2277 Capa Jobs - Page 27

Post - Sr QA / QC Engineer Location - Pune Alandi Markal Solu Contact - 9356395439 / 7666770622 Relocation can applying Education - BE / Diploma in Mechanical Engineering Experience - 4-08 yrs Industry - Fabrication / welding JD Experience in Quality Assurance and Quality Control . Heavy Fabrication and Welding industry ISO 9001 CERTIFILED ISO DOCUMENTATION AND QUALITY AUDIT OTHER RELEVANT QUALITY STANDARDS. strong knowledge of quality control principles , CAPA , SPC , MSA STRUDY ROOT CASE ANALYSIS.

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...

As a QA Chemist at Sinterx Pharma Private Limited, you will play a crucial role in ensuring that all API intermediate manufacturing operations adhere to established quality standards, GMP requirements, and regulatory guidelines. Your responsibilities will include: - Reviewing and approving GMP documentation such as BMRs, BPRs, SOPs - Overseeing batch records, managing deviations, and CAPA - Conducting internal audits and ensuring compliance throughout the production lifecycle Qualifications required for this role include: - Bachelor's or Master's Degree in Chemistry, Pharmaceutical Sciences, or Life Sciences - 5 to 8 years of experience in Quality Assurance within the API or API Intermediate...

Post - Sr. Engineer Quality Assurance Experience - Min 5-08 Years Industry - Plastic injection Moulding Email - jobpune25@gmail.com Contact - 9356395439 Skills QMS - overall Quality Management System IATF Automotive Plastics Domains CAPA SOP Plastic Injection Molding process 7QC, APQP, PPAP EHS systems Quality Assurance

Post - Sr. Engineer Quality Assurance Experience - Min 5-08 Years Industry - Plastic injection Moulding Email - jobpune25@gmail.com Contact - 9356395439 Skills QMS - overall Quality Management System IATF Automotive Plastics Domains CAPA SOP Plastic Injection Molding process 7QC, APQP, PPAP EHS systems Quality Assurance

Key Responsibilities Facilitate Scrum/Agile Frameworks Guide and coach teams to adopt Scrum practicesfacilitating stand-ups, sprint planning, reviews, and retrospectives; ensuring Agile values and principles are upheld. Lead and Oversee Workstreams Workstream A : Reporting, integrations, migration heavy focus on system integration deliverables. Workstream B : Front-end process drive cross-functional collaboration for requirements, design, development, and testing. Remove Obstacles & Enable Delivery Identify and eliminate impediments, manage dependencies, and coordinate across distributed teams to ensure smooth workflow. Drive Continuous Improvement Facilitate retrospectives, implement proces...

QA/AC Manager Sr. Manager (Plant) - Plastic PET BOTTLE Packaging Industry Location: Tamil Nadu/Telangana Position: QA & QC Manager Experience Required: 10+ Years Educational Qualifications: B.Sc, B. TECH, PGD-PPT, CIPET or equivalent Key Responsibilities Lead and Manage the Quality Team: Oversee a team of 25-30 quality professionals. Provide guidance and training to promote a culture of excellence and continuous improvement. Maintain and Improve Management Systems: Maintain and enhance the company's integrated management systems, including ISO 9001, and BRCGS for Packaging. Ensure compliance and readiness for all audits. Ensure Product Quality: Implement robust quality control processes for ...

Job Description Job Title: Specialist/Lead Quality Assurance Employment Type: Full time Location: Bengaluru, India About ClinChoice ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world. Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights, delivering the best strategies for product registration, and enhancing patient safety through real-world and clinical analysis. Our global delivery network has expanded to centers and satellite offices in t...

Who We Are At Kyndryl, we design, build, manage and modernize the mission-critical technology systems that the world depends on every day. So why work at Kyndryl? We are always moving forward – always pushing ourselves to go further in our efforts to build a more equitable, inclusive world for our employees, our customers and our communities. The Role Are you passionate about delivering exceptional service and revolutionizing the world of technology? We have an incredible opportunity for a talented individual to join our dynamic team as a Delivery Management Lead. In this customer-centric role, you will play a pivotal role in ensuring our customers receive top-notch service within a contract...

