We are looking for a young, energetic, organized, analytical, result-oriented individual who can work and meet deadlines in our medical device manufacturing company. Experience : 3 Years of experience in Accounts department with hands-on experience in Tally ERP 9, GST, TDS and MS Excel. Education : B. Com.(minimum) Job Responsibilities : 1. Handling Day-to Day Accounting and Book-keeping 2. Preparation & Maintenance of all records like Vouchers, Receipts, Bills, and Payments 3. Calculation & Deduction of TDS in Vendor payments 4. Monthly Bank Reconciliation, Payment Follow-up and Collection 5. Reconciliation of Sundry Debtors & Creditors 6. Preparation of Purchase Orders and planning payment to vendors 7. Physical Stock Keeping and monthly store reconciliation Job Types: Full-time, Permanent Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Work Location: In person
We are looking for a young, energetic, organized, analytical, result-oriented individual who can work and meet deadlines in our medical device manufacturing company. Experience : 3 Years of experience in Accounts department with hands-on experience in Tally ERP 9, GST, TDS and MS Excel. Education : B. Com.(minimum) Job Responsibilities : 1. Handling Day-to Day Accounting and Book-keeping 2. Preparation & Maintenance of all records like Vouchers, Receipts, Bills, and Payments 3. Calculation & Deduction of TDS in Vendor payments 4. Monthly Bank Reconciliation, Payment Follow-up and Collection 5. Reconciliation of Sundry Debtors & Creditors 6. Preparation of Purchase Orders and planning payment to vendors 7. Physical Stock Keeping and monthly store reconciliation Job Types: Full-time, Permanent Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Work Location: In person
1. Bid Preparation: Prepare and submit bids, tenders, and proposals in response to client requirements. 2. Tender Research: Identify and research potential tender opportunities, and analyze tender documents. 3. Client Relationship: Develop and maintain relationships with clients, and understand their requirements. 4. Bid Strategy: Develop and implement bid strategies to increase chances of winning tenders. 5. Team Collaboration: Collaborate with cross-functional teams, including sales, marketing, and operations. 6. Document Management: Manage and maintain bid documents, and ensure compliance with client requirements. 7. Risk Management: Identify and mitigate risks associated with bid submissions. 8. Quality Assurance: Ensure that bids meet client requirements and company standards. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹30,000.00 per month Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Location: Sithalapakkam, Chennai, Tamil Nadu (Preferred) Work Location: In person
1.Preparation of Quality Management system documents 2.Responsible of control of all level Master copy, Control copy, & Obsolete of QMS documents 3.Responsible for Retrieval of all level of Obsolete documents for disposition as per the control of documents. 4.Internal Quality Audit – Scheduling, Conducting, Monitoring and follow up for closure. 5.Responsibility to update level II, III & level IV documents of QA as per review period and maintenance of Index. 6.Management of change control and change request and maintenance of register 7.Document retrieval and support during external, internal and corporate audits. 8.Responsible for Handling of customer complaints 9.Scheduling Management Review Meeting 10.Responsible for Non-Conformance & CAPA implementation and its effectiveness. 11.Responsible to manage quality operation team to ensure quality of product lines and its deliverables 12.Customer Complaint Follow up 13.Batch Processing Record (BPR) Issuance, Storage and Retrieval 14.Batch Processing Record (BMR) Issuance, Storage and Retrieval 15.To prepare and maintain the Medical device File as per IMDR 2017 16. Responsible for preparation and submission of application to CDSCO and regular follow up for obtaining approval 17. Responsible and support implementation of Indian and applicable regulatory regulation 18.Reviewing the performance of Quality Management System and Liasoning with external parties on matters relating to the same. 19.Ensuring that processes needed for the quality management system are documented. Reporting to the top management non the effectiveness of the quality management system and any need for improvement 20.Ensuring the promotion of awareness of applicable regulatory requirements and management system requirements throughout the organization. 21.Responsible for batch release (COA) 22.Support any other additional responsibilities as when required. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per year Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Schedule: Day shift Work Location: In person
