2277 Capa Jobs - Page 24

Leadership Position to head Corporate Quality and report into the COO Lead Quality for 5+ Manufacturing Sites for a leading Automo Component Suppl About Our Client Our client is a leading Automotive Component Supplier headquartered in Delhi-NCR and has multiple plants across India in addition to dedicated R&D Centres Job Description Strategic Leadership Define and implement a unified Quality Vision and Strategy across all plants. Align quality goals with corporate objectives, customer expectations, and regulatory requirements. Lead cross-functional quality governance for new product development, launch, and lifecycle management Multi-Plant Oversight Oversee Quality Assurance and Control acro...

Job Title Sr Executive/Manager 2 Business Unit Sun Global Operations Job Grade G11B/G11A Location : Guwahati At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Key Responsibilities Responsible for Receipt of Raw, Packing & Misce...

Looking For highly motivated Engineer with Supplier Quality and Management skills. The Engineer is responsible for ensuring that all materials, components, and services provided by external suppliers meet the company's quality standards and regulatory requirements. This role is essential in evaluating, developing, and managing suppliers to improve product quality, reduce costs, and ensure on-time delivery. The SQME collaborates with cross-functional teams and suppliers to drive continuous improvement and operational excellence. Responsibilities Lead supplier qualification, development, and onboarding processes. Conduct supplier audits and assessments (initial, routine, and follow-up) in acco...

Role Purpose The purpose o central quality analyst role is to conduct quality audits and perform analytics in different areas as defined by central quality team, supporting the project teams in ensuring higher client satisfaction Do 1. Conduct process quality audits as per plan Conduct various process audits as per guidelines and SPOs defined in QMS Prepare findings from the report and share it with the account/ project leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridg...

Role Purpose The purpose o central quality analyst role is to conduct quality audits and perform analytics in different areas as defined by central quality team, supporting the project teams in ensuring higher client satisfaction Do 1. Conduct process quality audits as per plan Conduct various process audits as per guidelines and SPOs defined in QMS Prepare findings from the report and share it with the account/ project leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridg...

Role Purpose The purpose of this role is to conduct audits to ensure quality compliance within the account. Do Conduct process quality audits as per plan Conduct various process audits (1 audit/ agent/ week) as per procedure and guidelines For agents identified in the bottom quartile of performance, conduct 3 audits/ agent/ week Prepare findings from the report and share it with the client and the account leadership on daily/ weekly/ monthly, as required Conduct weekly analysis to identify the error trends and for top 2 errors, conduct root cause analysis (RCA) Conduct calibration communication to communicate any changes from the client and conduct refresher trainings to bridge any skill gap...

Before you apply to a job, select your language preference from the options available at the top right of this page. Explore your next opportunity at a Fortune Global 500 organization. Envision innovative possibilities, experience our rewarding culture, and work with talented teams that help you become better every day. We know what it takes to lead UPS into tomorrowpeople with a unique combination of skill + passion. If you have the qualities and drive to lead yourself or teams, there are roles ready to cultivate your skills and take you to the next level. About The Role : Job Summary The Healthcare Quality Assurance (QA) System Validation Supervisor provides guidance to UPS Supply Chain So...

Job Description Maintenance of GLP in the Laboratory Upkeep of Housekeeping in the Laboratory. Ensuring activity logs are maintained for all critical instruments /equipment’s. Timely preparation of Laboratory Documents. Timely review of analytical data generated in laboratory. Ensuring Analytical Technology transfer from transferring lab as per approved protocol. Review and approval of incident , out of specification ,out of trend report and approval of QC related activities. Involved in QAMS activities such as change control, CAPA , incidents, deviation etc. Approval of stability summery report. Timely review of Quality control procedures and initiation for up gradation of same. Compliance ...

Job Description As a Manager at Lupin Limited, positioned within the Mechanical (Unit I) division at our Pithampur facility, you will take the helm of our engineering operations, spanning the Mechanical, Electrical, and Instrumentation domains. Your role will be pivotal in ensuring the seamless functioning and reliability of pharmaceutical process equipment used in both formulation and active pharmaceutical ingredient (API) production processes. You will be responsible for the strategic oversight and execution of both preventive and breakdown maintenance activities, ensuring minimal downtime and optimal equipment performance. This will involve coordinating comprehensive maintenance schedules...