UNDERSTAND THE AUTOMOTIVE SUSPENSION SYSTEM COMPONENTS FUNCTIONING AND ANALYSE THE MARKET FAILURE [MAJOR PARTS ARE BOX ASSY STEERING GEAR, COLUMN ASSY COLLAPSIBLE STEERING, WHEEL ASSY STEERING ETC]. QUICK RESOLUTION OF SUSPENSION SYSTEM RELATED MARKET FAILURES THROUGH ROOT CAUSE ANALYSIS AND TAKING COUNTERMASURES. JOB RESPONSIBILITY DIAGNOSE AND RESOLVE CUSTOMER COMPLAINTS ACTION JUDGEMENT FOR CRITICAL MARKET ISSUES (HANDLING RECALLS, SERVICE CAMPAIGNS). WARRANTY DATA ANALYSIS INITATE PROACTIVE ACTION STRATEGIES FOR MARKET CLAIM REDUCTION. COMPETENCY REQUIREMENT: PROFOUND KNOWLEDGE ON VEHICLE STEERING SYSTEM. KNOWLEDGE OF AUTOMOTIVE-SPECIFIC GOVERNMENT REGULATIONS LIVE MOTOR VEHICLE ACT AND ...

Good knowledge of the inspection of sheet metal parts. Knowledge of measurement and reading drawing. Vernier Caliper , Height Gauges, Micrometer.Line Quality Inspection. Required Candidate profile Sheet metal or mechanical background.

Skill: CSV Manager Notice Period: Immediate . Employment Type: Contract Working Mode : Hybrid Job Description 12+ years of experience working in electronic based Computer System Validation in a GxP environment Demonstrated ability to maintain a CSV and Computer and Instrument System Change Control process Experience in employing risk-based approaches to CSV Experience in qualification of GLP Instrument Systems Ability to provide Quality oversight during implementation of GxP Software as a Service tools and systems Experience in perform

Responsibilities: Ensure compliance with QMS protocols in production and packing areas. Review and maintain batch records, SOPs, and documentation as per USFDA standards. Support deviation investigations, CAPA, and change control processes. Coordinate with cross-functional teams to uphold GMP and regulatory requirements. Key Skills: Knowledge of QMS and GMP in pharmaceutical manufacturing. Experience in USFDA-audited facilities preferred. Strong documentation and communication skills. Proffered Candidate Profile: Bachelors or Masters degree in Pharmacy or related field. 2–4 years of experience in pharmaceutical production or packing, preferably in a USFDA-audited facility. Strong understandi...

As a Manager Validation (Production) at the Mohali location, your role will involve the following responsibilities: - Build a cohesive team to support Validation activity at A-41 Mohali Location - Collaborate to create a robust Corrective and Preventive Action (CAPA) program - Conduct Equipment and facility Validation at A-41 Mohali Location, working with site-specific teams to prepare, review, and execute protocols and Master Validation documents - Prepare, review, and execute protocols & reports for facilities involving utilities, engineering, manufacturing operations, and cleaning. This includes HVAC, water, compressed air, and process/packing equipment qualification & validation - Ensure...

Role Overview: As a Safety Engineer/HSE Engineer, your primary responsibility will be to ensure a safe work environment for all personnel. You will play a crucial role in enhancing safety standards at project sites, conducting safety training, and implementing preventive measures to minimize risks and maintain a risk-free environment. Your expertise in identifying safety hazards, conducting surprise inspections, and driving compliance with HSE regulations will be key to the success of the organization. Key Responsibilities: - Identify potential safety hazards and risks at the site and implement appropriate risk mitigation strategies. - Regularly assess site conditions and practices to ensure...

As the Deputy General Manager of Quality Assurance, you will be responsible for overseeing the execution of quality assurance activities, collaborating with internal and external stakeholders to maintain high product quality, and representing management in regulatory audits, customer communications, and quality-related matters. Key Responsibilities: - Review, approve, and ensure alignment of key quality management system documents with relevant ISO standards and regulatory guidelines. - Drive continuous improvement and ensure full implementation and maintenance of the Quality Management System (QMS) across the organization. - Ensure adherence to statutory, legal, and international quality st...

As a Senior Executive at Syngene International Ltd. in Bangalore, you will be responsible for the commissioning & qualification, and QMS activities for biopharmaceutical manufacturing facilities. Your key responsibilities will include: - Performing validation of computerized systems and Electronic Records and Electronic Signature (ERES) Validation. - Timely preparation, review, and approval of URS, DQ, IQ, OQ, and PQ protocols and reports. - Coordinating the Calibration Program, Preventive Maintenance Program, and Alarm Management for manufacturing facilities. - Conducting investigation for equipment failure, root cause identification, and implementation of appropriate CAPA. - Participating ...

