Chemveda Life Sciences is hiring QA Freshers (M.Sc/M.Pharm) via walk-in on 27th June 2025 in Hyderabad. Join a USFDA-compliant CRO supporting global R&D.
💼 Chemveda Life Sciences Walk-In Drive 2025 for QA Executive Roles – Freshers Apply!
Are you a recent graduate in Chemistry or Pharmacy looking to kickstart your pharmaceutical career in Quality Assurance (QA)? Here’s your golden opportunity! Chemveda Life Sciences, a fast-growing CRO based in Hyderabad, is conducting a walk-in interview on 27th June 2025 (Friday) to hire Freshers and Executives for its QA department.
This is an exciting opening for candidates who are passionate about quality systems, compliance, and pharma documentation in a globally recognized contract research organization (CRO).
🏢 About Chemveda Life Sciences
Chemveda Life Sciences is a mid-sized, innovation-driven Contract Research Organization (CRO) offering integrated drug discovery, process R&D, and custom synthesis solutions to global clients. With a strong client base in pharma, biotech, and academia, Chemveda is renowned for its scientific rigor and client-centric approach.
From lab-scale synthesis to GMP manufacturing, Chemveda provides end-to-end chemistry support in drug development. The company operates out of USFDA-compliant facilities in Hyderabad and is known for building cost-effective, high-quality solutions across the drug development continuum.
🌍 Website: www.chemvedals.com
📌 Job Details – QA Executive (Freshers Can Apply)
| Position | QA Executive (Fresher/Experienced) |
|---|---|
| Experience | 0–5 Years |
| Qualification | M.Sc (Chemistry) / M.Pharm |
| Designation | Executive |
| Work Location | IDA Uppal, Hyderabad, Telangana |
✅ Job Type: Full-Time | On-site
🔍 Job Responsibilities: Quality Assurance Executive
As a QA Executive, you will play a critical role in maintaining compliance, quality documentation, and internal audits for regulatory and client requirements. Responsibilities include:
📋 Daily QA & Documentation
- Execution of day-to-day QA tasks as per SOP compliance
- Document issuance, retrieval, archival, and control
- Review and maintenance of equipment qualification records (IQ/OQ/PQ)
- Equipment/software compliance and backups
🧪 Quality System & QMS Monitoring
- Prepare QMS training modules and conduct training sessions
- Monitor CAPA, Change Control, Deviation, OOS/OOT, and risk assessments
- Internal audit coordination and tracking of non-compliances
🧫 Regulatory & Client Compliance
- Review of GMP projects, SOPs, Method Validation Protocols, and Specifications
- Support GMP facility audits and vendor assessments
- Scrutiny of GMP certifications, vendor questionnaires, and analytical reports
🧾 Reports & Compliance Verification
- Compile weekly/monthly QA reports
- Conduct lab rounds, circulate non-compliance alerts, and suggest CAPAs
- Coordinate internal audits and management review meetings
📈 Audit Handling & Closure
- Act as QA liaison during external and internal audits
- Compile and submit audit responses
- Ensure timely and successful audit cycle closure
🗓️ Walk-In Interview Details
| Event | Information |
|---|---|
| Date | Friday, 27th June 2025 |
| Time | 09:00 AM to 12:00 PM |
| Venue | Plot No. B-11/1, IDA Uppal, Hyderabad, Telangana, India |
| Contact Email | 📧 saivardhan.kothuri@chemvedals.com |
🗂️ Documents to Carry:
- Updated CV
- Academic Certificates
- Govt ID (Aadhar/PAN)
- Recent Passport-size photo
If you cannot attend the walk-in in person, email your profile to the HR contact above.
🌟 Why Join Chemveda Life Sciences?
✅ USFDA-Compliant Facilities: Work in globally recognized infrastructure adhering to top regulatory norms.
✅ Early Career Opportunity: Ideal for freshers to learn QA compliance, audits, and QMS in a real-time setup.
✅ Skill Development: Gain exposure to GMP, SOP writing, method validation, and vendor audits.
✅ Work Culture: Rated highly by employees for learning, mentorship, and career progression.
✅ Global Pharma Exposure: Serve biotech and pharma clients across USA, Europe, and Asia.
🎯 Who Should Apply?
This opportunity is best suited for:
- Freshers with a Master’s in Chemistry or Pharmacy (M.Sc/M.Pharm)
- Entry-level professionals with up to 5 years of QA or documentation experience
- Candidates aspiring to grow in pharma quality systems, regulatory compliance, or auditing
- Individuals looking for jobs in CROs, CDMOs, or API manufacturing companies.
📢 If you’re serious about building a high-impact career in pharmaceutical quality assurance, don’t miss this walk-in drive at Chemveda Life Sciences on 27th June 2025. With end-to-end exposure to QMS, documentation, and audit handling, this is the ideal launchpad for any QA fresher.
📝 Apply Now
Walk into the venue on the interview date or send your CV to:
📧 saivardhan.kothuri@chemvedals.com
Begin your journey with Chemveda – where science meets opportunity!
