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<h3>Job Description</h3>
Job DescriptionSalary: $22.26-$24.20 
Operates Injection Molding presses, performs secondary/value added tasks and operations within cycle times. Performs floor work/material handling duties. Operates various assembly, production, equipment and hand tools. Performs quality inspections and follows ISO procedures. Prepares and packs parts for material handling and/or shipping. Works with co-workers in a safe, professional and cooperative manner; Minimum qualifications; previous assembly/manufacturing experience preferred; HS diploma or GED

Weekend Molders 12 Hour Shift 1st and 2nd

<h3>Job Description</h3>
Job DescriptionSalary: 
Shawmut Communication Group is seeking a detail-oriented and reliable Night Shift Digital and Small Press Operator to join our team. The ideal candidate will be responsible for operating digital printing and small press equipment during night hours, ensuring high-quality production and timely completion of jobs.
Key Responsibilities:
<ul>
<li>Operate and monitor digital and small press printing equipment</li>
<li>Load, set up, and troubleshoot printing jobs</li>
<li>Ensure quality control and maintain print standards</li>
<li>Perform routine maintenance and clean equipment</li>
<li>Follow safety protocols and best practices</li>
<li>Document production activities and report any issues</li>
</ul>
Qualifications:
<ul>
<li>Previous experience with digital printing and small press operations preferred</li>
<li>Strong attention to detail and quality</li>
<li>Ability to troubleshoot technical issues quickly</li>
<li>Good time management skills</li>
<li>Ability to work independently during night shifts</li>
<li>Flexible and reliable attendance</li>
</ul>
Shift: Night hours, 2pm to 10pm - 4 day work week (flexible)
 
Join Shawmut Communication Group and play a crucial role in delivering outstanding print products. Apply today!

Digital & Small Press Operator

<h3>Job Description</h3>
Job DescriptionSalary: 
Automated NC Punch Operator - Essex Junction, VT
 
Pay:$23.50-$34.00 DOE
Shift: Monday through Thursday: 6:00 AM to 3:30 PM
 Fridays: 6:00 AM to 2:30 PM
 Saturdays: voluntary overtime from 6:00 AM to 12:00 PM
Duration:Temp to Perm
 
 
Duties and responsibilities include but not limited to:
<ul>
<li>Load machinery &amp; programs</li>
<li>Accurately measure parts</li>
<li>Execute first, middle, and last part check procedure</li>
<li>Assemble, install and remove dies</li>
<li>Knowledge of all tooling including maintenance</li>
<li>Load raw material and remove parts and scrap with forklift </li>
<li>Comes up with new or different ways to punch parts for ease of manufacturing and increased productivity</li>
</ul>
 
Qualifications/Essential Functions:
<ul>
<li>Adept at using small hand and power tools</li>
<li>Read blue print proficiently </li>
<li>Knowledge of shop measurement</li>
</ul>
 
Apply today!

Automated NC Punch Operator - Essex Jct, VT

<h3>Job Description</h3>
Job Description
Job Title: Assembler
Duration: 11 Months (temp to perm)
Location: Mansfield, MA 02048
Shift: 1st Shift
Pay Rate: $20/hr.
Job Description
Assembler- a temporary to permanent assignment; must have transportation to work on-site in Mansfield, MA.
EDUCATION and/or EXPERIENCE
Required:
 High School diploma, or equivalent
Desired:
<ul>
<li>Minimum of one (1) years' experience in manufacturing operations with medical devices.</li>
<li>Knowledge and experience with GMP, ISO, FDA, and quality standards</li>
<li>Experience with manufacturing documentation such as, but not limited to, Bill of Materials (BOM), shop orders, routers, and other relevant manufacturing documentation including the maintenance of manufacturing metrics.</li>
<li>Experience in a Clean Room environment</li>
</ul>
This position is responsible for the assembly, packaging, and other steps along the production line of various medical devices as required by clients. Adherence to Good Manufacturing Practices (GMP) and FDA, ISO, and environmental requirements.
This position must adhere to safety guidelines and standards to ensure the products are properly assembled and packaged. This role helps move a product towards the consumer market.
ESSENTIAL DUTIES AND KEY RESPONSIBILITIES:
Accountable for the day-to-day manufacturing activities, which include but are not limited to:
<ul>
<li>Work on the required manufacturing shop orders/workload</li>
<li>Maintain appropriate training as required by the company</li>
<li>Production accuracy and quality</li>
<li>Accurately follow manufacturing procedures and quality standards</li>
<li>Ensure that the proper material is available to perform the assigned manufacturing work</li>
</ul>
As required, work with Engineering personnel to assist and develop process and equipment validation/qualification plans and protocols
<ul>
<li>Assist/support in the execution of such plans, which include testing, data collection, etc.</li>
</ul>
Provide problem solving support to the manufacturing operation as required
Work closely with and play an integral role in the team building process with other cross-functional groups including, but not limited to, Quality Department and Development
Other responsibilities as required

Light Industrial - Assembler

<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting:
Vice President, Quality Assurance
 
Description: 
We are seeking an experienced Associate Director, Quality Systems to join Marianas Quality Assurance organization, advancing personalized medicine and radiopharmaceuticals.
 
