Find Your Dream Medical Job in India

Job Title: Medical Writer – Fixed Term Contract (12 months, Full Time)

Locations: India, Mexico, Brazil

Department: Scientific Operations

About the Role:

We are seeking a Medical Writer to join a dynamic scientific operations team supporting medical device projects. This is a full-time, site-based role on a 12-month fixed-term contract with the potential for extension. The Medical Writer will create, update, and manage a range of regulatory and clinical documents including Clinical Evaluation Reports (CERs), Summary of Safety and Clinical Performance Reports (SSCPs), State of the Art Reviews (SOAs), and Systematic Literature Reviews (LRRs) within their assigned therapeutic area.

Key Responsibilities:

• Write and update CERs, SSCPs, SOAs, and LRRs in compliance with applicable regulatory requirements and guidelines

• Participate in all core steps of systematic literature reviews, including search, screening, data extraction, analysis, and synthesis

• Summarize clinical, non-clinical, and regulatory data to perform risk/benefit analyses on medical devices

• Compare device safety and performance against the state of the art and investigate unexpected outcomes

• Utilize various software systems, including Microsoft Office, EndNote, Distiller, Wr

Job Title: Sales Representative

Experience: Minimum 2 years in Surgical

Industry: Medical Sales/Healthcare

Job Summary:

We are seeking a driven and experienced sales representative to join our team. The ideal candidate will have at least 2 years of experience in medical sales, with a proven ability to build strong client relationships and drive revenue growth.

Key Responsibilities:

• Promote and sell medical products and equipment to healthcare professionals, hospitals, and clinics.
• Identify new business opportunities and develop strategies to increase market share.
• Conduct product demonstrations and provide detailed information to customers.
• Build and maintain strong relationships with existing and prospective clients.
• Collaborate with internal teams to ensure smooth order processing and customer support.
• Meet or exceed sales targets and ensure customer satisfaction.

Key Requirements:

• Minimum 2 years of experience in medical sales or healthcare sales.
• Excellent communication and negotiation skills.
• Proven track record of meeting or exceeding sales targets.
• Bachelor’s degree in a relevant field (preferred: life sciences, business, or healthcare).

Be

JOB TITLE

TELE SUPPORT BIOMEDICAL ENGINEERS

Company Description

QUICKLAB SERVICES PRIVATE LIMITED is a company that started in 2012 as a service-oriented company specializing in laboratory machines. They have expanded globally and offer a range of products including Biochemistry Analyzer, Hematology Analyzer, Electrolyte Analyzer, Blood Gas Analyzer, and more.

Role Description

This is a full-time role for a Biomedical Engineer located in Chennai. The Biomedical Engineer will be responsible for Tele support for the equipment's sold by QUICKLAB and need to assist lab professionals and maintenance, managing medical equipment, performing preventive maintenance, and overseeing clinical engineering tasks.

Qualifications

• Equipment Maintenance and Preventive Maintenance skills
• Experience in Biochemistry Analyzer, Hematology Analyzer, Electrolyte Analyzer, CLIA, and more.
• Knowledge of Clinical Laboratory products
• Strong problem-solving and analytical skills
• Excellent communication and teamwork abilities
• Relevant certification or Bachelor's degree in Biomedical Engineering or related field

SDS Coder:

We are hiring experienced, certified Senior Same Day Surgery Medical Coders with extensive knowledge of CPT, HCPCS, ICD-10-CM, modifiers, units from the medical record documents and excellent communication skills.

Responsibilities:

⦁ A minimum of the last 5+ years’ experience required coding medical records for Inpatient and Outpatient Surgical Specialties which must include Orthopedics, General Surgery, Cardiology, Spine, Oral, etc.

⦁ Ability to assign ICD-10-CM & PCS diagnoses and procedure codes correctly and completely.

⦁ Requires advanced technical knowledge in specific inpatient and outpatient surgical and medical specialties as assigned.

⦁ Extensive knowledge of medical terminology.

