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<h3>Job Description</h3>
Overview ABOUT EAGLEPICHER EaglePicher Technologies and EaglePicher Electronic Packaging is driving the electrification of defense, aviation and space. We provide the broadest range of battery systems in the world for the most demanding applications. We develop leading-edge products that make drones fly higher, undersea vessels run longer, aircraft fly farther, rockets launch safely, and satellites operate longer. With our cutting-edge research and manufacturing, we continue to set new standards in the industry. For 100 years, we have provided mission-critical power solutions to the defense, aviation and space markets. EaglePicher's batteries power many U.S. missile and munition programs and are a key component of the U.S. space program, powering the Mars Rovers and the next crewed mission to the moon. EaglePicher provides custom battery assemblies, battery management systems, pyrotechnic devices and other power solutions. Our employees are passionate, dedicated and empowered to realize our vision. We strive for the right mix of people with diverse backgrounds, personalities and perspectives, and to ensure this works, we create an inclusive work environment that places a premium on communication and collaboration. At EaglePicher, we will give you the opportunity to harness all that is within you with access to the latest tools, information and training. EaglePicher is headquartered in St. Louis, MO with manufacturing and research and development facilities in Joplin, MO, Seneca, MO, Pittsburg, KS, East Greenwich, RI and in Southbridge, MA. For more information visit <a href="http://www.eaglepicher.com" target="_blank">www.eaglepicher.com</a> ABOUT THE POSITION The Toolmaker with a passion for customer service and excellence at EaglePicher is a key contributor in delivering first class tools, fixtures, and prototype parts for upcoming and ongoing projects. Successful execution of multiple projects ensures timely delivery of our products that safely and efficiently meet mission-critical, life-saving applications our Defense customers demand. The Toolmaker directly supports engineering and manufacturing to create, maintain, and repair precision tools, dies, jigs, and fixtures. These tools are essential in building components that meet product specifications. This role helps to ensure the efficiency and consistency of the manufacturing process. Responsibilities 
<ul>\n
<li>Designs, fabricates, constructs, assembles &amp; alters/repairs a wide range of tools, dies, fixtures , jigs and guages to tight tolerances</li>
\n
<li>Create precision tools, dies and fixtures based on technical drawings related documentation</li>
\n
<li>Set up and operate a variety of machine shop equipment: Lathe, vertical mills, drill presses, surface grinders, saws, welders, etc.</li>
\n
<li>Read and interpret drawings for tools, fixtures, and machines with a conceptual understanding of GD&amp;T.</li>
\n
<li>Diagnose and correct complicated machining and tooling issues </li>
\n
<li>Recommend repair or modificiations of tooling or equipment</li>
\n
<li>Conceptualize tooling from product requirements</li>
\n
<li>Actively learn new methods and techniques in machining, fabrication, welding, and additive manufacturing</li>
\n
<li>Must have strong focus on precision and quality, including tight tolerances</li>
\n
<li>Liaise wth engineering team and production team to ensure quality of product and functionality of tooling</li>
\n</ul>
\n Qualifications Hiring Requirements: 
<ul>\n
<li>U.S. Citizenship or U.S person status REQUIRED</li>
\n
<li>H.S. diploma or equivalent required, associates degree or higher preferred</li>
\n
<li>5+ years manufacturing or tooling experience required</li>
\n
<li>Mechanical understanding of machines and small parts tolerances</li>
\n
<li>Understanding of CNC and EDM equipment</li>
\n
<li>Solid written and verbal communication skills</li>
\n
<li>Understanding of theory and use of tools and fixturing in a production environment</li>
\n
<li>Ability to read and interpret detailed drawings for conversion into parts</li>
\n</ul>
\n Hiring Preferences: 
<ul>\n
<li>Tooling certification or technical degree in toolmaking, or related technical discipline</li>
\n
<li>Experience in semi-automated industrial environments</li>
\n
<li>Experience with high precision presses, tooling and dies</li>
\n
<li>Experience with welding/metal joining (TIG, solder)</li>
\n</ul>
\n PERKS OF BEING AN EAGLEPICHER EMPLOYEE Some of the great things about being an EaglePicher Electronic Packaging employee include: 
<ul>\n
<li>Medical, dental, vision, life, and disability insurance;</li>
\n
<li>11 paid holidays and PTO;</li>
\n
<li>Matching 401K;</li>
\n
<li>Tuition reimbursement;</li>
\n
<li>Dependent scholarship programs</li>
\n
<li>Hourly production bonuses</li>
\n</ul>
\n EaglePicher Technologies LLC is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.