Location - Jigani. compliance with AS9100 / ISO 9001 standards. conduct internal audits. Quality Management System documentation, certification audits, MRB (Material Review Board, activities. Required Candidate profile Location - Jigani. compliance with AS9100 / ISO 9001 standards. internal audits. Quality Management System documentation, certification audits, MRB (Material Review Board, activities.

Role Overview: As a Senior Manager / DGM - Sterility Assurance at our Halol - Vadodara location, you will be responsible for overseeing the Sterility Assurance and QMS elements for Sterile manufacturing Units. Your role will involve handling Regulatory Audit Queries and ensuring the implementation of contamination control strategies in compliance with regulatory standards. Key Responsibilities: - Own the Aseptic process simulation program of the site, including protocol development, operators training, intervention qualification program, and Trending analysis. - Develop and enhance the Sites Contamination Control Strategy to ensure robustness and continuous improvement. - Lead the Sterility ...

You are being hired for the role of Deputy Manager in Operational Excellence for the Chennai location. Your primary responsibilities will include: - Experience required: 5 to 8 years - Proficiency in Baselining, Benchmarking, Load Balancing, Resource Utilization, Cross Utilization, Business Analysis, SLA revision, etc. - Design, develop, and deploy a Quality Management System (QMS) framework aligned with customer expectations and business requirements. This includes SLA Management, Metric Management, setting targets, post-transition performance evaluation, reporting, sampling techniques, error definition (Critical & Non-Critical), FMEA, etc. - Schedule and manage customer interactions (VoC -...

As a Quality Assurance Manager at Apotex Inc., you will be responsible for ensuring the effective review and approval of various quality control processes. Your key responsibilities will include: - Reviewing and approving lab investigation reports, deviations, questionable results, out of specification (OOS) and out of trend (OOT) investigations. - Preparing and reviewing standard operating procedures. - Coordinating with cross-functional teams for the closure of investigations in a timely manner. - Reviewing and approving change controls, lab events, and temporary changes. - Coordinating with the regulatory department for submissions and post-approval changes. - Identifying system improveme...

You will be working as a Senior Executive - AQA at Jubilant Pharmova Limited located in Nanjangud, Mysore. Your role will involve the following key responsibilities: - Responsibility for analytical compliance in accordance with current regulatory guidelines, monograph requirements, customer needs, and internal procedures. - Reviewing laboratory metrics to identify areas for improvement in laboratory compliance and ensuring right first-time laboratory performance. - Reviewing and approving laboratory Quality Management System (QMS) documents such as Out of Specification (OOS), Out of Trend (OOT), Deviation, Change management, Incidents, Action items, Corrective and Preventive Actions (CAPA), ...

Post -Quality Manager-API Q1 & 6A 5CT knowledge Qualification Any graduate or DME / BE /BTECH Experience – in CNC & VMC Production line Experience - 8-10 yrs CTC -5.20 lpa Location Pune chakan contact -9356395439 Email jobpune22@gmail.com interview Arrangement Person must have following skills and Knowledge . • Sound knowledge and experience in ISO & IATF 16949 . • Communication skill in English is must Speaking , writing . • Automotive experience is must . • Person must have sound knowledge in 7 QC TOOLS . APQP , PPAP , 8D CAPA , CPK study etc . • Mass production and daily dispatch experience is preferred . • Person should have ability to lead the team of 20+ workman

As an experienced professional with 3~5 years of relevant experience in the automotive industry, you will be responsible for various key activities: - Conducting root cause analysis and simulating market failures of vehicle systems, with expertise in Brakes, Suspension, and ADAS systems. - Utilizing your work experience and knowledge of Electric vehicles and new technologies to your advantage. - Understanding and applying vehicle and component level testing standards for new models, and possessing basic knowledge of design-level interventions for quality problems. - Planning and executing fleet testing across India, and analyzing large amounts of test data to derive meaningful solutions. - D...

As a Document Controller at Ferring India Laboratories, your role involves handling the issuance, control, and retrieval of documents. You will be responsible for scanning and uploading approved paper-based documents in Veeva Vault. Additionally, maintaining master copies for SOPs, including issuance, control, and retrieval of SOPs will be a key part of your responsibilities. Your key responsibilities will include: - Managing and conducting training sessions - Organizing training programs - Maintaining vendor audit and technical agreement planners - Preparing and reviewing SOPs, Protocols, and other cGMP documents - Tracking Change control, CAPA, Deviation, OOS/OOT, and coordinating with sta...