Join SP Accure Labs for a walk-in interview on 27 December 2025. Exciting pharmaceutical careers in India await in QC, microbiology, and regulatory affairs. Immediate joiners preferred for oncology-focused roles in Telangana.
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About the Company
SP Accure Labs Pvt. Ltd. is a fully integrated, quality-led pharmaceutical company specializing in oncology. Committed to making high-quality, affordable anti-cancer medicines accessible worldwide.
With the motto “Touching Lives Globally,” the company focuses on innovation, stringent regulatory compliance, and global approvals (USFDA, EU-GMP, WHO-GMP).
Headquartered in Hyderabad, Telangana, SP Accure Labs operates a state-of-the-art facility in Biotech Park, Shamirpet, driving advancements in oncology formulations and injectables.
Job Details
- Company Name: SP Accure Labs Pvt. Ltd.
- Experience: Varies by role (2–10 years)
- Qualification: M.Sc, B.Pharm, M.Pharm, D.Pharm
- Location: Plot No. 12, Biotech Park, Phase II, Lalgadi Malakpet, Shamirpet, Medchal-Malkajgiri Dist., Telangana
- Work Type: On-site
Note: Formulation experience is mandatory. Preferred male candidates. Looking for immediate joiners.
Job Description
SP Accure Labs is hiring experienced professionals for key roles in Quality Control, Microbiology, and Regulatory Affairs.
These positions support the company’s global oncology operations and ensure compliance with international standards. Multiple openings available for immediate contribution in a fast-growing pharma environment.
Chemist/Executive – Environment Monitoring
- Department: Quality Control/Microbiology
- Role: Trend analysis of environmental monitoring (EM) and water data
- Experience: 2 to 5 years
- Education/Qualification: M.Sc, B.Pharm, M.Pharm
Chemist/Executive – Sterility & Bacterial Endotoxin Test
- Department: Quality Control/Microbiology
- Role: Sterility test analysis and Bacterial Endotoxin Test (BET) analysis
- Experience: 5 to 8 years
- Education/Qualification: B.Pharm, M.Pharm
Executive/Sr. Executive – Microbiology Supervisor/Section In-charge
- Department: Microbiology
- Role: Environment monitoring supervision, rational and risk assessment, MLT validations, BET validations, sterility test validation, microbial method validations
- Experience: 8 to 10 years
- Education/Qualification: B.Pharm, M.Pharm
Officer to Sr. Executive – Regulatory Affairs (Formulation)
- Department: Regulatory Affairs
- Role: Preparation, review, and compilation of CTD/eCTD/ACTD dossiers for global markets (EU, Canada, LATAM, GCC, ROW); ensure compliance with EMA, WHO, ICH guidelines
- Experience: 5 to 10 years
- Education/Qualification: M.Sc, B.Pharm, D.Pharm, M.Pharm
Officer – Regulatory Affairs (API)
- Department: Regulatory Affairs
- Role: Prepare, review, and compile DMF/ASMF/CEP and CMC sections for global submissions (EMA, MHRA, TGA, PMDA, WHO, ROW)
- Experience: 3 to 6 years
- Education/Qualification: M.Sc, B.Pharm, M.Pharm, D.Pharm
Skills/Qualifications
- Hands-on experience in environmental monitoring and trend analysis
- Proficiency in sterility testing and BET analysis
- Expertise in microbial limit test (MLT) and method validations
- Strong knowledge of CTD/eCTD/ACTD dossier preparation
- Familiarity with global regulatory guidelines (EMA, ICH, WHO, MHRA, TGA)
- Experience in DMF/ASMF/CEP and CMC documentation
- Formulation experience (mandatory)
- Excellent documentation and compliance skills
Key Responsibilities
- Perform trend analysis of EM and water data
- Conduct sterility and BET analysis
- Supervise microbiology operations
- Prepare risk assessment documents
- Validate microbial methods and tests
- Compile regulatory dossiers for submissions
- Ensure compliance with country-specific guidelines
- Review SmPC, labels, and artwork
Benefits/Perks
- Competitive salary packages
- Career growth in oncology pharma
- Global exposure and learning opportunities
- Supportive and innovative work culture
- Opportunity to contribute to life-saving medicines
- Professional development in regulatory compliance
How to Apply
Attend the walk-in interview with required documents or email your CV. Send resume to: jobs@spaccurelabs.com Contact: +91 73966 44772
Required documents: Resume, recent increment letter, 3 months payslips, bank statements, educational certificates, Aadhar & PAN copy.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the SP Accure Labs LinkedIn page.
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Walk-in Interview Details
- Date: 27 December 2025 (Saturday)
- Time: 08:30 AM – 11:00 AM
- Venue: Plot No. 12, Biotech Park, Phase II, Lalgadi Malakpet, Shamirpet Mandal, Medchal-Malkajgiri Dist., Telangana
- Contact/Email:jobs@spaccurelabs.com / +91 73966 44772
Why You Should Join
SP Accure Labs offers a dynamic environment focused on oncology innovation and global impact.
Employees enjoy long-term career stability, continuous learning, and recognition in a compliance-driven culture. Join a team dedicated to touching lives globally through high-quality anti-cancer medicines and cutting-edge research.
FAQs
What qualifications are required for these pharma jobs?
Candidates need M.Sc, B.Pharm, M.Pharm, or D.Pharm with relevant experience (2–10 years). Formulation experience is mandatory.
How can I apply if I can’t attend the walk-in interview?
Email your CV to jobs@spaccurelabs.com along with required documents. Outstation candidates are welcome to apply remotely.
Is this walk-in interview suitable for freshers?
No, all roles require 2–10 years of experience. Immediate joiners are preferred.
What growth opportunities are available?
SP Accure Labs offers competitive salaries, global exposure, and career advancement in regulatory affairs and microbiology within oncology pharma.