Job Description Evaluation of the processing products according to the specification (Master sample, Product Brief, VQG, SpecIT) Perform process audit Perform function test, when test failed, escalate the result. Support novelty process and SAT test Record
Additional Locations: N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our
Typical Accountabilities Responsible for Quality Supplier Management including but not limited to: Annual Assessments; Quality Agreements; trending and reporting of data; assessing, reviewing and improving quality systems at Suppliers; attendance at Quality and Business Review Meetings. Maintains a high level
Location:Shanghai, China Job ID: R0138671 Date Posted:2026-07-28 Company Name:HITACHI ENERGY SHANGHAI ELECTRICAL TRANSFORMER CO., LTD. Profession (Job Category):Quality Management Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy Transformer Business Unit in Greater China operates
At Jabil (NYSE: JBL), we are proud to be a trusted partner for the worlds top brands, offering comprehensive engineering, supply chain, and manufacturing solutions. With 60 years of experience across industries and a vast network
SummaryImagine what you could do here! At Apple, new insights have a way of becoming extraordinary products, services, and customer experiences very quickly. Bring passion and dedication to your job and theres no telling what you
About the Role As a Principal Senior Auditor of the Regulatory Audit China team in Group Internal Audit (GIA), you will operate within a dynamic, agile working environment — self-organizing with talented peers to deliver high-quality work, including
About the Role As a Principal Auditor of the Regulatory Audit China team in Group Internal Audit (GIA), you will operate within a dynamic, agile working environment — self-organizing with talented peers to deliver high-quality work, including not
Work ScheduleStandard (Mon-Fri) Environmental ConditionsAdherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job DescriptionAs part of the
Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your
Imagine your career taking you to the depths of innovation and the heights of impact. Our people enable continuous progress. Their commitment, collective expertise, and unique capabilities are the engine room behind SBM Offshore’s True. Blue.
Primary Function: To carry out and deliver the services to our customer in an efficient and professional manner as required by his Team Leader and/or formal agreements with clients. Responsibilities: • Responsible to meet his/her own
Location(s) Shijie Town, Dongguan, Guangdong Company Molex Career Field Quality Job Number 192122 PRIMARY PURPOSE: Supplier, including potential supplier, assessment/audit/qualification. Involve DFM review and PPAP process. Lead/coordinate “high risk” component PPAP process and support AQP/MIE on other
Location(s) Shijie Town, Dongguan, Guangdong Company Molex Career Field Quality Job Number 191691 PRIMARY PURPOSE: Supplier, including potential supplier, assessment/audit/qualification. Involve DFM review and PPAP process. Lead/coordinate “high risk” component PPAP process and support AQP/MIE on other
Typical Accountabilities (per AZ framework and regulatory expectations): Acting as the quality Approval / Decision maker for the GxP relevant procedure in Astrazeneca Distribution Facility. Ensure the compliance with internal Astrazeneca requirement and also relevant market Healthy
Job Description 1. Be responsible for the establishment of the IATF16949 quality system: (1) Prepare and revise system documents such as the quality manual and procedure documents (2) Conduct training for internal auditors in each department of the company
Company Description At QIMA, we are on a mission to offer our clients smart solutions to make products you can trust. Operating in over 100 countries, we serve the consumer products, food, and life sciences industries
Job Description SummaryThe Lead Supplier Quality Engineer – Mechanical Commodities is the technical authority and quality gatekeeper for GEV PCSs mechanical supply base, covering castings, large/heavy forgings, and precision-machined shafts. The role owns product and process qualification, defines
Job Summary Job Description 1. Perform QMS audit to vendors, write audit report, and follow-up supplier CAPA. 2. Work as project leader in Vendor FDA project, supervise vendor to adequately establish and maintain QMS based on