India's DMPLOI - Jobs & Networking AppBharat Parenterals Limited, a well-established pharmaceutical manufacturing company in India, has announced a Walk-In Interview Drive for multiple positions in Quality Control (QC), Quality Assurance (QA), and Analytical Development Laboratory (ADL) departments. This recruitment drive offers excellent opportunities for freshers and experienced pharmaceutical professionals looking to build their careers in the regulated pharma industry.
Walk-In Interview Details
Interview Dates: 6th June, 8th June & 9th June 2026
Time: 10:00 AM to 04:00 PM
Available Positions
1. Quality Control (QC)
Position: Trainee / Junior Officer
No. of Vacancies: 2
Qualification: B.Sc / M.Sc
Experience: 1 to 3 Years
Technical Skills: HPLC, GC
2. Quality Assurance (QA)
Position: Apprentice / Junior Officer / Senior Officer
No. of Vacancies: 4
Qualification: B.Pharm / M.Pharm
Experience: 0 to 3 Years
Technical Skills: IPQA, Lab-QA
3. Analytical Development Laboratory (ADL)
Position: Apprentice
No. of Vacancies: 1
Qualification: B.Sc / M.Sc
Experience: Fresher
Technical Skills: Basic knowledge of analytical techniques
Venue
Bharat Parenterals Limited
144-A, Village Haripura, Ta. Savli,
Jarod-Samlaya Road, Vadodara,
Gujarat – 391520
Important Instructions
Candidates attending the interview should carry:
Updated Resume/CV
Passport Size Photograph
Current CTC Details (if applicable)
Educational Documents
Experience Certificates (if applicable)
Note: Candidates must be willing to enter into a 3-year long-term association agreement with the organization.
Why Join Bharat Parenterals?
Opportunity to work in a reputed pharmaceutical manufacturing environment.
Exposure to quality systems, analytical testing, and regulatory compliance.
Career growth opportunities for both freshers and experienced professionals.
Hands-on experience with modern pharmaceutical quality and analytical instruments.
Technical FAQs
1. What is the role of HPLC in Quality Control laboratories?
HPLC (High-Performance Liquid Chromatography) is used to identify, quantify, and assess the purity of pharmaceutical compounds. It is one of the most important analytical techniques for drug testing and stability studies.
2. What are the primary responsibilities of an IPQA professional?
In-Process Quality Assurance (IPQA) professionals monitor manufacturing activities, verify compliance with SOPs, conduct line clearances, and ensure adherence to GMP requirements during production.
3. Why is GC (Gas Chromatography) used in pharmaceutical analysis?
GC is commonly used to detect and quantify volatile compounds, residual solvents, and impurities in pharmaceutical products according to regulatory guidelines.
4. What is the importance of laboratory documentation in QA and QC?
Proper documentation ensures data integrity, regulatory compliance, traceability of results, and successful audits by authorities such as USFDA, MHRA, and WHO-GMP.
5. What analytical knowledge is expected from ADL candidates?
ADL candidates should understand basic analytical concepts such as sample preparation, instrument calibration, method development principles, chromatography fundamentals, and data interpretation.
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