9 Qualification Testing Jobs

About River River is an electric vehicle company building multi-utility scooters. At River, were building scooters of tomorrow for the ambitious youth of today. Because we believe people only need two things to achieve success: the desire to make it to the top, and the means to get there. With our flagship product River Indie, SUVofScooters, is designed to help you get things done. Engineered to be a dependable ally on your road to success. We are backed by marquee international investors - these are mobility focused funds backed by Yamaha Motors, Al-Futtaim Automotive Group, Toyota VC and Maniv Mobility. Key Responsibilities Develop a risk-based test strategy, plan test procedures, and author test cases based on PRD, Field Failures and DFMEA documents for electronic components used in ECUs, power electronics and EV sub-systems. Provide expertise in regulatory compliance. Lead failure analysis (FA) efforts using techniques such as FMEA, Weibull analysis, Fault Tree Analysis (FTA), and Root Cause Analysis (RCA). Conduct signal integrity (SI), power integrity (PI), and thermal performance assessments for high-speed and power electronics To prioritize tasks and allocate resources effectively to meet project deadlines. Ideal Candidate B.E / B.Tech in EEE/ECE. 5 to 8 years of experience in Product development and Component Validation. Hands-on experience with electrical characterization, stress testing, and failure analysis Hands-on experience with semiconductor devices, ECUs, sensors, power electronics, chargers, GPS and GSM. Strong background in power electronics, analog/digital circuits, and embedded systems. Experience with qualification testing for Motor, MCU, charger and infotainment systems. Strong analytical and problem-solving skills for debugging component failures and optimizing designs. Show more Show less

IT- qualification , QMS in Pharma - Implement IT policies and coordinate with vendor ,Perform periodic maintenance of GxP system , Network configurations & infrastructure project , Cloud computing (SAAS, PAAS), backup, and user Management Free meal House rent allowance Travel allowance

Roles and Responsibilities Ensure compliance with quality management systems (QMS) through implementation, maintenance, and continuous improvement of ISO documentation. Prepare SOPs for various processes such as BMR, CAPA, Change Control, Cleaning Validation, etc. Conduct qualification testing and validation protocol execution to ensure product quality and regulatory requirements. Develop and maintain accurate records of test results, reports, and certificates related to quality assurance activities. Collaborate with cross-functional teams to identify areas for improvement in quality control processes. Desired Candidate Profile 5-10 years of experience in pharmaceutical industry with expertise in QMS implementation. Strong understanding of GMP regulations and industry standards like ISO 9001:2015. Proficiency in preparing documents like BMR, SOPs, Capas, Change Control procedures. Experience with cleaning validation process validation protocol execution.

Walk-in @ GOA We are hiring multiple positions for our manufacturing facility at AHMEDABAD as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Engineering (Instrumentation / QMS / Process Equipment maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech with relevant functional experience in Calibration / Instrumentation / QMS activities QUALITY ASSURANCE QMS / Documentation / Validation and Qualification / Market Compliance / IPQA - (injectables) (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. QUALITY CONTROL (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M.Sc. (Organic Chemistry / Analytical Chemistry) B. Pharmacy / M Pharmacy MICROBIOLOGY (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M. Sc (Microbiology) Injectable Manufacturing (Executive/Senior Officer / Officer / Associate) Experience - 01 to 06 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations/ Visual inspection / QMS activities OSD Manufacturing (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activities Time and Venue : 06th July 2025, 09:30 Hrs to 17:00 Hrs ______________________________________________________ The Fern Kesarval Hotel, Verna Plateau GOA -403710 _____________________________________________________ We would be very happy if you forward or refer any of your colleagues matching the requirement. *Having relevant qualification and experience only can attend the scheduled walk-in.

