field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
Job Overview
 
 The Quality Engineer is responsible for ensuring product quality, reliability, and compliance with industry standards by developing and implementing quality assurance processes. This role collaborates with cross-functional teams to drive root-cause problem solving, continuous improvement, and best practices in manufacturing.
 
Key Responsibilities
 
<ul>
<li>Oversee quality aspects of production projects through development, build, and testing phases.</li>
<li>Analyze data, perform root-cause investigations, and maintain accurate project documentation.</li>
<li>Define test requirements, acceptance criteria, and inspection standards.</li>
<li>Manage inspection data, reporting, and performance metrics for quality control.</li>
<li>Collaborate with engineering to capture and process design changes.</li>
<li>Develop and update work instructions to align with ISO 9001 standards.</li>
<li>Conduct internal quality audits and present findings.</li>
<li>Lead and document corrective and preventive actions (A3/8D).</li>
<li>Provide supplier quality support, including inspection, analysis, and corrective actions.</li>
<li>Partner with continuous improvement teams to reduce quality costs and improve process capability.</li>
</ul>
 
Qualifications
 
Education
 
<ul>
<li>Bachelor’s degree in Manufacturing, Mechanical, or Electrical Engineering, or related field.</li>
<li>Associate degree with equivalent experience may be considered.</li>
</ul>
 
Experience
 
<ul>
<li>7–10 years in heavy industrial or manufacturing environments.</li>
<li>5+ years in a quality-focused role preferred.</li>
<li>Experience with electrical, hydraulic, or mechanical systems a plus.</li>
</ul>
 
Preferred Certifications &amp; Skills
 
<ul>
<li>ASQ CQE or Six Sigma Green Belt certification preferred.</li>
<li>Strong understanding of GD&amp;T, CMM reporting, and inspection methods.</li>
<li>Proficient in quality tools, data analysis, and problem-solving methodologies.</li>
<li>Knowledge of fabrication, machining, welding, and assembly operations.</li>
<li>Excellent communication and leadership skills with the ability to train others.</li>
<li>Strong project management and continuous improvement mindset.</li>
<li>Ability to lift up to 40 lbs.</li>
</ul>

Quality Engineer

<h3>Job Description</h3>
Job Description We're seeking strong technical quality professional to develop and implement quality assurance standards into aerospace manufacturing processes and inspections.

Summary: Develops and implements quality assurance standards into manufacturing processes and inspection relating to the objectives of the RFC team. Responsible for dimensional verification of product though use of various inspection tools and techniques. Monitors data to keep processes in control; works with suppliers and customers to maintain day-to-day operations. 
Essential Duties and Responsibilities include the following. Others as assigned.
<ul>
<li>Applies modern quality principles, concepts, and methods to aerospace manufacturing operations through use of Lean Manufacturing and Six Sigma tools.</li>
<li>Interprets customer engineering requirements though use of customer drawings, specifications, and industry standards to ensure compliance.</li>
<li>Ability to operate and program CMM using PCDMIS software.</li>
<li>Ability to program and operate Leica tracker system using Polyworks software.</li>
<li>Manage quality information databases for gage calibration.</li>
<li>Manage outside service vendors/ suppliers for gage design, build, control, and calibration.</li>
<li>Proven ability to develop and improve dimensional inspection of product.</li>
<li>Ability to interpret and apply GD&amp;T principals to inspection of products.</li>
<li>Creates work instructions on use of inspection tools and inspection requirements for shop floor use.</li>
<li>Prepares reports, procedures, and presentations for customer/supplier review. </li>
</ul>
<ul>
<li>Initiate, recommend, investigate, trouble-shoot and provide solutions and actions to prevent the occurrence of any nonconformance relating to the products, process and quality system. </li>
</ul>
<ul>
<li>Requires strong interpersonal skills with the ability to effectively establish positive working relationships with various groups, across all levels of the company, suppliers, and customers. </li>
<li>Review proposed new products to ensure compliance with customer requirements and manufacturability standards through use of APQP process.</li>
</ul>

Physical Demands - The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this Job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. 

Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and fumes or airborne particles. The noise level in the work environment is usually loud.

Schedule: This overtime-exempt position will primarily work five days per week, eight or more hours per day. 

Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 
<ul>
<li>Five or more years’ related engineering experience working in a manufacturing environment. </li>
<li>Bachelor’s degree in Engineering or related technical field.</li>
<li>Experience with application of APQP</li>
<li>Experience with aluminum and metal forming processes.</li>
<li>Strong computer/technical skills including: PCDMIS, Microsoft office products and ability to learn others as needed, such as MRP or ERP.</li>
<li>US person as defined by ITAR/EAR.</li>
</ul>

Preferred:
<ul>
<li>Experience with leading or supervising team members in quality department(s) and six sigma.</li>
<li>Experience with Aerospace industry - customer specifications and requirements.</li>
<li>Experience with aluminum heat treating.</li>
<li>Experience with coordinating design and build of manufacturing inspection tools.</li>
<li>Hands-on experience with computer software: Autodesk Inventor, AutoCAD, GeoMagic and Polyworks software.</li>
</ul>

 
Who We Are 
voestalpine Roll Forming Corporation, or RFC as we call it, supplies custom roll formed metal components into several industries including Aerospace, Construction, Material Handling, Off-Highway, Office Furniture, Solar and Transportation. In 2000, Roll Forming Corporation was acquired by globally leading technology group voestalpine AG and became part of the Metal Forming, Tubes and Sections division. Today, voestalpine Roll Forming Corporation has seven production facilities across three states with five facilities and headquarters located in Shelby County, Kentucky and one facility each in Pennsylvania and Indiana.
 
What We Offer You
<ul>
<li>Several great benefit plans, including multiple health insurance options, vision, dental, life, short-term and long-term disability coverage, health-saving accounts, or flexible spending account</li>
<li>401K or 401K Roth up to 6% Match</li>
<li>Quarterly Profit-Sharing Bonus. </li>
<li>Apprenticeship programs &amp; tuition reimbursement opportunities</li>
<li>Leadership training opportunities</li>
<li>TogetherWeCare, a philanthropic volunteer program that allows employees to support their community while on company time</li>
<li>Countdown to Zero, a global environmental impact initiative that strives to make our work environments more efficient and environmentally friendly</li>
</ul>
Learn more at <a href="http://www.rfcorp.com/careers/life-at-rfc" target="_blank">www.rfcorp.com/careers/life-at-rfc</a>! 
 
voestalpine Roll Forming Corporation is an At Will employer. Employment will be at-will, which means that either the employee or the employer may terminate the employment relationship at any time, with or without prior notice, and with or without cause.
Roll Forming Corporation is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected Veteran status, and any other federal, state, or locally protected classifications. Please contact us at <a href="mailto:RFC.HR@voestalpine.com" target="_blank">RFC.HR@voestalpine.com</a> if you require any alternate application form or accommodation during our hiring process due to disability.

<h3>Job Description</h3>
Job DescriptionSalary: 
About 1HMX
At 1HMX, we are pioneering the future of Human Machine eXperience (HMX) through innovation, precision, and performance. Our diverse technology portfolio includes electro-mechanical assemblies, immersive virtual reality systems, wearable electronics, infection control solutions, and advanced medical and industrial touch interface products. As a trusted manufacturing partner serving global markets, 1HMX is committed to delivering high-quality, compliant, and reliable solutions that meet the evolving needs of our customers. We are driven by a passion for engineering excellence and a deep commitment to transforming how people interact with technology.
 
Job Summary
This position supports Advanced Input Systems a 1HMX Brand Quality activities for aerospace customers - Onboard entertainment, suppliers, and global manufacturing operations (U.S. &amp; Asia). The Quality Engineer ensures compliance with aerospace standards (AS9100, FAA, NADCAP, etc.), drives supplier and internal quality improvements, and maintains strong customer relationships by meeting or exceeding quality performance requirements.
Key Responsibilities
<ul>
<li>Customer Engagement: Build long-term partnerships with aerospace OEM and Tier 1 customers by addressing audits, surveys, complaints, and product performance metrics.</li>
<li>Supplier Quality: Evaluate and develop supplier capabilities to ensure compliance with aerospace regulations and customer-specific requirements.</li>
<li>Quality Systems: Maintain and enhance the AIS QMS in alignment with AS9100 and ISO9001.</li>
<li>Auditing &amp; Compliance: Plan, lead, and support internal, supplier, and customer audits. Participate in FAA, EASA, or NADCAP compliance efforts.</li>
<li>FAIR &amp; RCCA: Lead First Article Inspections (FAIR/AS9102) and structured Root Cause Corrective Actions (RCCA/8D).</li>
<li>Continuous Improvement: Apply Lean and Six Sigma methodologies to reduce defects, improve yield, and ensure production readiness.</li>
<li>Data Analysis: Collect, analyze, and act on quality data (SPC, capability studies, DOE) to prevent recurrence of defects and improve product reliability.</li>
<li>Collaboration: Work with Product Development, Manufacturing Engineering, and global operations to integrate quality into new product introduction (NPI) and sustainment programs.</li>
</ul>
Required Skills &amp; Abilities
<ul>
<li>Strong knowledge of aerospace quality standards and customer expectations.</li>
</ul>
<ul>
<li>Deep understanding of aerospace quality systems, regulations, and customer expectations.</li>
<li>Strong technical writing and reporting skills for customer and regulatory documentation.</li>
<li>Effective communicator with ability to present to both technical and executive audiences.</li>
</ul>
<ul>
<li>Excellent organizational skills and attention to detail.</li>
<li>Proven ability to manage multiple priorities under strict aerospace compliance timelines.</li>
<li>Strong analytical and problem-solving skills with experience in RCCA methodologies (8D, Fishbone, 5 Why, etc.).</li>
</ul>
<ul>
<li>Proficient in MS Office; knowledge of ERP/QMS software preferred.</li>
</ul>
Education &amp; Experience
<ul>
<li>Bachelors degree in Engineering, Quality, or related technical field required.</li>
<li>Minimum 4+ years applicable experience, preferably in aerospace electronics and manufacturing.</li>
<li>Experience with AS9100, ISO9001:2015, and internal auditing processes.</li>
</ul>
<ul>
<li>Demonstrated experience with FAIR/AS9102, PPAP, FMEA, SPC, and process capability.</li>
<li>Lean/Six Sigma Green Belt or equivalent preferred.</li>
</ul>
<ul>
<li>Experience supporting or leading aerospace customer audits and compliance reviews highly desirable.</li>
</ul>
AIS is an equal opportunity employer. We are committed to creating an inclusive environment for all employees and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected characteristic. We encourage applicants of all backgrounds to apply.

