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Tuesday, 2 August 2016

Wipro - Hiring for Pharmacovigilance Officer

Wipro BPS (A division of Wipro Limited)
0 - 5 yrs
Delhi
Walkin Interview
3rd August - 4th August 11 PM

Job Description

    Dear Candidate,

    Wipro BPS is Hiring for Pharmacovigilance Business.

    - CANDIDATE SHOULD BE COMFORTABLE FOR VOICE PROCESS

    - CANDIDATE SHOULD BE OKAY FOR NIGHT SHIFTS & REGISTERED PHARMACIST.

    Please find the JD below, if interested please walk-in to the below address with the required documents.

    Interview Address:

    Wipro,A- 23, Mathura Road, Sarita Vihar, Near Sarita Vihar Metro Station, New Delhi - 44 

    Walk-in Date: 3rd & 4th August , 2016

    Walk-in Time: 11am - 4pm

    Contact Person: Ritu Mishra

    Qualification: Education:

    * Bachelors / Masters in Pharmacy + Registered Pharmacist

    * Valid PAN CARD available

    * minimum 1 year experience required in case processing
    * Freshers can also apply.

    Skills:
    - Excellent English Communication both written and Spoken
    Performing preliminary step of Pharmcovigiliance that case intake
    - Doing research work on adverse events or product complaints, or with an inquiry about the human health product
    - Receiving calls from consumers and health care professionals with reports
    - Verbal Probing for necessary information including but not limited to the adverse event(s), the patient's medical history, - Suspect product, concomitant drugs involved if any, and medication history of patient
    - Answering to the inquiries, and respond to inquiries in a knowledgeable manner
    - Completing various safety reports regarding the contact through computer based database system
    - Receiving adverse drug reaction or adverse event information Medical coding of terms according to Med DRA. WHO medical dictionary Filling AEM (Adverse event management) forms and generating adverse event reports according to ICH-guidelines E2A, E2B, E2E Writing narratives for adverse events
    - Ability to work under pressure and deliver

    - Comfortable working in Voice Process
    - Comfortable with night shifts
    - Immediate Joining

    Documents Required -

    - Updated and Printed Resume
    - 2 Passport Sized Colored Photographs
    - Govt. Photo ID
    - Certificate of Registration

    MENTION RUPSHIKHA RAY ON THE TOP OF YOUR RESUME.Company Profile:
Wipro BPS (A division of Wipro Limited)

Wipro BPS
At Wipro BPS, you will get a in-depth understanding about the best way to service the customer requirements by leveraging Quality, Innovation, a self-sustaining Process Framework, IT expertise and Domain knowledge.
In addition to our intensive new-hire training program and our scheduled development-oriented programs, we provide Learn and Earn options to fast track your career by offering a variety of paid education programs (SEED) affiliated with various reputed universities - these programs include both graduate and post-graduate options.
While best-of-breed facilities and infrastructure is a given, we believe that our iconic brand, our industry leading position and the exciting career opportunities differentiate us from the rest of the industry.  

Pharmacovigilance Team Manager

Novartis Healthcare Pvt. Ltd.


Hyderabad / Secunderabad

Job Description
    1. Manage and lead processing team and ensure that all tasks are performed according to business rules, guidelines and standard operating procedures.
    2. Monitor workload and allocates resources appropriately. Ensure that incoming Adverse Events are processed by the team according to internal timeframes to meet Health Authorities requirements.
    3. Monitor the quality of work produced by the team and support quality improvement initiatives as appropriate. Provide feedback to team members on quality and train team members as appropriate to improve quality.
    4. Set up yearly objectives and review performances of team ensuring best use of available resources. Discuss and set up development plans with/for all team members to further develop individuals skills and potentials.
    5. Set up the training plans for new hires according to the individuals experience and job role and ensure that training is provided to team as appropriate. Support the training of other departments in clinical safety related procedures/regulatory obligations.
    6. QC periodic regulatory safety reports before submission to management approval and ensure compliance with required timelines and co-author, together with the Medical Safety Physicians, periodic regulatory safety reports, as appropriate.
    7. Interact with the Medical Safety Physicians on project activities in specific therapeutic areas, compatibly with the timely processing/production of individual case reports and regulatory periodic reports.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.  

