Showing posts with label Jobs in Chennai. Show all posts
Showing posts with label Jobs in Chennai. Show all posts
Monday, 26 September 2016
By Anuj Tripathi / Posted on 10:31 / Categories: Jobs in Bangalore, Jobs in Chennai, Medical Coding, Medical Terminology
Job Description
- Immediate Openings for IP-DRG Medical Coding @ Vee Technologies
Job Description:
1+ Years of experience in IP-DRG Coding.
Coding certification like CIC, CPC, CCS, CPC-H, CCS-P. is added advantage.Apply here
Tuesday, 20 September 2016
Accenture is a global management consulting, technology services and outsourcing company, with approximately 275,000 people serving clients in more than 120 countries. Combining unparalleled experience, comprehensive capabilities across all industries and business functions, and extensive research on the world’s most successful companies, Accenture collaborates with clients to help them become high-performance businesses and governments. The company generated net revenues of US$28.6 billion for the fiscal year ended Aug. 31, 2013.

Job Description
Ph.D. in Life Sciences or Pharmacy/M.D. in Pharmacology or Physiology or Public Health/ M.B.B.S. /B.D.S. /B.A.M.S with working knowledge of safety report generation, reconciliation of Serious Adverse Events, patient narrative writing may apply.
Apply here

Job Description
Ph.D. in Life Sciences or Pharmacy/M.D. in Pharmacology or Physiology or Public Health/ M.B.B.S. /B.D.S. /B.A.M.S with working knowledge of safety report generation, reconciliation of Serious Adverse Events, patient narrative writing may apply.
Apply here
Thursday, 15 September 2016
By Anuj Tripathi / Posted on 10:13 / Categories: 1-6 Years, BIOTECH JOBS, Jobs in Bangalore, Jobs in Chennai, Medical Coding, Medical Terminology, Pharma
Job Description
- Immediate Openings for IP-DRG Medical Coding @ Vee Technologies
Job Description:
1+ Years of experience in IP-DRG Coding.
Coding certification like CIC, CPC, CCS, CPC-H, CCS-P. is added advantage.
Specialty : IP-DRGExperience : 1- 6 Years.
Designation : Medical Coder/ Sr.medical Coder/QA & TL
Location : Chennai / Bangalore/ Salem
Attractive salary & joining bonus for the immediate joiner's.
Interested Candidate Call Immediately to the below contact number
Regards,
Ramesh - HRD
9443238706
mail: ramesh.m@veetechnologies.com
Company Profile:
Vee Technologies
Vee Technologies a Sona Group Company has been operating in the BPO space for in various domains like Insurance, Healthcare, Logistics, Engineering Services, Finance & Accounts and News tracking successfully for the last 14 years. The Sona Valliappa Group owns and runs a group of educational institutions like the Sona College of Technology, Sona School of Management and Thiagarajar Polytechnic. The Valliappa Software Technological Park is a pioneer in the infrastructure and incubation services. We work with major physician groups, billing companies and hospitals.
Saturday, 10 September 2016
By Anuj Tripathi / Posted on 09:58 / Categories: 1-5 Years, Biotech, Healthcare, Jobs in Chennai, Jobs in Hyderabad, Life Science, Medical Coding, Pharma
Openings For Medical Coding!!!
1 - 5 Years
Job Description
Greeting from Sutherland Health care Services!!!
We are currently hiring for E&M-inpatient & outpatient (min 1year of exp).
Job Description:
Good written and verbal communication skills.
Good analytical and domain skills
Well versed in MS office and ability to work online with multiple navigation systems and various coding software(s).
Coding Certification (CPC/CCS): Preferred
ICD-10 training completed - Preferred
Free transportation
Good written and verbal communication skills.
Good analytical and domain skills
Well versed in MS office and ability to work online with multiple navigation systems and various coding software(s).
Coding Certification (CPC/CCS): Preferred
ICD-10 training completed - Preferred
Free transportation
Sat & Sun- Fixed off
Salary: As per company norms
Work Location: Hyderabad
Interested candidates mail your resume to marysandana.nikhita @sutherlandglobal.com
Regards,
HR Team
Sutherland Global Services
Hyderabad
Company Profile
Apollo Health Street (AHS) is an end-to-end healthcare outsourcing focused services company, with impeccable credentials, proven track record and unwavering commitment aimed at delivering value added services to its clients
Tuesday, 6 September 2016
Huge Openings for Denial Coding ( Medical Coding ) - Chennai
Access Healthcare Services Pvt Ltd
1 - 6 yrs
Chennai

