131 Ipqc Jobs - Page 4

Good knowledge about sampling plan and IQC control plan,Should know the Incoming quality control lab process in any EMS industry,Should know prepare the SOP & SIP and LRR,Daily basic process schedule & Tracking.Skill in yield and production process in EMS. Incomming Quality Control, Supplier Quality Engineering,,Online Relaiability Test,Process Quality Control, 1. Responsible for Leading the Quality function and day to day In-process Quality verification with consistent result both in terms of Quality and Quantity to meet daily plant output/customer requirements. 2. Performing in-process quality inspection for accuracy, specification parameters and workmanship. Develop and implement best qua...

Role & responsibilities : • Responsible for Leading the Quality function and day to day In-process Quality verification with consistent result both in terms of Quality and Quantity to meet daily plant output/customer requirements. • Performing in-process quality inspection for accuracy, specification parameters and workmanship. Develop and implement best quality processes in production • Tabulate and document data relating to products, processes, materials, its qualities, and reliabilities. • Train staff, technicians, and professionals on the aspects of quality control activities. • Troubleshoot and resolve problems relating to quality using quality tools ( analysis of COPQ in order to achie...

IQC (Incoming Quality Control) SQA (Supplier Quality Assurance) IPQC ( In Process Quality Control) Strong SMT Components Knowledge Must

IQC (Incoming Quality Control) SQA (Supplier Quality Assurance) IPQC ( In Process Quality Control) Strong SMT Components Knowledge Must

Urgent Requirement for Rabale MALE Candidate Knowledge Required:- Good knowledge of 21 CFR Part 11 / Annexure 11 (Must) Good knowledge of CSV,GAMP 5 (Must) Good knowledge of Data Integrity requirements for Pharma (Must) Experience of working at Pharma Site QC,QA,IT,CSV etc Must Experience Candidate with 3 - 5 years of experience in Pharma/Life science domain working knowledge in authoring on Computer System Validation Deliverables, Part 11/Annex 11, Data Integrity Work experience in Pharmaceutical Sector will be desirable Experience in Authoring all CSV deliverables e.g. URS, FRS, CS, IQ, OQ, PQ, RTM, VSR, Risk assessment, etc Experience on validation of any of the enterprise level applicati...

Roles and Responsibilities: ONLY FOR MALE CANDIDATES Conduct quality assurance activities such as BPR review, BMR review, SOP preparation, validation, cleaning validation, equipment qualification, process validation, stability analysis, and OOS/OOT investigations. Ensure compliance with regulatory requirements by maintaining records of batch manufacturing, testing results, and other relevant documents. Develop and implement quality control procedures for bulk drugs production. Perform analytical testing of APIs using HPLC/GC techniques.

Job Description Candidate should have sound knowledge about upstream process development (Cell culture and Fermentation). Hands on experience of shake flask studies including sample analysis and documentation. Experience in handling and operation of cell culture and microbial related experiments in bioreactor including sample analysis and documentation. Aseptic handling of seed inoculum and its maintenance Independently handle media and feed preparation for conducting studies. Should be able to trouble shoot in case of any deviation from process/parameter. Good documentation practice. Should be able to perform cell culture (IPQC) analysis. Preparation of SOP, Support for Equipment qualificat...

Inprocess Quality control engineer required at kundli sonipat Qualification- Diploma/ b.tech electronics Exp- min 2 yrs Salary- upto 25k- 30k Skills- Power bank, charger, earphone timing- 9 to 6

To handle DCS as operator. Ensure batch charging other manufacturing operations should be strictly as per BMR/SOP in line with current GMP practices. To maintain manufacturing records online should comply data integrity practices. To take out sample of intermediate/in-process material and send to IPQC/QC lab. To ensure the production related inputs in SAP system. To be check and ensure the PISCADA reports generation review of DCS alarms. Transfer finished goods through Finished Goods Transfer Note. To Check and ensure minimum stock of consumables, Logbooks status labels. Ensuring preventive maintenance of all equipment as per schedule. Co-ordinate with service departments (QA, QC, stores, E ...