Walk In on 6/8/2016 @ Hyderabad - 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 รข„¢. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world

 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  

Immediate Opening for Medical Coding Manager @ Vee Technologies, Salem

Vee Technologies

Job Description

    Immediate Opening for Medical Coding Assistant Manager/ 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 trainings 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

    If interested kindly fwd your updated profile to ramesh.m@veetechnologies.com


    Regards,

    Contact:
    Ramesh-HRD
    Mobile: 9443238706


    Venue :
    Vee Technologies Private Limited,
    4/14, Reddipatty road,
    Mamangam,
    Salem-636302Company 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  

Over a period of 30 years, Suguna Food Limited ( formerly Suguna Poultry ) has gone from strength to strength and has become a Rs. 5350+ crore company that makes it India's No. 1 broiler producer. Along the way, Suguna's pioneering efforts in contract farming helped create thousands of rural entrepreneurs who share the growth successfully. 'Poultry Integration' introduced and pioneered by Suguna in the country has energized the livelihoods of farmers in rural India. Suguna ranks among the top ten poultry companies worldwide. With operations in 11 states across India, it offers a range of poultry products and services. The fully integrated operations cover broiler and layer farming, hatcheries, feed mills, processing plants, vaccines and exports. Suguna markets live broiler chicken, value added eggs, ready-to-eat and ready-to-cook chicken products. With the intent to provide consumers with fresh, clean and hygienic packed chicken, Suguna has set up a chain of modern retail outlets in the name of 'Daily Fressh'.
DesignationMicrobiologist - 1 Opening(s)
Job Description* Standardizing the bacteriological culture procedure for local lab  conditions.

* Periodical monitoring and maintenance of lab hygiene.
Monitoring of water hygiene - Qualitative/Quantitative method.

* Measuring of physical qualities of water - PH & Hardness in newly started farms.

* Sampling and Monitoring of empty shed hygiene - Plate exposure test.

* Monitoring of hatchery hygiene - Drags, Swabs, Plate exposure test, microbial load in water, etc.

* Bacteriological culture in field organ samples and Antibiotic sensitivity test.

* HA and HI test in broiler serum samples
Desired Profile* M.Sc (Microbiology) Graduate with 1 Year to 5 Year Experiences
* Male Candidates only Preferred
Apply here

Microbiologist, Biotechnology, walk in 1 Aug 2016 to 13 Aug 2016

Eagle System
0 - 5 yrs
Pune

Job Description
    Candidate can work on all stages of a production, from research and development to design and manufacture, through to installation and final commissioning
    B.E/B.Tech, M.Tech, B.Sc ,Are any degree
Company Profile:
Eagle System

We are one of the fastest growing company in todays

competitive world.
walk in venue:-
Timing :-10 am to 4 pm
Eagle System
flat no 205, A-wing,
second floor,chaurang Building,
Opp Annsaheb Magare college,
Hadpasar, pune
HR
9689146883
View Contact Details

 Medical Writing Document Specialist

Quintiles
2 - 6 yrs
Mumbai

Job Description
    Opening for Medical Writing Document Specialist Grade 29 and Medical Writing Document Associate Grade 28
    Medical Writing
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 0E2201E0A2. A career with Quintiles connects you to great opportunity to achieve professional success and impact healthcare around the world.  