Illustrative Breadth of Responsibilities:
<ul>
<li>Lead the integration from Marianas legacy QMS to Novartis QMS platform.</li>
<li>Be the system owner and Subject Matter Expert for quality systems (EDMS, EQMS, LMS) at Mariana.</li>
<li>Review GMP documentation to support the Quality Systems including Document Management, Change Control, Deviations, CAPA, Supplier Management, Risk, and Audits.</li>
<li>Collaborate cross-functionally, including but not limited to liaising with QA, Regulatory Affairs, CMC, Preclinical Development, Manufacturing, etc.</li>
<li>Liaise between IT and Operations for QMS process/system enhancements and process improvements.</li>
<li>Author, review, and, when appropriate, approve policies, procedures, and other related documents for the QMS processes.</li>
<li>Lead the implementation and/or evolution and execution of QMS GxP training program..</li>
<li>Manage GxP document archive.</li>
<li>Manage internal and external audit documentation, while acting as an SME for electronic QMS.</li>
<li>Establish and/or refine systems governance KPIs and create a culture of continuous improvement.</li>
</ul>
 
Requirements/Skills:
<ul>
<li>Bachelors or Masters degree in relevant scientific or engineering discipline with at least eight years of experience working within Quality Assurance in the pharmaceutical or biotechnology industry. Experience working with radiopharmaceuticals and/or oncology will be considered as a plus.</li>
<li>Experience working in an onsite GMP manufacturing facility is highly preferred.</li>
<li>Must have experience implementing an electronic Document Management System.</li>
<li>Strong understanding of industry quality management tools, quality systems.</li>
<li>Experience navigating large, complex pharmaceutical organization(s) is preferred.</li>
<li>System integration experience and/or company integration experience is highly preferred.</li>
<li>Must be willing to work onsite in Watertown 4 days per week.</li>
</ul>
 
Mariana Oncologys Principles
<ul>
<li>Building a Legacy</li>
<li>Execution Excellence</li>
<li>Courage of our Convictions</li>
</ul>

Associate Director, Quality Systems

<h3>Job Description</h3>
Job DescriptionOverview:&nbsp;&nbsp;&nbsp;&nbsp;TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.&nbsp; &nbsp;Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.&nbsp;&nbsp;&nbsp;&nbsp;Job Title:&nbsp;&nbsp;&nbsp;&nbsp; MES Engineer / Project EngineerLocation:&nbsp;&nbsp;&nbsp;&nbsp; Portsmouth, NH - 03801Duration:&nbsp;&nbsp;&nbsp;6 MonthsJob Type:&nbsp;&nbsp;Temporary AssignmentWork Type: Onsite&nbsp;&nbsp;Summary&nbsp;MES Engineer is responsible for supporting activities such as requirements gathering, testing, implementation and use of Manufacturing Execution Systems (MES). Position is expected to operate with some supervision and some autonomy.&nbsp;Safety
<ul>
<li>Performs all work safely and meets the requisite training requirements</li>
</ul>
Manufacturing Support
<ul>
<li>Develop technical knowledge on manufacturing equipment and process automation systems</li>
<li>Manage resolution of equipment breakdowns and quality issues in the suites</li>
<li>Provide SME support to Manufacturing and other departments for the design and operation of process equipment.</li>
<li>Conduct troubleshooting and technical analyses on manufacturing equipment and process control systems including PI data analyses, CIP/SIP circuit review, flow path analyses, code review/troubleshooting, etc.</li>
<li>Assist with tech transfer of new processes into the facility</li>
<li>Complete change request lot assessments to support lot release</li>
<li>Participates in IPT/JPT meetings as MES representative</li>
</ul>
Projects
<ul>
<li>Planning and execution of plant projects involving automation changes and process improvements including lump sum capital projects</li>
<li>Execute test scripts (design, execution, simulation, wet testing)</li>
<li>Own change requests and complete change request tasks to support project completion</li>
<li>Perform change request assessments</li>
</ul>
Deviations / RCAs
<ul>
<li>Assist the Quality department with deviation investigations</li>
<li>Participate in RCAs as MES representative</li>
<li>Assist with completion of CAPA actions</li>
<li>Participates in quality risk assessments</li>
</ul>
Documentation
<ul>
<li>Review/revise automation and Manufacturing related SOP’s, Functional Specifications, and work instructions as a result of CAPA, equipment/process changes, error prevention activities, etc.</li>
<li>Complete MES review/approval of batch records</li>
<li>Author and review test protocols</li>
</ul>
Required Skills &amp; Qualifications
<ul>
<li>Prior experience in &nbsp;supporting MSE Projects is required</li>
<li>Must have experience in planning and executing changes to automation or process improvements</li>
<li>Strong experience in performing change request assessments is required</li>
<li>Should have experience in supporting or leading deviation investigations and root cause analyses (RCA)</li>
<li>Strong hands on experience in authoring or reviewing technical documentation such as SOPs, functional specifications, or test protocols is required.</li>
</ul>
TekWissen® Group is an equal opportunity employer supporting workforce diversity. 
TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.
Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.
TekWissen® is an equal opportunity employer supporting workplace diversity.&nbsp;

