2277 Capa Jobs - Page 39

General Summary: Job Overview This is a unique opportunity to join Qualcomms finance and accounting organization based in Hyderabad in the Corporate Internal Audit & Advisory Services (IA & AS) team. The department focuses on assisting the Audit Committee and management teams in the improvement of processes that manage risks related to achieving Qualcomms business objectives. Using Qualcomms risk-based audit methodology, the senior auditor will assist in the execution of internal audits. Specifically, the responsibilities include: Providing U.S. based time zone coverage as needed (up to 50% of time) Supporting the creation of initial planning memos and process flowcharts Identifying and asse...

As a Quality Control Specialist, your main responsibility will be to handle customer complaints in a timely manner by implementing Corrective and Preventive Actions (CAPA) and communicating with customers using the 8D format. You will also be required to upload relevant documents related to quality issues on the customer portal to ensure transparency and efficiency. Monitoring the effectiveness of the action plans derived from customer complaints will be crucial, along with ensuring the implementation of all internal quality procedures. Conducting audits on products, processes, and docks will be necessary to identify and address non-compliances effectively. Additionally, you will be responsi...

Job Responsibilities: You will be responsible for managing workers and delegating them respective work in the sheet metal manufacturing processes. It will be your duty to integrate systemic documentation periodically and handle internal and customer quality issues with an immediate action plan. Your decision-making skills will be crucial for addressing quality issues related to sheet metal stamping, welding, and powder coating processes. Additionally, you will be in charge of handling customer and ISO audits, as well as managing incoming inspection procedures. You will analyze data by completing hypothesis and process capability analysis tests and prepare reports by collecting, analyzing, an...

You will be responsible for meeting the production schedule in terms of quality and quantity. It is essential to maintain discipline in the Packaging area and department while ensuring the implementation of EHS practices. Planning daily activities in the area and allocating different jobs to workmen and machine operators will be part of your routine. Your duties will also include verifying the transfer of Primary Packing Material, maintaining Good Packaging Practices, and adhering to SOPs to uphold product quality standards. Effective control of manpower, machinery, and materials is crucial in the department. You will need to coordinate validation activities, conduct on-the-job training, and...

As a member of our team at Meteoric Biopharmaceuticals, your role will involve various responsibilities related to Human Resources. You will be responsible for Talent Acquisition and Management, ensuring we have the right individuals on board to drive our organization forward. Additionally, you will oversee Onboarding and Offboarding processes, ensuring a smooth transition for new hires and departing employees. Employee Relations and Engagement will be a key focus of your role, as you work to foster a positive and inclusive work environment. Performance Management will also fall under your purview, as you support employees in reaching their full potential through feedback and development opp...

As the Pharmacovigilance (PV)/GCP Auditing & QMS Manager, you will be responsible for independently performing QA activities in collaboration with the Quality Head. This includes managing quality issues, events, deviations, and CAPAs. You will be involved in performing Root Cause Analyses (RCAs) or guiding staff in conducting RCAs, as well as developing CAPA plans or assisting staff in implementing CAPAs. Planning audits based on risk assessments, maintaining audit schedules, and conducting internal audits and vendor audits are also part of your role. Your responsibilities will encompass maintaining controlled documents like SOPs and templates, liaising with Project Leads/Functional Heads to...

We are seeking an experienced Supplier Quality Professional Trainer with 10+ years of expertise in managing supplier quality assurance , supplier development, and compliance in regulated industries (pharmaceutical, biotech, or medical devices). The role involves ensuring suppliers meet company , industry, and regulatory standards by leading audits, driving quality improvement initiatives , and building strong supplier partnerships. Job Responsibilities: Develop and manage supplier quality strategies, policies, and risk management processes. Lead supplier qualification, selection, and approval in alignment with regulatory standards (FDA, EMA, ISO 13485, ICH Q10, GMP). Conduct supplier audits,...

About The Role The Quality Process Professional establishes and runs the quality process. They have various responsibilities which include architecting, defining and maintaining Quality Management Systems to enable standard way of working, developing and managing process assets methods, PoVs best practices, enablers to facilitate delivery and acting as SMEs in areas such as Agile, Service Management, Six Sigma etc. They are responsible for creating and maintaining process metrics baselines and prediction models accountBU level to support data driven delivery execution and governance and support creation of estimation models. They will plan and drive external quality certification initiatives...

1. Monitor raw material dispensing activity. 2. Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations. 3. Conduct validation sampling as per approved validation protocols. 4. Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance. 5. Perform ERP-related transactions of IPQA. 6. Check BSR (Batch Summary Record) and Shipper inspection as per SOP. 7. Manage issuance, review, and reconciliation of formats across all departments. 8. Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance. 9. Ensure cleaning, sanitation, and hygiene in all departments to maint...

About The Role Skill required: Marketing Operations - Quality Management Designation: Quality Auditing Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years About Accenture 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 worlds 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 cou...

We are looking for a highly skilled and experienced Officer, Quality Assurance to join our team in India. The ideal candidate will have 2-5 years of experience in the field. Roles and Responsibility Develop and implement quality control processes to ensure compliance with regulatory requirements. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve quality-related issues and improve overall performance. Analyze data to identify trends and opportunities for quality improvement. Develop and maintain quality metrics and reports to track performance. Ensure all products meet required standards before release...

Should have worked for 2 wheeler OEM Like Hero, Honda , Bajaj, TVSM, Royal Enfield Knowledge about Quality core tools, IMDS, Process & Product Audit, Layout Inspection Calibration, Incoming, Process & Final Inspection, SPC, MSA ,Injection Molding

About The Role Skill required: Membership - Life Sciences Regulatory Operations Designation: Health Operations Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years About Accenture 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 worlds 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 th...

