Unlock regulatory affairs jobs at Macleods’ walk-in drive in Mumbai. Explore senior pharma roles in global markets with a leader in innovative, compliant therapeutics.
Contents
About the Company
Macleods Pharmaceuticals Ltd., established in 1989 and headquartered in Mumbai, India, is a vertically integrated global pharmaceutical powerhouse. Renowned for its R&D-driven innovation, the company develops, manufactures, and markets a diverse portfolio of affordable, high-quality therapies across multiple dosage forms.
With state-of-the-art facilities approved by stringent bodies like USFDA and EMA, Macleods ensures unwavering regulatory compliance while expanding its footprint in over 100 countries, fostering sustainable growth and patient-centric excellence.
Job Details
- Company Name: Macleods Pharmaceuticals Ltd.
- Experience: 2 to 15 years (varies by role)
- Qualification: M.Pharm, M.Sc
- Location: Mumbai, Maharashtra
- Work Type: On-site
Job Description
Macleods Pharmaceuticals is hosting an exclusive walk-in drive at its R&D facility in Mumbai to bolster its Regulatory Affairs team. This recruitment targets experts in global dossier management and compliance to support product lifecycles across key international markets. Join a dynamic environment driving pharmaceutical innovation and regulatory success.
Sr. Executive/Executive (Europe, South Africa, MENA, AU, NZ & Canada)
- Department: Regulatory Affairs
- Role: Leadership in global regulatory strategy and submissions
- Experience: 6 to 15 years
- Education/Qualification: M.Pharm, M.Sc
Sr. Officer/Officer (CIS, LATAM & MENA)
- Department: Regulatory Affairs
- Role: Product lifecycle management and dossier handling
- Experience: 2 to 5 years
- Education/Qualification: M.Pharm, M.Sc
Skills/Qualifications
- Deep expertise in FDA, EMA, and ICH regulatory guidelines
- Proficiency in dossier preparation, variation filing, and query responses
- Strong leadership experience in pharmaceutical regulatory affairs
- Knowledge of global market requirements for Europe, MENA, and emerging regions
- Excellent analytical and documentation skills for post-approval changes
- Familiarity with product lifecycle management in diverse international markets
Key Responsibilities
- Lead regulatory submissions for Europe, South Africa, and key regions
- Prepare and file dossiers with accuracy and timeliness
- Manage queries and variations to ensure compliance
- Oversee post-approval changes across product lifecycles
- Collaborate on strategies meeting FDA, EMA, and ICH standards
- Drive team efforts in global market expansions
Benefits/Perks
- Accelerated career growth in a global R&D leader
- Access to cutting-edge training and innovation programs
- Competitive salary packages with performance bonuses
- Inclusive work culture promoting work-life balance
- International exposure through cross-market projects
How to Apply
Walk in with your updated CV, salary structure (CTC breakup), and Aadhar card to the venue. For queries, contact 8291054728, 8291331272, or 7208877803. Explore more regulatory affairs jobs and tips at Pharma Recruiter. Seize this opportunity—apply now and shape global pharma compliance!
Verified Post
The post is released by the Macleods Pharma LinkedIn page. Click here to visit the post
Walk-in Interview Details
- Date: 1st November 2025
- Time: 09:30 AM onwards
- Venue: Plot 60, Street No 14, MIDC Phase II, Andheri East, Mumbai 400093
- Contact/Email: 8291054728 / 8291331272 / 7208877803
Why You Should Join
Macleods fosters a culture of innovation and integrity, recognized globally for its compliant, patient-focused operations and rapid expansion into new markets. Benefit from long-term stability with clear promotion pathways and skill-building in regulatory excellence.
In this R&D-centric hub, you’ll contribute to affordable therapies while gaining exposure to cutting-edge compliance strategies—ideal for ambitious professionals eyeing sustainable pharma careers.
FAQs
Who qualifies for these regulatory affairs jobs at Macleods?
M.Pharm or M.Sc holders with 2-15 years in pharma regulatory affairs, specializing in global guidelines like FDA and EMA. Leadership experience preferred for senior roles.
How does the walk-in interview process work?
Arrive post-09:30 AM on 1st November 2025 with CV, CTC details, and Aadhar. On-site screening and interviews; contact numbers for pre-queries.
Can candidates from outside Mumbai apply?
Yes, on-site roles in Mumbai welcome interstate applicants. Prepare documents and plan travel for the November 1 drive.
What career growth awaits in these pharma positions?
Macleods offers mentorship, global projects, and advancement in regulatory leadership, backed by a compliant, innovative ecosystem for long-term success.