The pharmaceutical and contract research industry in India continues to expand rapidly, creating thousands of career opportunities for skilled science and pharmacy professionals. If you are searching for a promising career in analytical testing, quality control, method validation, or pharmaceutical research, then this latest hiring announcement from Accuprec Research Labs Pvt. Ltd. could be the perfect opportunity.
Accuprec Research Labs has officially announced a Mega Walk-In Interview Drive for multiple positions in its Analytical Development (AD) and Quality Control (QC) departments. The recruitment drive is being organized to support the company’s new facility expansion and will offer opportunities for both freshers and experienced professionals.
Candidates from Pharmacy, Chemistry, Life Sciences, and related backgrounds are encouraged to attend this walk-in interview and explore exciting career prospects with one of India’s leading Contract Research Organizations (CROs).
🏢 About Accuprec Research Labs Pvt. Ltd.
Accuprec Research Labs Pvt. Ltd. is a reputed pharmaceutical testing and research organization headquartered in Ahmedabad, Gujarat. The company is widely recognized for delivering high-quality analytical services to pharmaceutical companies across India and international markets.
The organization operates under various quality certifications and regulatory approvals, including:
✅ FDCA Approved Laboratory
✅ OECD-GLP Compliant Facility
✅ NABL Accredited Laboratory
✅ ISO 9001:2015 Certified Organization
With branch operations extending into the United States and Canada, Accuprec has established itself as a trusted name in pharmaceutical testing, analytical research, quality assurance, and regulatory compliance services.
Working with Accuprec provides professionals with exposure to advanced analytical instruments, international quality standards, and challenging research projects that contribute to the development of safe and effective pharmaceutical products.
📢 Why This Walk-In Drive is Important
The pharmaceutical industry is increasingly investing in analytical development, method validation, elemental impurity testing, and advanced instrumentation technologies.
As a result, companies require trained professionals capable of handling sophisticated instruments such as:
- HPLC
- GC
- LC-MS/MS
- Q-TOF
- ICP-MS
- ICP-OES
- Ion Chromatography
- Particle Size Analyzers
This recruitment drive offers candidates an opportunity to join a growing CRO and work with cutting-edge technologies used across pharmaceutical research and development.
Whether you are a fresher seeking your first industry exposure or an experienced analyst looking for career growth, this hiring drive offers positions across multiple experience levels.
📅 Walk-In Interview Details
Candidates planning to attend should note the following information carefully:
| Particulars | Details |
|---|---|
| Interview Date | 6th June 2026 (Saturday) |
| Interview Time | 09:00 AM to 05:00 PM |
| Job Location | Ahmedabad, Gujarat |
| Employment Type | Full-Time |
| Industry | Pharmaceutical / CRO |
| Departments | Analytical Development (AD) & Quality Control (QC) |
📍 Walk-In Venue
Candidates must report directly to:
Accuprec Research Labs Pvt. Ltd.
Opposite Zydus Pharmez
Near Matoda Patiya
Post: Matoda
Ahmedabad, Gujarat – 382213
India
Candidates are advised to arrive early to avoid registration delays and complete documentation formalities smoothly.
🔬 Department-Wise Job Openings
The company has announced multiple openings across several technical and non-technical functions.
Let’s explore each category in detail.
1️⃣ QC (Certificate of Analysis Preparation)
Experience Required
0–1 Year
Educational Qualification
- BA
- B.Com
- BCA
- B.Sc
- B.Pharm
- Equivalent Graduation Degree
Job Responsibilities
The selected candidates will primarily work on:
- Preparation of Certificates of Analysis (COA)
- Data compilation
- Documentation support
- Report generation
- Record maintenance
- Coordination with analytical teams
Freshers Can Apply
One of the biggest highlights of this recruitment drive is that fresh graduates are eligible for these positions.
Candidates seeking entry-level jobs in the pharmaceutical industry can use this opportunity to begin their careers in quality documentation and laboratory support functions.
2️⃣ HPLC, IC & Analytical Method Validation Positions
Experience Required
3–5 Years
Qualification
- B.Sc
- M.Sc
- B.Pharm
- M.Pharm
- Equivalent Technical Qualification
Open Roles
HPLC – QC
Professionals experienced in High-Performance Liquid Chromatography will perform routine testing and quality control activities.
IC – QC
Candidates familiar with Ion Chromatography techniques can apply for specialized analytical testing roles.
HPLC – AMV
Analytical Method Validation professionals with hands-on experience in validation studies are encouraged to attend.
Key Responsibilities
- Method development
- Method validation
- Sample analysis
- Instrument calibration
- Regulatory compliance
- Data review and reporting
3️⃣ LC-MS/MS and Q-TOF Analyst Openings
Experience Required
3–5 Years
Qualification
- B.Sc
- M.Sc
- B.Pharm
- M.Pharm
Positions Available
LC-MS/MS (QC + AMV)
Candidates with expertise in Liquid Chromatography-Mass Spectrometry systems can apply.
LC-MS / Q-TOF
Professionals experienced in Quadrupole Time-of-Flight Mass Spectrometry will have opportunities to work on advanced analytical projects.
Skills Preferred
- Method development
- Impurity profiling
- Bioanalytical testing
- Instrument troubleshooting
- Data interpretation
These are highly specialized roles offering excellent growth opportunities for experienced analysts.
