Pharmaceutical

Job Opening for Manager Finance with 2 -5years post qualification experience @ AstraZeneca, Bangalore

Posted on December 26, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

AstraZeneca, Bangalore
 
AstraZeneca is one of the world’s leading pharmaceutical companies. Backed by a strong research base and extensive manufacturing and commercial skills, the company provides a powerful range of products for six important areas of healthcare – gastrointestinal, cardiovascular, cancer, respiratory, neurosciences and infection. With its headquarters based in UK, AstraZeneca has its R&D facilities basedin Sweden, USA, Japan & India. The company sells its products in over 100 countries, manufactures in 27 and has major research centres in 11. It employs over 65,000 people worldwide and values the diversity of skills and abilities that they bring to the business. R&D is based in Sweden, the UK, the USA, Canada, France, India & Japan. The company is recognised as having one of the best development pipelines in the industry and spends over $14 million each working day to maintain a flow of new medicines designed to meet patients’ needs. AstraZeneca invests over US$ 3.4 billion a year on R&D activities including Discovery Research. The company worldwide sales in 2005 totalled $24 billion.
 
This Job is posted in http://www.astrazenecaindia.com
 
Job Description: 
Position Manager Finance
Work Location Bangalore
Date Posted Monday, November 10, 2008
 
Responsibilities

  • To prepare and submit group and local management reports on timely basis;
  • To work as a team leader in company budgeting process
  • To support various functions and Senior Management members in business analysis, budgeting, forecasting and strategic planning.
  • Provide Budget v\s Actual to various Department heads

Requirements

  • Organization structure – Functionally reports to: Sr.Finance Manager (Corp.Info.group)
  • Academic / Professional qualification : Bachelor’s Degree (Finance or related)
  • Technical / skills training: Qualified CA
  • Good business understanding
  • Working experience: (No. Of years job function business types)
  • Desirable: 2 -5years post qualification experience in Accounting/ MIS/ Planning
  • Language ability: Fluent written and verbal English
  • Computer literacy :
  • ERP knowledge is Must
  • Good command of Excel and PowerPoint
  • Good communication skill
  • Pleasant personality and able to work with senior management

 

AstraZeneca Pharma India Limited
Avishkar
Bellary Road
Hebbal
Bangalore – 560 024 India
Tel : +91 80 23622021- 27

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Manager Procurement – 5+ Years – AstraZeneca, Bangalore

Posted on December 26, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

AstraZeneca, Bangalore
AstraZeneca is one of the world’s leading pharmaceutical companies. Backed by a strong research base and extensive manufacturing and commercial skills, the company provides a powerful range of products for six important areas of healthcare – gastrointestinal, cardiovascular, cancer, respiratory, neurosciences and infection. With its headquarters based in UK, AstraZeneca has its R&D facilities basedin Sweden, USA, Japan & India. The company sells its products in over 100 countries, manufactures in 27 and has major research centres in 11. It employs over 65,000 people worldwide and values the diversity of skills and abilities that they bring to the business. R&D is based in Sweden, the UK, the USA, Canada, France, India & Japan. The company is recognised as having one of the best development pipelines in the industry and spends over $14 million each working day to maintain a flow of new medicines designed to meet patients’ needs. AstraZeneca invests over US$ 3.4 billion a year on R&D activities including Discovery Research. The company worldwide sales in 2005 totalled $24 billion.
This Job is posted in http://www.astrazenecaindia.com
Job Description: 
Position Manager Procurement
Work Location Bangalore
Date Posted Monday, November 17, 2008
 
Responsibilities

  • Procurement:
  • Excellent understanding of Procurement Process & the current Best Practices in pharmaceutical industry.
  • Managing production related tasks including planning, procurement, and control & for achieving the planned periodic schedules, within budgeted parameters.
  • Should have Complete knowledge of working on ERP system preferably SAP
  • Should have excellent knowledge of MS Office & MS project
  • Should Have In depth knowledge on Pharmaceuticals API/Packing Material –related to sourcing & pricing
  • Contract Management :
  • Identifying & Managing Contract Manufacturer & negotiating & finalizing cost with the contract Manufacturers.
  • Assessing, auditing & executing the agreements as per company policy to ensure smooth operations.
  • Formulating, validating & adhering to the SOP’s designed for efficient production, Purchase, Quality, Warehousing & Distribution.
  • Coordination:
  • Coordination with contractors, to ascertain technical specifications, Production related essentials, based on the prevalent rules.
  • Internal coordination with Marketing, Regulatory, Supply chain & Distribution for new product launches etc
  • Supplier Relationship management on an ongoing basis
  • Assessing annual requirement of material; coordinating with the Procurement Dept for identifying a reliable Vendor base in India & overseas for cost effective Procurement of quality material.
  • Managing Inventory of Raw material & Finished to ensure timely delivery of materials
  • Managing Logistics to & from the contract-manufacturing site.
  • Liaising with Govt Depts. For sanctions / approvals as well as ensuring seamless flow of operations.

Requirements

  • Candidate must possess at least a Bachelor of Pharmacy or equivalent.
  • At least 5 year(s) of working experience.
  • Should have experience in Procurement & Contract Management.

 

AstraZeneca Pharma India Limited
Avishkar
Bellary Road
Hebbal
Bangalore – 560 024 India
Tel : +91 80 23622021- 27

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Data Analyst – 4 Years Experience in clinical research, drug development @ PharmaNet, Mumbai

Posted on December 24, 2008. Filed under: Pharmaceutical | Tags: , , , , |

PharmaNet

PharmaNet, a global, drug development services company, provides a comprehensive range of services to the pharmaceutical, biotechnology, generic drug, and medical device industries. PharmaNet offers clinical-development solutions including consulting services, Phase I clinical studies, bioequivalency and pharmacodynamic studies, bioanalytical analyses, and Phase II, III, and IV clinical development programs. In addition, PharmaNet offers technology tools for managing clinical trial data.

