6 Test Methods Jobs

As an Electrical Design Engineer at ViewRay Systems, you will play a crucial role in the innovation and development of novel cancer therapy systems, contributing to the mission of conquering cancer. Your primary responsibilities will include developing a deep understanding of Embedded control system/sub-system solutions, designing electrical schematics, and testing proof of concept and prototype modules using Altium designer tool. Additionally, you will be involved in testing prototypes, analyzing data using basic software skills and OEM tools, and operating a variety of control systems. You will be expected to develop effective test methods to ensure various design requirements are met, adhere to technical documentation and design analysis processes, and follow internal design controls and change control procedures. Managing design files and materials as per guidelines will also be a part of your responsibilities. To qualify for this role, you should have a BSEE or a related degree, with a demonstrated interest in circuit design, FPGA, and software. Excellent communication, troubleshooting, and problem-solving skills are essential for success in this position. You must also be comfortable working around strong magnetic fields and have familiarity with Microsoft Office tools. Preferred qualifications include a BSEE with 3 years of experience, technical leadership capabilities in integration activities, and proficiency in software such as C, C++, Python, Linux, and Shall script. Effective oral and written communication skills are highly valued for this role. This is a full-time position based in Chandigarh, India, requiring relocation before starting work at the office located at Plot No. A-40A, Industrial Focal Point, Phase 8-Extn, Sector 59, S.A.S. Nagar (Mohali), Distt. Mohali, Punjab -160059. In return for your contributions, ViewRay Systems offers a competitive salary and benefits package to support your professional growth and well-being.,

You are seeking a Lead Engineer - System Verification to join our team. In this role, you will be responsible for executing verification tests, developing test methods, analyzing measurement data, and reporting test results in compliance with international standards. Your tasks and responsibilities will include translating requirements into verification plans and protocols with a focus on traceability. You will develop reproducible and maintainable verification test methods, test set-ups, and tools. It will be your responsibility to define and document the impact on system-level behavior resulting from design changes and ensure thorough verification. You will create, implement, and enhance product test plans/protocols to ensure that product design meets specifications and quality system requirements in alignment with reference standards. Collaboration with the system team and development team to design test descriptions and acceptability criteria is essential. Familiarity with the medical device regulatory environment, including FDA regulations, MDR, and IEC standards, is required. You will conduct product tests using laboratory tools such as a multimeter and oscilloscope, performing statistical analysis of test results. Additionally, you will design test methods, conduct test method validation activities including Measurement System Analysis (MSA), and prepare relevant documentation. Providing the test area with parameters for sample testing and specifying tests to be performed will be part of your responsibilities. You will also perform and report verification and validation tests, write test reports, and create technical documentation in compliance with applicable standards and regulations. Your role will involve guiding project members in documenting development activities, coordinating the work and progress of the development team, and mentoring and supporting team members in the development of test methods and test equipment. **Work Experience:** **Skills and Qualifications:** - Bachelor's degree in Mechatronics or Electrical Engineering - 6-9 years of industry experience in a similar role with a strong understanding of the design verification process - Knowledge of international (medical) standards and regulations - Proficiency in writing and maintaining test requirements from Customer level to System Level, decomposed into subsystems, modules, software levels - Understanding of statistical methods, test method validation, and the use of MiniTAB - Broad knowledge of available market test equipment - Excellent written and spoken English skills - Quality-oriented mindset with comfort in documentation practices and understanding of objective evidence.,

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

The Chemist role involves performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. As a Chemist, you will contribute by conducting laboratory testing, preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation, reviewing product certificates of analysis, maintaining Certificates of Analysis (C of A) files, and providing input on Standard Operating Procedures (SOPs), Test Methods, and laboratory documents. You will also participate in investigations, address Out of Specifications (OOS), resolve deviations, and implement CAPA with general supervision while strictly adhering to current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP). Key responsibilities include interpreting test results, maintaining a safe, clean, and efficient laboratory environment, and ensuring routine calibration and performance verification of lab equipment and instrumentation. Although there are no supervisory responsibilities, you should possess the ability to adapt as the external environment and organization evolve. Successful candidates will demonstrate the ability to complete testing according to established methods, proficiency in lab instrumentation and multiple test methods, problem-solving skills, and the capacity to coordinate workload effectively. The ideal candidate will hold a Bachelor/Master of Science in Chemistry, Biochemistry, or related scientific fields, or equivalent experience. Additionally, knowledge of LC/MS and GC/MS, previous cGMP regulation and compliance knowledge, nutraceutical or pharmaceutical laboratory work experience, and familiarity with ISO17025 Lab Management are preferred. Join us in this exceptional opportunity to contribute to world-class research and shape the future of nutritional science.,

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. (qualitative and quantitative chemical and collect/physical analysis of raw materials, finished products and/or stability samples Required Candidate profile 6+ yrs of Agrochemicals/chemicals in Green field/brown field Projects Exp in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD & DSC capitalplacement04@gmail.com P- 9315507817

Role & responsibilities Responsible for overall functioning of the Quality department. Developing Quality Management System, maintenance, internal audits, auditor qualification & co-ordination with external certification agency in the capacity of Management Representative. Responsible for developing of test methods and procedures Responsible for new product validation and testing Analysing various processes/ applications and recommending process modifications and equipment calibrations to enhance operational efficiency. Approval of new materials. Internal audits. Responsible for developing tools for keeping MIS up-to-date and monthly reporting of Quality data to the Customer and Management team. Handling of customer issues and indepth investigation of root cause analysis. Participating in continual improvement and kaizen activities SKILLS REQUIRED Exposure to Six Sigma, SMETA & PIP Projects Adept at Process improvements, problem analysis, root case elimination. Exposure to driving certifications for QMS