SP Accure Labs Hiring for Regulatory Affairs Jobs professionals in Hyderabad 2025 for CTD, eCTD, and DMF submissions – Apply now.
SP Accure Labs Hiring Regulatory Affairs Professionals – Walk-In Interview 2025
If you are an experienced Regulatory Affairs professional looking for pharma jobs in Hyderabad, this is your opportunity to grow with one of the leading companies in the industry. SP Accure Labs, a reputed pharmaceutical company known for its expertise in global regulatory submissions, has announced a walk-in interview on 8th November 2025 (Saturday) for Regulatory Affairs Officer to Senior Executive positions. SP Accure Labs Hiring for Regulatory Affairs Jobs
This recruitment is ideal for candidates with hands-on formulation experience, strong understanding of CTD/eCTD dossier compilation, DMF/ASMF preparation, and familiarity with international regulatory guidelines such as EMA, WHO, and ICH. The company is offering excellent career growth prospects for professionals eager to work on global regulatory projects. SP Accure Labs Hiring for Regulatory Affairs Jobs
SP Accure Labs is inviting immediate joiners with 1–8 years of relevant experience for its Regulatory Affairs department located in Biotech Park, Shameerpet, Telangana. SP Accure Labs Hiring for Regulatory Affairs Jobs
About SP Accure Labs
SP Accure Labs Pvt. Ltd. is an established pharmaceutical company specializing in formulations and API manufacturing with a strong foothold in regulated and semi-regulated markets across Europe, Canada, LATAM, GCC, and ROW. The company focuses on developing high-quality, compliant products that meet the stringent requirements of international health authorities. SP Accure Labs Hiring for Regulatory Affairs Jobs
SP Accure Labs has built a reputation for its robust regulatory operations, innovation-driven R&D, and efficient global submissions. Its Regulatory Affairs team plays a key role in preparing, reviewing, and managing product registration dossiers for multiple markets, making it an excellent workplace for professionals aiming to build expertise in global pharmaceutical regulations. SP Accure Labs Hiring for Regulatory Affairs Jobs
Why Work with SP Accure Labs?
Choosing SP Accure Labs means joining a company with a strong focus on regulatory excellence and career advancement. Here’s why you should attend this walk-in interview: SP Accure Labs Hiring for Regulatory Affairs Jobs
- Global Market Exposure: Work on submissions for regulated and semi-regulated markets including EU, Canada, GCC, and LATAM.
- Skill Enhancement: Get hands-on experience with CTD/eCTD dossier preparation and DMF documentation.
- Competitive Salary: Attractive pay structure with performance-based growth.
- Dynamic Work Environment: Collaborate with skilled professionals in an innovation-driven setup.
- Career Progression: Clear advancement path in the Regulatory Affairs domain.
- Supportive Team: Learn from experienced professionals and gain international exposure.
Available Positions – Regulatory Affairs Jobs at SP Accure Labs
SP Accure Labs is hiring candidates for both Formulation and API Regulatory Affairs tracks. Below are the details of the available roles: SP Accure Labs Hiring for Regulatory Affairs Jobs
1. Regulatory Affairs – Formulation Track (Officer to Senior Executive)
Qualification:
B.Pharm, M.Pharm, M.Sc, or D.Pharma
Experience:
3 to 8 years in formulation dossier compilation and submission
Key Responsibilities:
- Preparation, review, and submission of CTD/eCTD/ACTD dossiers for regulated and semi-regulated markets.
- Manage new product registrations, renewals, and post-approval variations.
- Handle MOH and client queries related to regulatory submissions.
- Ensure all regulatory documentation complies with EMA, WHO, ICH, and country-specific guidelines.
- Manage product information documents (SmPC, PIL, labels, IFU, SPC, artwork, etc.).
- Maintain regulatory databases, submission trackers, and track product registration statuses.
- Coordinate with R&D, QA, and Production teams for technical documentation and compliance.
2. Regulatory Affairs – API Track (Officer)
Qualification:
B.Pharm, M.Pharm, M.Sc, or D.Pharma
Experience:
1 to 5 years in API Regulatory Affairs / DMF preparation
Key Responsibilities:
- Prepare and update DMF (Drug Master File), ASMF (Active Substance Master File), and CEP dossiers.
- Draft and review CMC sections (S.1 to S.7) for API documentation.
- Compile stability data and support filings with regulatory authorities such as EMA, MHRA, TGA, PMDA, and WHO.
- Review impurity profiles, manufacturing processes, and control strategies per ICH guidelines.
- Manage initial filings, amendments, and annual reports for global submissions.
- Maintain proper document version control and ensure data integrity in all submissions.