Openings For Medical Writing in Kolkata

Adventures International Pvt Ltd
1 - 3 yrs


Job Description
    Designation: Medical Writing
    Experience: 1-3 Yrs
    qualification: M.Pharm/BHMS/BAMS/MSc
    Location: Mumbai
    Skills:
    Draft Narratives
    Review and QC all deliverables

    Drop ur resume to: sravanthi@adso.com
    Contact Person: sravanthi
    Contact number: 720714000
Company Profile:
Adventures International Pvt Ltd

Advansoft International is a Recruitment & Search firm, well recognized in the market as amongst top manpower consulting firms. We have continuously provided resources to many Indian MNC's.We have committed relationships with our strategic partners  

What Are the Different Types of Clinical Research?

Different types of clinical research are used depending on what the researchers are studying. Below are descriptions of some different kinds of clinical research.
Treatment
Treatment research (also called “clinical trials”) generally involves an intervention such as medication, psychotherapy, new devices, or new approaches to surgery or radiation therapy.
Prevention
Prevention research looks for better ways to prevent disorders from developing or returning. Different kinds of prevention research may study medicines, vitamins, vaccines, minerals, or lifestyle changes.
Diagnostic
This refers to the practice of looking for better ways to identify a particular disorder or condition.
Screening
Screening research aims to find the best ways to detect certain disorders or health conditions.
Quality of life
Also known as “supportive care,” this research explores ways to improve comfort and the quality of life for individuals with a chronic illness.
Genetic studies
Genetic studies aim to improve the prediction of disorders by identifying and understanding how genes and illnesses may be related. Research in this area may explore ways in which a person’s genes make him or her more or less likely to develop a disorder. This may lead to development of tailor-made treatments based on a patient’s genetic make-up.
Epidemiological studies
Epidemiological studies seek to identify the patterns, causes, and control of disorders in groups of people.
An important note: some clinical research is “outpatient,” meaning that participants do not stay overnight at the hospital. Some is “inpatient,” meaning that participants will need to stay for at least one night in the hospital or research center. Be sure to ask the researchers what their study requires.
Phases of clinical trials: when clinical research is used to evaluate medications and devices
Clinical trials are a kind of clinical research designed to evaluate and test new interventions such as psychotherapy or medications. Clinical trials are often conducted in four phases. The trials at each phase have a different purpose and help scientists answer different questions.
Phase I trials
Researchers test an experimental drug or treatment in a small group of people for the first time. The researchers evaluate the treatment’s safety, determine a safe dosage range, and identify side effects.
Phase II trials
The experimental drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase III trials
The experimental study drug or treatment is given to large groups of people. Researchers confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the experimental drug or treatment to be used safely.
Phase IV trials
Post-marketing studies, which are conducted after a treatment is approved for use by the FDA, provide additional information including the treatment or drug’s risks, benefits, and best use.
Examples of other kinds of clinical research
Many people believe that all clinical research involves testing of new medications or devices. This is not true, however. Some studies do not involve testing medications and a person’s regular medications may not need to be changed. Healthy volunteers are also needed so that researchers can compare their results to results of people with the illness being studied. Some examples of other kinds of research include the following:
  • A long-term study that involves psychological tests or brain scans
  • A genetic study that involves blood tests but no changes in medication
  • A study of family history that involves talking to family members to learn about people’s medical needs and history.

Monday, 1 August 2016

Product Specialist - Oncology Sales

Job Description

Job Description
To attain or exceed the targeted sales volume in the assigned territory.
To develop relations with the select doctors in the assigned territory.
To implement HO strategies on the field

Sale Target:
To generate sales through regular doctor visit.
To meet all the doctors as defined in the doctors list
Responsible for product detailing and discussions with the customers for prescription generation
Maintain healthy secondary to primary sales ratio.

Implementation of marketing strategies:
Effective planning for territory coverage
Conduct CMEs and activities as defined in cycle meetings
Keeping self updated with the scientific knowledge

Stock management:
Monitoring the stock levels with the stockists
Taking orders and collecting payment timely
Ensuring liquidation of stocks

Feedback on Competitor information:
To provide regular feedback on competitor activity through market survey/ field interaction to the HO

Therapy Knowledge: Oncology,Critical care exposure is preferable.
    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 .

