Omya fosters a diverse and inclusive culture where employees are encouraged to learn, grow and innovate, while making a meaningful difference for millions of people. Inspired by our mission, we continue to shape medical devices with breakthroughs in products that expand access to care, enhance quality care and improve patient & provider satisfaction.
Culture
Our teams are made of creative, accomplished and dynamic people.
Medical technology development is a challenging but rewarding business that needs talented, motivated, and multi-disciplinary teams. Omya fosters an inclusive culture that connects talent of diverse disciplines into agile and cross-functional teams. We value team players from design, biomedical engineering, medicine, regulatory, and manufacturing who can contribute, collaborate and add value across multiple domains.
Omya prides itself on delivering performing and reliable devices, and successful value-driven clinical outcomes for our patients and providers. If you are tenacious, resourceful, and thrive in a fast-paced but supportive environment, we invite you to be part of the Omya family.
Because here you have an opportunity to make a difference in the world
Inspired by our vision, we continue to shape healthcare with breakthroughs in technologies and products that expand access to care, redefine the quality of care delivery, and improve patient and provider satisfaction.
Our employees are encouraged to learn, grow and innovate to create transformative technologies that make a meaningful difference for millions of people around the world. If you want a career that goes beyond corporate ladder-climbing and provides access for you to have a direct impact on patients’ lives in every job function, we welcome the opportunity to engage with you.
Career
People of Omya
Omya has diverse roles to offer. With our guiding principle of ‘Innovating for value’, we leverage on collective knowledge and passion of individuals to create value for our patients and customers worldwide.
From our interns to our senior management, follow rewarding and meaningful career paths and maintain a strong sense of job satisfaction. You will be part of a collaborative team environment across multi-functional areas dedicated to innovation, creative problem solving, teamwork, and lifelong learning. Our fast-changing and growing business offer new opportunities for building an impactful career at all levels.
People of Omya
Omya has diverse roles to offer. With our guiding principle of ‘Innovating for value’, we leverage on collective knowledge and passion of individuals to create value for our patients and customers worldwide.
From our interns to our senior management, follow rewarding and meaningful career paths and maintain a strong sense of job satisfaction. You will be part of a collaborative team environment across multi-functional areas dedicated to innovation, creative problem solving, teamwork, and lifelong learning. Our fast-changing and growing business offer new opportunities for building an impactful career at all levels.
Explore Our Current Vacancies
We are in an exciting phase of growth and have several stimulating positions.
If you are interested in any of our vacancies or to view our privacy notice for applicants please click here.
Experience
Minimum of 4 – 6 years experience in Marketing & Digital Communications
Location
Bengaluru, Karnataka, India
Education
Education Graduate / Post graduate in Management
Job Description
The Manager is responsible for the implementation and management a range of on-line & off-line communication strategies targeting media and industry engagement, to promote the value of the products developed and marketed by Omya Healthcare in Critical care segment.
Primary Responsibilities
– Develop strategic communications planning for promotion and dissemination of corporate and marketing content of devices in critical care segment
– Develop corporate promotions and communications liaising with R&D departments and the Management Team.
– In conjunction with the web team, create, adapt, improve and optimize web communication for SEO and organic and keyword search
– Manage the corporate branding
– Develop/maintain social media profiles and quality content on Twitter, Facebook, and LinkedIn.
– Develop other, relevant social media outlets to support and expand our digital presence
– Email campaign development and implementation
– Manage inbound marketing system, including campaign development and data analysis – Develop compelling custom content
– Craft email campaigns Print and Social Media
– Optimize print, social media and blog campaigns to generate interaction, brand exposure, and sales
Skill Set
Profile/Professional skills:
– Hands-on experience with inbound marketing systems, and familiarity with marketing automation practices
– 3-4 years of experience in Digital Marketing with a focus in content development and/or reporting, knowledge of Search Engine Marketing (SEM)
– Ability to forge relationships with distributors
– Expert knowledge in the latest in digital and social media technology and channels and how to best leverage for marketing programs as part of an overall social business strategy
– Excellent project and deadline management skills
– Proficiency in MS Office Suite, Mac environment
– Highly motivated, quick-learner, self-starter College degree in marketing, communications and/or technical areas
– Excellent knowledge of English (both speaking and writing)
– Must be able to present portfolio of work, including writing and digital samples
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Experience
3-4 years of experience in Quality Assurance & Regulatory affairs preferably in the medical device Industry
Location
Bengaluru, Karnataka, India
Education
B.Tech/BE, Graduate / Technical Graduate
Job Description
Candidate with a Degree in Engineering or equivalent and about 3-4 years of experience in Quality Assurance and Exposure/Knowledge of Regulatory affairs in the medical device industry.
“In depth understanding of latest revisions of ISO 13485, CFR 820, CE & ISO 14971, GMP, preferred certified Internal Auditor.
