2270 Capa Jobs - Page 9

KGVK (NGO & CSR Arm of Usha Martin Limited) is looking for Quality Control/Assurance Professional to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control systems to ensure products meet regulatory and customer standards. Conduct inspections, audits, and testing to identify deviations or defects. Collaborate with production and R&D teams to address quality issues and implement corrective actions. Maintain documentation and compliance with ISO and GMP standards for continuous improvement. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourag...

KGVK (NGO & CSR Arm of Usha Martin Limited) is looking for Quality Control/Assurance Professional to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control systems to ensure products meet regulatory and customer standards. Conduct inspections, audits, and testing to identify deviations or defects. Collaborate with production and R&D teams to address quality issues and implement corrective actions. Maintain documentation and compliance with ISO and GMP standards for continuous improvement. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourag...

Job Description JOB Responsibilities: - Location: Ahmedabad 1. Ensuring the GMP compliance at CMO and Release of batch manufactured for US market at CMU. 2. Monitoring of process starting from dispensing to packing including witness analysis of Lupin products manufactured at CMO for US market and Domestic market. 3. Handling of market complaint with root cause identification and ensuring the CAPA implementation. 4. New product review to be carried out at manufacturing site after availability of all the documents. 5. Review and authorize Master Batch Records, stability protocol, process validation protocol, temperature cycling protocol, specification of in-process, intermediate and finished p...

Responsibilities Formulation and filling in-charge Planning of Formulation and Filling area Indenting of raw materials from store Availability of raw materials, consumables required for Formulation and Filling area Maintain Raw and PPM inventory as per the production schedule Product changeover in Formulation and Filling Media fill simulation activity Coordinate with other department for equipment qualification / requalification / revalidation and equipment calibration activity Supervision of online documentation Review of documentation Preparation of new SOPs, Annexures, BMRs and summary protocols Awareness about deviation, investigation, change control, CAPA cGMP practices Heath hygiene Qu...

Job Title: Senior QC + QA Trainer (Pharma / Biotech Laboratory) Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced and knowledgeable QC + QA Trainer to design, develop, and deliver technical training programs for quality control and quality assurance teams. The trainer will be responsible for building competence in analytical testing, documentation practices, GMP compliance, and QA/QC systems within a regulated laboratory environment. Key Responsibilities: Training & Development Develop and deliver structured training programs on QC laboratory techniques, QA systems, and GMP compliance . Conduct practical laboratory training (analytical instruments, wet che...

This job is with Pfizer, an inclusive employer and a member of myGwork the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Everything we do every day is driven by an unwavering commitment to delivering safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the customer first. Whether you are engaged in development, maintenance, compliance, or analysis through research programs, your contribution will have a direct impact on patients. Our dedication to quality and safety ensures that every product we deliver meets the highes...

Job Title: Sr Officer – Production Business Unit: Sun Global Operation Job Grade G12B Location : Gangtok 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: To ensure operation & Preventive Maint...

Responsibilities: Prepare SOPs, manage quality systems, conduct customer audits. Ensure compliance with ISO standards through documentation. Implement QMS, prepare CAPAs, document quality actions. Annual bonus

Role Overview: You will play a crucial role in leading downstream manufacturing compliance and ensuring quality management systems in line with cGMP and regulatory requirements at a sterile pharmaceutical manufacturing unit. Your contribution will directly impact patients by maintaining the excellence of every product delivered by the company. Your responsibilities will include handling change control management, coordinating with investigators for CAPA identification, reviewing and approving manufacturing records, ensuring compliance to audit observations, monitoring training metrics, and supporting site inspection readiness programs. Key Responsibilities: - Lead downstream manufacturing co...

As the Manager - API at Dishman Carbogen Amcis Limited, located in Bavla, Gujarat, IN, your role involves the following responsibilities: - Preparation and review of Standard Operating Procedures. - Issuance, review of OOS, OOT, Deviation, CAPA, Change Control & its Management. - Handling and monitoring of control samples. - Imparting internal trainings to DCAL Employees. - Reviewing Calibration records, Instrument Logs of Quality Control. - Reviewing Analytical Method Validation protocols and reports. - Reviewing the Instrument qualifications and re-qualifications protocols of Quality control. - Preparation and review of quality risk assessment documents. - Reviewing and approving analytica...

"QMS Knowledge of Regulatory standards CFR820 , ISO 13485 & 14971, 60601 Hands on experience on Risk Management Good understanding of Post Market Survey and complaint handling Design plan Medical Process DQC Deviation and CAPA preferred " " Be a part of core project team and support the quality engineering across the entire development cycle Lead product risk management, usability, reliability and design validation efforts for new product development and design change projects, Lead the development and implementation of design verification and validation plans with project design lead, Lead the development of Critical to Quality (CTQs), design input and output documents, Lead the fixture qua...

"QMS Knowledge of Regulatory standards CFR820 , ISO 13485 & 14971, 60601 Hands on experience on Risk Management Good understanding of Post Market Survey and complaint handling Design plan Medical Process DQC Deviation and CAPA preferred " " Be a part of core project team and support the quality engineering across the entire development cycle Lead product risk management, usability, reliability and design validation efforts for new product development and design change projects, Lead the development and implementation of design verification and validation plans with project design lead, Lead the development of Critical to Quality (CTQs), design input and output documents, Lead the fixture qua...