Job Description
- Greetings from Access Healthcare!!
Hope you are doing well...
About Us: Access Healthcare Services Pvt Ltd is a Healthcare revenue cycle management, business process outsourcing firm. We are US based Multi-National Company and are located in Chennai, Manila, Pune and Coimbatore To know more about us, kindly visit our website, www.accesshealthcare.org
Job Role: Medical Coding
Specialty: Denial Coding / Denial Management Coding
Experience: 1 to 6 Years
No. of Openings: 135
Job Location: Chennai
Interview Location: Chennai
Compensation: We offer highly competitive work environment with best in the business compensation package
Walk-In Interview on 8th July and 9th July 2016
Time: 11.00AM - 4.00PM
*Interested candidates please walk-in directly for Face to Face Interview with your updated profile.
It's a Spot Offer interview, all the levels of interview are happening on the same day
Note: Kindly ignore this email if your profile does not matches this requirement.
Thanks and look forward to meet you up soon.
Interview Venue:
HQ
Access Healthcare Services Pvt Ltd.
A9, First Main Road,
Ambattur Industrial Estate
Ambattur
Regards,
Santhosh
Human Resource
7395973888
Company Profile:
Access Healthcare Services Pvt Ltd
Access Healthcare Services Pvt Ltd is a Healthcare revenue cycle management, business process outsourcing firm. We are US based Multi-National Company and are located in Chennai, Manila, Pune and Coimbatore
Saturday, 3 September 2016
Work as CLS Associate @ Kemin | M.sc Biochemistry / Microbiology & Chemistry Eligible

Work as CLS Associate I @ Kemin | M.sc Biochemistry / Microbiology & Chemistry Eligible
Kemin combines sound molecular science with the human qualities of creativity, curiosity and collaboration to improve the lives of humans and animals around the world. Using superior science, Kemin manufactures more than 500 specialty ingredients that deliver important nutrition and health benefits through products consumed by people and animals.
Job Title : CLS Associate I
Job ID : 2016-4311
Qualifications : Master of science (chemistry, biochemistry or microbiology) with 1 – 2 years of experience
No. of Positions : One
Location : Chennai
Category : Customer Service/Support
Position Type : Regular Full-Time
Position Objective : Provide lab service to our customers with an objective to retain the customers above 90%, to develop new business 25% of the total sales and to demonstrate the superiority of our products over competitive brands.
Responsibilities:
Kemin combines sound molecular science with the human qualities of creativity, curiosity and collaboration to improve the lives of humans and animals around the world. Using superior science, Kemin manufactures more than 500 specialty ingredients that deliver important nutrition and health benefits through products consumed by people and animals.
Job Title : CLS Associate I
Job ID : 2016-4311
Qualifications : Master of science (chemistry, biochemistry or microbiology) with 1 – 2 years of experience
No. of Positions : One
Location : Chennai
Category : Customer Service/Support
Position Type : Regular Full-Time
Position Objective : Provide lab service to our customers with an objective to retain the customers above 90%, to develop new business 25% of the total sales and to demonstrate the superiority of our products over competitive brands.
Responsibilities:
- Responsible to conduct lab analysis of feed sample for top 20 customers and complete minimum of 90 % of annual projects without errors with no more than 50% supervision.
- Ensure to deliver the reports on time to customers (minimum of 98% report within 5 days.
- Should play active role as a team member in the project team in new product Innovative Process ( PIP)
- Maintain the lab account for chemical and test charges in a proper ledger.
- Maintain and operate the lab equipment effectively and handle the trouble shoot, basic repair of the lab equipment’s independently.
- Responsible to conduct method validation of the lab equipment at regular intervals.
- Ensure to send weekly and monthly reports to manager – CLS
- Responsible to maintain etiquette of the lab
Friday, 2 September 2016
By Anuj Tripathi / Posted on 11:38 / Categories: 1-3 Years, B Pharm, Biotech, Jobs in Chennai, Life Science, Medical Coding, Medical Terminology
Job Description
Dear Candidate,
e4e Healthcare Business Services Pvt Ltd
Unit 1-5-2, Block A (the Eastern Front Wing)
TECCI Park No:285, Old Mahabalipuram Road,
Sholinganallur, Chennai - 600 119
Greetings!
Urgent Opening for Experienced Medical Coder - HCC Coding
Job Description :-
1. Any life Science graduate (Should be certified).
2. Should have minimum experience of 1 year in HCC coding.
3. Understand the client requirements and specifications of the project.
4. Ensure that the deliverables to the client adhere to the quality standards.
5. Immediate joinee will be an added advantage.
Interested candidates can directly walk-in to e4e office in Chennai or send me the updated resume to the mentioned ID.
Timings: 11 am - 05 pm
Job Location :- Chennai
Contact Person :-Sowmithry Devi Jayakumar
Venue :-
Unit 1-5-2, Block A (the Eastern Front Wing)
TECCI Park No:285, Old Mahabalipuram Road,
Sholinganallur, Chennai - 600 119
Contact : 8754444001
Email :- sowmithrydevi.jayakumar@e4e.com
By Anuj Tripathi / Posted on 11:36 / Categories: 1-3 Years, Jobs in Chennai, Medical Writing, Pharmacovigilance, Regulatory Affairs
H and LS Medical Writer

