154 QA Engineering Jobs in Hyderabad, India

Role highlights

• In this vital role you will act as the Quality Engineering representative on multi-functional teams, employ quality principles and company’…
• The Sr Quality Engineer will be an integral part of the design and development of combination products, providing quality oversight…

Role highlights

• Key Responsibilities: As a Quality engineer, you’ll be responsible for : Shall be responsible to implement Client and execute Quality…
• Oversee on-job quality control processes, including inspection of materials received from factories and suppliers to ensure they meet the r…

Role highlights

• We are seeking an Engineer III - Quality Systems & Documentation to lead quality documentation standardization, supplier quality governance…
• This role will partner with Quality, Manufacturing Engineering, Regulatory, Procurement, Operations, and external manufacturing partners to…

Role highlights

• Main responsibilities: Handle Product Technical Complaints (PTC) for medical devices, pharmaceutical products, biologics, and combination p…
• Process Toll out manufacturing complaints in QualiPSO (Intake and closure) – As applicable.

Role highlights

• ABOUT THE ROLE Role Description: The senior associate will work within R&D Quality’s Business Intelligence and Data Analytics (BIDA) team…
• This role contributes to ensuring Amgen’s pursuit of life-saving medication is done with the highest regard for quality and compliance…

Role highlights

• Role Overview We are seeking a mid-level specialist to lead and sustain GMP-compliant SDLC activities for the Our product platform…
• Required Skills: Agile SDLC, Asset Management, Atlassian Confluence, GMP Compliance, GMP Validation, JIRA Tool, Product Management, Softwar…

Role highlights

• Process: 1) Author, review, act as an expert in the field of medical regulatory writing and maintain the regulatory requirement…
• 11) Support Health Authority inspections/audits and development of corrective and preventive actions (CAPA) to address findings Stakeholder…

Role highlights

• Strong collaboration and change management skills, experience of working with and aligning multiple stakeholders such as Global Quality, ou…
• Good understanding of System Development Lifecycle (SDLC) activities and Computer System Assurance (CSA) Required experience within a regul…

Role highlights

• Skills/Knowledge: Data Standards & Technical Expertise Strong experience in medical or regulatory writing, including protocol authoring and…
• Collaborate cross-functionally with Global Regulatory Writing (GRW), Clinical Development, Regulatory, TA SMEs, Dev IS, and other stakehold…

Role highlights

• Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall SZ str…
• Generate and support in evaluation and interpretation of results including investigations on SST failures, OOX/Deviations/Change controls a…

Role highlights

• Process Toll out manufacturing complaints in QualiPSO (Intake and closure) – As applicable.
• Main responsibilities: Handle Product Technical Complaints (PTC) for medical devices, pharmaceutical products, biologics, and combination p…

Role highlights

• Validation & QA Analyst in Hyderabad, - Syneos Health Career Areas Advertising Operations & Leadership Consulting Field Medical Medical Com…
• Careers Job Search Join Our Talent Network Early Career Veterans Working at Syneos Health Why Work Here About Us Our…

Role highlights

• Extensive experience with application of Quality by Design and Quality risk management principles and tools as well as a strong…
• You will use your strong communication, stakeholder management and influencing skills to effectively lead the drug product subteam and the…

Role highlights

• This position may support one or more areas including Drug Substance, Drug Product, Finished Drug Product & Packaging, or Facilities…
• The Manager, C&Q Document Preparation will lead a blended team of employees and contingent workers responsible for preparing compliant, ins…

Role highlights

• The Manager, C&Q Document Preparation will lead a blended team of employees and contingent workers responsible for preparing compliant, ins…
• This position may support one or more areas including Drug Substance, Drug Product, Finished Drug Product & Packaging, or Facilities…

Role highlights

• Act as a trusted GxP quality partner with internal and external stakeholders to resolve compliance issues, monitor trends, strengthen quali…
• Provide independent GxP quality advice to Consumer Safety, Clinical Development, Regulatory, Medical, Quality, Commercial and other relevan…

Role highlights

• Act as a trusted GxP quality partner with internal and external stakeholders to resolve compliance issues, monitor trends, strengthen quali…
• Provide independent GxP quality advice to Consumer Safety, Clinical Development, Regulatory, Medical, Quality, Commercial and other relevan…

Role highlights

• As a Specialist in Regulatory Affairs (CMC), you will be responsible for site and customer CMC writing actvities for clinical…
• Strong knowledge of global regulatory requirements and CMC documentation (clinical and commercial submissions).

Role highlights

• Qualifications Job Purpose To perform preventive and breakdown maintenance of analytical instruments to ensure maximum equipment uptime, re…
• Key Responsibilities Perform preventive maintenance (PM) and breakdown maintenance for analytical instruments.

Role highlights

• Role Overview We are seeking a mid-level specialist to lead and sustain GMP-compliant SDLC activities for the Our product platform…
• Required Skills: Agile SDLC, Asset Management, Atlassian Confluence, GMP Compliance, GMP Validation, JIRA Tool, Product Management, Softwar…

Role highlights

• Good understanding of clinical trial process across Phases II-IV and/or post-marketing safety requirements, ICH GCP, GVP and regulations re…
• Assists in the processing of ICSRs according to Standard Operating Procedures (SOPs) and project/program-specific safety plans as required.

Role highlights

• Monitor evolving, region-specific regulations and proactively provide strategic guidance to cross-functional teams to ensure compliance COR…
• Oversee the end-to-end preparation, review, and filing of regulatory dossiers (NDAs, NDSs, and MAAs (CP, DCP, MRP, NPs) etc.

Role highlights

• As a Regulatory Compliance senior actively establish, maintain and strengthen internal and external relationships.
• Demonstrated track record in project management, governance, and reporting Exposure to Data Integrity requirements and other applicable reg…

Role highlights

• This role requires close collaboration with Quality Assurance, Regulatory Affairs, Manufacturing, Laboratory Operations, IT, Validation, Au…
• This role will be responsible for managing enterprise-wide quality transformation programs, regulatory compliance initiatives, and digital…

Role highlights

• This role requires close collaboration with Quality Assurance, Regulatory Affairs, Manufacturing, Laboratory Operations, IT, Validation, Au…
• This role will be responsible for managing enterprise-wide quality transformation programs, regulatory compliance initiatives, and digital…