Toolmaker

<h3>Job Description</h3>
MACOM designs and manufactures semiconductor products for Data Center, Telecommunication and Industrial and Defense applications. Headquartered in Lowell, Massachusetts, MACOM has design centers and sales offices throughout North America, Europe and Asia. MACOM is certified to the ISO9001 international quality standard and ISO14001 environmental management standard. MACOM has more than 75 years of application expertise with multiple design centers, Si, GaAs and InP fabrication, manufacturing, assembly and test, and operational facilities throughout North America, Europe, and Asia. View our facilities at <a href="https://www.macom.com/" target="_blank">https://www.macom.com/</a> In addition, MACOM offers foundry services that represents a key core competency within our business. MACOM sells and distributes products globally via a sales channel comprised of a direct field sales force, authorized sales representatives and leading industry distributors. Our sales team is trained across all of our products to give our customers insights into our entire portfolio. Semiconductor Manufacturing Technician 2 Semiconductor visual die inspection to ensure MIL-STD 883 and customer specification compliance. Job Responsibilities: 
<ul>
<li>Heavy use of microscope and other die inspection tools.</li>
<li>Handles semiconductor wafers and die.</li>
<li>Visually inspects to customer criteria and MIL-STD - die level.</li>
<li>Familiarity with AOI, die sorting equipment (manual, semi and full auto).</li>
<li>Capable of binning defects.</li>
<li>Capable of interpreting wafer map.</li>
<li>Familiarity with FOD management.</li>
</ul>
\n Skills and Qualifications: 
<ul>
<li>Must be able to sit in a long period of time.</li>
<li>Must be able to work under a microscope for an extended period of time - optical and digital.</li>
<li>Must pay attention to details, being meticulous.</li>
<li>Must be well organized and detail oriented.</li>
</ul>
\n Experience and Education: 
<ul>\n
<li>High school diploma or equivalent.</li>
\n
<li>Comfortable working with automated equipment.</li>
\n
<li>Previous semiconductor inspection experience helpful.</li>
\n
<li>Computer skills and knowledge in excel.</li>
\n
<li>Prior work experience in a lean manufacturing environment a plus.</li>
\n
<li> Due to ITAR regulations, only candidates who are U.S.Persons (U.S. citizens, U.S. nationals, lawful permanent residents, orindividuals granted asylum or refugee status) will be considered for thisposition. </li>
\n</ul>
\n The Salary Range for this position is $37,000 - $58,000. Actualsalary offered to candidates will depend on several factors, including but notlimited to, work location, relevant candidates' experience, education, andspecific knowledge, skills, and abilities. EEO: MACOM is an Equal Opportunity Employer committed to adiverse workforce. MACOM will not discriminate against any worker orjob applicant on the basis of race, color, religion, sex, gender identity,sexual orientation, national origin, age, disability, genetic information,veteran status, military service, marital status, or any other categoryprotected under applicable law. Reasonable Accommodation: MACOM is committed to working with and providing reasonableaccommodations to qualified individuals with physical and mentaldisabilities. If you have a disability and are in need of a reasonableaccommodation with respect to any part of the application process please call+1-978-656-2500 or email [email&nbsp;protected]. Provide your name, phonenumber and the position title and location in which you are interested, andnature of accommodation needed, and we will get back to you. We also workwith current employees who request or need reasonable accommodation in order toperform the essential functions of their jobs. Benefits: Thisposition offers a comprehensive benefits package including but not limitedto: • Health, dental, andvision insurance. • Employer-sponsored401(k) plan. • Paid time off. • Professional developmentopportunities.

Semiconductor Manufacturing Technician - Inspection

<h3>Job Description</h3>
#2531 Validation Engineer - Pharmaceutical
 
Our client is a Fortune 500 Pharmaceutical Company with Global reach. They are currently looking for a strong Validation Engineer to join their tenured Validation team.
 
