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<h3>Job Description</h3>
Job Description
Who we are:
Charter Medical, LLC is a life sciences company that is committed to designing, developing, and manufacturing quality products to support cell and gene therapy, bioprocessing, and blood management. 
About the role:
The Operator performs assembly, runs manufacturing lines, label printing functions, and/or packaging tasks in accordance with applicable Work Instructions (WI), Visual Inspection Criteria, Standard Operating Procedures (SOP), and internal specifications in an FDA regulated environment. There are four (4) levels within this position, defined by the Operator Career Ladder. The incumbent is assigned to workstations based on successful completion of training and may be primarily assigned to one area or functional task.
1st Shift: Monday-Friday 7:00 am-3:00 pm
What you will do:
<ul>
<li>Follows Standard Operating Procedures (SOP) and Work Instructions (WI’s) to manufacture and package components of medical devices.</li>
<li>Performs assembly, machine operation, label printing, and packaging as required. May be cross trained in multiple areas or focus in a primary area.</li>
<li>Performs responsibility in accordance with production standards and rates while adhering to quality requirements.</li>
<li>Conducts in-process inspection and testing of material to ensure it meets criteria, elevating to management and documenting/reporting defects into the production records. May require measuring and simple mathematical calculations to ensure product meets specification requirements.</li>
<li>Labels and packages product as per internal specifications.</li>
<li>Performs leak-testing and operates pouch sealing equipment according to product work instructions and company procedures.</li>
<li>Maintains clean machinery, parts, and surrounding area.</li>
<li>Completes all paperwork associated with daily tasks.</li>
<li>Carries out job requirements and operates equipment within safety guidelines and reports any nonconformance.</li>
</ul>
<ul>
<li>May perform Inventory/cycle counts</li>
</ul>
Who you are:
<ul>
<li>High school graduate or equivalent.</li>
<li>Ability to effectively communicate with coworkers and management. Business communication is conducted in English.</li>
<li>Ability to comprehend and follow SOP’s, WI’s, policies, and procedures such a safety, quality, and HR that are written in English.</li>
<li>Possess basic mathematical skills to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, and decimals.</li>
<li>Basic understanding of Good Manufacturing Practices (GMP) and working within FDA regulated industries preferred.</li>
<li>Basic computer skills including ability to use MS Outlook and automated manufacturing and quality systems. </li>
<li>Excellent interpersonal skills with ability to get along well with others and work in a team environment.</li>
<li>Ability to properly complete paperwork as required according to work instructions, standards, or other specifications.</li>
<li>Excellent dependability and reliability</li>
<li>Willingness to accept change, learn, and work with new processes</li>
<li>Familiarity with an ERP system and Quality Management System (eQMS) preferred</li>
<li>Must be able to work extended hours when required</li>
</ul>
Perks / Benefits:
<ul>
<li>Generous Paid Time Off</li>
<li>Paid Breaks</li>
<li>Quarterly Bonuses</li>
<li>401k with excellent company match</li>
<li>Health Insurance with multiple plans to choose form</li>
<li>Paid Short Term and Long Term Disability</li>
</ul>

1st shift Operator I (Monday-Friday 7:00 am-3:00 pm)

<h3>Job Description</h3>
Job Description
Press Brake Operator 
***REQUIRES PRIOR PRESS BRAKE OPERATING EXPERIENCE*** Shift: 1st shift Area: Erlanger, KY Pay: $19-$22/hr starting range - based on experience and interview 
RESPONSIBILITIES:
<ul>
<li>Reads prints to select the appropriate tools, machines, and materials to be used in of fabrication work.</li>
<li>Sets up, adjusts, and operates press brakes.</li>
<li>Installs, aligns, and secures tools, attachments, fixtures, and work pieces on Press Brake</li>
<li>Skilled in hand tools and precision measuring instruments</li>
<li>Forms parts to specifications indicated on prints</li>
</ul>
 QUALIFICATIONS: 
<ul>
<li>Ability to lift 30 to 50 pounds</li>
<li>Minimum of three years experience with a CNC hydraulic brake press</li>
<li>Ability to read, calibrate gauges, select tools, use a protractor, angle finder tape measurer.</li>
<li>Possesses practical application of fractions, percentages, ratio and proportion, measurement, practical algebra, and essentials of shop trigonometry </li>
</ul>

