India's DMPLOI - Jobs & Networking AppEris Therapeutics Ltd. is inviting applications from experienced professionals for its Quality Control (QC) department at the Bavla, Ahmedabad manufacturing facility. Candidates with experience in HPLC analysis, method validation, and laboratory operations are encouraged to apply.
Job Details
Company: Eris Therapeutics Ltd.
Department: Quality Control (QC)
Designation:
- Officer
- Executive
- Senior Executive
Job Location: Bavla, Ahmedabad, Gujarat
Experience Required: 0–7 Years
Key Responsibilities
- Analysis of raw materials, in-process samples, and finished products using HPLC.
- Calibration and preventive maintenance of HPLC instruments.
- Method validation activities.
- Stability sample analysis.
- Ensure compliance with laboratory procedures and quality standards.
Eligibility Criteria
- B.Pharm, M.Pharm, B.Sc, M.Sc, or other relevant Life Science qualification.
- 0–7 years of experience in Quality Control within the pharmaceutical industry.
- Hands-on experience in HPLC operation and analytical testing.
- Knowledge of GMP, GLP, and pharmaceutical quality systems will be an added advantage.
How to Apply
Interested candidates can send their updated resume to:
Email: recruitment@eristherapeutics.com
For More Information: +91 9558001555
Quick Highlights
- Company: Eris Therapeutics Ltd.
- Department: Quality Control
- Positions: Officer, Executive & Sr. Executive
- Experience: 0–7 Years
- Location: Bavla, Ahmedabad, Gujarat
- Apply Via: recruitment@eristherapeutics.com
Related Basic Interview Questions for Advance Preparation
1. Tell me about yourself.
Answer: Briefly introduce yourself, your educational qualification, QC experience, instruments handled (HPLC, UV, FTIR, Dissolution), and current role.
2. Why do you want to join Eris Therapeutics?
Answer: Mention Eris’ reputation in the pharmaceutical industry, quality standards, learning opportunities, and career growth.
3. What are your current job responsibilities?
Answer: Discuss sample analysis, HPLC operation, documentation, instrument calibration, stability testing, and GMP compliance.
HPLC Interview Questions
4. What is HPLC?
Answer: High Performance Liquid Chromatography is an analytical technique used to separate, identify, and quantify components in pharmaceutical samples.
5. What are the major components of HPLC?
- Solvent Reservoir
- Degasser
- Pump
- Injector/Autosampler
- Column
- Detector
- Data Processing System
6. What is the difference between Isocratic and Gradient Elution?
- Isocratic: Mobile phase composition remains constant.
- Gradient: Mobile phase composition changes during the run.
7. What is Retention Time (RT)?
Answer: The time taken by a compound to travel through the column and reach the detector.
8. What is Tailing Factor?
Answer: It measures peak symmetry. Acceptance criteria are generally ≤ 2.0.
9. What is Resolution?
Answer: Resolution indicates the degree of separation between two adjacent peaks. Generally, Rs ≥ 2.0 is acceptable.
10. What is Theoretical Plate?
Answer: It indicates column efficiency. Higher plate count means better separation.
Method Validation Questions
11. What are the parameters of method validation?
- Specificity
- Accuracy
- Precision
- Linearity
- Range
- Robustness
- Ruggedness
- Detection Limit (LOD)
- Quantitation Limit (LOQ)
12. Difference between Accuracy and Precision?
- Accuracy: Closeness to the true value.
- Precision: Reproducibility of results.
13. What is Robustness?
Answer: The method’s ability to remain unaffected by small deliberate changes in analytical conditions.
Stability Questions
14. What is Stability Testing?
Answer: Stability testing determines how the quality of a drug changes over time under environmental factors.
15. Types of Stability Studies?
- Long-Term
- Accelerated
- Intermediate
- Photostability
Instrument Questions
16. Which instruments have you handled?
- HPLC
- UV Spectrophotometer
- FTIR
- Dissolution Apparatus
- pH Meter
- Analytical Balance
- Karl Fischer
- GC (if applicable)
17. How do you calibrate an HPLC?
Explain system suitability, pump flow verification, wavelength accuracy, injector precision, and documentation as per SOP.
GMP & Documentation
18. What is GMP?
Answer: Good Manufacturing Practices ensure medicines are consistently produced and controlled according to quality standards.
19. What is GDP?
Answer: Good Documentation Practices ensure accurate, complete, and traceable documentation.
20. What should you do if an OOS result occurs?
- Inform the supervisor.
- Do not discard data.
- Follow the OOS investigation procedure.
- Identify the root cause.
- Document all findings.
21. Difference between OOS and OOT?
- OOS (Out of Specification): Result outside the approved specification.
- OOT (Out of Trend): Result within specification but significantly different from historical data.
HR Interview Questions
22. Why should we hire you?
Highlight your analytical skills, HPLC experience, GMP knowledge, teamwork, and willingness to learn.
23. What are your strengths?
- Analytical thinking
- Attention to detail
- Documentation
- Time management
- Problem-solving
24. What are your weaknesses?
Choose a genuine but manageable weakness and explain how you’re improving it.
25. Are you willing to work in shifts?
Answer: Yes.
26. What are your salary expectations?
State that you’re open to discussing a package based on company standards and your experience.
Frequently Asked Technical Questions
- What is System Suitability Test (SST)?
- What is Blank, Standard, Sample, and Placebo?
- What is Relative Standard Deviation (RSD)?
- Difference between Assay and Content Uniformity.
- What is Forced Degradation?
- What is LOD and LOQ?
- What is a Chromatogram?
- Difference between Assay and Dissolution.
- Difference between Calibration and Validation.
- What precautions should be taken while operating HPLC?
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