⦁ Experience in researching and applying coding rules and regulations.

⦁ Must have experience with data entry of codes into a database and/or software tool.

⦁ Proficiency in Microsoft Excel, Word, and a variety of EMR (Electronic Medical Record) systems.

⦁ Excellent oral and written communication skills.

⦁ Have a positive, respectful attitude.

Minimum Requirements:

· Education: Science Graduate or Postgraduate.

· Credentials: Must possess current AHIMA/ AAPC certificate(s).

· Communication: Possess outstanding verbal and written proficiency in English.

Roles and Responsibilities

The resource will lead the clients through the implementation of PracticeSuite’s practice management software. He/she will manage multiple projects to ensure the client and the internal departments/teams are completing tasks on schedule as outlined in the client’s project plan. This is a skilled position that requires experience in a related field.

Job duties include the below:

· Assess client/project need and build relationships with the client.

· Develop and manage implementation project lifecycles.

· Manage client expectations, outcomes and timelines.

· Ability to effectively communicate with the client to define what is in scope versus out of scope.

· Keep the project in scope and on time.

· Effectively lead meetings and direct team/client solutions to anticipate and overcome obstacles.

· Serve as a liaison between internal departments and the client during implementation.

· Update client and internal management on project status, issues, additional scope

· Manage issue escalations and provide direction as necessary.

· Effectively communicate recommendations to management

· Promote team and client collaboration to establish and improve best practices.

· Serve as a trusted advisor by advocating for client needs and product requests to PracticeSuite support, product and engineering t

Key Responsibilities

1. Storyboard Development

• Create structured clinical storyboards for videos, infographics, and graphical articles.
• Collaborate with design and animation teams to ensure scientific accuracy and narrative flow.
• Interpret data and research to build engaging, compliant visual content.

2. Scientific Writing

• Draft manuscripts, CME content, and short/long-form medical articles.
• Ensure accuracy, referencing, and adherence to scientific and regulatory standards.
• Summarize complex data into clear, clinician-focused communication.

3. Content Ideation

• Generate topic descriptions and content ideas for client projects.
• Identify emerging therapy trends to develop new scientific content.
• Support campaign and CME theme conceptualization.

Qualifications

• Master’s or PhD in Life Sciences / Pharmacy / Medicine.
• 1–5 years’ experience in medical writing or scientific communication.
• Strong understanding of clinical research, publication standards, and evidence-based medicine.
• Excellent research, writing, and communication skills.

Core Competencies

• Scientific accuracy and attention to detail.
• Ability to simplify complex medical concepts.
• Creative storytelling within clinical contexts.
• Collab

Role: Medical Surveillance Specialist 1

Skill: Clinical research,

Mode: Hybrid (3 days Work form Office)

Shifts: 2 shifts- morning shift 5.30-2.30pm and 2nd shift from 2.30-11.30pm

Experience: 2- 6 years

Job Location: Kochi/Bangalore/Thane

Job Description Summary:

Provide a wide range of medical surveillance support (including monitoring of clinical laboratory data for subjects in clinical studies and composing medical narratives and interfacing with investigator sites.)

Qualifications:

• Bachelor's Degree Life Sciences or allied health sciences, ie pharmacy, biochemistry, microbiology, biotechnology, nursing, biotechnology, medical laboratory sciences, physiotherapy health care ie medical (allopathy, homeopathy, ayurveda), or dentistry, 2 to 6 years relevant experience with a minimum 2.5 years of medical surveillance experience (req) equivalent combination of education, training and experience.
• Strong technical ability to comprehend and integrate scientific data from a variety of sources.
• Strong communication skills, both written and verbal. Demonstrated computer skills, especially word processing and data management.
• Strong analytical and organizational skills and attention to detail required.
• Ability to establish and maintain effective working relationships with coworkers, man

1. Job description:

Applications are invited for the position of Maintenance Engineer from Medical device/Pharmaceutical background at EffecMed Private Limited for its New Manufacturing facility (ISO Cleanrooms) at Rabale, Navi Mumbai location.

