Huge Openings for Pharmacovigilance !! Pune "A"

 Huge Openings for Pharmacovigilance !! Pune

Adventures International Pvt Ltd

Job Description

Min 2 years of exp for PV , Case Processing, Drug Safety, MEDDRA.

Interview Mode:Telephonic
Work Location: Pune


If Interested drop your CV to ravali@adso.com call to 9032912255

Company Profile:

Adventures International Pvt Ltd

SAP Services Partner and an advanced Information Technology consulting firm with over 15 years of industry experience. Since 1998, we have partnered with Fortune 500, mid-size and PublMNC's.We have committed relationships with our strategic partners  

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Pharmacovigilance Associate required "A"

Designation

Pharmacovigilance Associate / Drug Safety Physician

Job Description

Looking for Professionals from Pharmacovigilance for a leading CRO in Delhi NCR - Pharmacovigilance Associate (Day Shift) BDS / B.Pharm / M.Pharm 1-2 years experience - Pharmacovigilance Associate (Rotational Day & Night Shift) BDS / B.Pharm / M.Pharm 1-2 years experience - Sr. Pharmacovigilance Associate (Day Shift) BDS / B.Pharm / M.Pharm 3-4 years experience - Sr. Pharmacovigilance Associate (Rotational Day & Night Shift) BDS / B.Pharm / M.Pharm 3-4 years experience - Drug Safety Physician (Day Shift) MBBS / MD 1-3 years experience - Drug Safety Physician (Roational Day & Night Shift) MBBS / MD 1-3 years experience Key Skills: Drug Safety, Pharmacovigilance, ICSR, case narrative, PSUR, Aggregate reports, Data entry into Safety Database, ADR, Medical Reviewer Apply here

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Walkins to Quintiles on 6th August "A"

Walk - In to Quintiles on 6/8/2016 - Pharmacovigilance (2 to 8 Years)

Quintiles

2 - 7 yrs

Bengaluru/Bangalore

Job Description

Dear  All,

We are pleased to invite you for the Walk In , which will be conducted on 6 /8/2016 at Quintiles , Hyderabad for Pharmacovigilane role.


Skill Sets Required - Case Processing , Drug Safety , Medical Coding, ICSR.


Experience - 2 to 8 years 


Job Location - Bangalore


 Company Profile:

Quintiles

Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health â„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Apply here

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Massive Walkin drive @ Biocon "A"

Massive Walk-in Drive By Syngene For Discovery Biology @ Biocon Park, Bangalore | 10 Openings Available

2 - 6 YearsBengaluru/Bangalore Openings: 10

Walkin Interview on 30th July from 9 AM

Job Description

1) Cell Biology: Sound knowledge in Cell Biology - Cell Culture , Generation of stable cell lines, Transient Transfection and experience in Flow Cytometry.


2) Protein Science: Expert knowledge and experience in Protein Biochemistry including construct design, Protein expression and purification from multiple systems.
Analytical techniques: Gel electrophoresis, Western Blot, FPLC, HPLC, Mass Spectroscopy


3)DMPK :  
A) Should Conduct in vitro ADME studies such as buffer solubility, metabolic stability, plasma protein binding,CYP450 inhibition etc. Prepare samples for LC-MS/MS analysis, data upload in specific templates

B) Hands-on experience in rodent PK, pre-formulation work, dosing via different routes & plasma preparation for bioanalysis.Expertise in rodent surgery such as cannulation (dual cannulation for PK) is required.


4) BIACore: Well versed technically with BIA Core, pharmacokinetic assays.



Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Bio-Technical Research Associate/Scientist
Role: Bio-Technical Research Associate/Scientist
Keyskills:

Cell BiologyProtein ScienceInvitro ADMEInvivo PK studiesMass specBIACORE

Desired Profile

Syngene International, Bangalore conduct Walk-In drive for Discovery Biology @ Biocon Park,Bangalore

Date : 30-July-16
Time: 08.30 AM to 04.00 PM
Venue: Syngene International Ltd
             Biocon Park
             Bommasandra Phase-IV
             Jigani Link Road
             Bangalore
       
Qualification- M.Sc/ M.Tech  (Biotechnology/Biochemistry)with 2-6 years relevant experience

For DMPK - M.Pharm Pharmacology with 2-5 years relevant experience

Freshers not allowed

Education:UG -B.Sc - Any Specialization, B.Tech/B.E. - Bio-Chemistry/Bio-Technology
PG - M.Sc - Bio-Chemistry, M.Tech - Bio-Chemistry/Bio-Technology, M.Pharma - Pharmacy
Doctorate - Doctorate Not Required

Company Profile

Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with  Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.

To advance its programs and expand its capabilities, Syngene is looking to recruit outstanding scientific talents.

So come and join us in our journey of scientific innovation.

For further details, please visit www.syngeneintl.com.

Apply now

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Medical Coding freshers required "A"

 Medical Coding - Freshers in Nursing and Pharmacy

Nestem Technologies

0 - 0 yrs

Chennai

Job Description

Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD10-CM, CPT & HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders.