Key responsibilities for this role include:
<ul>
<li>Provide direction, reviews and provides Quality approval for design qualification documents, validation protocols, summary reports, discrepancy reports and CPV reports.</li>
<li>Provides the Quality Assurance review and approval of Engineering, Calibration, Facility Maintenance, Production Support (Maintenance), Technical Services and IT procedures and forms.</li>
<li>Authors protocols and reports as required/assigned.</li>
<li>Perform validation planning and tracking.</li>
<li>Assist in the development and maintenance of the procedures defining the validation program at MTI.</li>
<li>Participates in the evaluation of changes to validated systems to ensure the validate state is maintained. Provides direction, reviews and approves proposed changes and facilitates decision making regarding the extent of any re-validation requirements.</li>
<li>Assist in the compilation of periodic reports required by the validation program.</li>
</ul>
 
The minimum qualifications for this role are:
<ul>
<li>Bachelor of Science degree (or equivalent) and 7 + years in a pharmaceutical cGMP environment is required. A combination of experience and/or education will be taken into consideration.</li>
<li>Must possess a working knowledge of Pharmaceutical validation and cGMP concepts.</li>
</ul>

Validation Engineer - Pharmaceutical

<h3>Job Description</h3>
Research Associate, QC
Location:&nbsp;Woburn, MA
Vaxess Technologies is developing next-generation vaccines and therapies based on its microneedle array patch (MAP) platform. The Vaxess microarray patch enables intradermal delivery of vaccines and therapeutics to enhance efficacy and simplify administration. We are committed to enabling products that are not only more effective but also more accessible to patients around the world. &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
Research &amp; Development at Vaxess is cross-disciplinary, integrating biology, chemistry, immunology, materials science, and engineering to address important unmet medical needs in vaccines and therapeutics. We are seeking a talented, collaborative, and highly motivated individual with expertise in environmental monitoring and cleanroom QC operations to join our core team of scientists and engineers. The Research Associate will execute environmental monitoring, support cleanroom operations, and contribute to analytical testing to ensure compliance with cGMP requirements. This is a unique opportunity to be part of an emerging early-phase clinical company bringing innovative technology to the global market.
 
Key Responsibilities
Essential duties and responsibilities include the following. Other duties may be assigned.
·Conduct viable and non-viable environmental monitoring in classified cleanroom areas, including air, surface, and personnel monitoring.
·Perform routine and non-routine cleanroom qualification, including particle counts, viable air sampling, and surface swabbing.
·Support environmental monitoring trending, data review, and deviation investigations.
·Maintain detailed, accurate records in compliance with cGMP and data integrity requirements.
·Support cleanroom gowning, aseptic technique, and contamination control training programs.
·Collaborate with Quality and Operations teams to ensure compliance with facility and product requirements.
·Prepare detailed reports and summaries of findings for management.
·Assist in the development and execution of protocols for cleanroom and facility qualification.
·Participate in audits and inspections as needed.
·Support routine and non-routine analyses of drug substances, intermediates, and drug products using techniques such as pH, HPLC, SEC, viscometry, and UV-Vis spectroscopy.
·Work effectively in a fast-paced, team-oriented environment with strong oral and written communication skills.
·Maintain accurate, detailed laboratory records and ensure compliance with data integrity standards in electronic lab notebooks.
·Collaborate cross-functionally to support project success and meet organizational goals.
 
Qualifications&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;
·Bachelor’s degree with at least 2 years of relevant experience, or a master’s degree in microbiology.
·Proficient in environmental monitoring techniques, including viable/non-viable particle monitoring, surface sampling, and cleanroom qualification.
·Familiarity with aseptic processing, contamination control, and cGMP cleanroom operations.
·Strong analytical, problem-solving, and critical-thinking skills.
·Excellent attention to detail and organizational skills.
·Effective written and verbal communication skills.
·Ability to work both independently and collaboratively in a team environment.
·Experience in a QC/GMP laboratory is a plus.
 
Vaxess, a venture-backed life sciences company, is building a team of exceptional people to rapidly advance products on its microneedle array platform.&nbsp;We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you’re interested in joining the Vaxess team, please submit your CV/resume to <a href="mailto:careers@vaxess.com" target="_blank">careers@vaxess.com</a>.&nbsp;&nbsp;

Research Associate, QC

<h3>Job Description</h3>
Job Description &amp; Skill Requirement:
<ul>
<li>Work with quality and Operations on new part costing/quoting process</li>
<li>Work on improvement projects in terms of 5S, Process improvement, fixturing/tooling</li>
<li>Design fixturing /tooling for work holding</li>
<li>Make Parts in ERP system for Shop floor</li>
<li>Work with CNC machines on automation/robotics implementation</li>
<li>Variance(Waste) reduction activities on shop floor</li>
<li>Work on making machine maintenance checklist/works instructions</li>
</ul>
Qualification:
<ul>
<li>Bachelor’s degree in Industrial, Manufacturing Engineering</li>
</ul>

