CAREERS
JOB SUMMARY:
- To handle Accounts related work of a manufacturing unit.
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- 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.
ACADEMIC QUALIFICATION:
- B Com. / M Com. / Inter C.A.
EXPERIENCE:
- 1-3 Years’ experience in Accounts.
JOB LOCATION:
- Thane (Ambernath) & Mumbai (Suburban)
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Accounts Executive’.
JOB SUMMARY:
- 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.
- Customers would include hospital (purchase departments), corporate hospital chains, international distributors & importers of healthcare & medical devices,
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
- Proven experience as a Sales Executive or relevant role
- Thorough understanding of marketing and negotiating techniques
- Fast learner and passion for sales
- Self-motivated with a results-driven approach.
REQUIRED BACKGROUND & CRITERIA:
- Graduation / Post Graduation in any degree from recognized University (Science/Commerce background preferred).
- Experience of 1-3 Yrs in Marketing Department preferably from a healthcare company.
- Fluency & proficiency of English Language is must.
- Strong communication and negotiation skills.
- Proficient in working with Computer including MS Word/Excel/Power Point etc.
ACADEMIC QUALIFICATION:
- Graduation / Post Graduation in a ‘science’ degree from a recognized University.
- Candidates in Biomedical Engineering, Nursing Professional, Medical Professional, Healthcare professional, MBA in Marketing, MBA in Digital Marketing, would be preferred.
WORK EXPERIENCE:
- 1 to 3 years in sales & marketing, preferably in Medical and Healthcare Industries.
JOB LOCATION:
- Thane (Ambernath) & Mumbai (Suburban)
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Online Marketing Executive’.
JOB SUMMARY:
- 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.
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- Should have degree in Biomedical/Biotechnology or degree in a related field.
- Should have experience working in the regulatory team of a medical device industry.
- 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.
QUALIFICATION:
- Bachelors / Master’s in Biomedical, Biotechnology Engineering or related field.
- Candidates with a background from Biomedical Engineering, Medical Professional, Healthcare professional, would be preferred.
EXPERIENCE:
- 2-5 Years’ experience in FDA regulated Medical and Healthcare Industries.
JOB LOCATION:
- Thane (Ambernath) & Mumbai (Suburban).
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Regulatory Affairs Specialist’.
JOB SUMMARY:
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.
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- B-Tech or a related field.
- Proven work experience as a production 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.
- 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.
ACADEMIC QUALIFICATION:
- B Tech (Production Engineering)
WORK EXPERIENCE:
- 1 to 3 years in engineering industry, preferably in medical disposable assembly.
JOB LOCATION:
- Thane (Ambernath)
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Production Engineer’.
JOB OVERVIEW:
We are looking for an experienced and talented candidate to join us as a Biomedical Engineer in our Medical Device Manufacturing Facility at Ambernath East, Thane District.
JOB SUMMARY:
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
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
OTHER RESPONSIBILITIES WOULD INCLUDE:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- 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.
ACADEMIC QUALIFICATION:
- 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.
WORK EXPERIENCE:
- 2-5 years’ experience in FDA regulated Medical & Healthcare Industries.
JOB LOCATION:
- Thane (Ambernath) & Mumbai (Suburban).
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Biomedical Engineer’.
JOB SUMMARY:
- 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.
JOB DETAILS:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- Background in Mechanical Engineering.
- Should have experience handling Quality Control operations.
- 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.
QUALIFICATION:
- Tech / B.E in Polymer Engineering, Mechanical Engineering, Polymer Engineering
EXPERIENCE:
- 2-5 Years’ experience in quality control.
JOB LOCATION:
- Thane (Ambernath)
JOB SUMMARY:
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.
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- Electronic engineer with Diploma in Electronics.
- 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.
ACADEMIC QUALIFICATION:
- B Tech / Diploma in Electronics
WORK EXPERIENCE:
- 1 to 3 years in electronic industry, preferably in assembly, testing & production of components & boards.
JOB LOCATION:
- Thane (Ambernath)
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Electronic Engineer’.
JOB SUMMARY:
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
JOB DETAILS, REQUIREMENTS & SKILLS:
- 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.
REQUIRED BACKGROUND & CRITERIA:
- CIPET, B-Tech or a related field.
- 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.
ACADEMIC QUALIFICATION:
- CIPET (Plastic Processing, Production Engineering), B-Tech
WORK EXPERIENCE:
- 1 to 3 years in plastic processing industry.
JOB LOCATION:
- Thane (Ambernath)
HOW TO APPLY:
- Email ‘Cover Letter’ & Resume to ‘hrd@georgephilips.com’
- Address the email as ‘Application for the post of ‘Polymer Engineer’.