<h3>Job Description</h3>
Job Description
Are you a skilled CNC Setup Machinist looking for a great opportunity? Join our team and work with state-of-the-art equipment in a dynamic and growing company!
We are a pharmaceutical tooling company
We are not a job shop. Design and build our own product.
What We Offer:
✅ Competitive pay based on experience
✅ Full-time, stable work schedule with Overtime
✅ Benefits package (health, dental, 401k, etc.)
✅ Opportunity for growth and advancement
Job Responsibilities:
Set up and operate CNC machines (Haas)
Read and interpret blueprints and technical drawings
Adjust machine settings to meet tight tolerances
Perform inspections
Work closely with programmers and engineers
What We’re Looking For:
✔️ 5+ years of CNC setup experience
✔️ Strong knowledge of G-code and machining processes
✔️ Ability to use precision measuring tools
✔️ Attention to detail and problem-solving skills
✔️ Team player with a strong work ethic
If you’re ready to take your machining career to the next level, apply today!
Please contact me at <a href="mailto:Jeff.ferguson@Prodieco.com" target="_blank">Jeff.ferguson@Prodieco.com</a>
215-355-2174

CNC Setup Machinist

<h3>Job Description</h3>
Job Description
Are you a skilled mechanic with a passion for small engine repair? Groundhog Landscaping in Derry, NH is seeking a talented individual to join our team as a full-time Mechanic - Small Engine Repair. As a member of our company, you'll have the opportunity to work in a dynamic and collaborative environment that values your expertise and dedication. You will enjoy competitive pay ranging from $22 to $28 per hour and a wide range of benefits, including:
<ul>
<li>Health, dental, and vision insurance</li>
<li>Paychecks every Friday</li>
<li>Growth opportunities</li>
<li>Company parties</li>
<li>Company vehicle</li>
<li>Uniforms</li>
</ul>
If you're ready to take the next step in your career, keep reading to learn more about what Groundhog Landscaping has to offer!
 
WHAT'S YOUR DAY LIKE?
As our Mechanic - Small Engine Repair, you dive into performing routine maintenance and repairs on various small engine equipment. Your expertise shines as you deftly diagnose and resolve mechanical and electrical issues, ensuring that each tool and machine operates at its best. Keeping detailed records of all maintenance and repair work comes naturally to you, reflecting your commitment to accountability and excellence. You take charge of managing the inventory of parts and supplies, knowing that a well-stocked workshop is pivotal in maintaining operational efficiency. Through your hard work and dedication, you ensure all equipment complies with safety regulations and company standards.
 
WHO ARE WE?
As one of the largest full-service landscape companies in southern New Hampshire, Groundhog Landscaping provides high-quality, reliable, and affordable grounds maintenance and construction services. Since 1995, we have served our residential and commercial clients to the best of our abilities. Our team is passionate about their work, and we encourage continual growth and professional advancement. Whether you're looking to build a fulfilling landscaping career or want an opportunity to grow with a dynamic, thriving team, we have something to offer you!
 
WHAT'S NEEDED FROM A MECHANIC - SMALL ENGINE REPAIR?
We're looking for someone who can work Monday to Friday from 6:30 AM to 5:00 PM while meeting the following qualifications:
<ul>
<li>Strong knowledge of mechanical, electrical, and fuel systems in small engines</li>
<li>Detail-oriented and well-organized</li>
<li>Ability to work independently and as part of a team</li>
</ul>
Having a valid driver's license and being skilled in using a variety of tools and diagnostic equipment is a plus!
Join our team as a Mechanic - Small Engine Repair at Groundhog Landscaping and kickstart your career in a dynamic and growing company! The initial application should take you less than 3 minutes to complete. Good luck!
 
