Quality Assistant Salary at Mektec Europe Gmbh BETA

Job Title: Medical Device Manufacturing Engineer Starting Pay: $50-$75 per hour Duration: 3+ months PURPOSE OF JOB: Provide assistance in the implementation and ongoing support of manufacturing lines and maintain compliance with Quality System. MAJOR DUTIES AND RESPONSIBILITIES: Perform, coordinate, and provide guidance on: o Development and documentation of manufacturing processes o Design and development of assembly tooling and equipment o Process and product validations and documentation Support of: o Internal audits o Supplier audits o Material Review Board o Complaints investigation Analyzes returned products for failure modes and works with Quality Engineering to improve product quality and prevent future failures o CAPA and NCR documentation and investigation Train manufacturing and quality staff and associates Performs data collection and analysis to monitor trends in testing and manufacturing process results Develop inspection and sampling plans with Quality Engineering Develo

This position is responsible for the general management of the overall plant operations, plant facilities and the production of manufactured products. Responsible for managing the activities of various functions which may include some or all of the following: production, quality control, maintenance, environmental, engineering, mining, human resources, safety, yard operations, customer service, and financial operations. Manages activities of a team which may include supervisors, managers and/or individual contributors. Responsible for hiring, firing, performance appraisals, and pay reviews. Resolves critical issues and contributes to unit development. Make decisions based on company and functional objectives and allocated resources. Essential Duties And Responsibilities Leads special projects such as plant improvements or expansions, new product design, process changes and trend analysis of production and quality. Participates in the overall strategic planning for both the location and

Meet is working with a clinical stage biotechnology company looking to hire an Associate Director of CGMP Quality Assurance. Reporting to the Head of Quality, you will be working with cross-functional teams to manage external vendors and CDMOs. The role involves providing quality support and contributing to the development of quality systems. Expertise in GMP and related regulations is required. RESPONSIBILITIES: Serve as the technical expert on CGMP-related regulations and guidelines, specifically for manufacturing, testing, and controls. Review and approve drug substance and drug product manufacturing, packaging, and labeling documents within defined timelines. Lead and support external quality activities, including batch record reviews, analytical method validations, tech transfers, deviations, quality agreements, supplier qualifications, and audits. Participate in CDMO team meetings, providing quality feedback and collaborating on complex investigations for the company's global pro

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility. Job Overview We are seeking a highly skilled and professional Executive Assistant to provide comprehensive support to our VP of Quality Assurance (QA) and the QA department. The ideal candidate will demonstrate exceptional organizational skills, discretion, and the ability to thrive in a fast-paced biotech environment. This is an opportunity to bring your ideas, energy, and leadership to the table, helping to shape the future of Quality at Cytokinetics. Key Responsibilities Act as

Job Title: Sr. Manufacturing Engineer Location: San Jose, CA Zip Code: 95134 Start Date: Right Away Job Type: Contract - 6 months Pay Rate: $70.00 - $80.00 /hr DoE Shift: 8am-4:30pm M-F with some weekend work Keywords: #SrEngineeringJobs #ManufacturingEngineeringJobs #SanJoseJobs A Sr. Manufacturing Engineer job is available with our client in San Jose, CA. As a Manufacturing Engineer, you will learn and Apply knowledge of electrical components, interiors, systems integration or structural assembly and installation to collaborate and influence our multidisciplinary Product Design Engineering, Quality, Manufacturing and Facilities teams in the development of a new aircraft. To be considered for this role, you will have a Bachelor's Degree and 5+ years of relevant work experience in the aerospace industry. US Citizenship is required. JOB RESPONSIBILITIES: Assist on and off aircraft builds for electrical components, interior closeouts, metallic and composite assemblies, wiring harnesses,

Job Title: Composite Manufacturing Engineer Location: San Jose, CA Zip Code: 95134 Start Date: Right Away Job Type: Contract - 6 months Pay Rate: $55.00 - $70.00 /hr DoE Shift: 2nd - 3pm-11:30pm W-Sun OR Tues-Sat A 2nd Shift Composite Manufacturing Engineer job is available with our client in San Jose, CA. As a Manufacturing Engineer, you will learn and Assist aircraft build up and modifications to electrical components, mechanical composite assemblies, and wiring harnesses and to collaborate and influence our multidisciplinary Product Design Engineering, Quality, Manufacturing and Facilities teams in the development of a new aircraft. To be considered for this role, you will have a Bachelor's Degree and 5+ years of relevant work experience in the aerospace industry. US Citizenship is required. JOB RESPONSIBILITIES: Assist aircraft build up and modifications to electrical components, mechanical composite assemblies, and wiring harnesses. Utilizes various forms of engineering and techni

Discover International are currently partnered with a leading Pharmaceutical Company based around 30 Minutes from San Jose, CA who are seeking a Quality Assurance Specialist to be work fully onsite. This role will be an 18 Month Contract. **Please only consider applying if you are located within this area and happy to work onsite** Key Responsibilities: Quality Control (QC): Conduct routine and non-routine testing of raw materials, in-process samples, and finished products to ensure compliance with specifications. Manufacturing Support: Collaborate with production teams to identify and resolve quality issues during the manufacturing process. Batch Release: Review and approve batch records for product release, ensuring all manufacturing and quality control steps have been completed per regulatory standards. LIMS (Laboratory Information Management System): Utilize LIMS to manage and track laboratory data, ensuring all information is accurate and up-to-date. Lab Work: Perform lab testing

Director of Quality - Quality Management Representative Well-Funded 25-Person Start-up Medical Device company Devices: Neurovascular & Endovascular devices (US Market, 510K) Location: San Jose, CA (near SJ Airport) Responsibilities: Will serve as the company's first Quality Management Representative Draft and manage a complete QMS Own and ensure Quality Compliance for the company FDA & ISO Audits Incoming & Receiving Inspections CAPA & NCR Supplier Audits Write and revise SOP's, WI's Will establish the Quality function at the company, and soon add a small support team (likely Doc Control and/or Quality Specialist or Manager) Requirements: **Must Have served as a Quality Management Representative** BS Degree, preferred in an Engineering or Lifesciences discipline 10-15+ years Quality Assurance experience in a MEDICAL DEVICE company 5+ years People Leadership experience Startup experience preferred, or mix of startup & larger company experience Hybrid Position: Requirement to be in-offic