Roles and Responsibilities Conduct BMR reviews, CAPAs, GMP audits, and IPQC activities to ensure compliance with quality standards. Perform incoming inspection, process validation, and equipment qualification tasks as per SOPs. Identify and report deviations/OOS/OOT events during production runs. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of QMS documentation and participate in training programs. Desired Candidate Profile 3-8 years of experience in pharmaceutical industry with expertise in IPQA (In Process Quality Assurance). Strong understanding of Good Manufacturing Practices (GMP) regulations. Proficiency i...

Mainly focus on IN PROCESS QUALITY, REJECTION CONTROL, REJECTION ANALYSIS, ZERO REJECTION at CUSTOMER END, CALIBRATION of RECEIVING GAUGES by CMM, SUB ASSEMBLY SETUP APPROVAL, CHILD PARTS INSPECTION, SUB ASSEMBLY, IN-HOUSE VALIDATION of PARTS et Required Candidate profile DIP/BE Mech 3+yrs exp into IN PROCESS QUALITY CONTROL Responsible for LINE QUALITY, REJECTION CONTROL, CHILD PARTS QUALITY APPROVAL etc Wiring Harness exp preferred Mail CV to hr@adonisstaff.in Perks and benefits Excellent Perk. Work @ Oragadam, Walajabad etc

QC Chemist Qualification - B.Sc Chemistry/B.Pharm with 2 years of previous experience in medical devices/pharma. Tasks : IPQC, RM/PM testing, Stability studies, BMR issuance & review, Monitoring of calibration of instruments & validation of equipments

Sanmina is seeking a highly motivated and experienced Quality Manager to lead our In-Process Quality Assurance (IPQA) activities. In this role, you'll be instrumental in ensuring product and process quality, fostering strong customer relationships, and driving continuous improvement initiatives. If you're a proactive leader with a passion for quality excellence and a proven track record in manufacturing environments, we encourage you to apply! Role & responsibilities Lead and Coordinate IPQA: Lead and coordinate the In-Process Quality Assurance (IPQA) team and Cross-Functional Teams (CFTs) to ensure robust quality control throughout the manufacturing process. Strategic Quality Planning: Coll...

Key Responsibilities: Lead and manage the plants quality team while fostering a culture of accountability and continuous improvement. Oversee quality testing and inspection activities across the factory and assembly lines. Ensure full compliance with ISO audits and maintain relevant certifications. Liaise with clients to meet audit and pre-delivery inspection requirements. Proactively identify and address quality issues in a timely manner. Continuously enhance quality systems, processes, and overall performance. Requirements: Degree or diploma in engineering (preferably mechanical, electrical, or industrial). Minimum 5 years of managerial experience in manufacturing quality. Strong communica...

Focus on NPD, IPQC & CUSTOMER QA handling 8D, PPAP, APQP Methodology, Customer Handling, EMS Product knowledge, PCBA, IPC 610 & 620 Standards , Expertise in Soldering, ISO 9001:2015, IATF Knowledge, DFMEA, PFMEA, R&D, Product & Process Specification Required Candidate profile Only BE EEE Only FEMALE 8+yrs exp into NPD, In-Process QA & Customer Quality with EMS industry Good understanding of EMS Products & PCBA Willing to work @ ORAGADAM Send CV to cv.ch2@adonisstaff.in Perks and benefits Excellent Perk. Send CV to cv.ch2@adonisstaff.in

Company - Sahajanand Laser Technology Ltd. Designation - Fresher - IPQC/R and D/QA/Production Work Location - Sector 25, Gandhinagar Interested please Mail your CV at placement@SLTL.com/7490055612 (Only WhatsApp) with Subject - "Your Name - Qualification - Location - Position Applying For"

Role & responsibilities : 1.English Communication skills, 2.Good local launguage Communication Skills 3.Good Knowledge in Excel & PPT IQC Job Description: 1.Should know the Incoming quality control lab process in any EMS industry 2.Good knowledge about sampling plan and IQC control plan 3.Should know about inventory management and ageing control. 4.Have knowledge about conduct MRB meeting for rejection 5.Should know prepare the SOP & SIP and LRR. 6.Familiar with smartphones and process 7.should know about 5s/ESD/7QC tools knowledge 8.Should know the yield and production basic knowledge 9.Need manpower handling near 30x operators 10.Need strong knowledge on supplier quality process in EMS ind...