 This Job is posted in http://www.pharmanet.com/aboutus/html/ for more details visit https://www.ultirecruit.com/pha1001/JobBoard/SearchJobs.aspx?__SVRTRID=B83DF025-78B0-457B-8A55-E71AF5DA1A6C

Job Details

Requisition Number 340
Post Date 12/3/2008
Title Data Analyst
City Mumbai
Country India
Description · Perform data review and query generation
· Define edit checks to be programmed for the study/project
· Review programmed edit checks
· Track study progress and issue periodic status reports
· Update the database to correct errors
· Code Case Report Form (CRF) verbatim terms using PharmaNet or sponsor-supplied dictionaries
· Process electronic data received from outside vendors
· Identify the achievement of milestones to the project team or Lead Data Analyst, e.g., database status as “draft” or “final”
· Participate in the completion of all quality control measures necessary for the finalization and transfer of the database and related materials to the sponsor
· May act as the Lead Data Analyst for assigned studies or projects
· May coordinate the work of Associate Data Analysts assigned to the project
· May provide training on data management procedures and systems
· May create the data management plan for the study/project
· May assist in the review of the database design
· May develop and design CRFs, or participate in the review of sponsor-generated CRFs

Requirements · Bachelor’s Degree or RN; in lieu of Bachelor’s Degree or RN, four years experience in clinical research, drug development, or other healthcare environment, including eighteen months experience in data management
· Eighteen months of relevant clinical or data management experience
· Proven data management skills
· Effective communication skills
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Clinical Research Associate II – 2 Years Experience – PharmaNet, Bangalore

Posted on December 24, 2008. Filed under: Pharmaceutical | Tags: , , , , |

PharmaNet

PharmaNet, a global, drug development services company, provides a comprehensive range of services to the pharmaceutical, biotechnology, generic drug, and medical device industries. PharmaNet offers clinical-development solutions including consulting services, Phase I clinical studies, bioequivalency and pharmacodynamic studies, bioanalytical analyses, and Phase II, III, and IV clinical development programs. In addition, PharmaNet offers technology tools for managing clinical trial data.

 This Job is posted in http://www.pharmanet.com/aboutus/html/ for more details visit https://www.ultirecruit.com/pha1001/JobBoard/SearchJobs.aspx?__SVRTRID=B83DF025-78B0-457B-8A55-E71AF5DA1A6C

Job Details

Requisition Number 378
Post Date 12/3/2008
Title Clinical Research Associate II
City Bangalore
Country India
Description Job Functions:
• Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 – 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines
• Recruit investigators for participation in clinical trials
• Negotiate study budgets with investigators
• Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites
• Review draft protocols for completeness and feasibility
• Develop Case Report Forms for clinical trials
• Present (e.g. study specific guidelines and procedures, case report forms, and monitoring conventions) at Investigators’ Meetings
• Prepare and process Serious Adverse Event (SAE) reports
• Prepare project management reports for clients, project personnel, and PharmaNet management
• Review and verify CRFs and other clinical data, in-house, for completeness and accuracy; generate queries
• Resolve queries of CRF data with study site personnel
• Review Tables and Listings generated from study data
• Assist in writing Clinical Study Reports
• Train junior CRAs on monitoring, internal procedures, and query resolution
• When allocated by study management, submit essential/required documents to a central IRB or a country’s central Ethics Committee, and, if necessary based on local requirements, the Competent Authority
Requirements Minimum Requirements:
• Bachelor’s Degree or RN
• Two years’ work experience in clinical research, data management, regulatory affairs, or other relevant healthcare research position
• Eighteen months’ experience in field monitoring of clinical trials. Alternatively, twelve months’ experience in field monitoring of clinical trials, plus at least one of the following qualifications:
1. Twelve months’ prior experience as a clinical study coordinator
2. Relevant post-graduate doctoral degree (e.g., PharmD, PhD, MD)
3. Five years of relevant work experience as a nurse or pharmacist
• Excellent written and verbal communications skills
• Ability and willingness to travel up to 50%
• Excellent organizational skills and ability to manage time and work independently
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Interactive Trials Analyst I – 4+ Years Relevant Experience – PharmaNet, Mumbai

Posted on December 24, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

PharmaNet, A Global, Drug Development Services Company

This Job is posted in http://www.pharmanet.com/   for more details visit https://www.ultirecruit.com/pha1001/JobBoard/SearchJobs.aspx?__SVRTRID=70775E21-C026-4FC4-A154-CF21AAA8F8A1

Job Details

Requisition Number 380
Post Date 12/5/2008
Title Interactive Trials Analyst I
City Mumbai
Country India
Description • Answer IVRS help calls from system users, resolve issues and track resolutions
• Resolve issues/problems relating to client and investigator requests and supply shipments
• Document validation plans and other required materials for IVRS projects
• Assist manager with data modifications/loads for IVRS projects
• Monitor and re-submit failed confirmation reports to ensure receipt
• Provide administrative support to management
• Train support staff
Requirements • Bachelor’s Degree; in lieu of degree, a minimum of four years of relevant technical and or clinical/health related experience
• MS Office experience
• Excellent verbal and written communication skills
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Job Opening for Pharmaceutical Analyst with 2 to 3 Years Experience @ Arbro, Pharmaceuticals Ltd, New Delhi

Posted on December 24, 2008. Filed under: Pharmaceutical | Tags: , , , , |

Arbro, Pharmaceuticals Ltd, New Delhi

A World Class R&D and Analytical Services Organization

Arbro provides research and development services, technical problem solving and contract analytical services to industry, government and academia and is an ISO9001:2000 registered company. Arbro specialises in spectroscopy, microscopy, chemical analysis and instrumentation development to provide tailored, innovative solutions to client requirements.

World Class Integrated Solutions

Arbro can provide analytical services, apply these techniques to commercial problem solving and develop innovative methods and instrumentation in-house. Within a single organization, Arbro provides an integrated approach that ensures cost effective solutions, delivered on schedule and clearly focused on the requirements of the client.

From pharmaceuticals to food and fine chemicals, Arbro has worked closely with hundreds of companies in the India and overseas to apply our expertise in analytical chemistry to meet their specific challenges.