Press Brake Operator- 1st Shift

<h3>Job Description</h3>
Job Description
Amphenol Communications Solutions (ACS), a division of Amphenol Corporation, is a world leader in interconnect solutions for Communications, Mobile, RF, Optics, and Commercial electronics markets. Amphenol Corporation is one of the world’s largest designers and manufacturers of electrical, electronic and fiber optic connectors and interconnect systems, antennas, sensors and sensor-based products and coaxial and high-speed specialty cable. ACS has an expansive global presence in research and development, manufacturing, and sales. We design and manufacture a wide range of innovative connectors as well as cable assemblies for diverse applications including server, storage, data center, mobile, RF, networking, industrial, business equipment, and automotive.
Position: Global Quality Director, CBS
Location: Valley Green, PA (Etters PA)
Amphenol High Speed Products Group is the market leader for high speed, high bandwidth electrical connectors for the Telecom/Datacom market (Mobile Networks, Storage, Servers, Routers, Switches, etc.). Our products help to enable the electronics revolution and remain a key enabler for all the major Tier 1 OEMs globally. Our global headquarters are located in Nashua, NH and we have design, sales and manufacturing locations globally. We are currently seeking a Global Quality Director to join our team. The position will be located at our Valley Green site location.
RESPONSIBILITIES: 
<ul>
<li>Oversee all aspects of the quality management system across multiple manufacturing sites globally</li>
<li>Set and drive global quality strategy to meet customer expectations</li>
<li>Manage product and process quality to meet customer satisfaction metrics through formal continuous improvement program</li>
<li>Manage customer quality requirements through documentation review, process capability/control, and detailed inspection plans</li>
<li>Responsible for presentation of business unit level quality metrics to corporate management</li>
<li>Manage all quality related aspects of customer and supplier relationships, including management of both customer and supplier corrective action processes</li>
<li>Participate in customer audits / site visits to support local manufacturing teams</li>
<li>Communicate effectively with cross-functional teams and senior management, distilling complex technical information into clear, concise presentations to drive aligned decisions on quality issues and initiatives, and obtain buy-in from key stakeholders</li>
<li>Manage product and process quality, with a primary focus on new product introduction, to meet customer satisfaction and business unit metrics.</li>
<li>Lead or facilitate continuous improvement initiatives across both development engineering and manufacturing organizations.</li>
<li>Manage customer quality requirements through documentation review, process capability/control, and development engineering phase gate management.</li>
<li>Responsible for quality planning of customer programs which involves leading cross functional teams in a global capacity.</li>
<li>Responsible for managing all quality related aspects of customer and supplier relationships, including management of both customer and supplier corrective action processes.</li>
</ul>
QUALIFICATIONS: 
<ul>
<li>BS in Engineering, or an equivalent mix of education and experience.</li>
</ul>
<ul>
<li>15+ years of progressive experience in quality operations working with a global team</li>
<li>Knowledge of cable manufacturing processes is preferred</li>
<li>Quality management experience with strong leadership skills</li>
<li>Working knowledge and proven leadership in continuous improvement activities and formal programs</li>
<li>Experience working directly with customers and suppliers</li>
<li>Quality management experience with strong supervisory and leadership skills.</li>
<li>Working knowledge and proven leadership in continuous improvement activities and formal programs.</li>
<li>Ability to travel up to 25-50%</li>
</ul>
Amphenol Corporation is proud of our reputation as an excellent employer. Our main focus is to provide the highest level of support and responsiveness to both our employees and our customers, the world's largest technology companies. Amphenol Corporation offers the opportunity for career growth within a global organization. We believe that Amphenol Corporation is unique in that every employee, regardless of his or her position, has the ability to positively impact the business.
Amphenol is an “Equal Opportunity Employer” - Minority/Female/Disabled/Veteran/Sexual Orientation/Gender Identity/National Origin
For additional company information please visit our website at <a href="https://www.amphenol-cs.com/" target="_blank">https://www.amphenol-cs.com/</a>

