2277 Capa Jobs - Page 32

Skill required: Membership - Life Sciences Regulatory Operations Designation: Health Operations New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years Language - Ability: English(International) - Intermediate About Accenture 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 countries. Visit us at www.accenture.com What would you...

About The Role The Quality Engineer is a member of the Quality department. Primary Skill Functional expert for Change Management process. Knowledge of CAPA ,NC and Investigations along with change control process Resolve issues on SmartSolve for Change and Documentation Modules. Liaise with Master Data Team on resolving issues in SAP for the ECO notifications. Maintain procedures for Document Control and Change Control processes. Maintain Change Management process as per procedure. Review approvals and implement updates in a timely manner to support the various business units. Secondary Skill Strong computer literacy skills in Microsoft Office, drawing package (e.g. CAD) and an ERP (preferab...

About The Role Skill required: Marketing Operations - Quality Management Designation: Quality Auditing Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designAct of overseeing all activities and tasks needed to maintain a desired level o...

About The Role Job Title - Internal Audit Analyst Management Level :11 Analyst Location:Bangalore Must have skills: Chartered Accountant with 2 - 3 years of post-qualification experience in external or internal auditing, preferably in Big 4 or a global organization. Good to have skills: Internal Audit experience with Big 4 or a global organization Job Summary : An agile, highly motivated, innovative thinker with a background in audit, risk, or compliance looking to join a fast-paced, global Internal Audit department that has embraced transformative capabilities including advanced analytics, dynamic risk assessment, and automation to retain its role as a trusted advisor to the business. You a...

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

Responsibilities: Act as the primary point of contact for customers on all quality-related matters. Handle customer complaints, conduct root cause analysis (RCA), and implement effective corrective & preventive actions (CAPA). Monitor and analyze customer feedback, warranty claims, and field issues to identify trends and drive continuous improvements. Ensure compliance with customer-specific quality standards, IATF 16949, ISO 9001, or other applicable certifications. Conduct customer audits, support customer visits, and ensure timely closure of audit findings. Coordinate cross-functional teams (Production, Engineering, Supply Chain) to resolve customer quality issues. Track and report custom...

leadership quality,Review line inspectors ,and plan their work and monitor,documentation as per ISO ,CMM INSPECTION ,inward to Final Inspection Handling. Perks and benefits EL,CL,BONUS,MEDICLAIM,GRAUDITY,

NEED TO HANDLE LINE INSPECTION AS WELL CMM ,DRAWING STUDY Perks and benefits EL,CL,BONUS,MEDICLAIM,GRAUDITY,

Role Overview: As a GLP-Quality Assurance Personnel at Syngene International Limited, Bengaluru, you will play a crucial role in contributing to the GLP Quality Assurance Unit. Your primary responsibility will be to ensure compliance with OECD principles of Good Laboratory Practices (GLP), as well as ICH and WHO-GCLP guidelines. You will be tasked with handling inspections and audits, managing QMS activities such as change controls, deviations, and CAPA, and reviewing SOPs and study plans. Your core purpose in this role is to align laboratory practices with GLP guidelines to uphold the integrity and reliability of non-clinical safety and clinical studies. Furthermore, you will work in a regu...

Role Overview: You will be responsible for item attribute extraction and content enrichment, following the defined process steps as per the SOP (Statement of Process) and executing the final QC/sign off to the customer. Working on RCA/CAPA for any quality issues that may arise will also be part of your responsibilities. Your accountability for the success and quality of the process will be crucial, with your input playing a valuable role in improving defined processes, especially as more automation is introduced and information is gathered. Maintaining a high degree of confidentiality while completing tasks within strict deadlines will be essential. Flexibility and willingness to work in any...

