Careers at George Philips
Join a team that's improving healthcare outcomes worldwide. We offer challenging work, growth opportunities, and a mission that matters.
8 open positions
Growth
Clear career paths and continuous learning opportunities in a growing company.
Impact
Your work contributes to medical devices used in hospitals across 50+ countries.
Culture
Inclusive, collaborative workplace that values every team member.
Current Openings
Finance & AccountsFull-time
Account Executive
Thane (Ambernath) & Mumbai (Suburban)1–3 years
To handle Accounts related work of a manufacturing unit.
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Key Responsibilities
- • Should have Knowledge of TALLY ERP 9 and be able to update entries in Tally
- • Preparing Proforma Invoice, Sales Invoices of domestic and export sales
- • To maintain Banking, Payroll Accounts
- • Service Tax, Excise, Provident Fund, ESIC
- • Audit, Preparation of Balance Sheets, Profit & Loss Statements
- • Income Tax, GST Returns/Fillings, TDS Fillings
- • Import / Export documentation, EOU Requirements, EOU – QPR / APR Filings
- • Other Skills related to the Applied Post
Requirements
- • B Com. / M Com. / Inter C.A.
- • Experience of 1-3 Yrs in Accounts Department
- • Should have Knowledge of TALLY ERP 9
- • Proficient in working with Computer including Word/Excel/Power Point etc.
- • Strong oral and written communication skills in English Language is must
Sales & MarketingFull-time
Online Marketing Executive
Thane (Ambernath) & Mumbai (Suburban)1–3 years
To assist the Marketing Director in all routine activities, process orders, coordinate for delivery of goods and develop/maintain amicable relationships with customers. Actively seeking out new sales opportunities through cold calling, networking and social media.
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Key Responsibilities
- • To find potential distributors / traders in every country (Domestic & Export)
- • To identify competitors, study their pricing strategies, distribution discount offers etc, and collect their quotations and technical datasheets as part of market intelligence
- • Responsible to prepare invoice orders and customer agreements
- • Communication with customers on order status and details regarding dispatch of materials
- • Identify product enhancements or opportunities of new products as per customer requirements
- • Responsible for all activities related with import and export including customs clearance
- • Enquiring and gathering information about markets, deal with international customers and quote for tenders within the stipulated time along with the required document formalities
- • Manage Offers and Enquiries
- • Should negotiate terms of payment / delivery
- • Strong Knowledge of marketing strategies, social media, managing marketing campaigns and business development
Requirements
- • Graduation / Post Graduation in any degree from recognized University (Science/Commerce background preferred)
- • Candidates in Biomedical Engineering, Nursing Professional, Medical Professional, Healthcare professional, MBA in Marketing, MBA in Digital Marketing, would be preferred
- • Experience of 1-3 Yrs in Marketing Department preferably from a healthcare company
- • 1 to 3 years in sales & marketing, preferably in Medical and Healthcare Industries
- • Fluency & proficiency of English Language is must
- • Strong communication and negotiation skills
- • Proficient in working with Computer including MS Word/Excel/Power Point etc.
Quality & RegulatoryFull-time
Regulatory Affairs Specialist / Quality Assurance Engineer (Medical Devices)
Thane (Ambernath) & Mumbai (Suburban)2–5 years
Manage all regulatory affairs activities in support of medical device product development including, Pre-Clinical, Risk Analysis, Clinical Evaluation, Biocompatibility, Post market surveillance & Post Market Vigilance issues.
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Key Responsibilities
- • Preparing & Implementing Quality Systems & Quality Control documentation
- • Design Verification & Validation activities
- • GMP & ISO Requirements & activities
- • Risk Management activities
- • Represent or lead the RA function on assigned cross-functional project teams
- • Develop and execute regulatory plans for the Critical Care product portfolio, including new products and maintenance of licenses/authorizations for existing marketing authorizations
- • Monitor applicable regulatory requirements; assure compliance with external standards (ISO 13485, CE certification, FDA certification & MDR requirements)
- • US-FDA Establishment registration & 510K preparation & submissions
- • Inspection Test Plan & Good Manufacturing Practices
- • Facing & conducting Internal Audits
- • Develop and document sound regulatory decisions and justifications
- • Ensure project teams and business objectives and deliverables are aligned with regulatory strategy
- • Review promotional material or SOP's for compliance with local and global regulations
- • Support product owner in assembly of process/product regulatory submission and assist in follow up questions
- • Perform gap analysis and propose solutions
- • Support in GMP or pre-licensing inspections conducted by authorities
- • Conducting Internal Audits & Preparation of documentation for the same and facing External Audits
- • Identify the Nonconformities within the Internal system at each stage of product development and close the same
Requirements
- • Bachelors / Master's in Biomedical, Biotechnology Engineering or related field
- • Candidates with a background from Biomedical Engineering, Medical Professional, Healthcare professional, would be preferred
- • Should have experience working in the regulatory team of a medical device industry
- • 2-5 Years' experience in FDA regulated Medical and Healthcare Industries
- • Experience in medical device listing / establishment registration / ISO Documentation / medical device reporting
- • Understanding of international regulatory requirements for medical devices (ISO 13485/MDD 93/42 EEC/ MDR)
- • Proven track record in writing dossiers for regulatory device submissions
- • Knowledge of creating and making a Design History File (DHF)
- • Fluency & proficiency of English Language is must
- • Proficient in working with Computer including MS Word/Excel/Power Point etc.
