VNAI Specialities Pvt Ltd is an equal opportunity employer. We welcome and value high caliber, talented and result oriented professionals with excellent teamwork & communication skills and strong work ethics.
Warehouse - AGM / DGM - 1 No
Experience: Min 15+Yrs
Industry Exp: API (Bulk Drugs)
Education: B.sc/M.sc Chemistry (Mandatory), MBA
Responsibility:
- Leading, planning and monitoring of day-to-day activities of Warehouse
- Maintain API, Bulk drugs and Chemical warehouses as per ISO, cGMP and regulatory guidelines
- To prepare and lead the department during Financial Audits-Yearly Stock Audit with Monthly Stock Statements
- Preparation of stores SOP’s
- Monthly planning with production and co-ordinate with the planning department
- Responsible for warehouse security and accountability
- Liasioning with PCB
Location: Factory
Microbiology - Asst. Manager - 1 No
Experience: Min 10 Yrs
Industry Exp: API (Bulk Drugs)
Education: B.sc/M.sc Microbiology (Mandatory)
Responsibility:
- Maintaining the microbiology lab in compliance and presentable manner
- Exposure towards compliance and GAP assessment
- Management and leading of various sections in microbiology lab
- Sound experience in Microbiology, Aseptic behavior, Sterility assurance, implementation of Quality Systems, cGMP, Preparation of SOP’s, review ofValidation protocols, media fill protocol, BMR , MPR
- Protocol preparation and execution for Qualification of equipment’s, Area Qualifications and Water system Qualifications
- Preparation & review of specifications
Location: Factory
R&D - Executive / Sr.Executive - 6 Nos
Experience: Min 5 Yrs
Industry Exp: API (Bulk Drugs)
Education: B.sc/M.sc Chemistry (Mandatory)
Responsibility:
- Product Development & Process research
Location: Factory
QA - Executive - 1 No
Experience: Min 5 Yrs
Industry Exp: API (Bulk Drugs)
Education: B.sc/M.sc Chemistry (Mandatory)
Responsibility:
- Analysis of both instrumental and chemical of all the finished products, Intermediates, Raw materials, In- process and Stability Samples followed by the standard test procedures (STP’s) & standard operating procedures (SOP) and documentation as per USFDA & cGMP.
- Exposure in prepare and review of Incidents, QMS Investigations and CAPA, SOP’s, Protocols & reports.
Location: Factory
Project - Head - 1 No
Experience: Min 15 Yrs
Industry Exp: API (Bulk Drugs)
Education: BE/B.Tech – Chemical / Mechanical Engineering
Responsibility:
- Responsible for leading Project & Technical team to meet new project initiation requirements, technical evaluations of the equipment and project feasibility studies.
- End to End Project completion from starting Conceptual to Detailed designs including technical / design summaries, preparation of execution Drawings & executing / commissioning.
- Technical comparisons for Major Equipment’s & Vendor evaluation. Co-ordination with Supply chain team to ensure the availability of materials on time
- Budget tracking and Project Schedule tracking.
- Follow up to Implement, monitor projects execution plan, and provide weekly reports.
- Co-ordination with Consultants/contractors / vendors for on time completion of the projects.
Location: Factory
Finance & A/C - Executive - Costing - 1 No
Experience: Min 4 Yrs
Industry Exp: Manufacturing (Preferably Pharma)
Education: ICWA Qualified
Responsibility:
- Maintenance of Cost Auditing records
- Reconciliation of Logs
- Reviewing of BOM on monthly basis
- Reconciliations of Inventory records with Financials
Location: HO
Finance & A/C - Manager - Projects Accountant - 1 No
Experience: 10 Yrs
Industry Exp: Pharma
Education: CA-Inter / ICWA Inter
Responsibility:
- Monitoring of Projects & Progress updation
- Review of CAR form with Project team
- Ensure GRN Preparation on time
- Ensure timely capitalisation of FA & depreciation
Location: HO
Production - Executive - 1 No
Experience: 10 Yrs
Industry Exp: API (Bulk Drugs)
Education: B.sc/M.sc Chemistry, BE/B.tech Chemical
Responsibility:
- Manufacturing the drug products as per Batch Production Record (BPR) and performing process operation as per Standard Operating Procedures (SOP).
- Maintain documents and records as required by the manufacturing department
- To report to the seniors available in case of any abnormalities observed at work
- Responsible for attending cGMP, EHS and otherTrainings
Location: Factory