408 Quality Assurance Analysts jobs in Hyderabad

Experience Required: 2–4 years

Salary Offered: ₹20,000 per month

We are seeking motivated QA Executives with 2–4 years of experience to support daily quality assurance activities in a GMP-regulated pharmaceutical facility. The role will focus on documentation review, QA activities, and ensuring compliance with regulatory standards.

• Review batch manufacturing and packing records
• Line clearance for production and packaging activities
• Support in handling deviations, change controls, CAPA, and incident reports
• Ensure compliance with cGMP and Revised Schedule M requirements
• Participate in in-process checks and quality monitoring
• Assist in preparation and review of SOPs, logbooks, and other controlled documents
• Support internal audits and regulatory inspection readiness

• B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry)
• 2–4 years of experience in QA in a pharmaceutical company
• Good understanding of cGMP and QMS principles
• Strong documentation and communication skills

Experience Required: 4–8 years

Salary Offered: ₹30,000 per month

We are looking for experienced QA Executives with 4–8 years of experience to take responsibility for advanced QA functions, including compliance management, documentation oversight, and training of junior QA staff.

• Review and approval of batch records, logbooks, and controlled documents
• Oversee line clearance, in-process checks, and QA compliance
• Lead and investigate deviations, OOS, OOT, change controls, and CAPA
• Coordinate with production, QC, and engineering for quality compliance
• Handle document control, issuance, archival, and retrieval systems
• Support vendor qualification and raw material quality compliance
• Prepare for and participate in internal audits and regulatory inspections
• Mentor and guide junior QA team members

• B.Pharm / M.Pharm / B.Sc / M.Sc (Life Sciences/Chemistry)
• 4–8 years of QA experience in a pharmaceutical manufacturing unit
• Strong knowledge of QMS, regulatory compliance, and cGMP
• Experience in facing audits (USFDA/WHO/other regulatory bodies is an advantage)
• Excellent analytical, communication, and leadership skills

Job Insights:

· 3–5 years’ experience in Medical Writing Quality Control/Review, with additional exposure to creative/digital assets QC.

· Bachelor’s degree is a must.

· Strong background in reviewing medical content and ensuring its correct integration into creative outputs.

· Experience with proofreading, copy editing, and QC for both text-based and creative materials.

· Familiarity with referencing tools (e.G., EndNote, Mendeley)

Experienced in project management tool (Jira/ Hive /Adobe Workfront)

· Good understanding of creative asset formats (email templates, videos, static images, HTML banners).

· Proficiency in basic QC of creative assets—checking layout, alignment, copy placement, and regulatory footnotes.

· Good communication skills and ability to collaborate with cross-functional teams to meet deadlines.

· Ensuring timely completion of project, understanding process requirements and providing use cases for the business, functional & technical requirements

· Able to review and annotate 3-5 assets per day with first time right from the agency/brand.

EOE:

Our client is an Equal Opportunity Employer, committed to a workplace free from discrimination and harassment. Employment decisions are based on business needs, job requirements, and individual qualifications without regard to race, color, religion, gender, age, disability, sexual orientation, gender identity, marital status, military service, genetic information, or any other status protected by law.

About Earthful

Earthful i s an FMCG company focused in the health and wellness space. The founders (Sudha Gogineni and Veda Gogineni) are graduates from IIT Kharagpur and ISB with a multitude of experience across multinational companies & startups, such as Uber, Meesho, Deutsche Bank, ITC. Earthful is an early stage startup and hence the candidate will have the opportunity to work closely with the founders. We are looking for a candidate passionate about scaling a startup.

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About Role

Earthful is looking for a Quality Assurance Specialist, who has attention to detail and commitment to maintaining consistent quality that will play a vital role in upholding the brand's reputation and delivering safe, high-quality products.

Location: Full-time, on-site position, Hyderabad

Responsibilities

● Set up and maintain quality control protocols and SOPs across manufacturing, warehousing, and packaging.

● Audit and approve manufacturers and raw material suppliers;
ensure GMP, FSSAI, and Earthful standards are met.

● Manage quality checks for raw materials, blends, and finished goods through both internal and third-party labs. Able to evaluate sensory parameters of the products

● Successfully complete Hazard Analysis Critical Control Point (HACCP), Good Manufacturing Practice (GMP), and Food Security Training.

● Lead issue resolution through Root Cause Analysis (RCA), implement Corrective and Preventive Actions (CAPA), and collaborate cross-functionally with R&D, Production, and Supply Chain to improve quality processes.

Education:

● Bachelor's in Food technology / Masters in Food technology or any related field

● Total work Experience: : 2-3 years minimum

Be a part of Earthful’s Family!