Self Supportive Training ll be provided for Fresher

Company Profile:

Nestem Technologies

Nestem Technologies is an ISO 9001:2008 Certified Leading Healthcare BPO Service Provider. Nestem Technologies is offering different services like Direct Placement, Training and Assured Placement in Medical Coding field with major US MNC BPO's.  

Apply here

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Syngene hiring "A"

Associate Scientist, PCO Toxicology

0 - 5 YearsBengaluru/Bangalore Openings: 1

Job Description

Principal Accountabilities/ Responsibilities (Describe in bullet points, the duties and tasks of this position)

-The candidate must possess a strong background and experience in the theory and practice of discovery pathology -Ability to conduct necropsies and recognize, describe and interpret findings at necropsy -Strong background in animal models of diseases and experience in evaluating tissues from discovery biology studies including immunotechniques -Ability to evaluate tissue sections from discovery toxicity studies, including the interpretation of microscopical findings is preferable -Excellent verbal and written communication skills -Excellent interpersonal and teamwork skills


Qualification & Experience:

MVSc/PhD in Veterinary Pathology (0-5 years)

Skills :
The candidate should be having the expertise in multiple areas within the industrial pathology and drug discovery biology domains. Pathology- Should have basic understanding of principles involved in characterizing the pathology of efficacy models. Ability to read and understand the published literature of the respective animal models and applying the concepts to characterize them in house. Should have experience as a study pathologist in preclinical efficacy studies, data analysis, interpretation, preparation of reports and communication of findings with perspective to the cross functional teams. Should have a thorough knowledge in comparative anatomy, histology and histopathology. Should have directed a pathology lab with good understanding of the procedures such as necropsy and descriptive gross pathology. Good collaboration with various cross functional stakeholders, excellent communication skills and core behaviors should be must.


Key behaviors to be demonstrated for success in the role :

Innovation, team work and quick learner


Interfaces and Dependencies (Describe briefly the functions and people with whom the job-holder in this position will need to interact and coordinate with)
 Company Profile

Incorporated in the year 1994, Syngene International is one of India's premier contract research and manufacturing organizations in providing customized service. Our services encompasses all across discovery chain: early stage discovery, process development, cGMP manufacturing and formulation development both in the small molecule and novel biologics area. Based in Bangalore, Karnataka, the Company is situated in a 90 acre Special Economic Zone with over 100000 sq. mt of built up facilities. The state-of-the-art research facilities have been qualified by various pharmaceutical majors & regulatory agencies and has received various certifications including ISO 9001: 2008, ISO 14001:2004, OHSAS 18001:2007, GLP and AAALAC.

Over the past 16 years, Syngene has successfully partnered with leading pharmaceutical companies, large biotech companies, crop protection companies and cosmetics companies. Syngene together with  Bristol-Myers Squibb has set up a dedicated research facility in Bangalore to help advance Bristol-Myers Squibb's work in discovery and early drug development.

To advance its programs and expand its capabilities, Syngene is looking to recruit outstanding scientific talents.

So come and join us in our journey of scientific innovation.

For further details, please visit www.syngeneintl.com.

Apply here

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Assistant professor for Microbiology required "A"

 Assistant Professor (UG) - Microbiology

University of Mysore

Job Description

Qualifications:

i. Good academic record as defined by the concerned university with at least 55% marks (or an equivalent grade in a point scale wherever grading system is followed) at the Master’s Degree level in a relevant subject from an Indian University, or an equivalent degree from an accredited foreign university.

ii. Besides fulfilling the above qualifications, the candidate must have cleared the National Eligibility Test (NET) for Lecturer/Assistant Professor conducted by the UGC, CSIR or similar test accredited by the UGC like SLET/SET.

iii. Notwithstanding anything contained in sub-clauses (i) and (ii) to this Clause 4.4.1, candidates, who are, or have been awarded a Ph. D. Degree in accordance with the University Grants Commission (Minimum Standards and Procedure for Award of Ph.D. Degree) Regulations, 2009 or the subsequent Regulations if notified by the UGC, shall be exempted from the requirement of the minimum eligibility condition of NET/SLET/SET for recruitment and appointment of Assistant Professor or equivalent positions in Universities /Colleges / Institutions.

Further, the award of degrees to candidates registered for the M.Phil/Ph.D programme prior to July 11, 2009, shall be governed by the provisions of the then existing Ordinances/ By laws/ Regulations of the Institution awarding the degrees and the Ph.D candidates shall be exempted from the requirement of the minimum eligibility condition of “NET/SLET/SET for recruitment and appointment of Assistant Professor or equivalent positions in Universities / Colleges / Institutions subject to the fulfillment of the following conditions: -

(a) Ph.D. degree of the candidate awarded in regular mode only;

(b) Evaluation of the Ph.D. thesis by at least two external examiners;

(c) Candidate had published two research papers out of which at least one in a refereed journal from out of his/her Ph.D. work;

(d) The candidate had presented two papers in seminars/conferences from out of his/her Ph.D. work;

(e) Open Ph.D. viva-voce of the candidate had been conducted.

(a) to (e) as above are to be certified by the Vice- Chancellor/ Pro-Vice-Chancellor/ Dean (Academic Affairs)/Dean (University Instructions)”

iv. iv. NET/SLET/SET shall also not be required for such Masters Programmes in disciplines for which NET/SLET/SET is not conducted.