Role & responsibilities Designation: Sr. executive Exp.: 5-7 years Preferred candidate profile He should have understanding in Upholding regulatory compliance (GMP, ICH), Mastering robust documentation and record-keeping, Implementing quality systems like CAPA and change control, Conducting thorough internal and supplier audits, Ensuring effective quality training for personnel, Maintaining a proactive approach through risk assessment, and a strong understanding of product release processes and continuous improvement. This Is Minimum requirement for this position, eligible candidates can apply. We will schedule interview after discussion Email- ShubhamUpadhyay.Sanat@schwabeindia.com

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview As a senior Supplier Quality Engineer with over 6 years of hands-on experience in managing supplier with respect to quality, ensuring part conformance, handling customer complaints, and leading process improvements across diverse commodities including casting, PCB, plastic molding, rubber, and plating. Proven ability to implement robust incoming inspection systems, conduct supplier audits, and drive sustainable quality improvements that align with organizational goals. Responsibilities Lead incoming inspection activities; ana...

NUMEROS MOTORS PRIVATE LIMITED is looking for Deputy Manager - Quality to join our dynamic team and embark on a rewarding career journey Assist the Manager in the day-to-day operations of the business, including setting goals, developing strategies, and overseeing the work of team members Take on leadership responsibilities as needed, including managing team members and making decisions in the absence of the Manager Identify and address problems or challenges within the business, and develop and implement solutions Collaborate with other departments and teams to ensure smooth and efficient operations Maintain accurate records and documentation Contribute to the development and implementation...

At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world. Job Overview The Aerospace Defence & Marine (AD&M) business of TE Connectivity is uniquely qualified to provide innovative solutions for a variety of applications from ruggedized interconnects, fiber optic products, and sealed harness assemblies to high-performance relays and power distribution units. Responsible for the inspection of incoming components, Sub-assemblies,Finished goods and piece parts based on the Specifications, control Plans, or Customer specific requirements. Responsibility: Clearing the lots based on priority on daily ...

Objective To support supplier quality assurance, new product development, lab validation, and quality system improvements. Ensure product reliability and compliance with industry standards through effective audits, documentation, and testing processes. Key Responsibilities Conduct supplier audits and analyze supplier quality performance. Support New Product Development (NPD) activities with documentation such as APQP and FMEA. Collaborate with R&D teams to validate new components and ensure quality standards. Coordinate lab testing of components and ensure adherence to testing protocols. Conduct internal audits for ISO 9001 / IATF 16949 compliance. Implement process improvements to reduce de...

Job Description Summary The Lead Engineer, Quality Development will focus on performing tests (eg NDT) and defining controls (eg SPC). Ensure correct alignment with quality requirements. Ensure that manufactured or procured products meet specified standards before they progress to next phase of production or customer delivery. (Verification/Checking) 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. Job Description Essential Responsibilities: Competency Development & Resource Adequacy: Develop training materials as well as Plan, execute and mon...

Experience : 10 + years Role & Responsibilities: Procurement of plastic moulded components, planning, scheduling and follow up suppliers. Expertise in costing of Moulded, Sheet metal / MS, Painting /Powder coating components. Inventory management : Monitoring of inventory level , forecasting inventory needs as per rolling plan , supplier capacity planning and ensuring adequate stock availability as per plan. Ensure the purchased material meet the required quality standard and specification, Co ordination with QA and suppliers on non conformities and related CAPA. New supplier selection , evaluation of Supplier performance , Supplier Audits Expertise in work -SAP( HANA)

Manage day-to-day quality operations and documentation reviews related to contract/loan-license manufacturing of soft gel capsules. Review and ensure timely closure of: Deviations and Investigations Change Controls CAPAs Coordinate the review of Batch Documentation, Certificates of Analysis (CoAs), and related product quality documentation. Facilitate communication and resolution of quality matters between: Manufacturing sites (CDMO/LL partners) Internal departments (Supply Chain, QC, RA) External customers (on quality queries/documentation) Support management of product-specific documentation such as: Specifications and Test Methods Master Manufacturing Records (MMRs) Packaging components a...

QA Manager OSD/Liquid formulation background.Must have experience in BMR, batch release,validations,qualifications,SOPs,GMP,audits,QMS(Deviation,OOS, OOT, CAPA), tech transfer. Analytical exposure is an added advantage Resume to hrd@stedmanpharma.com

Serve as Quality Lead for outsourced manufacturing operations (CDMO/LL), ensuring robust compliance with cGMP (FDA, EU, ICH, PIC/S). Draft, review, negotiate, and manage Quality & Technical Agreements with contract manufacturers. Oversee and approve Change Controls, Deviations, Investigations, and CAPA activities; ensure timely and risk-based closure. Lead technical review and approval of batch documentation, including BMR/MMR, COAs, specifications, test methods, artworks, and master records. Act as key interface between contract manufacturing sites, internal teams (Supply Chain, Regulatory, QC), and customers to resolve quality issues and queries. Conduct or support audit readiness activiti...

About The Role About The Role ( Team Member - Customer Service) Responsible to provide adequate and quick resolution to all the cases assigned Analyze the complaint trend and present to the senior management Preparing RCA ,Monitoring the cases and initiating corrective action Liaise up and coordinate with business stakeholders to close the cases end to end Job Requirement: Banking knowledge is must (Loan division knowledge is preferred) Good Communication skill (Verbal & Written) Microsoft office hands-on knowledge (Excel/Powerpoint/Word etc.) Graduate n above Min. experience of 5 years n plus