MES Engineer

<h3>Job Description</h3>
Job DescriptionSalary: 
 IMMEDIATE OPENING FULL TIME POSITION 
 Experienced Mechanical Engineer
Local Candidates Only
 
Diversified Technologies, Inc. (DTI) is an international leader in the design and manufacture of high-power electrical equipment. Our exceptional engineers and scientists collaborate to develop the worlds most powerful radar transmitters, pulsed power units for state-of-the-art processing in food, energy and wastewater, and advanced R&amp;D for national laboratories. 
Join a team where your professional development will be rapid. We offer an opportunity to engage with world-class engineers and scientists through the entire product cycle from design through production and installation for industrial and government applications. Through teamwork and innovation, we strive to consistently deliver reliable, high-quality products. We seek an experienced Mechanical Engineer to join our systems design and development team at our headquarters in Bedford, Massachusetts.
___________________________________________________________________________
 
Responsibilities:
<ul>
<li>Team with other engineers, scientists, technicians</li>
<li>Assist in developing new designs</li>
<li>Develop production documents (drawings, travelers, test plans)</li>
<li>Assist with fabrication, assembly of systems</li>
<li>Support system and subsystem testing, evaluate results, prepare reports</li>
<li>Participate in on-site installations </li>
</ul>
 
Requirements:
<ul>
<li>Bachelors degree in Mechanical Engineering</li>
<li>Two to five years experience as an engineer</li>
<li>Proficient with SolidWorks</li>
<li>Demonstrated analytical skills and hands-on aptitude</li>
<li>Experience with and effective in a team setting leading small groups</li>
<li>Good written and oral communication skills</li>
<li>Able to travel (domestic and abroad, occasional)</li>
<li>U.S. Citizen</li>
</ul>
 
Compensation:
<ul>
<li>Salary commensurate with experience.</li>
<li>Excellent benefits including health, dental, life, and disability insurance; 401K Plan; tuition reimbursement; paid holidays, sick leave and fifteen vacation days beginning year one. </li>
</ul>
 
DTI is an Equal Opportunity Employer: Female / Male / Disabled / Veteran
DTI makes reasonable accommodation(s) for persons with disabilities
Visit Career Opportunities on our website at <a href="http://www.divtecs.com" target="_blank">www.divtecs.com</a> to learn more and apply

Experienced Mechanical Engineer

<h3>Job Description</h3>
Job DescriptionPosition Description&nbsp;The 2nd Shift Supervisor&nbsp;will have responsibility for all operations of a particular functional area within the manufacturing/operations organization, that produces a high volume of small-run custom products. This position spends time on the production floor planning work for each employee in the area, performing area operations, training new employees, and organizing each area. In addition to performing daily area activities, this position will have direct reports and be responsible for the day-to-day management of associates and will support the company’s operational goals. This role requires a roll-up-your-sleeves, hands on approach. &nbsp;&nbsp;Responsibilities&nbsp;•Responsible for the daily performance of the department, with a focus on safety, quality and on-time metrics.•Manage the workload of the area, recommending overtime as needed, additional labor as identified, and perform operations as required.•Cross train the team on all products.•Support quality assurance programs.•Maintain area tools, fixtures, and other equipment.•Ensure proper coverage of the area by managing employee time appropriately.•Perform employee annual appraisals, recommend merit increases and handle all employee disciplinary issues.•Approve and manage vacation and sick time. &nbsp;Flex resources as required.•Support process improvements and a lean culture.•Developing, support, analyzing and improving key metrics such as productivity, efficiency and utilization.•Ability to troubleshoot Milling, Turning issues.&nbsp;Requirements&nbsp;•Ability to work in team oriented environment.•Must possess clear and concise written and verbal communication skills, with the ability to effectively communicate with all levels of the corporation.•Proficient in the use of Microsoft Office•Ability to understand and track metrics and key performance indicators.•Ability to read and understand blueprints•Proficient in CNC Lathe and Milling programming and set ups. Mastercam a plus•Familiar with metals and composites and corresponding speeds and feeds for them•Ability to read programs and adjust as needed. G-code and M-code•Familiarity with HAAS, Mazak , Okuma and Hitachi controls&nbsp;Education and Experience&nbsp;•High school diploma•Minimum of 5 years’ experience in a CNC job shop manufacturing environment•Strong planning, organizational skills•Experience in a leadership position•Familiarity with lean/continuous improvement concepts•Positive, Energetic attitude