Role Overview: You will be responsible for initiating, reviewing, and approving various quality management systems such as Change Controls, Deviations, Investigations, CAPA, OOS, and Complaints. In addition, you will handle Return Goods and ensure the proper functioning of the quality system by performing risk assessments as needed. Conducting regular internal audits will also be part of your duties. Key Responsibilities: - Review and approve all documents including SOPs, Spec & STPs, Forms, protocols, and reports to ensure compliance. - Review annual product quality review reports and provide training on cGMP topics to employees at the site. - Support customer audits/visits and regulatory a...

As a Manufacturing Supervisor, your role involves ensuring efficient line clearance activities, preventive maintenance of machines, cleaning and sanitizing visual inspection and packing areas, operating machines, and maintaining logs as per SOPs. You are also expected to uphold cGMP, GDP standards, and enforce discipline within the department to ensure uniform compliance among all employees. Key Responsibilities: - Perform line clearance activities before commencing operations - Follow the preventive maintenance schedule of machines - Clean and sanitize visual inspection and packing areas - Operate machines and maintain logs according to SOP - Ensure adherence to cGMP, GDP, and discipline st...

Role Overview: As a Production Manager in the Pharma industry, you will be responsible for overseeing the daily operations of a production team. Your primary goal will be to ensure that production schedules, quality standards, and safety regulations are consistently met to achieve organizational objectives. Key Responsibilities: - Supervising and coordinating daily production activities to meet output, quality, and delivery targets. - Leading all production activities in compliance with Good Manufacturing Practices (GMP) and Current Good Manufacturing Practices (CGMP). - Overseeing the completion targets of intermediate and finished products, including the filling and completion of Batch Pro...

As a Manufacturing Specialist in our company, your responsibilities will include: - Performing line clearance activities before commencing operations to ensure a clean and sanitized visual inspection and Packing area - Following the preventive maintenance schedule of machines - Operating the machines efficiently and filling the log of general areas as per SOP and work execution - Adhering to cGMP, GDP, and maintaining discipline in the department - Ensuring that all employees comply with the same standards Your role will also involve: - Ensuring that all equipment and production lines are in validated and calibrated status - Preparing daily production reports based on achieved targets - Crea...

Key Responsibilities: Lead preparation and implementation of ISO 13485, MDSAP, and 21 CFR Part 820 compliance. Manage the preparation of the Design Dossier along with other documents and ensure compliance with EU MDR requirements. Conduct gap analysis of client QMS and MDD/MDR documentation. Draft, review, and approve stability study protocols, reports, and validation documentation. Organise and oversee Internal Quality Audits (IQA) and Management Review Meetings (MRMs). Plan and execute predefined visits based on client needs and predetermined agendas. Conduct internal audits of systems and processes to identify non-conformances and drive closure. Update technical documentation (CER, PSUR, ...

SENIOR QUALITY ENGINEER QMS -FO A GREEN FIELD KOREAN MNC AT CHENNAI Qualification : Bachelors Degree in Electronics and Communication Engineering (ECE) Experience : 08 -10 Years CTC : 06 LPA to 10 LPA ( Salary is not a constraint for a deserving candidate ) Job Description A Senior Engineer Quality (QMS) for Quality Management System roles in the automotive sector is responsible for developing, maintaining, and auditing the companys QMS processes in line with international standards (ISO 9001, IATF 16949, etc.), leading audits, and driving continuous improvement of quality performance. Lead the implementation, maintenance, and continual improvement of the Quality Management System (QMS) as p...

1.Strong experience in heavy fabrication and machining processes. 2.Experience with PPAP, FMEA, SPC, MSA, and CAPA. 3. NDT LEVEL -II certification in VT,RT, UT, PT, MPT will be prefer. 4. Knowledge fabrication / machining Drawing Reading. Required Candidate profile 5. Control & monitoring on the quality of every Stage Inspection As per QAP. 6.knowledge of Fabrication Processes & machining processes (turning, milling, grinding, drilling, CNC operations).

