GeneSys Biologics Recruitment 2026 for Freshers | R&D Jobs for MSc Biotechnology, Biochemistry, B.Tech & M.Tech Candidates (GeneSys Biologics Recruitment 2026 for Freshers) Introduction GeneSys Biologics Pvt. Ltd. has announced new Research & Development (R&D) job openings for freshers and early-career professionals in Telangana. Candidates with qualifications such as MSc Biotechnology, MSc Biochemistry, B.Tech, and M.Tech can apply for these exciting opportunities in the biologics research sector. This recruitment is particularly suitable for candidates interested in Upstream Processing (USP), Downstream Processing (DSP), microbial platform technologies, biologics manufacturing, and biotechnology research. Professionals with 0–2 years of experience and fresh graduates looking to start their careers in biologics R&D are encouraged to apply. If you are searching for Biotechnology Jobs 2026, Biologics R&D Careers, Freshers Biotech Jobs in Telangana, or Researc...
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In today’s global pharmaceutical industry, regulatory compliance plays a vital role in ensuring that every medicine and clinical trial follows strict international standards. If you’re a science or pharmacy graduate looking for a rewarding career in documentation, compliance, and global collaboration — this opportunity is for you!
PPD, a part of Thermo Fisher Scientific, is hiring for the position of Regulatory Affairs Specialist (Admin) to support Regulatory Compliance Review (RCR) operations. This role allows you to work remotely while being part of one of the world’s most trusted names in clinical research and pharmaceutical development.
Let’s explore this exciting career opportunity in detail 👇
About the Role:-
The Regulatory Affairs Specialist (Admin) plays a crucial part in maintaining regulatory compliance across global studies. This professional ensures that essential clinical and regulatory documents meet global standards, such as ICH-GCP, FDA, and EMA guidelines, while coordinating with multiple project teams.
If you enjoy managing documentation, reviewing compliance data, and ensuring process integrity, this position offers a perfect balance of analytical, technical, and administrative skills in a global environment.
Key Responsibilities:-
As a Regulatory Affairs Specialist (Admin), your day-to-day responsibilities will include:
Conducting Global Regulatory Compliance Reviews for essential clinical documents based on Essential Document Checklists (EDCs).
Managing Essential Document Checklist Processes efficiently and ensuring version control and accuracy.
Responding to queries from project teams and clarifying EDC requirements.
Ensuring all regulatory documents meet country-specific and global guidelines.
Facilitating discussions related to deviations from RCR processes, ensuring compliance and process transparency.
Maintaining a deep understanding of PPD SOPs, client directives, and international regulatory standards.
Supporting document consistency, finalization, and timely posting across internal systems.
This position offers a chance to work with a global team of experts while helping ensure that new medicines reach patients safely and ethically.
Qualifications and Experience:-
Educational Background:
Bachelor’s degree in Science, Pharmacy, Life Sciences, or a closely related field.
Experience Required:
1–3 years of experience in regulatory affairs, clinical documentation, or regulatory compliance review.
Fresh graduates with strong documentation and organizational skills may also apply, depending on company requirements.
Key Skills:
To succeed in this role, candidates should have:
Excellent written and verbal communication skills in English.
Strong attention to detail and editorial accuracy.
Proficiency in Microsoft Word, Excel, PowerPoint, and other digital tools.
Ability to interpret and apply global regulatory requirements.
Analytical mindset with excellent problem-solving and coordination skills.
Team-oriented approach with the flexibility to adapt to new systems and processes.
Why Join PPD (Thermo Fisher Scientific)?
Global Impact:
By joining PPD, you become part of a world-renowned organization that contributes to improving global health through high-quality research, innovation, and compliance.
Remote Work Flexibility:
Enjoy the convenience of working from home while staying connected to international projects and teams across multiple time zones.
Career Growth and Learning:
PPD offers extensive career development programs, training modules, and exposure to diverse regulatory environments. You’ll gain hands-on experience with cutting-edge tools used in regulatory submissions and compliance reviews worldwide.
Inclusive and Collaborative Culture:
The company promotes a supportive environment that values teamwork, transparency, and respect for every employee.
Work-Life Balance:
With standard weekday schedules and remote flexibility, this role ensures you can maintain a healthy balance between work and personal life.
Ideal Candidate Profile:
This position is best suited for professionals who:
Are passionate about regulatory documentation and global compliance.
Have a keen eye for detail and accuracy.
Enjoy working in a structured, process-driven environment.
Seek remote opportunities that provide both flexibility and international exposure.
If you’re a B.Pharm, M.Pharm, or Life Sciences graduate who wants to make an impact in the global pharma industry, this could be your next career step!
How to Apply:-
Interested candidates can apply directly through the official Thermo Fisher Careers portal using the link below:
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