- SP Accure Labs Hiring for Regulatory Affairs Jobs
Eligibility Criteria
Educational Qualification:
B.Pharm, M.Pharm, M.Sc, or D.Pharma (as per role)
Experience Range:
1–8 years depending on the track (Formulation or API)
Mandatory Requirements:
- Must have formulation experience for Formulation RA roles.
- Should be an immediate joiner.
- Male candidates preferred.
- Strong understanding of international regulatory guidelines and submission formats (CTD, eCTD, ACTD).
Preferred Skills:
- Experience in regulatory dossier compilation for global markets.
- Knowledge of GMP, GLP, and pharmaceutical documentation systems.
- Proficiency in regulatory databases, submission portals, and dossier management.
- Good communication and coordination skills with cross-functional teams.
Key Markets Covered by SP Accure Labs
Professionals at SP Accure Labs get exposure to a wide range of global regulatory markets, including:
- European Union (EU)
- Canada
- LATAM countries
- GCC (Gulf Cooperation Council)
- ROW (Rest of the World)
This international exposure makes the organization one of the most sought-after places for regulatory professionals aiming for global-level experience in dossier management and compliance. SP Accure Labs Hiring for Regulatory Affairs Jobs
Benefits of Joining SP Accure Labs
- Attractive Salary Packages: Competitive compensation for qualified professionals.
- Global Exposure: Opportunities to handle regulatory submissions for major international markets.
- Professional Growth: Structured career development in the regulatory field.
- Positive Work Culture: Supportive leadership and team-based collaboration.
- Location Advantage: Located in Hyderabad’s Biotech Park, providing a research-oriented atmosphere.
- Long-Term Stability: Work with a well-established, compliance-focused organization.
- SP Accure Labs Hiring for Regulatory Affairs Jobs
Walk-In Interview Details – SP Accure Labs Regulatory Affairs Jobs 2025
Date: Saturday, 8th November 2025
Time: 08:30 AM – 11:00 AM
Venue:
SP Accure Labs Pvt. Ltd.
Plot No. 12, Biotech Park, Phase II,
Lalgadi Malakpet, Shameerpet Mandal,
Medchal-Malkajgiri District, Telangana, India.
Documents Required for the Walk-In Interview
Candidates attending the interview should carry the following documents:
- Updated Resume / CV
- Recent Increment Letter (if applicable)
- Last 3 months’ Payslips and Bank Statements
- Educational Certificates (Degree and Marksheets)
- Aadhaar Card and PAN Card copies
- Any additional regulatory or compliance certifications
For Outstation Candidates
If you are unable to attend the walk-in interview in person, you can still apply by sending your resume via email or contacting HR directly. SP Accure Labs Hiring for Regulatory Affairs Jobs
- Email ID: jobs@spaccurelabs.com
- Contact Number: +91 73966 44772
Ensure that your email subject line clearly mentions the role you are applying for (e.g., Application for Regulatory Affairs Officer – API).
How to Apply for SP Accure Labs Jobs 2025
Follow these simple steps to apply for regulatory affairs positions at SP Accure Labs: SP Accure Labs Hiring for Regulatory Affairs Jobs
- Update Your Resume: Highlight your formulation or DMF experience and regulatory exposure.
- Gather Your Documents: Keep educational and employment proofs ready.
- Attend the Walk-In Interview: Visit the venue on 8th November 2025 between 8:30 AM and 11:00 AM.
- Unable to Attend? Send your resume to jobs@spaccurelabs.com.
- Follow Up: Contact the HR team at +91 73966 44772 for updates on your application.
Frequently Asked Questions (FAQs)
1. What is the eligibility for SP Accure Labs Regulatory Affairs jobs?
Candidates must have 1–8 years of experience in regulatory affairs, with mandatory formulation experience. Qualifications accepted include B.Pharm, M.Pharm, M.Sc, or D.Pharma. Only immediate joiners are considered, and male candidates are preferred. SP Accure Labs Hiring for Regulatory Affairs Jobs
2. Can outstation candidates apply for these roles?
Yes. Outstation candidates who cannot attend the walk-in interview can apply online by sending their resumes to jobs@spaccurelabs.com.
3. What kind of submissions will I work on?
You’ll work on CTD, eCTD, and ACTD dossier compilation for regulated and semi-regulated markets, along with DMF preparation for APIs.
4. What is the work location for these jobs?
The positions are based at SP Accure Labs, Biotech Park, Shameerpet, Telangana.
Start your journey with SP Accure Labs and advance your career in global pharmaceutical regulatory affairs.
Join a company that values expertise, innovation, and regulatory precision.
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