1476 Capa Jobs - Page 18

JOB PROFILE OF SR. TECHNICAL OFFICER-QUALITY ASSURANCE MENDINE PHARMACEUTICALS PVT LTD Job Title / Designation- SENIOR TECHNICAL OFFICER - QA Qualifications- M.PHARM Experience- 5 to 10 years experience in QUALITY ASSURANCE Job Objective- The ideal candidate will be responsible for implementing and maintaining quality systems, ensuring compliance with cGMP guidelines, conducting internal audits, reviewing batch records, and supporting regulatory inspections. This role demands strong documentation skills, a sound understanding of pharmaceutical quality standards, and the ability to work collaboratively across departments to uphold product integrity and safety throughout the manufacturing proc...

Key Job description requirements : BE / B tech Mechanical with overall 7-12 Years experience Sound knowledge on GD & T basic concepts Capability of Gauge / Fixture designing / giving strong inputs in this area 'Exposure in handling CMM / OMM Equipements Basic programming knowledge on CMM / OMM Additional advantage if exposure in the equipment like ATOS Q / Sensofar etc Lead in Quality lab oratory Have Min 3-5 Years of experience in Lab oratory Management , as lead Exposure in handling of NABL accredited lab , will be additional advantage Sound knowledge in Concepts like SPC/ MSA - GRR / PFMEA / APQP Exposure in handling high end customers / Customer audits etc Developing team / Multiskilling...

Role & responsibilities Data analysis - Analysing data using statistical techniques and providing reports. Identifying, analyzing and interpreting trends or patterns and guide Team for improvements. Lead CFT for non-conforming products. Reporting of daily testing /inspection MIS Dealing with external labs for material testing Should drive process quality issues for permanent resolution. Developing and implementing databases and data collection systems. Ensure continuous improvement in Quality system & Quality assurance Monitoring Quality KPI, Quality Objectives for Business Cost reduction initiatives: Cost reduction in testing / calibration / rejection. To identify new test requirements, new...

We make real what matters. About the role: Candidate should have sound knowledge in acquisition, verification & analysis of asset performance data (SAP etc.), development of optimal maintenance plans (preventive, predictive, condition based monitoring (CBM), reliability maintenance etc.), development of optimal strategies based on economic cost-benefit analysis to improve asset performance & maximize OEE, Perform criticality analysis and determine risk priority for various assets. Candidate will be responsible for implementation of AO by maintaining liaison with technicians and other management regarding work execution, ensure adequate processes, schedules, task list, tools etc. are availabl...

Position Level 10 Job family: Quality Management Your new role challenging and future-oriented: Analyze non conformances (NCR) occurring at different stages (In- process, Testing, Supplier, etc.), identify root cause of failure and define CAPA. Prepare and update Procedures, Guidelines, and other documents in the Manufacturing assembly line, also ensure correct documents are used in Manufacturing line Perform Product audits on ready to pack products to conform compliance to Design and Customer requirements. Support SQM, Operations excellence, purchasing to establish new supplier evaluation/assessment, qualification, and development of parts and equipment. Work closely with suppliers in devel...

* Conduct in-process and final quality inspections of switchgear/control panels. * Ensure adherence to quality standards (IS/IEC) and customer specifications. * Maintain quality records, inspection reports, and test certificates.

•5-6 years' experience in professional experience in medical device regulatory , Experience with systems for quality management, product development, and follow-up of procedures. •Responsible for Quality compliant Investigation. • Evaluation of compliant event and device allegation of customer and determine adverse event or report failure. • Investigating the Complaints and prepare technical investigation summary as per the GDP. • Investigating and Failure analysis of Recalled products and devices, Identifying the root cause and analysis of CAPA, Codes of failure. •Be able to handle ad-hoc changes in priority/planning and independently. •Be able to think from customer expectation perspective...

Quality Planning & Systems: Own and maintain the QMS, draft SOPs, conduct FMEA, CAPA, COC Certification. Incoming & InProcess Control: Define inspection standards, drive supplier quality improvements. Should have knowledge in documentation.

