38 QA Engineering Jobs in Delhi, India

Role highlights

• Drive continuous improvement initiatives and identify opportunities to improve quality, efficiency, and consistency of deliverables.
• Experience- 4 years -7 years Experience of working in regulated environment such as FDA QSRs, ISO 13485 Design Control Procedures,…

Role highlights

• Hands on experience of problem-solving methodology and root cause analysis, 7 QC tools, Problem Solving & CAPA, Strong Analytical ability…
• Sound knowledge on complaint handling process of medical devices will be an added advantage.

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• Education & Work Requirements Bachelor’s Degree with 5-8 years of related experience Education & Work Preferences ASQ Certified Quality Eng…
• Responsibilities Guide cross-functional teams in the appropriate application of design controls in compliance with global regulatory requir…

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• You will collaborate with cross-functional teams to enhance product quality and regulatory compliance, conduct internal audits, and analyze…

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• Engineer to join our Quality team.
• I must have good knowledge and experience of Quality Tools as APQP, FMEA, MSA, SPC and PPAP.

Role highlights

• Conduct department level training, as necessary, to educate subordinates in the department on regulatory requirements, policies, and proced…
• Support new technology development within our Company People Leadership & Stakeholder Management Build and mentor a high-performing global…

Role highlights

• Quality Processes/ Tools - Working knowledge of basic and advanced Quality tools such as; PPAP, Six Sigma, SPC, FMEA, Control…
• Executes/implements/ improve all supplier quality tools/ Processes.

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

• Job Purpose The Clinical Process and Quality Manager (CPQM) is responsible for enabling Sponsor Oversight, Quality Control, and Risk-Based…
• Proven experience in clinical quality management, including QMS, risk-based quality oversight, trend analysis, and CAPA.

Role highlights

• Represent Regulatory Affairs on cross-functional project teams and collaborate with Global Regulatory Affairs, Quality, Commercial, Supply…
• Lead and oversee regulatory submissions, authority queries, approvals, and post-approval activities with health authorities, including mana…

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• This position reports to the Manager, Commercial Regulatory Affairs (SWA) and is part of the Commercial Regulatory Affairs Center of…
• Provide regulatory assessments for anticipated analytical, manufacturing and packaging changes.

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• Experience supporting regulated Life Sciences organizations.
• Familiarity with Agile delivery methodologies.

Role highlights

• Assist with the implementation and maintenance of a quality control system and ensure that equipment, reagents, and supplies are maintained…
• Validate new assays under a quality system and participate in the test and evaluation of new technologies as necessary.

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• Should be able to handle team 6\. QA Document management * Lab Equipment PM and Calibration Planner * Reviews Operational,…
• Ensure smooth system integration across manufacturing, QC, and QA functions.

Role highlights

• Based within the R&D structure the role is positioned to support development and help in bringing compliance from both quality…
• Written communication skills for accurate data entry and concise documentation Timely execution of multiple project objectives Knowledge of…

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• Certification in regulatory affairs, clinical safety preferred.
• Job Details Develop and maintain client relationships and highlight opportunities for increased service support to the respective lead.

Role highlights

• Provide guidance to manufacturing partners’ QC and production on in-line production quality control, assisting first production qualificati…
• Quality control experience in a manufacturing environment and/or field quality experience.

Role highlights

• Partner with Global Regulatory Affairs, Quality Assurance, Pharmacovigilance, Medical Affairs, Supply Chain, and Commercial teams to suppor…
• 8+ years experience in Regulatory Affairs Desired Characteristics Strong verbal and written communication skills, with the ability to effec…

Role highlights

• You will perform quality surveillance and hands on inspections to verify that supplier equipment, material, documentation, and personnel ac…
• Assists in the development of the final bid list and the selection of a recommended bidder Assists with the establishment…

Role highlights

• Collaborate with cross-functional stakeholders (Clinical Operations, Regulatory Affairs, Quality, and external CROs/vendors) to ensure cons…
• The Documentation Specialist plays a central part in maintaining inspection and audit readiness across the clinical study portfolio.

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• Key Responsibilities: Project Leadership Lead life sciences projects from conceptual design through construction and validation.
• Team Leadership Lead, mentor, and develop engineering and project management teams.

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• Lead SET development at Co-man sites Support driving Quality & Food safety systems in plant for NPD and other R&D…
• The role will ensure consistent compliance to QFS systems, enhance supervision with additional support, direction & guidance to ensure cons…

Role highlights

• This role will involve working closely with cross-functional teams, including Design, Engineering, and Manufacturing, to ensure that our pr…
• Experience: Minimum 4-6 years of experience in IMDS compliance, product design, or related field, preferably in a manufacturing environment.

Role highlights

• 3-5 years of experience in quality assurance/control within the automotive industry.
• Proficient in using quality tools such as 8D, FMEA, SPC, and Root Cause Analysis.