Global Quality Director

<h3>Job Description</h3>
Job Description
As a global organization, PharmEng Technology has been providing quality services to leading manufacturers of the Pharmaceutical and Biotech industries since 1997. Our employees come from diverse backgrounds where we value unique talents and work together to support our clients. In addition, our consultants have extensive experience obtained from world-class organizations across the globe, and the development of our staff continues to grow PharmEng Technology.
We are seeking an experienced Validation Engineer.
Objectives of this Role:
<ul>
<li>Write and execute, Installation Qualification (IQ), and Operational Qualification (OQ) protocols and Summary Reports including thorough resolution of protocol discrepancies.</li>
<li>Assess potential sources of variation in materials, processes, facilities, equipment, products, and packaging processes that may impact consistent performance or product quality; where needed, design studies to characterize impact of identified sources.</li>
<li>Maintain an up-to-date knowledge of validation requirements, practices, and procedures.</li>
<li>Interpret existing Validation Plans and Project Plans and apply concepts to the task at hand.</li>
<li>Working with a team to ensure all aspects of activity within the Process Development and Validation group adhere to required policies and procedures, including safety and training.</li>
<li>Investigate/troubleshoot validation problems, as well as, conduct some statistical analysis of testing results.</li>
</ul>
Skills and Qualifications:
<ul>
<li>Bachelor’s degree in engineering, life science discipline, or equivalent experience in the pharma/biotech industries.</li>
<li>Highly capable of developing, executing, and reviewing validation life cycle protocols.</li>
<li>Knowledge of validation principles, standard concepts, practices, procedures, and requirements in GMP regulated environments.</li>
<li>Proven capability to assess processes, equipment, and products for sources of variation, ability to analyze data and reach appropriate conclusions, and to perform and appropriately document deviations and investigations.</li>
<li>Experience with validation and working knowledge of production is a plus.</li>
<li>Familiarity with FDA regulatory requirements for the Pharmaceutical/biopharmaceutical industry (i.e. GMP and GLP).</li>
<li>Experience with Microsoft Office Suite.</li>
<li>Experience Programing LabView require </li>
</ul>
 
PharmEng Technology is committed to attracting and retaining world-class employees valued for their contributions to achieving business objectives. PharmEng offers continuous career growth, competitive wages, travel opportunities, a team mentality that sets us apart from our competitors, and more!