1. What is Medical Coding?


Let me start with the core responsibilities of a Medical Coder (be it India or elsewhere). These core responsibilities would help us understand how well one can fit into the role per se. How a medical procedure is coded determines the financial reimbursement for that particular procedure, and accuracy in coding also ensures quality data for future sound medical decisions. It affects everything in a healthcare organization.

Patients receive medical care or services. And it the responsibility of the Medical Coder to convert or translate the services received into a bunch of codes which will later help in billing, administration, fraud detection and investigation, recovery etc.. This line of work mandates experience in ICD 9 and 10 codes, CPT codes and HCPCS codes. Certifications add to ones' experience as well knowledge.

2. How are the prospects?
Now, coming to your core question : Yes, the prospects look good.

Primary reasons:

  1. The level of coding work outsourced to India
  2. Existing medical coding jobs in India (non-outsourced i.e.)
  3. The growing Healthcare sector in India


3. What is the career path?
If you are currently employed as a Medical Coder, it would perhaps make sense to gain considerable work and domain related experience first i.e. at least 1-2 years of experience. This experience coupled with the right certification (refer point #4 below) should give you a head-start on your career progression.

The US healthcare industry is in the middle of a shift from ICD9 to ICD10 and having experience in the latter is a valuable asset right now and for the next couple of years.

With increase in your expertise and experience, you can expect your pay-scale to go up (either in the same company or when you switch jobs). Down the line, from what I have researched, you can get into Medical office Management or Medical office Operations.

4. How to prepare to succeed?

  1. Well you can start by gaining as much Coder work experience as possible
  2. Get comfortable with and then gain expertise on CPT codes, the ICD 9 and 10 coding systemMedical Charts
  3. Once you feel you are comfortable with the coding terminology, research and choose an appropriate certification:
    CCA aka Certified Coding Associate (offered by AHIMA i.e. American Health Information Management Association)
    CPC aka Certified Professional Coder (offered by AAPC i.e. American Academy of Professional Coders)
    - Other certifications (COC aka Certified Outpatient Coding, CIC aka Certified Inpatient Coder, CRC aka Certified Risk Adjustment Coder, CPC - P aka Certified Professional Coder - Payer)
Work in the Exciting Field of Biotechnology Sales with Biogenuix Medsystems Pvt. Ltd.


Biogenuix Medsystems is national private firm whose existence has been in the Biotech market for last 10 years. Differentiating through quality products & top class service & support to the customers, Biogenuix has been catering to the Biotech industry’s demands aggressively. Biogenuix has been associated as channel partners with several US & European companies. We have been quite successful in creating a name for ourselves in this competitive market & now looking for expansion in our Sales & Marketing team at different locations all over India.
Biogenuix deals in distribution of Life Science & Diagnostic Products & Instrumentation mainly in the research industry. For further details please visit our website www.biogenuix.com
Designation -Technical Sales/ Sr. Sales Executive (Field Sales)
Location – Delhi, Bangalore, Jaipur
Vacancy – 04
Experience – Fresher can apply
Preference– Candidates with experience in Sales will be preferable
Qualification B.Tech/M.Tech/M.Sc. – Biotechnology/ Microbiology or related field
CTC– 3.5 lac- 4.2 lac (depending upon qualification & experience in the mentioned field)
Job Description: 
Roles & Responsibility
(Life Science, Diagnostic Products & Instrumentation)
  1. Responsible for entire sales cycle starting from lead identification, proposal & presentations, techno-commercial negotiations and order closures.
  2. Maintaining strong customer relationships
  3. Ensure timely collection of Receivables/ Payables
  4. Building a strong network in the industry.
  5. Keeping a close watch on competitors & defining strategies to hold the market share.
  6. Managing Key Accounts
  7. Responsible to establish new products in the market with the existing or new clients.
Key Skills & Perquisits :
  1. Technically sound (Biotechnology/related field is a must)
  2. Energetic & Enthusiastic
  3. Sales Oriented, willing to travel & must have a two wheeler with a valid license .
  4. Ability to take challenges
  5. Good Communication skills
  6. Positive attitude & a Team player.
Candidates who have an aptitude for Sales & Marketing may only apply.
How to Apply :
Interested candidates may mail their updated CVs to HR at careers@biogenuix.com mentioning the location preference in the subject line.