2. Essential Duties and Responsibilities include:

a. Perform preventive, predictive, and Breakdown/ Corrective maintenance on Plant utilities (e.g. HVAC, ELVs, Purified Water systems, ETP, etc), Facility equipment (e.g., Autoclave, LT panel, Compressors etc.) and MEP systems.

b. Diagnose and resolve Mechanical, Electrical, Pneumatic, and Instrumentation issues to minimize Downtime, saving Energy and improve Efficiency of Plant Machinery.

c. Prepare and Maintain records of maintenance, calibration, and validation as per audit and compliance requirements.

d. Participate in engineering activities for process improvements and new equipment commissioning, qualification (IQ/OQ/PQ) and validation activities.

e. Ensure adherence to EHS (Environment, Health & Safety) standards during maintenance operations.

f. Coordinate with production and quality teams to plan maintenance schedules with minimal disruption.

g. Manage spare parts inventory, equipment documentation, and vendor coordination for technical services.

h. Provide technical training to technicians and operators on equipment maintenance and

Medical Counselor / Clinical Doctor

Location: Pune, India

Experience: 3–7 years

Employment Type: Full-time

Position Title : Manager/ Senior Manager – Global Medical Information

Function : Global Medical Services

Location : Bangalore

About Viatris:

At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.

Viatris empowers people worldwide to live healthier at every stage of life.

We do so via:

• Access – Providing high quality trusted medicines regardless of geography or circumstance;
• Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
• Partnership – Leveraging our collective expertise to connect people to products and services.

Every day, we rise to the challenge to make a difference and here’s how the Manager/Senior Manager- Global Medical Information role, will make an impact:

Role Purpose:

As a Manager – Global Medical Information, you will lead and support a team of Medical Information professionals while also contributing individually to the development of scientific content, literature analysis, and customer response strategies. This hybrid role combines leadership with hands-on operational responsibilities to ensure the delivery of high-quality, compliant, and customer-centric medical information globally.

Ke

Key Responsibilities for AR:

• Review account thoroughly, including any prior comments on the account, EOBs / ERAs / Correspondence, and perform pre-resolution analysis.
• Understand the reason for rejection, denials, or no status from the payer.
• Work on the resolution of the claim by performing follow-up with the payer using the most optimal method, i.e., calling, IVR, web, or email.
• Take appropriate action to move the account towards resolution, including rebilling the claim, sending claims for reprocessing, reconsideration, redetermination, appeal (portal/web, fax, mail), verifying eligibility and benefits, and managing management hand-off with the client and internal teams.
• Documentation of all the actions on the practice management system and workflow management system, and maintain an audit trail.
• Ensure adherence to Standard Operating Procedures and compliance.
• Highlight any global trend/pattern and issue escalation with the leadership team.
• Meet the productivity and quality target on a daily/monthly basis.
• Upskill by learning new/additional skills and enhancing competencies. Active participation in all process/client-specific training and refresher training.

Requirements:

• Undergraduate / Graduate in any stream with 2 to 4 years of experience in US Healthcare RCM for Account Receivable / Denial Management Resoluti

TITLE : QA/Process Specialist – Medical Coding

REPORTS TO : General Manager - Medical Coding

DEPARTMENT : Huron Healthcare RCM Group

WORK HOURS : 5 days week and flexible to work in different shifts

LOCATION : Chennai & Bangalore

SUMMARY :

Responsible for the day-to-day production and quality functions of a team of coders specializing in meeting client production goals and coding accuracy goals. Help supervisor in preparing daily operational reports, provide feedback about the challenges and participates in the client interactions and internal stakeholder meetings.

Excellent communication skills, attention to detail, and strong technical and problem solving skills are essential aspects of this role.

