates with a bachelor’s degree in pharmacy or life sciences such as B.Pharm, M.Pharm, Pharm.D, Biotechnology, Microbiology, Biochemistry, or related disciplines can apply if they meet the experience requirements.

Is regulatory affairs experience mandatory?

Yes. Candidates with approximately 2–3 years of experience in pharmaceutical regulatory affairs or regulated industry environments are preferred for this role.

What skills are important for regulatory affairs jobs?

Important skills include regulatory documentation management, knowledge of international guidelines like ICH, product lifecycle management, electronic regulatory submissions, and strong attention to detail.

Where is the job located?

The role is located in Mumbai with a hybrid work arrangement, allowing flexibility between office and remote work.

How do I apply for the Orion Pharma vacancy?

Candidates must send their CV along with current salary, expected salary, and notice period details to the official Orion Pharma recruitment email address.

Summary

Company	Orion Pharma
Vacancies	Officer – Regulatory Affairs
Required Education	B.Pharm, M.Pharm, Pharm.D, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, BSc Life Sciences, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Pharmaceutical Sciences, MSc Clinical Research
Experience	2–3 Years Pharmaceutical Regulatory Affairs / Regulated Industry Experience

Tagged as: Pharma Jobs in Mumbai