Role & responsibilities 1. Routine and Stability analysis of development batches. 2. Analytical support for development of new or existing APIs. 3.Analytical method development and validation of raw materials, intermediates, finished APIs, under close supervision of senior analyst. 4.Qualification, Calibration and maintenance of analytical instruments. 5.Perform Calibration of analytical instruments and online documentation as per GDP requirement. 6. Preparation / Review of test method specification, method development protocol, method development report and analytical reports. 7. Work as per Good Laboratory Practices (GLP). 8. Maintaining log books, column usage cards and calibration records. 9. Following safety in the laboratory premises by using personal protective equipment and guiding to the subordinates to follow safety norms.

BASIC SUMMARY: Responsible for technical support for Endosafe (including automated NEXUS system) and/or Celsis and their associated systems. Support customers on Endosafe® and/or Celsis™ instrument installation, qualifications and product validation. Provide on-site training, sample testing or troubleshooting for continued customer satisfaction of our clients. Manage activities to help meet revenue targets and goals for the business. ESSENTIAL DUTIES AND RESPONSIBILITIES: Understanding and application of one or more of the product lines under the Microbial portfolio (Endosafe® and/or Celsis™) Applies technical/scientific skills to develop existing accounts and compete for customers together with the Account Management team whether for products sales or services sales. Supports customer onboarding, provide customer training, qualify leads, perform test demonstrations and help close new business opportunities during customer start up and continued account management. Responsible for the initial training and validation/application development support for customers, ensuring full and continued utilization of Microbial Solutions products. Recommends or performs remedial actions to troubleshoot customer issues related to application, reagents and software for the assigned product line. Performs instrument qualification and installation for new customers Establishes regular interface and communication with the Account Management and Field Services team to relay shared goals and targets; develop co-strategies to achieve defined targets; and work cohesively as a team to provide excellence in service to clients Builds relationships with customers to influence the acceptance and use of Microbial portfolio Input, manage and monitor cases on Service Cloud or SFDC. Ensures activities of the Technical Services team are continuously compliant to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. General requirements Maintains confidentiality of all Client information according to internal SOPs, Quality Service Agreements, and regulatory requirements. Maintains appropriate records and documentation of activities to facilitate continuous compliance to ISO 9001, Company local & global SOPs and data integrity principles and requirements, where appropriate. Actively seeks improvement within area of responsibility and takes necessary action to implement such improvements. Must be willing to travel domestically and internationally to customers’ sites Adheres to Company Policies and Procedures, including Code of Ethics and to Health and Safety requirements. Performs all other related duties as assigned. Preferred candidate profile QUALIFICATIONS: Education: Minimally M.Sc. or equivalent in Biology, Botany, Microbiology, Life Sciences, Biotechnology or any other related scientific discipline. Experience: 0-5 years of relevant industry experience, preferably involving customer-facing responsibilities. Understanding of Biology/Microbiology in the Pharma setting is an advantage An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above. Other: Must possess excellent communication and presentation skills. Proficient in the use of Microsoft Office applications

1)Good understanding in Environmental, EMI/EMC Qualification as per DO-160/MIL/IEC/EN standards 2)Experience in conducting successful environmental tests, and producing reports and technical data 3) Experience in writing Qual test reports, Procedure and Planning documents 4) Skilled in writing and defusing of MTRs 5) Good in American English writing and MS word formatting etc. 6) Highly skilled in operating and handling automated test stands and general lab equipments E.g.: Data loggers, oscilloscope, Power supplies, Signal analyzers etc. 7) Good understanding of vibration, shocks and experience in performing vibration test as well as post test data analysis . 8) Good skill in post test data analysis in excel and plotting different graphs to show test results for Qual test reports. 9) Evaluation of test data to establish correctness through reduction analysis and interpretation of instrumentation data 10)Knowledge about ABD0100 and Boeing Qualification standards will be added advantage

quality checks on raw materials, in-process, and finished product proper documentation as per GMP standard stability studies, sampling, and lab testing compliance with SOPs, regulatory, and safety guideline audits and assist in CAPA implementation

compliance with GMP and quality policie Approve RM/PM vendors and conduct regular quality audit validation, qualification, and batch release. GMP training $ support factory-wide implementation. Manage change control, deviation, and QMS execution.