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$500k–$700k/yr
Other
postgraduate degree
Posted 7d ago
~40 hrs/week
Responsibilities
The Research Associate is responsible for analytical method development, feasibility studies, and ensuring compliance with cGLP/cGMP standards. They also manage documentation, instrument calibration, and support method transfer activities to CMO locations.
Requirements
Candidates must hold a M. Pharm degree to be considered for this role. A minimum of 4-6 years of relevant experience in analytical research and development is required.
Full job description
Job DetailsJob Location: Prashanti Nagar IE Kukatpally Hyderabad, TELANGANA 500072Salary Range: $500,000.00 - $700,000.00 Salary/yearJob Shift: Day• Responsible for execution of Analytical Method Development (Assay, Dissolution, Related substances, content, UOD, PSD.), Analytical method feasibility activities of drug substance / drug product / excipients. • Responsible for execution of activities related to Regulatory query and performing RLD analysis and COA generation. • Responsible for preparation of assessment report, Method Development report, Method Equivalency report of drug product. • Responsible for performing the qualification and calibration of analytical instruments like HPLC, IR and other standalone instruments (like water content, pH meter, Balances etc.,). • Responsible for preparation of protocols / reports / standard operating procedures and Standard Testing Procedures. • Responsible for following cGLP/cGMP compliance of the Analytical Laboratory, ensuring laboratory safety, good laboratory practices, Good Documentation practice in the lab and general cleanliness and Training & development activities. • Monitoring and supporting all method transfer related activities from ARD to the CMO locations. • Responsible for to execute authorized to sign (as prepared and checked by) for, Certificate of analysis, Calibration record, Specification and Standard test procedure, Method Validation / transfer/Reverse Engineering / protocols and reports, Method equivalency report.
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
Offices: 3250 Commerce Parkway, Miramar, FL 33025, US
AVEVA is a global leader in transdermal drug delivery located in the United States. The company has an extensive history of providing pharmaceutical partners with fully integrated, controlled-release transdermal products that fulfill unmet market needs or supply high-quality, affordable brand equivalents. By leveraging this experience, AVEVA offers a full range of research, development and manufacturing capabilities to produce transdermal pharmaceutical products that can improve the quality of life, usage and compliance rates for patients.
Offices: 3250 Commerce Parkway, Miramar, FL 33025, US