Qureos Mentor

Azurity Pharmaceuticals

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 Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company&rsquo;s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
 
 
 Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
 
 
 
 Brief Team/department Description
 
 
 
 The analytical team in Azurity Pharmaceutical is responsible for support of formulation development and related analytical activities for various formulations intended primarily for US market.
 
 
 
 Principle Responsibilities
 
 
 
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 Minimum 6 to 8 Years working experience in analytical research and development lab with hands on experience of Method development, Stability analysis in Solid Oral (tablets, Capsules), Oral suspension and Oral solution.
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 Hands on experience on at least HPLC/ UPLC, GC, UV, IR, pH meter, Dissolution, KF titrator etc.
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 Should have potential exposure on method validation/method transfer of different analytical test methods.
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 Good understanding of GLP, GDP, Data integrity and Documentation practices in lab work.
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 Preparation of SOP, Test methods, Validation/Transfer protocols and reports knowledge is added advantage.
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 Good knowledge and exposure on Related test and impurity profile methods development is needed.
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 Knowledge about regulatory requirements on analytical methods, characterization of standards, and impurities is needed.
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 Experience in calibration of different instruments like HPLC, GC, UV, IR, pH meter, Dissolution, KF titrator is required.
 
 
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 Qualifications And Education Requirements
 
 
 
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 M.Sc. Chemistry/ Analytical sciences or M. Pharmacy (Chemistry, Analysis or Pharmaceutics
 
 
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 </ul>
 By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
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Analytical Development Scientist

<div>
 Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company&rsquo;s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
 
 
 Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Opportunity Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
 
 
 
 Brief Team/department Description
 
 
 
 The Analytical Development department in the science organization at Azurity Pharmaceuticals is responsible for developing new analytical methods for the new dosage forms to ensure their quality.
 
 
 
 Principal Responsibilities
 
 
 
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 <li>
 Responsible for the development of analytical methods for product development, primarily for sterile dosage forms and/or oral dosage forms.
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 Responsible for the preparation of method development reports, validation protocols and reports, and test methods.
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 Accountable for performing routine analytical testing for assigned projects, as per requirements.
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 Responsible for executing Analytical ATR (Analytical Testing Reports), documenting results, and sharing findings with the concerned formulation development (FD) team.
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 Accountable for the calibration of assigned equipment, qualification of working standards, and maintenance of standards per storage conditions.
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 Responsible for conducting forced degradation studies and identifying unknown impurities.
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 Responsible for executing experiments to address and respond to regulatory queries.
 
 
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 </ul>
 
 Qualifications And Education Requirements
 
 
 
 <ul>
 <li>
 6-8 years of experience in Analytical Development of Formulation
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 <li>
 M. Pharm or MSc Chemistry
 
 
 </li>
 </ul>
 By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.
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Join Azurity Pharmaceuticals and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Azurity Pharmaceuticals

ABOUT_COMPANY

Analytical Development Scientist

Analytical Development Scientist