2258 Capa Jobs

Manufacturing engineering tasks that do not require 4 year degree. Primarily tactical responsibilities. This does not include general administrative work. Developing in-depth knowledge of a technical discipline. Uses prior experience and acquired technical expertise to execute policy/strategy. In-depth understanding of key business drivers; uses this understanding to accomplish own work. In-depth understanding of how work of own team integrates with other teams and contributes to the area. Uses some level of judgment and has ability to propose different solutions outside of set parameters but with guidance. Uses prior experience and on-the-job training to solve straightforward tasks. Has acc...

QA Documentation Validation / Qualification Documents Control and Archival of documents Retain Sample Handling and Observation SOP Preparation and Revision related Activities BMR Preparation and Review Monitoring of all the QA activities, test results, leaked defects, and identifying areas of improvement. Handling of QMS Related Activities (change control, deviation, Market Complaint, incident, OOS). Knowledge of regulatory guidelines and requirements, such as FDA, MHRA, and ICH & ISO Standard.

To check documents like equipment log books, temperature & humidity records, Collect in-process and Finished sample as per Specifications and Protocol. Supervision of RM/PM Sampling and dispensing procedure. Machine Line clearance of Production Area. Area Line Clearance of Production area Checking online tablet weight variation, hardness, friability, thickness & DT Time & check informality of weight. Verification of granulation, Compression, Coating, & Packing process & also release for same. Able to fill And Check BMR. Able to Give Batch Approval, verify various Documents. Able to finalize Quality of Finished goods. DOCUMENTATION

Line clearance of Various in process stage such as Dispensing, Granulation, Compression, Coating, Packaging and Sampling. Routine monitoring of all functional area to ensure adherence to the SOPs. Co-ordination & Ensuring timely execution of Sampling activity of Raw and Packing materials. Co-ordination of daily activities in Manufacturing and packaging areas. Create signature and methods for raw materials by using Truscan RM analyzer. Approved / Rejected labels affixing for API, Excipients, Primary packing and secondary packing materials finished goods and operation supplies. Verification of Temperature and Relative Humidity reports generated from TESTO software. Co-ordination & ensuring tim...

A. Product Certification Act as EU Authorized Person for PED Module D, B & H Coordinate certifications: SiTAs, TSG, CCOE & PESO Formerly authorized for ATEX and CCC product certifications B. Quality Management Certification Serve as Management Representative for API Spec Q1 6D Coordinate ISO systems: 9001, 14001, 45001 Develop QMS processes, documentation, SOPs Manage welder certifications and records C. Customer Support Provide quality documentation during quotation, PO, and FAT stages Offer technical support for customer claims Conduct RCA and implement CAPA for claim resolution Support customer audits and registration processes D. Additional Duties Perform internal audits and report QMS e...

Accountable for being Management representative with Responsibility & Authority forthe Quality and Regulatory requirements; ensuring compliance to Abbott Global Quality/Regulatory Framework, Divisional Policies/ Procedures. Responsible for proactively creating Quality Culture w.r.t People, Process, Products & Services to meet customer needs. Maintain QMS in the market and continually evaluate and monitor the quality system for suitability and adequacy for the commercial business. Must interface and represent commercial leader in areas of quality decisions, such as escalations, field actions and/or other significant quality issues. Engage as required for the Quality Complaints for Abbott prod...

PRODUCTION PLANNING & EXECUTION MANPOWER MANAGEMENT QMS KNOWLEDGE 4M,KAIZEN,14Q,QCC OEE MONITORING Risks & Risk mitigation plan in the manufacturing process to achieve smooth material flow

To ensure timely and thorough investigation of quality-related events such as deviations, OOS, and OOT results in compliance with regulatory standards and internal SOPs, thereby maintaining product quality and patient safety. Deviation Handling: Initiate and lead investigations for laboratory and manufacturing deviations. Identify root causes using tools like 5 Whys, Fishbone, or CAPA analysis. Collaborate with cross-functional teams to implement corrective and preventive actions (CAPA). OOS Investigations: Conduct Phase I and Phase II investigations for OOS results. Review analytical data, equipment logs, and analyst performance. Coordinate retesting and reanalysis as per SOPs. Document fin...

