2270 Capa Jobs - Page 3

The Quality Auditor will be responsible for conducting systematic inspections and audits across production processes, components, and finished goods. The role ensures that all products meet required quality standards and comply with internal procedures, customer specifications, and regulatory norms. Perform incoming, in-process, and final product audits based on defined checklists and standards Conduct process audits within the production line to ensure compliance with SOPs and work instructions Report non-conformities and assist in root cause analysis & corrective actions Maintain audit records, quality reports, and inspection data Verify calibration status of measuring & inspection equipme...

1.Manager- 10+yrs exp 2.Asst Manager- 10+yrs exp Review of audit trail for chromatographic and non chromatographic systems 3.Sr.Executive- 7+yrs exp ONLY MALE CANDIDATES ARE PREFFERED

Roles and Responsibilities Conduct breakdown analysis to identify root causes of failures and implement corrective actions (CAPA). Perform predictive maintenance activities to minimize downtime and optimize equipment performance. Collaborate with cross-functional teams for effective manufacturing processes and product quality improvement. Develop and maintain documentation related to maintenance procedures, work instructions, and standard operating practices (SOPs). Ensure compliance with safety regulations, industry standards, and company policies.

Should have exposure in ensuring compliance, documentation, preparing / reviewing SOPs, assisting in submission of regulatory documents, coordination with cross functional teams.

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Your role and responsibilities In this role, you will have the opportunity to deploy and lead the quality strategy for a local organizational unit, including quality culture, systems, tools, and competent teams, with the aim to achieve and exceed customer expectations while ensuring sustainable operations. Each day, you will drive the local quality system through the right mix of prevention, continuous improvement, robust root cause analysis, quick response, and sustainable solutions to problems. You will also showcase your expertise by coordinating the efforts of all necessary local functions that impact the quality results to reach the targets for the organizational unit and aim for world-...

You will be responsible for the inspection of all raw materials including Electronics Parts and Mechanical Parts with AQL (Acceptable Quality Level) standards. Your role will also involve verifying CKD and SKD materials, maintaining the 5S & ESD practices in the allotted area, and verifying BPCB. In addition, you will need to communicate with suppliers regarding material defects through email. Your tasks will include maintaining all Incoming Quality Control (IQC) documents like Certificates of Conformance (COC), Corrective and Preventive Actions (CAPA), rejection records, and golden samples of critical parts. You will also be required to prepare quality audit documents and maintain equipment...

Role Overview: As a Senior Executive in the Quality Assurance department at ZLL-SEZ Oncology Injectable (Alidac), your role is critical and involves responsibilities such as reviewing and authorizing testing work sheets for various materials, ensuring compliance with Good Laboratory Practices, handling stability samples, reviewing analytical data, initiating change controls and investigations, participating in regulatory audits, and ensuring calibration and maintenance of equipment. Key Responsibilities: - Review and authorize testing work sheets for Raw Material, Packaging Material, In-process, Finished product, and stability studies - Ensure compliance with Good Laboratory Practices and re...

Bachelor's degree with over 8 years of experience in designing and developing solutions in Trackwise Proven track record of successfully completing Trackwise project implementations, including stages such as discovery, design, development, testing, and deployment. Experience working in a GMP environment, 5+ years in an IT Systems Role. Expert knowledge of GMP Quality Management to include CAPA/Deviation, Lab Exception, Product Complaint, Audit, and Supplier Management. SDLC/GAMP, Business Analysis, and Enterprise Systems Management. General knowledge of GxP Quality Processes and Systems (GMP, GLP, GCP, GVP, GDP) Familiarity with other enterprise systems and modules such as ERP, SCM, and PLM,...

Role Overview: As an Associate Quality Engineer, Quality Engineer, Sr Quality Engineer, or Principal Quality Engineer at ABB, you will play a crucial role in contributing to successful project results in technology, software, product, and solution development. Your main focus will be on deploying the quality strategy, ensuring quality culture, systems, tools, and competent teams are in place to exceed customer expectations. You will collaborate with cross-functional teams to define and execute comprehensive test strategies and plans, identify and address risks and opportunities, and utilize quality data analytics to enhance quality management. Key Responsibilities: - Deploying and leading st...

Location - Jigani , Bommasandra. Conduct incoming, in-process, and final inspection of precision machined parts, Knowledge in VMM , CMM must with CAPA, FMEA,GD& T, quality documentation, and audit report preparation, internal, supplier. Required Candidate profile Location - Jigani , Bommasandra. Conduct incoming, in-process, and final inspection of precision machined parts, Knowledge in VMM , CMM must with CAPA, FMEA,GD& T, quality documentation.

As a Supervisor in the Sterile manufacturing department, your role involves preparing, reviewing, revising, controlling, and implementing standard operating procedures related to activities such as Change control and CAPA. You will be responsible for ensuring the smooth functioning of the department. Your key responsibilities will include: - Preparation, review, revision, control, and implementation of standard operating procedures for the Sterile manufacturing department - Document preparation for activities like CCF, SOP, Investigation, Risk Assessment, Protocol, etc. Qualifications required for this role: - M.Sc in Pharmacy or M.Pharm - Minimum 8 to 11 years of relevant experience in the ...

We are looking for competent, dynamic and motivated candidates for Manufacturing- QMS Injectable department for Amneal Pharmaceutical Pvt. Ltd ( Injectable units, SEZ-Matoda Plant,Ahmedabad) Job Description Key Responsibilities: Responsible for preparation & review of the master documents of sterile manufacturing for parenteral facility. Responsible for preparation and review of protocols and reports based on the requirements. Responsible for document management and preparation like BMRs, BPRs, master SOPs etc. Responsible for the handling of change control, deviations, CAPA, investigation etc. Responsible to give training to all the subordinates, technicians and operators of the department....