Industrial Engineer

<h3>Job Description</h3>
POSITION SUMMARY:
 
The Plant Manager is directly responsible for leading and driving all operational activities at the facility to ensure consistent levels of production excellence are achieved and sustained while developing a fully engaged and talented workforce. In this role, the Plant Manager will provide clear direction and leadership to the plant staff through goal setting, performance and metric reviews, action planning and Continuous Improvement execution. Collaborating with all cross-functional groups within the organization, this role must maintain a clear focus on the tactical and strategic plans of the facility and ensure that they are aligned with corporate goals and objectives.
 
 essential functions, Job duties and responsibilities:
 
<ul>
<li>Manage and optimize the performance of the production, maintenance and continuous improvement teams and supervisors enhancing workflow efficiency.</li>
<li>Champion continuous improvement and embed operational excellence principles within manufacturing as the foundation of EPIC’s culture.</li>
<li>Demonstrate adeptness in troubleshooting production challenges and facilitating effective resolutions.</li>
<li>Oversee the initiation of new production lines as well as the seamless operation of existing lines.</li>
<li>Foster a Safety First, Quality Always culture focused on operational excellence while developing direct reports.</li>
<li>Coach, manage and develop a high performing leadership team by setting high standards for selection, communicating, and delegation of key responsibilities.</li>
<li>Improve the capabilities of all plant personnel and develop a highly motivated workforce.</li>
<li>Lead facility to achieve Key Performance Indicators (KPIs) and use performance data to drive improvement and provide optimal production performance</li>
<li>Implement cost-effective control systems over capital assets, operating expenditures, and labor costs</li>
<li>Develop and execute upon a site capital plan, addressing both short-term and long-term opportunities</li>
<li>Control and minimize overtime labor costs, maintenance/repair costs, downtime and product re-work.</li>
<li>Optimize ingredient and packaging material usage to minimize scrap loss.</li>
<li>Identify and eliminate potential sources of food safety risk. </li>
<li>Effectively communicate urgent issues both internal and external to the management team as needed. </li>
<li>Identify issues quickly, develop action plans and coordinate team member activities, so that these issues are communicated upward, and dealt with quickly &amp; effectively.</li>
<li>Identify root causes of issues and develop and implement corrective actions to prevent repeat problems.</li>
<li>Ensure accurate and timely communication across all departmental functions.</li>
<li>Support and comply with GMP’s; understand and follow emergency action plan</li>
<li>Support food safety, quality, and legality.</li>
<li>Ensure the operation provides food-safe, quality products which meet or exceed all product specifications and regulatory requirements.</li>
</ul>
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Comply with FDA regulations, other regulatory requirements, company policies, operating procedures, contracts and task assignments.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Assist in all regulatory audits of manufacturing at the facility.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Guide and develop processes/procedures related to Capital Equipment repair and refurbishment.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Occasional travel as business needs demand.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Other duties as assigned.
 
EDUCATION/EXPERIENCE DESIRED:
 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;College degree is preferred 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Minimum 7+ years of applicable manufacturing experience in high-speed beverage manufacturing plant or similar plant management/operations management role.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Manufacturing experience with companies engaged in the manufacture of FDA regulated products.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proven success leading, managing and developing a staff.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Strong interpersonal skills and ability to work with others in a positive and collaborative manner.
 
KEY SKILLS DESIRED:
 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Leader, self-starter and team player.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Excellent speaking, writing and listening skills.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Proven ability to work in a fast-paced and high-demand environment.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to utilize MS Office applications, Outlook, Word, Excel.
PHYSICAL DEMANDS:
 
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to work in an office and plant environment with exposure to noise, equipment, and&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;machinery
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Ability to stand for long periods of time.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Able to perform repetitive movements (e.g. twisting, gripping, lifting, bending, reaching)
 
 
 
 
WORK ENVIRONMENT: 
The work environment’s characteristics described here are representative of those an employee encounters while performing the essential duties of this job.&nbsp;Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;The noise level in the work environment is usually moderate to high.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;The environment can be wet, dry, hot, cold, sticky and dirty.