Whether it is quality control testing, non-routine analysis or advice and consultancy, clients can trust Arbro to provide the right outsourcing solution – enabling them to concentrate on the development of their business.

This Job is posted in http://www.arbropharmaindia.com  for more details visit http://www.arbropharmaindia.com/careers.htm

If you wish to apply please send an email with your Bio-Data in email.

If you are applying to TestLab Send Email to: arbrolab@arbropharma.com

Job Description:

Pharmaceutical Analyst
Nature Of work: Analysis of pharmaceuticals and cosmetics
Qualification: Science graduat or Postgraduate
Experience: 2-3 years in analysis of pharmaceuticals and/or cosmetics products
No of Post: 3
Department Testing Lab

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Job Opening for 2-3 years experience in analysis of food products as Food Analyst @ Arbro, Pharmaceuticals Ltd, New Delhi

Posted on December 24, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

Arbro, Pharmaceuticals Ltd, New Delhi

A World Class R&D and Analytical Services Organization

Arbro provides research and development services, technical problem solving and contract analytical services to industry, government and academia and is an ISO9001:2000 registered company. Arbro specialises in spectroscopy, microscopy, chemical analysis and instrumentation development to provide tailored, innovative solutions to client requirements.

World Class Integrated Solutions

Arbro can provide analytical services, apply these techniques to commercial problem solving and develop innovative methods and instrumentation in-house. Within a single organization, Arbro provides an integrated approach that ensures cost effective solutions, delivered on schedule and clearly focused on the requirements of the client.

From pharmaceuticals to food and fine chemicals, Arbro has worked closely with hundreds of companies in the India and overseas to apply our expertise in analytical chemistry to meet their specific challenges.

Whether it is quality control testing, non-routine analysis or advice and consultancy, clients can trust Arbro to provide the right outsourcing solution – enabling them to concentrate on the development of their business.

This Job is posted in http://www.arbropharmaindia.com  for more details visit http://www.arbropharmaindia.com/careers.htm

If you wish to apply please send an email with your Bio-Data in email.

If you are applying to TestLab Send Email to: arbrolab@arbropharma.com

Job Description:

Food Analyst
Nature Of work: Analysis of Food
Qualification: Science graduat or Postgraduate
Experience: 2-3 years in analysis of food products
No of Post: 3
Department Testing Lab

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Job Opening for Quality Manager with 5 to 6 Years Experience @ Arbro, Pharmaceuticals Ltd, New Delhi

Posted on December 23, 2008. Filed under: Pharmaceutical | Tags: , , , , , , , , |

Arbro, Pharmaceuticals Ltd

A World Class R&D and Analytical Services Organization

Arbro provides research and development services, technical problem solving and contract analytical services to industry, government and academia and is an ISO9001:2000 registered company. Arbro specialises in spectroscopy, microscopy, chemical analysis and instrumentation development to provide tailored, innovative solutions to client requirements.

This Job is posted in http://www.arbropharmaindia.com for more details visit  http://www.arbropharmaindia.com/careers.htm

If you wish to apply please send an email with your Bio-Data in email.

If you are applying to TestLab Send Email to: arbrolab@arbropharma.com

Job Description:

Quality Manager
Nature Of work: ISO/IEC 17025 Quality system
Qualification: Science graguate/post graduate.
Experience: 5-6 years experience in analytical lab. Should have atended 4 days training on 17025. Able to independently iiplement the system.
No of Post: 1
Department Testing Lab

 

 

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Job Opening for Project Manager (s) @ Aurigene, Bangalore

Posted on December 22, 2008. Filed under: Pharmaceutical | Tags: , , , , , , , |

Aurigene

Established in Bangalore, India, in 2002, Aurigene is a drug discovery biotech with a proven track record of successful partnerships with 10 collaborators globally. Aurigene has a pipeline of 15 discovery programs, at various stages from Hit Generation to late-stage Pre-Clinical Optimization, and has filed multiple patents in these Discovery Programs.

With proprietary Structural Biology and Fragment-based Drug Design technology platforms, and experienced scientific leadership, Aurigene is a fully integrated operation with expertise in Target Validation Biology and Hit Generation to IND nomination. Focus TAs includes Oncology, Metabolic disorders and Autoimmune/ Inflammatory diseases.

This Job is posted in http://www.aurigene.com/index.php?option=com_content&view=article&id=51&Itemid=128 for more details visit  http://www.aurigene.com/index2.php?option=com_content&view=article&id=97

Position Description:  Project Manager(s)      

Position Code:
   005

Location:
   Bangalore

Project Manager (s)

3 positions are available for immediate recruitment for Project Management in Small Molecule Chemistry, Peptide Chemistry and Protein Crystallography.

Key Responsibilities – The candidates will serve as interface between the technical team at the client site and Aurigene. Cross-functional responsibilities include working with procurement and suppliers to ensure raw materials availability; working with technical teams in drafting and reporting the findings of studies and interfacing the client and internal teams for tech support / discussions. The candidate will have proficient communication as most of Aurigene clients are large MNCs from Europe and USA. The position reports to heads of Business Development and respective technical field and requires a high energy, dynamic, solutions oriented personality who is willing to go the extra mile.

Qualifications – Successful candidate will have very good people skills and team forming abilities especially MS preferably with MBA.

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Job Opening for Fershers in Post Doctoral Fellowship @ Aurigene , Bangalore

Posted on December 22, 2008. Filed under: Pharmaceutical | Tags: , , , |

Aurigene

Established in Bangalore, India, in 2002, Aurigene is a drug discovery biotech with a proven track record of successful partnerships with 10 collaborators globally. Aurigene has a pipeline of 15 discovery programs, at various stages from Hit Generation to late-stage Pre-Clinical Optimization, and has filed multiple patents in these Discovery Programs.

With proprietary Structural Biology and Fragment-based Drug Design technology platforms, and experienced scientific leadership, Aurigene is a fully integrated operation with expertise in Target Validation Biology and Hit Generation to IND nomination. Focus TAs includes Oncology, Metabolic disorders and Autoimmune/ Inflammatory diseases.

