Research and Development jobs

The primary focus of the Area Development Manager (ADM) is to support the attainment of area sales performance objectives. The position is responsible for monitoring operations and identifying and pursuing opportunities to improve business results with the area.
The incumbent must strictly abide by all Wyeth policies, Wyeth Code of Conduct and government regulations.

Job Responsibilities

Operational

Evaluate field sales resource alignment (MyPA) and make recommendations to ABD
Manage field sales resource distribution and program funding requests (MDRA Tool)
Provide input into the POA meeting structure and content
Manage logistics for POA Meeting
Take lead on area projects, e.g. surveys, rebate programs and recognition programs
Participate in job fairs and other recruiting opportunities
Take leadership role in area level convention management.

Manage a program in the development of safe, economical and scaleable processes for the commercial manufacture of active pharmaceutical ingredients (APIs). Provide expertise to the solution of problems that arise in the preparation of APIs. Assemble and write transfer of technology packages for Pilot Plants and Production units.

Job Responsibilities
Conduct experimentation aimed at devising and optimizing safe, economical and scaleable processes for the synthesis, isolation and purification of APIs. Develop research programs that lead to robust chemical processes.
Manage and carry out process development activities to support further scale-up of API for transfer to internal scale-up facilities or 3rd party suppliers.
Prepare technical reports and documents for technology transfer packages, assist in the transfer of chemical processes to scale-up facilities, and troubleshoot large-scale API manufacturing processes.

Plan and implement projects with minimal supervision. Conduct laboratory work aimed at developing processes for the manufacture of pharmaceutical ingredients (APIs). Solve problems that arise during process optimization activities. Prepare technical reports and technology transfer documents for technology transfer to external 3rd party plant operations. Support preparation of API for late stage development and manufacturing.

Job Responsibilities
Evaluate and optimize synthetic routes for APIs.
Propose alternate synthetic options
Develop robust conditions for scale up of chemical reactions
Identify process by-products and devise appropriate in-process tests.
Analyze mechanistic interpretation of competing process pathways
Keep abreast of breaking technical developments in organic chemistry, process development, automated reaction screening.
Provide technical reports and technical transfer documents.

Provide veterinary support to the Research and Development and Quality Control animal colonies

RESPONSIBILITIES:
• Coordinate required animal health related documentation for Research and Development and Quality Control.
• In conjunction with Bio QC and Animal Care personnel, coordinates animal testing activities.
• Collect and process diagnostic samples.
• Maintain Veterinary Services equipment and drug stocks.
• Provide assistance to the Veterinary Services veterinarians in performing animal work and other tasks as assigned. Such as vaccinations and animal test challenges, as well as assistance to plant veterinarians and investigators.
• Facilitate Research and Development and Quality Control animal matters whenever possible.

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Plan, coordinate and conduct molecular microbiology and animal studies for developing biotechnology-derived new generation vaccines.
• Develop and improve the testing methods of virology, immunology, and molecular biology.
• Write study protocols, IACUC and reports.
• Organize, analyze and present research data to supervisor and working group.
• Supervise scientists working within the laboratory and perform technical trouble-shooting..

BASIC QUALIFICATIONS
• Within a field of microbiology, immunology, animal vaccinology, or related scientific discipline, Bachelor of Science and 8 years relevant experience or Master of Science and 6 years relevant experience or PhD.

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Maintain and operate high capacity automated cell culture system

Maintenance and passage of cell lines

Detailed tracking of large cell line inventory and all the associated components

Develop, implement, and operate high throughput cell based screening systems

Utilize and optimize automated data analysis software

Develop and optimize new cell based assay technologies using traditional and novel formats
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Serve as counsel to Wyeth Consumer Healthcare, a leader in the research, development, manufacturing and marketing of a broad range of consumer healthcare products (e.g., Advil®, Centrum®, Caltrate®, ChapStick®, Robitussin®, Dimetapp®, etc.) operating in over 65 countries, with 2006 sales of $2.5 billion. Work closely with Senior Vice President & Chief Counsel as part of a small-dedicated legal team servicing the global consumer healthcare business.

Job Responsibilities

*Manage a diverse range of important legal issues while providing legal counsel and analysis to help accomplish business objectives; and,

GSK R&D China (Shanghai) will focus on research in neurodegenerative diseases including multiple sclerosis, Alzheimer's disease and Parkinson's disease. The site will direct GSK global drug discovery and development activities in the above disease indications, from drug target identification to late-stage clinical studies, while collaborating with research institutions elsewhere in China and other countries. We offer internationally-competitive salary, benefit and relocation package.

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1. Together with CEDD, CEEDD and MDC members, identify potential in-licensing opportunities and where appropriate co-ordinate pitch meetings to partners with assets of strategic interest to GSK. Provides a WWBD point of scientific accountability to CEDD and/or MDC. Contributes broadly to the therapeutic area strategy based on technical expertise and knowledge of GSK in-house projects and work ongoing external to GSK.
Lead technical evaluation of in-licensing opportunities in line with CEDD and MDC therapy area strategic focus. Provides an in-licensing context to the therapeutic area strategy.
2. Leading a GSK Matrix team (encompassing CEDD/DDM, CEEDD and MDC employees) that carries out a technical evaluation of potential in-licensing candidates.