India's DMPLOI - Jobs & Networking AppHonour Lab Ltd, a leading API pharmaceutical company, has announced a Walk-In Drive on 07 June 2026 for multiple positions in Quality Control (QC), Quality Assurance (QA), and Production departments. This recruitment drive offers an excellent opportunity for both freshers and experienced professionals looking to build a career in the pharmaceutical manufacturing industry.
The company is seeking candidates with educational backgrounds in M.Sc, B.Pharm, B.Sc, B.Com, B.A, B.Tech (Chemical Engineering), and Diploma streams. Professionals with 0–8 years of experience are eligible to attend the walk-in interview.
Job Details
Details
Company Name
Honour Lab Ltd
Departments
Quality Control, Quality Assurance, Production
Qualification
M.Sc, B.Pharm, B.Sc, B.Com, B.A, B.Tech (Chemical Engineering), Diploma
Experience
0–8 Years
Walk-In Date
07 June 2026
Location
Sangareddy, Hyderabad, Telangana
Key Highlights
Opportunity to work with a reputed API pharmaceutical organization.
Hands-on exposure to advanced analytical instruments such as HPLC, GC, and LCMS.
Involvement in Method Validation, Quality Management Systems (QMS), Quality Assurance, and Production Operations.
Suitable for both freshers and experienced candidates.
Excellent learning environment with career growth opportunities.
Areas of Work
Quality Control (QC)
Selected candidates may be involved in:
HPLC & GC analysis
LCMS techniques
Raw material and finished product testing
Analytical method development and validation
Stability sample analysis
Quality Assurance (QA)
Responsibilities may include:
Documentation review
GMP compliance monitoring
QMS activities
Deviation and CAPA management
Internal audits and validation support
Production
Candidates may work in:
API manufacturing operations
Process monitoring
Batch execution
Equipment handling
Compliance with SOPs and GMP requirements
Walk-In Interview Instructions
Interested candidates should attend the walk-in drive with:
Updated resume
Educational certificates
Experience documents (if applicable)
Recent passport-size photographs
Government ID proof
This recruitment drive provides an excellent platform for candidates aspiring to gain experience in analytical laboratories, quality systems, and pharmaceutical production operations.
Technical FAQs
1. What is the difference between HPLC and GC in pharmaceutical analysis?
HPLC (High-Performance Liquid Chromatography) is primarily used for non-volatile and thermally sensitive compounds, whereas GC (Gas Chromatography) is used for volatile substances. Both techniques are widely used for impurity profiling and assay testing.
2. What is method validation in a pharmaceutical laboratory?
Method validation is the documented process of proving that an analytical method consistently produces accurate, precise, specific, and reliable results according to regulatory requirements.
3. What is the purpose of a Quality Management System (QMS)?
A QMS ensures that pharmaceutical products are consistently manufactured and controlled according to quality standards, regulatory guidelines, and GMP requirements.
4. Why is LCMS important in Quality Control?
LCMS (Liquid Chromatography-Mass Spectrometry) provides highly sensitive and accurate identification of impurities, degradation products, and trace-level compounds in pharmaceutical samples.
5. What is GMP and why is it critical in production?
Good Manufacturing Practices (GMP) are regulations that ensure products are consistently produced and controlled according to quality standards. GMP helps maintain product safety, efficacy, and compliance with regulatory authorities.
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