This Job is posted in http://www.aurigene.com/index.php?option=com_content&view=article&id=51&Itemid=128 for more details visit  http://www.aurigene.com/index2.php?option=com_content&view=article&id=54

Position Description:  Post Doctoral Fellowship      

Position Code:
   002

Location:
   Bangalore

Post Doctoral Fellowship

 

Postdoctoral fellowships are available for outstanding and ambitious synthetic organic chemists in the Medicinal Chemistry Department. Successful candidates must be highly motivated and able to work as part of an interdisciplinary team focused on drug discovery. Since candidates will be required to undergo an interview

Key Responsibilities

Ø      Organic synthesis, purification, and analysis of novel small molecule compounds

Ø      Utilize various methods to perform synthesis under general direction

Ø      Independently evaluate and troubleshoot synthesis problems

Required Skills

     Ø      Multi-step synthesis of small molecules and their characterizations by techniques such as Chromatography, NMR, IR, MS & Spectrophotometry

Ø      Parallel or combinatorial synthesis

Ø      Medicinal Chemistry knowledge is desirable

Qualifications

      Ø      Fresh Ph. D in Organic / Medicinal Chemistry

Ø      Knowledge of scientific principles and concepts in the field is expected

Ø      Experience in the pharmaceutical industry will be considered advantageous

Ø      Good oral and written communication skills

Ø      Ability to work in teams

Duration:  The position is for one year

Application

Interested candidates should send curriculum vitae, brief summary of research experience and the names, email addresses with contact number of 3 references, one of whom must be your current supervisor. Please send application by email to the following address:   careers@aurigene.com 

 

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Research Assistant/ Associate and Lab Leaders – 2+ Years Relevant Experience – Aurigene, Bangalore

Posted on December 22, 2008. Filed under: Pharmaceutical | Tags: , , |

Aurigene

Established in Bangalore, India, in 2002, Aurigene is a drug discovery biotech with a proven track record of successful partnerships with 10 collaborators globally. Aurigene has a pipeline of 15 discovery programs, at various stages from Hit Generation to late-stage Pre-Clinical Optimization, and has filed multiple patents in these Discovery Programs.

With proprietary Structural Biology and Fragment-based Drug Design technology platforms, and experienced scientific leadership, Aurigene is a fully integrated operation with expertise in Target Validation Biology and Hit Generation to IND nomination. Focus TAs includes Oncology, Metabolic disorders and Autoimmune/ Inflammatory diseases.

This Job is posted in http://www.aurigene.com/index.php?option=com_content&view=article&id=51&Itemid=128 for more details visit  http://www.aurigene.com/index2.php?option=com_content&view=article&id=53

Position Description:  Research Assistant/ Associate and Lab Leaders      

Position Code:
   001

Location:
   Bangalore

Research Assistant/ Associate and Lab Leaders

We are seeking highly motivated entry level and experienced research assistants/ associates in our medicinal chemistry group. This individual will be a critical member of our chemistry team focused on the preparation of small molecule therapeutics for targeted proteins.

Key Responsibilities

  • Organic synthesis, purification, and analysis of novel small molecule compounds
  • Utilize various methods to perform synthesis under general direction
  • Independently evaluate and troubleshoot synthesis problems

    Required Skills

  • Multi-step synthesis of small molecules and their characterizations by techniques such as     Chromatography, NMR, IR, MS & Spectrophotometry
  • Parallel or combinatorial synthesis
  • Medicinal Chemistry knowledge is desirable

    The selected candidates will become members of our Multidisciplinary Drug Discovery teams for the development of novel therapeutic entities.

    Qualifications
     

  • MS/ Ph. D in chemistry
  • Knowledge of scientific principles and concepts in the field is expected
  • Experience in the pharmaceutical industry will be considered advantageous
  • Good oral and written communication skills
  • Ability to work in teams

    Experience
    2-3 years in the relevant areas. Candidates with more than 5 years’ experience and post-doc experience abroad will be considered for the role of Lab Leader managing a team of chemists.

 

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Job Opening for Consultant Pathologist with 3 Years Experience @ Dr Lal PathLabs (LPL), Delhi / NCR

Posted on December 22, 2008. Filed under: Pharmaceutical | Tags: , , , , , |

Dr Lal PathLabs (LPL), a centre of innovation and a premier clinical pathology laboratory was established in 1949 by the late Dr (Major) S K Lal, a pioneer in the field of pathology who had been trained in the Army and later at the Cook County Hospital, Chicago, USA . He used his expertise and knowledge to establish an organisation that was destined to become the first Pathology Laboratory of repute in Delhi and Northern India.

Dr Arvind Lal, the present Chairman and Managing Director took over the reins of LPL In 1977. His mission is to provide the best laboratory services to patients in India at the most economical costs. He embarked upon a modernisation programme keeping in view the rapid global advancements in the field of laboratory medicine. Constant upgradation of equipment, introduction of newer diagnostic parameters, automation and strict quality assurance were the hallmarks of his able guidance. These practices enabled LPL to emerge as the Number One Pathology laboratory in India providing diagnostic services to patients, doctors, hospitals, pharmaceutical companies and government agencies.

This Job is posted in http://www.lalpathlabs.com for more details visit  http://www.lalpathlabs.com/NewlplSite/career_currentopenings.aspx?PGID=2

Job Description:

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Designation Consultant Pathologist
 Location

Delhi / NCR

 Qualifications
 Experience

MBBS, MD with min three yrs of exp of handling fully automated pathology laboratory

 Job Posted Date
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Job Opening for Phlebotomist with 3 yrs of exp of Sampling @ Dr Lal PathLabs (LPL), Ahmedabad, Baroda

Posted on December 22, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

Dr Lal PathLabs (LPL), a centre of innovation and a premier clinical pathology laboratory was established in 1949 by the late Dr (Major) S K Lal, a pioneer in the field of pathology who had been trained in the Army and later at the Cook County Hospital, Chicago, USA . He used his expertise and knowledge to establish an organisation that was destined to become the first Pathology Laboratory of repute in Delhi and Northern India.

