Trainee Intern Regulatory Affairs Job at GeneDrift in Uttarakhand. Apply for trainee internship role with hybrid work opportunity.
About the Company
GeneDrift is a growing pharmaceutical organization committed to quality, compliance, and innovation in drug development and regulatory operations. The company focuses on maintaining high regulatory standards while supporting young professionals through structured training, mentorship, and real-world exposure. Trainee Intern Regulatory Affairs Job
With operations aligned to Indian and global regulatory expectations, GeneDrift provides an environment where fresh graduates can learn the fundamentals of pharmaceutical regulatory affairs, documentation practices, and cross-functional collaboration. The organization values accuracy, ethics, and continuous learning, making it a suitable workplace for candidates who want to build a long-term career in regulatory affairs.
This opportunity is designed especially for pharmacy graduates who are at the beginning of their professional journey and are eager to understand how regulatory systems function within the pharmaceutical industry. Trainee Intern Regulatory Affairs Job
Job Details
- Job Title: Trainee Intern – Regulatory Affairs
- Company: GeneDrift
- Job Location: Uttarakhand, India
- Work Mode: Hybrid
- Employment Type: Internship / Trainee
- Experience Required: Freshers or up to 6 months (R&D / Formulation & Development preferred)
- Educational Qualification: B.Pharm or M.Pharm
- Industry: Pharmaceutical / Regulatory Affairs
- Job Category: Regulatory Affairs Fresher Jobs
This role is ideal for candidates searching for regulatory affairs internships in India, entry-level pharma regulatory jobs, or fresher opportunities in Uttarakhand. Trainee Intern Regulatory Affairs Job
Job Description
The Trainee Intern – Regulatory Affairs position at GeneDrift is an entry-level role focused on building a strong foundation in pharmaceutical regulatory processes. Selected candidates will work closely with experienced regulatory professionals and gain practical exposure to documentation, compliance, and submission-related activities.
As a trainee, you will be introduced to regulatory frameworks governing pharmaceutical products and will assist in preparing, reviewing, and organizing regulatory documents. The role requires attention to detail, willingness to learn, and effective communication with cross-functional teams such as R&D, Quality Assurance, and Formulation departments.
This position is structured to help freshers understand regulatory expectations, industry guidelines, and internal compliance systems while developing skills that are essential for long-term growth in regulatory affairs. Trainee Intern Regulatory Affairs Job
Skills and Qualifications
To be successful in this role, candidates should meet the following qualifications and skill requirements:
Educational Qualifications
- Bachelor’s degree in Pharmacy (B.Pharm) or
- Master’s degree in Pharmacy (M.Pharm)
Experience Requirements
- Freshers are encouraged to apply
- Candidates with up to 6 months of experience in R&D or Formulation & Development will be considered
Required Skills
- Basic understanding of pharmaceutical regulatory affairs concepts
- Strong written and verbal communication skills
- Good documentation and formatting abilities
- Basic knowledge of pharmaceutical guidelines and compliance requirements
- Ability to work with regulatory records and data
- Willingness to learn regulatory processes and industry standards
Candidates with an academic interest in regulatory affairs and compliance will find this role particularly beneficial. Trainee Intern Regulatory Affairs Job
Key Responsibilities
As a Trainee Intern – Regulatory Affairs, your key responsibilities will include:
- Assisting in the preparation and compilation of regulatory dossiers
- Supporting regulatory submissions and documentation activities
- Maintaining regulatory records, logs, and internal databases
- Coordinating with R&D, Quality Assurance, and other departments for document collection
- Ensuring documents align with applicable regulatory guidelines and internal standards
- Assisting in the review, formatting, and quality checking of technical and regulatory documents
- Supporting day-to-day regulatory operations under senior team guidance
- Learning regulatory workflows and compliance processes applicable to pharmaceutical products
These responsibilities are designed to gradually build regulatory knowledge while providing hands-on experience. Trainee Intern Regulatory Affairs Job
Benefits and Perks
GeneDrift offers several advantages for freshers entering the regulatory affairs domain: Trainee Intern Regulatory Affairs Job
- Entry-level exposure to pharmaceutical regulatory affairs
- Hybrid work model offering flexibility and work-life balance
- Structured learning environment with practical training
- Opportunity to work with experienced regulatory professionals
- Development of strong documentation and compliance skills
- Foundation for long-term career growth in regulatory affairs
- Exposure to cross-functional pharmaceutical operations
This role is particularly valuable for candidates aiming to transition into permanent regulatory affairs positions in the pharmaceutical industry.
Why You Should Join GeneDrift
Joining GeneDrift as a Trainee Intern – Regulatory Affairs gives you an opportunity to start your career in one of the most critical domains of the pharmaceutical industry. Regulatory affairs professionals play a key role in ensuring product compliance, quality, and approval readiness. Trainee Intern Regulatory Affairs Job
For freshers, gaining early exposure to regulatory documentation and submissions can significantly improve future job prospects. GeneDrift’s learning-oriented environment supports professional development, helping candidates understand real-world regulatory challenges beyond academic knowledge.
If you are looking for a regulatory affairs fresher job in Uttarakhand with structured learning and hybrid flexibility, this opportunity provides a strong career starting point. Trainee Intern Regulatory Affairs Job
Frequently Asked Questions (FAQs)
Is this position open to freshers?
Yes, this role is open to fresh B.Pharm and M.Pharm graduates. Candidates with up to 6 months of relevant experience may also apply.
Is prior regulatory affairs experience mandatory?
No, prior regulatory affairs experience is not mandatory. Basic knowledge and interest in regulatory concepts are sufficient.
What type of work mode is offered?
The role offers a hybrid work mode, combining on-site and remote working as per organizational requirements.
Is this a permanent role or internship?
This is a trainee internship role designed to provide foundational regulatory affairs experience. Performance-based growth opportunities may be available.
Which location is this job based in?
The position is based in Uttarakhand, India.
How to Apply
Interested and eligible candidates can apply online through the official application link provided in the job listing. Ensure that your resume highlights your pharmacy qualification, basic regulatory knowledge, and interest in regulatory affairs before submitting your application. Trainee Intern Regulatory Affairs Job
Candidates are advised to apply at the earliest, as regulatory affairs fresher jobs and trainee internships are highly competitive. Trainee Intern Regulatory Affairs Job
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