2371 Qms Jobs - Page 29

Role & responsibilities Prepare document as when required like SOP, BMR/BPR/Process validation Protocol/Report in Production Department Handling of QMSs (Change control, Deviation and CAPA) Maintain cGMP requirements. Execution of batches and maintain BMRs. Perform SAP related activities Execute trainings Regulatory audit exposure

Alembic Group is looking for Manager - Quality Control to join our dynamic team and embark on a rewarding career journey A QC Manager is responsible for managing the quality control process within a company or organization They oversee the quality assurance procedures for products, services, and processes to ensure they meet the required standards and specifications The QC Manager must be skilled in analyzing data, identifying trends, and implementing corrective actions to improve quality control Develop, implement, and maintain quality control policies and procedures Establish quality control metrics and benchmarks to monitor product and service quality Develop and oversee quality control inspection and testing procedures Analyze quality control data and trends to identify areas for improvement Develop and implement corrective actions to improve quality control processes Ensure compliance with industry standards and regulatory requirements

Supreme Universal is looking for Quality Manager to join our dynamic team and embark on a rewarding career journey Develop, implement, and maintain quality assurance policies, procedures, and processes to ensure product or service quality Oversee the inspection and testing of products and services to ensure they meet the required standards and specifications Maintain accurate and up-to-date documentation of quality assurance activities, including test results, inspection reports, and corrective action plans Prepare regular reports on quality assurance activities, including performance metrics, trends, and areas for improvement

Kalol Institute & Research Center is looking for QA & Pharma. Chemist Faculty to join our dynamic team and embark on a rewarding career journey Developing and teaching plans Advising and mentoring students Conducting research and publishing findings in academic journals Participating in departmental and university-wide committees Engaging in professional development activities to stay current in the field Excellent communication and interpersonal skills

Alembic Group is looking for Senior Executive to join our dynamic team and embark on a rewarding career journey Leading the full audit cycle by checking tax compliance, verifying financial records, and inspecting accounts. Analyzing the results of the audit and presenting possible solutions for ineffective financial practices to management. Evaluating company accounting procedures, payroll, inventory, and tax statements to guide financial policymaking. Conducting risk assessments to recommend aversion measures and cost savings. Following up with management to ensure remediations are implemented into the company's financial practices. Supervising junior auditing personnel and implementing their research work into the auditing process. Preparing and reviewing annual audit memorandums. Researching applicable federal and state laws and regulations to ensure the company's books are compliant.

Role & responsibilities Inspection coordination at Branch level Executing Physical /Remote inspection at various locations upon request from IC coordinator, verifying that all information provided for inspection execution is complete and allows executing inspection without problem. Observance of inspectors manual (handout) and IJO for inspection execution. Reporting of inspection results according to standard TFS Inspection Report form. On time submission of inspection report to TFS IC office, according to deadlines provided by KPIs. Reporting to Inspection Coordinator/Inspection Manager of any risky information detected by during inspection process, according to risk detection guidance provided by IC management. Taking care of Security Material supplied by the IC coordinator; reporting all Security Material movement to IC Coordinator (used, damaged, and lost) for prompt registration/action. Careful use of tools and materials provided by the company for inspection execution. Using of standard security elements for personnel protection to make the execution under safety conditions. Reporting to IC Coordinator/Inspection Manager any deviation of standard procedures according to inspectors manual, IJO, SGS Policy, SGS Ethic Code, and any other mandatory document applicable to TFS. Timely reporting to IC Coordinator of expenses related to inspection execution. Any other task assigned by local IC office. Preferred candidate profile Computer literate and at ease with technological innovations. Familiarity with Quality management systems and auditing procedures and international standards Field Job which requires extensive travelling Good communication skills

** Responsible for Wet Lab In charge ** Responsible for HPLC Lab In charge ** Responsible for QMS related to Wet / HPLC lab