Validation Engineer

<h3>Job Description</h3>
Job Description
Plastipak Production Technicians operate equipment to manufacture plastic containers in a clean &amp; safe work environment.&nbsp; Associates take pride in maintaining our high quality standards &amp; our positive team culture.
We Offer
<ul>
<li>Set Schedules:&nbsp; 12-hour shifts &amp; a unique rotating schedule with 12-14 days off per month! </li>
<li>Stability:&nbsp; Enjoy our food-grade clean &amp; climate-controlled facility with an industry leader identified as an essential business! </li>
<li>Advancement: We follow a strong promote-from-within business practice!</li>
<li>Premium pay &amp; benefits, including 18 days of paid time off a year!&nbsp;</li>
</ul>
You Will
<ul>
<li>Operate automated blow-molding and injection-molding equipment in a safe manner</li>
<li>Monitor &amp; troubleshoot equipment, making adjustments &amp; repairs to assure optimal production/operating performance</li>
<li>Assure customer requirements are always met by performing quality checks for specifications such as bottle weights &amp; dimensions</li>
<li>Grow your knowledge &amp; skills through a wide-variety of training &amp; on-the-job experiences</li>
</ul>
You Have
<ul>
<li>Ability to work a schedule cycle of 3 days on, 2 day off, 2 days on, 3 days off, repeat</li>
<li>Experience in blow-molding or injection molding is preferred.</li>
<li>Able to use basic hand tools, such as wrenches, hammers, screwdrivers, etc.</li>
<li>Mechanical, electrical or other technical/machine operation ability.&nbsp; </li>
<li>Able to operate a computer to enter &amp; retrieve data</li>
<li>Strong interpersonal skills &amp; desire to be a productive team member&nbsp;</li>
<li>Ability to lift up to 50 pounds with or without a reasonable accommodation</li>
</ul>
As a Plastipak Associate, you receive a benefits package offering the following:
<ul>
<li>Wellness Programs</li>
<li>Health Insurance Coverage, including Medical, Dental &amp; Vision</li>
<li>EAP, Employee Assistance Program</li>
<li>Life Insurance</li>
<li>Accidental Death &amp; Dismemberment Insurance</li>
<li>Disability Insurance:&nbsp; Short-Term &amp; Long-Term</li>
<li>Accidental Insurance</li>
<li>Critical Illness Insurance</li>
<li>Hospital Indemnity Insurance</li>
<li>401(k) Plan, with Company Matching Contribution &amp; Profit Sharing feature</li>
<li>Paid Time Off&nbsp;&nbsp;&nbsp; - 80 hours within 1st year &amp; subsequent increases</li>
<li>Paid Company Holidays</li>
<li>Dependent Care Flexible Spending Account</li>
<li>Caregiving via Care.com</li>
<li>Pet Insurance</li>
<li>Tuition Assistance Program</li>
<li>Sons and Daughters Scholarship Program</li>
<li>Travel Assistance</li>
<li>Employee Discount Programs</li>
</ul>
*Some benefits are subject to eligibility requirements
Plastipak is an Equal Opportunity Employer
In order to process your job application, Plastipak collects and stores the personal information that you submit via this website. Please refer to Plastipak’s Privacy Policy to understand how Plastipak uses and protects the information that you provide.

Machine Operator / Production Technician - Pay starting at $22 per hour

<h3>Job Description</h3>
Job Description PRODUCTION SUPERVISOR The Supervisor is responsible for supervising production employees in a manufacturing and assembly/packaging environment.&nbsp; This position plans and assigns work, implements policies and procedure and recommends improvements in production methods, equipment, operating procedures and working conditions. The Supervisor may be responsible for supervising multiple production lines while achieving optimal performance of their assigned tasks; helping to solve problems; meeting quality and production standards and maintaining a safe, clean and organized work area. Duties:
