Job Description: Blister Packing Machine Operator ( BQS- Primary & Secondary) ( No. of positions- 02 nos.) To perform daily activities of Blister Packing area. Well versed with the BQS Primary or Secondary machine handling. (Make BQS Primary- ACG Pam pack, BQS Secondary- ANTRAS). To perform weighing balance calibration & verification activities. To record and maintain proper documentation of production area along with area log books. 2. Coating Operator (No. of positions - 01 nos.) To perform daily activities of Coating area. Well versed with the Coating machine handling. (Make Kevin Autocoater). To perform weighing balance calibration & verification activities. To record and maintain proper documentation of production area along with area log books. Interested candidates can share their resumes on below mentioned E-Mail ID's: n32admin@v-ensure.com career@v-ensure.com a.salunkhe@v-ensure.com Interested candidates can also reach on 8356911996 for further details. While sending the resume mention your expertise area in the subject line & mention below details in the mail body: Current CTC Expected CTC Notice period Total Experience Reason for change
Dear Candidates, We are looking for our USFDA & EUGMP approved plant located at Rasayani, Patalangana MIDC for QMS -Sr. Officer/ Executive. Role & Responsibilities 1.Coordination and evaluation of QMS (Change control, Deviation, CAPA 2.Training Management- Approval of training, allocation of training followed by tracking. 3. New product initiation and evaluation/tracking. 4. Preparation and review of sectional and cross functional department SOPs 5. To carry out all responsibilities assigned by section head as per cGMP, GDP and zero data integrity. Preferred candidate profile: Candidate must have experience in Pharma Formulation Company and exposure in Regulated Market (USFDA & EU - GMP). Interested candidate can share CVs on: n32admin@v-ensure.com
Dear Candidates, We are looking for our USFDA & EUGMP approved plant located at Rasayani, Patalangana MIDC for Manager / Section Head IPQA. Role & responsibilities 1. To Lead IPQA activities. 2. Strategies, plan and organize the team's resources to perform day to day operations 3. Ensure Quality compliance as per CGMP requirement in manufacturing facility and inspection readiness at all times and represent in regulatory audits. 4. Review and approval of all SOPs, protocols, reports related to IPQA section. 5. To provide Line clearance by ensuring clearance of documents as per requirement. 6. To verify and coordinate In process and finished product, cleaning validation and any other sampling. 7. Investigation of critical deviations, Incidents, OOS, OOTs, market complaints, recalls and any other related to the manufacturing facility. 8. Ensure acceptance quality level and certification of inspectors as per respective SOP. 9. Initiation, review and approval of QMS documents (Change control, Deviation, CAPA but not limited to). 10. To prepare and review Quality Risk Assessment. 11. Evaluation and Approval of Qualification documents (Area/ facility/ equipment), Risk assessment, protocols, reports and Annual product review. 12. Monitoring execution of calibrations of IPQA equipment / instrument as per calibration schedule with respective SOPs. Preferred candidate profile Candidate must have experience in Pharma Formulation Company and exposure in Regulated Market(USFDA & EU - GMP). Team handling experience is mandatory. Interested candidates can share Cv on : n32admin@v-ensure.com
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