Quality Engineer - Aerospace

<h3>Job Description</h3>
Job DescriptionWe are seeking a skilled Manufacturing Quality Engineer to join our team. Our company operates in a regulated environment and adheres to ISO9001 and AS9100 standards. We specialize in manual manufacturing processes, emphasizing precision and reliability in every aspect of our operations. Work Authorization: Due to US Govt and our Clients rules and regulations - candidates must be able to provide proof of US Citizenship and or Permanent Residence. Day to Day Responsibilities:
<ul>
<li>Lean Manufacturing Tools and Technologies – The use of tools, techniques and processes specifically designed to increase value added work, including daily routines and tasks, to eliminate waste, decrease cost, and create a culture of continuous improvement&nbsp;</li>
<li>Gather, Analyze, and Report information – Observing, receiving or otherwise obtaining information from all available resources. Identifying the underlying principles, reasons, or facts within the information to provide meaningful results for the given audience&nbsp;</li>
<li>Implement and maintain quality control procedures in accordance with ISO9001 and AS9100 standards.</li>
<li>Perform inspections and audits to identify areas for improvement and ensure compliance with regulatory requirements.</li>
<li>Collaborate with cross-functional teams to address quality issues and implement corrective actions.</li>
<li>Provide guidance and training to production teams on quality standards and procedures.</li>
<li>Conduct root cause analysis and implement preventive measures to minimize defects and non-conformances.</li>
<li>Drive continuous improvement initiatives to enhance overall quality and efficiency in manufacturing operations.</li>
</ul>
Qualifications and Skills
<ul>
<li>Bachelor's degree in Engineering or related field.</li>
<li>4+ years of professional experience in Quality Engineering, preferably in a regulated environment.</li>
<li>Strong knowledge and experience with ISO9001 and AS9100 standards.</li>
<li>Proven track record in manual manufacturing environments, with a focus on quality assurance and process improvement.</li>
<li>Prefer candidates with a solid Data background and organizing Data</li>
</ul>

Quality Engineer (Manufacturing)

<h3>Job Description</h3>
Job Description
As the largest pureplay adhesives company in the world, H.B. Fuller’s (NYSE: FUL) innovative, functional coatings, adhesives and sealants enhance the quality, safety and performance of products people use every day. Founded in 1887, with 2024 revenue of $3.6 billion, our mission to Connect What Matters is brought to life by more than 7,500 global team members who collaborate with customers across more than 30 market segments in over 140 countries to develop highly specified solutions that enable customers to bring world-changing innovations to their end markets. Learn more at <a href="http://www.hbfuller.com" target="_blank">www.hbfuller.com</a>.
 
 
Join H.B. Fuller as a Production Operator I
<ul>
<li>Location: Blue Ash, Ohio (On-Site)</li>
<li>Schedule: All shifts available</li>
<li>Pay: $23.00 per hour + $2.00 shift differential for 2nd and 3rd shifts</li>
<li>Benefits: Comprehensive package including health, dental, and vision insurance, 401(k) contributions, PTO, paid holidays, and more. Eligibility may vary.</li>
<li>Career Development: Effective training, learning tools, and development programs to help you grow at every level of the organization.</li>
</ul>
 
H.B. Fuller is a leading global adhesives provider focusing on perfecting adhesives and sealants across all industries throughout the world. While our products are virtually invisible, they play a vital role in ensuring the quality of modern life and we are dedicated to connecting what matters to solve some of the world's biggest adhesion challenges.
 
