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Hyderabad City Police Recruitment 2014
Hyderabad City Police Vacancy Details:
Total No. of Posts: 150
Name of the Post:
1. Home Guard (Men)
2. Technical (Drivers)
Total No. of Posts: 150
Name of the Post:
1. Home Guard (Men)
2. Technical (Drivers)
Age Limit: Candidates age should be between 18-50 years as on 29-10-2014.
Educational Qualification: Candidate should possess 7th class or equivalent examination (candidates who possess higher qualification than the prescribed will also be considered) & Valid LMV/ HMV license issued by the Govt.
Selection Process: Selection will be based on Physical Standard Test & Qualifying test of Driving.
Application Fee: Candidates has to pay Rs.25/- in cash should be remitted at the time of submission of each application form towards registration fee. There is no Fee for SC/ ST candidates.
How to Apply: Eligible candidates can send their application in prescribed format & Hall Ticket (in Duplicate) along with the copies of all necessary documents by hand to Goshamahal Stadium, Hyderabad on any working day between 10-11-2014 to 22-11-2014 (excluding public holidays) in between 10:00 am to 02:00 pm.
Last date for Submission of Applications: From 10-11-2014 to 22-11-2014 (excluding public holidays) in between 10:00 am to 02:00 pm.
For more details like age limit, educational qualification, selection process, application fee, how to apply and other information click on the following link …
Safety Medical Writer
- Pharmacovigilance
- Bangalore
Looking for Safety Medical Writers!
Are you looking for a job to unlock your Medical Writing skills? Apply for the position of Safety Medical Writer to have life changing career!
About the department
Novo Nordisk Service Centre India Pvt Ltd, responsible for the development of diabetes medicines. Novo Nordisk has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. We are located at Bangalore.
The Job
Be responsible for the planning and preparation of:
Development Safety Update Reports (DSURs)
Periodic Safety Update Reports (PSURs/PBRERs
Risk Management Plans (RMPs)
Are you looking for a job to unlock your Medical Writing skills? Apply for the position of Safety Medical Writer to have life changing career!
About the department
Novo Nordisk Service Centre India Pvt Ltd, responsible for the development of diabetes medicines. Novo Nordisk has a long and outstanding track-record of developing the best, most innovative and widely-used injection devices in the world. We are located at Bangalore.
The Job
Be responsible for the planning and preparation of:
Development Safety Update Reports (DSURs)
Periodic Safety Update Reports (PSURs/PBRERs
Risk Management Plans (RMPs)
- through development to submission
- post-marketing
- Responses to any safety questions raised in connection with assessment reports
Other relevant ad-hoc documents
Contribution to knowledge sharing, skill building and good collaboration with stakeholders and colleagues:
You will also have an opportunity to participate in internal/external marketing/medical activities, e.g., expert meetings, lectures and conferences
Contribute to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge
Contribute to process improvements
Maintain up-to-date knowledge and competencies within relevant therapeutic and professional areas
Actively participate in relevant meetings, training sessions and seminars in the department, competency anchor and relevant project(s)
As Product responsible Safety Medical Writer, you will:
Act as mentor/trainer for other safety medical writers working with the product, as required.
Plan, drive, and co-ordinate preparation of documents to ensure submission according to the submission plan, or as otherwise agreed with Regulatory affairs.
Contribute to continuous resource planning process in collaboration with immediate superior – including identifying medical writing tasks and assist in the prioritisation of tasks
Perform consistency review of documents as back-up SMW
contribute to the evaluation of safety data from clinical trial and spontaneous sources
Qualifications
Graduate (MSc, MBBS, BDS/MDS, B.Pharm/M.Pharm, B.V.Sc.&A.H or equivalent)
≥3 years of experience in Pharmacovigilance as Medical Writer/Pharmacovigilance writer/Advisor.
Experience with scientific writing in English (publications or equivalent)
Novo Nordisk is an organisation with many international employees. Here, you will get the opportunity to be a part of a global team that fosters great work culture, work independently and play an active role in the growth of the team through knowledge sharing and skill building and in addition enhance your career, benefiting from the possibilities for professional and personal development provided by Novo Nordisk.