Job Title: Quality and Regulatory Affairs Specialist Quality Management Systems Location : Bangalore / Hybrid Department : Quality & Compliance Reports to: Head Quality & Regulatory Affairs / Legal Counsel About Ultrahuman Ultrahuman is a health-tech company building the worlds most advanced metabolic fitness platform through connected wearable technology and science-backed insights. Our products including the Ultrahuman Ring, M1 CGM, and Blood Vision diagnostics — combine hardware, software, and physiology to help users optimise sleep, movement, and nutrition. We are expanding our Quality and Regulatory Affairs (QARA) function to support the implementation of a Quality Management System (QM...

Responsible for implementing and maintaining ISO & BIS quality systems, conducting audits, managing QMS, CAPA, and supplier quality. Ensure product compliance, process improvement, and zero-defect standards. Required Candidate profile Experienced Quality Manager with strong knowledge of ISO/BIS standards, audits, CAPA, and manufacturing quality. Proven expertise in QMS implementation and team leadership. Perks and benefits Company Accommodation, EPF, Health Insurance

About The Role Skill required: Talent Development - Learning Operations Designation: Learning Operations Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song"” all powered by the world's largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We ...

Hi, Greetings from Avani consulting !! We have opening for Production Associate role with Pharma Mysore location. Exp : min 3 yrs in Production in API Mfg Industry Education: B.tech Chemical. Msc chemistry Work Loc- Mysuru Interview- First round virtual If interested , kindly share an updated resume to ruchi.r@avaniconsulting.com or whatsapp@7050851748 Referrals most accepted and preference given. Job Description 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherenc...

The Head of Quality Assurance & Quality Control (QA/QC) will lead and oversee the organizations quality management functions across all projects. The role is responsible for ensuring strict adherence to contract specifications, IS codes, and ISO 9001:2015 standards while fostering a strong culture of quality, compliance, and continuous improvement. The incumbent will ensure that all project deliverables meet or exceed client expectations through effective quality systems and leadership. Key Responsibilities: 1. Quality Planning and Documentation Develop and implement project-specific QA/QC plans aligned with contract requirements, IS codes, and ISO 9001:2015 standards. Ensure all quality doc...

Job Title: Quality Manager Location: Bhiwandi, Thane Purpose: To ensure adherence to quality standards across all production processes. This role oversees incoming quality control, panel assembly inspections, documentation, and customer audits, while driving continuous improvement, maintaining product integrity, and enhancing overall operational efficiency. Key Responsibilities: Oversee inspection and approval of incoming materials including numerical relays, meters, electronic devices, and fabrication items. Ensure that all required test certificates and reports, as specified in the Quality Assurance Plan (QAP), are verified at the point of receipt. Assist in developing, implementing, and m...

SUMMARY ASSOCIATE PRODUCTION - ASSEMBLY & SFT Requirements PLANNING AND EXECUTION MANPOWER MANAGEMENT OEE MONIOTORING QMS KNOWLEDGE KAIZEN,4M,14Q TROUBLE SHOOTING

Own plant-wide quality systems and drive audits and improvements. Gain exposure across teams and stakeholders to grow leadership skills. About Our Client The hiring company is a well-established large organization operating in the FMCG industry, particularly in the Food sector. They are known for their commitment to delivering premium products and maintaining high standards of quality in their manufacturing processes. Job Description Ensure compliance with quality parameters across all production stages and escalate deviations as needed. Maintain accurate records in SAP and ensure timely compliance with certifications related to quality and food safety. Coordinate with stores for material is...