What makes a successful Production Operator at H.B. Fuller:
<ul>
<li>Prepare raw materials and packaging by identifying and transporting the correct quantities to the production area, reporting any deviations, and documenting processes.</li>
<li>Operate processing equipment following detailed instructions and procedures.</li>
<li>Monitor equipment to ensure smooth operations and maintain desired production rates.</li>
<li>Perform initial product testing to ensure specifications are met.</li>
<li>Check labels and packaging materials to ensure accuracy and compliance with standards.</li>
<li>Package final products in line with H.B. Fuller’s high-quality expectations.</li>
<li>Maintain a clean and organized work environment.</li>
<li>Follow all company safety, environmental, and quality standards.</li>
<li>Complete additional duties as requested by the Production Manager or Supervisor.</li>
</ul>
 
Vital Ingredients of a Production Operator:
<ul>
<li>HS diploma/GED</li>
<li>Familiarity with common software programs (e.g., MS Office).</li>
<li>Ability to read and comprehend work orders, safety regulations, and quality procedures.</li>
<li>Experience in an industrial environment (chemical background preferred) with exposure to mixing or batching processes.</li>
<li>Basic English comprehension</li>
<li>Availability to work in shifts.</li>
</ul>
 
Physical Environment:
<ul>
<li>Ability to stand for extended periods and move freely, including climbing stairs, stretching, and reaching.</li>
<li>Comfort lifting up to 50 pounds regularly and up to 100 pounds with assistance.</li>
<li>Willingness to work in a chemical manufacturing environment with exposure to varying temperatures, dust, noise, and odors.</li>
</ul>
 
Ready to Grow with Us? At H.B. Fuller, we ensure our employees are equipped with meaningful opportunities, comprehensive benefits, and a simple application process. Keep an eye on your email after applying, and we’ll guide you to the next steps.
 
Join H.B. Fuller Today! Be a vital member of our team and help us Connect what matters.
 
Pay is based on several factors including but not limited to education, work experience, certifications, and geographic location.
 
The salary for this role is $23.00/hr.
 
In addition to your salary, H.B. Fuller offers employees a competitive total rewards package including comprehensive benefits, incentive and recognitions programs, health &amp; wellness benefits, 401K contributions, paid time off and paid holidays. Eligibility may vary.
 
 
H.B. Fuller is an Equal Employment Opportunity employer and proud to have created a collaborative culture where employees around the world are seen, heard, and respected. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, national origin, disability, or marital status or status as a protected veteran, or any other legally protected classification.
 
H.B. Fuller does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with H.B. Fuller, a written service agreement must be executed by Human Resources prior to submitting any information relating to a potential candidate. Without a signed service agreement, H.B. Fuller shall not be obligated for payment of any fee or compensation.
Company DescriptionH.B. Fuller is a leading global adhesives provider focusing on perfecting adhesives, sealants and other specialty chemicals across all industries throughout the world. While our products are virtually invisible, they play a vital role in ensuring the quality of modern life and we are committed to connecting what matters to solve some of the world's biggest adhesion challenges. Offering you: Medical, dental, and vision insurance for you and your family FREE medical insurance coverage – all or a portion of your medical premiums will be reimbursed by the company 3 weeks paid vacation (increases to 4 weeks after 48 months of employment) 11 paid Holidays per year Quarterly bonuses based on site performance Competitive 401k, with up to 4% dollar-for-dollar company matching contributions, 1% automatic company contribution, and additional profit-sharing contribution. And MORE!

Production Operator

<h3>Job Description</h3>
Job Description
Job Overview
 
The Electrical Quality Engineer ensures product quality and reliability by developing, implementing, and maintaining quality assurance processes within electrical assembly and wiring environments. This role collaborates with cross-functional teams to drive root cause analysis, continuous improvement, and compliance with industry standards. The position primarily focuses on electrical systems—wiring, harnesses, and cabling—but may also include mechanical and fabrication processes.
 
Key Responsibilities
<ul>
<li>Oversee quality aspects of electrical and production projects from development through testing.</li>
<li>Inspect and verify wiring, harness, and cable assembly processes to ensure compliance with IPC/WHMA standards.</li>
<li>Analyze data, resolve issues, and maintain accurate inspection and test records.</li>
<li>Define and justify machine test requirements and acceptance limits.</li>
<li>Manage Work In Progress (WIP) and Operation Acceptance Test (OAT) data and prepare performance reports.</li>
<li>Lead root cause analysis, corrective actions (8D, CAPA), and continuous improvement initiatives.</li>
<li>Collaborate with the Continuous Improvement team to reduce quality costs and enhance process capability.</li>
<li>Ensure materials traceability and manage Pre-Check and Factory Acceptance Test (FAT) reporting.</li>
<li>Coordinate with Engineering to process design and “redline” drawing changes.</li>
<li>Update and maintain work instructions related to the ISO 9001 Quality Management System.</li>
<li>Conduct internal audits, report findings, and ensure compliance with quality standards.</li>
<li>Drive supplier quality improvement through inspection, data analysis, and corrective feedback.</li>
</ul>
 