JOB DETAILS:

• Monitors performance of all coding staff using key metrics including, but not limited to daily coding volume, assignments worked, client project deadlines and coding accuracy performance to achieve and maintain a 95% coding quality accuracy rate.
• Escalate Production and QA concerns or roadblocks to the Manager for involvement as needed. Work closely with the Training teams members to communicate progress across the Team to the Manager.
• Reviews both production and quality accuracy

Location: Bengaluru / Hybrid 

Experience: 5 - 8 years

Overall Package: 8 - 10 LPA

Role Summary:

The Regulatory Affairs senior specialist will be responsible for planning, preparing, and managing regulatory submissions and compliance activities for medical devices under CDSCO (India), EU MDR, and US FDA frameworks. The role involves working cross-functionally with design, quality, clinical, and manufacturing teams to ensure regulatory compliance throughout the product lifecycle and to maintain an effective Quality Management System (QMS) aligned with ISO 13485 and other applicable standards.

Key Responsibilities:

• Prepare, review, and submit regulatory dossiers and applications to  CDSCO , including:
• Manufacturing and import licenses, Test licenses, Device registration dossiers,  Post-approval variations and renewals
• Prepare  Technical Documentation and  Design Dossiers as per EU, India requirements.
• Prepare  US FDA submissions , including:
• 510(k) ,  PMA ,  De Novo , and  Q-Submission documentation.
• Address queries, deficiencies, and audits of  Notified Bodies, CDSCO, and FDA reviewers
• Support implementation and maintenance of  ISO 13485:2016, 21 CFR Part 820

Company Description (RXpress - Medicine in 20 Minutes)

We’re building Pharmacy 2.0 - India’s fastest, smartest 20-minute medicine delivery platform.

Powered by dark stores, AI-driven SKU-alternatives, in-app doctor consultations and prescription management. RXpress is redefining how healthcare reaches every household - Fast. Smart. Zero-Hassle.

What You’ll Do

You’ll play a core role in ensuring RXpress dark stores never run out of what customers need - from prescription medicines to wellness SKUs. This isn’t just about purchasing; it’s about building India’s smartest pharmacy supply chain from the ground up.

Own Procurement Across Dark Stores

• Manage end-to-end sourcing and replenishment for Rx, OTC, and wellness categories across RXpress’s hyperlocal dark stores.
• Develop and refine reorder triggers based on real-time sales velocity, expiry tracking, and store-level consumption patterns.
• Maintain a live inventory availability of >98% on top 1,000 SKUs, enabling 20-min delivery reliability.

Manage Multi-Channel Vendor Network

• Build and manage supplier relationships across pharma distributors, wholesalers, and digital B2B platforms such as RetailIO, Pharmarack, MedleyMed, Tata 1mg Partner, etc.
• Ensure each dark store has access to a multi-vendor supply chain, with redundancy for

Medical Affairs Writer JD

1. Writing, editing, reviewing, formatting, publishing regulatory (clinical and post marketing) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO, ICH, CONSORT guidelines and other similar standards.

2. Collaborating with the clinical team in developing and strategizing the Clinical Development Plan.

3. Collaborating across line functions in preparing SOPs for Regulatory documents.

4. Interpreting, representing and summarizing clinical and scientific data

5. Planning, organizing, tracking, and archiving clinical and post-marketing regulatory dossiers.

6. Managing stakeholders across line functions and geographies.

7. Managing assigned individual projects and holding complete responsibility throughout the document/project lifecycle.

8. Ensuring consistency at all times with compulsory and voluntary codes of conduct, appropriate legislations and compliance with internal SOPs.

9. Building-up newer competencies and enhance existing competencies; analyzing skill/process gaps and bridging the gaps by developing expertise/process maps.

10. Developing cross-functional skills in publication writing.

11. Training peers in regulatory writing.

12. Mentoring and coaching of direct reportees, if any

About This Role

Position Overview

This Senior Lead Engineer is responsible for providing technical leadership and direction across Sustaining and Innovation Engineering projects, overseeing design changes, product enhancements, and new solution development. This role drives complex problem-solving, mentors junior engineers, and ensures design integrity from concept to validation. Senior Lead Engineer partners with engineering leadership to define strategies for product improvement, cost optimization, and innovation while maintaining compliance with engineering standards and business objectives.

