Wexford Laboratories Walk-in Interview 2025.Wexford Laboratories Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Vacancy details:
- Department: QC
- Experience: 2-7 YERAS
- Qualification: Bsc,Msc,Bpharm,Mpharm
- Salary: ₹Not Disclosed
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description: Greeting from Wexford Laboratories !!!
Role & responsibilities
1. Analytical Testing using HPLC
- Operate and maintain HPLC systems for quantitative and qualitative analysis.
- Perform routine testing of raw materials, finished products, in-process samples, and stability samples.
- Analyse active pharmaceutical ingredients (API) for assay, impurities, degradation products, dissolution profiles, etc.
2. Method Execution
- Perform analysis using pharmacopeial (USP, BP, IP, Ph. Eur.) or validated in-house methods.
- Prepare mobile phases, standards, and sample solutions as per method protocols.
- Adhere to system suitability criteria before sample analysis.
3. Data Handling and Documentation
- Record and document chromatograms, peak integrations, system suitability, and raw data accurately.
- Prepare analytical reports, calculation sheets, and ensure entries in logbooks and LIMS (if applicable).
- Ensure compliance with ALCOA+ principles of data integrity.
4. Instrument Maintenance and Calibration
- Perform routine instrument checks and minor maintenance (e.g., flushing, degassing).
- Document instrument usage and maintenance logs.
- Coordinate with engineering/QA for scheduled calibration and preventive maintenance.
5. Compliance and Good Laboratory Practices (GLP)
- Follow GMP and GLP guidelines in all laboratory operations.
- Ensure correct labelling, storage, and disposal of chemicals and reagents.
- Maintain personal protective equipment (PPE) usage and safety protocols in the laboratory.
6. OOS, OOT, and Deviation Handling
- Immediately report abnormal results (Out of Specification/Out of Trend) to supervisors.
- Assist in root cause analysis and CAPA implementation.
- Participate in re-analysis, investigation, and documentation of any laboratory incident.
7. Stability & Validation Support
- Perform stability study testing at predefined intervals.
- Assist in method validation/verification activities using HPLC.
- Document test results for inclusion in stability or validation reports.
8. Reagent and Column Management
- Label, prepare, and store reagents and mobile phases properly.
- Maintain column inventory, usage logs, and cleaning schedules.
- Ensure traceability and suitability of reference standards and working standards.
9. Regulatory and Audit Preparedness
- Ensure laboratory readiness for audits (USFDA, WHO, MHRA, etc.).
- Maintain proper archiving and traceability of HPLC test data.
- Present analytical data and records during internal and external inspections.
Preferred candidate profile
Educational Qualifications & Experience
- Qualification: B.Pharm / M.Pharm / M.Sc. in Analytical Chemistry, Pharmaceutical Chemistry, or equivalent.
- Experience: 14 years of experience operating HPLC in a regulated pharmaceutical QC environment.
- Technical Knowledge: Proficiency in operating HPLC systems (Waters, Shimadzu, Agilent) and software (Empower, Lab solutions).
Walk-In Interview Alert – Wexford Laboratories Pvt Ltd 🚨
Time and Venue
15th November – 30 November , 9.30 AM – 5.30 PM
Sujyo Arcade no. 3987, 3989, 80 feet road, Dr. Muthu IV phase,, Dr Raj Rd, 1st phase Girinagar, Srinivasnagar, Banashankari, Bengaluru, Karnataka 560050
Contact – Sahana ( 9845106656 )