At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working at Novo Nordisk is not just a way to make a living, but a way to make a difference.
Contact
For further information, contact Lavanya Sadashiva at +91 80 39988645
Deadline
1 December 2014
Career as Associate Project Manager @ Icon Clinical Research
Post: Associate Project Manager
Job Description:
Functions as primary contact to sponsors for assigned projects in the maintenance phase
Assists in the development of project related documentation.
prepares project summary report and analyses as needed
Assists in monitoring the quality within departments / projects
Assists callers to the IVRS Helpdesk
Functions as primary contact to sponsors for assigned projects in the maintenance phase
Assists in the development of project related documentation.
prepares project summary report and analyses as needed
Assists in monitoring the quality within departments / projects
Assists callers to the IVRS Helpdesk
Candidate Profile
Background in Medicine, Science or other relevant discipline
Minimum of 2 yrs in IVRS or equivalent
Ability to manager multiple tasks and timelines
ability to prioritise tasks and delegated workload
ability to liase professionally with clients and system users
forien language skills desirable
Other responsibilities may be assigned as required.
Background in Medicine, Science or other relevant discipline
Minimum of 2 yrs in IVRS or equivalent
Ability to manager multiple tasks and timelines
ability to prioritise tasks and delegated workload
ability to liase professionally with clients and system users
forien language skills desirable
Other responsibilities may be assigned as required.
Additional Information:
Education: Background in Medicine, Science
Location: Chennai
Industry Type: Pharma/ Biotech/Clinical Research
Job Code: 011241
End Date: 30th Nov, 2014
Education: Background in Medicine, Science
Location: Chennai
Industry Type: Pharma/ Biotech/Clinical Research
Job Code: 011241
End Date: 30th Nov, 2014
Work as Analyst-Forecasting at Novartis - MBA with Graduate / Post Graduate in Pharmacy
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 them one of the most rewarding employers in their field.
Post: Analyst-Forecasting
Job Description:
• Provide forecasting support to Novartis internal customers (CPOs & Regional marketing and sales teams) on various low-medium complexity forecasting reports.
• Support and facilitate data enabled decision making for Novartis internal customers by providing and communicating qualitative and quantitative analytics.
• Support GBS-GCO business in building practice by involving in various initiatives like knowledge sharing, on-boarding and training support, support team lead in all business related tasks / activities, building process documentation and knowledge repositories.
• Create and deliver below customer requirements as per agreed SLAs (timeliness, accuracy, quality, etc) and drive excellent customer service
o Strategic 5 year forecasts for in-line / pipeline products
o Lifecycle management forecasts for inline / pipeline products
o BD&L market & product revenue forecasts
o Pipeline product forecasts
o Monthly revenue forecasts by indication for 24 months
o Ad-hoc Forecasting support
• Deliver services through structured project management approach with appropriate documentation and communication throughout the delivery of services
• Support in creation and maintenance of standard operating procedures (SOPs), quality checklists that will enable excellent quality outputs for all outputs within the function
• Support in developing and maintaining knowledge repositories that captures qualitative and quantitative reports of brands, disease areas, macroeconomic trends of Novartis operating markets, etc
• Support team leaders in recruitment and on-boarding of new associates within the organization
• Participate in various knowledge sharing sessions that enables growth and improves quality of GCO Hyd deliverables across the function
• Comply with all internal functional operating procedures like time tracking, KPI tracking and reporting, and other internal systems and processes
• Comply to all Novartis operating procedures as per legal / IT / HR requirements.
• Provide forecasting support to Novartis internal customers (CPOs & Regional marketing and sales teams) on various low-medium complexity forecasting reports.
• Support and facilitate data enabled decision making for Novartis internal customers by providing and communicating qualitative and quantitative analytics.
• Support GBS-GCO business in building practice by involving in various initiatives like knowledge sharing, on-boarding and training support, support team lead in all business related tasks / activities, building process documentation and knowledge repositories.