Education
<ul>
<li>Bachelor’s degree in Electrical, Mechanical, or Manufacturing Engineering, or related field.</li>
<li>Associate degree with relevant hands-on experience may be considered.</li>
</ul>
 
Experience
<ul>
<li>7–10 years in a heavy industrial or electrical manufacturing environment.</li>
<li>5+ years in a Quality Engineering role focused on electrical systems, wiring, or assembly.</li>
<li>Hands-on experience with wire terminations, harnesses, and cabling required.</li>
<li>Experience in board or transformer manufacturing a strong plus.</li>
</ul>
 
Certifications &amp; Standards
<ul>
<li>ASQ CQE or ASQ SSGB certification preferred.</li>
<li>Familiarity with industry standards:</li>
<li>IPC-A-610 – Acceptability of Electronic Assemblies</li>
<li>IPC/WHMA-A-620 – Cable &amp; Wire Harness Assembly Requirements</li>
<li>ANSI/ESD S20.20 – Electrostatic Discharge Control</li>
<li>ISO 9001 – Quality Management Systems</li>
</ul>
 
Skills
<ul>
<li>Strong understanding of GD&amp;T, CMM measurement, and inspection layout techniques.</li>
<li>Proficient in quality tools and methodologies (PPAP, 8D, CAPA).</li>
<li>Skilled in problem-solving, data analysis, and process improvement.</li>
<li>Effective written and verbal communication skills.</li>
<li>Strong organizational and project management capabilities.</li>
<li>Proficient in Microsoft Office and ERP systems.</li>
</ul>

Electrical Quality Engineer

<h3>Job Description</h3>
Job Description
C &amp; Q
PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning &amp; Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products.   At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals.
   These positions will be responsible for the generation of design documents (i.e. URS, C&amp;Q Plan, risk assessments), authoring protocols, execution of commissioning and qualification activities, along with moving these methodologies towards digitization of C&amp;Q and validation processes into the Knead Gx Platform. The position will also can provide client support for C&amp;Q projects either independently or as part of a site team. This position will have the ability to interpret the needs, expectations, and limitations of each stakeholder, and bring them together with the goal of meeting project timelines. They should have familiarity with risk assessments and overall project safety. They must have prior experience in pharmaceutical or similar regulated cGMP environments and experience in supporting fast-paced C&amp;Q/validation projects, development of documentation, and/ or execution of various C&amp;Q/validation projects. They should be able to build a high level of trust with internal and client personnel. Candidates must operate with honesty, integrity, accountability, teamwork, and commitment.
In this position, the ideal candidate will be integrated into VEQTOR’s C&amp;Q group and Kneat Services &amp; Support group working on the projects (internal and external) for our US and EU clients.
Kneat Gx platform digitizes and manages life cycle documentation, including design documentation, risk management, commissioning and qualification, validation documentation and testing. It releases groups from paper and is presently being used by 12 of the world’s top 20 pharma companies. Being part of the VEQTOR team, you will be trained on Kneat and assist our clients with implementation.
These roles are primarily on-site but there may be hybrid or remote options available depending on client and project need.
The ideal candidate should have the following skills:
<ul>
<li>Ability to identify project requirements from client stakeholders to achieve the desired outcome.</li>
<li>Ability to generate a detailed plan that can be implemented by a project team.</li>
<li>Plan, communicate and lead scientifically sound C&amp;Q strategies for small to large scale projects.</li>
<li>Familiarity with risk-based C&amp;Q strategies, procedures, policies, and guidance and its practical application based on process knowledge and product requirements.</li>
<li>Aptitude to plan (i.e., budget/scheduling) and forecast a project from a C&amp;Q and/or Validation perspective.</li>
<li>Capable of understanding project needs.</li>
<li>Liaising with contractors, suppliers, and internal company stakeholders.</li>
<li>Ability to perform system walk-downs, as well as other engineering pre-commissioning activities, if required.</li>
<li>Able to perform commissioning, qualification, and validation testing on manufacturing process equipment, such as:
<ul>
<li>Incubators/Coolers/Freezers/Freezer Dryers/Autoclaves</li>
<li>Isolators</li>
<li>Lyophilizers</li>
<li>Mixers including single-use</li>
<li>Bioreactors/Product Vessels/Buffer Vessels</li>
<li>Fume Hoods/Biosafety Cabinets</li>
</ul>
</li>
<li>Able to perform commissioning, qualification and validation testing on facilities and utilities, such as:
<ul>
<li>Nitrogen, Clean Compressed Air, Vacuum, RODI, Purified Water, Water-For-Injection, Clean Steam</li>
<li>HVAC, Cleanroom Qualification</li>
</ul>
</li>
<li>Knowledge of minimal protocol requirements and ability to author various life cycle documents associated with C&amp;Q and Validation.</li>
<li>Perform a review of design and requirement specifications to establish fit-for-purpose for systems.</li>
<li>Perform a review of engineering drawings for accuracy.</li>
<li>Provide summary and analyses reports.</li>
<li>Perform ongoing reporting of the project progress to client and VEQTOR management.</li>
<li>Ensuring all aspects of the project proceed while adhering to company SOPs as well as external regulations, including maintenance of project documentation.</li>
<li>Ability to troubleshoot problems as they arise on a project – finding efficient and effective solutions.</li>
</ul>
Desired Skills &amp; Experience:
<ul>
<li>Knowledge of Validation policies and documentation for various systems and processes</li>
<li>B.S. in Science or Engineering discipline</li>
<li>Minimum of 3 – 5+ years related experience preferred, however candidates with related experience will be considered.</li>
<li>Kneat Gx platform experience is preferred but not required.</li>
<li>Proficient in English</li>
</ul>
 Communication and Influence: Communicates primarily and frequently with internal contacts. External interactions are less complex or problem solving in nature. Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision making. 
  Company Response to Covid-19 While we serve industries deemed essential businesses, PharmEng Technology will follow safe business practices and adhere to local, state, and federal guidelines. When possible, PharmEng Technology will allow remote work from home.   EEOC Statement At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.

