About Us


Arni Medica was founded in December 2019 in Hyderabad, India. With over 15 years of cumulative experience in this field and a core team of highly skilled professionals, Arni Medica caters to the needs of Global Medical Device Industry. The company meets these needs adequately and produces highly reliable Medical Devices with its in-house design and manufacturing skills along with the support from contract manufacturing companies. Arni Medica strictly follows the implementation of standard regulatory, quality guidelines and policies of the industry like Quality Management System (QMS) as per Schedule-V of Medical Device Rules 2017 issued by CDSCO, ISO 13485, ISO 15223-1 and 21 CFR 820 issued by US FDA.

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The product portfolio of Arni Medica includes


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.

Let's Get In Touch!


Give us a call or send us an email and we will get back to you as soon as possible!

V-Square, 4th Floor, Plot No. 50, Sai Nagar Colony, Madhapur, Hyderabad 500 081.
+91 965 226 6200