1 - 3 Years
Chennai
Job Description
OVERALL PURPOSE OF JOB
Writing, Reconciling, editing and/ or managing the production of high quality clinical documents that are components of regulatory marketing approval. Knowledge of clinical terminology is a must. They ensure that documents are written consistent with company and regulatory guidelines.
PROCESSES :
.
Responsibilities/ Authorities :
oWriting first draft of Aggregate Report (e.g. RMP, PVP, PSURs, PADERs, ASRs, QSUSARs)
oLiterature Search
oNewly analyzed, ongoing and completed study information from, but not limited to, clinical, non-clinical, and epidemiology studies.
oCurrent Reference Safety Information (e.g., CCSI/ CCDS/ CPLP)
oConduct analysis of singles cases extracted
oEnsure consistency with quality, accuracy, and medical safety standards
oReview and follow-up reports with relevant stakeholders internally (Lead TA, local market PV, Global Regulatory Teams, Medical Surveillance Team, Pharmaco-epidemiology, etc.)
-Attaches/ reviews all letters and queries for appropriateness and completeness.
-Oversees all the team resources in the work.
-Oversee execution of Quality Control and discrepancy management for outputs
-Assist in training for new resources and as a part of continuous improvement
-Assist in the development of documentation such as work instructions or task checklists for readiness activities as required
-Ensure compliance with client and company policies
-Own assist and comply to all SLAs (Cycle time and quality)
Requirements:
- No special physical demands.
- Major part of work done in office environment.
- High degree of accuracy and attention to detail.
- Good decision making ability.
- Demonstrated strong writing skills and has written publications.
- Ability to analyze, understand and interpret complex scientific data from a broad range of scientific disciplines
Writing, Reconciling, editing and/ or managing the production of high quality clinical documents that are components of regulatory marketing approval. Knowledge of clinical terminology is a must. They ensure that documents are written consistent with company and regulatory guidelines.
PROCESSES :
.
Responsibilities/ Authorities :
oWriting first draft of Aggregate Report (e.g. RMP, PVP, PSURs, PADERs, ASRs, QSUSARs)
oLiterature Search
oNewly analyzed, ongoing and completed study information from, but not limited to, clinical, non-clinical, and epidemiology studies.
oCurrent Reference Safety Information (e.g., CCSI/ CCDS/ CPLP)
oConduct analysis of singles cases extracted
oEnsure consistency with quality, accuracy, and medical safety standards
oReview and follow-up reports with relevant stakeholders internally (Lead TA, local market PV, Global Regulatory Teams, Medical Surveillance Team, Pharmaco-epidemiology, etc.)
-Attaches/ reviews all letters and queries for appropriateness and completeness.
-Oversees all the team resources in the work.
-Oversee execution of Quality Control and discrepancy management for outputs
-Assist in training for new resources and as a part of continuous improvement
-Assist in the development of documentation such as work instructions or task checklists for readiness activities as required
-Ensure compliance with client and company policies
-Own assist and comply to all SLAs (Cycle time and quality)
Requirements:
- No special physical demands.
- Major part of work done in office environment.
- High degree of accuracy and attention to detail.
- Good decision making ability.
- Demonstrated strong writing skills and has written publications.
- Ability to analyze, understand and interpret complex scientific data from a broad range of scientific disciplines
Company Profile
By Anuj Tripathi / Posted on 11:34 / Categories: 2-5 Years, BIOTECH JOBS, Jobs in Chennai, Pharma Jobs
Research Associate

2 - 5 yrs
Chennai
Job Description
- Responsibilities
- Strong technical expertise in protein analytical method, formulation development, biophysical characterization of protein aggregation and/or protein stability.
- A minimum of two years working experience with characterization of degradation mechanisms of proteins especially using chromatographic techniques and development of analytical methodologies for characterization of drug product attributes is required.
- Experience in formulation and/or fill/finish process development for biological drug products demonstrating interpretation of analytical data and writing reports is required.
- Strong working knowledge of size-exclusion and reverses phase HPLC, HIAC and or MFI particle characterization techniques is preferred.
- Experience with frozen liquid, liquid in vials or pre-filled syringe and lyophilization cycle development is preferred.
- Some working knowledge of GMP requirements, process analytical technologies (PAT) and Quality by design (QbD) is also preferred.
- Experience implementing and maintaining high quality standards for all aspects of work conducted including adherence to regulatory GLP/GMP, departmental, and safety guidelines is preferred
Company Profile:
Thursday, 1 September 2016
Pharma Data Entry Associate
1 - 5 Years
Chennai