C&G Engineer

<h3>Job Description</h3>
Job Description
Overall Purpose of the Role:
Responsible for ensuring that the products produced meet quality standards required to minimize quality costs and maximize customer satisfaction whilst ensuring that procedures and processes are adhered to. Ensure incoming materials meet required quality standards. Responsible for identifying and
raising quality issues and for speedily resolving them to ensure zero impact to the customer. Work closely with Engineering on new product introductions to ensure the robustness of product builds. Work in a team environment to develop and implement best practices that emphasize defect prevention, reduction in variation and waste and provide for continuous improvements in meeting all customer requirements. Maintain Metrological equipment that generates quality data. Manage the customer specific requirements and offer technical support. Technical expertise on composites manufacturing will be taught on the job, but the Quality Engineer will be leading work to define and establish quality processes in pursuit of an ISO 9001 certification.
Key Responsibilities:
<ul>
<li>Lead team in pursuing an ISO 9001 certification</li>
<li>Manage all quality-related issues within the manufacturing team (e.g. internal, supplier, customer and customer warranty)</li>
<li>Identify root cause and instigate permanent corrective actions for product quality issues</li>
<li>Carry out product and process auditing</li>
<li>Ensure control plans and associated documentation are implemented effectively and maintained</li>
<li>Monitor and report on quality-related key performance indicators including scrap monitoring, rework levels, parts per million (PPM) figures</li>
<li>Stop production in the event of manufacture of unacceptable goods/processes</li>
<li>Work closely with engineering on developing product layup instructions</li>
<li>Assist with training of quality awareness</li>
<li>Participate in cross-functional teams in the development of new products or changes related to current products in meeting customer requirements</li>
<li>Participate in the development and refinement of Design and Process FMEA's (Failure Mode and Effects Analysis)</li>
<li>Lead quality audits</li>
<li>Drive continuous improvement activities</li>
<li>Support and lead process improvement activities</li>
<li>Conduct benchmarking studies to determine best practices/designs and future trends</li>
<li>Independently determine approach and assigned tasks</li>
<li>Lead and/or support groups of technicians</li>
<li>Support any customer visits with facility tours and demonstration of quality controls</li>
<li>Communicate efficiently throughout the shop floor and with own and customer's management</li>
<li>Comply with the Health, Safety and Environmental Policies</li>
</ul>
Requirements and Qualifications:
<ul>
<li>4 year college degree or 5 years equivalent experience</li>
<li>Knowledge of ISO 9001 and IATF 16949</li>
<li>Strong knowledge of Advanced Product Quality Planning (APQP), Production Part Approval Process (PPAP), Failure Mode and Effect Analysis (FMEA)</li>
<li>3-5 years experience of working in Quality Assurance or Obtention</li>
<li>Technical writing experience preferred</li>
<li>Exercise substantial initiative/judgement in work methods and interpreting goals</li>
<li>Work independently and is reviewed infrequently with minimal supervision</li>
<li>Knowledge of quality systems and measurement</li>
<li>Knowledge of Metrology</li>
<li>Understanding of engineering drawings and manufacturing processes</li>
<li>Ability to work in a diverse and dynamic environment</li>
<li>Planning and prioritizing activities</li>
<li>Good communication and interpersonal skills</li>
<li>Negotiation skills</li>
<li>Ability to present data effectively</li>
<li>Strong problem-solving skills</li>
<li>Team working skills</li>
<li>Strong Analytical skills</li>
<li>Relevant manufacturing/engineering degree preferred</li>
<li>Experience of dealing with customers and suppliers</li>
<li>OEM Supplier Portal experience</li>
<li>Familiarity with compliances and legal requirements of automotive seating regulations</li>
<li>Proficient in use of Microsoft Word, Excel, and Outlook.</li>
<li>Experience in PLEX ERP software system is desired.</li>
</ul>