CNC 2nd Shift Supervisor

<h3>Job Description</h3>
Job DescriptionSalary: 
PURPOSE:
<ul>
<li>The Mechanical Quality Inspector is responsible for REXA product quality by ensuring that material channeled through inspection complies with defined requirements and does not enter REXA operations, or is not released for shipment. The ideal candidate shall be a team player, have good communication skills, be thorough, methodical, and detail oriented. This position reports to the Senior Quality Engineer and is responsible for the following: </li>
</ul>
 
RESPONSIBILITIES:
<ul>
<li>Ensure that both supplier provided material/product entering operations or inventory; and manufactured product for shipment meets all design and customer requirements by inspecting and confirming dimensional characteristics, visual / cosmetic attributes, functional requirements and supporting documentation review</li>
<li>Conduct inspection of parts and packaging utilizing all standard tools and methodologies</li>
<li>Compare measurement outputs against established design requirements, determines pass/fail, and documents any non-conforming material according to standard practices</li>
<li>Maintains inspection tooling and equipment to ensure results reliability and repeatability</li>
<li>Conduct Coordinate Measuring Machine (CMM) part setup and operation utilizing fixturing and probe calibration</li>
</ul>
<ul>
<li>Develops inspection methods and set-ups</li>
</ul>
<ul>
<li>Develop and use Inspection Sampling Plans with assistance of the QA Manager and QA Engineering</li>
<li>Provides Inspection guidance and support to Engineering, Supplier Quality, and Suppliers as required</li>
<li>Originate and maintain all inspection records including vendor inspection reports and certificates as required</li>
</ul>
<ul>
<li>Originate Nonconformance Reports in the Syteline Business System</li>
<li>Support MRB (Material Review Board) activities</li>
<li>Perform Liquid Penetrant Inspection to verify weld quality and workmanship</li>
<li>Performs mechanical calibration of inspection and measurement tools and administers calibration system</li>
</ul>
<ul>
<li>Conduct all responsibilities in compliance with the REXA Quality Management System</li>
<li>Identifies potential project candidates for continuous improvements and provides project support</li>
</ul>
<ul>
<li>Acts as a mentor for other Inspection team members</li>
</ul>
EDUCATION AND EXPERIENCE:
<ul>
<li>High School Diploma required</li>
<li>Associate Degree in related field or certificate from technical school highly preferred.</li>
<li>ASQ Certified Inspector preferred</li>
<li>Minimum 2 years-experience inspecting product in an ISO 9001 manufacturing environment</li>
<li>Liquid Penetrant Level I or Level II Certification / Training to SNT-TC-1A preferred</li>
</ul>
KNOWLEDGE AND SKILLS:
<ul>
<li>Proficient in the use of inspection and measurement hand tools (calipers, micrometers, height gauge, etc.)</li>
</ul>
<ul>
<li>Working level understanding of Metrology concepts including Blueprint layout &amp; GD&amp;T.</li>
<li>Working level and complex (independent) CMM programming software.</li>
</ul>
<ul>
<li>Ability to read electrical/mechanical diagrams, spec sheets, and outline drawings</li>
<li>Good communication skills, verbal and written</li>
<li>Strong organizational skills and the ability to successfully complete multiple tasks within established and changing deadlines</li>
</ul>
WORKING CONDITIONS:
<ul>
<li>Standing 95%</li>
<li>Lifting up to 50 lbs.</li>
</ul>
 
We offer full benefits and competitive compensation.
 