- • Ability to successfully manage projects to deadlines
ManufacturingFull-time
Production Engineer
Thane (Ambernath)1–3 years
As a Production Engineer, you will be responsible for supporting in house manufacturing process of 'Medical Device Manufacturing' in the following areas: Production Planning, (Injection Moulding, Assembly, Packaging, Labelling), Assembly Room Supervision, Product Testing, Quality Assurance (Regulatory Affairs Documentation), Setting up Production Process & Controls, Clean Room Protocols & Maintenance of Sterility, Timely completion of work, Clean Room Operating protocol.
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Key Responsibilities
- • Will be responsible for setting up & monitoring the production process & ensuring that the set manufacturing & testing standards are being adhered to during & after production
- • To plan and co-ordinate production process on daily basis to produce high quality products
- • Should easily identify the problems, analyze root cause
- • Implement the solution and to design efficient equipment and process
- • Should have excellent communication skill so that you can exceed project expectations
- • Exceptional attention that comes when design complex
- • Should be multi-tasker who can handle numerous activities in the Manufacturing process
- • Will be responsible for troubleshooting in all production areas and as well as maintaining the test equipment's on a regular basis
- • To perform engineering analysis to reduce down time
- • Provide training and guidance to the team members to accomplish production goal
Requirements
- • B Tech (Production Engineering)
- • B-Tech or a related field
- • Proven work experience as a production Engineer or a similar role in the Engineering department
- • 1 to 3 years in engineering industry, preferably in medical disposable assembly
- • Ability to create a safe working environment
- • Excellent communication and organization skills
- • Outstanding leadership and time management skills
- • Ability to work in a team environment as well as independently
- • Fluency & proficiency of English and local Language is must
- • Proficient in working with Computer including MS Word/Excel/Power Point etc.
- • Ability to successfully manage projects to deadlines
EngineeringFull-time
Bio-Medical Engineer (Medical Devices)
Thane (Ambernath) & Mumbai (Suburban)2–5 years
As a Biomedical Engineer, you will be responsible for supporting our inhouse 'Medical Device Manufacturing' in any of the following areas: Production Supervision (Injection Moulding, Assembly, Packaging, Labelling, Sterilization), Product Testing, Quality Control, Quality Assurance (Regulatory Affairs Documentation), Setting up Production Process & Controls, Clean Room Protocols & Maintenance of Sterility, Microbiology & Sterilization, Online Sales & Marketing.
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Key Responsibilities
- • You will be responsible for setting up & monitoring the production process & ensuring that the set manufacturing & testing standards are being adhered to during & after production
- • You will also be responsible for troubleshooting and maintaining the test equipment's on a regular basis
- • You will support the regulatory affairs activities with documentation in support of medical device product development including, Pre-Clinical, Risk Analysis, Clinical Evaluation, Biocompatibility, Post market surveillance & Post Market Vigilance issues
- • To succeed in this job role, you should possess excellent problem-solving skills and the ability to keep a close eye on details
- • You should also have an extraordinary ability to manage multiple tasks simultaneously
- • Analysing information & documentation skills
- • Infection control & working knowledge of the sterility & clean room protocols
- • Preparing technical documentation on how to use the equipment
- • Writing reports and documents detailing procedures and policies
Requirements
- • Bachelors / Master's in Biomedical, Biotechnology Engineering or a similar related field
- • Candidates with a background of/from Biomedical Engineering, Medical Professional, Healthcare Professional, would be preferred
- • 2-5 years' experience in FDA regulated Medical & Healthcare Industries
- • Bachelor's degree in Biomedical Technology, Electronics Engineering, or a related field
- • Proven work experience as a Biomedical Engineer or a similar role in the Engineering department
- • Ability to create a safe working environment
- • Excellent communication and organization skills
- • Outstanding leadership and time management skills
- • Good analytical and research abilities
- • A keen eye for details and accuracy
- • Ability to work in a team environment as well as independently
- • Fluency & proficiency of English Language is must
- • Proficient in working with Computer including MS Word/Excel/Power Point etc.