4️⃣ GC & GC-MS/MS Professionals
Experience Required
3–5 Years
Qualification
- B.Sc
- M.Sc
- B.Pharm
- M.Pharm
Open Positions
- GC – QC
- GC – AMV
- GC-MS/MS Analyst
Major Responsibilities
- Gas Chromatography testing
- Method validation
- Stability studies
- Residual solvent analysis
- Instrument qualification
- Regulatory documentation
GC and GC-MS experts remain highly sought-after across CROs and pharmaceutical manufacturing organizations.
5️⃣ Elemental Impurity Testing Positions
Elemental impurity analysis has become increasingly important due to stringent global regulatory requirements.
Accuprec is currently hiring professionals for:
ICP-OES (QC + AMV)
Experience
3–5 Years
Responsibilities
- Heavy metal analysis
- Elemental impurity testing
- Method validation
- Compliance with ICH guidelines
ICP-MS (QC + AMV)
Experience
3–5 Years
Responsibilities
- Trace element analysis
- Method development
- Validation protocols
- Instrument maintenance
- Data review
Professionals skilled in ICP technologies often command excellent career growth and salary progression within the pharmaceutical sector.
6️⃣ Wet Lab Operations
Experience Required
1–3 Years
Qualification
- B.Sc
- M.Sc
- B.Pharm
- M.Pharm
Responsibilities
Wet Lab Analysts will perform:
- Chemical testing
- Titrations
- Identification tests
- Reagent preparation
- Laboratory documentation
- Sample handling
This role is ideal for professionals who enjoy hands-on laboratory work and traditional analytical chemistry techniques.
7️⃣ Particle Size Distribution (PSD) Analyst
Experience Required
1–3 Years
Qualification
- B.Sc
- M.Sc
- B.Pharm
- M.Pharm
Responsibilities
Selected candidates will work with:
- Malvern Particle Size Analyzer
- Zeta Potential Instruments
- PSD Studies
- Characterization activities
- Data interpretation
Particle size analysis is a critical aspect of pharmaceutical formulation development, making this a valuable specialization.
8️⃣ Reviewer & Documentation Specialist Positions
Experience Required
5–8 Years
Qualification
- B.Sc
- M.Sc
- B.Pharm
- M.Pharm
These senior-level positions are designed for experienced professionals capable of handling audits, compliance reviews, and technical documentation.
Reviewer – QC
Responsibilities include:
- Data review
- Analytical report verification
- Compliance checks
- Regulatory readiness
Reviewer – AMV
Candidates will oversee:
- Validation protocols
- Validation reports
- Analytical compliance
Reviewer – GC & GC-MS
Responsibilities include:
- Chromatographic data review
- Technical verification
- Documentation assessment
Reviewer – QC (GLP Activities)
Professionals with strong Good Laboratory Practice experience will review laboratory records and ensure compliance with regulatory standards.
Documentation Specialist – AMV
Responsibilities include:
- Validation documentation
- Protocol preparation
- Report review
- Regulatory submissions support
🎓 Educational Qualifications Accepted
The company is accepting applications from candidates with qualifications such as:
- B.Sc Chemistry
- M.Sc Chemistry
- B.Pharm
- M.Pharm
- BA
- B.Com
- BCA
- Other relevant graduation degrees
Candidates possessing practical laboratory experience will receive preference for technical positions.
📑 Documents Required for Walk-In Interview
Applicants should carry the following documents:
Essential Documents
✅ Updated Resume/CV
✅ Passport Size Photographs
✅ Academic Certificates
✅ Government ID Proof (Aadhar/PAN)
✅ Experience Certificates
For Experienced Candidates
✅ Last 3 Months Salary Slips
✅ Current CTC Details
✅ Latest Increment Letter
✅ Offer Letter (if available)
Carrying complete documentation helps speed up the evaluation process and salary discussions.
💼 Why Consider a Career at Accuprec?
Working at Accuprec can offer several professional advantages:
Exposure to Advanced Instruments
Employees gain practical experience on:
- HPLC
- GC
- LC-MS/MS
- Q-TOF
- ICP-MS
- ICP-OES
Career Growth
The organization continues expanding its analytical operations, creating long-term growth opportunities.
Learning Environment
Professionals work alongside experienced scientists and subject matter experts.
Regulatory Exposure
Employees gain experience with:
- GLP
- NABL
- ISO Standards
- Pharmaceutical Compliance Systems
International Client Exposure
The company serves both domestic and multinational pharmaceutical organizations.
📧 Unable to Attend the Walk-In?
Candidates who cannot visit Ahmedabad on the interview date may submit their profiles through email.
Recruitment Email
When sending your application, mention:
- Department Name
- Position Applied For
- Total Experience
- Current Location
in the email subject line.
☎️ HR Contact Details
For additional information regarding the recruitment process, candidates may contact:
📞 +91 7600138060
📞 +91 9099932105
Applicants are encouraged to contact during official working hours for faster assistance.
🎯 Final Thoughts
The Accuprec Research Labs Mega Walk-In Interview Drive 2026 presents an excellent opportunity for freshers and experienced pharmaceutical professionals seeking career advancement in Analytical Development, Quality Control, Method Validation, Elemental Impurity Testing, Documentation, and Review functions.
With vacancies ranging from entry-level COA preparation roles to senior reviewer positions, candidates across multiple experience brackets can participate in this hiring event. The company’s strong reputation, advanced analytical infrastructure, regulatory compliance standards, and expanding operations make it an attractive destination for professionals looking to build a successful career in the pharmaceutical and CRO industry.
If your expertise aligns with HPLC, GC, LC-MS/MS, ICP-MS, Wet Lab, PSD, QC Documentation, or Analytical Method Validation, ensure you attend the walk-in drive on 6th June 2026 and take the next step toward a rewarding pharmaceutical career.
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