Role & responsibilities Quality Engineer Quality Engineering: Knowledge on GD&T Engineering Drawing Reading Knowledge on Final Inspection Knowledge in instrument handling - Vernier calipers, Micrometers, Height gauge 7 QC, 8D, SPC & Quality Tools Supplier Quality Management Qualification: Diploma in Mechanical or NTTF / Experience 1-2 Year CMM Programmer: Experience 0-2 Year Proficient in CMM programming with PC-DMIS software / Calipro Experienced in operating the Coordinating Measuring Machine, Make-Hexagon Knowledge about GD&T, Drawing interpretation & Inspection VMS Programmer (Video Measuring System): Experience 0-2 Year Proficient in VMS or OMM programming with any software Experienced ...

Position : Vice President - Operations / Plant Head / Vice President - Operations_Winding Wires / Wires & Cables / Any other process Industry / Manufacturing Industry or similar industry. Industry : Copper & Aluminium Wire Manufacturing Location : Anand, Gujarat Reports To: Managing Director / CMD Role Objective: To provide strategic leadership, operational excellence, and overall management of the Copper & Aluminium Wire Manufacturing plants. The role focuses on driving productivity, efficiency, quality, cost optimization, compliance, and employee engagement to ensure smooth and profitable operations. Key Responsibilities: Plant Operations Management Lead end-to-end operations of all the ma...

Roles and Responsibilities 1. Responsible for implementation & monitoring of cGMP/GDP practices at site. 2. Responsible for periodic review of all quality Documents for appropriateness. 3. Preparation of SOPs and handling of QMS tools like deviation change control, CAPA. 4. Responsible for approval/rejection of deviations /change controls pertaining to corporate activities. 5. Oversee the team of technical personnel handling order processing artworks finalization BOM updating of products and follow ups. 6. Responsible for co-ordination and submission of Quality documents for regulatory submissions. 7. Responsible for maintenance, periodical update and review of technical agreements with dome...

As an experienced Quality Control Manager in the plastics industry, you will play a crucial role in leading the quality department to new heights. Your responsibilities will include: - Minimum 3 years of experience in the plastics industry, with a focus on Quality Control/Assurance. - Demonstrated expertise in quality documentation processes, standards, and regulatory compliance. - Proven track record as a team leader, showcasing excellent organizational and communication skills. - Implementation and maintenance of quality systems to ensure consistent product excellence. - Knowledge and experience in audits, root cause analysis, CAPA, and continuous improvement initiatives are advantageous. ...

Role Overview: You will be responsible for ensuring the establishment, implementation, and maintenance of processes needed for the Quality Management System at the company. Reporting on the quality system's performance to the Head-QA for review and improvement will be a key part of your role. Additionally, you will plan and execute clinical activities, conduct audits, review equipment maintenance, data analysis, and support regulatory inspections. Key Responsibilities: - Ensure establishment, implementation, and maintenance of processes for the Quality Management System. - Report on the performance of the quality system to the Head-QA and suggest improvements. - Plan and execute clinical act...

Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong ...

As a candidate for this role, you will be responsible for various tasks related to self-hygiene and the sterile manufacturing department. Your key responsibilities will include: - Updating on self-hygiene - Preparation, review, revision, control, and implementation of standard operating procedures - Preparation and review of protocols and reports - Document management including BMRs, BPRs, Master SOPs, etc. - Handling of Change Control, Deviations, CAPA, Investigation - Generating general purchase indents for departmental items - Preparation of production planning on a monthly and daily basis - Preparation of daily production reports - Ensuring validation and calibration status of equipment ...

Role Overview: You will be responsible for coordinating and preparing for internal and external audits such as ISO, GRS, OCS, Intertek, etc. You will also develop and maintain compliance checklists and audit documentation. Monitoring HR policies and practices to ensure alignment with certification standards will be a key part of your role. Additionally, you will be involved in training and supporting internal teams on compliance protocols and audit readiness. Liaising with certification bodies and auditors during audits and identifying gaps to propose corrective and preventive actions (CAPA) will be crucial. Staying up to date with regulatory and certification standard changes and promoting ...