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Greetings from MSN Laboratories...! We are conducting a walk-in interview for Experienced candidates in Our APICHEM Unit Vangapalli (Near to Yadagirigutta) on 27th Sept 2025 (Saturday). Department- Quality Assurance- AQA& QMS Req Exp- 3 to 8 Yrs Qualification- B. Sc Chemistry/ Any Graduate Designations- Executive/ Jr. Executive/ Sr. Executive Department- TSD Req Exp- 03 TO 08 Yrs Qualification- B. Tech Chemical Designations- Executive/ Jr. Executive/ Sr. Executive Venue Details- APICHEM Laboratories Pvt. Ltd, Vangapalli (V), Yadagirigutta (M), Yadadri Bhuvangiri (D), Telangana. Date- 27th Sept 2025 (Saturday)

Role & responsibilities Strategic & Technical Leadership Define and implement the overall quality strategy for LV and MV switchgear products, including AIS, GIS, and VCB technologies. Ensure compliance with applicable international and national standards such as IEC 62271, IEC 60947, IS standards, and ISO 9001. Set quality goals and drive a culture of continuous improvement through Six Sigma, Lean, and Kaizen practices. Product & Process Quality Oversee the quality control and assurance of all products: AIS (Air Insulated Switchgear) panel fabrication, insulation testing, dielectric testing. VCB (Vacuum Circuit Breakers) – assembly accuracy, vacuum integrity, contact resistance. In Process &...

Role Overview: As a PV Physician at Dr. Reddy's Laboratories Ltd., you will be primarily responsible for overseeing and providing medical input for benefit-risk assessment activities. Your role will involve ad hoc data analysis, preparation and review of aggregate reports, signal detection and evaluation, support for benefit-risk evaluation efforts, and more. Your contribution will be crucial in ensuring the safety and efficacy of pharmaceutical products. Key Responsibilities: - Ensure quality control of medical assessment of individual case safety reports, including coding, seriousness, expectedness, and company causality assessments conducted by the vendor. - Contribute to scheduling of ag...

1. Oversee and coordinate the daily operations of the QA department, ensuring all activities align with business goals and customer requirements. 2. Carry out Lay out inspection, Process, Product & ESD audit on shop floor. 3. Lead the development and execution of quality assurance plans for products, including both manual and automated testing strategies. 4.Identify opportunities for process improvement, implement changes to enhance product quality and efficiency. 5. Monitoring in-process & Final quality inspection with QMS documentation. 6. Ensure compliance with regulatory standards, industry best practices, and company policies regarding quality assurance processes. 7. Managing out fault ...

Job Summary The Policy Servicing Specialist will be responsible for managing and maintaining life and annuities insurance policies. This role requires a keen eye for detail and proficiency in MS Office to ensure accurate policy servicing. The candidate will work in a hybrid model primarily during day shifts with no travel required. The role is crucial in supporting the companys mission to provide exceptional insurance services. Responsibilities Manage and maintain life and annuities insurance policies to ensure accuracy and compliance with company standards. Utilize MS Office tools to efficiently process and update policy information. Collaborate with internal teams to resolve policy-related...

Responsible for managing customer quality requirements, ensuring product and process compliance, and driving continuous improvement to achieve zero-defect deliveries Maintain IATF 16949 & QMS compliance, internal & external audits Support NPD plans Required Candidate profile This role acts as the key interface between customers, internal quality teams & production to resolve issues & maintain high customer satisfaction Knowledge of SPC, MSA, PPAP, FMEA & problem-solving

Build sustainable relationships and trust with customer via open and interactive communication Regular & timely interaction with the customer via various modes like calls, whatsapp, EDMs etc. as decided per the business plan Explain customized proposition to the customer basis the important dates (Birthday, Term Renew etc.) Perform annual protection review calls as per the timelines Campaign Calling Perform Segmented product based campaigns including GLIP, SWP, FWP and others Perform Service Request Calls Keep records of customer interactions and ensuring timely processing of client service request Handle customer complaints, provide appropriate solutions and alternatives within the time lim...