Send your application to The Registrar, University of Mysore, Viswavidyanilaya Karya Soudha Crawford Hall, Mysore - 570005


The last date for receiving the duly filled in application forms in the office of the Registrar, University of Mysore, Mysore is 30-07-2016 (upto 5.00 P.M.)


For more information visit: http://uni-mysore.ac.in/sites/default/files/content/04_last_date_extension_for_submission_of_application.pdf, http://www.uni-mysore.ac.in/sites/default/files/content/1_teaching_post_backlog_and_current_vacacny_notification_-_2016.pdf

Company Profile:

University of Mysore

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Dupont Jobs "A"

Biotech and Regulatory Affairs Manager

Job Description

REPORTS TO: Country Manager

BRIEF JOB DESCRIPTION:

• The position is responsible for planning, initiating, and managing registration and regulatory affairs activities for timely approval of biotech (GMO) crop products in India.
• This includes understanding the regulatory processes and requirements at the national level, developing regulatory strategies for specific biotech crop products, preparing and managing high quality regulatory submissions for trialing and commercial approvals, and responding to complex technical questions from government reviewers against tight schedules.
• This position would also be responsible for conventional (non-Biotech products) registration and Freedom-to-Operate (FTO) activities such as PPV FR&A, NBA, and related policy matters.
• The position will establish and maintain professional contacts with regulatory authorities in India, lead discussions with regulatory bodies such as RCGM, GEAC and other relevant regulatory groups that may come into picture time-to-time, build academic and industry contacts, stay up-to-date with latest developments in science and agricultural biotechnologies, and promote pragmatic science-based legislation.
• The position will also lead technical discussions internally with the Regulatory Sciences and Operations groups to conduct biosafety studies to meet current and anticipated requirements, and ensuring all technical issues related to biotech product approvals are fully addressed.
• Conventional registration would need continued engagement with internal stakeholders, mainly Research, Agronomy and Business, and also with external stakeholders such as PPVFRA and NBA.

JOB QUALIFICATIONS:

• MSc or PhD preferably in biological or agricultural sciences with 8- 10 years research and regulatory experience, or equivalent

 Company Profile

DuPont Pioneer is the world leader in the plant biotechnology area including the discovery, development and delivery of elite crop genetics.

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Jobs in Novartis "A"

 Manager Supply Chain Mgmt

Novartis Healthcare Pvt. Ltd.

4 - 7 yrs

Hyderabad / Secunderabad

Job Description

1. Being the Drug Supply Management representative in Technical Research and Development sub team, drives Drug Substance/ Drug Product supply process, ensures key project milestones are met. 2. Creates and updates Drug Substance/ Drug Product supply plan on global project level, reviews supply plan in Technical R&D sub-team and ensures agreements with stakeholders on Drug Substance/ Drug Product delivery quantity/ timeline. 3. Maintains overall supply plans, optimizing overage/ drug usage, minimizing waste, allowing the flexibility to accommodate changing demand.4. Has key role at demand planning meetings, responsible for coordination of delivery of drug substance, drug product and packaged goods according to plan. 5. Looks for available options for comparators based on Clinical demand, triggers technical feasibility testing and procures selected comparator 6. Plans budget for associated external costs for comparators and commercial drug products and is-sues related grants and purchase orders. 7. Coordinates and maintains the Drug Supply Management project budget in SUCCEED (planned and actual costs). 8. Aligns with Trial Manager on clinical supply to ensure that supply meets the changing demand on project level. 9. Supports internal/ external inspections and audits. 10. Actively contributes to SOP creation, revision and update

Company Profile:

Novartis Healthcare Pvt. Ltd.

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding employers in our field.  

Apply now

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Walkins at Biocon "A"

Walkins for Production - API Manufacturing - Hyd

0 - 5 YearsHyderabad / Secunderabad

Job Description

WALK-INS - BIOCON : The difference lies in our DNA!!!

We are hiring the Fresher and Experienced Candidates for our API Plant-Hyderabad. 

Role Description:

  A. Duties & Responsibilities 

1. Monitoring and control of production operations 

2. Following SOP's, EOP's, SCP's and OCP's 

3. Should be responsible for compliance wrt cGMP & EHS 

4. Should be responsible for Shift Activities 

5. Maintain & control process parameter as per BPR & perform activity safely. 

6. Allocation of work to workmen as per days plan 

7. Looking after daily Production activities and shift work execution in Effective Manner 

8. To enhancement in production by studying time cycle of the batch. 

9. Maintaining and updating the batch production records. 

10. To implement and maintain cGMP guidelines during production activity. 

11. Trouble shooting process and quality issues. 

12. Production planning and optimization in the production. 

13. Continuous improvement so as to reduce production cost, get better yield and Quality Product. 

14. Handling manpower effectively and efficiently. 

15. Reporting production and plant details to the Manager. 

16. To take care of inter departmental Co-ordination to get done work in plant. 

17. To provide on the job training and guidance to the operators if required. 

18. Must have API Pharma Production Experience. 

 B. Key Skills / Competencies 

19. Experience in Product handling, Packing & Labelling 

20. Maintenance of Production Equipment in cooperation with E & M Dept. 

21. Should be a team player. 

Qualification : 

B.Sc/M.Sc (Chemistry /Biochem) / Diploma in Chemical / Petrochemical Eng. 

