India's DMPLOI - Jobs & Networking AppSP Accure Labs has announced a Walk-In Interview Drive for experienced pharmaceutical professionals at its Telangana manufacturing facility. The company is seeking skilled candidates from multiple departments including Packing Injectables, OSD Production, Engineering, Quality Control (QC), Analytical Research & Development (AR&D), and Information Technology (IT).
This recruitment drive offers an excellent opportunity for candidates with formulation pharmaceutical experience who are looking for career growth in a reputed pharma organization.
Walk-In Interview Details
Details
Company
SP Accure Labs
Interview Date
13 June 2026 (Saturday)
Time
09:30 AM – 12:30 PM
Location
Plot No. 12, Biotech Park, Phase II, Lalgadi Malakpet, Shamirpet Mandal, Medchal-Malkajgiri Dist., Telangana, India
Experience Required
3–10 Years
Industry
Pharmaceutical / Formulation Manufacturing
Departments Hiring
1. Packing Injectables
Designation: Operator / Executive
Experience: 3–6 Years
Required Skills:
QMS activities
BMR preparation
Labeling operations
Injectable packing processes
Qualification:
ITI
Diploma
B.Sc
M.Sc
B.Pharm
M.Pharm
2. OSD Production
Designation: Operator
Experience: 3–7 Years
Required Skills:
Granulation
Compression
Coating
HME operations
Bottle packing
Blister packing
Qualification:
ITI
Diploma
M.Sc
B.Pharm
M.Pharm
3. Engineering
Designation: Officer / Jr. Executive / Executive
Experience: 4–8 Years
Required Skills:
Mechanical process engineering
Instrumentation and calibration
Injectable equipment maintenance
HVAC systems
Electrical systems
Water system operations
Qualification:
Diploma
B.Tech
4. Quality Control (QC) – Stability
Designation: Executive / Sr. Executive
Experience: 6–10 Years
Required Skills:
Stability testing
ICH guideline compliance
OOS investigation
Stability data review
Method validation
Regulatory documentation
Qualification:
B.Sc
M.Sc
B.Pharm
M.Pharm
5. Analytical Research & Development (AR&D)
Designation: Officer / Executive
Experience: 3–6 Years
Required Skills:
HPLC operation and troubleshooting
GCMS analysis
LCMS analysis
Analytical method development and validation
Qualification:
B.Pharm
M.Pharm
M.Sc
6. Information Technology (IT)
Designation: Officer / Executive
Experience: 3–8 Years
Required Skills:
Server management
System maintenance
Network administration
Backup management
Application support
QMS software support
Empower software knowledge
Qualification:
Diploma
B.Tech
Documents Required
Candidates attending the walk-in interview should carry:
Updated Resume/CV
Recent Increment Letter
Last 3 Months Payslips
Last 3 Months Bank Statements
Educational Certificates
Aadhaar Card Copy
PAN Card Copy
Email ID: jobs@spaccurelabs.com
Contact Number: +91 73966 44772
Why Join SP Accure Labs?
SP Accure Labs is a growing pharmaceutical organization known for its focus on quality manufacturing, regulatory compliance, and innovation. Professionals joining the company get exposure to advanced formulation technologies, quality systems, and a collaborative work environment that supports career development.
Technical FAQs
1. What is the importance of BMR preparation in pharmaceutical manufacturing?
Batch Manufacturing Record (BMR) documents every manufacturing step, material usage, equipment details, and process parameters. It ensures traceability, regulatory compliance, and product quality according to GMP requirements.
2. Why is HPLC widely used in AR&D and QC laboratories?
High-Performance Liquid Chromatography (HPLC) is used for quantitative and qualitative analysis of pharmaceutical products. It helps determine assay, impurities, degradation products, and content uniformity with high accuracy and precision.
3. What is an OOS (Out of Specification) result?
An OOS result occurs when a test result falls outside predefined acceptance criteria. A detailed investigation is conducted to identify laboratory errors, manufacturing issues, or analytical method problems before final disposition.
4. What role does HVAC play in pharmaceutical manufacturing?
HVAC systems maintain controlled temperature, humidity, pressure differentials, and air cleanliness levels. Proper HVAC operation prevents contamination and ensures compliance with GMP standards.
5. What are ICH stability testing guidelines?
ICH stability guidelines define storage conditions and testing requirements used to establish a product’s shelf life, packaging suitability, and storage recommendations under various environmental conditions.
Note: Candidates with relevant formulation pharmaceutical experience are encouraged to attend the walk-in interview and explore career opportunities with SP Accure Labs.
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