Dr Arvind Lal, the present Chairman and Managing Director took over the reins of LPL In 1977. His mission is to provide the best laboratory services to patients in India at the most economical costs. He embarked upon a modernisation programme keeping in view the rapid global advancements in the field of laboratory medicine. Constant upgradation of equipment, introduction of newer diagnostic parameters, automation and strict quality assurance were the hallmarks of his able guidance. These practices enabled LPL to emerge as the Number One Pathology laboratory in India providing diagnostic services to patients, doctors, hospitals, pharmaceutical companies and government agencies.

This Job is posted in http://www.lalpathlabs.com for more details visit  http://www.lalpathlabs.com/NewlplSite/career_currentopenings.aspx?PGID=2

Job Description:

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Designation Phlebotomist
 Location

Ahmedabad, Baroda

 Qualifications
 Experience

DMLT with three yrs of exp of sampling. Should have knowledge of vaccutainer.

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Job Opening for Lab Administrator with 3+ Years Experience @ Dr Lal PathLabs (LPL)

Posted on December 22, 2008. Filed under: Pharmaceutical | Tags: , , , , |

Dr Lal PathLabs (LPL), a centre of innovation and a premier clinical pathology laboratory was established in 1949 by the late Dr (Major) S K Lal, a pioneer in the field of pathology who had been trained in the Army and later at the Cook County Hospital, Chicago, USA . He used his expertise and knowledge to establish an organisation that was destined to become the first Pathology Laboratory of repute in Delhi and Northern India.

Dr Arvind Lal, the present Chairman and Managing Director took over the reins of LPL In 1977. His mission is to provide the best laboratory services to patients in India at the most economical costs. He embarked upon a modernisation programme keeping in view the rapid global advancements in the field of laboratory medicine. Constant upgradation of equipment, introduction of newer diagnostic parameters, automation and strict quality assurance were the hallmarks of his able guidance. These practices enabled LPL to emerge as the Number One Pathology laboratory in India providing diagnostic services to patients, doctors, hospitals, pharmaceutical companies and government agencies.

This Job is posted in http://www.lalpathlabs.com for more details visit  http://www.lalpathlabs.com/NewlplSite/career_currentopenings.aspx?PGID=2

Job Description:

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Designation Lab Administrator
 Location

Location all across the county

 Qualifications
 Experience

min three yrs of exp of handling a small lab , preferably science background. Candidate would be required to take care of general administrative functions, accounts, stores purchase, logistics, customer care at the lab level

 Job Posted Date
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Job Opening for Assistant Manager – Production with 4+ Years Experience @ Claris Lifesciences

Posted on December 18, 2008. Filed under: Pharmaceutical | Tags: , , , , , , , , |

Claris Lifesciences

Claris Lifesciences is an international pharmaceutical company, in the business of manufacturing and marketing of high end injectables with focus on New Drug Delivery Systems for treatment of critical illnesses and diseases.

Having established its presence in India in 1999, Claris continues to grow from strength to strength with every passing year.

Claris enjoys market leadership across several products and categories in India including propofol, parenteral nutrition and IV fluids. The company continuously endeavours to support upgrade of medical care in the country with the introduction of breakthrough new products and technologies. It has several firsts to its credit including

This Job is posted in http://www.clarislifesciences.com/  for more details visit http://www.clarislifesciences.com/currentopenings_Manuf.asp

Job Title :   Assistant Manager – Production

Location : Ahmedabad

Description :

B Pharm / MSC with 4 – 6 years of experience is required to handle entire function of production of a particular plant. The candidate would be responsible for managing, manufacturing through target achievement, accurate housekeeping and inventory management.Should also have minimum 2 years of experience in Injectable with exposure of working in MHRA / TGA approved plant.
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Job Opening for QA Manager with 6+ Years Experience @ Claris Lifesciences, Ahmedabad

Posted on December 18, 2008. Filed under: Pharmaceutical | Tags: , , , , , , , , , |

Claris Lifesciences

Claris Lifesciences is an international pharmaceutical company, in the business of manufacturing and marketing of high end injectables with focus on New Drug Delivery Systems for treatment of critical illnesses and diseases.

Having established its presence in India in 1999, Claris continues to grow from strength to strength with every passing year.

Claris enjoys market leadership across several products and categories in India including propofol, parenteral nutrition and IV fluids. The company continuously endeavours to support upgrade of medical care in the country with the introduction of breakthrough new products and technologies. It has several firsts to its credit including

This Job is posted in http://www.clarislifesciences.com/  for more details visit http://www.clarislifesciences.com/currentopenings_Manuf.asp

Job Title :   Manager QA

Location : Ahmedabad

Description :

B Pharm / MSC with 6 – 8 years of experience, is required to handle entire function of QA of a particular plant. He would be responsible for In-process QA, Process Validation and Micro Validation. The candidate should have experience of working in Injectables, at least for 2 years.

Should have exposure of reviewing & authorizing SOPs, documentation of CC and other critical situations and internal quality audits.

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Job Opening for TRAINEE RESEARCH ASSOCIATES @ Jubilant Chemsys , Noida

Posted on December 18, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

Jubilant Chemsys , Noida

Jubilant Chemsys Limited offers medicinal chemistry services for the global pharmaceutical and biotech industries. We are a wholly owned subsidiary of Jubilant Organosys Limited, a composite pharmaceutical industry player with a turnover of over US$ 250 million and ~2300 employees. Jubilant Organosys is the largest custom research and manufacturing services (CRAMS) company and a leading manufacturer of active pharmaceutical ingredients in India.

We at Jubilant Chemsys are striving to be a world leader in offering discovery chemistry solutions and are actively looking for top-class talent to be a part of our team.

Jubilant Chemsys provides freehanded work environment, a culture that is open, transparent and performance oriented, a place where you are provided with countless opportunities to learn and grow. We thrive on teamwork and encourage creativity and out of the box thinking in order to deliver innovative, world-class products and services to our clients.