Experience :  0-10yrs. in API Production/Bulk Drugs. 

Note: All the above mentioned positions would require working in shifts. 

 If the opportunity excites you,

Please walk in on : 

Date: 28th July & 4th Aug 2016, Time 8:30AM 03:00PM 

Venue : 

Biocon Limited

Plot Number 213-215,Phase II 

IDA,Pashamylaram, 

Near Patancheru, Via Insapur, 

Medak Dist-502307 

Ph: 08455224310/11/12. 

 Hyderabad 

 Visit our website: www.biocon.com 

Carry a copy of updated resume and your recent salary slip for walk in. 

Only Male Candidates Candidates unable to attend the walk-in may mail their resumes.

Company Profile

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approxmimately Rs 2500 crore turnover and is expected to grow further during the current financial year .

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Parexel jobs for Medical Writers "A"

Medical Writer II

3 - 6 Years

Bengaluru/Bangalore

Job Description

Summary:
Under departmental supervision, the Medical Writer II will research, create, edit, and coordinate the production of clinical documents associated with submissions to regulatory authorities including but not limited to: study protocols, model informed consents, interim and final clinical study reports and safety updates. The Medical Writer II will also be responsible for the production of clinical study documentation associated with clinical trials that may not be included in a regulatory submission. The Medical Writer II may serve as primary technical contact with client under appropriate departmental supervision.

Write clinical documents associated with submissions to regulatory authorities including but not limited to: study protocols, model informed consents, interim and final clinical study reports and safety updates.
Serve as the primary client contact, negotiating deliverable timelines, and resolving project related issues, under departmental supervision.
Provide medical editing review of draft and final documents prepared by other writers before internal or external distribution. This includes both copyediting and content review.
Ensure document content and style adheres to FDA/ EMA or other appropriate regulatory guidelines, and complies with departmental and corporate or client SOPs and style guidelines

Salary: Not Disclosed by Recruiter
Industry: Pharma / Biotech / Clinical Research
Functional Area: Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category: Documentation/Medical Writing
Role: Documentation/Medical Writing
Keyskills:

medical writingclinical trialsdocumentationfdadocumentsregulatory authoritiesmedical writerclinical studybeedit

Desired Profile

Medical writing experience: experience in writing multiple clinical study reports or other regulatory documents
Education:UG -Any Graduate - Any Specialization
PG - Any Postgraduate - Any Specialization
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required

Company Profile

PAREXEL International Corporation is a leading global bio/ pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Perceptive Informatics, Inc., a subsidiary of PAREXEL, provides advanced technology solutions, including medical imaging, to facilitate the clinical development process. Headquartered near Boston, Massachusetts, PAREXEL operates in approximately 70 locations throughout over 50 countries around the world, and has more than 13,000 employees. At PAREXEL, we have a passion for making a profound difference. As an expertise-based business, the caliber of our people and their dedication directly impacts our success, the success of our clients, and the ability to make a difference in the lives of patients worldwide. You'll be surrounded by supportive leadership and a brilliant team who share a common goal - to improve the lives of millions of patients.

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Vee technologies is hiring Medical Coders "A"

 Immediate Opening for Medical Coding Manager @ Vee Technologies, Salem

Vee Technologies

Salem

Job Description

Immediate Opening for Medical Coding  Manager/ Assistant Manager @ Vee Technologies 

Job Description:

Experience in Multi-Specialty & Specific to E&M, HCC, OP, IP & Radiology Coding


Job Location: Salem

• Responsible for the entire division or the projects assigned
• Completely accountable for the Service Levels Agreed
• Accountable for Team performance and Quality
• Mentor and Coach the team to achieve better efficiency at all times
• Responsible for all process documentation and project planning
• Conduct and recommend training to improve team performance
• Manage Customer Engagement and Client Interaction when needed
• Coordination with Internal and client teams as per requirement
• Work towards continual improvement of processes and knowledge enhancement at all times
• Ensure the TAT and Quality of projects handled

Interested can send their updated resume to saravanan.rl@veetechnologies.com and can reach us @ 9901326413


Regards,
Saravanan.R - HR

Company Profile:

Vee Technologies

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  

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QC Officer job

QC Officer job


Job Description
Sampling of Raw materials, Packing materials, in process samples and Finished Goods Samples
Preparation and Standarization of  Volumetric solution and other laboratory reagents
Analysis of Raw materials , Packing materials , In-process samples , Finished goods samples, Validation and stability Samples
Qualification and calibaration of QC Instruments/ Glasswares
SOP Management  (Preparation Review / Implementation
Documentation of all activities as per cGMP Process.