• Perform routine and advanced analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods according to established protocols and regulatory guidelines.
• Analyze test results, interpret data, and prepare accurate and comprehensive reports.
• Investigate out-of-specification (OOS) results and deviations, documenting findings and recommending corrective and preventive actions (CAPA).
• Maintain laboratory equipment, ensuring calibration, qualification, and routine maintenance are performed.
• Ensure adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.
• Prepare and review standard operating procedures (SOPs) for analytical testing and laboratory operations.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues and support product development.
• Manage laboratory inventory, including chemicals, reagents, and consumables.
• Participate in internal and external audits as required.
• Stay updated with the latest advancements in pharmaceutical analysis and quality control techniques.
• Contribute to continuous improvement initiatives within the Quality Control department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Proficiency in wet chemistry techniques and compendial testing (USP/EP/BP/IP).
• Strong understanding of GMP, GLP, and ICH guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.
• Proficient in Microsoft Office Suite and LIMS (Laboratory Information Management System) software.
• Strong written and verbal communication skills.
• Experience with method validation and transfer is highly desirable.

• Develop, implement, and maintain comprehensive quality control systems and procedures throughout the manufacturing lifecycle.
• Conduct rigorous inspections and testing of raw materials, in-process components, and finished products to ensure compliance with specifications.
• Analyze quality data, identify trends, and implement corrective and preventative actions (CAPA) to address deviations.
• Collaborate with engineering, production, and R&D teams to define quality standards and acceptance criteria.
• Lead root cause analysis investigations for quality issues and implement effective solutions.
• Develop and maintain quality documentation, including inspection reports, test procedures, and quality manuals.
• Oversee the calibration and maintenance of quality control equipment and instrumentation.
• Train and mentor junior quality control personnel on quality standards and procedures.
• Stay updated on industry best practices, regulatory requirements, and emerging quality control technologies.
• Conduct internal audits and participate in external supplier audits to ensure quality compliance.
• Contribute to the continuous improvement of manufacturing processes and product quality.
• Ensure all activities are performed in accordance with relevant quality management systems (e.g., ISO 9001).
• Prepare detailed reports on quality performance and present findings to management.

• Bachelor's degree in Mechanical Engineering, Industrial Engineering, Manufacturing Engineering, or a related technical field.
• Minimum of 5-7 years of progressive experience in quality control or quality assurance within a manufacturing environment.
• Proven expertise in developing and implementing quality control plans and methodologies.
• Strong understanding of statistical process control (SPC), Six Sigma, and Lean Manufacturing principles.
• Experience with various inspection and testing techniques and equipment.
• Proficiency in quality management software and data analysis tools.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong documentation and reporting abilities.
• Effective communication and interpersonal skills, with the capacity to collaborate with cross-functional teams in a remote setting.
• Detail-oriented, methodical, and highly organized.
• Experience in the specific manufacturing sector of our client (e.g., automotive, electronics, consumer goods) is a strong advantage.
• Knowledge of relevant international quality standards.

• Perform a variety of chemical and physical tests on raw materials, in-process samples, and finished pharmaceutical products.
• Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Analyze test results, interpret data, and prepare accurate and concise laboratory reports.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Validate analytical methods and instruments according to established protocols.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
• Maintain laboratory equipment and ensure calibration is up-to-date.
• Manage inventory of laboratory supplies and reagents.
• Collaborate with other departments, including R&D, production, and regulatory affairs, to resolve quality issues.
• Contribute to the continuous improvement of quality control processes and procedures.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in a pharmaceutical quality control laboratory.
• Hands-on experience with analytical techniques and instrumentation commonly used in pharmaceutical QC.
• Thorough understanding of GMP, GLP, and regulatory requirements (e.g., FDA, EMA).
• Proficiency in data analysis and report writing.
• Excellent attention to detail and problem-solving skills.
• Strong organizational abilities and the capacity to manage multiple tasks.
• Ability to work effectively both independently and as part of a team.

• Develop, implement, and manage the company's quality management system (QMS) in accordance with relevant industry standards (e.g., ISO 9001).
• Establish and oversee quality control procedures for raw materials, in-process production, and finished goods.
• Lead and mentor the quality control team, providing training, guidance, and performance management.
• Conduct regular audits of production processes and quality systems to identify areas for improvement.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA) to resolve quality issues.
• Ensure compliance with all applicable regulatory requirements and industry specifications.
• Collaborate with production, engineering, and R&D departments to integrate quality considerations into product development and manufacturing processes.
• Manage product non-conformance and customer complaint resolution processes.
• Develop and maintain quality control documentation, including SOPs, work instructions, and inspection records.
• Stay updated on the latest quality control technologies and best practices.
• Drive continuous improvement initiatives to enhance product quality, process efficiency, and customer satisfaction.
• Prepare reports on quality performance metrics for senior management.
• Oversee calibration and maintenance of quality control equipment.
• Champion a quality-focused culture throughout the organization.

• Bachelor's or Master's degree in Engineering (Mechanical, Electrical, Chemical), Science, or a related field.
• Minimum of 8 years of experience in quality control and assurance within a manufacturing setting, with at least 3 years in a managerial role.
• In-depth knowledge of quality management systems (QMS) such as ISO 9001.
• Proven experience in implementing and managing CAPA systems.
• Strong understanding of statistical process control (SPC) and other quality tools.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional leadership, team management, and communication skills.
• Ability to interpret technical specifications and regulatory standards.
• Experience with auditing (internal and external) is essential.
• Proficiency in quality management software is a plus.
• Detail-oriented with a strong commitment to quality and accuracy.