Job Responsibilities: 1) Manage and control all documentation related to the Integrated Management System (IMS), including policies, procedures, manuals, and records. 2) Coordinate activities related to the implementation and maintenance of IMS across departments and teams within the organization. 3) Assist in the implementation of IMS standards (ISO 9001, ISO 14001, ISO 45001) within the organization, ensuring compliance and continuous improvement. 4) Coordinate training sessions related to IMS and other relevant topics for employees within the organization. 5) Assist in maintaining and improving the quality management system (QMS) as per ISO 9001 standards. 6) Support the implementation and maintenance of environmental management system (EMS) as per ISO 14001 standards. 7) Assist in implementing and maintaining the occupational health and safety management system (OHSMS) as per ISO 45001 standards. 8) Proven experience in document control, coordination, and implementation of IMS. 9) Ability to coordinate plant trainings related to IMS and other relevant topics. Skills Needed: Strong communication, organizational, and interpersonal skills. Attention to detail and ability to work effectively in a team environment. Interested Can share their resume on- Vaibhavi.songadkar@fujisilvertech.com

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical products to ensure they meet established quality standards. They work in laboratories, using analytical Techniques to test raw materials, in-process samples, and finished products. Quality assurance analyst Responsible for ensuring compliance with regulatory requirements by conducting audits, inspections, and assessments Preferred candidate profile Qualification B.Pharma , B.Sc or B.Tech Biotech D.Pharma Divya ( 9736044662 ) (9:30 AM to 7:30 PM ) Preferred candidate profile Company - Top Pharmaceuticals Companies based at Baddi HP. Fresher & Experience. Job Location- Chanigarh,Panchkula, Paonta Sahib ,BADDI ( Himachal Pradesh ) Functional : QC,QA & Production.Industry: Pharma manufacturing unit/ Food Technology The Saksham Success Enterprises Near Sunder Ayan by pass solan 173212 Himachal Pradesh Contact us Divya ( 9736044662 ) (9:30 AM to 7:30 PM )

Min 2yr BPO Quality Manager Exp on the paper, AM/DM cannot apply Manage BPO Quality Team Call Callibration, Audit, Score , CSAT Call/whatsapp CV Amit 8851792136, Neha 8287267407 Required Candidate profile WFO-Hyderabad only not for Bangalore ..Apply those who can relocate in Hyderabad Must Knows-English and Telugu

Key Responsibilities Process Improvement & Automation Identify repetitive and manual processes ripe for automation across reporting, documentation, and administrative workflows Lead initiatives to streamline operational tasks and improve capacity management Collaborate with cross-functional teams to implement scalable efficiency solutions Reporting & Analytics Own monthly reporting cycles, including dashboards, benchmarking, and methodology-based tracking Proactively refine reporting methods for better transparency and time savings Document & Site Management Maintain and manage SharePoint and Sphere sites, including user permissions, file structures, and content consistency Support migration planning and execution from legacy platforms (Box) to MyDocs (DocShare) Policy Alignment Cycles (PAC) Coordinate PAC verification and documentation efforts twice annually, ensuring change-tracking and comment logging are consistent Business Impact Assessment (BIA) Support Verify and update application lists and organizational structures by location Ensure data integrity and audit-readiness of structured documentation Required Skills & Qualifications Strong eye for identifying automation opportunities and driving operational efficiency Highly organized, detail-oriented, and independently driven Familiarity with platforms like SharePoint, DocShare, Sphere, and other enterprise documentation tools Competence in reporting tools and dashboard creation (Excel, Power BI preferred) Excellent communication and collaboration skills

The ideal candidate for this position should preferably hold a Diploma or B.Tech degree with a minimum of 3-5 years of relevant experience. You should have the capability to independently handle all operations of Quality Management System (QMS). If you are a committed and results-oriented individual with the drive to take on challenges, we encourage you to apply in confidence with your CV to info.hyd@qualityprofiles.in. Please make sure to clearly mention your Current Cost to Company (CTC) and expected Salary in your application. Interviews will be conducted shortly for shortlisted candidates.,