Click here to apply

Apply Now

Walk-in Drive- Water plant operations & Utility Maintenance on 30th July

Walk-in Drive- Water plant operations & Utility Maintenance on 30th July


Job Description
  Operation of water plant:
Experience in handling purified water system
Experience in handling Reverse osmosis unit
Experience in handling Electrode ionization (EDI) unit
Experience in water for injection (WFI) generation plant
Experience in pure steam generation (PSG) plant
Understanding the GMP requirements for water system
Facility management:
Maintenance and supervision of Clean room facility
Operation of Autoclave
Operation of Dry heat sterilizer (DHS)
Experience in handling fumigation and preparation of disinfection solution
Experience in handling kill tank unit and bio disposable waste
Understanding the GMP concepts of the cleanroom facility
Experience in handling GMP documents and Archival
Experience in handling GMP Audit would be added advantage

Click here to apply directly

Apply Now

Ultimate source for Medical Coding "A"

"Get employed during training period"



Code MeDica is a proliferating healthcare training institute located in Bangalore. We are a Institute focused entirely on Medical Coding and Medical Billing.  Our in-depth healthcare training expertise enables us to provide end-to-end solutions to successfully resolve our students’s coding and  billing challenges.

We give a wonderful opportunity to Life Sciences students to develop a outstanding career in Healthcare industries. Healthcare industry is an emerging one in present scenario and is something which will keep on emerging in coming years.


It is the Mission of our institute  to strengthen and promote excellence in medical coding, billing, and also for CPC certification.

Code medica is committed to prepare a highly skilled health workforce made up of health care professionals, health management and support workers.
It will strive to produce health care professionals who will integrate the advances in research healthcare industries with their best accuracy.
It will promote health services, which incorporate the latest advances in scientific knowledge in a manner that supports education for the benefit of the industry..

The institute aspires to attract the best of students by offering a variety of excellent programs supported by quality administration and student support services.
The institute aspires to be known for excellence and impact of its research on the educational milieu of the country  and the outcomes of healthcare.
 The University aspires to be an integral part of the community through transfer of knowledge, continuous dialogue with the country’s health care planners and enhanced community service.

“Join Us Today…Make this your Best decision ever”

Contact Us Now

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Openings in Quintiles "A"

 Openings for Medical Data Reviewer@quintiles (2-5 Years Exp)-only MBBS

Quintiles

2 - 5 yrs

Bengaluru/Bangalore

Job Description

Multiple Job Openings for Medical Data Reviewers having Mbbs degree


PURPOSE
Review structured clinical patient data output without direct access to medical charts to ensure medical plausibility and determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level of review.
RESPONSIBILITIES
Serve as a Subject level Data reviewer (SLDR) and identify any anomalies in patient reported data by performing Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy
Review all inclusion and exclusion criteria to ensure each patient meets minimum level of acceptance into the clinical trial
Review investigation product dosing records to determine adherence to protocol and identify possible inaccurate / missed dosages
Review all reported Adverse Events (AEs) , Concomitant Medication and medical history information to ensure all supporting information is expected and/or implausible data is verified and adherence to protocol expectations and its impact on other patient reported/observed information (e.g., laboratory results, AEs, etc.)
Ensure end-of-treatment (EOT) and end-of-study (EOS) information is correctly documented to determine primary reason for the patient ending treatment or ending participation in the clinical trial
Review all laboratory results to ensure completeness of information and adherence to protocol schedule of events and determine if reported laboratory values represent a potential safety condition not reported in the AE information for the patient
Review any other information as necessary to determine overall readiness of the patient information for next level review
Interaction with other Medical review staff to verify information and/or triage new data issues or prior identified action items
Serve as POC/ Back-up POC
Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
May act as a Clinical Data Scientist for performing data analytics by reviewing the visualizations and identify potential issues of concern
All responsibilities are essential job functions unless noted as nonessential (N).
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Understanding of clinical/medical data.
Background in Medical Terminology, Pharmacology, Anatomy, and Physiology
Excellent motivational, influencing and coaching skills
Ability to work on multiple projects and manage competing priorities
Strong customer focus skills
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Ability to establish and maintain effective working relationships with coworkers, managers and clients

PHYSICAL REQUIREMENTS
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time

Company Profile:

Quintiles

Quintiles
Quintiles is the world's largest provider of biopharmaceutical development and commercial outsourcing services. We bring a fully integrated approach to build biopharma and life sciences solutions - from pipeline through portfolio to population health . A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Apply now

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Work as a Food Technologists "A"

Get Placed As A Food Technologist At A Top MNC in Maharashtra | ETA invites Applications

Food Technologist - R&D, New Product Development - MNC in Maharashtra

4 - 9 YearsMumbai Openings: 1

Job Description

New product development, Managing R&D product pipeline/Portfolio planning for new recipes

• Recipe formulation development by within defined constraints of shelfstability & other technical aspects
• Analyze the impact of packaging material on the food & alter recipe formulation accordingly
• Conducting lab & pilot trials
• Benchmarking products with competition and research & analyze for claims/claim validation

Product/Recipe validation process

• Assess sterilization & shelfstability of food by conducting thermal process validation studies
• Developing SOPs for recipe validation
• Define process for & manage Chemical & Microbiological Analysis of Food

Quality & Compliance processes

• Lead FSSAI regulatory application filing, documentation & follow up process
• Ensure compliance of GMP & HACCP requirements
• Develop Quality standards for products & processes
• QA audits compliance by external agencies including regulatory bodies

Production & Operations

• Maintaining quality records
• Identify, characterize and control food allergens
• Investigate nonconforming material and products for causes and ensure corrective action
• Assist in supplier validation & development by raw material screening

 Company Profile

Food Technologist- New product dev R&D - MNC in Maharashtra

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Opportunity to work @NIT,Karnataka "A"

Opportunity to work in KIST, Korea funded project @ NIT, Karnataka

To facilitate transformation of students into good human beings, responsible citizens and competent professionals, focusing.

