Interested candidates must share their CVs on talent@v-esnure.com & a.salunkhe@v-ensure.comRole & responsibilities 1. To guide the team for experimental trials and review stability study results compilation and interpretation.2. To prepare product development study protocols and reports as per regulatory requirement.3. To prepare technology transfer documents like MF, Risk assessment based upon CPP & CQA.4. To execute scale up/ exhibit at plant and prepare scale up summary report.5. To prepare PDR and support for regulatory submission.6. To prepare pre- ANDA documentsPreferred candidate profile Candidate must have experience in Formulation Development for Injectable dosage forms.Perks and benefits Best of Industry

-We are looking out candidates for different sections and positions in Quality Assurance department. Such as IPQA, QMS, Lab QA, AMV QA.Interested candidates can share their resumes on a.salunkhe@v-ensure.com & n32admin@v-ensure.com Role & responsibilities 1) IPQA- In process Checks.- Line clearance- Review of BMR, BPR2) QMS- Handling and review of Change control, deviations, CAPA of different departments.- Document issuance, archival, retrieval.- Facing the Audits.3) Lab QA & AMV QA- Managing Analytical QA activities.- Review of documents related to QC i.e. Raw material, finished products, stability.- Review of documents of Method validation, Assay.Preferred candidate profile - Candidates must have experience in Pharma formulation plant.- Must have good communication skills.- Candidates from Regulatory plant will be given preference.- Immediate joiners will be preferred.Perks and benefits Best in the industry