Ensure quality parameters are maintained at each stage of manufacturing, testing, and inspection Review and interpret the technical requirements of customers to align production accordingly Handle and resolve technical customer complaints effectively Coordinate with TPI (Third Party Inspection), certification agencies, and consumer representatives for inspections and approvals Review and address non-conformity reports and ensure appropriate corrective actions Approve Quality Assurance Plans (QAP), Inspection and Test Plans (ITP), and final test certificates Maintain CAPA (Corrective and Preventive Actions) records for all customer complaints Hold overall authorization to release final produc...

This Position reports to: Supply Quality Manager Your role and responsibilities You will be working as SQA Specialist and will involve some or all the activities mentioned in the job description. (Please note that the list is only indicative not exhaustive) . The engineer must travel / visit Suppliers in Bengaluru & suppliers across India, for Problem Solving, technical discussions, trials, Process /Assessment /Channel Partner Audits, Improvement Projects and support wherever necessary . The stay outside could depend on the Criticality of the project. It could be for 2-3 days at initial stages could extend. He will not resist the same. This role is contributing to the ABB India, Smart Power,...

This Position reports to: Supply Quality Manager Your role and responsibilities In this role, you engineer must travel / visit Suppliers in Bengaluru & suppliers across India, for Problem Solving, technical discussions, trials, Process /Assessment /Channel Partner Audits, Improvement Projects and support wherever necessary This role is contributing to the ABB India, Smart Power, Electrification, Business, for Supplier Quality function for Bangalore Nelamangala Location. You will be mainly accountable for: Promote Supplier Quality & Zero-Defect Culture: Enhance supplier quality awareness, ensuring a Zero Defect mindset while supporting incoming quality control and process reliability. Audit &...

This Position reports to: Quality Manager Your role and responsibilities In this role, you will have the opportunity to deploy and lead the quality strategy for a local organizational unit, including quality culture, systems, tools, and competent teams, with the aim to achieve and exceed customer expectations while ensuring sustainable operations. Each day, you will drive the local quality system through the right mix of prevention, continuous improvement, robust root cause analysis, quick response, and sustainable solutions to problems. You will also showcase your expertise by coordinating the efforts of all necessary local functions that impact the quality results to reach the targets for ...

Role Description The Group Audit (GA) function comprises c. 880 staff who take a proactive, risk based and independent approach to assist the Bank's business and infrastructure functions to identify key control weaknesses. GA prides itself in ensuring the highest standard in professional delivery. Being DB's 'third line of defense GA have a high internal profile, acting as an independent and forward-looking challenger and adviser to Senior Management. We are strongly rem/lied upon by the Regulators. We are a diverse and inclusive global division where culture is at the core of our team dynamic; GA is inextricably linked to promoting strong corporate and ethical governance, a philosophy that ...

Post* *QMS- Sr. Engineer/Assit Manager *Urgent Opening @ Ranjangaon MIDC, Karegaon, Shirur* . *Interview arrangement* *Contact -9356395439* *Experience* -06-08 yrs *CTC -4.20-5.00 lpa* 1) *ISO-9001/14001 Compliance* : Maintain an organization's quality management system to ensure compliance with ISO standards 2) *Documentation* : Ensure that all quality-related documentation, including policies, procedures, work instructions, and records, are maintained and updated as required by ISO standards. 3)Co-ordinate with all departments for system compliance 4) Closing of audit Internal and External. 5) Maintain MR/System Records. 6) *Internal Audits* : Plan, conduct, and report on internal audits t...

Designation - Manager - Quality Assurance Company - Leading Pharma Raw Material Mfg. Company Job Location - Dahej, Bharuch Qualification - B.Sc. / M.Sc. / B.E.- Chemical / B.Pharm Experience - Min. 8yrs. and above share with your friends Required Candidate profile company will provide transportation facility from Bharuch. Responsible for handling QA / GMP Related documentation QMS, Audit Preparation, Vendor Questionnaire, Market Compliant & Customer Compliance

Conduct process documentation as per ISO standards, conduct and review sampling strategy in the process. Conduct root cause analysis for process improvements, conduct MSA as per schedule, Drive and conduct process compliance, Drive and conduct audits, conduct baseline and analyze CTQs, Drive brainwave in the process, Drive open forums/best practice sharing sessions, YB six sigma improvement project to be certified, successfully completed GB DMAIC training and YB test within 12 months of role. Successfully complete ISO training. Working on the product and helping the team members to achieve deadlines. Provided timely reports, provide the daily update to all team members, updates and system en...