This Job is posted in http://www.jchemsys.com   for more details visit http://www.jchemsys.com/po.htm

Job Description : TRAINEE RESEARCH ASSOCIATES

Education : M.Sc. in Organic/ Medicinal Chemistry
The candidate should be first division holder and from an institute of repute.

Location : Noida

Experience :  Fresher

Contact Details
    
If a promising career with Jubilant Chemsys excites you, then please email your resume to careers@jchemsys.com

Or post at the following address:

Jubilant Chemsys Ltd.
D – 12, Sector 59
NOIDA – 201 301.
INDIA.

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Job Opening for RESEARCH ASSOCIATES with 2 to 3 Years Experience @ Jubilant Chemsys , Noida

Posted on December 18, 2008. Filed under: Pharmaceutical | Tags: , , , , , |

Jubilant Chemsys , Noida

Jubilant Chemsys Limited offers medicinal chemistry services for the global pharmaceutical and biotech industries. We are a wholly owned subsidiary of Jubilant Organosys Limited, a composite pharmaceutical industry player with a turnover of over US$ 250 million and ~2300 employees. Jubilant Organosys is the largest custom research and manufacturing services (CRAMS) company and a leading manufacturer of active pharmaceutical ingredients in India.

We at Jubilant Chemsys are striving to be a world leader in offering discovery chemistry solutions and are actively looking for top-class talent to be a part of our team.

Jubilant Chemsys provides freehanded work environment, a culture that is open, transparent and performance oriented, a place where you are provided with countless opportunities to learn and grow. We thrive on teamwork and encourage creativity and out of the box thinking in order to deliver innovative, world-class products and services to our clients.

This Job is posted in http://www.jchemsys.com   for more details visit http://www.jchemsys.com/po.htm

Job Description : RESEARCH ASSOCIATES

Education : M.Sc. in Organic/ Medicinal Chemistry
The candidate should be first division holder and from an institute of repute with 2-3 years of relevant work experience.

Location : Noida

Experience :  2-3 years of relevant work experience.

Contact Details
    
If a promising career with Jubilant Chemsys excites you, then please email your resume to careers@jchemsys.com

Or post at the following address:

Jubilant Chemsys Ltd.
D – 12, Sector 59
NOIDA – 201 301.
INDIA.

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Job Opening for TRAINEE RESEARCH SCIENTIST @ Jubilant Chemsys , Noida

Posted on December 18, 2008. Filed under: Pharmaceutical | Tags: , , , , |

Jubilant Chemsys , Noida

Jubilant Chemsys Limited offers medicinal chemistry services for the global pharmaceutical and biotech industries. We are a wholly owned subsidiary of Jubilant Organosys Limited, a composite pharmaceutical industry player with a turnover of over US$ 250 million and ~2300 employees. Jubilant Organosys is the largest custom research and manufacturing services (CRAMS) company and a leading manufacturer of active pharmaceutical ingredients in India.

We at Jubilant Chemsys are striving to be a world leader in offering discovery chemistry solutions and are actively looking for top-class talent to be a part of our team.

Jubilant Chemsys provides freehanded work environment, a culture that is open, transparent and performance oriented, a place where you are provided with countless opportunities to learn and grow. We thrive on teamwork and encourage creativity and out of the box thinking in order to deliver innovative, world-class products and services to our clients.

This Job is posted in http://www.jchemsys.com   for more details visit http://www.jchemsys.com/po.htm

Job Description : TRAINEE RESEARCH SCIENTIST

Education : Fresh Ph.Ds in specializing in Organic/ Medicinal Chemistry from a Reputed Institute/Universities

Location : Noida

Experience :  Fresher

Contact Details
    
If a promising career with Jubilant Chemsys excites you, then please email your resume to careers@jchemsys.com

Or post at the following address:

Jubilant Chemsys Ltd.
D – 12, Sector 59
NOIDA – 201 301.
INDIA.

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Job Opening for SENIOR SCIENTISTS with 2 to 3 Years @ Jubilant Chemsys , Noida

Posted on December 18, 2008. Filed under: Pharmaceutical | Tags: , , , , |

Jubilant Chemsys , Noida

Jubilant Chemsys Limited offers medicinal chemistry services for the global pharmaceutical and biotech industries. We are a wholly owned subsidiary of Jubilant Organosys Limited, a composite pharmaceutical industry player with a turnover of over US$ 250 million and ~2300 employees. Jubilant Organosys is the largest custom research and manufacturing services (CRAMS) company and a leading manufacturer of active pharmaceutical ingredients in India.

We at Jubilant Chemsys are striving to be a world leader in offering discovery chemistry solutions and are actively looking for top-class talent to be a part of our team.

Jubilant Chemsys provides freehanded work environment, a culture that is open, transparent and performance oriented, a place where you are provided with countless opportunities to learn and grow. We thrive on teamwork and encourage creativity and out of the box thinking in order to deliver innovative, world-class products and services to our clients.

This Job is posted in http://www.jchemsys.com   for more details visit http://www.jchemsys.com/po.htm

Job Description : SENIOR SCIENTISTS
    
Education :
Ph.Ds in specializing in Organic/ Medicinal Chemistry from a Reputed Institute/Universities .

Location : Noida

Experience :  2-3 Yrs Postdoc experience abroad and working experience in Pharma Industry.

Contact Details
    
If a promising career with Jubilant Chemsys excites you, then please email your resume to careers@jchemsys.com

Or post at the following address:

Jubilant Chemsys Ltd.
D – 12, Sector 59
NOIDA – 201 301.
INDIA.

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Job Opening for Clinical Safety Team Leader @ India Novartis Healthcare Private Limited, Hyderabad

Posted on December 17, 2008. Filed under: Pharmaceutical | Tags: , , , |

Novartis

Novartis offers a wide range of healthcare products through our Pharmaceuticals, Vaccines and Diagnostics, Sandoz and Consumer Health Divisions.

