SP Accure Walk-in Production, QA, AR&D & RA
- Company Overview
- Walk-In Interview Details
- Job Role & Responsibilities
- OSD Production & QMS
- Production – Injectables
- Packing – Injectables
- Engineering – Process Engineering (Injectables)
- AR&D – Analytical Research & Development
- Regulatory Affairs (RA)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Consider SP Accure Labs?
- Frequently Asked Questions (FAQs)
- Summary
BPharm/MSc Vacancies at SP Accure Telangana
B.Pharm, M.Pharm, M.Sc vacancies at SP Accure Labs Telangana. Walk-in on 20 Feb 2026 for Production, QA, AR&D & RA roles.
SP Accure Labs is conducting a walk-in interview for experienced professionals in OSD and Injectable manufacturing, Quality Systems, AR&D, Regulatory Affairs, and Engineering. Candidates with strong formulation plant exposure and regulatory compliance experience are invited to attend the hiring drive at the Telangana facility. Immediate joiners with hands-on pharmaceutical manufacturing experience will be given preference.
This opportunity is ideal for professionals searching for OSD production jobs, injectable manufacturing vacancies, pharmaceutical QMS executive roles, AR&D method development openings, CTD dossier preparation jobs, and pharma engineering plant maintenance careers in Telangana.
Company Overview
SP Accure Labs is a formulation-focused pharmaceutical manufacturing company with a growing global footprint. The organization supports regulated and semi-regulated markets and operates with strict compliance to cGMP, QMS, data integrity, and global regulatory frameworks including EMA, WHO, and ICH guidelines.
The Shamirpet facility handles oral solid dosage (OSD) and sterile injectable manufacturing with advanced process equipment, cleanroom systems, and compliance-driven quality systems. The company emphasizes regulatory documentation, validation protocols, and global dossier submission standards.
Professionals joining SP Accure Labs gain exposure to regulated pharmaceutical manufacturing environments, deviation management systems, root cause investigations, change control processes, and global regulatory submission practices.
Walk-In Interview Details
Date: 20 February 2026 (Friday)
Time: 10:30 AM – 03:00 PM
Venue: Plot No. 12, Biotech Park, Phase II, Lalgadi Malakpet, Shamirpet Mandal, Medchal-Malkajgiri District, Telangana, India
Formulation experience is mandatory. Immediate joiners are preferred.
Outstation candidates may share their CV at: jobs@spaccurelabs.com
Contact: +91 73966 44772
Job Role & Responsibilities
OSD Production & QMS
Designation: Jr. Executive / Executive
Qualification: ITI, Diploma, B.Pharm, M.Pharm
Experience: 3–10 Years
Key Responsibilities:
- Execute granulation, compression, coating, and packing operations.
- Handle deviation, CAPA, root cause analysis, incident investigation, and change control.
- Manage batch manufacturing records (BMR) and documentation review.
- Support recall handling and market complaint investigation.
- Ensure compliance with cGMP and SOPs.
Production – Injectables
Designation: Operator / Chemist / Executive
Qualification: ITI, Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm
Experience: 3–8 Years (Operators), 4–8 Years (Chemist/Executive)
Key Responsibilities:
- Operate compounding systems including CIP/SIP.
- Manage vial filling, vial washing, PFS filling operations.
- Perform granulation, HME, compression, capsule filling activities.
- Maintain sterile area documentation and compliance.
- Ensure adherence to injectable GMP standards.
Packing – Injectables
Designation: Officer / Executive
Qualification: B.Sc, M.Sc, Diploma, B.Pharm, M.Pharm
Experience: 3–6 Years
Key Responsibilities:
- Perform optical/visual inspection activities.
- Handle BMR preparation and review.
- Manage QMS activities including deviation and recall documentation.
- Ensure compliance with sterile packing guidelines.
Engineering – Process Engineering (Injectables)
Designation: Executive
Qualification: Diploma, B.Tech, M.Tech (Mechanical)
Experience: 5–8 Years
Key Responsibilities:
- Handle injectable process equipment maintenance.
- Support preventive and breakdown maintenance.
- Ensure equipment validation and qualification compliance.
- Maintain HVAC and utility system documentation.
AR&D – Analytical Research & Development
Designation: Research Associate
Qualification: M.Sc, B.Pharm, M.Pharm
Experience: 3–6 Years
Key Responsibilities:
- Perform analytical method development and validation.
- Operate GC, HPLC, and LCMS systems.
- Prepare analytical reports and validation protocols.
- Support regulatory submission documentation.
Regulatory Affairs (RA)
Designation: Officer to Sr. Executive
Qualification: M.Sc, B.Pharm, D.Pharm, M.Pharm
Experience: 6–12 Years
Key Responsibilities:
- Prepare and compile CTD, eCTD, and ACTD dossiers.
- Submit product registrations for EU, Canada, LATAM, GCC, and ROW markets.
- Ensure compliance with EMA, WHO, ICH, and country-specific guidelines.
- Review SmPC, labels, artwork, PIL, SPC, and IFU documentation.
- Handle renewals and post-approval variations.
Eligibility / Qualifications
Eligible qualifications include:
ITI, Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm, D.Pharm, B.Tech, M.Tech (Mechanical).
Candidates must have prior formulation manufacturing experience. Freshers are not eligible.
Strong documentation skills, regulatory awareness, and QMS exposure are essential.
Location & Salary
Location: Shamirpet, Telangana
Salary: Competitive and based on experience. Industry-aligned compensation for regulated pharmaceutical manufacturing roles.
Application Process
Walk in on 20 February 2026 with:
- Updated Resume
- Recent Increment Letter
- Last 3 Months Payslips
- Last 3 Months Bank Statement
- Educational Certificates
- Aadhaar & PAN Card Copies
Outstation candidates may email their CV to jobs@spaccurelabs.com.
Why Consider SP Accure Labs?
Professionals here gain exposure to:
- Sterile injectable manufacturing systems
- Global regulatory dossier preparation
- Analytical method validation platforms
- QMS documentation and CAPA systems
- EU and ROW market regulatory compliance
Such exposure strengthens long-term career prospects in pharmaceutical manufacturing, regulatory affairs, analytical research, and quality management.
Frequently Asked Questions (FAQs)
1. Is formulation experience mandatory?
Yes. Only candidates with formulation plant experience are eligible.
2. Are freshers eligible?
No. All roles require prior pharmaceutical experience.
3. Are immediate joiners preferred?
Yes.
4. Can outstation candidates apply?
Yes, by emailing CV to jobs@spaccurelabs.com.
5. What documents are required for walk-in?
Resume, increment letter, payslips, bank statement, educational certificates, Aadhaar and PAN copies.
Summary
| Company | SP Accure Labs |
|---|---|
| Vacancies | OSD Production (Jr. Executive/Executive), Production Injectables (Operator/Chemist/Executive), Packing Injectables (Officer/Executive), Engineering (Executive), AR&D (Research Associate), Regulatory Affairs (Officer to Sr. Executive) |
| Required Education | ITI, Diploma, B.Sc, M.Sc, B.Pharm, M.Pharm, D.Pharm, B.Tech, M.Tech |
| Experience | 3–12 Years (Role Dependent) |

To apply for this job email your details to jobs@spaccurelabs.com