Must have the ability to pass a background check and drug screening test.
 Job Posted by ApplicantPro

Mechanic - Small Engine Repair

<h3>Job Description</h3>
Job Description
Summary:
Responsibilities for this role include spooling, visual inspection, installation and packaging of coiled tubing for both domestic and international shipments. Working in small teams, spooling technicians utilize proprietary spooling equipment to execute tasks for both internal and external customers while interacting with operational departments throughout Global Tubing. 

Job Duties/Responsibilities
<ul>
<li>Perform work in a professional and safe manner, report unsafe work practices</li>
</ul>
<ul>
<li>Prepares work to be accomplished by studying assembly instructions, blueprint specifications, and parts lists.</li>
<li>Gathers parts, subassemblies, tools, and materials.</li>
<li>Assembles parts and spool equipment as instructed.</li>
<li>Maintains safe and clean work environment.</li>
<li>Conserves resources by using equipment and supplies as needed to accomplish job results.</li>
<li>Other duties as assigned.</li>
</ul>
Skills/Knowledge
<ul>
<li>Have knowledge of safe work practices</li>
<li>Ability to read and understand training materials and work instructions</li>
<li>Work in a fast paced environment</li>
<li>Have physical strength and ability to perform moderate to heavy duty manual labor</li>
</ul>

Education
<ul>
<li>High School Diploma or equivalent.</li>
</ul>

Experience
<ul>
<li>6 months - 1 year of experience</li>
<li>Valid drivers license</li>
</ul>
About FET FET (Forum Energy Technologies, Inc.) is a global company, serving the crude oil, natural gas, and renewable energy industries. FET is headquartered in Houston, TX with quality manufacturing, efficient distribution, and service facilities conveniently located to support the major energy-producing regions of the world. Forum’s products and services range from the underwater reservoir to the refinery, from the sea floor to the above ground transportation line. We pride ourselves on giving you a comprehensive offering of solutions to maximize your operations and improve your bottom line. Our customers are our partners and we work with them to solve their ever-changing challenges.
FET is an Equal Opportunity Employer. FET does not discriminate on the basis of race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected under federal, state, or local law. All employment decisions and practices at FET are subject to the foregoing non-discrimination provisions and are based solely on merit, competence, performance, and business needs at the time.

Assembler I

<h3>Job Description</h3>
Job Description
Position: Outdoor Scheduling Representative
Start Your Career in the Field – No Experience Needed Earn $50K–$75K!
Canvass neighborhoods identify storm damage roofs and schedule inspections - no selling.
Responsibilities: • Canvass neighborhoods identify storm damage roofs • Explain and educate homeowners that they will get a brand new roof paid for by their insurance • Schedule Inspections
Requirements: • No experience needed • Strong communication, negotiation, and closing skills • Self-motivated
Position Offers: • Earning Potential: $50K-$75K+ annually • Growth Opportunities
To Apply: All applicants must submit their updated resume along with their contact phone number. Qualified candidates will be contacted for a phone interview.
 #hc215323

Outdoor Scheduling Representative Immediate Start!

<h3>Job Description</h3>
Job DescriptionLeading architectural and engineering firm is adding a Senior Electrical Engineer to their Washington, D.C. team! 
 
Responsibilities: 
<ul>
<li>Prepare scope, budget and staff after assessing project requirements </li>
<li>Using preliminary review and client meetings, write scope of work for electrical design </li>
<li>Prepare engineering studies/schematic design for new systems </li>
<li>Analyze operation of existing systems </li>
<li>Effectively present complex engineering analysis to owner/design team </li>
<li>Troubleshoot/resolve complex problems (conflicting design requirements, code issues, varying design options, and difficult condition requirements) </li>
<li>Research non-routine code issues and obtain interpretations from code officials </li>
<li>Prepare sketches/system schematics for complicated design tasks </li>
<li>Prepare calculations including whole building electrical loads, lighting calculations, power distribution calculations, equipment sizing, editing specification sections, and creating punch lists </li>
<li>Review contractor cost estimates after preparing engineering opinion of probable cost for electrical systems </li>
<li>Develop/maintain a thorough understanding of construction processes and delivery methods </li>
<li>Review drawings/documents for compliance </li>
<li>Mentor/train junior staff </li>
</ul>
 