• Create and deliver below customer requirements as per agreed SLAs (timeliness, accuracy, quality, etc) and drive excellent customer service
o Strategic 5 year forecasts for in-line / pipeline products
o Lifecycle management forecasts for inline / pipeline products
o BD&L market & product revenue forecasts
o Pipeline product forecasts
o Monthly revenue forecasts by indication for 24 months
o Ad-hoc Forecasting support
• Deliver services through structured project management approach with appropriate documentation and communication throughout the delivery of services
• Support in creation and maintenance of standard operating procedures (SOPs), quality checklists that will enable excellent quality outputs for all outputs within the function
• Support in developing and maintaining knowledge repositories that captures qualitative and quantitative reports of brands, disease areas, macroeconomic trends of Novartis operating markets, etc
• Support team leaders in recruitment and on-boarding of new associates within the organization
• Participate in various knowledge sharing sessions that enables growth and improves quality of GCO Hyd deliverables across the function
• Comply with all internal functional operating procedures like time tracking, KPI tracking and reporting, and other internal systems and processes
• Comply to all Novartis operating procedures as per legal / IT / HR requirements.
andidate Profile:
MBA with Graduate / Post Graduate in Medicine (MD/MBBS/BDS) Pharmacy / Life Sciences Fluency in English is prerequisite, while knowledge of other in-scope country languages would be an advantage
- Experience (2-3 years) in forecasting in a market research firm or pharmaceutical company or Pharma KPO
- Should have an understanding of Pharmaceutical business including its regulatory environment
- Strong analytical thinking with problem solving approach
- Should have worked in an international company with exposure to working in cross-cultural environment
- Should be customer service oriented
- Strong and proactive business results-focus, and proven ability to provide insights that increase productivity
MBA with Graduate / Post Graduate in Medicine (MD/MBBS/BDS) Pharmacy / Life Sciences Fluency in English is prerequisite, while knowledge of other in-scope country languages would be an advantage
- Experience (2-3 years) in forecasting in a market research firm or pharmaceutical company or Pharma KPO
- Should have an understanding of Pharmaceutical business including its regulatory environment
- Strong analytical thinking with problem solving approach
- Should have worked in an international company with exposure to working in cross-cultural environment
- Should be customer service oriented
- Strong and proactive business results-focus, and proven ability to provide insights that increase productivity
Additional Information:
Job ID: 153543BR
Experience: 2-3 Year
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: other
End Date: 9th Dec, 2014
Job ID: 153543BR
Experience: 2-3 Year
Industry Type: Pharma/Biotech/Clinical Research
Functional Area: other
End Date: 9th Dec, 2014
India to double drug inspectors to boost oversight
A rash of import bans imposed by the U.S. Food and Drug Administration on leading Indian generic drugmakers due to lapses in production processes over the past year has triggered concerns about the quality of drugs sold in other markets, including in India.
The government will increase the number of inspectors at the Central Drugs Standard Control Organization (CDSCO) to 1,000 from 500 now, Drugs Controller General of India G.N. Singh said in a statement on Wednesday.
The number of officials at state regulatory departments will be raised to 3,000 from 800 now, he said.
"India's reference system (for drug testing and intellectual property) will be at par with the top world standards in two to three years and will even match the U.S. in three to five years," Singh said.
In India, states regulate the manufacture and distribution of drugs, while CDSCO, which is the federal authority, handles approvals of new drugs and clinical trials, oversees drug imports and coordinates the activities of state regulators.
A chronic shortage of inspectors has made it difficult for regulators to monitor the more than 10,000 drug manufacturing factories in India, which supply to more than 200 countries.
Multiple state drug regulators told Reuters in April that skeletal staff and lack of enough drug testing laboratories had rendered their departments unequipped to carry out their duties.
($1 = 58.7600 Indian Rupees)
(Reporting by Zeba Siddiqui in Mumbai; Editing by Prateek Chatterjee)
Opening for Team Lead - Pharmacovigilance in Global Safety at Novo Nordisk
About the department
Pharmacovigilance in the area within Global safety and responsible for processing ICSRs. Global safety has an outstanding track-record in case processing. You will join a team of highly motivated employees, responsible for the safety of the patients.
Pharmacovigilance in the area within Global safety and responsible for processing ICSRs. Global safety has an outstanding track-record in case processing. You will join a team of highly motivated employees, responsible for the safety of the patients.
