For more than 20 years, as Albany Molecular Research Inc. (AMRI), we have provided fully integrated drug discovery, development and manufacturing services – all while adapting to the rapidly changing needs of our customers within the pharmaceutical, biotechnology and related industries.
With locations in the United States, Europe and Asia, AMRI SMARTSOURCING™ offers you a versatile and strategic way of partnering with us that is designed to deliver reduced risk, greater flexibility and a better return on investment. AMRI has successfully partnered R&D programs and is actively seeking to out-license its remaining programs for further development.
Post: Research Scientist; Analytical Development - 1000385
Job Description
The principal responsibility of the Research Scientist is the analysis by multiple procedures of intermediates and target compounds. The Research Scientist I is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist's performance rating will be based on productivity.
RESPONSIBILITIES:
• Develop, establish and validate analytical methods as assigned.
• Develop and maintain working knowledge of instrumentation, equipment and scientific methodologies necessary to perform assigned analytical development tasks. Demonstrate expertise in at least one technique.
•Plan, execute, analyze and troubleshoot laboratory work related to analytical/pharmaceutical development.
• Provide high-quality ideas and contributions to solve difficult analytical development problems as assigned; exercise judgment within broadly defined practices and policies
• Use sound judgment and previously acquired knowledge and experience to develop new procedures for new compounds.
• Use and maintain equipment in a neat and orderly manner. Report any malfunction immediately to supervisor. Repair minor problems. Maintain service and calibration records.
• Provide analytical development expertise and act as a technical consultant to both internal and external customers.
• Interface with other departments and customers and keep supervisor informed of activities.
• Keep contemporary, accurate, legible, and complete experimental records in accordance with GMP and GLP practices.
• Use technical and regulatory knowledge and judgment to validate procedures to comply with internal SOPs and regulatory needs with minimal supervision.
• Submit complete, documented, and legible reports of analytical testing. Ensure that data is properly filed and accessible for review in accordance with appropriate SOP’s.
• Discuss routinely with supervisor the status of assigned programs and potential problems.
• May supervise one or more employees and train and mentor junior level team members, although primary role is that of individual contributor.
• Organize work time so that multiple activities run concurrently. Use time efficiently to accomplish immediate task and perform other needed activities.
• Volunteer to assist with other tasks in the analytical function not directly related to specific projects.
• Exhibit safety awareness and conduct laboratory operations and chemical disposal in a safe manner; maintain a clean and organized work environment free of safety hazards.
• Maintain familiarity with current, relevant scientific literature.
• Maintain compliance with regulations at all levels as well as strict adherence to standard operating procedures and cGMP’s as necessary.
• Demonstrate professionalism, enthusiasm, dedication and productivity.
•Prepare presentations and present data and analytical development services to internal and external customers.
• Suggest improvements for safety, work quality, and productivity.
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Candidate Profile
M.S. degree in Analytical Chemistry or related scientific field with at least 5 - 7 years of industrial analytical development experience in a pharmaceutical environment.
• Demonstrated expertise in instrumentation techniques (HPLC, LC-MS, GC, and GC-MS etc.) and wet chemistry techniques.
• Experience working in analytical development.
• Ability to work under minimal supervision and in a team environment.
• Demonstrated excellence in verbal and written communications.
• Ability/willingness to work with potent compounds and controlled substances
Additional Information:
Experience: 5-7 years
Qualification: Master's Degree
Location: Hyderabad
Industry Type: Pharma/Biotech/Vaccines
Requisition Code: 1000385
Last Date: 30th October, 2016
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