Mandatory Skills:

• 5+ years’ experience in driving execution of complex design changes including model and drawing revisions, design justifications, tolerance stack-ups, verification testing, and root cause analyses.
• 5+ years & Advanced proficiency in SolidWorks (or equivalent CAD software) for complex assemblies, tolerance stack-up analysis, and design optimization.
• 3 to 5 years’ experience in deep understanding of GD&T per ANSI Y14.5, tolerance analysis, and mechanical stress evaluation for high-precision components.
• Strong communication & interpersonal skills and ability to work in a fast-paced environment and manage multiple priorities.

Desired Skills:

• Lead and oversee Change Request and Change Order processes, ensuring effective prioritiza

Job Description:

Position : Territory Sales Manager / Area Sales Manager

Division : Orthotics Products

Location : Hyderabad

Reports to : Regional Sales Head

Role Objective:

To drive sales growth, develop and manage key accounts, and expand market share for the orthotics product portfolio in the assigned territory.

Key Responsibilities:

• Achieve monthly, quarterly, and annual sales targets for assigned territory.
• Develop and implement territory sales plans aligned with company objectives.
• Identify and onboard new customers (orthopaedic surgeons, physiotherapists, hospitals, and distributors).
• Strengthen relationships with existing accounts to maximize revenue and customer satisfaction.
• Manage distributor / dealer network and ensure their performance in terms of coverage and sales.
• Conduct product presentations, demonstrations, and training sessions for customers and partners.
• Monitor competitor activities, market trends, and provide feedback to management.
• Support marketing initiatives, conferences, and local promotional activities.
• Ensure timely reporting of sales data, forecasts, and customer interactions.

Candidate Profile

• Graduate in Science / Pharmacy / Physiotherapy / Business. MBA preferred.
• 3–6 year

About Triomics:

Triomics is building the modern technology stack for oncology trial sites and investigators that unifies the workflows of clinical care and clinical research, moving the healthcare industry closer to the vision of Clinical Research as a Care Option. Our platform, which is based on our proprietary oncology-focused large language model (OncoLLMTM) co-developed with several leading cancer centers, eliminates the operational inefficiencies in patient recruitment, data curation, and other laborious tasks involved in clinical research, thus enabling the generation of high-quality data and speeding up the clinical trials.

Job Description:

Part of the Oncology Clinical Team, working on building Oncology Data dictionaries, Curation/Abstraction, SOPs, clinical trial - study build, etc.

Position Summary:

The Person navigates electronic medical record systems and other medical databases. This role involves reviewing clinical trial data for consistency, completeness, and compliance with study protocols and regulatory requirements. reviews medical records, and abstracts medical record data related to specified disease and project requirements.

Essential Job Functions:

• Screen patient cases for eligibility across multiple oncology clinical trials, applying trial-specific inclusion/exclusion criteria.
• Interpret diagnostic, pathology, imaging, and other clinic

Non-Clinical Job in US based MNC located in Vadodara, Gujarat Location (On-site job)

Company budget: 6,20,000 PA. (For FRESHER'S)

1-2 year experienced 8,50,000 PA.

3+ years' experience can get up to 12,00,000 PA.

About the Role - The role will be to review and verify large volumes of patient's full medical records with precision, perform clinical reviews as defined by the specific review methodologies and prepare a detailed report that includes chronologies and timelines, summaries, mass tort matrix and medical opinions on case validity and valuation.