Benefits:
<ul>
<li>401(k) with generous match</li>
<li>Dental insurance</li>
<li>Employee discount</li>
<li>Flexible spending account</li>
<li>Health insurance</li>
<li>Life insurance</li>
<li>Paid time off</li>
<li>Parental leave</li>
<li>Tuition reimbursement</li>
<li>Vision insurance</li>
</ul>
 
Equal Opportunity Employer - Minorities/Women/Veterans/Disabled
*This organization participates in E-Verify.*

Mechanical Quality Inspector

<h3>Job Description</h3>
Job DescriptionSalary: $65,000 minimum 
Mack Moldingis recognized as one of the worlds premier custom manufacturers of high quality complex parts, assemblies, and total products in plastic and metal.We have been in business since 1920, and have grown to over 2000 employees in seven plants located throughout the eastern United States.
Mack Moldingoffers a variety of services throughout its numerous facilities,resulting in many diverse career paths and advancement opportunities. And when new opportunities arise, whether on the manufacturing floor, out in the field, or in the corporate offices, Mack strives to promote its talent from within.
<ul>
<li>This role involves working in an ITAR-controlled environment. The successful candidate will have a strong technical background, problem-solving skills, and the ability to work within the strict compliance requirements of ITAR regulations.</li>
</ul>
Essential Responsibilities:
<ul>
<li>Support new business development
<ul>
<li>Provides support to new business development relating to quality matters as needed</li>
<li>Draft preliminary Quality Plan, if appropriate</li>
<li>Provides cost and time estimates for anticipated quality department services such as metrology or validation services</li>
<li>Functions as a resource for applicable ISO Program and QSR Program requirements</li>
</ul>
</li>
</ul>
<ul>
<li>Support Program Launch and Product Realization as functional department representative assigned to team and Program Manager
<ul>
<li>Reviews new program drawings/information/customer specifications to understand program requirements</li>
<li>Determines quality and reliability standards and ensures dimensional and cosmetic requirements, as well as customer specifications, are defined and understood.</li>
<li>Drafts program Quality Plan (as required) and metrology labor plan to include definition of required fixtures, calibration and metrology requirements and measurement methods needed to meet customer requirements for approval</li>
<li>Drafts other required quality documentation such as Dimensional Visual Quality Requirements (DVQRs) and new product inspection techniques</li>
<li>Confirms customer agreement on GD&amp;T callouts/interpretations and all critical dimensions of program when required</li>
<li>Prepares Failure Mode Effects Analysis (FMEA), as needed</li>
<li>Prepares Traveler Document</li>
<li>Develops required Control/Test methods</li>
<li>Ensures First Article Inspection (FAI) and Capability Studies are scheduled and completed</li>
<li>Completes FAI and capability study analysis for submission to customer</li>
<li>Authors operational qualification (OQ) and performance qualification (PQ) protocols and provides training for protocol participants</li>
<li>Oversees the execution of assigned OQ and PQ studies to ensure compliance with protocol requirements and completion of study tasks</li>
<li>Authors OQ and PQ Completion Reports to include resolution of any deviations recorded and overall study conclusion</li>
<li>Establishes golden sample standards and prepares and submits to customer via customer approval form (CAF) as required</li>
<li>Attends program team meetings to address quality-related matters</li>
<li>Performs assigned activities in a timely manner</li>
</ul>
</li>
</ul>
<ul>
<li>Provide continuous quality engineering support through program end of life.
<ul>
<li>Completes Certificates of Conformance (CoC) for outgoing products, where required</li>
<li>Collects and analyzes production line data to monitor yield and defect performance</li>
<li>Ensures golden samples are retained and controlled</li>
<li>Maintains Device History Records (DHR) as necessary</li>
<li>Performs periodic risk assessments, as required</li>
<li>Assists Purchasing Department with maintaining vendor quality requirements</li>
<li>Continuously monitors production to identify quality-related customer issues and supports corrective action plans when necessary</li>
<li>Issue or authorize CCRs as needed. Manages the return of goods, assignments and close out of RC/CA.</li>
<li>Conducts root cause investigation and develops corrective action plans for assigned problem reports (PSRs) and quality issues</li>
<li>Manages product and process change control and notification to ensure required Engineering Change Orders (ECOs) are generated and approved by the customer prior to implementation.</li>
<li>Attends program team meetings as necessary to resolve program quality issues to maintain customer satisfaction</li>
<li>Support QBRs with customer and provides/presents quality-related topics</li>
<li>Participates in customer, certified body, and regulatory audits as a subject matter expert for assigned products and processes</li>
</ul>
</li>
</ul>
 Working knowledge of Statistical techniques &amp; sampling plans and of Quality Systems Regulations. Bachelors degree (B.A.) in technical field desired, plus 2 years related experience preferred. Experience in medical device-manufacturing environment, and experience with Six Sigma or Lean are preferred.

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