Requirements: 
<ul>
<li>BS or MS degree in electrical engineering </li>
<li>12+ years of design experience for a variety of projects (corporate, higher education, or performing arts projects) </li>
<li>Documented experience providing electrical design to an MEP engineering firm or A/E firm </li>
<li>PE License </li>
<li>Extensive knowledge of National Fire Protection Association Codes (NFPA) </li>
<li>Understanding of applicable (city, state, federal) requirements/pertinent standards </li>
<li>Knowledge of IECC, LEED and ASHRAE requirements </li>
<li>Working knowledge of Revit software </li>
<li>Familiar with electrical analysis software (SKM, Easy Power) </li>
<li>Knowledge of the current sustainable technologies applicable to the design of commercial electrical systems </li>
</ul>
 
Salary is commensurate with experience. 
 
Successful applicants must be authorized to work in the USA without sponsorship. 
 
All qualified applicants will receive consideration for employment without regard to protected veteran status, disability, race, color, religion, sex, sexual orientation, gender identity, or national origin. 
 
Please contact Laura Harrison for further information! 
 
<a href="http://www.harrisonconsultingsolutions.com" target="_blank">www.harrisonconsultingsolutions.com</a> 
 
517-906-6926

Electrical Engineer

<h3>Job Description</h3>
Position Summary:
The CQM Supervisor oversees non-clinical auditors in the Clinical Quality Management (CQM) department, ensuring regulatory compliance and the quality of processes in daily Non-Clinical Utilization Management (UM) activities, under the direction of a manager. This Supervisor is responsible for conducting live audits of UM case files, assigning drivers and presenters, and ensuring their performance is appropriate. The role also involves monitoring UM system controls and processes, specifically those that do not require clinical decisions. A solid understanding of comprehensive regulations, UM policies and procedures, the UM system, UM auditing, and quality improvement is essential for this position.
 
Essential Duties and Responsibilities:
 
- Familiarity with Non-Clinical UM regulations, processes, and systems.
- Ability to assign workloads effectively while managing staff.
- Proficient in presenting case files and conducting interviews regarding non-clinical questions.
- Skilled in designing audit tools to monitor Non-Clinical UM processes completed by non-clinical staff.
- Strong communication skills for effective interaction with internal clients and external customers.
- Capable of training employees using Policies &amp; Procedures (P&amp;Ps) and audit tools.
- Provide constructive feedback and exhibit strong active communication skills.
- Summarize quality monitoring findings, analyze root causes, and propose quality improvement plans.
- Suggest and design focused audits that help improve compliance in Non-Clinical UM processes.
- Request decision support for creating and enhancing Non-Clinical UM monitoring reports based on changes to UM P&amp;Ps.
- Ensure auditors complete audits and necessary remediation within specified timeframes.
- Collaborate with the Non-Clinical UM team to ensure monitored focus areas are addressed and that process quality is tracked.
- Work with operational teams to evaluate the effectiveness and efficiency of process changes made for quality improvement.
- Ensure that new processes are accurately implemented through reports and case file reviews.
- Report issues identified to the Prior Authorization Compliance Director based on findings.
- Review updated policies and procedures, and be able to update the quality monitoring tool accordingly.
- Maintain all evidence related to quality monitoring projects.
- Track and manage daily reports received from the decision support team.
- Report any issues related to internal processes (e.g., timeliness) to the CQM manager.
- Attend department meetings, in-house services, and trainings, completing acknowledgments within the required timeframe.
- Perform all other duties as directed by management.
 