The job
You will become a member of the safety team which is responsible for processing of ICSRs. You will especially focus on defining and integrating user/stakeholder requirements and safety risk management. You will be given a number of different responsibilities and experience a variety of tasks, working with both internal and external stakeholders. The job will enhance your professional and personal development, providing you with an opportunity to develop skills within specialist expertise and project management.
You will become a member of the safety team which is responsible for processing of ICSRs. You will especially focus on defining and integrating user/stakeholder requirements and safety risk management. You will be given a number of different responsibilities and experience a variety of tasks, working with both internal and external stakeholders. The job will enhance your professional and personal development, providing you with an opportunity to develop skills within specialist expertise and project management.
To contribute to the collection, medical evaluation and reporting (to the authorities) concerning adverse events/technical complaints from clinical use of Novo Nordisk’s preparations and products whether the product is in clinical development or Primary driver of process optimisation of the operational case handling
Contribute to the build-up of a strong team, which can work professionally in the operational handling of adverse events in close collaboration with affiliates and other partners.
Maintain a network of safety contacts within safety operations and affiliates.
Conduct performance management, individual development plans, job descriptions and performance evaluation.
Ensure continuous development of employees, training/coaching in pharmacovigilance and in departmental functions as well as provision of knowledge about NN business.
To negotiate processes for collaboration with Contract Research Organisations regarding SAE reporting and establish excellent working relationships with these.
To participate in the development and maintenance of departmental and functional procedures which have to ensure the observance of internal and external requirements for the management of safety information
To supervise the daily activity of the team, including vacation, planning and other activities.
Monitor and ensure that KPIs for evaluation and reporting of adverse events are maintained.
To have extensive knowledge of Novo Nordisk safety database (Argus).
Close co-operation with other groups in Global Safety. Liaise with the Safety Reporting and IT in all aspects of E2B reporting; database and application management; data retrieval; custom reporting.
Measure and present internal and regulatory compliance.
Maintenance of MOMs related to case processing and QC feedbacks.
Responsible for providing inputs for updates of SOPs
Provide input to safety data exchange agreements and pharmacovigilance system description documents regarding the post marketing surveillance process.
Conduct safety trainings for new pharmacovigilance staff and other company units.
Establish and maintain a thorough understanding of safety requirements of the project protocol, and safety reporting workflow, set up and maintain project materials such as project files, forms, templates, databases and workflow.
Establish and maintain effective project communications by representing department at interdepartmental project team meetings to understand and adhere to specific safety reporting requirement.
The tasks demand self-dependence and competence in making decisions, as well as flexibility, a good comprehensive view and a many-functioned, often international, co-operation.
Contribute to the build-up of a strong team, which can work professionally in the operational handling of adverse events in close collaboration with affiliates and other partners.
Maintain a network of safety contacts within safety operations and affiliates.
Conduct performance management, individual development plans, job descriptions and performance evaluation.
Ensure continuous development of employees, training/coaching in pharmacovigilance and in departmental functions as well as provision of knowledge about NN business.
To negotiate processes for collaboration with Contract Research Organisations regarding SAE reporting and establish excellent working relationships with these.
To participate in the development and maintenance of departmental and functional procedures which have to ensure the observance of internal and external requirements for the management of safety information
To supervise the daily activity of the team, including vacation, planning and other activities.
Monitor and ensure that KPIs for evaluation and reporting of adverse events are maintained.
To have extensive knowledge of Novo Nordisk safety database (Argus).
Close co-operation with other groups in Global Safety. Liaise with the Safety Reporting and IT in all aspects of E2B reporting; database and application management; data retrieval; custom reporting.
Measure and present internal and regulatory compliance.
Maintenance of MOMs related to case processing and QC feedbacks.
Responsible for providing inputs for updates of SOPs
Provide input to safety data exchange agreements and pharmacovigilance system description documents regarding the post marketing surveillance process.
Conduct safety trainings for new pharmacovigilance staff and other company units.
Establish and maintain a thorough understanding of safety requirements of the project protocol, and safety reporting workflow, set up and maintain project materials such as project files, forms, templates, databases and workflow.