- • Ability to successfully manage projects to deadlines
Quality & RegulatoryFull-time
Quality Control Engineer (Mechanical Engineering)
Thane (Ambernath)2–5 years
To handle all Quality Control operations of the production process in the factory. To ensure that all the raw materials coming into the factory, the goods produced in the factory & finished goods leaving the factory are upto the set quality standards of the company, as dictated in the quality manuals of the QMS.
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Key Responsibilities
- • Should be familiar with working with ISO 9001 standards & systems
- • Should be familiar & proficient in the use of all test instruments
- • Should be an expert in record keeping & should be able to independently investigate complaints and identify root causes for the same
- • Is expected to address quality issues proactively & ensure appropriate corrective action is taken for timely and effective closure for issues
- • Monitoring of supplier quality performance & execute validation activities associated with incoming inspections
- • Provide support to validation teams to achieve project milestones
- • Develop & improve incoming & in-process QC inspection methods
Requirements
- • B Tech / B.E in Polymer Engineering, Mechanical Engineering, Polymer Engineering
- • Background in Mechanical Engineering
- • Should have experience handling Quality Control operations
- • 2-5 Years' experience in quality control
- • Should have expertise in Technical Writing & have adequate Computer skills
- • Should be good in communication, co-ordination and planning
- • Attention to details, would be a pre-requisite
ManufacturingFull-time
Electronics Engineer (Production Engineer)
Thane (Ambernath)1–3 years
An Electronic engineer will be responsible for Designing, Testing, Troubleshooting and modifying Electronic devices The Electronics engineer should also be skilled to applying the principles and Theories of electronics and as well as you should knowledge of electrical engineering also.
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Key Responsibilities
- • Expert in soldering
- • Electronic testing
- • Extensive experience in inspection of electronic devices
- • Define & execute testing maintenance procedures for electronic software and maintain records
- • Inspect electronics to ensure compliance with regulatory standards
- • Should be effective contributor beating deadline and targets
- • Knowledge of safety case major accident and hazards
- • Should have Analytical skills to follow logic of electronic circuits and interface with software
- • Should have good leadership skills
Requirements
- • B Tech / Diploma in Electronics
- • Electronic engineer with Diploma in Electronics
- • 1 to 3 years in electronic industry, preferably in assembly, testing & production of components & boards
- • Should Design, built and installed electrical instrumentation systems in a variety of projects
- • Carried out surveys to determine the condition of existing systems and made recommendations for further improvement
- • Devised requirements for improvement and modification of work and procedure
- • Tested equipments and machine tools and reported any discrepancies
- • Trained and supervised assistant electricians in all divisions regarding proper handling and installation of electrical/electronic equipment
- • Report daily to your superior and kept in informed of the status of all the area and responsibility
ManufacturingFull-time
Polymer Engineer
Thane (Ambernath)1–3 years
Polymer Engineer you will be responsible for processing medical disposable products and supporting in house Manufacturing in the following areas: Vast experience in polymer processing, Familiarity with various types of polymers and it's processing, Sound knowledge of reduction of scrap, Reducing down time, Increasing polymer product performance, Prepare reports and Documentation.
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Key Responsibilities
- • Injection Moulding Room Supervision & production
- • To plan and co-ordinate production process on daily basis to produce high quality products
- • Should easily identify the problems, analyze root cause
- • Co-ordinate with process engineering team and provide technical support
- • Co-ordinate with tool room engineer / Tool maker
- • To ensure that the product produce were flash free component with no defects
Requirements
- • CIPET (Plastic Processing, Production Engineering), B-Tech
- • CIPET, B-Tech or a related field
- • 1 to 3 years in plastic processing industry
- • Proven work experience as a polymer Engineer in processing field
- • Ability to operate and set parameter of injection moulding machine
- • Ability to create a safe working environment
- • Excellent communication and organization skills
- • Outstanding leadership and time management skills
- • Ability to work in a team environment as well as independently
- • Fluency & proficiency of English and local Language is must
- • Proficient in working with Computer including MS Word/Excel/Power Point etc.
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