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
Dear Candidates, V-Ensure Pharma (USFDA & EU GMP approved Formulation plant ) located at additional Patalganga MIDC near Panvel is hiring for Sr. Officer / Executive HR & Admin role. Role & responsibilities 1. Talent Acquisition & Management 2. Employee life cycle management 3. Supervision of Time office Management 4. Supports to PMS activity 5. Handling QMS activities such as SOP Preparation, SOP Compliance & Pharma Audits 6. Sound Knowledge of Statutory compliances. Preferred candidate profile Candidate having experience in Pharmaceutical Company is preferable
Role & responsibilities 1.Led end-to-end project management for EU, US and CMO projects, ensuring on-time, in-scope, and on-budget delivery. 3. Responsible for tracking & monitoring each step in the process & managing projects (Dosage form: OSD, Nasal) so that project milestones are completed as per planned timelines 4. To create & track detailed project plan in MS Projects 5. Preparation of project budgets & quarterly reconciliations
Role & Responsibilities Candidate Profile: A highly skilled professional with strong knowledge of project planning and project management , along with hands-on experience in the pharmaceutical industry (Formulation) Key Responsibilities Project Planning & Management Develop comprehensive project plans, timelines, and resource allocations. Monitor project progress and ensure adherence to industry standards and regulatory requirements. Coordinate with cross-functional teams to ensure smooth project execution. AutoCAD Drawings Prepare, review, and interpret AutoCAD drawings for facility layout, equipment placement, and utility routing. Ensure all drawings comply with GMP, safety, and engineering standards. Equipment Installation & Qualification Oversee installation, commissioning, and validation of pharmaceutical equipment. Perform IQ/OQ/PQ documentation and ensure compliance with regulatory guidelines. Coordinate with vendors and engineering teams for timely execution. MEP (Mechanical, Electrical, and Plumbing) Systems Management Manage and supervise MEP activities, including HVAC , water systems , and utility systems for upcoming projects. Ensure proper design, installation, and validation of MEP systems in line with pharma regulatory requirements. Troubleshoot and resolve technical issues to maintain operational efficiency. Preferred candidate profile : Formulation industry background.
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