Sravani Mutyala

An 9-years Quality control analyst with experience in Quality control department and Method validations and method transfer, for supporting and maintaining Quality Management Systems (QMS) to levels of GMP and regulatory compliance within the pharma sector. Skilled in performing laboratory experiments, data interpretation, and conformity to regulatory levels like ICH, MHRA and GMP.

Documentation & Product Release: Skilled in batch record review, product release operations and management of correct and timely documentation. Seeking pharmaceutical industry job to apply experience in developing and validating analytical methods of sound quality. Renowned for attention to detail, consistency and practical, team-oriented approach to laboratory operations.

Senior Quality Control Analyst - ACE Laboratories limited - London, United Kingdom

(2025-08)

• Performed routine and non-routine analysis of finished pharmaceutical products (Tablets and Capsules), and stability samples using HPLC, Dissolution, and other analytical techniques.
• Ensured all testing is carried out in compliance with GMP, SOPs, and regulatory requirements
• Accurately documented all analytical data, observations, and deviations in accordance with ALCOA+ principles.
• Performed equipment calibration, qualification, and routine maintenance as required
• Troubleshoot analytical methods and instruments and escalate issues when necessary.
• Assisted in method development and method transfer activities where applicable.
• Supported laboratory investigations, OOS, and deviation reports with technical input.
• Provided support and guidance to junior analysts and contributed to their technical development.
• Maintained lab cleanliness, safety, and regulatory compliance always.
• Training to Juniors during the analysis.

Research Associate (Junior Manager Level 3) - Neuland Laboratories Ltd - Hyderabad, India

(2020-03 - 2023-08)

• Led and executed method validation and transfer activities for analytical methods (e.g., HPLC and UPLC), contributing to [quantifiable achievement, e.g., a 25% increase in testing efficiency].
• Dealing with Site managers while transfer the methods from AR &D to manufacturing site.
• Validated and optimised analytical methods for [Specific analytes, e.g., KSM's (Key starting materials) and intermediate's drug substances, impurities], resulting in [positive outcome, e.g., improved assay sensitivity].
• Prepared and reviewed validation protocols and reports ensuring compliance with ICH guidelines and GMP regulations.
• Conducted rigorous data analysis and interpretation, identifying trends and strongly addressing potential issues, leading to [positive impact, e.g., the prevention of batch failures].
• Effectively troubleshot analytical method issues, providing effective technical support and training to junior team in 5.0 members.
• Maintained accurate and detailed laboratory records, adhering to GLP standards and contributing to successful audits.
• Coordinated to the implementation of new analytical technologies and equipment, enhancing laboratory capabilities.

Senior Analyst - Megsan Labs Pvt Ltd - Hyderabad, India

(2016-09 - 2020-02)

• Executed method validations for analytical methods for Related substances and Assay by HPLC contributing to [quantifiable achievement, e.g., a 15% increase in testing efficiency] with ICH guidelines and GMP regulations. Maintenance and calibration of HPLC periodically.
• Prepared, documented and maintained validated excel sheets for Related substances, assay, content uniformity for different paraments (System suitability, specificity, Method precision, LOD and LOQ, Linearity and Accuracy, solution stability)
• Validations are conducted for Key starting materials (KSM's), intermediates, Active pharmaceutical ingredients (API's) and Finished products like Solid dosage forms (Tablets and Capsules) and Liquid dosage forms (Injectables), Semisolid dosage forms (Suspensions).
• Experinced FDA (Food and Drug Administration) audit and number of customer audits.
• Exposed different customer-based client routine audits on every week.

Chemist - Nasense Labs Pvt Ltd - Hyderabad, India

(2015-08 - 2016-09)

• Executed Manual titrations like (Acid- Base titrations, Precipitation titrations) and Solubility tests.
• Conducted Description of the raw materials, melting point and boiling point test and Loss on drying (LOD) etc.

Master's in pharmacy - Pharmaceutical Analysis, Quality Assurance and Regulatory Affairs - Acharya Nagarjuna University (2013-08 - 2015-09)

Bachelor's in pharmacy - Pharmaceutical Science - Acharya Nagarjuna University (2009-09 - 2013-04)