Vital Therapeutics & Formulations Private Limited is a dedicated effort to be a reliable partner by offering products and services with highest quality standards in the domains of Contract Manufacturing, Vitamins & Food Ingredients, Aqua Culture and Animal Health.
We at Vital understand and appreciate the importance of meeting the customer requirements and aim towards customer delight.
DATE AND TIME:
- Date: 27th September ‘2025
- Time: 9:30am to 12:30pm
- Venue: Vital Therapeutics and Formulation Pvt. Ltd. Plot No:47 B/2, St. No.4, Phase-I, IDA, Cherlapally, Secunderabad.
Contact:
- E-mail Id: hr@vitalpharma.in
- HR: 9666 977 644
POSITIONS:
1. Department: Production Chemist – Male
- Qualification: B. Pharmacy / M. Pharmacy
- Experience: Fresher’s
- Passed Out: 2024 & 2025
- Note: Telugu language mandatory
2. Department: Production Operator – Male
- Qualification: ITI/Diploma – Mechanical /Fitter
- Experience: 0 to 2years
- Passed Out: 2023 to 2025
- Skills: Liquid Filling and Sealing Operator
3. Department: QA – Sr. Executive / Asst. Manager – Male
- Qualification: MSc / M. Pharmacy
- Experience: 5 to 10 years
- Salary: Up to 6 LPA
JOB DETAILS: –
- To assist the Management in executing all GMP / GLP related activities.
- To provide the all documentation support to meet the local and national regulatory requirements and filings
- To coordinate with the regulatory and customer’s auditors for timely completion of auditing, compliance reports etc.
- Handling of Market Complaints, Returns /Recall, Deviations, OOS, Validation report review.
- To review and approve all specifications, STPs, SOPs, BMR, BPR, MFR.
- To review and approve of all validation protocols and reports.
- To ensure quality related complaints are investigated and resolved in coordination with QC, QA, and production departments.
- To handle critical quality systems like deviations, change control, CAPA, training, OOS, validations and Qualifications.
- To review and approve annual product quality reviews.
- To carryout self-inspection (internal audits) of the facility to ensure GMP systems are being adhered to.
- To review and approve of contract laboratories, critical starting materials vendors, API manufacturers and Quality Agreements Management.
- To Review and approve Certificate of Analysis as per the customer requirement.
- To Review and approve Vendor Qualification documents.
- To provide the GMP trainings to build awareness on the site.
- Excellent communication and writing skills
- Take care of QA All Activities
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