Plant Manager-Beverage Manufacturer

<h3>Job Description</h3>
Industry: Pharmaceuticals
Title: Manufacturing Contractor I
Job ID: NORT000013
Location: Norton, MA
Duration: 12+ months contract (+Possibility of extension)
 
Shift: 4x10 Weds-Sat 6am-4pm
 
Overview:
With direct supervision, this individual will perform routine clinical manufacturing operations at the Norton Manufacturing Facility, ensuring safe, efficient, and cGMP-compliant operations at all times. Responsibilities include, but are not limited to, operation of production equipment in the areas of weigh/dispense, solution preparation, equipment CIP/COP and small parts cleaning, and materials stocking in manufacturing suites. Operates production equipment according to SOPs for the production of clinical products. Requires interaction with support groups (Facilities, QC, QA, Materials Management, EHS) to ensure accurate completion of activities.
 
Top 3 Must-Have Skills / Experience:
Strong communication skills – able to retain and apply information effectively.
Troubleshooting skills – should be able to speak to specific examples.
Team player – works well in a collaborative, fast-paced environment.
 
Nice-to-Have Skills / Experience:
Experience with TFF or UFF operations
Familiarity with HPLC systems
 
Tools / Technologies:
DeltaV
Basic automation experience preferred
 
Soft Skills / Cultural Fit:
Outgoing and communicative – fits into an outspoken team environment
Proactive, self-motivated, and eager to learn
Comfortable working with diverse personalities

Manufacturing Contractor I

<h3>Job Description</h3>
Responsibilities: &nbsp;
\n
<ul>\n
<li>Observe and record production operations</li>
\n
<li>Review operational schedules and coordinate manufacturing activities to ensure minimum costs and prevent operational delays. i.e.: SMED development, ergonomics, LDR improvement.</li>
\n
<li>Inspects machines and equipment to ensure specific operational performance and optimum utilization</li>
\n
<li>Seeks methods to improve standard operational and working practices</li>
\n
<li>Observe workers, molding machinery, and conveyors to ensure compliance with safety standards and operating efficiency</li>
\n
<li>Coordinates with mold set technician, department supervisors and production personnel for parts, tooling, equipment, and machinery</li>
\n
<li>Performs preventative maintenance on tooling and equipment as directed</li>
\n
<li>Works with the machine attendants and supervisors in training personnel</li>
\n
<li>Follows all safety rules and procedures</li>
\n
<li>Drive scrap reduction on the production floor</li>
\n
<li>Assist process engineer with optimizing cycle times</li>
\n
<li>Ensure presses are running at optimized&nbsp; cycle</li>
\n
<li>Troubleshoot injection molding machines as issues arise&nbsp;</li>
\n</ul>
\n
Requirements:
\n
<ul>\n
<li>A minimum of a High School diploma. Bachelor’s degree in manufacturing, engineering, or related area and at least one year's work experience preferred.</li>
\n
<li>Lean Six Sigma or Kaizen experience/certification a plus</li>
\n
<li>Good verbal and written communication skills</li>
\n
<li>Good Mathematical and organizational skills</li>
\n
<li>Working knowledge of OSHA standards and GMPs</li>
\n
<li>Good interpersonal skills</li>
\n
<li>Experience and demonstrated knowledge of troubleshooting skills, preferably in injection and blow molding processes</li>
\n
<li>Ability to work for up to 12 hours at a time on Day shift or Night shift</li>
\n</ul>
\n
The pay range is $20–$30/hour. Exact salary offered will depend on candidate’s experience, work location, skills, etc.
\n
Mauser Packaging Solutions offers a comprehensive benefits package, including medical, dental, paid time off, and other competitive benefits.
Do you want to work with people who are dedicated to innovation and making the world a better place? Do you want to build a career with a company that provides opportunities for growth and development? Mauser Packaging Solutions is that company. Our mission is to help our customers achieve better sustainability with their packaging. And we do that by giving our people the opportunity to do important work, solve interesting problems and be part of a diverse, forward-looking team. At Mauser Packaging Solutions, you can be proud to work for a company that’s always striving to innovate and serve customers better—and help them be better stewards of the environment. Whether you’re a seasoned professional—or just beginning your career—there’s a place where you can help make a difference at Mauser Packaging Solutions. Join us!\n\n \n\n\n
Mauser Packaging Solutions is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.
\n
Benefits:
Mauser Packaging Solutions offers a comprehensive benefits package, including medical, dental, paid time off, and other competitive benefits.

