Job Overview
Regulatory Affairs Associate
Company: Teva Pharmaceuticals
Navi Mumbai Maharashtra
Work Mode: Hybrid
Job Type: Full-Time
Experience: 2–4 Years
Regulatory Affairs Associate Job at Teva Pharmaceuticals Navi Mumbai Offers Hybrid Work
A new beginning right after your pharmacy or life sciences degree? Could be time to explore something different – especially if you already have experience in regulatory work. One opportunity shows up at Teva Pharmaceuticals, active across the globe in making medicines. They’re looking for someone to step into a Regulatory Affairs Associate position. Location: Navi Mumbai. A standout in healthcare, hiring now for a sharp eye on details. Right at home with regulations? This role matches that strength. People who thrive here understand the ins and outs of compliance deeply.
Every now then comes a role like this one – steady movement forward possible, especially if rules and systems are your thing. Not stuck in one place: some days near others, some far. What builds you up? Actual work. Real pieces handed over, not talk. Imagine balance struck – not too tight, never loose either. Space given because trust matters when organizing effort across screens or desks.
Starting with a pharmacy degree can lead you into B.Pharm, perhaps stepping later into M.Pharm for more depth. Holders of an MSc in life sciences also find their way in, coming straight from science backgrounds. One route might build strong foundations, another sharpens expertise – each shapes experience differently. Still, they often arrive at comparable roles in the field
It’s official – this job exists. Verified and given the green light
Salary Details
Wages here tend to land somewhere in this range
₹5.5 LPA ₹9 LPA
Right now, most folks in Indian regulatory roles – two to four years on the job – show numbers like this one. People just a few years into regulation work across the country tend to land here when measured.
About the Role
Right away, you take charge of following drug regulations. Working closely with different teams happens all the time as you track documents and required actions. Getting forms right for government agencies depends on careful checking. Each change or filing moves forward under your watch. Mistakes tend to slow things down, after all. When details stay clear, work follows without hiccups. Laws shift often – keeping up means less friction later. Progress likes precision, quietly pushing each step ahead.
Starting out in regulatory affairs? Real learning comes from doing things yourself. Some days might feel uncertain, though improvement still moves forward quietly. People focused on long-term goals begin seeing changes after a while. Slowly, understanding grows even when there is no rush to get results fast.
Key Responsibilities
Prepare and review regulatory documents
Support submission of dossiers to health authorities
Ensure compliance with regulatory guidelines
Coordinate with cross-functional teams
Maintain accurate regulatory records and documentation
Qualifications and Skills Needed
Hold a science degree? You’re in. A B.Pharm also opens the door. Life sciences M.Sc? That counts. Even an M.Pharm lines up. Each qualification finds its place
2–4 years of experience in regulatory affairs
Good understanding of regulatory guidelines
A story finds its match in fine paper. When words flow well, the moment stays light. Staying clear means nobody loses the thread
Focused on small details plus knowing the rules well
Balanced Hours Growth Chances Teamwork Support Skills
Work with a globally recognized pharmaceutical company
Hybrid work model for better work-life balance
Competitive salary package
Exposure to international regulatory standards
Career growth opportunities in regulatory affairs
Reasons to Think About Applying
Growth seekers often land here first. Higher ambitions? This path lines up just right. New hurdles call out to some – this answers loud and clear. Learning never stops when curiosity shows up. Forward motion finds its match inside this setup
✔ Build a strong career in regulatory affairs
✔ Work in a reputed pharmaceutical company
✔ Gain hands-on experience in regulatory submissions
✔ Enjoy flexibility with hybrid working
How to Apply
Got a resume ready? Send it over to get into the running. Use the email listed right here to connect. Once sent, materials head directly to those doing the hiring. Make sure your phone number and address are up to date before you press send. That wraps things up – at least for today
📧 ankita.sonawane@teva.co.in
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Email CV to: ankita.sonawane@teva.co.in