Responsibilities

• Analyzing and summarizing medical records for pre and post settlement projects.
• Interpreting clinical data in terms of medical terminology and diagnosis.
• Adhering to company policies & principles, hence taking good care of Company culture.
• Adhere to Health Insurance Portability and Accountability Act (HIPPA) all the time.
• Daily reporting to Medical team lead for productivity & quality

Qualifications - MBBS (Freshers & Experienced both can apply)

Required Skills

• Knowledge of basic level of health care data analysis and clinical review.
• Sound knowledge of medical terminology, assessments, patient evaluation, and clinical medici

Origin Nutrition is a premium plant-based nutrition brand dedicated to creating products that fuel a healthier lifestyle while being kind to the planet. Our flagship product line includes high-quality, plant-based protein powders designed to support health-conscious individuals, athletes, and patients with special nutritional needs. We are expanding our footprint in the medical and retail nutrition space and are

looking for a dynamic Sales Manager to lead this growth.

Role Overview

We are seeking an experienced and driven Sales Manager to lead our efforts in

promoting and selling our plant-based protein powder through medical and nutritional

channels. This role will focus on developing and executing sales strategies,

managing a team of medical sales representatives, and building strong relationships

with healthcare professionals and institutions.

Key Responsibilities:

• Develop and execute sales strategies to promote plant based nutrition products to doctors within the assigned city or region.
• Build and maintain strong relationships with key healthcare professionals, including doctors, pharmacists, and other medical personnel.
• Identify new business opportunities and develop plans to expand market reach and penetration.
• Provide product information, educational materials, and training to healthcare professionals to increase awareness and usage of

Role Description

This is a full-time remote, clinical role for a Medical Illustrator . You'll work closely with medical writers, subject matter experts, and designers to create high-quality visuals for a range of medical and scientific content, including:

• Creating accurate, engaging, and visually appealing illustrations of human anatomy, surgical procedures, pathophysiology, and medical devices
• Translate scientific information into accessible visual formats for both technical and non-technical audiences
• Meet deadlines while maintaining high artistic and scientific standards
• Contribute to brainstorming and concept development for new projects

What we are looking for:

• Candidates who have strong attention to detail and accuracy
• Excellent communication and collaboration skills
• Ability to work independently in a remote environment
• Experience with medical imaging software is a plus

About the Team

The Process Excellence team at Navi is focused on maintaining and elevating the quality of customer interactions. As the quality audit function, the team conducts regular audits of agent communications—across calls, chats, and other channels—to ensure accuracy, consistency, and compliance. The team also ensures compliance across different verticals and runs multiple initiatives in coordination with business team stakeholders to drive key business metrics. Insights from these audits are used to drive continuous improvement through targeted training, helping agents close knowledge or process gaps and deliver a consistently excellent customer experience.

About the Role

We are seeking an experienced doctor with medical knowledge, analytical skills for process excellence to join our dynamic team..The ideal candidate will be responsible for strategic claim auditing, insight-driven reporting, stakeholder engagement, and improvement areas. The auditor should be able to identify patterns and process gaps. will collaborate with cross-functional teams like claims, network providers, and investigations. product, analytics, automation & compliance to ensure successful delivery of initiatives.

What We Expect From You

• Review submitted health claims for accuracy, completeness, and compliance with insurance policies and applicable regulations.
• Identify any inconsis

ABOUT US:

Firstsource Solutions Limited, an RP-Sanjiv Goenka Group company (NSE: FSL, BSE: 532809, Reuters: FISO.BO, Bloomberg: FSOL:IN), is a leading provider of transformational solutions and services spanning the customer lifecycle across Healthcare, Banking and Financial Services, Communications, Media and Technology, and other industries. The Company's Digital First, Digital Now approach helps organizations reinvent operations and reimagine business models, enabling them to deliver moments that matter and build competitive advantage. With an established presence in the US including over a dozen offices, and multiple sites in the UK, India, the Philippines and Mexico, we act as a trusted growth partner for over 150 leading global brands, including several Fortune 500 and FTSE 100 companies.

Website:

• Job location : RMZ Perungudi, Chennai
• Position : Senior Certified Coding Associate
• Industry : ITES/BPO
• Category : Medical Coding
• Work Mode : Work From Office
• Role : E&M Medical Coder
• Shift Timing : 8 AM - 6 PM

Eligibility Criteria:'

• Candidates should have experience in Evaluation & Management (OP / IP)
• Must have strong knowledge of ICD-10 CM/PCS and CPT coding
• Anesthesia coding & Surgery Cod

Company Description

We suggest you enter details here.