Role & responsibilities Personality Traits: Strong leadership and decision making abilities Excellent problem solving and analytical skills Ability to handle customer concerns and audits effectively Detail oriented with strong process improvement focus Strong communication, coordination, and interpersonal skills Preferred candidate profile Work Experience: 8+ years of experience in quality management within a manufacturing environment, Strong knowledge of ISO standards, IATF 16949, and customer specific quality requirements, Experience in handling internal, customer, and third party audits, Leadership experience in managing quality teams

Pune, Maharashtra, India Department Vendor Development Job posted on Mar 05, 2025 Employment type Permanent Manage the tool , fixture, gauge development process, including planning, scheduling, and execution. Conduct tool inspections, Tool trials & Manage First Piece approvals of duplicate Tooling. (FPA submission to tool productionised). Troubleshoot and resolve tooling & process impelmentation. Collaborate with tool maker & Part maker team to ensure accurate, FTR, on time development. Collaborate with CFT to ensure seamless transition from tooling to production Collaborate with Part maker team to identify and address & resolve the issue. Develop and implement corrective action plans to address quality defects Strrong knowledge of injection moulding, process parameter setting, right tool specification implementation, EGP & mould flow, painting process , powder coating process, materlization process, APQP & PPAP, QMS.,

As a Process Engineer at Syngene International Limited in Mangalore, you will play a crucial role in contributing to the development of procedures, practices, and systems that ensure safe operations and compliance with the company's integrity and quality standards. You will be responsible for driving a corporate culture that promotes an environment, health, and safety (EHS) mindset and operational discipline at the workplace. Your primary focus will be on ensuring all safety precautions are followed and adhering to EHSS policies. Your educational background should include a BE in Chemical Engineering, and you should have a minimum of 2 to 3 years of experience as a Process Engineer with Pharma experience. You will be involved in activities such as scale-up, reactor mapping, QMS, EHSS, and more. It is essential that you comply with Syngene's quality standards at all times and ensure operations are carried out in accordance with current Good Manufacturing Practices, Good Documentation Practices, and Data Integrity policy. Your responsibilities will include evaluating the process with respect to critical chemicals, volumes, and process conditions, mapping the process in the MSEZ facility, preparing batch sizes and calculating capacity, and determining operating costs for the mapped product. You will also be involved in preparing a list of modifications/facilities required in the production facility, coordinating with the CFT to plan and execute these modifications/facilities, and supporting the Production team for scale-up and execution of initial batches and validation. Additionally, you will work on process improvement in running products, contribute to improvements in utilities and energy management, attend training on standard operating procedures, and maintain good health and hygiene practices. Your behavioral skills should include adhering to company systems and policies with dedication to work, having a result-oriented approach, being self-driven, and possessing strong team coordination skills. Syngene International Ltd. is an equal opportunity employer, and as a Process Engineer, you will have the opportunity to be part of an innovative culture driven by a passionate team of scientists. If you are a detail-oriented individual with a strong background in chemical engineering and a passion for process improvement, this role may be the perfect fit for you.,

Handle quality assurance/control, inspections, customer coordination, QA documentation. Ensure compliance with ISO standards and welding codes across all production stages. Required Candidate profile BE/B.Tech (Mech) with 5+ yrs or DME with 10 yrs in QA/QC. Strong in welding codes, inspections, QA documentation, ISO standards, and customer coordination.