Ph: 011-48754862

Sr. Research Scientist

JOB PURPOSE


  • Responsible for generation and establishment of Double Haploid programs in biofuel plants.

KEY ACCOUNTABILITIES
  • Standardize, establish and implement the programme for production of Double Haploid perennial biofuel plants.
  • Establish lab infrastructure and equipment for developing double haploids
  • Cytological studies to determine the genome of biofuel plants
  • Develop genotype specific protocol for generating double haploids by means of anther culture, microspore culture, haploid cell culture followed by chromosome doubling, etc.
  • Optimize protocols to improve production efficiency
  • Manage an operational budget at or below budgeted amounts
  • Coordinate with breeders to design program and plan production of double haploids for important crosses
  • Coordinate the production of double haploid plants with tissue culture lab and breeders
  • Manages activities associated with growing double haploid plants including plant rooms, incubators and greenhouses
  • Train and supervise lab personnel in all phases of double haploid production
  • Co-ordination with external research & development agencies to continuously upgrade technology
  • Co-ordination with internal teams for effective implementation of project assignments

QUALIFICATIONS
  • Knowledge of double haploid production and genetics & breeding.
  • M.Sc degree in science related field (necessary)
  • Ph. D in biological science (desirable)
  • Skill in tissue culture techniques to produce double haploid plants.
  • Expertise in microscopy, imaging, karyotyping and statistical analysis.
  • Demonstrated experience in in vitro cell biology.
  • Experience in tissue culture, media preparation and working in or management in a laboratory setting.
  • Experience with double haploids, tissue culture and demonstrated capability of doing independent research
  • Experience with double haploids in perennial plants and basic cytological studies
  • Proven by one or two publications in renowned journal in field of plant tissue culture and double haploids.
  • Strong organization capabilities, excellent interpersonal skills, interaction with various research teams for designing, improving and implementing the program, capable of implementing and driving a strong research and development program with double haploid plant production.


Job Segment: Scientific, Statistics, R&D, Engineering, Research, Data          

EMPRI - Govt of Karnataka Hiring Multiple Research Scientists / Microbiologists With Excellent Salary Packages

Aishwarya Facility Services invites applications form the eligible candidates for outsourcing the following technical posts on annual contract basis to Environmental Management & Policy Research Institute (EMPRI) which is an autonomous institution under Government of Karnataka, Bangalore. Applications are to be sent by email to Aishwarya Facility services (aishwarya.facility@gmail.com) and EMPRI (admin-empri@karnataka.gov.in) by 5:00pm before August 15th 2016. Applications by post are also accepted if email is not available. Every application must include:
1. A Duly filled Application Form (download from​).
2. Recent Curriculum Vitae.
Selection procedure is based on CV, written examination followed by technical interview of the shortlisted candidates.
Candidates will be shortlisted on the basis of CV, eligibility criteria for the examination and be notified.
Original / Attested degree certificates and marks sheets will be required at the time of interview.
No TA/DA will be paid for attending the written test and interview. 
AFS or EMPRI shall not be responsible for the non-receipt of information due to lack of internet/ wrong email id of the candidates.
​Incomplete applications will be rejected.

