Career’s

 

PHP DEVELOPER CUM DIGITAL MARKETING

 

 Job Summary

Good Experience in JavaScript,, HTML/CSS, Php, Photoshop, WordPress, Analytical Skills, SEO, Responsive Design, ecommerce with Payment Plugins, Subscription plugging. Etc

Responsibilities and Duties

 

  • Manage Website Front-End Development.
  • Design website layouts and add content.
  • Proficiency in languages like HTML and CSS.
  • Research with users on how they use the website.
  • Customize changes to the user experience to make the website more visually appealing and user-friendly.
  • Manage Back-End Development on the server side.
  • Manage integration with databases and servers.
  • Work on features like structure, security, and content management.
  • Coding in languages like PHP.
  • Generation of Plug-Ins and Themes.
  • Performance Monitoring of website and response to error codes and troubleshooting.
  • Passion for web technology, problem-solving, and creativity.
  • Solid Website design skills – Programming and development skills.
  • Front-end technologies (such as HTML, JavaScript, CSS, and jQuery).
  • Back-end technologies (such as PHP).
  • Website creation tools (Word Press).

Experience:

Web Designing, Web Development and Web Hosting Mentainace: 0 to 2 year (Preferred).

Required Experience, Skills and Qualifications

Good Experience in JavaScript,, HTML/CSS, Php, Photoshop, WordPress, Analytical Skills, SEO, Responsive Design, ecommerce with Payment Plugins, Subscription plugging. Etc

 

Salary: ₹25,000.00 to ₹35,000.00 /month

 

Office Address :-
Lars Medicare Pvt.Ltd.
136, 2nd Floor, Avtar Enclave,
Paschim Vihar. New Delhi 110063, India
Tel: + Mob: + 91 9910014706
Fax: + 91-11-45652878

 

Export & Logistic Officer

 

Responsibilities and Duties

 

  1. Knowledge of banking and international banking.
  2. Knowledge of export documents (Shipping Bill, Bill of Lading, COO, GSP etc).
  3. Preparation of Commercial Invoice & Packing List.
  4. Coordinating with PPC, Excise & Marketing Team.
  5. GR documents to be prepared and submitted to bank.
  6. Knowledge of GST, e-way bill and other taxes.
  7. Knowledge of Bank Realization Certificate.
  8. Knowledge of invoice, bills.
  9. Export benefits (MEIS/Advance License)
  10. Prepare monthly MIS.

 

Industry:   Medical / Healthcare / Hospitals

Functional Area:  Export & Logistic Officer

Role Category: Export & Logistic Officer

Role:  Logistic Officer

Sales Coordinator

 Required: Experience 3-4 years

 

Job Description:

  1. Assist with office related work & making proper documentation of records.
  1. Maintaining Data in Excel in a systematic manner.
  2. Data entry & data analysis.
  3. Coordination with different departments.
  4. Coordination with sales team for various day to day activities.
  5. Ensure proper supply and stock of goods.

Candidate Profile:

Candidate should have hands on experience on MS office, MS excel and documentation and should be able to coordinate among internal and external customers for data collection and approvals.

Making data, updating information, handling work with lots of patience. Good communication skills to form letters, reply emails, good management skills. Dedicated, hardworking, focused, quick learner, Long term job stability.

 

Industry:   Medical / Healthcare / Hospitals

Functional Area:  Sales

Role Category:  Sales Professional

Role:  Sales Cordinator

 

Medical Representative 

Experience –0 – 1 year

Qualification – Graduation

Job Description

Visiting distributors and hospitals on a daily basis;
Offering, Promoting and presenting of medical disposable products; Building positive and professional relations with clients and tracking of market trends;

Industry: Medical / Healthcare / Hospitals

Functional Area: Sales, Retail, Business Development

Role Category: Retail Sales

Role: Medical Representative

Quality Assurance Regulatory Affairs Manager

 Required: Experience 3-4 years

 

Job Summary

As a Quality Assurance , he will be responsible for performing a variety of QA duties to determine if materials, products, and or processes are in accordance with specifications and requirements Roles Validation of process Validation of machines Validation of product Clinical Evaluation Statistical techniques Corrective and Preventive Action CAPA with log MDR procedures with log Non-conformance with log To handle customer complaint with log Maintaining all required records documentation Risk Management.

Responsibilities and Duties

As a Quality Assurance, he will be responsible for performing a variety of QA duties to determine if materials, products, and or processes are in accordance with specifications and requirements Roles Validation of process Validation of machines Validation of product Clinical Evaluation Statistical techniques Corrective and Preventive Action CAPA with log MDR procedures with log Non-conformance with log To handle customer complaint with log Maintaining all required records documentation Risk Management

  1. Conduct internal audit for ISO and CE Certification.
  2. Handle External Audit for ISO and CE Certification
  3. Implement MDR new regulations in Plant.
  4. Must be from Medical Device Company.
  5. We are looking for experienced Quality Assurance & Regulatory Affairs to ensure that our products and services meet all necessary requirements before they reach the consumer.
  6. The Regulatory Affairs Officer will inspect the final product to make sure it has been built with compliance with legal standards and meets customer expectations. A great Regulatory Affairs Officer is thorough and observant with an eye for detail.
  7. They must fully understand the requirements for the product or service and have a sense of responsibility towards our potential and existing customers as well as the competition.
  8. The goal is to help preserve our reputation by ensuring that our products and services are capable to drive sustainable growth.

Responsibilities:

  1. Understand customer needs and requirements to develop effective quality control processes.
  1. Supervise inspectors, technicians and other staff and provide guidance and feedback.
  1. Oversee all product development procedures to identify deviations from quality standards.
  1. Keep accurate documentation and perform statistical analysis.
  1. Be on the lookout for opportunities for improvement and develop new efficient procedures.
  2. Knowledge of the Production process of medical device manufacturing (IV Cannula).
  3. Implementing and maintaining Quality Management System (QMS), that complies with ISO 13485, ISO 14971 and FDA 21 CFR Part 820,
  4. Develop and implement quality control and inspection procedures for receipt and control of incoming materials, in-process materials and final product acceptance activities.
  5. Support the quality inspection to ensure, products and processes comply with the relevant requirements of the QMS.
  6. Analyze failure, corrective and preventive action to respond to internal/external customer complaints.
  7. Manage, coordinate and oversee all validation studies, cleaning validation, change controls, protocol revisions, equipment validation, and documentation of results for manufacturing equipment.
  8. Data analysis, continuously improve QA processes and procedures.
  9. Establish and maintain test instrument calibration procedures and maintenance schedules.
  10. Data and record maintenance according to ISO 13485 & GMP certification.

Industry:   Medical / Healthcare / Hospitals

Functional Area:  Quality Assurance

Role Category: Quality Assurance & Regulatory Affairs

Role:  Quality Assurance Regulatory Affairs Manager

 

Please send your CV at :-  Sales@larsmedicare.com

For Enquiries call at: 9910014706/ 011- 45733068

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