Novartis Vaccines & Diagnostics is a new division of Novartis consisting of two business focusing on the development of preventive treatments and tools. Novartis Vaccines is the world’s fifth-largest vaccines manufacturer and second-largest supplier of flu vaccines in the United States. Chiron, the blood testing and molecular diagnostics business, is dedicated to preventing the spread of infectious diseases through the development of novel blood-screening tools that protect the world’s blood supply.

This Job is posted in http://www.novartis.com  for more details visit http://www.novartis.com/careers/job-search/brassring/index.shtml

Job ID 31786BR
Posting Title Clinical Safety Team Leader
Division Pharmaceuticals
Business Unit General Medicines
Country India
Work Location India – Hyderabad
Company/Legal Entity India Novartis Healthcare Private Limited
Posting Functional Area Development
Job Type Full Time
Employment Type Permanent
Job Description 1. Manage and lead his/her team and ensure that all tasks are performed according to business rules, guidelines and standard operating procedures; Monitor workload and allocate resources appropriately.
2. Ensure the development of processes and procedures to meet global safety reporting requirements and the management of incoming adverse event reports.
3. Maintain high level of compliance for processing of incoming adverse events reports by the team according to internal timeframes and Health Authorities requirements.
4. Communicate achievements, issues and actions regularly with Global Management
5. Set up yearly objectives and review performances of team ensuring best use of available re-sources. Discuss and set up development plans with/for all team members to further develop individual’s skills and potentials.
6. Facilitate training for new hires according to the individuals’ experience and needs.
7. Review entered case reports and monitor the quality of work produced by the team and implement quality improvement initiatives as appropriate.
8. Alert global management to potential safety signals based on incoming case reports
9. QC periodic regulatory safety reports before submission to management approval and ensure compliance with required timelines.
10. Promote working relationships between Integrated Medical Safety and other groups such as; other members of Integrated Medical Safety, medical personnel, Clinical Data Management, Clinical Research, Marketing.
11. Play an active/leading role in cross-functional teams on safety matters/ Integrated Medical Safety special projects relating to investigational and marketed drugs.
12. Facilitate the training of other departments in clinical safety related procedures/regulatory obligations.
13. Support and work closely with manager to set group strategy and achieve group objectives.
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Job Openings for Sr. Instrument Mechanics / Instrument Mechanics with 2 to 9 Years @ Ochoa Laboratories Limited

Posted on December 10, 2008. Filed under: Pharmaceutical | Tags: , , , , , , |

Ochoa Laboratories Limited one of the fastest growing pharmaceutical Company in India, commenced operations in 1995. In the past one & a half decade the company has grown at a rapid pace and has today made a respectable position in the organized Indian Pharmaceutical Sector. The company is set to become one of the top Indian pharmaceutical companies by 2015 and is rapidly moving towards becoming a globally recognized company through strategic alliances & partnerships with global pharma companies.

The Company is highly respected by the medical profession and trade. Ochoa Products are widely prescribed by the medical profession in India and some of the top products like Dobesil, Ivermectol, Carnivit, Essvit, tacrovate, Wormectol & Zincoa feature among the top brands of the Industry.

Ochoa’s new world class formulation manufacturing facility will be operational by April 2008 which conforms to UKMHRA USFDA norms and the company is gearing itself towards obtaining USFDA, UKMHRA regulatory approvals by mid of 2009.

This JOb is posted in http://www.ochoalabs.com/ for more details visit http://www.ochoalabs.com/careers/careers_job.php?career_sid=3

Sr. Instrument Mechanics / Instrument Mechanics (OCPL-ME010)

Maintenance & Engineering

Qualification : ITI Instrument / Electronic / Electrical. Experience : 2 to 9 years, knowledge of instrumentation , calibration, troubleshooting of PLC, AC/DC drives and other instrument related equip. pharma plant machineries maintenance (Capsule/Tablet/Ointment/Syrup). Knowledge of instrumentation and computer preferable.

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Job Opening for Quality Assurance Executive with 3 to 4 Years experience @ Ochoa Laboratories Limited

Posted on December 10, 2008. Filed under: Pharmaceutical | Tags: , , , |

Ochoa Laboratories Limited one of the fastest growing pharmaceutical Company in India, commenced operations in 1995. In the past one & a half decade the company has grown at a rapid pace and has today made a respectable position in the organized Indian Pharmaceutical Sector. The company is set to become one of the top Indian pharmaceutical companies by 2015 and is rapidly moving towards becoming a globally recognized company through strategic alliances & partnerships with global pharma companies.

The Company is highly respected by the medical profession and trade. Ochoa Products are widely prescribed by the medical profession in India and some of the top products like Dobesil, Ivermectol, Carnivit, Essvit, tacrovate, Wormectol & Zincoa feature among the top brands of the Industry.

Ochoa’s new world class formulation manufacturing facility will be operational by April 2008 which conforms to UKMHRA USFDA norms and the company is gearing itself towards obtaining USFDA, UKMHRA regulatory approvals by mid of 2009.

This JOb is posted in http://www.ochoalabs.com/ for more details visit http://www.ochoalabs.com/careers/careers_job.php?career_sid=2

Executive (OCPL-QA008)

Quality Assurance

Qualification : Pharmacy Graduate / Post Graduate in microbiology / Biochemistry. Experience : 3 to 4 years process validation and cleaning validation for oral dosage forms.

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Job Openings for Dy. Manager / Asst. Manager with 6 to 10 Years experience in Maintenance & Engineering @ Ochoa Laboratories Limited, Noida

Posted on December 10, 2008. Filed under: Pharmaceutical | Tags: , , , , , |

Ochoa Laboratories Limited one of the fastest growing pharmaceutical Company in India, commenced operations in 1995. In the past one & a half decade the company has grown at a rapid pace and has today made a respectable position in the organized Indian Pharmaceutical Sector. The company is set to become one of the top Indian pharmaceutical companies by 2015 and is rapidly moving towards becoming a globally recognized company through strategic alliances & partnerships with global pharma companies.