3rd Shift Process Technician

<h3>Job Description</h3>
Job DescriptionDescription:
The TSUBAKI name is synonymous with excellence in quality, dependability and customer service. U.S. Tsubaki Automotive, LLC is an international tier-one supplier of high-speed chain drive systems to the automotive industry.&nbsp;&nbsp;
This role is responsible for set up and operation, changeover, adjusting and troubleshooting cold heading, cold forging, and bushing forming equipment used in the manufacture of bushing, rolls, pin cut-off for Automotive Timing Chain and Components, and following established work standards.&nbsp;
Essential Duties and Responsibilities: The essential duties and responsibilities of this job are included but not limited to this job description – other tasks may be assigned and expected to be performed.
<ul>
<li>Quality of all components is maintained by each machine operator using statistical quality control methods and defined in the work standard.&nbsp;</li>
<li>Changeovers and adjustments exacting, but not difficult.&nbsp;</li>
<li>Work to specifications, schedules, orders and general instructions of department group leader or supervisor.</li>
<li>Perform preventive maintenance inspection before the start of each shift as outlined on the Preventive Maintenance Check Sheet. Apply oil or grease to specified areas. Confirm the operability of all detectors.</li>
<li>The ability to perform a more comprehensive PM on the machines including but not limited to oil changes.&nbsp;</li>
<li>Basic troubleshooting of chain assembly equipment to understand the alarm messages, identify what this issue is and how to correct the issue.&nbsp;</li>
<li>Adhere to work standards and statistical quality control methods must be followed.&nbsp;</li>
<li>Must have complete knowledge of the cold header equipment, cold forging, bushing forming, and pin cut-off work standards and SQC methods.&nbsp;</li>
<li>Adhere to work standard. Responsible for maintaining production schedules, quality control records, and accurate reporting of production volumes. Refers any unusual problems to the departmental supervisor.</li>
<li>Prepare test samples for quality control per work standard.&nbsp;</li>
<li>Record production, traceability, and any other data required utilizing various forms as directed.&nbsp;</li>
<li>Utilize machine-monitoring system to record down time.&nbsp;</li>
<li>Use material handling devices such as hand truck, hydraulic lift truck.</li>
<li>Maintain work area and equipment in a clean and orderly condition and follow standard safety regulations.&nbsp;</li>
<li>Detect faulty operation or defective material and report these and other unusual conditions to group leader or supervisor.</li>
<li>Perform other similar and associated duties as required or directed.&nbsp;</li>
</ul>
Requirements:
<ul>
<li>High school diploma or equivalent preferred; equivalent relevant experience may be considered</li>
<li>2-5 Years of experience running multiple machines and performing preventative maintenance.</li>
<li>Safety First mindset.&nbsp;</li>
<li>Strong focus on Quality.</li>
<li>Ability to work well in a team environment.</li>
<li>Ability to work in a fast-paced environment.</li>
<li>Must have good mechanical aptitude and problem-solving skills.</li>
<li>Ability to use material handling devices such as hand trucks, and hydraulic lift trucks.</li>
<li>Basic computer Skills.&nbsp;</li>
<li>Ability to read and comprehend simple instructions, short correspondence, and memos.&nbsp;&nbsp;</li>
<li>Ability to write simple correspondence.&nbsp;&nbsp;</li>
<li>Ability to effectively present information in one on one and small group situations to customers, clients, and other employees of the organization.</li>
<li>Ability to add, subtract, multiply, and divide into all units of measure, using whole numbers, common fractions, and decimals.&nbsp;&nbsp;</li>
</ul>
U.S. Tsubaki offers:
<ul>
<li>A competitive compensation package, including medical and dental benefits, life insurance, and generous 401(k) match and profit sharing.</li>
<li>Paid vacation time</li>
<li>Step increases</li>
<li>Shift differential pay</li>
<li>Weekly pay</li>
</ul>
Tsubaki is an Equal Opportunity Employer - Minorities/Females/Veterans/Disability
PM21
 
Compensation details: 24.29-26.92 Hourly Wage
 
PIb45bbbb2ad62-25405-38942011

Fabrication, Set Up & Operate - 2nd Shift

<h3>Job Description</h3>
Advance has an immediate opening for Manufacturing Engineers to develop manufacturing processes planning and coordinate the production of complex machined, mechanical, and welded assemblies. Must be able to understand customer PO Requirements, specifications, and evaluate machine part and assembly engineering drawings to understand the processes to produce the part. Develop machining and assembly processes, operation sheets and tooling. 
Recognize customer quality and inspection requirements. Must have a comprehensive understanding of CAD and working with CAD drawings. Autodesk products a plus. 
Must have min 5 years experience as manufacturing engineer, CNC programmer, or estimator. Experience with engineering drawings, specifications, GD&amp;T, and close tolerance manufacturing processes.

8,513 Manufacturing Jobs