Job Description
Position PurposeReview, analysis, preparation, and completion of safety-related reports within scope of the DSU to determine the safety profile of Clients products and to meet regulatory requirements. Provide specific pharmacovigilance knowledge and experience, as required by the business, and mentor colleagues accordingly. Manage resources in the safety team depending on local organization and safety group size.Primary Responsibilities Organize, manage, and actively carry out as appropriate, local PV activities, such as adverse event monitoring, safety reporting, risk management, local safety monitoring activities as required by local agency, local contractual agreements, process documentation and training, inspection preparedness, and any other required country-specific safety activity. Carry out all case management activities as appropriate.Ensure regulatory compliance with timelines for individual expedited case report submissions and timely delivery of information for aggregate reports and other regulatory documents as requestedReview processed cases to verify accuracy, consistency, and compliance with process requirements, and review case data for special scenariosEnsure complete and timely forwarding of ICSR to Core Determine if appropriate case follow-up has been considered. Conduct follow-up activities when needed.Consistently apply regulatory requirements and Client policies Analyze and monitor activities, define and implement corrective actions, where applicable.Develop and maintain expertise of all assigned products, of applicable corporate policies and local regulations, guidelines, Standard Operating Procedures and writing practices, of data entry conventions, and of search functions in the safety database.Provide oversight and team mentoring on case handling aspects, data extraction, and analyses. Manage, where applicable, safety resources in th
Company Profile
Accenture is a leading global professional services company, providing a broad range of services and solutions in strategy, consulting, digital, technology and operations. Combining unmatched experience and specialized skills across more than 40 industries and all business functionsunderpinned by the worlds largest delivery networkAccenture works at the intersection of business and technology to help clients improve their performance and create sustainable value for their stakeholders. With approximately 373,000 people serving clients in more than 120 countries, Accenture drives innovation to improve the way the world works and lives. Visit us at www.accenture.com
By Anuj Tripathi / Posted on 10:38 / Categories: 0-1 Years, Biotech, Freshers, Jobs in Chennai, Life Science, Pharma
Intelenet Hiring for Hiring for life Science Graduate

0 - 1 yrs
Chennai
Job Description
- Greetings from Intelenet Global Services!!
We are urgently hiring for life science Graduate for medical coding
Eligibility:
* Minimum Graduate (2016 passout can also apply)
*Any life science graduates (Biotechnology ,Bio chemistry, botany,Zoology,Microbiology and pharma)
*Should have excellent knowledge in medical terminology,anatomy and physiology
Interview Date: 01/9/2016 To 02/09/2016
Interview Timing: 11.00 AM to 3.00 PM
Venue:
Intelenet Global services
Ambit IT Park
32 A&B Industrial Estate
Ambattur Chennai-600058
Land Mark-Ambit IT Park
Refer your friends. Dont miss the right opportunity.
Company Profile:
Intelenet Global Services Private Limited
Intelenet® is a large global Business Process Outsourcing player, committed to delivering our client's strategic goals and helping in enhancing, broadening, and deepening the relationship to add value.
Backed by The Blackstone Group, a leading Global Private Equity player, with a current portfolio of clients that includes Fortune 500 companies, we are a 55,000 people organization spread across 66 global delivery centers across USA, UK, India, Poland, and Philippines; supporting 100+ clients in over 50 languages.
Backed by The Blackstone Group, a leading Global Private Equity player, with a current portfolio of clients that includes Fortune 500 companies, we are a 55,000 people organization spread across 66 global delivery centers across USA, UK, India, Poland, and Philippines; supporting 100+ clients in over 50 languages.
Thursday, 30 June 2016
By Anuj Tripathi / Posted on 11:10 / Categories: 0-3 Years, 2-6 years, 5-9 years, Biochemistry, Biotech, CDM, Clinical Research, Immunology, Jobs in Ahmedabad, Jobs in Bangalore, Jobs in Chennai
Massive Recruitment Drive @ Syngene For R&D Positions in Upstream & Downstream Process
Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations .
Subscribe to:
Posts (Atom)
www.CareerBiotech.com. Powered by Blogger.





