India's DMPLOI - Jobs & Networking AppShilpa Medicare Ltd. has announced a Walk-In Interview in Hyderabad for experienced pharmaceutical professionals. The recruitment drive is being conducted for positions in the Analytical Services (Quality Control – Formulation) and Quality Assurance (Formulation) departments.
Candidates with M.Pharm, B.Pharm, M.Sc, or B.Sc qualifications and 2 to 6 years of relevant pharmaceutical industry experience can explore this opportunity. Candidates from QC Formulation backgrounds are also eligible for Quality Assurance positions, as mentioned in the official recruitment notification.
The walk-in interview is scheduled for 11th July 2026 (Saturday) at the Shilpa Medicare facility in Nacharam, Hyderabad.
Shilpa Medicare Walk-In Interview – Overview
Particulars Details
Company Name
Shilpa Medicare Ltd.
Industry
Pharmaceutical / Healthcare
Recruitment Type
Walk-In Interview
Departments
Analytical Services (QC – Formulation) & Quality Assurance (Formulation)
Designations
Executive / Senior Executive
Qualifications
M.Pharm, B.Pharm, M.Sc, B.Sc
Experience Required
2 to 6 Years
Job Location
Nacharam, Hyderabad
Walk-In Date
11th July 2026 (Saturday)
Interview Time
10:00 AM to 1:00 PM
Candidate Preference
Male candidates preferred, as stated in the official advertisement
Additional Eligibility
QC Formulation candidates are eligible for the QA opening
Available Positions and Eligibility Details
1. Analytical Services – Quality Control (Formulation)
Shilpa Medicare is recruiting experienced candidates for its Analytical Services (Quality Control – Formulation) department.
Designation: Executive / Senior Executive
Qualifications: M.Pharm, B.Pharm, M.Sc, or B.Sc
Experience: 2 to 6 years
Job Location: Nacharam, Hyderabad
Required Skills and Experience
Candidates should have hands-on experience in executing analytical method validation and monitoring validation parameters according to ICH and ANVISA guidelines.
Applicants should be proficient in the preparation and review of:
Analytical method validation protocols
Raw analytical data
Method validation reports
Regulatory-compliant documentation
Candidates should possess strong knowledge of formulation finished product analysis, covering both oral dosage forms and injectable products.
Practical experience in handling analytical instruments and techniques is required, including HPLC, GC, LC/GC, FTIR, UV-Visible Spectrophotometer, and Karl Fischer water content determination techniques.
The official notification specifically mentions that if candidates refer to LBPC, they should clarify whether it relates to LC/GC.
2. Quality Assurance – Formulation
Shilpa Medicare is also hiring candidates for its Quality Assurance (Formulation) department.
Designation: Executive
Qualifications: M.Pharm, B.Pharm, or M.Sc
Experience: 2 to 6 years
Job Location: Nacharam, Hyderabad
Important Eligibility Note: Candidates with experience in QC Formulation are eligible to apply for this position.
Required Skills and Responsibilities
Candidates should have experience in the review and approval of various analytical and quality documents, including:
Analytical documents and raw data
Audit trails
Calibration and Preventive Maintenance (PM) records
Analyst qualification documents
Reference and working standard qualification records
Applicants should understand Good Manufacturing Practices (GMP) and data integrity requirements applicable to pharmaceutical quality systems.
The position also requires experience in monitoring:
Laboratory Information Management System (LIMS) data
Chromatographic systems
Stability chamber performance
Candidates should be capable of ensuring data accuracy, regulatory compliance, and adherence to pharmaceutical quality standards.
Shilpa Medicare Walk-In Interview Date and Time
The recruitment drive will be conducted according to the following schedule:
Interview Date: 11th July 2026 (Saturday)
Interview Time: 10:00 AM to 1:00 PM
Candidates are advised to arrive at the interview venue on time with all required documents.
Walk-In Interview Venue
Shilpa Medicare Ltd.
Plot No. 79, Road No. 15,
Survey No. 125, IDA Mallapur,
Nacharam, Uppal Mandal,
Telangana – 500076
Documents Required for the Interview
Candidates attending the Shilpa Medicare walk-in interview should carry the following documents:
Updated Resume/CV
Recent Increment Letter or Offer Letter with complete CTC breakup
Latest 3 months’ salary slips and 6 months’ bank statement
Copies of all educational certificates
Copy of Aadhaar Card and PAN Card
Candidates should carry clear and updated copies of all documents to facilitate the recruitment and verification process.
Unable to Attend the Walk-In Interview?
Candidates who are unable to attend the walk-in interview can send their updated resumes to the email address mentioned in the official recruitment advertisement:
Email: karthik.kumar@vbshilpa.com
Applicants should mention their relevant department, total experience, current location, and current designation in the email subject or resume for better clarity.
Why Join Shilpa Medicare?
Shilpa Medicare Ltd. operates in the pharmaceutical and healthcare sector with a focus on delivering affordable healthcare products. This recruitment drive offers experienced QC and QA professionals an opportunity to work in areas involving analytical method validation, formulation analysis, pharmaceutical quality systems, GMP compliance, data integrity, LIMS, and chromatographic systems.
Candidates looking to develop their careers in pharmaceutical Quality Control, Analytical Services, or Quality Assurance can consider attending this recruitment drive if they meet the required eligibility criteria.
How to Apply for Shilpa Medicare Recruitment
Interested and eligible candidates can directly attend the walk-in interview at the specified venue on 11th July 2026.
Before attending the interview, candidates should carefully review the required qualifications, experience, technical skills, and documentation requirements.
Candidates unable to attend can forward their updated resumes to the email address provided in the official recruitment notification.
5 Technical FAQs for Shilpa Medicare QC & QA Interview
1. What is analytical method validation, and which parameters are commonly evaluated?
Analytical method validation is the documented process used to demonstrate that an analytical procedure is suitable for its intended purpose. Common validation parameters include accuracy, precision, specificity, linearity, range, robustness, detection limit (LOD), and quantitation limit (LOQ). The applicable parameters depend on the analytical method and regulatory requirements.
2. What is the difference between Quality Control and Quality Assurance in the pharmaceutical industry?
Quality Control (QC) focuses mainly on sampling, testing, analytical activities, laboratory investigations, and confirming that materials and finished products meet predefined specifications.
Quality Assurance (QA) focuses on establishing and maintaining systems that ensure pharmaceutical products are consistently manufactured, tested, documented, and released according to GMP requirements and approved procedures.
3. What is an audit trail in pharmaceutical computerized systems?
An audit trail is a secure, computer-generated, time-stamped electronic record that allows the reconstruction of events related to the creation, modification, or deletion of electronic data. Audit trail reviews are important for ensuring data integrity, traceability, accountability, and regulatory compliance.
4. What is the purpose of system suitability testing in HPLC analysis?
System suitability testing verifies that the chromatographic system is performing adequately before or during sample analysis. Common parameters include retention time reproducibility, theoretical plates, tailing factor, resolution, and percentage relative standard deviation (%RSD).
Acceptance criteria are defined in the analytical method, pharmacopoeia, or approved procedure.
5. What is the role of Karl Fischer titration in pharmaceutical Quality Control?
Karl Fischer titration is an analytical technique used to determine the water or moisture content of pharmaceutical raw materials, intermediates, and finished products. It is widely used because it provides selective and accurate moisture determination. The two primary techniques are volumetric Karl Fischer titration and coulometric Karl Fischer titration.
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