Opening as Senior Chemists - QC in Wings Pharmaceuticals

WINGS PHARMACEUTICALS PVT. LTD.  is a Delhi based fast growing, professionally managed pharmaceutical company.From a humble beginning through wholesale shop, the burning desire to serve the society, crystallised into a modern manufacturing output in 1989 under the able leadership of the Managing Director Mr. R.P. Arora, a man of great vision. He always believed in very cautious but firm steps in matters of expansion and advancement of the company.
Post: Senior Chemists - QC
Job Description:
1) Responsible for Analysis of intermedates, Raw materials, inprocess samples, stabilty samples finished products with help of HPLC,FTIR etc.,
2) Qualitative & Quantitative analysis, Documentation, Validation etc.
3) Should have good exposure to face Audits
Additional Information:
Experience: 3-4 years
Location: Baddi
Education: B.Pharm, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: QC
End Date: 24^th March, 2012
Forward CVs to, hrbaddi@wingspharma.com

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Career as State Business Manager at Piramal Healthcare Ltd

Piramal Healthcare Ltd, a Piramal Group company, is a globally integrated healthcare company that fulfills unmet medical needs across the world. It has a growth track record of above 29% CAGR since 1988. Piramal Healthcare had consolidated revenues of US$ 656 million in FY2009. PHL is currently ranked 4th in the Indian market with a diverse product portfolio spanning several therapeutic areas. It is also one of the largest custom manufacturing companies with a global footprint of assets across North America, Europe and Asia.

Post: State Business Manager

Job Description:
The person will be primarily responsible for:
Driving sales across Bio chemistry, Immunology and Haematology range of Products in Mumbai region
Managing Key Accounts and ensuring Profitability from those accounts
Should have knowledge of analyzers of leading diagnostic companies and troubleshooting of minor problems

Candidate Profile:
The desired candidate should have 6-7 years of dynamic sales experience in Diagnostics Products from the related organizations.
The Candidate will be responsible for managing a team and therefore should have excellent Man Management and Communication Skills.

Interested candidates may send their CVs on phl.careers@piramal.com

Additional Information:
Experience: 6-7 years
Location: Mumbai
Education: B.Pharm, B.Sc, Any
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Sales, BD
End Date: 12^th March, 2012

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Opportunity as Clinical Data Manager - CDM @ Novartis Healthcare

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: Clinical Data Manager - CDM

Job Description:
1. Provide professional DM input on Clinical Trial Team(s)
2. Input to and review of clinical trial database design including User Acceptance Testing (UAT).
3. Responsible for the Validation and Analysis Plan (VAP) meeting for the clinical trial, which includes chairing the meeting, writing the study specific validation checks and necessary reports to ensure high quality and consistent data.
4. Identify errors and inconsistencies; resolve them or initiate their resolution either via the field monitor or directly with the investigational site, to ensure high quality and timely database locks.
5. Review and contribute to preparation of protocols, specifically related to the data management section, visit schema and study design.
6. Prepare Case Report Forms (CRFs) and CRF completion Guidelines (CCGs), electronic or paper.
7. Support and provide leadership for data management staff for allocated trials.
8. Freeze and lock data as appropriate in time for statistical review, blinded interim quality review, interim and final database lock.
9. Perform training on data management software and practices or trial specific topics as required.
10. Prepare training materials for data management activities and processes as required.
11. Travel is required as needed.

Candidate Profile:
University Science Degree in life sciences, pharmacy, nursing or equivalent relevant experience.

1. 2 or more years experience in drug development with at least 2 years experience in Data Management.
2. University Science Degree in life sciences, pharmacy, nursing or equivalent relevant experience.
3. Excellent written and oral English skills
4. Understanding of clinical trial methodology, GCP and medical terminology
5. Good computer skills
6. Good organizational and project management skills.
7. Good communication and interpersonal skills
8. Intermediate presentation and problem solving skills
9. Ability to work well in a team
10. May coordinate and provide direction on task to other data management team members.

Additional Information:
Location: Hyderabad
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
Division: Pharma
Job Type: Full Time
Employment Type: Permanent
Job ID: 92624BR
End Date: 6^th March, 2012

To Apply  CLICK HERE

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Abbott invites applications for Regulatory Quality Compliance Associate - AV

Abbott India Limited is a subsidiary of Abbott Laboratories, USA, a global, iversified health care company devoted to the discovery, development, manufacture and marketing of pharmaceutical, diagnostic, nutritional and hospital products. The company now employs approximately 70,000 people and markets its products in 130 countries worldwide.

Post: Regulatory Quality Compliance Associate - AV

Job Description:

• To strategies for regulatory approvals as per annual registration plans 
• To prepare dossiers and submissions for various regulatory fillings
• To deal efficiently and effectively with regulatory agencies for regulatory issues.
• Management of the complaint handling system and the adverse event reporting systems
• To assist in handling various regulatory queries
• To prepare and submit PSURS for four years after approval to the regulatory authority
• To prepare and submit all PMS reports, Adverse Event Reports and other safety reports to the regulators
• Technical Evaluation of the dossiers and files obtained from US regulatory for submission in India
• Regularly gets updated and self trained with the latest regulations on Medical devices in the country
• Liasioning with the Regulatory agencies both at centre and state level
• Scrutiny and internal regulatory Audits of Quality system as per guidelines and SOPs
• Creates / develops regular checklists based on overall business regulatory plans as assigned.
• Evaluates the adequacy and compliance of systems, operations and practices against regulations and company documentation 
• Tracks issues through to closure including reviewing corrective action taken 
• To implement/coordinate changes per field notifications received from Manufacturing sites (stop shipment, recalls etc)

Additional Information:
Exp: 2-6 yrs
Location: Mumbai
Education: B.Sc. or B.Pharma with Diploma in Regulatory Affairs
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: DRA
Keyword or Job ID: 108593BR
End Date: 5^th March, 2012

To Apply , Click Here

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