Experience in QMS, SOPs, IQ,PQ,OQ, CE submissions, other global regulatory requirements.”
Demonstrate strong Communication, Verbal and Written skills
Skill Set
Responsible for Establishment and Implementation of QMS as per ISO 9001, ISO 13485, and ICMED. CE, FDA etc other Regulatory approvals and working on Class II, III medical devices
Conducting Audits internally and externally with sub-contractors, Notified bodies, MRM review on quality systems, processes, and products to ensure compliance with regulations and Internal specifications
Participate in the development of corrective & preventative action plans and coordinate closure of actions with assigned responsible parties. Assure and track the timely closing of all variances, CAPAs and audit findings
Interface between multidisciplinary departments, managers, regulatory agencies and vendors to ensure expectations are met like ISO, CE marking, FDA, Indian regulations etc.
Keeps current on global directives, harmonized standards, procedures and communicates changes that may affect R&D and cross-functional team.
Assist in risk management plan, perform product risk assessment, facilitate the failure mode effects analysis, and create a final risk management report.
Review MDF, DHR, DMR Files and Technical Files for conformance to applicable regulatory requirements. Maintain Regulatory Affairs product files to support compliance with regulatory requirements and Approvals to introduce new and modified products to the market.
Assist in regulatory strategies, preparing CE / US FDA submissions, providing documentation for international submissions, evaluating proposed product changes for regulatory impact and preparing necessary documentation
Provide on-going support to core and project teams for regulatory issues and questions. Find, interpret and apply regulations and guidance appropriately for situations.
Effective problem-solving skills, excellent analytical skills, strong attention to detail, structured and methodical. Independent judgment.
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Experience
6 to 10 years relevant field experience on any medical equipment preferably critical care equipment’s.
Location
Bengaluru, Karnataka, India
Education
Diploma in Engineering/BE/Equivalent Technical Qualification in Electrical / Electronics / Physical Sciences.
Job Description
Roles and Responsibilities:
Planning , Organising & Managing team of Sales and Service People
Executing the assigned target through the team members and maintain the customer delight.
Understanding requirements , submission of appropriate proposals &
Participation in the negotiating process towards successful closure.
Customer Engagement.
Understand and applicable knowledge of pre tender work to execute facilitate tender orders
Monitoring & guiding the team on a daily basis to achieve the Sales goals on weekly /monthly/quarterly basis.
Manage and deliver profit for the zone.
Create and maintain relationship with KOL for business growth
Penetrate and establish existence in various hospitals and fall upon the business of Rate contract basis.
Capable of handling high volume/ turn over business and deliver proper profit to the Organisation and to create growth opportunities for the team members.
Mentoring coaching and giving proper motivation to the team to help achieve and execute the targets.
Feedback to the R&D team regarding the competition, products in market, technology trends & potential new products for future development/business.
Establishing & Implementing the systems & process as per the company CRM & generation of timely reports needed for MIS.
Liasoning & participating in the Post Market Surveillance study.
Implementation of the QMS & the applicable regulatory systems & procedures.
Skill Set
Omya is looking for a Leader who is very Aggressive, Dynamic personality with very strong competencies in Marketing, Sales and service in Medical Device Field and to take Omya’s branded Medical Devices to Indian and International Markets, Should be fluent in English, Hindi and regional languages – Should have an expert knowledge in MS office – Graduate in any discipline.
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Experience
Minimum of 5 years experience in regulatory medical device industry products regulations
Location
Bengaluru, Karnataka, India
Education
Education Graduate / Post graduate in Engineering / Bio Medical / Electronics. Post graduate in Management
Job Description
An experienced, high caliber Senior Regulatory Specialist to lead project submissions for regulatory approvals and who acts independently to identify and resolve problems. Applies advanced regulatory expertise to guide cross-functional teams and partners , demonstrates strategic thinking and creativity in support of programs.
In depth experience in Medical Device Directive, ISO 13485, IEC 60601, includes ISO 14971, IEC 62304 etc., with FDA requirements, guidance documents, 510(k) submissions, and other global regulatory requirements and quality standards involvement with regulatory submissions, interactions with regulatory agencies, and working with cross-functional project teams.
Skill Set
The position will participate in the development of product specifications, ensuring project compliance to internal and external standards, and regulatory compliance, coordinating the risk analysis activities, and creating and managing the quality engineering deliverables.
Devising solutions in product design to meet the regulatory requirements like CE marking, FDA etc.
Ensuring that the design process meets the Regulatory Compliance Plan by reviewing the process throughout the Product Life Cycle.
Identifying and incorporating regulatory requirements in the design of new Products and process in coordination with the cross functional teams from India and overseas for medical products
Product support to currently marketed products. Work with engineers and technical experts to evaluate proposed changes to products for regulatory impact and to develop necessary documentation
Governmental approvals to introduce new and modified products to the market
Regulatory submissions and negotiates their approval
Developing regulatory strategies, preparing CE / US FDA submissions, providing documentation for international submissions, evaluating proposed product changes for regulatory impact and preparing necessary documentation
Prepare submissions for new products and their product changes as required to ensure timely approval for clinical studies and market release
Provide on-going support to core and project teams for regulatory issues and questions. Find, interpret and apply regulations and guidance appropriately for situations.
