ProductLife Group (PLG) is hiring a Regulatory Affairs Officer – UK Regulations in India, with remote work possible. This is a permanent opportunity for regulatory affairs professionals with 4–6 years of experience in UK and European regulations.
The role focuses on regulatory activities across the product lifecycle, including pre-licensing, new registrations, post-licensing submissions, regulatory dossiers, health authority interactions, labelling, and ongoing regulatory support. ProductLife Group’s regulatory operations services cover areas such as regulatory information management, dossier publishing, labelling, translations and other lifecycle activities.
Position: Regulatory Affairs Officer – UK Regulations
Company: ProductLife Group
Location: India
Work Arrangement: Remote work possible
Employment Type: Permanent
Experience: 4–6 years
Specialization: Regulatory Affairs & Operations
Regulatory Expertise: UK & European Regulations
By PharmaBharat Editorial Team
ProductLife Group Regulatory Affairs Officer Job – Key Highlights
| Job Detail | Information |
|---|---|
| Company | ProductLife Group |
| Job Role | Regulatory Affairs Officer |
| Regulatory Focus | UK & European Regulations |
| Location | India |
| Remote Work | Possible |
| Experience | 4–6 years |
| Education | Bachelor’s degree or higher in a science-related field |
| Employment | Permanent |
| Function | Regulatory Affairs & Operations |
Regulatory Affairs Officer Responsibilities
The selected candidate will support regulatory activities performed through ProductLife Group’s RA Platform and Hub. Key responsibilities include:
- Contribute to regulatory activities throughout the product lifecycle.
- Support pre-licensing regulatory activities.
- Assist with new registrations involving sites and medicinal products.
- Support post-licensing regulatory submissions.
- Interact with health authorities on behalf of ProductLife Group customers.
- Prepare client administrative documents and reports for regulatory submissions.
- Compile or supervise the compilation of regulatory dossiers according to national requirements.
- Manage and administer regulatory systems and documentation.
- Document and track regulatory submissions and regulatory authority approvals.
- Support activities required to obtain regulatory authority approval.
- Provide regulatory support to clients and associate companies.
- Liaise with sponsor head offices and affiliate departments on regulatory matters.
- Communicate with external regulatory authorities when required.
- Review the format and content of packaging texts, Summary of Product Characteristics (SmPC), Patient Information Leaflets (PILs), and product labelling.
- Review tasks and support or mentor Regulatory Affairs Associates.
- Provide ongoing regulatory support to Regulatory Affairs Specialists and project teams.
- Help ensure regulatory requirements are incorporated into project planning.
- Support generation of relevant regulatory data required to meet project objectives.
- Contribute regulatory data to PLG systems for KPI and service-performance measurement.
Eligibility Criteria
Experience
Candidates should have 4–6 years of professional experience in Regulatory Affairs, particularly with:
- UK regulatory requirements
- European regulatory requirements
- Pharmaceutical regulatory submissions
- Regulatory dossier compilation
- Health authority interactions
- Product lifecycle regulatory activities
- Labelling and packaging review
- Post-approval regulatory activities
Experience working with UK and European pharmaceutical regulations is specifically required for this Regulatory Affairs Officer position.
Educational Qualification
Applicants should have a Bachelor’s degree or higher in a science-related field, or equivalent relevant experience.
Suitable academic backgrounds may include pharmaceutical sciences, life sciences, chemistry, biology, or other relevant scientific disciplines, subject to the employer’s requirements.
Skills Relevant to This Regulatory Affairs Job
Candidates looking for Regulatory Affairs Officer jobs should ideally demonstrate knowledge or experience in:
- UK Regulatory Affairs
- European Regulatory Affairs
- Pharmaceutical regulations
- Regulatory submissions
- Regulatory dossier management
- Health authority communication
- Product registration
- Post-licensing activities
- Lifecycle management
- Pharmaceutical labelling
- SmPC review
- Patient Information Leaflet review
- Regulatory operations
- Regulatory information management
- Submission tracking
- Regulatory documentation
- Stakeholder management
- Client communication
- Regulatory project coordination
Salary for Regulatory Affairs Officer in India
ProductLife Group has not specified a salary range in the supplied job description. Therefore, candidates should confirm compensation directly with the employer during the recruitment process.
For general market context only, a Regulatory Affairs Officer with 4–6 years of experience in India and specialized UK/European regulatory expertise may commonly encounter compensation in approximately the ₹8–14 lakh per annum range, depending on location, specialization, employer, and experience.
This is a market estimate and not a salary offered or confirmed by ProductLife Group.
Why This Role May Interest Regulatory Affairs Professionals
This opportunity involves regulatory work across multiple stages of the pharmaceutical product lifecycle rather than focusing solely on a single submission activity.
The responsibilities span registration, post-licensing activities, regulatory documentation, health authority interactions, labelling, regulatory systems and client support. ProductLife Group describes its regulatory operations offering as supporting products from preparation for registration through ongoing post-approval compliance.
Professionals with UK and European regulatory experience can therefore apply their existing regulatory knowledge across client projects and lifecycle activities.