Are you a passionate Regulatory Affairs professional with hands-on formulation experience searching for pharma jobs in Hyderabad? SP Accure Labs, a leading pharmaceutical company specializing in global regulatory submissions, is conducting a walk-in interview on 08th November 2025 for Regulatory Affairs Officer to Senior Executive roles. This is an excellent opportunity for immediate joiners with expertise in CTD dossier compilation, eCTD submissions, DMF preparation, and compliance with EMA, WHO, ICH guidelines. Don’t miss this chance to advance your career in pharmaceutical regulatory affairs jobs in Telangana!
With mandatory formulation experience and preferred male candidates, these positions offer growth in a dynamic environment focused on international markets like EU, Canada, LATAM, GCC, and ROW.
Key Responsibilities for Regulatory Affairs Roles
As a Regulatory Affairs Expert at SP Accure Labs, you’ll play a crucial role in ensuring seamless global product registrations. Primary duties include:
- Preparation, review, and compilation of CTD/eCTD/ACTD dossiers for regulated markets (EU, Canada, LATAM, GCC, ROW).
- Timely submission of new product registrations, renewals, variations, and handling customer/MOH queries.
- Ensuring product information (SmPC, labels, artwork, PIL, SPC, IFU) complies with EMA, WHO, ICH, and country-specific guidelines.
- Maintaining regulatory databases, submission trackers, and product registration status.
- For API-focused roles: Prepare DMF/ASMF/CEP, CMC sections (S.1-S.7), stability data, and support filings with EMA, MHRA, TGA, PMDA, WHO.
- Review impurities, manufacturing details, and control of drug substance per current ICH guidelines.
- Manage initial filings, updates, amendments, annual reports, and version control of documents.
These responsibilities demand precision and up-to-date knowledge of global regulatory affairs in pharmaceuticals.
Qualifications and Experience Required
SP Accure Labs is hiring for two tracks with mandatory formulation experience:
Formulation Track (Officer to Sr. Executive):
- Experience: 3-8 years in regulatory affairs dossier compilation.
- Qualification: B.Pharm, M.Pharm, M.Sc, D.Pharma.
API Track (Officer):
- Experience: 1-5 years in DMF/ASMF/CEP preparation.
- Qualification: B.Pharm, M.Pharm, M.Sc, D.Pharma.
Candidates must be immediate joiners and preferably male. Strong understanding of pharmaceutical regulatory affairs jobs involving international submissions is essential.
Benefits of Joining SP Accure Labs
- Competitive salary package with growth opportunities in a globally focused pharma company.
- Exposure to high-profile submissions for EU, Canada, and emerging markets.
- Supportive work environment in Hyderabad’s Biotech Park.
- Career progression in regulatory affairs careers in pharma.
How to Apply – Walk-in Interview Details
Attend the walk-in interview for regulatory affairs jobs:
- Date: 08th November 2025 (Saturday)
- Time: 08:30 AM – 11:00 AM
- Location: Plot No. 12, Biotech Park, Phase II, Lalgadi Malakpet, Shameerpet Mandal, Medchal-Malkajgiri Dist., Telangana, India.
Documents Required:
- Resume
- Recent Increment Letter
- 3 Months Payslips & Bank Statements
- Educational Certificates
- Aadhaar & PAN Card copies
Outstation candidates: Email CV to jobs@spaccurelabs.com or call +91 73966 44772.
This SP Accure Labs walk-in interview 2025 is your gateway to rewarding pharma regulatory affairs jobs in Hyderabad.
Frequently Asked Questions (FAQs)
1. What is the eligibility for SP Accure Labs Regulatory Affairs jobs? Candidates need 1-8 years experience in dossier compilation or DMF preparation with mandatory formulation background, B.Pharm/M.Pharm/M.Sc/D.Pharma qualification, and must be immediate joiners. Preferred male candidates.
2. Is this a walk-in or can I apply online for regulatory affairs officer roles? It’s a walk-in on 08 Nov 2025, 08:30 AM-11:00 AM. Outstation applicants can email CV to jobs@spaccurelabs.com for consideration.