Evaluating proposed product changes for regulatory impact and preparing necessary documentation
Provide regulatory support by reviewing labeling, promotional materials, training materials, changes to existing devices and documentation. Prepare submissions and reports for regulatory agencies as required.
Maintain Regulatory Affairs product files to support compliance with regulatory requirements.
Keeps current on global directives, harmonized standards and procedures and communicates changes that may effect cross functional areas.
Knowledge and experience with Class II, III medical devices will be desirable
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Experience
6 to 10 years relevant field experience on any medical equipment preferably critical care equipment’s.
Location
Bengaluru, Karnataka, India
Education
Graduate / Post graduate in Engineering / Bio Medical / Electronics. Post graduate in Management
Job Description
Master’s/Bachelor’s degree in Engineering plus 2-5 years Medical Device field experience and Research and Development of a technological product is required
Use multidisciplinary engineering knowledge to lead and contribute to a team designing and developing innovative mechanical and electro-mechanical medical devices or components/subsystems in support of company’s strategic plan.
Skill Set
Professional experience with in-depth knowledge and hands-on experience of the bio medical theories, principles and practices of Critical Care Medical Equipment’s, Preferably experience in product such us Medical Ventilator, Syringe pump, volumetric pump and Patient Monitor.
Work along with design and development team for NPD studies such us Competitor product study, Product technology and Configuration, Tear down, Technical and user requirements, defining Product specification for new products.
Support R&D cross functional team in developing and bringing the next generation Life Saving Equipment medical devices to market.
Visiting the healthcare professionals, other medical professionals, such as doctors and therapists as well as with end-users to collect their need, findings and requirements,
Participating in R&D, Marketing meeting and provide input for product design and development specification, provides innovative new ideas and features for new products.
Support on product development life cycle through concept and feasibility, risk analysis, prototyping, design V&V and designs transfer as needed for NPI process and quality systems, requirements.
Creating, Defining and Writing technical specifications for each NPD product, Product specific reports and creates presentations as required to document and market communication purpose.
Organising and maintaining the database of all orginational product lineup.
Developing the validation & verification protocol and test methods, manual and service procedure’s.
Identifying the risk hazards associated with the products, analysed and mitigated, using FMEA method
Working with the medical standards such as ISO 13485, ISO 14971 and IEC 60601-1, as required.
Skilled in detecting problems in medical equipment by providing troubleshooting solutions for problems arise in existing products.
Familiar with the standards, codes, and regulations related with biomedical engineering
Proficient with MS Office suite and Internet search
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Experience
3-4 years of experience in conducting clinical research & clinical trial in the medical device industry
Location
Bengaluru, Karnataka, India
Education
Bachelor’s Degree in Science or Healthcare Related Field or Biomedical Engineering
Job Description
Strong knowledge and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Working knowledge of regulations and standards applied in clinical area and medical devices is essential.
Knowledge and experience with ISO 14155, ISO 13485, ISO 14971, 21CFR 820, etc.,
Experience monitoring approval and surveillance studies in support of 510(k) clearance
Demonstrated strong communicator, verbal and written, across all levels of the organization as well as cross functionally.
Skill Set
Performs scientific literature searches as needed to support team members, Review and provide feedback on collateral material in development.
Participates in the design, administration and oversight of clinical and human factor/ergonomic studies. Studies may be conducted as either Investigator Initiated or Sponsor initiated studies.
Perform comprehensive literature searches to develop and maintain in-depth knowledge and understanding of current scientific literature required to support assigned product lines and related clinical studies, staying informed about applicable clinical landscapes and trends.
Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution
Perform site selection (if applicable), initiation, monitoring and close-out visits in accordance with contracted scope of work and good clinical practice.
Supporting development of project subject recruitment plan on a per site basis. Work with sites to adapt, drive and track subject recruitment plan in line with project needs to enhance predictability.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
May provide assistance with design of study tools, documents and processes.
Collaborate and liaise with study team members for project execution support as appropriate.
Must have ability to travel for Clinical relevance/studies
Perform statistics, statistical methods, and design of experiment.
Maintain responsibility for site management for pre- and post-market studies ensuring successful conduct of clinical programs, and cross- functional strategies.
Disclaimer
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.
Student Internship Opportunities
As a student intern at Omya, you will be part of a growing team and developing organization. You will work alongside committed professionals in a fast-paced, challenging, hands-on work environment, allowing you to maximize your learning experience during your six to twelve-month placement.
Omya regularly recruits student interns, with start dates in January and July. Apply through your university’s career portal or our career page linked below.
Policies & Statements
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