Responsibilities: • Equipment Engineer is responsible for Testing Equipments (Standard & Special Purpose, customized Equipments). • Equipment Engineer to work on Mechanical and Electrical Testing of Medical Equipment products (CT/MR). Work on testing, troubleshooting during testing, also coach operators on testing and troubleshooting. • Define Equipment Requirement Specifications (ERS) for Testing equipment. • Work with Engineering, Manufacturing team, Supplier to finalize on equipment designs. Also interface with sourcing team for procurement of a new equipment. • Work with supplier on equipment development, manufacturing. • Own Equipment FMEA, trials, installation at manufacturing floor. • Own Equipment IQ (Installation Qualification), OQ (Operational Qualification) & PQ (Performance Qualification) as per Quality Management System (QMS) procedures/norms. Qualifications: • Bachelors degree in electrical/ electrical and Electronics Engg. / Electronics & Communication Engineering • Sound knowledge of Electromechanical (PLC integration) equipments and its parts for example Servo motor, Encoder systems, NI Hardware’s ,PCB etc. • Hands on experience on Equipment’s, Special Purpose Machines troubleshooting. • Hands on experience on Microsoft office applications • Good communication skills (Oral/Written) • Strong bias for documentation & technical reports • Effective multitasking and ability to deliver on time and with quality. • Ability to work in a team with good Interpersonal skills. Interested candidates can share their resume to mahesh.b@harita.co.in

Quality Management System (QMS) Implementation & Adherence: In-process Quality Control: Supplier Quality Management (with MACE contexT Leverage knowledge of MACE (Maruti Suzuki Centre for Excellence) Required Candidate profile New Product Introduction (NPI) & PPAP: MSA Strong working knowledge and implementation experience of Quality Management Systems (QMS), specifically IATF 16949 and ISO 9001.

1.As per QMS, implement, and maintain process controls and procedures 2.Identify, analyze, and resolve process-related quality issues through root cause analysis techniques (Fishbone, 5 Whys, FMEA 3.Work with cross-functional teams to identify CAPA Required Candidate profile 7. Conduct layout, process and product audits, report compilation and reporting. 8. Knowledge of GD&T. 3. Utilize (SPC, Control Charts) to track process stability and capability.

Oversee multiple Precast Projects execution to set benchmarks, audit projects for standardized compliance across L&T Construction, track and showcase Precast Technology benefits in various infrastructure as well as buildings Precast Construction projects across India for all L&T Construction ICs. The role does not include direct execution responsibility but to monitor and catalyse QA/QC in Precast Construction. The role includes unique additional responsibilities of leading the EHS responsibilities specific to Precast Works QA/QC Responsibilities: Liaise with the Project Team/Site/Cluster/IC QC Teams on the quality related activities of the project to achieve established benchmarks. Establish global QA/QC benchmarks for Precast Construction across L&T Construction Establish standardized Method Statements for Precast Works and enforce the same at all sites using the Quality Teams at IC/Sites. Establish QA/QC Evaluation Criteria for Precast Yards and Site Installation Conduct periodic Audits to ensure compliance Setup QA/QC training programs for Precast Construction Build Knowledge Bank for QA/QC related issues/case studies/challenges and disseminate the same across L&T Construction Ensure implementation of Quality Management System in the project through QC Engineers / discipline QC Inspectors. Review all QA/QC Procedures / QC Plans and Work Instructions for adequacy against scope of work and revise, where required. Ensure relevant Codes & Standards, Specifications are available at site for reference. Based on the feedback from QC Engineers help develop project specific Procedures, Plans and Work Instructions, where required incorporate in the PQP and issue controlled copies of the same. Ensure Quality System documents viz: QA/QC Procedures, QC Plans, Work Instructions etc., are available at pertinent locations of use. Safety Responsibilities: Responsible for the overall EHS organization for Precast Works and facilitate in achieving benchmark performance. Ensure the implementation of EHS Policy & Integrated Management System for EHS at the project site specifically for Precast. Network with EHS teams such that Precast works requirements are adopted across L&T Construction. Develop & facilitate implementation of project specific guidelines & procedures Review project specific risk assessments on Precast Safety. Identify, design and impart site specific Precast Works training for site EHS staff and ensure the requirements are translated to site further with subsequent trainigns. Continually monitor the proactive & reactive EHS performance at project and facilitate operations to take necessary corrective & preventive action. Establish, implement and maintain emergency preparedness and response procedure at project. Support in Standardization and Modularization efforts of PWCC by collecting and analysing data of IC wide demands and challenges to deliver superior quality and safe product Support in building innovative data collection and analysis options using IoT and AI

Role & responsibilities Corporate Quality Management Customer Audits QMS Quality Improvements Preferred candidate profile Candidated from stamping / sheetmetal parts manufacturing company having good PR with OEM customers and exposure of handeling MACE Audits with geen score card.