Details of the vacancies are as given below

I. Research Scientist (1 Position)
          (40,000 CTC / 1 Year, renewable)
Essential Qualification:
•      Ph.D. in Forestry/ Wildlife/ Zoology/ Botany/ Agriculture/ Environmental Science /Life Sciences and 1 to 2 years of relevant research experience.  Should be well versed in MS office applications.  Working knowledge of Kannada is essential.
       Desirable:  Preference would be given to candidates with expertise/knowledge in Climate Change.
                                                                                                                                                                                                                                                                

II. Research Associate  (2 Positions)
          (24,000 pm(CTC), 1 Year, renewable)
Essential Qualification:
M.Sc. in Forestry/ Agriculture/ Wildlife/ Zoology/ Entomology/Life Sciences with 1 year of research experience
Desirable : Experience in Butterfly identification
M.Tech in Environmental Engineering or M.Sc in Environment Sciences/ B.Tech in Environmental Engineering with 1 year of research experience.
       Should be well versed in MS office applications. Working knowledge of Kannada is essential.
                                                                                                                                                                                                                                                                

III. Research Assistant (4 Positions)
          (18,000 – 20,000 pm(CTC), 1 Year, renewable)
Essential Qualification:
M.Sc. in Zoology/ Entomology/ Life Science/ Botany/ Forestry / Agriculture/ Environment Sciences. Desirable: Experience in field forestry  / Butterfly identification. 
Should be well versed in MS office applications. Working knowledge of Kannada is essential
                                                                                                                                                                                                                                                                

IV. Microbiologist (1 position) 
          (22,000 pm(CTC), 1 year, renewable)
Essential Qualification:
M.Sc Microbiology/Applied/ General/ Industrial/ Medical Microbiology. 2 to 3 years of relevant work experience. Working knowledge of Kannada is essential. Proficiency in MS Office applications.
                                                                                                                                                                                                                                                                 

V. Lab Technician (1 Position)
          (18,000 pm(CTC), 1year, renewable)
Essential Qualification:
Graduate in Science with chemistry specialization. Working knowledge of kannada essential. Proficiency in MS Office applications.
                                                                                                                                                                                                                                                                

VI. IT Assistant (1 Position)
          (21,028 pm(CTC), 1 year, renewable)
Essential Qualification: 
BE/ B.Tech/ BCA (Computer Science) Graduate with good knowledge of computer technology (Website development, designing, internet, publications etc.) with 1 year of relevant work experience. Working knowledge of Kannada is essential. Proficiency in MS Office applications is must.
Age Bar - upto 35 years
                                                                                                                                                                                                                                                                

VII. Programme Co-ordinator – National Green Crops (1 position)
          (25,000 - 30,000 CTC / 1 year, renewable)
Essential Qualification:
MEd/ BEd with 1 year of experience in environmental education / Teaching. Working knowledge of Kannada is essential. Proficiency in MS Office applications - Willingness and ability to travel extensively.
​                                                                                                                                                                                                                                                                 

VIII. Programme Associate (1 position)
          (20,000 - 25,000 CTC / 1 year, renewable)
Essential Qualification:
Post-Graduation in Science / humanities. Working and typing knowledge of Kannada is essential. Proficiency in MS Office applications - Willingness and ability to travel extensively.
​                                                                                                                                                                                                                                                                 

IX. Training Associate (1 position)
          (22,000 pm(CTC), 1 year, renewable)
Essential Qualification:
M.Sc. /B.Sc. Environment Science - 2 years for B.Sc. / 1 year for M.Sc. of relevant work experience. Working knowledge of Kannada is essential. Proficiency in MS Office applications - Willingness and ability to travel extensively.

Executive - Regulatory Affairs

1 - 5 YearsBengaluru/Bangalore

Job Description

reparation & Review of Registration Dossiers as per either of US/European Union/CANADA/Australia requirements (In CTD format).

Preparation of Module-3 and Module-2 of Registration dossiers in CTD format. [Solid Orals]

Updation of registration dossiers, evaluation of the queries received from respective country agencies.

Review of documents such as product manuals, batch manufacturing records, stability protocols, specifications, validation protocols and Validation reports of process as well as analytical method for regulatory compliance.