<ul>
<li>Provides line set ups that best accommodates each employee and the product being run on a particular line while maintaining production efficiencies. </li>
<li>Meeting quality standards set forth by the Bill of Material (BOM) Specifications administered by Quality Control Personnel. </li>
<li>Enter labor electronically, production and quality data within our software system.</li>
<li>Train, coach, encourage and motivate employees and workers to efficiently perform their assigned tasks. </li>
<li>Provide protective oversight of employees through encouragement, moral support and patient direction.</li>
<li>Report any employee behaviors, incidents and/or accidents to Production Manager. .</li>
<li>Maintain work area in a safe, clean and organized manner.</li>
<li>To comply with all SQF procedures and policies, and is responsible to report food safety problems.</li>
<li>Follow all policies and procedures established by Company.</li>
<li>Maintain a professional appearance and demeanor that reflects the company’s commitment to quality, continuous improvement and respect for individuals.&nbsp;</li>
<li>Other related duties as directed by management.</li>
</ul>
 Qualifications: High School Diploma or GED required.&nbsp; Intermediate Microsoft Office skills required. Experience: Prior experience working with people with disabilities or related experience desired.&nbsp; Excellent&nbsp; communication verbal and written skills required.&nbsp; Attention to detail required. Experience with Nulogy software preferred. Physical Requirements: 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the essential functions of this position, Supervisor must regularly communicate effectively, both verbally and through active listening. The role frequently requires walking, sitting, reaching with hands and arms, climbing, balancing, and occasionally stooping, kneeling, crouching, or crawling. The position involves both fine and gross motor skills, as well as the ability to reach, turn, and twist above and below waist level. The Supervisor must be able to push or pull up to 25 pounds and lift and carry up to 30 pounds of static weight. Vision requirements include close, distance, color, and peripheral vision; depth perception; and the ability to adjust focus. Work Environment/Conditions: The work environment characteristics will vary depending upon the work environment of the customer.&nbsp; Specific characteristics, representative of those an employee will encounter while performing the essential functions of the job will be described. &nbsp;Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.&nbsp;
<ul>
<li>Work is performed in a warehouse environment with varying temperatures.</li>
<li>Regular handling of materials; may involve repetitive motions.</li>
<li>Exposure to moderate noise levels and occasional dust.</li>
<li>Personal protective equipment (PPE) such as gloves, safety glasses, and closed-toed shoes must be worn.</li>
<li>Must be able to work in a paced environment and meet production deadlines.</li>
</ul>
Reports to:&nbsp; Production Manager Hours: Full Time&nbsp; M-Th 7:00AM to 3:30PM&nbsp; Fri 6AM - 2:30PM No nights, no weekends Pay: $19-$21 BCI helps with the cost of your benefits by covering part of your insurance premiums.&nbsp; PTO It is the policy of BCI to provide equal employment opportunities. BCI will not discriminate against any staff member or applicant for employment with regard to compensation, terms, conditions or privileges of employment because of race, color, age, sex, sexual orientation, marital status, national origin, religion, disability, military status, or any other status protected by law. &nbsp;
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Production Supervisor