Apply now 

Apply Now

Join Biocon "A"

Join Biocon As A  Executive/Senior Executive QC

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing

.

Apply now

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Zydus Cadila Jobs "A"

Assistant Mgr / Dy. Mgr- Medical Writing- Pharmacovigilance

4 - 7 YearsAhmedabad Openings: 1

Job Description

1. Act as a Subject matter expert (SME) and Mentor for Aggregate Report Team
2. Lead/co-lead cross functional expert teams to fulfill Periodic Safety Report accountability (Clinical, Marketing).
3. Prepare and maintain aggregate reports schedule.
4. Preparation, review and submission of Periodic Safety Update Reports (PSURs)/Periodic Adverse Drug Experience Reports (PADERs)/Risk Management Plan (RMP)/other periodic report.
5. Responding regulatory assessment reports on RMPs and PSURs.
6. Performing signal management activities.
7. Ensure compliance (quality, procedures, regulations, timeliness, consistency) of aggregate reports
8. Assist in preparation/revision of SOP, Work instructions, templates and guidance training documents.
9. Support Health Authorities inspections and audits, and development of Corrective & Preventative Actions (CAPA) to address safety findings.
10. Handling queries of local affiliates/regulatory agency.
 Company Profile

Zydus Cadila is an innovative global pharmaceutical company that discovers, develops, manufactures and markets a broad range of healthcare products. The groups operations range from API to formulations, animal health products and cosmeceuticals. Headquartered in the city of Ahmedabad in India, the group has global operations in four continents spread across USA, Europe, Brazil, South Africa and other emerging markets.

In its mission to create healthier communities globally, Zydus Cadila delivers wide ranging healthcare solutions and value to its customers. With a strong dedicated employees worldwide, a world-class research and development center dedicated to discovery research and eight state-of-the-art manufacturing plants, the group is dedicated to improving peoples lives.

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Access Healthcare hiring "A"

 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  

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Cactus hiring Freshers "A"

Quality Control Specialist, Publications

Cactus Communications

0 - 4 yrs

Mumbai , Mumbai Suburbs

Job Description

CACTUS is currently looking to add a dynamic, detail-oriented, and self-motivated QC specialist to our world-class medical communications delivery team in Mumbai. The medical communications team at CACTUS partners with some of the largest global pharmaceutical companies across a wide range of communications needs including writing, graphics, animation, and publication strategy. As a QC specialist, you will:


• Evaluate manuscripts, posters, slide decks, educational material, medical literature, etc, provided by clients for data accuracy
• Check documents (mentioned above) developed by medical writers for scientific data errors by checking the developed material against annotated references, CSRs, other source data 
• Check for discrepancy within text, discrepancy between figures/tables, and between text and supplementary material, and make suggestions for improvements
• Identify missing sources documents and gaps in scientific logic 
• Check for grammar, syntax, style, and compliance with style guides, regulatory guidelines, and publishing requirements
• Be responsible for the quality of the documents/projects fact checked/QCed
• Ensure effective communication of QC/fact check findings with the client/medical writers 
• Deliver QC reports to the stakeholders, and identify quality trends
• Ensure 100% timely delivery of documents
Job Location: Andheri/Vashi/Tele-commute

Company Profile:

Cactus Communications

Cactus Communications is a leading provider of scientific communication services to more than 60,000 clients across 116 countries. In line with its mission-to enable growth through effective communication-CACTUS offers specialist academic editing, medical communications, publication support, transcription, translation, and training services to individuals and corporations across sectors such as academia, publishing, and pharmaceuticals.

Combining the rich experience of a multi-national, multi-functional team; the peerless capabilities of over 1400 language and business professionals; and ingenious technological innovation, CACTUS helps researchers, journals, universities, and corporations achieve their publication goals. The CACTUS culture is an eclectic yet inclusive one, where people from different countries and professional backgrounds come together to form a global team that pursues excellence, prizes integrity, and works as a unified client-focused organization.

Offices
United States | Japan | Brazil | India | South Korea | Taiwan | China

Awards and Recognition

*2014: Ranked 1st in the Professional Services category and as India's 10th best workplace overall in the Great Place to Work Institute survey (Ranked among top 20 from 2011- 2013)

*2010: Red Herring Global 100 Award, for innovation in business

*2008: Featured among the Top 15 Exciting Emerging Companies 2008, in a NASSCOM survey  

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Novartis hiring "A"

Medical Safety Writer

Novartis Healthcare Pvt. Ltd.