Opening in Medicamen Biotech Ltd(ANVISA & EU), Bhiwadi, Raj. Pharma formulation exp. Preferred Qualification: B.Sc./B.Pharma Vacant Post: 10 Nos. QA - IPQA/Documentation/Validation QC - IPQC/HPLC/Chemical Testing/GC/KF Mail-ID: hrd@medicamen.com Required Candidate profile Immediate joiner prefer Experience : 2 to 6 Years Ready to Relocate Bhiwadi Self Motivated/ Team Player/ Committed for Performance. E-Mail: hr-ho@medicamen.com Mob: +91 7240001632/ 9992395009

Complete analysis of Paddy & Rice - all varieties (Basmati & Non-Basmati).Sampling and analysis of rice during milling and packaging process to ensure that it meets with predefined criteria. Only from rice Industry Perks and benefits CANTEEN FACILITIES,BACHELOR ACCOMMODATION

Position Executive / Sr. Executive- QC Grade : A3 A4 Business Unit / Function Department - Quality Control Location Bharuch; SEZ;;;; Reports to Lab In charge-QC; Summary of Job (Purpose/ objective of the job Department Organogram to be enclosed) candidate is required having complete experience in API/Bulk/ Intermediates industries as per global regulatory requirements and responsible for implementation and compliances of ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP / global QMS requirements at SEZ site. Key Responsibilities (Performance Indicators) Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP, USFDA, FSSC - 22000, NABL. Analytical skill for QC instrume...

Quality Management System: Oversight/Handling of Handling of Change Control, Incident / Deviation and CAPA. Following and tracking of Change Control, Incident /Deviation and CAPA. Involved in the investigation activity whenever required. Ensure that products are manufactured in compliance to Regulatory requirements and as per Good Manufacturing Practices. Ensure that production and manufacturing activities are undertaken in compliance to SOPs, systems, procedure and GMP/GLP requirements. Maintain GMP compliance in various departments to manage the production in line with the current GMP requirement. Handling of Change Control, Deviation, risk assessment and CAPA as per company procedure Veri...

Coordinating the daily operation and management of the QC team (OQC/, rationally arranging manpower supplements according to actual production schedules, and improving work efficiency. Required Candidate profile Engineering quality tools, Problem solving tools, 8D, 6Sigma, SPC and other quality tools. Core tools knowledge ERP/ SAP/ Oracle hands on experience Master the skills , Minitab, email etc.

Handling customer complaints Lead customer audits Lead engineering change management NPILead team & quality risk controlling Participate Process quality abnormality handling, control quality risk points, and promote quality improvement Required Candidate profile Proficient in quality negotiation & crisis quality incident management, product failure analysis, Engineering quality tools Abilities: Problem solving, customer handling, Communication skills

Roles and Responsibilities Perform quality control checks on electronic components and semiconductors using SMT process, THT/PTH process, Surface Mount Technology, IPQC, and Inprocess Quality techniques. Conduct regular inspections to ensure compliance with industry standards and company policies. Identify defects or anomalies in products and report them to relevant teams for rectification. Collaborate with production staff to resolve issues related to product quality. Maintain accurate records of testing results and inspection reports. Desired Candidate Profile 1-3 years of experience in electronics manufacturing or a related field (diploma holders preferred). Strong understanding of electr...

Department: Quality Control Location: Tehsil Inodra, Kangra (HP). Near by Pathankot Reporting to: QC Manager / Head Quality Department Key Responsibilities: Conduct routine testing of raw materials, in-process materials, and finished products as per approved specifications and standard test procedures (STPs). Perform chemical and instrumental analysis using HPLC, UV, IR, GC, KF, etc. Maintain accurate and up-to-date laboratory records, worksheets, and logbooks. Ensure timely calibration and maintenance of laboratory instruments and equipment. Review and follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Assist in method development and method validation activities...