<h3>Job Description</h3>
Job Description
Position: Development Quality Engineer
Location: Valley Green, PA
Amphenol High Speed Products Group is the market leader for high speed, high bandwidth electrical connectors for the Telecom/Datacom market (Mobile Networks, Storage, Servers, Routers, Switches, etc.). Our products help to enable the electronics revolution and remain a key enabler for all the major Tier 1 OEM’s globally. Our global headquarters are located in Nashua, NH and we have design, sales and manufacturing locations globally. The CBS team is looking for a Quality Engineer to join them in the Valley Green, PA location. The Quality Engineer will help to plan and facilitate quality related activities for manufacturing development projects by fulfilling the duties associated with FMEA’s, Product Quality Planning, Process Qualification Planning, Metrology Planning, Control Plans, Inspection Plans and Methods, Workmanship Standards, DOE’s and other necessary studies within a development protocol in developing Statistical Process Control.
RESPONSIBILITIES:
<ul>
<li>Act as a team member to manage projects to assess quality aspects, report process feasibility &amp; risks and make quality recommendations on how to proceed.</li>
<li>Interface with vendors, process engineering, product engineering and manufacturing to assure capability levels and documentation compliance are achieved in meeting quality deliverables.</li>
<li>Partner with cross-functional teams to investigate deviation events, recommend corrective actions and product disposition, and develop improvements using Lean tools and analytical skills (e.g., FMEA, SPC, 5-Why, 12 Step, DMAIC, Risk Assessments, Fishbone Diagram, etc.)</li>
<li>Interface with site quality, engineering, and other departments throughout final phases of development and pre-release to manufacturing.</li>
<li>Participate in definition of respective project plan qualification tasks and schedules for development projects that meet time to market (TTM) objectives.</li>
<li>Determine initial inspection methods based or best-known methods (where applicable) and manage metrology requirements.</li>
<li>Facilitate process qualification planning assuring conformance to standards and specifications. Define process qualification plans, inspection plans, inspection workflow, metrology requirements and workmanship standards for process engineering.</li>
<li>Participate in quality readiness at the site by providing the inspections plans, metrology, Cpk requirements and any special qualification requirements.</li>
<li>Support the analysis of defined risk areas and experimentation, proof of principle tooling, feasibility studies, capability studies, detailed design and analysis, DOE, passive data collection (PDC) and or basic technology searches and development.</li>
<li>Participate in product &amp; process FMEA, characterization of product and process critical features and respective risk assessment activities.</li>
<li>Develop, facilitate and control standards and methods both internally and externally for the inspection of CTF’s inclusive of accuracy, linearity, R&amp;R’s, long term stability, FAI’s, Cmk’s and Cpk’s.</li>
<li>Ability to analyze operating data, including yield, cycle time, and throughput to identify and action opportunities, utilizing the appropriate tools to achieve desired outcome (e.g., Six Sigma, Lean etc.)</li>
<li>Assist product and process engineering in the reconciliation of First Article Inspections, Capability Studies and Comparison Studies through corrective actions driven by root cause analysis that incorporate process improvement tools.</li>
<li>Assist process development engineers and mechanical Integrity engineers in the (data &amp; statistical) analysis of feasibility studies, DOE’s, passive data collection’s (PDC) and capability studies.</li>
<li>Advance capabilities of Operations Team and partners with Quality Team to understand and implement new test methods and best practices</li>
<li>Coordinate and or participate in the metrology transfer and training to respective personnel.</li>
</ul>
QUALIFICATIONS:
<ul>
<li>Bachelor's degree from four-year College in engineering, Quality Assurance; or six to eight years related experience and/or training; or equivalent combination of education and experience.</li>
<li>Ability to read, analyze, and interpret professional journals, technical procedures, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, customers, and the internal Amphenol groups.</li>
<li>Ability to effectively identify and eliminate common cause variation within continuous or batch processes through the use of solid practices and analysis in establishing statistical process control (SPC)</li>
<li>Ability to define and generate Quality Plans, Control Plans and Workmanship Standards.</li>
<li>Ability to provide qualification assessments related to product/process risks, capability and manufacturability.</li>
<li>Ability to effectively present information and respond to questions from managers, customers, vendors, engineers and manufacturing site representatives.</li>
<li>Should have knowledge and skills using:
<ul>
<li>Microsoft Suit (Power Point, Excel, Word, SharePoint)</li>
<li>Measurement System Analysis</li>
<li>Statistical analysis software (Minitab)</li>
<li>Geometric Dimensioning &amp; Tolerancing</li>
<li>Strong Knowledge of Gage Repeatability and Reproducibility</li>
</ul>
</li>
<li>Demonstrated skill and knowledge to train individuals and teams.</li>
<li>Demonstrated ability to operate with minimal supervision and provide updates on project status where issues or problems can be reviewed, discussed and resolved.</li>
<li>Ability to travel internationally to support product development and process ramps. </li>
</ul>
Amphenol Corporation is proud of our reputation as an excellent employer. Our focus is to provide the highest level of support and responsiveness to both our employees and our customers, the world's largest technology companies. Amphenol Corporation offers the opportunity for career growth within a global organization. We believe that Amphenol Corporation is unique in that every employee, regardless of his or her position, has the ability to positively impact the business.
Amphenol is an “Equal Opportunity Employer” - Minority/Female/Disabled/Veteran/Sexual Orientation/Gender Identity/National Origin
For additional company information please visit our website at <a href="https://www.amphenol-cs.com/" target="_blank">https://www.amphenol-cs.com/</a>