5 - 7 yrs

Hyderabad / Secunderabad

Job Description

Lead global cross-functional teams responsible for writing periodic safety reports within agreed timeframes and to a high standard of accuracy, in compliance with DS&E business rules, standard operating procedures and global regulatory requirements. Responsible for supporting the Global Medical Safety Physicians in the monitoring of the safety profile of newly launched Novartis products. 1. Lead cross functional expert teams to fulfill Periodic Safety Report accountabilities (DRA, Cli n- ical, Marketing). 2. Author along with Global Medical Safety Physicians, regulatory periodic safety reports (Period- ic Safety Update Reports, US Periodic Reports) for newly launched Novartis products: collect- ing, organizing, analyzing, presenting the data and drafting safety medical evaluations by means of DS&E templates and procedures. 3. Collaborate with the Medical Safety Physicians and other line functions to monitor the safety profile of newly launched products emerging from aggregate reporting or large data set anal- yses. 4. Review emerging regulatory guidelines and legislations and identification of impact to DS&E processes. 5. Drive and Lead DS&E projects to develop new PSUR processes in alignment with international regulations. 6. Lead the development and maintenance of safety documents templates and Standard Operat- ing Procedures pertaining safety aggregate reports. 7. Lead sessions during Health Authorities inspections and audits as Subject Matter Expert, and lead the development and implementation of Corrective and Preventative Actions (CAPA) to address safety findings. 8. Review global marketing programs and establish process for AEs collection with global mar- keting teams. 9. Review Risk Management Plans in close coordination with Pharmacovigilance Compliance and Global Medical Safety groups and assess the operational feasibility and implications of phar- macovigilance commitments. 10. Contribute to Safety Profiling Teams to newly launched products to ensure that case reports are accurately evaluated and databased, and have reliable and exploitable data sets when preparing aggregate reports. 11. Proactively collaborate with licensing partners and Clinical Research Organizations to meet joint accountabilities. 12. Act as Subject Matter Expert in cross-functional projects and external meetings. 13. Train and mentor new DS&E associates and associates from other line functions on medical safety writing & periodic reporting matters. 14. Deputize for Team Leader/ Group Head and assist with the recruitment of new staff.

Key Performance Indicator(s) (HR Core IT9102 ST9003) 

Company Profile:

Novartis Healthcare Pvt. Ltd.

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes us one of the most rewarding employers in our field.  

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Parexel hiring Medical Writers "A"

Medical Writing Support Coordinator

2 - 4 YearsBengaluru/Bangalore

Job Description

The Medical Writing Support Coordinator (MWSC) will provide support on Medical Writing Services (MWS) projects as appropriate, including administrative and filing support. . The MWSC must be conscientious, able to work with minimal supervision and accept work direction from Lead Medical Writers and MWS management, have an aptitude for working with a variety of different software packages, exhibit a high degree of flexibility and initiative, demonstrate the ability to follow up on multiple tasks and projects, and possess the ability to handle matters of a confidential nature. - Organize and track delivery of all project documents as required
- Assist Medical Writers in all billable project-related tasks, as required. This includes assisting with client communication, set up and maintenance of project files and archiving.
- Provide administrative support, including coordination of meetings, recording and distribution of meeting minutes, photocopying, faxing, and maintenance of project trackers, as required.Company Profile

PAREXEL International (India) Pvt. Ltd.

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Medical Coding Specialist required "A"

Medical Coding Specialist I

Chiltern Clinical Research India Private Limited

1 - 4 yrs

Bengaluru/Bangalore

Job Description

1. Perform coding using web-enabled dictionary and coding management system (eg. OC TMS or dsNavigator) or other system as required.
2. Perform Coding in accordance with study specific coding conventions as outlined in the Data Management Plan (DMP) for assigned projects.
3. Perform coding using MedDRA and WHO Drug or other Sponsor specified dictionaries.

Company Profile:

Chiltern Clinical Research India Private Limited

Chiltern is a leading CRO that listens to client needs in order to customize solutions for the Biopharma industry. With a 32 year history, Chiltern delivers globally with therapeutic expertise in oncology, respiratory, anti-infectives / vaccines, ophthalmology and dermatology. Chiltern operates two specialty units: Chiltern Oncology is led by physicians, scientists and clinicians to uniquely manage all phases of hematologic and oncologic clinical drug development; and Chiltern Source is a world leader in tailored relationships for FSP, resourcing and staffing solutions. Chiltern’s 2,200 engaged professionals work across 45 countries to deliver flexible, responsive solutions that are “Designed Around You”.  

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Dell hiring Medical Coders "A"

Medical Coder - Surgery or Denial Coding for Chennai Location

Dell International Services India Private Limited

1 - 5 yrs

Chennai

Job Description

Designation         :        Medical Coder Associate
Experience          :        1 years to 5 years
Location              :         Chennai
Functional Area  :         Medical Coding
Notice Period      :         Any
Specialty             :         Surgery Or Denial Coding


Job Requirement : 

- 1.5+ years of coding experience along with strong knowledge in anatomy and physiology
- Thorough knowledge in the specialty - ED coding with live coding experience in both professional and facility billing
- Active CPC certification is mandatory
- Willing to learn concepts quickly and develop in the area of specialization
- Should possess skill sets to code and audit reports
- ICD-10 knowledge and should have cleared proficiency assessment
Interested Candidates Kindly contact 09884355140 or walkin to the below mentioned venue with your updated resume.