Role Description

This is a full-time on-site role for a professional in Medical Billing, Insurance Accounts Receivable (AR), and Patient calling, located in Ahmedabad. Responsibilities will include handling medical claims processing, reviewing insurance denials, resolving AR discrepancies, supporting accurate patient scheduling, and ensuring compliance with relevant policies and regulations. The role also requires effective communication with insurance companies and patients to address billing queries and payment resolutions efficiently.

Qualifications

• Strong knowledge of Medical Terminology and familiarity with ICD-10 coding
• Experience in managing insurance claims, including handling Medicare-related tasks
• Proficiency in analyzing and resolving insurance denials and Accounts Receivable discrepancies
• Capacity to work in a fast-paced environment with attention to detail and organizational skills
• Excellent communication skills for liaising with insurance providers and patients
• Understanding of healthcare reimbursement processes and regulatory compliance
• Previous experience in medical billing, patient scheduling, or similar healthcare roles is beneficial
• Bachelor's degree or relevant certification in medical billing, healthcare administration, or a related field is preferre

Company Description

We are situated at Farakka, Murshidabad,West Bengal.

Role Description

This is a full-time on-site role for a Medical Doctor at Farakka Medical Diagnostic Centre Pvt. Ltd. The Medical Doctor will be responsible for providing medical care, diagnosing and treating patients, conducting examinations, prescribing medications, and collaborating with other healthcare professionals.

Qualifications

• Medical degree and valid license to practice
• Experience in patient care and treatment
• Strong diagnostic and decision-making skills
• Excellent communication and interpersonal abilities
• Ability to work well in a team
• Knowledge of medical software and tools
• Specialization in a specific area of medicine is a plus
• Completion of residency program

Role Overview:

Responsible for implementing and maintaining the Quality Management System (QMS) in compliance with ISO 13485 and regulatory standards. Ensures product quality, process integrity, and audit readiness across all manufacturing operations.

Key Responsibilities:

• Oversee incoming, in-process, and final product inspections .
• Ensure compliance with ISO 13485, ISO 14971, and GMP guidelines.
• Review and approve SOPs, batch records, and quality documentation .
• Manage deviations, CAPA, and root cause analysis .
• Support validation and qualification of equipment and processes.
• Lead internal and supplier audits , and support regulatory inspections.
• Drive continuous improvement initiatives in quality systems.

Qualifications:

• B.Pharm / M.Pharm / B.Tech (Biomedical, Biotechnology, or Life Sciences).
• Minimum 6 years’ QA/QC experience in medical device manufacturing .
• Strong understanding of QMS documentation and validation protocols .
• Internal auditor certification (ISO 13485) preferred.

Job Description:

Position : Territory Sales Manager / Area Sales Manager

Division : Orthotics Products

Location : Kochi, KL

Reports to : Regional Sales Head

Role Objective:

To drive sales growth, develop and manage key accounts, and expand market share for the orthotics product portfolio in the assigned territory.

Key Responsibilities:

• Achieve monthly, quarterly, and annual sales targets for assigned territory.
• Develop and implement territory sales plans aligned with company objectives.
• Identify and onboard new customers (orthopaedic surgeons, physiotherapists, hospitals, and distributors).
• Strengthen relationships with existing accounts to maximize revenue and customer satisfaction.
• Manage distributor / dealer network and ensure their performance in terms of coverage and sales.
• Conduct product presentations, demonstrations, and training sessions for customers and partners.
• Monitor competitor activities, market trends, and provide feedback to management.
• Support marketing initiatives, conferences, and local promotional activities.
• Ensure timely reporting of sales data, forecasts, and customer interactions.

Candidate Profile

• Graduate in Science / Pharmacy / Physiotherapy / Business. MBA preferred.
• 3–6 year