Development Quality Engineer

<h3>Job Description</h3>
Job Description
Position: Quality Engineer
Location: Valley Green, PA
Position summary:
The Quality Engineer will provide quality leadership and support to the operations area in achieving quality objectives and effective problem resolution. This person will Identify and lead continuous improvement initiatives, contributing to business growth and cost reduction and ensure customer satisfaction through responsive complaint resolution, including root cause analyses and implementing corrective and preventive actions.
This position requires access to controlled technology that is subject to US export controls. Qualified candidates must be a US Person (including US Citizen, lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3)) or eligible to obtain required authorization(s) from the U.S. Government.
Position responsibilities: 
<ul>
<li>Develop, implement and maintain quality planning of components and products.</li>
<li>Provide technical support to the organization for implementation of process control techniques, methods and quality methodologies.</li>
<li>Manage and report quality performance indices, including process capabilities, cost of quality and outgoing quality levels.</li>
<li>Lead investigation of customer complaints and/or concerns, implementing solutions with internal functions, suppliers and other Company sites, as necessary.</li>
<li>Perform regular and routine auditing to ensure compliance to requirements of the quality management system and the processes.</li>
<li>Conduct internal auditing in support of ISO 9001 certification.</li>
</ul>
Requirements:
<ul>
<li>Bachelor's Degree in technical field</li>
<li>Effective use of APQP methodologies, including MSA, FMEA, SPC, etc</li>
<li>5+ years' experience in production environment is required</li>
<li>Familiarity with Quality Management Systems standards (e.g. ISO 9001, TS 16949, etc)</li>
<li>Ability to effectively investigate and resolve problems, including use of 8D Problem Solving, Ishikawa Fishbone, and 5-Why methodologies.</li>
<li>Effective use of problem prevention tools, including Quality Planning, Poka Yoke, D-FMEA, P-FMEA, SPC, MSA, etc.</li>
<li>Effective communication skills with all levels of the organization.</li>
<li>Able to travel, domestically and internationally, when required</li>
<li>Basic SPC knowledge, including X-Bar/R Charting, Cp/Cpk, R&amp;R, etc.</li>
<li>Internal auditing skills.</li>
<li>Proficient in Microsoft Office</li>
<li>Minimum of 5 years' experience in connector / electronics manufacturing is preferred</li>
<li>ASQ Certified Quality Engineer is preferred</li>
<li>5+ years' experience in Quality Assurance is preferred</li>
<li>ASQ Certified Quality Auditor is a bonus</li>
</ul>
Physical demands and work environment:
<ul>
<li>Lifting requirements of Operations area, as defined. </li>
</ul>
This position requires access to controlled technology that is subject to US export controls. Qualified candidates must be a US Person (including US Citizen, lawful permanent resident, or protected individual as defined by 8 U.S.C. 1324b(a)(3)) or eligible to obtain required authorization(s) from the U.S. Government.
Amphenol Corporation is proud of our reputation as an excellent employer. Our main focus is to provide the highest level of support and responsiveness to both our employees and our customers, the world's largest technology companies. Amphenol Corporation offers the opportunity for career growth within a global organization. We believe that Amphenol Corporation is unique in that every employee, regardless of his or her position, has the ability to positively impact the business.
Amphenol is an "Equal Opportunity Employer" - Minority/Female/Disabled/Veteran/Sexual Orientation/Gender Identity/National Origin
For additional company information please visit our website at<a href="https://www.amphenol-cs.com/" target="_blank">https://www.amphenol-cs.com/</a>