Education and Experience:
 
- Three to five (3-5) years of experience in non-clinical utilization management.
- Preferred: at least two (2) years of experience in non-clinical UM supervision or auditing.
- Proficiency in MS Office programs (Word, Excel, Outlook, Access, PowerPoint).
- Typing speed of 60 words per minute with accuracy.
- Ability to handle confidential matters responsibly.
- Strong analytical, creative problem-solving, and organizational skills.
- Capacity to work in a multi-tasking, high-stress environment.
- Effective strategy execution within timelines, delivering quality results.
- Ability to adapt and thrive in a fast-paced environment, demonstrating proactivity.
- Capable of managing multiple projects simultaneously, adjusting priorities daily, and knowing when to seek assistance with conflicting priorities.
- Self-motivated, assertive, ambitious, and possessing high personal ethics.
- Ability to collaborate with all levels of management and establish positive working relationships across various divisions in the company.
 
Compensation:
 
The pay range for this position at the start of employment is expected to be between $70,304 and $72,000 annually, depending on experience. However, the base pay offered may vary based on multiple individual factors, including market location, job-related knowledge, licensure, skills, and overall experience.
 
The total compensation package for this position may also include other elements, such as a sign-on bonus and discretionary awards, along with a full range of medical, financial, and other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), depending on the position offered.
 
Details regarding participation in these benefit plans will be provided to employees who receive an employment offer. If hired, the employee will be in an “at-will position,” and the company reserves the right to modify base salary (along with any other discretionary payments or compensation programs) at any time, including for reasons related to individual performance, overall company performance, or market factors.
 
As one of the fastest-growing Independent Physician Associations in Southern California, Regal Medical Group, Lakeside Community Healthcare, and Affiliated Doctors of Orange County offer a dynamic and fast-paced work environment.
 
Employer will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of the LA City Fair Chance Initiative for Hiring Ordinance.

Supervisor , Continuous Quality Monitoring

<h3>Job Description</h3>
&amp;#x1F527; Maintenance Planner / Scheduler
 &amp;#x1F4CD; Sumter County, South Carolina
 &amp;#x1F3ED; Global Manufacturing Company
 
A large, global manufacturing organization is seeking a Maintenance Planner / Scheduler to support high-volume plant operations. This role is critical to planning, scheduling, and coordinating maintenance activities to improve equipment reliability and minimize downtime.
 
What You’ll Do
• Plan and schedule preventive, corrective, and outage maintenance activities
 • Develop work plans including labor, materials, tools, and time estimates
 • Manage maintenance work orders, backlog, and on-time completion
 • Partner with Production to optimize technician and resource utilization
 • Track maintenance KPIs, costs, and planning effectiveness
 • Ensure compliance with safety, quality, and regulatory standards
 
What We’re Looking For
✔ High School Diploma required; additional education preferred
 ✔ 3–5 years of maintenance experience (technician or supervisor)
 ✔ Experience with processing/packaging equipment and facilities maintenance
 ✔ Formal training in maintenance planning, scheduling, and work control
 ✔ CMMS experience required (SAP preferred)
 ✔ Strong communication and organizational skills
 ✔ GMP experience preferred
 
Additional Info
• U.S. work authorization required
 • No visa sponsorship available
 
Interested or know someone who might be a fit?
 &amp;#x1F4E9; Feel free to message me directly to learn more or start a confidential conversation.