Role & responsibilities To follow and adhere to Company Policy. Monitoring of all warehouse activities at Vizag Sites (Unit-1, 3, 4, 5, 6&LSPL). Monitoring of all Commercial Department activities at Unit-1, 2, 3,4,5,6 & LSPL. Liaising with Govt.Authorities like Excise, Customs, Narcotics & Explosive Departments. Co-ordination with QA Department during the Internal, Customer and Regulatory Audits. Responsible for Audit Compliance and cGMP implementation in warehouse. Review of Warehouse SOPs and related documents. Lead the investigation of failures pertaining to raw materials. Ensure to initiation of deviations, change controls, CAPA for Quality System implementation is inline with the cGMP. ...

SUMMARY 1. Conducting In-process Inspection activities as per the control plans and ensuring that parts are accepted at each stage before transferred to the subsequent stage. 2. Precision Measurement CMM and Micrometers CNC/VMC Knowledge GD T and Drawing Interpretation. 3. Problem - solving to implement corrective and preventive actions (CAPA) to address issues and reduce scrap. Requirements Proficiency in using a variety of precision measuring instruments Strong ability to read and interpret engineering drawings . Familiarity with programming and operating CMMs Knowledge of quality control standards and methodologies. Familiarity with quality management systems (QMS), Experience with Statis...

Plan, organize & control production activities to meet daily monthly& annual targets Lead production team to achieve quality productivity & efficiency goals Implement lean manufacturing, Kaizen, 5S Ensure quality & preventive actions are implemented

Key Requirements: Young, energetic, and self-motivated professional with 57 years of experience , preferably in Plastic Processing Machinery Manufacturing . Proven experience in Export Sales is mandatory . Willingness to travel extensively – minimum 100 to 125 international travel days per year (Asia Pacific, Africa, Gulf, etc.) and additional domestic travel as required. Hands-on experience in After-Sales Service and customer support. Strong communication and client-handling skills for managing international customers. Ability to read and interpret electrical wiring diagrams . Roles & Responsibilities: Act as the single point of contact for receiving, registering, and resolving export servi...

Looking for Senior Engineer/Engineer–Quality with 4–6 yrs experience in Auto Component industry. Responsible for QA/QC, PPAP, ISO 9001:2015, inspections, audits, CAPA, and 5S implementation at Noida plant. Required Candidate profile - Diploma/B.Tech in Mechanical Engineering - 4–6 years exp in QA/QC - Knowledge of PPAP & ISO 9001:2015 - Skilled in inspection & audits - Strong in CAPA & RCA - Good documentation & analytical skills

Responsibilities: * Lead QMS implementation and audits * Ensure compliance with ISO standards * Manage CAPA process for non-conformances * Collaborate on continuous improvement initiatives * Develop and maintain quality procedures Health insurance Provident fund Annual bonus

Job Title: QA Officer Department: Quality Assurance Location: Neemrana, Rajasthan Company: VRB Consumer Products Pvt. Ltd. About the Company: VRB Consumer Products Pvt. Ltd. is a fast-growing FMCG company focused on producing safe, high-quality, and innovative consumer products. With strong manufacturing capabilities and a commitment to continuous improvement, we are expanding our quality team at our Neemrana plant. Job Summary: We are looking for a detail-oriented QA Officer to support daily quality assurance activities, including in-process checks, documentation, and implementation of quality systems. The ideal candidate will ensure adherence to company standards, GMP, and regulatory requi...

Role & responsibilities 1. Manage quality documentation (policies, procedures, records) 2. Ensure compliance with ISO 9001 and regulatory requirements 3. Support internal audits, management review meetings, and external audits 4. Maintain accurate records and identify areas for improvement 5. Provide training and awareness on quality procedures Preferred candidate profile 1. Quality management certification (e.g., ISO 9001 Lead Auditor) 2. Excellent communication and analytical skills 3. Ability to work independently and as part of a team

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.