As a Production Operator at ACG Group Company in Dahanu, India, your primary responsibilities will include: - Checking the allocated post production (ATS/Printing/camera) line(s) in each shift as per the CTQ (critical to Quality) /CTP (Critical to Productivity) checklist. - Following the plan as per color change note by ensuring minimal change over time at each sub section. - Following instructions from the shift lead for timely change over by ensuring availability of roller(s)/ink etc. - Executing IPQC after every roller cleaning and checking of rejections of camera(s) after every hour to achieve zero defects. - Operating cameras as per SOP to achieve productivity and quality. - Coordinatin...

Key Responsibilities Monitor and ensure compliance with quality standards during all stages of solar module production (cell sorting, stringing, lamination, assembly, and final testing). Conduct in-process and final inspections, audits, and testing of PV modules as per IEC/UL standards. Perform root cause analysis and corrective & preventive actions (CAPA) for quality issues and customer complaints. Collaborate with production, maintenance, and R&D teams to improve process capability and product quality. Support implementation of ISO 9001, ISO 14001, and ISO 45001 management systems within the plant. Ensure adherence to reliability testing protocols (EL testing, IV curve measurement, thermal...

HI, We have an opening for Assistant Manager - QC (Analytical Reviewer & QMS) in Nerul, Navi Mumbai Location. Experience - 10 - 15 yrs Qualification - M.Sc. (Chemistry/Analytical Chemistry) Interested Candidate may forward his resume on ankit02.kumar@usv.in Job Responsibilities: 1. Review of Logbooks, Test data sheets, and data generated in Quality control Analytical department. 2. Routine inspection of Quality control department to check and ensure compliance as per cGMP. 3. Routine inspection of QC schedule for execution. 4. Preparation and review of protocol and report for validation, verification, Characterization, hypothetical testing and Force degradation studies. 5. Initiation of devi...

Responsibilities: * Lead quality initiatives at foundry site. * Implement PPAP process & ISO standards. * Conduct Why-Why analysis & RCA investigations. * Ensure compliance with IATF requirements.

Roles & Responsibilities: Quality Oversight Supervise and implement quality control measures across manufacturing operations to ensure compliance with ISO 13485, FDA QSR, and other applicable regulatory standards. Conduct regular in-process and final inspections of products to identify defects and ensure they meet specifications. Manufacturing Process Monitoring Collaborate with manufacturing teams to monitor and control production processes, ensuring adherence to Good Manufacturing Practices (GMP). Review and approve manufacturing process documentation, including SOPs, work instructions, and validation protocols. Quality Systems Management Maintain and support the quality management system ...

Role & responsibilities 1. Preparation of COA for Dispatch of APIs and Excipients. 2. Reviewing of completed Batch Production Records and laboratory records (Test data sheet). Distribution and Release of batches. 3. Review and Approval of validation/qualification protocols and reports. 4. Preparation and Review of change control that potentially impact intermediate or API quality. 5. Formal investigation of laboratory incidents, deviation and out-of-specification laboratory results and documentation. 6. Investigation of Market complaints, Market returns and Product recalls. 7. To give proper training of GMP and of other subjects to all related employees. 8. Review and qualification of any ne...

Developing and implementing quality standards. Monitoring and analyzing quality performance. Inspecting and testing materials, equipment, processes, & ensure customer quality specification. Awareness of IATF, VSA & Red Bin Analysis.

Quality Inspector (QA/QC) Education & Experience: Diploma with 2 - 5 years Work Location: Jigani, Bengaluru Key Responsibilities: 1. Candidates should have knowledge in Aerospace Manufacturing, handling instruments & inspection methods for receiving, in-process & final inspections, calibrated instruments process & stamping activities. 2. Good knowledge on RCCA, CAPA, 7QC tools, GD&T, Kaizen, Calibration & handling Internal Audits 3. Adherence to Quality Management System in accordance with AS9100 & AS9102 requirements.