1.Preparation of Quality Management system documents 2.Responsible of control of all level Master copy, Control copy, & Obsolete of QMS documents 3.Responsible for Retrieval of all level of Obsolete documents for disposition as per the control of documents. 4.Internal Quality Audit – Scheduling, Conducting, Monitoring and follow up for closure. 5.Responsibility to update level II, III & level IV documents of QA as per review period and maintenance of Index. 6.Management of change control and change request and maintenance of register 7.Document retrieval and support during external, internal and corporate audits. 8.Responsible for Handling of customer complaints 9.Scheduling Management Review Meeting 10.Responsible for Non-Conformance & CAPA implementation and its effectiveness. 11.Responsible to manage quality operation team to ensure quality of product lines and its deliverables 12.Customer Complaint Follow up 13.Batch Processing Record (BPR) Issuance, Storage and Retrieval 14.Batch Processing Record (BMR) Issuance, Storage and Retrieval 15.To prepare and maintain the Medical device File as per IMDR 2017 16. Responsible for preparation and submission of application to CDSCO and regular follow up for obtaining approval 17. Responsible and support implementation of Indian and applicable regulatory regulation 18.Reviewing the performance of Quality Management System and Liasoning with external parties on matters relating to the same. 19.Ensuring that processes needed for the quality management system are documented. Reporting to the top management non the effectiveness of the quality management system and any need for improvement 20.Ensuring the promotion of awareness of applicable regulatory requirements and management system requirements throughout the organization. 21.Responsible for batch release (COA) 22.Support any other additional responsibilities as when required. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Work Location: In person
1.Preparation of Quality Management system documents 2.Responsible of control of all level Master copy, Control copy, & Obsolete of QMS documents 3.Responsible for Retrieval of all level of Obsolete documents for disposition as per the control of documents. 4.Internal Quality Audit – Scheduling, Conducting, Monitoring and follow up for closure. 5.Responsibility to update level II, III & level IV documents of QA as per review period and maintenance of Index. 6.Management of change control and change request and maintenance of register 7.Document retrieval and support during external, internal and corporate audits. 8.Responsible for Handling of customer complaints 9.Scheduling Management Review Meeting 10.Responsible for Non-Conformance & CAPA implementation and its effectiveness. 11.Responsible to manage quality operation team to ensure quality of product lines and its deliverables 12.Customer Complaint Follow up 13.Batch Processing Record (BPR) Issuance, Storage and Retrieval 14.Batch Processing Record (BMR) Issuance, Storage and Retrieval 15.To prepare and maintain the Medical device File as per IMDR 2017 16. Responsible for preparation and submission of application to CDSCO and regular follow up for obtaining approval 17. Responsible and support implementation of Indian and applicable regulatory regulation 18.Reviewing the performance of Quality Management System and Liasoning with external parties on matters relating to the same. 19.Ensuring that processes needed for the quality management system are documented. Reporting to the top management non the effectiveness of the quality management system and any need for improvement 20.Ensuring the promotion of awareness of applicable regulatory requirements and management system requirements throughout the organization. 21.Responsible for batch release (COA) 22.Support any other additional responsibilities as when required. Job Types: Full-time, Permanent Pay: ₹30,000.00 - ₹35,000.00 per month Benefits: Food provided Health insurance Leave encashment Paid sick time Provident Fund Work Location: In person
You will be responsible for various aspects of the Quality Management System (QMS) including preparation, control, retrieval, and disposition of documents. This will involve managing Master copies, Control copies, and Obsolete documents effectively. Additionally, you will be in charge of scheduling, conducting, and monitoring Internal Quality Audits, as well as following up for closure. Another key aspect of your role will be updating QA documents at different levels and maintaining the Index. You will also be involved in change control management, document retrieval during audits, handling customer complaints, and implementing Non-Conformance & CAPA procedures. Furthermore, you will manage the quality operation team to ensure the quality of product lines and deliverables. Responsibilities also include managing Batch Processing Records, maintaining the Medical Device File as per IMDR 2017, and submitting applications to CDSCO for approval. You will review the performance of the Quality Management System, liaise with external parties on related matters, and ensure that processes are documented. Reporting to top management on the effectiveness of the QMS and identifying areas for improvement will be part of your role. Promoting awareness of regulatory and management system requirements throughout the organization is also expected. Other duties may include batch release, supporting regulatory compliance, and handling any additional responsibilities as required. This is a full-time, permanent position with benefits such as food provision, health insurance, leave encashment, paid sick time, and Provident Fund. The work location is in-person.,