Vital Therapeutics and Formulations – Walk in Interviews for QC / Production Department On 23rd Aug’2025 @ Cherlapally ‘Hyderabad.
1. Department: Production Chemist – Male
- Qualification: BSc / B. Pharmacy / M. Pharmacy
- Experience: 1- 2years
- Skills: Liquid Orals’ Manufacturing Chemist.
2. Department: Production Operator- Male
- Qualification: Diploma / ITI – Mechanical /Fitter
- Experience: 1- 2years
- Skills: Liquid Filling and Sealing Operator
3. Department: QC – Male
- Qualification: B. pharmacy / M. Pharmacy /MSc
- Experience: 1- 4 years (Pellets Exposer)
- Skills: Wet /RM/HPLC / Stability / validation
Walk-In Interview Details:
- Date: 23rd Aug’ 2025
- Time: 10:00am to 12:30pm
- Interview Venue: Vital Therapeutics and Formulation Pvt. Ltd. Plot No:47 B/2, St. No.4, Phase-I, IDA, Cherlapally, Secunderabad.
- E-mail Id: [email protected]
- HR: 9666 977 644
Vital Therapeutics and Formulations – Walk in Interviews for QA – Sr. Executive / Asst. Manager On August’2025 @Hyderabad – Apply Now.
- Department: QA – Sr. Executive / Asst. Manager
- Qualification: MSc / M. Pharmacy
- Experience: 5 to 10 years
- Working Location: Cherlapally (Nearby Habsiguda, ECIL, Kushaiguda)
- Salary UP to 6 LPA
JOB DESCRIPTION: –
1) To assist the Management in executing all GMP / GLP related activities.
2) To provide the all documentation support to meet the local and national regulatory requirements and filings
3) To coordinate with the regulatory and customer’s auditors for timely completion of auditing, compliance reports etc.
4) Handling of Market Complaints, Returns /Recall, Deviations, OOS, Validation report review.
5) To review and approve all specifications, STPs, SOPs, BMR, BPR, MFR.
6) To review and approve of all validation protocols and reports.
7) To ensure quality related complaints are investigated and resolved in coordination with QC, QA, and production departments.
8) To handle critical quality systems like deviations, change control, CAPA, training, OOS, validations and Qualifications.
9) To review and approve annual product quality reviews.
10) To carryout self-inspection (internal audits) of the facility to ensure GMP systems are being adhered to.
11) To review and approve of contract laboratories, critical starting materials vendors, API manufacturers and Quality Agreements Management.
12) To Review and approve Certificate of Analysis as per the customer requirement.
13) To Review and approve Vendor Qualification documents.
14) To provide the GMP trainings to build awareness on the site.
How to Apply:
- Interested Candidates with relevant experience @ qualification can share their update resume to E-mail Id [email protected]