Job Description QC Manager (Plastic & Protective Packaging) Department: Quality Assurance / Quality Control Reporting To: Plant Head / General Manager Operations Location: Surajpur Industrial area ( Greater Noida ) Job Summary The QC Manager is responsible for planning, implementing, and overseeing all quality control activities within the packaging plant. This includes ensuring that plastic packaging products such as thermoformed trays, cutlery, foam, and shrink/poly wraps meet customer requirements, industry standards, and internal quality benchmarks. The role demands leadership in team management, process improvement, and compliance to regulatory and certification norms. Key Responsibilit...

Job Description To follow the safety rules in the premises according to the company norms. Responsible for production plan, inventory and timely delivery from production to packing. Responsible to carry out all activities in manufacturing area in compliance with cGMP. Daily work allocation to supervisor & workmen. Achieving set targets of daily/weekly /monthly manufacturing/packaging plan To discuss production plans with team mates and scheduling weekly plans / allocation of weekly shift schedule. Control on GMP documents /log books and other relevant documents of manufacturing To review of documents like log books, BMR, BPR for error free online documentation and timely submission to QA. To...

Department: Quality Assurance Location: Ahmedabad / Mehsana (with travel across India sites) Reports To: Global Head- Quality Assurance Team Size: ~50 QA professionals (Bioanalytical QA & Clinical QA) Position Summary: The Head QA (India) will lead and oversee Quality Assurance functions across Veedas Gujarat facilities (Ahmedabad & Mehsana), covering Bioanalytical QA and Clinical Research QA operations. This role ensures compliance with global quality standards, regulatory requirements, GCP/GLP and internal quality systems while strengthening a culture of quality, continuous improvement, and operational excellence. The role acts as the primary QA leadership point in India and collaborates c...

Job Title: Assistant Manager Quality Assurance (Oral Solid Dosage) Department: Quality Assurance Location: Bangalore- Harohalli Reporting To: Manager / Head Quality Assurance Job Overview: The Assistant Manager – QA will be responsible for overseeing and executing qualification, validation, and Quality Management System (QMS) activities for oral solid dosage (OSD) manufacturing. The role involves ensuring GMP compliance, maintaining documentation, and supporting regulatory readiness through effective implementation of quality systems and validation programs. Key Responsibilities: 1. Qualification & Validation Plan, execute, and review equipment, utility, and facility qualification protocols ...

1) To do the FSSC 22000 Ver 6.0 certification related documentation which includes preparing of SOP's, Formats, Annexures & records 2) To prepare the Standard Operating Procedures w.r.t. Quality and Food Safety requirements so as to improve the Quality Systems at the Site. 3) To prepare and update schedules of the implemented procedures and imparting trainings to the Food Handlers. 4) To Prepare Audit planner and preparing/reviewing Audit Checklist 5) Implementation of CAPA & follow up of same. Essential Skills : Should have Hands on Experience in Handling the Quality & Food Safety Systems and Documentations. Desirable Skill s: Good Communication

Responsible for planning, organizing, coordinating, and controlling production activities to meet the monthly production plan. Oversee machine qualifications and review BMR during manufacturing and after completion to ensure documentation. Perks and benefits Accommodation, Travelling Mediclaim Policy

Urgently Required CSV Trainer For Part Time Basis and Online Training Sessions. Should have Experience in Computer system validation and LIMS Functional Specifications (FS)Design Specifications (DS) Validation Protocols (IQ, OQ, PQ) (FDA, EMA, GAMP 5 Required Candidate profile Experience in employing risk-based approaches to CSV Experience in qualification of GLP Instrument Systems Classes Mode Online or Remote Mode Interested Directly Please Contact - 9133469786

To ensure that quality standards are maintained during the manufacturing process, monitoring and improving in-process quality control activities, reducing defects, and ensuring adherence to customer specifications.

Description Customer Care-----Call center Operations Specialist-One to Three Years,Frontend Helpdesk-One to Three Years Named Job Posting? (if Yes - needs to be approved by SCSC) Additional Details Global Grade A Level To Be Defined Named Job Posting? (if Yes - needs to be approved by SCSC) No Remote work possibility No Global Role Family To be defined Local Role Name To be defined Local Skills help desk;call center Languages RequiredENGLISH Role Rarity To Be Defined

Job Overview: We are looking for a dedicated and detail-oriented Quality Engineer / Quality Manager to oversee the quality management system, ensure process compliance, and drive continuous improvement initiatives across manufacturing operations. The ideal candidate should have strong technical knowledge of machining processes, quality audits, and team leadership capabilities. Key Responsibilities: Develop, implement, and maintain quality management systems (QMS) and production standards to ensure consistent manufacturing quality. Possess in-depth knowledge of manufacturing processes such as CNC, VMC, conventional, and grinding machines. Conduct quality inspections for raw materials, in-proc...

Handling Quality management system and regulatory support & reviewer. Change control, CAPA,OOS,APQR. Compliance verification at Site. Dispatch compliance. BMR and Work sheet compliance before release. Document and Data control and training.

Handling Quality management system and regulatory support & reviewer. Change control, CAPA,OOS,APQR. Compliance verification at Site. Dispatch compliance. BMR and Work sheet compliance before release. Document and Data control and training.