<h3>Job Description</h3>
Job Description
Responsibilities:
<ul>
<li>Identify, develop, and implement continuous improvement projects and contribute to developing necessary operation and maintenance procedures.</li>
<li>Develop standard work practices from process limits and corrective actions and ensure operators and supervisors are engaged and trained in running plant processes.</li>
<li>Effectively address and resolve customer complaints and issues through corrective and preventative actions.</li>
<li>Develop and manage the quality system to ensure products are manufactured within specification.</li>
<li>Understand and manage ISO &amp; QS current standards.</li>
<li>Responsible for site ISO &amp; QS certifications.</li>
<li>Manage the site document control process.</li>
<li>Manage the site Management of Change Process.</li>
<li>Analyze statistical data and material laboratory test results to evaluate process operation and develop process improvement that would improve the quality and quantity of the company’s product.</li>
<li>Work with plant operators, coordinators, and contractors to develop scope of work for projects. Prepare drawings, evaluate bids, procure material, and equipment and supervised the installation and startup.</li>
<li>Apply safety and good environmental practices on the floor. Includes maintaining the cleanliness of work areas.</li>
<li>Other duties as assigned.</li>
</ul>
 
Knowledge, Skills &amp; Abilities:
<ul>
<li>Strong computer skills, including Microsoft Office Suite, Adaptive, I-Series, PeopleSoft, and Ultimate.</li>
<li>Knowledge of general maintenance of electrical systems and smelting equipment.</li>
<li>Knowledge of lean principles.</li>
<li>Knowledge and practice of general chemistry.</li>
</ul>
 
Education &amp; Experience:
<ul>
<li>Bachelor’s degree in mechanical, chemical, metallurgical or industrial engineering.</li>
<li>Minimum 3 years of experience in process engineering, continuous improvement or quality management.</li>
<li>Quality &amp; Six Sigma experience preferred.</li>
</ul>
 
Work Environment, Physical &amp; Lifting Requirements:&nbsp;
<ul>
<li>Occasionally exposed to wet, humid, or hot (non-weather) conditions. Occasionally required to work near moving mechanical parts. Occasionally required to wear personal protective equipment, including but not limited to, fall protection, a respirator, hearing protection, and eyewear. May be exposed to loud noise levels.</li>
<li>Regularly required to sit, stand, and walk for extended periods, talk and hear; occasionally required to use repetitive motion and reach with hands/arms. Requires clarity of vision and three-dimensional vision.</li>
<li>Occasionally required to lift up to 15 pounds.</li>
</ul>
 
Education:
<ul>
<li>Required</li>
<li>Bachelor or better in Engineering or related field.</li>
</ul>
 
Experience:
<ul>
<li>Required</li>
<li>3-5 years: Experience in mechanical, chemical, metallurgical or process engineering.</li>
</ul>