Responsible 4 smooth functioning in processing of various products & systems as per the laid down procedure.Customer Complaint Handling.Corrective & Preventive Action for External & internal Product Quality Issues.Suppliers audit & Internal Audit,QMS Required Candidate profile Problem solving tools,knowledge of workshop kaizen, knowledge of system standards.Identifying & solving problems,Setting goals & targets,Commitment,Time management & Prioritizing,Training & Delegating

Nuti Food Science is looking for Quality Control Manager to join our dynamic team and embark on a rewarding career journey Developing, implementing, and maintaining quality control procedures, policies, and systemsManaging and overseeing the quality control team and providing guidance, direction, and training to team membersDeveloping and monitoring quality control metrics and key performance indicators (KPIs) to ensure compliance with quality standards and customer requirementsConducting quality control audits and inspections to identify non-compliance issues, defects, and areas for improvementDeveloping and implementing corrective and preventive actions to resolve quality issues and preven...

Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

Key Responsibilities: Administer and maintain SQL Server databases, ensuring high availability (HA) and optimizing performance. Perform regular database backups, monitoring, and auditing to maintain data integrity and security. Utilize PowerShell scripting to automate routine database tasks, streamline processes, and improve operational efficiency. Perform performance tuning to optimize database systems for improved speed and responsiveness. Monitor and troubleshoot database-related issues, ensuring quick resolution of any operational problems. Implement and maintain disaster recovery procedures to ensure data availability and minimal downtime. Collaborate with other IT teams to ensure datab...

Key Responsibilities Develop and maintain supply chain analytics to monitor operational performance and trends. Lead and participate in Six Sigma and supply chain improvement initiatives. Ensure data integrity and consistency across all analytics and reporting platforms. Design and implement reporting solutions for key supply chain KPIs. Analyze KPIs to identify improvement opportunities and develop actionable insights. Build and maintain repeatable, scalable analytics using business systems and BI tools. Conduct scenario modeling and internal/external benchmarking. Provide financial analysis to support supply chain decisions. Collaborate with global stakeholders to understand requirements a...

Job Title: Solar Cell Quality Integrated PV Manufacturing Location: Kavali/Ramayapatnam, Andhra Pradesh (Location near to Nellore, AP) Position: Manager / Associate Manager /Deputy Manager Solar Cell Quality About the client: INDOSOL Solar Private Limited is a Special Project Vehicle (SPV) of Shirdi Sai Electricals Limited (SSEL), who is a leading Indian Conglomerate (Manufacturing B2B) in Transformer manufacturing, headquartered in Hyderabad. Having qualified in PLI (Production linked incentive) scheme through MNRE, Government of India is keenly materializing to set-up 10GW Integrated PV manufacturing for the entire value chain (Polysilicon, ingot, wafer, cell, Module & Glass manufacturing)...

QMS and it's implementation Review and approval of NCs, CAPA, Change Controls, Validation Master Plan, SMF, BMR, BPR, Quality Manual, Vendor qualification. Lead and manage internal/ external audits, QA compliance, continuous improvement, MRM data Required Candidate profile Bachelor’s/Master’s in Mechanical/ Biomedical 10+ years of exp. QA & QMS in the medical devices Strong knowledge of QMS, GMP, regulatory guidelines (ISO, USFDA, CE, WHO),handling audits, QA practices.

Issuance & retrieval of BPCRs/ ECRs/ formats/ log books etc. Preparation of QA SOPs and list of SOPs. Follow-up cross functional team for periodic review and review of other departmental SOPs as and when required. Distribution of controlled documents e.g. SOPs, specification etc. QC Analytical Raw data and sampling and review checklist Issued. Ensure all the activities comply with EHS regulations and policies. Ensure Zero accident / Incident at work place Ensure all the activities / documentation as per the cGMP guideline

Requisition for Executive for the implementation and monitoring of GLP in TIC. Skills Required : Good Laboratory Practice, Quality Assurance, MS Office Package, Communication Skills Roles and Responsibilities : Preparation of documents related to applying GLP (Good Laboratory Practices). Ensure the upkeep and maintenance of the laboratory by implementing GLP. Ensure compliance with GLP standards. Logbook management, sample management, SOP management, and other document management related to GLP. Any other work related to Quality assurance assigned by the manager. GLP-trained person or experience working in GLP labs. Must have good verbal and written skills.