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 - (1000162)
Job Description
The principal responsibility of the Research Scientist I 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.
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- AP
Industry Type: Pharma/Biotech/Vaccines
Requisition Code: 1000162
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