Establish and maintain effective project communications by representing department at interdepartmental project team meetings to understand and adhere to specific safety reporting requirement.
The tasks demand self-dependence and competence in making decisions, as well as flexibility, a good comprehensive view and a many-functioned, often international, co-operation.
Qualifications
Bachelor/Master in life science (Health care professional)
Working knowledge of MS Windows applications including MS Office tools, good written an spoken English, extensive knowledge of medicinal terminology and clinical pharmacology. Knowledge of basic and advanced GCP (Good Clinical Practice) & GMP (Good Manufacturing Practice) Self-motivated and proactive, Quick learning and analytical skills, ability to motivate and engage individuals, ability to take up initiatives.
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.
Bachelor/Master in life science (Health care professional)
Working knowledge of MS Windows applications including MS Office tools, good written an spoken English, extensive knowledge of medicinal terminology and clinical pharmacology. Knowledge of basic and advanced GCP (Good Clinical Practice) & GMP (Good Manufacturing Practice) Self-motivated and proactive, Quick learning and analytical skills, ability to motivate and engage individuals, ability to take up initiatives.
At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development.
Contact
For further information, please contact Aparna +91 80 33549289
For further information, please contact Aparna +91 80 33549289
Deadline
31 October 2014
31 October 2014
MOHFW Kanpur Jobs 2014 Pharmacist, Nurse, Clerk
MOHFW Kanpur Jobs 2014 Pharmacist, Nurse, Clerk
Ministry of Health and Family Welfare (MOHFW) Kanpur (Government of India) invites applications from Indian National for the temporary posts of Pharmacist, Staff Nurse and Pharmacists Cum Clerk. Eligible candidates are required to apply within 21 Days from the date of publication in Employment News Paper (4th January 2014).
Post Name No of Vacancies Age Limit Pay Scale
1.Pharmacist (Allopathic) 08 (UR-06 SC-2) 18- 30 years
PB-1 Rs.5200-20200+2800
2.Staff Nurse Grade I 03 (SC-01, UR-01, OBC-01) 21 – 35 years
PB-2 Rs.9300-34800+4600
3.Pharmacists Cum Clerk (Homeopathic) 01 (SC-01) 18 - 30 years
PB-1 Rs.5200-20200+2800
4.Pharmacists Cum Clerk (Ayurvedic) 01 (BCC-01) 18 - 25 years
PB-1 Rs.5200-20200+2800
Educational Qualifications:
Pharmacist (Allopathic) -> 10+2 with science stream (Physics / Chemistry / Biology). Technical Qualification – Approved diploma in Pharmacy from an institute recognized by the pharmacy council of India and registered as a pharmacist under the pharmacy Act. 1948.
Staff Nurse -> 10+2 OR its equivalent. Diploma in General nursing and Mid Wifery from a recognized Institution. Registered Nurse and registered Mid-Wife in Lieu of mid wifery, a six month duration course as prescribed by Indian Nursing Council (For male Nurse). Desirable - one years Experience in Mid Wifery. Or one years Experience in general Nursing.
Pharmacists Cum Clerk (Homeopathic) -> Matriculation or equivalent. At least 2 years Experience as a homeopathic pharmacist in government OR recognized private homeopathic Hospital / dispensary or 3 years Experience under registered Homeopathic practitioner.
Pharmacists Cum Clerk (Ayurvedic) -> Matriculation or equivalent. Training in upavaidya (Kalpada) Course, Duration of which should not be less than 2 years form a govt. organization or recognized private institution like all India ayurvedic congress or its equivalents. Atleast 2 years Experience as Ayurvedic pharmacist in a recognized Ayurvedic dispensary, Hospital or Pharmacy.
How To Apply: Application on the prescribed format. Completed application should attach recent passport size photo that must be attested by a Gazetted officer along with required documents reach to "Office of the Additional Director, Ministry of Health and Family Welfare, Central Government health scheme, Plot No. 8-11, Rattan Lal Nagar, Kanpur- 208022” within 21 Days from the date of advertisement (Employment News Paper 04/01/2014).
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