The Company is highly respected by the medical profession and trade. Ochoa Products are widely prescribed by the medical profession in India and some of the top products like Dobesil, Ivermectol, Carnivit, Essvit, tacrovate, Wormectol & Zincoa feature among the top brands of the Industry.

Ochoa’s new world class formulation manufacturing facility will be operational by April 2008 which conforms to UKMHRA USFDA norms and the company is gearing itself towards obtaining USFDA, UKMHRA regulatory approvals by mid of 2009.

This JOb is posted in http://www.ochoalabs.com/ for more details visit http://www.ochoalabs.com/careers/careers_job.php?career_sid=2

Dy. Manager / Asst. Manager (OCPL-PR002)

Maintenance & Engineering

Qualification: B.E / Diploma in Electrical Instrument. Experience : 6-10 years, Knowledge of Pharma plant machineries maintenance (Capsule/Tablet/Ointment/Syrup)and utilities maintenance, documentation, awareness of SAP and cGMP.

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Job Openings for Asst. Manager / Section Head in Production with 5 to 8 Years experience @ Ochoa Laboratories Limited, Noida

Posted on December 10, 2008. Filed under: Pharmaceutical | Tags: , , , , , , , |

Ochoa Laboratories Limited one of the fastest growing pharmaceutical Company in India, commenced operations in 1995. In the past one & a half decade the company has grown at a rapid pace and has today made a respectable position in the organized Indian Pharmaceutical Sector. The company is set to become one of the top Indian pharmaceutical companies by 2015 and is rapidly moving towards becoming a globally recognized company through strategic alliances & partnerships with global pharma companies.

The Company is highly respected by the medical profession and trade. Ochoa Products are widely prescribed by the medical profession in India and some of the top products like Dobesil, Ivermectol, Carnivit, Essvit, tacrovate, Wormectol & Zincoa feature among the top brands of the Industry.

Ochoa’s new world class formulation manufacturing facility will be operational by April 2008 which conforms to UKMHRA USFDA norms and the company is gearing itself towards obtaining USFDA, UKMHRA regulatory approvals by mid of 2009.

This JOb is posted in http://www.ochoalabs.com/ for more details visit http://www.ochoalabs.com/careers/careers_job.php?career_sid=2

Asst. Manager / Section Head (OCPL-PR001)

Production

Qualification : B Pharma / M Pharma. Experience : 5 to 8 years in semisolid preparations in both steroidal & non steroidal. Must be approved as “Competent Technical Staff” in manufacturing of semisolid dosage form(Ointment) and oral liquid from state drug authority.

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Project Manager -Clinical Trials, 5-6 years of overall experience – PAREXEL International, Hyderabad

Posted on December 29, 2006. Filed under: Hyderabad, Pharmaceutical, Project Manager |

My Client, PAREXEL International, is one of the largest pharmaceutical services companies in the world, delivers a full range of services and solutions through their 37 offices worldwide. My client is actively on look out for a Project Manager (Clinical Trials)

Job Title: Project Manager -Clinical Trials
Job Location: Hyderabad ,INDIA
Service Unit:Clinical Research Services

Essential Functions:
Provide overall management of clinical trials or clinical programs. General areas of responsibility include: Sponsor liaison, project assessment and initiation, resource procurement and planning, project implementation, leading and motivating a cross-functional team, milestone planning and tracking, ensuring that projects are progressing according to contract and quality standards, SOPs, ICH-GCP and/or other guidelines to fulfill local regulations, production of key project progress reports, management of communication between PAREXEL project team, Sponsor, contract and financial management.

Primary Role of the Project Manager:
· Manage domestic or international projects. May be part of a global project management team. Requires some interaction/supervision by Line Manager or Senior Project Manager or Director.
· May mentor Associate Project Managers and FLs for specific project.
· Participate in proposal development teams, giving input to particular indication and operational structure for the proposal.
· Represent Project Management at marketing/new business meetings.

Relationships:
Works Closely With: Sponsor Project managers, Clinical Research Directors, Quality, Process and Training (QPT), Project Assistants, Functional Leads, Line Managers, Project Team Members, all groups within Consulting and Clinical Research Services, WW Business Operations (BusOps), Account Management, Perceptive Informatics and Finance.

External Relationships: Sponsor counterparts and management, investigators, third party contractors, regulatory authorities.

Qualifications:
• Bachelor of Science degree required, Masters Degree preferred
• 5-6 years of overall experience out of which 3 + years must be in project management
• Willingness/comfort with 60% to 80% travel
• Demonstrated project management skills including the ability to plan a project and operate within plan and budget
• Demonstrated ability to perform assessments and present findings to audiences of varying skill set and knowledge base
• Clinical implementation experience preferred
• Solid understanding of the implementation and client services process and the various interdependencies between operations and technology, both internal and external
• Mastery of the following Microsoft Office applications, including Outlook, Excel, and Word; proficiency with PowerPoint and Access
• training techniques, excellent client-facing skills and the ability to simultaneously champion the cause of the client and serve as an advocate for the company.

Responsibilities:
• Independently develop, manage, execute, and own overall project plan and timelines for key deliverables
• Lead and manage project team to ensure timely and effective completion of project assignment and other tasks
• Direct implementations and serve as primary client contact on implementations
• Establish clear definition of clients’ implementation responsibilities and company’s responsibilities with each client
• Establish a clear understanding of client’s key metrics prior and determine clear quantifiable expectations for the customer once fully implemented
• Perform general practice, workflow, and staffing assessments of prospective client organizations
• Collaborate in the ongoing development of the implementation process and other client services the team provides
• Collaborate in the ongoing development of training materials and curricula
• Organize and lead training sessions
• Administer end user proficiency tests
• Provide on site support during the “go live” period

Thanks
Anil Shrivastava
Kenexa®
HIRING & RETENTION
Outsourcing | Employee Research | Software
# 603, 6th Floor, Aditya Trade Centre,
Ameerpet, Hyderabad – 500038.
Tel: +91 40 39113911 x 105
Cell: 9949358856
610.971.6911 v

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