Quality Engineer

<h3>Job Description</h3>
Job Description
We are looking for a Production Scheduler! 
WE OFFER GREAT BENEFITS!
<ul>
<li>A trimester (four-month period) monetary incentive based on meeting standard operating margin and inventory turn goals while meeting delivery and quality commitments.</li>
<li>Weekly payroll</li>
<li>Start accruing vacation from day one! Accrued each pay period, you will receive 96 hours of vacation in your first year. That increases to over three weeks of vacation (136 hours) after three years. </li>
<li>Anniversary paid day off awarded each year.</li>
<li>Nine (9) paid holidays including the day after Thanksgiving, Christmas Eve, and New Year's Eve.</li>
<li>Complete benefits package including Health, Dental, Vision, and Voluntary Life.</li>
<li>Benefits Paid 100% by Seyer Industries: HealthiestYou (Teledoc services), Basic Life Insurance, Accidental Death and Dismemberment, Employer Assistance Program (EAP), Short-term disability, Long-term disability, and Parental Leave. </li>
<li>401(k) with employer match - Seyer Industries will match 100% of the first 3% of pay you contribute to the plan; plus 50% of next 2% contributed.</li>
</ul>
Working at Seyer Industries isn't like working at other manufacturing companies. Our commitment to employee engagement, collaborative spirit, emphasis on achieving results, dedication to continuous improvement, and high expectations offer a different culture. At Seyer Industries, our annual average turnover rate is mind-blowingly low at 6.37% (the industry average is 39.9%). And there is a good reason why our average tenure is 8.98 years - people that come to work at Seyer Industries end up staying. 
ABOUT SEYER INDUSTRIES
Founded in 1957, Seyer Industries is a small business located in St. Peters, Missouri, specializing in high-complexity machined parts and assemblies for the aerospace and maritime industries. Seyer is a turnkey supplier with extensive capabilities, including CNC machining, design engineering, mechanical assembly, chemical processing, painting, kitting, welding, and NADCAP-certified penetrant and magnetic particle inspection. Our team is comprised of individuals proudly committed to the objectives of quality and productivity. 
Duties and Responsibilities:
<ul>
<li>Engage with Production Control Manager to review and assess system settings to assure scheduling parameters are aligned with Customer obligations</li>
<li>Work with Production Control Manager to balance safety and buffer stocks with business Inventory Turn objectives</li>
<li>Keep Production Manager informed of critical issues which affect production schedule
<ol>
<li>Progress/Issues of jobs</li>
<li>Identify delays in Production; Machine issues, Quality issues, Planning/Programming issues, etc.</li>
</ol>
</li>
<li>Collaborate with Customer Account Manager (CAM) to proactively address schedule risk items to develop and implement plans to maintain delivery schedules</li>
<li>Monitor Non-recurring Engineering efforts are completed to support production schedules</li>
<li>Monitor and manage job release queues to assure on time start to Epicor Scheduled start dates</li>
<li>Review/Manage Job Scheduling Factors in Epicor ERP to more efficiently schedule individual jobs</li>
<li>Adjust schedules/machine priorities when necessary, utilizing Resource Scheduling Board/Part Queue's to manage machine loads</li>
<li>Communicate with Planning/Programming when changes are needed as driven by schedule</li>
<li>Monitor progress of critical path and Late Jobs using Job Notifications/Follow Ups</li>
<li>Assign actions to functional groups in response to system suggestions or to raise awareness of schedule risk items</li>
<li>Build, compile &amp; analyze production reports</li>
<li>Conform to all requirements of Seyer Industries Quality System and any and all customer invoked quality requirements (AS9100, for example).</li>
<li>Maintain safe and clean working environment by complying with 6S standards.</li>
<li>Contribute to team effort by accomplishing related results as required.</li>
<li>Support continuous improvement initiatives</li>
</ul>
Requirements, Skills, and Qualifications:Associate's degree or equivalent technical training in manufacturing, engineering, or supply chain required
<ul>
<li>Associate's degree or equivalent technical training in manufacturing, engineering, or supply chain required</li>
<li>Experience with MRP/ERP systems required; Epicor Kinetic highly desirable</li>
<li>Professional certification by the American Production and Inventory Control Society (APICS) desirable</li>
<li>Production Control experience highly desirable</li>
<li>General familiarity with manufacturing operations</li>
<li>Comfortable with PC and Apple devices</li>
<li>Work well in a team environment, but capable of self-managing/initiation as needed</li>
<li>Strong communication &amp; interpersonal skills</li>
<li>Must possess solid organizational skills and be able to multitask</li>
<li>Possess leadership skills and ability to lead with a positive attitude </li>
<li>Attention to detail, with a strong work ethic</li>
<li>Strong critical thinking and problem-solving skills</li>
</ul>
All job offers are contingent on the successful completion of a pre-employment drug test and background check.
EOE disability/veteran - We are an Equal Opportunity Employer and do not discriminate. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Production Scheduler

<h3>Job Description</h3>
Job DescriptionAre you a skilled metalworker with a passion for craftsmanship? Do you want your work to mean something? At Re-View Historic Windows, we don’t just build windows — we restore the architectural soul of America. From century-old steel to classic wood details, we preserve history one window at a time. Now, we’re looking for a dedicated Metal Fabricator to join our expert team and help breathe life back into some of the nation’s most iconic buildings. What You’ll Do:You’ll work with irreplaceable, original materials — no big box store parts here. This is precision work with a purpose.
<ul>
<li>MIG weld steel (typically 1/8” or thinner)</li>
<li>Drill, tap, and grind to paint-ready finishes</li>
<li>Make seamless splice repairs that replicate the original structure</li>
<li>Lift and maneuver up to 50 lbs.</li>
<li>Read tape measures and calipers accurately</li>
<li>Follow detailed processes — consistency is key in preservation</li>
</ul>

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