Quality Process Engineer

<h3>Job Description</h3>
Job DescriptionCompany Description 
Nemera is a world leader in the design, development and manufacturing of drug delivery devices for the pharmaceutical, biotechnology and generic industries. We leverage a long-standing experience to provide our clients with leading-edge drug delivery devices for different application areas, from services, design to large scale manufacturing.
Job Description 
The Quality Validation Engineer is responsible for planning, coordinating and managing through completion, assigned projects to ensure the development and production of products meets customer and internal quality deliverables. Coordinate and lead investigations regarding customer complaints. Work with Supply Chain management to evaluate and manage supplier performance. Duties and responsibilities are accomplished personally or through collaboration with other staff.
Description for Internal Candidates
Responsibilities:
<ul>
<li>Assists the Quality Manager in coordinating and executing objectives throughout the company in cooperation with other departments, to maximize product quality and operating system efficiency/effectiveness while minimizing cost</li>
<li>Identify and coordinate resolution of system inefficiencies that contribute to increased quality costs.</li>
<li>Coordinate and manage the execution of validations and creation of written protocols.</li>
<li>Coordinate and manage the execution of change control activities.</li>
<li>Assess results of Customer Complaint investigations and Corrective Actions for application, validity and conformance to FDA regulatory, QSR, ISO and Customer requirements.</li>
<li>Utilize CAPA problem solving techniques to reduce internal and external failures, selects sound techniques (FMEA, Design of Experiments, Cause and Effect, Flow Charts, SPC) to solve problems effectively, and assess results for application, validity and conformance to specifications.</li>
<li>Develop and analyze statistical data in relationship to assigned tasks to determine adequacy of present standards and establish proposed quality improvements, including analysis of current inspection methods and sample plans.</li>
<li>Evaluate compliance using relevant information and individual judgment to determine whether events or processes comply with specifications, operating procedures or standards.</li>
<li>Develop product specifications for existing products and assess existing specifications for accuracy and compliance.</li>
<li>Plan, coordinate, and manage assigned Supplier Quality evaluations through scheduling and auditing of suppliers.</li>
<li>Interact with suppliers and ensures mutual interpretation of specified requirements to make certain customer requirements and objectives are met.</li>
<li>Support implementation and management of quality agreements with assigned suppliers.</li>
<li>Plan, promote, perform and organize training activities for internal departments related to quality activities, including basic statistics, DOE, GR&amp;R and Sample Plan designation.</li>
<li>Interact with customers to assure mutual interpretation of specified requirements to ensure fulfilment of customer requirements and objectives are met.</li>
<li>Assist the Quality Managers during customer audits and lead to final resolution any findings/observations resulting from the audits.</li>
<li>Assist in maintaining ISO and FDA QSR quality systems compliance.</li>
<li>Execute specific responsibilities as defined within the company quality operating system.</li>
<li>Support and maintain all policies of the company, including but not limited to applicable FDA regulatory and ISO requirements, Health and Safety Requirements and Continuous Improvement initiatives.</li>
<li>Identify and complete continuous improvement projects utilizing Six Sigma tools and methodologies.</li>
<li>Other duties as assigned.</li>
</ul>
Preferred/Required Education/Skills:
<ul>
<li>Bachelor’s degree in Engineering, Science or related field.</li>
<li>3+&nbsp;years' of experience in a Quality position strongly preferred.</li>
<li>Experience in the Medical Device industry strongly preferred (ISO13485)</li>
<li>Experience with technical writing, IQ/OQ/PQ is preferred</li>
<li>Experience with equipment validation is preferred</li>
<li>Experience working onsite in Manufacturing is strongly preferred</li>
<li>Excellent communication skills with the ability to understand, read, write and speak English required.</li>
<li>Must have the ability to apply advanced mathematical concepts and intermediate statistical (SPC) knowledge.</li>
<li>Six-sigma experience, training or certification preferred.</li>
<li>Intermediate level computer skills, including Microsoft Office applications required.</li>
<li>&nbsp;SAP experience preferred.</li>
<li>Ability to work independently from verbal and/or written instructions required.</li>
<li>Ability to understand and articulate how individual role and responsibilities tie into Quality department function, goals and objectives</li>
</ul>
Work Environment
<ul>
<li>Works in a clean manufacturing environment that may include moderate noise levels and required appropriate PPE and cleanroom apparel.</li>
<li>Ability to regularly lift up to 30 lbs with repetitive movements.</li>
<li>Ability to push and pull items.</li>
<li>Ability to stand, sit, walk up to 80% of a shift.</li>
<li>Ability to travel between office and production departments as well as company buildings required.</li>
<li>Up to 25% travel required (some international)</li>
</ul>
Qualifications 
<ul>
<li>Bachelor’s degree in Engineering, Science or related field required</li>
<li>3+&nbsp;years' of experience in a Quality position strongly preferred.</li>
<li>Experience in the Medical Device industry strongly preferred (ISO13485)</li>
<li>Experience with technical writing, IQ/OQ/PQ is preferred</li>
<li>Experience with equipment validation is preferred</li>
<li>Experience working onsite in Manufacturing is strongly preferred</li>
<li>Excellent communication skills with the ability to understand, read, write and speak English required.</li>
<li>Must have the ability to apply advanced mathematical concepts and intermediate statistical (SPC) knowledge.</li>
<li>Six-sigma experience, training or certification preferred.</li>
<li>Intermediate level computer skills, including Microsoft Office applications required.</li>
<li>&nbsp;SAP experience preferred.</li>
<li>Ability to work independently from verbal and/or written instructions required.</li>
<li>Ability to understand and articulate how individual role and responsibilities tie into Quality department function, goals and objectives</li>
</ul>
 Additional Information 
Why Join Nemera?
At Nemera, we prioritize patients when creating drug delivery devices, understanding that accurate dosing and ergonomics are crucial for treatment adherence. Joining Nemera means becoming part of a team that enjoys working together and consistently delivers on its commitments. We take pride in our work because it improves patients’ lives.
We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group, if you want to discover more about Nemera, please look at our website <a href="http://www.nemera.net" target="_blank">www.nemera.net</a>
Know someone at Nemera? We have a Referral Program so, be sure to have them submit you as a referral prior to applying for this position!
PAY RANGE:&nbsp;$95,000 - $110,000 USD Salaried&nbsp;(This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.)
For US Benefits, CLICK HERE.
Nemera is an equal opportunity employer and does not discriminate against any person on the basis of race, religion, color, gender, gender identity, sexual orientation, age, national origin, disability, veteran status, or any other protected class indication. This company is required by federal law to hire only persons who can establish they are eligible to work in the United States.

5,242 Manufacturing Jobs in California