Careers


APPLY HERE: Please submit your profiles to jobs@arnimedica.com
QUALIFICATION: B- Pharma/ B.Sc. (Biology, Biotech and Botany), MBA. Excellent English Communication and thorough Scientific Knowledge is a MUST.

EXPERIENCE: Minimum 5 years of work experience with Medical Device Sales.

RESPONSIBILITIES:
Product Sales and Marketing:
  • To Achieve Sales Objectives using marketing skills effectively to generate the demand and business from doctors
  • Demonstrating or presenting demo of the products to healthcare staff including Doctors, nurses, and pharmacists
  • To promote critical care range of Medical devices to Doctors, Hospital Pharmacist, Stockiest, Distributors and achieve maximum marketing
  • Organizing appointments and meetings with community and hospital-based healthcare staff
  • Assess clients’ needs and present suitable promoted products
  • Monitor and analyse data and market conditions to identify competitive advantage
  • Ability to develop Customer Relationship
  • To ensure proper implementation of marketing strategies
  • Daily updating stock details to the higher management.
Product marketing and Market research:
  • Appoint Distributors in the assigned Regions and negotiate contracts
  • Plan and implement the most effective distributor & Dealer Network for placement of Company Products in the market
  • Identify market needs & capture through product & brand line extension with the support of product development team
  • Identify opportunities in the market through new channel creation & ensure product availability in that region
  • Design schemes for Trade & execute in the market to achieve organizational goals
  • Analyse sales data & implement necessary models to ensure analytics driven decision making
  • Assess clients’ needs and present suitable promoted products
  • Monitor and analyse data and market conditions to identify competitive advantage
  • Candidates with an experience in a Medical devices company are preferred
QUALIFICATION: B- Pharma/ B.Sc. (Biology, Biotech and Botany), MBA. Excellent English Communication and thorough Scientific Knowledge is a MUST.

EXPERIENCE: 2 to 3 years of work experience in Medical Devices.

RESPONSIBILITIES:
  • To Achieve Sales Objectives using marketing skills effectively to generate the demand and business from doctors
  • Demonstrating or presenting demo of the products to healthcare staff including Doctors, nurses and pharmacists
  • To promote critical care range of Medical devices to Doctors, Hospital Pharmacist, Stockiest, Distributors and achieve maximum marketing
  • Organizing appointments and meetings with community and hospital-based healthcare staff
  • Assess clients’ needs and present suitable promoted products
  • Monitor and analyse data and market conditions to identify competitive advantage
  • Ability to develop Customer Relationship
  • To ensure proper implementation of marketing strategies
  • Daily updating stock details to the higher management.
  • Identify market needs & capture through product & brand line extension with the support of product development team.
  • Identify opportunities in the market through new channel creation & ensure product availability in that region.
QUALIFICATION: Bachelor s degree in a technical discipline or equivalent combination of education and experience in medical device quality systems and/or biomedical engineering

EXPERIENCE: Minimum of 3 to 5 years experience with the above-specified responsibilities in a regulated medical device environment.

RESPONSIBILITIES:
  • Support executing system level test protocols using good documentation practices in a regulated environment System level testing of both software, hardware, & documentation
  • The Senior Verification and Validation Engineer will be responsible for various Verification and Validation during the development lifecycle of complex devices.
  • Participating in design reviews and code inspections and will support the development of documentation required for FDA device approval.
  • Participation in other quality assurance functions, including, but not limited to, process audits, static code analysis, risk/hazard analysis, and test automation development.
  • Defining of new product, implementing operational profiles, preparing for test, executing test, and guiding the test. Support the Validation / qualification of third-party components and tools used for development and verification/validation
  • Active Participation in team meetings, discussions and customer meetings.
  • Frequent interaction with Developers, team members from other disciplines, particularly hardware engineers, to develop test requirements and other project artifacts. Possible interaction with third-party vendors, subcontractors and another user.
  • Involvement in Innovation, technical discussion’s, product/process improvements.
QUALIFICATION: M-Pharm/ B- Pharma/ Pharma- D/ B.Sc. (Biology, Biotech and Botany). Excellent English Communication and thorough Scientific Knowledge is a MUST.

EXPERIENCE: : 2 to 5 years of work experience in Medical Devices.

RESPONSIBILITIES:
  • Expertise in QMS documentation.
  • Preparation of Quality Policy, Quality Objectives, Quality Manual and Validation Master Plan.
  • Preparation of documents required for ISO, QA, and other regulatory bodies.
  • Preparation of documents for plant validation, Qualification, and self-inspection.
  • Ensure the procedures are in place for performing the activities, operating and calibrating the equipment.
  • Review of batch manufacturing records and QC testing data prior to release of any batch.
  • Ensure that all deviations, OOS/OOT & Market complaints are logged, investigated to identify the root cause so as to take CAPA to prevent recurrence.
  • Arrange and conduct the self-inspection, identify gaps and take CAPA.
  • Ensure that all the records are retained as per the requirement.
  • Preparation of Annual product quality reports, trending of data, determining product and process performance.
  • To extend the support to Regulatory Affairs as per their requirements for registration of products in different countries.
  • To take the other responsibilities from time to time as suggested by Higher Management.
QUALIFICATION: Bachelor s degree in a technical discipline or equivalent combination of education and experience in medical device quality systems and/or biomedical engineering

EXPERIENCE: Candidates with an experience in a Medical devices company are preferred

RESPONSIBILITIES:
  • Candidates should have good experience & exposure in Domestic Licensing Procedure, Loan Licensing, Licensing / approvals in Regulated Countries / ROW Markets.
  • Exposure in Dossier Preparation for Europe Market.
  • Create and maintain company quality documentation, such as manuals, procedures, etc.
  • Continuously improve QA processes and procedures.
  • Preparation of QA reports.
  • Well versed with ISO 13485, Implementation of ISO 13485 Quality Management System and maintaining related documentation for the periodic audits.
  • Fulfilling regulatory requirements for Registration of Medical Devices in various countries.
  • Efficient Implementation and management of ISO 13485, US FDA - 21 CFR, MDD 93/42/EEC, MDR 2017/745, CER, ISO 14971.
  • Preparation of Technical File, Instruction Manual, Post Market Surveillance and Clinical Evaluation Report for medical devices.
  • Good co-ordination & interpersonal skills.
  • Willing to Learn and implement ideas.
Experience of ISO 13485:2016 and preferably USFDA audit.