Role Overview: As a Quality Head at our manufacturing facility in Noida, you will play a crucial role in leading the Quality Assurance & Control function. Your expertise in quality systems within the television and home appliances sector will be essential in ensuring product excellence and compliance with national and international standards. Key Responsibilities: - Lead end-to-end Quality Assurance (QA) and Quality Control (QC) operations within the plant. - Design, implement, and maintain robust quality systems and SOPs to uphold product reliability and enhance customer satisfaction. - Monitor in-process quality controls, supplier quality, and conduct final product audits. - Drive initiati...

Handling of Manufacturing Compliance i.e. IPQA Activity Handling of QMS Documents like CAPA, and OOS and Change control Handling of APQR Handling of Batch release activity Good in communication skills Exposure of Regulatory audit

Jindal Advance Materials is looking for Quality - QMS Associate - Patherheri (- yrs) to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Job Title: Manager - Regulatory Affairs / Quality Assurance Company: GreenSignal Bio Pharma Pvt Ltd Location: Gummidipoondi, Chennai, Tamil Nadu Experience: 10-15 years in Quality Assurance and Regulatory Affairs, specifically within the Vaccine, Injectable, and Sterile Industry Educational Qualification: Bachelors or Masters in Pharmacy M.Sc in Biotechnology, Microbiology, or a related field Additional qualifications in life sciences or pharmaceutical sciences are a plus Job Overview: As the Manager QA / Regulatory Affairs , you will play a pivotal role in ensuring that our vaccine , injectable , and sterile pharmaceutical products meet global regulatory requirements and quality assurance (...

First Piece Inspection Report Active participation in RCA/why-why analysis/CAPA Material inspection before and after plating Incoming RM / Tooling inspection Ensure proper and timely disposal of NG material Maintain NC product data KHED SHIVAPUR. Required Candidate profile feedback to Purchase team regarding supplier quality issues Conduct hourly In-process inspection on all machines Properly maintain all inspection instruments as per list of IMTE JR ENGINEER . Perks and benefits ALL BASIC BENEFITS ,TRANSPORT CANTEEN ETC

Role & responsibilities - Quality Engineer for Assembly process line inspection & documentation Preferred candidate profile Quality Engineer for Auto parts industry

Lead QA team, ensure product quality, maintain IATF/ISO systems, handle APQP & PPAP, manage inspections, resolve complaints, audit suppliers, track quality metrics, and drive continuous improvement. Salary Range:-35k to 45k

1 INCOMING MTLs INSPECTION Prepare control paln for all items procure from out side Incoming inspection as per set control plan for all received items. RC Management and Physical Rejected Materials Control Vendor audit and vendor inspection Vendor rating system updation Improvements in Vendor supplies Quality 2 INPROCESS INSPECTION Prepare and maintain Control Plans for all manufactured parts In process audits for all manufecturing areas to check abidance of processes with SOP's. Rework management 3 OUT GOING INSPECTION Prepare and maintain Control Plans for all FG SKUs FG Products Inspection as per sampling plan Rejection / Rework management Packed goods audit on sampling basis Inspection r...

1. Quality System Management: Establish, implement, and maintain the Quality Management System (QMS) as per cGMP, WHO, and regulatory norms . Oversee activities related to change control, deviations, CAPA, OOS/OOT investigations, and risk assessments . Ensure all QA processes align with company policies and current regulatory requirements. 2. Documentation & Compliance: Review and approve SOPs, BMRs, BPRs, validation protocols , and analytical reports. Ensure all documentation complies with Good Documentation Practices (GDP) and data integrity requirements. Supervise document control , issuance, archival, and version management systems. 3. Batch Release & In-Process Quality Assurance: Ensure...

Job Title: Senior Automation Engineer Medical Device Manufacturing Experience: 10+ years Industry: Medical Devices / Life Sciences / Manufacturing Location: Remote Summary: Senior Automation Engineer responsible for developing, implementing, and sustaining automation systems that support manufacturing, assembly, and testing of medical devices in compliance with ISO 13485 and FDA 21 CFR Part 820. The role involves managing PLC, SCADA, and robotic systems, ensuring process reliability, data integrity, and regulatory compliance across production operations. Responsibilities: Designed and implemented automation solutions for medical device manufacturing and test systems to improve reliability an...

QA, QC, Maintenance, Production

Associate - Clinical Quality Assurance (CQA) Department: QA - MakroCare and DDi Job Roles and Responsibilities: Perform maintenance, review, and approval of company Standard Operating Procedures (SOPs) in compliance with ISO standards and applicable international and national regulations. Prepare and review Quality Management System (QMS) documents, CQA procedures, and assist in reviewing department SOPs as needed. Manage SOPs in mLMS, create users, review training records, and escalate non-compliance issues to the Head of CQA or relevant department heads. Maintain the CQA document repository and archive validation protocols and documents in line with regulatory requirements. Conduct interna...

Role & responsibilities Urgent hiring for Engineer, Sr Engineer, Assistant Manger Strong knowledge of injection moulding machine operation and mould setup. Ability to identify and troubleshoot common moulding defects (e.g., flash, short shot, burn marks). Familiarity with different plastic materials (PP, ABS, HDPE, etc.). Understanding of process parameters like temperature, pressure, and cycle time. Good mechanical aptitude and attention to detail. Basic knowledge of 5S, Kaizen, and lean manufacturing principles. Effective communication and teamwork skills. Shop-floor environment with rotating shifts. Machine uptime and production efficiency. Product quality and rejection rates. Adherence t...