Initiation, review and approval of all types of quality management systems (Ex: Change controls, Deviations, Investigations, CAPA, OOS, and Complaints etc.) Handling of Return Goods. Handling of quality system and perform risk assessment to the required quality system. Conduct regular internal audits as per the need basis. Reviewing and approving of all documents (SOPs, Spec & STPs, Forms, protocols and reports etc.) Review of annual product quality review reports. Providing training on all cGMP topics to employees at site. Supporting to customer audits/ visits and regulatory audits. Support to provide necessary documents for amendments, annual updates and regulatory filings and CMC supporting documentation. Filling of questionnaires, declarations & quality agreements. Execution of additional responsibilities assigned by HO

responsible for MR function for ISO certification (QMS,EMS & OHSAS) responsible for ISO documentation responsible for 5 S implementation Will do safety audit of factory provide safety training and conduct mock drill Required Candidate profile Min 5 years in above profile. In-depth knowledge of ISO 9001, 14001, and 45001 standards ISO Lead Auditor (preferred)(Graduation/MSW/RLI/CLI + Auditor/Lead auditor certification is a added advantage) Perks and benefits Food & Accommodation

• Follow up with supplier for Quality documents required as per IS standard. • Performed root cause analysis to identify and resolve defects with the help of ,Ishikawa, 7QC,8D, Why-Why analysis. • Conducting meeting with supplier for CAPA to reduce overall rejection. • Timely coordination with supplier ,Internally sharing rejection report, queries regarding test certificate . • Prepare Quality Assurance Plane (QAP) as per scope of work. • Inspection of Pre & Post fabrication activity. • Preparation of Welding procedure Specification (WPS,WPQR,WPQ) • Handling all measuring instrument as well as Tachometer, Sound level, Vibration measuring Instruments. • Conduct FAT with the customers to get the acceptance before delivery . • Vender inspection, Coordinating third party inspection agency, Prepared MOM with clients. • Incoming material Inspection ,Stage Inspection, Final Inspection prepared all documents as per ISO,API and ASME standard. • Coordinating and Guide at the time of final Inspection with Client . • Attend ISO9001:2008,ISO9001:2015Internal And External Audit

To follow safety rules in the premises according to the company norms. Operation and Cleaning of glove integrity and filter integrity testers. Responsible to perform the in process checks during operation. Responsible for Dispensing, checking and receiving of PPM from warehouse on need basis. To ensure cleaning and storage of change parts as per the procedures. To maintain the BMRs and other log books in the compounding area as per cGMP and SOP Cleaning and maintenance of compounding area as per GMP and SOP Operation and cleaning of dynamic pass box in compounding area Responsible for Cleaning and sanitization of drain points in compounding area Responsible for manufacturing and supervising of Media fill and Drug products batches as per BMR To carry out CIP & SIP of the vessels related to compounding and flitration area. Responsible for operation, calibration and cleaning of weighing balance, pH meter, DO meter and conductivity meter, Compounding isolator, Manufacturing and filtration vessels, Heating & cooling skid, Air shower. Table mounted LAF and ceiling mounted LAF, Filter integrity tester, Sonicator , TFF, Homogenizer, Lipid extruder, Fogger, Heating magnetic stirrer with thermometer, SART system, Strip chart recorder Preparation and periodic revision of SOPs related to compounding area. Responsible for the co-ordination with cross functional departments like QA,QC, warehouse Engineering, HR and administration for the day to day activities. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instructions and guidance.