Dell International Services,
Ambit IT Park
3rd Floor, 32 A& B, Industrial Estate
Ambattur,
Chennai - 600058
Contact: Karthikeyan Karunakaran
Please send your resume to k_karunakaran@dell.com


Note:
NTT DATA plans to acquire Dell Services as announced on 28th March 2016.
If you are selected for a Dell Services position and the transaction closes, your future employment will be with NTT DATA. Dell recruiters can provide you with additional information about any applicable changes upon request.\Company Profile:

Dell International Services India Private Limited

Dell is a Technology driven company with a unique Dell Direct model. Dell Information Technology department (Dell I/T) plays a key role in enabling the Dell Direct model by creating, deploying and supporting global industry-leading I/T assets and services that reliably deliver the best customer experience and competitive edge.  

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Walkin at Cadila "A"

 Walk-in for Quality Control on 22nd July 2016 at API Ankleshwar

Cadila Healthcare Limited - Akleshwar

3 - 8 yrs

Ankleshwar

Job Description

Walk-in for Quality Control on 22nd July 2016 at Cadila Healthcare Ltd, API Ankleshwar Multi Product Plant


Here is a chance to join Zydus at our API Manufacturing located at Ankleshwar as.


Candidates having experience of 3 to 8 years in Quality Control API pharma can Walk-In for Interview along with their CVs and relevant documents at

Date : 22nd July 2016 (Friday)

Time: 09:30 AM to 04:00 PM

Venue : Plot No 291, Cadila Healthcare Ltd,
Industrial Estate , GIDC
Dist :Bharuch,
Ankleshwar,
Gujarat
 
Contact No of HR representative: 02646-660408 / 660507
Key Responsibilities are mentioned as below:


QUALITY CONTROL : Sr.Executive / Executive : M.Sc /B.Sc (Chemistry / Microbiology) with 3 - 8 years of hands on experience and relevant exposure in handling instruments like HPLC, GC, UV , wet lab, micro lab and chemical analysis of Raw Material . Must be familiar with cGMP requirements. Shop floor Operation in API / Bulk Drug Manufacturing.



Candidates having experience of working in regulatory approved plants and possesses sound knowledge of documentation, cGMP and SAP will be preferred.

Those who are unable to attend the Personal Interview may send their resume through e-mail at reema.patel@zydusmail.com

Please mention the position applying for on the top of envelope or subject in case of e-mail.

Preference will be given to candidates having API - Pharmaceutical Industries experience.

Company Profile:

Cadila Healthcare Limited - Akleshwar

Zydus Cadila is a fully integrated, global healthcare provider, with strengths all along the pharmaceutical value chain. With a core competence in the field of healthcare, Zydus Cadila provides  total healthcare solutions ranging from formulations, active pharmaceutical ingredients and animal healthcare products to wellness products. From a turnover of Rs. 250 crores in 1995, the group posted  revenues of over Rs. 8600 crores in FY15. The group had posted a turnover of Rs. 4600 crores in FY 11, making it a billion dollar company. Recently, the group launched Exemptia, the world's first biosimilar for Adalimumab, the largest selling therapy worldwide for inflammatory arthritis.

Zydus is also the only Indian pharma company to launch its own patented NCE - Lipaglyn, the world's first drug to be approved for the treatment of diabetic dyslipidemia. The Zydus group was one amongst the top five companies worldwide at the FT ArcelorMittal Boldness in Business Awards 2014 in the Developing Markets category and was declared as the 'Emerging Company of the Year' by the Economic Times Awards for Corporate Excellence 2010. The group aims to be a leading global healthcare provider with a robust product pipeline and aspires to post revenues of Rs. 10000 crore by 2015-16 and be a research-based pharmaceutical company by 2020.  

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Biocon jobs "A"

Executive- Utility Maintenance

2 - 5 Years

Bengaluru/Bangalore Openings: 1

Job Description

Execution of all maintenance jobs as per the laid safety standards of the group.
To carry out Predictive , Breakdown, predictive and corrective maintenance activities & preventive maintenance as per schedule.
Interdepartmental Coordination
Variance Analysis
Maintaining Stationary & Rotating Equipment's in shift basis,
Sewage Treatment plant, Effluent treatment plant, Utility equipment's (D.G sets, Chillers, Compressors, Boilers and its accessories),Pumps (Centrifugal), Compressors, Valves, Cooling TowersCompany Profile

Biocon is an integrated biotechnology enterprise focused on the development of biopharmaceuticals. With successful initiatives in drug discovery and development, bioprocessing, manufacturing and global marketing, Biocon delivers products and solutions to partners and customers in over 75 countries. Biocon has the defining science, world class capabilities and a focused vision to deliver the promise of innovative and affordable medicine to a waiting world. Today, Biocon together with group companies employs more than 5000 employees with approxmimately Rs 2500 crore turnover and is expected to grow further during the current financial year .

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