Liaison with various departments like R&D, Analytical Development, QC, QA, Production and Corporate affairs

Evaluation of gap-analysis for line-extension products

Handling the query received from various countries and customers

Review the documents as per specific country requirementCompany Profile
Medreich is a pharmaceutical company that has been in existence since 1976, manufacturing generic and branded drugs in several therapeutic areas. With more than 2900 employee's worldwide, exceptional quality standards and a client base that is spread across 54 countries, Medreich has built a reputation for raising the bar on product superiority with every undertaking.
Medreich's Research & Development and manufacturing facilities have received the seal of approval from leading global regulatory bodies such as -UK MHRA, Australia TGA, SA MCC, Health Canada, French FDA. The company produces drugs for leading, global pharmaceutical companies such as GSK, Pfizer, Sanofi Aventis, Wyeth, Merck, among others.
Medreich has 8 manufacturing facilities built to comply International regulatory standards. Two newly added facilities are State of the art technology driven plants. One among them has the capacity to produce 9 billon tablets and capsules per annum.

Pharmacovigilance Team Manager

Novartis Healthcare Pvt. Ltd.
8 - 13 yrs
Hyderabad / Secunderabad

Job Description
    1. Manage and lead processing team and ensure that all tasks are performed according to business rules, guidelines and standard operating procedures.
    2. Monitor workload and allocates resources appropriately. Ensure that incoming Adverse Events are processed by the team according to internal timeframes to meet Health Authorities requirements.
    3. Monitor the quality of work produced by the team and support quality improvement initiatives as appropriate. Provide feedback to team members on quality and train team members as appropriate to improve quality.
    4. Set up yearly objectives and review performances of team ensuring best use of available resources. Discuss and set up development plans with/for all team members to further develop individuals skills and potentials.
    5. Set up the training plans for new hires according to the individuals experience and job role and ensure that training is provided to team as appropriate. Support the training of other departments in clinical safety related procedures/regulatory obligations.
    6. QC periodic regulatory safety reports before submission to management approval and ensure compliance with required timelines and co-author, together with the Medical Safety Physicians, periodic regulatory safety reports, as appropriate.
    7. Interact with the Medical Safety Physicians on project activities in specific therapeutic areas, compatibly with the timely processing/production of individual case reports and regulatory periodic reports.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.  

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.

Senior Medical Writer

2 - 4 YearsBengaluru/Bangalore

Job Description

Essential Function
The Senior Medical Writer researches, creates, and edits all documents associated with clinical research. Responsibilities also include: acting as primary client contact for medical writing projects, working with other PAREXEL departments and clients to set and meet internal and external deliverable timelines, leadership, training and support of junior medical writing staff.

Relationships
Reports To Departmental Line Management, Medical Writing Services
Directly Supervises None
Provides Work Direction to Medical Writers, Associate Medical Writers, Medical Writing Assistants
Works Closely with Project Managers/ Leaders, Physicians, Biostatisticians, Data Managers, Regulatory Associates, Medical Writing staff
External Relationships Client technical representatives

Key Accountabilities
Write clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, clinical development plans, previous human experience summaries, human pharmacology summaries, investigator brochures, study protocols, model informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/ aggregate reports, integrated summaries of safety and efficacy.
Act in the capacity of project manager/ lead for medical writing projects. This may entail serving as the primary client contact, negotiating deliverable timelines, and resolving project-related issues. Project management of contractual and financial aspects may only be performed with the guidance of medical writing management.
Serve as the Medical Writing representative on assigned project teams, providing proactive support to Project Leadership for planning efficient work plans and timelines for medical writing deliverables, and medical writing input into other departmental deliverables. Identify any potential project challenges to departmental line management and project leader including changes in project plan, timeline or out of scope requests, and suggest possible resolution options.
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 guidelinesCompany Profile
PAREXEL International (India) Pvt. Ltd.

H and LS Medical Writer


2 - 6 YearsChennai

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

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

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