India's DMPLOI - Jobs & Networking AppSynokem Pharmaceuticals Ltd., a well-established pharmaceutical company committed to delivering quality healthcare solutions, has announced a recruitment drive for Quality Control (HPLC) professionals at its SIDCUL, Haridwar manufacturing facility. This opportunity is ideal for candidates with HPLC analysis experience who are looking to build their careers in a regulated pharmaceutical environment.
Job Overview
Particular Details
Company
Synokem Pharmaceuticals Ltd.
Department
Quality Control (QC)
Position
Quality Control (HPLC)
Job Location
SIDCUL, Haridwar, Uttarakhand
Experience Required
1–4 Years
Salary
₹3.50 LPA CTC
Industry
Pharmaceutical Manufacturing
Employment Type
Full-Time
About Synokem Pharmaceuticals
Synokem Pharmaceuticals Ltd. is known for manufacturing high-quality pharmaceutical formulations while maintaining strict quality standards. The company offers employees opportunities to work with modern analytical instruments, professional development programs, and a safe working environment.
Key Responsibilities
Perform HPLC analysis of raw materials, finished products, and stability samples.
Prepare mobile phases, standard solutions, and test samples.
Operate, calibrate, and maintain HPLC systems.
Review chromatograms and ensure compliance with analytical specifications.
Maintain analytical documentation according to GMP and regulatory guidelines.
Follow laboratory safety procedures and Good Documentation Practices (GDP).
Support investigations related to Out of Specification (OOS) and Out of Trend (OOT) results.
Desired Candidate Profile
B.Pharm, M.Pharm, B.Sc., M.Sc., or equivalent qualification in a relevant discipline.
1–4 years of experience in Quality Control with HPLC operation.
Knowledge of cGMP, GLP, and pharmaceutical quality systems.
Good analytical and documentation skills.
Ability to work in a manufacturing environment.
Salary & Benefits
Annual Package: ₹3.50 LPA CTC
Career growth opportunities
Learning and development programs
Safe and quality-focused workplace
Exposure to regulated pharmaceutical manufacturing
How to Apply
Interested candidates can send their updated CV to:
Email: job.p2@synokempharma.com
WhatsApp: 7417052714
Ensure your resume includes your educational qualifications, experience, current CTC, expected CTC, notice period, and contact details.
Technical FAQs
1. What is HPLC in pharmaceutical Quality Control?
Answer: High Performance Liquid Chromatography (HPLC) is an analytical technique used to identify, separate, and quantify pharmaceutical compounds. It is widely used for assay, impurity profiling, dissolution testing, and stability studies.
2. What GMP documentation should a QC analyst maintain?
Answer: QC analysts should maintain analytical worksheets, instrument logbooks, calibration records, chromatograms, raw data, standard preparation records, and test reports while following Good Documentation Practices (GDP).
3. What should be checked before starting an HPLC analysis?
Answer: Before analysis, analysts should verify system suitability, column condition, mobile phase preparation, detector wavelength, flow rate, pressure, instrument calibration, and sample preparation.
4. What is System Suitability Testing (SST)?
Answer: System Suitability Testing confirms that the HPLC system is performing correctly before sample analysis. Typical parameters include resolution, tailing factor, theoretical plates, retention time, and %RSD of replicate injections.
5. What is an Out of Specification (OOS) result?
Answer: An OOS result occurs when a test result falls outside the predefined specification limits. It requires a documented investigation to determine the root cause and appropriate corrective and preventive actions (CAPA).
Why Join Synokem Pharmaceuticals?
Work with advanced HPLC analytical instruments.
Gain experience in a GMP-compliant pharmaceutical facility.
Excellent learning and career advancement opportunities.
Competitive salary package.
Professional and safe working environment.
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