Maintenance Planner

<h3>Job Description</h3>
Job Description
We are seeking a highly skilled Quality Assurance Technician III - Metrology with demonstrated expertise in Coordinate Measuring Machines (CMM) and Industrial CT Scanning to support dimensional inspection and quality assurance activities in a medical plastic injection molding environment. This role serves as a technical authority for advanced measurement technologies, ensuring critical medical device components meet stringent dimensional, regulatory, and customer requirements.
The ideal candidate has deep experience in CMM programming, CT scan data interpretation, GD&amp;T analysis, and process capability, and thrives in a regulated manufacturing environment.
Key Responsibilities
Advanced Metrology &amp; Dimensional Inspection
<ul>
<li>Perform complex dimensional inspections of medical injection molded components using CMMs and industrial CT scanning systems, as well as other precision measurement tools.</li>
<li>Develop, program, and optimize CMM inspection programs (e.g., PC-DMIS or equivalent).</li>
<li>Execute and analyze CT scan measurements for internal geometry, wall thickness, porosity, and complex features not accessible through traditional measurement methods.</li>
<li>Interpret and apply GD&amp;T (ASME Y14.5) to ensure accurate and repeatable measurement strategies.</li>
</ul>
Inspection Planning &amp; Measurement Strategy
<ul>
<li>Lead development of inspection plans, measurement strategies, and sampling methodologies for new and existing products.</li>
<li>Partner with Engineering, Tooling, and Manufacturing during NPI, First Article Inspection (FAI), PPAP, and validation activities to define appropriate measurement approaches using CMM and CT technologies.</li>
<li>Evaluate part design and tooling for measurability and provide feedback to Engineering.</li>
</ul>
Calibration &amp; Equipment Management
<ul>
<li>Perform calibration, verification, and routine maintenance of CMM and CT scanning systems, ensuring ongoing accuracy and compliance.</li>
<li>Maintain calibration and verification records in accordance with ISO 13485 and internal Quality Management System (QMS) requirements.</li>
<li>Support measurement system analysis (MSA) for CMM and CT equipment.</li>
</ul>
Statistical Analysis &amp; Problem Solving
<ul>
<li>Apply SPC, MSA, and capability studies (Cp/Cpk) to evaluate manufacturing process performance.</li>
<li>Lead root cause investigations related to dimensional nonconformances and measurement system issues using structured problem-solving methodologies.</li>
<li>Drive and support CAPA activities tied to metrology and inspection findings.</li>
</ul>
Documentation &amp; Regulatory Compliance
<ul>
<li>Document inspection results, CT scan analyses, deviations, and investigations in compliance with FDA 21 CFR Part 820, ISO 13485, and internal procedures.</li>
<li>Support internal, customer, and regulatory audits related to metrology, CMM, and CT scanning processes.</li>
</ul>
Training, Mentorship &amp; Technical Leadership
<ul>
<li>Serve as the site subject matter expert (SME) for CMM and CT scanning technologies.</li>
<li>Train and mentor Quality Technicians and Manufacturing personnel on metrology principles, GD&amp;T, and equipment operation.</li>
<li>Establish and improve standardized work and best practices for advanced metrology.</li>
</ul>
Continuous Improvement &amp; Cross-Functional Collaboration
<ul>
<li>Lead continuous improvement initiatives focused on measurement accuracy, efficiency, and automation.</li>
<li>Collaborate with Engineering, Quality, Operations, and Tooling to resolve quality issues and improve process robustness.</li>
<li>Communicate metrology findings clearly and effectively to cross-functional teams and leadership.</li>
</ul>
 
Qualifications &amp; Experience
Education
<ul>
<li>Bachelor's degree in Engineering, Metrology, Quality, or related technical field preferred</li>
<li>Equivalent experience in advanced metrology will be considered</li>
</ul>
Experience
<ul>
<li>3-5+ years of experience in metrology or quality roles within medical device manufacturing, plastic injection molding, or other regulated industries</li>
<li>Hands-on experience with CMM programming and industrial CT scanning required</li>
</ul>
Technical Skills
<ul>
<li>Proficiency with CMM programming software (PC-DMIS or equivalent)</li>
<li>Experience analyzing CT scan data for dimensional inspection, wall thickness, internal features, and defect detection</li>
<li>Strong knowledge of GD&amp;T (ASME Y14.5)</li>
<li>Working knowledge of SPC, MSA, Cp/Cpk</li>
<li>Familiarity with ISO 13485 and FDA QSR (21 CFR Part 820)</li>
</ul>
Core Competencies
<ul>
<li>Exceptional attention to detail and precision</li>
<li>Strong analytical and problem-solving skills</li>
<li>Ability to work independently and as a technical leader</li>
<li>Clear written and verbal communication skills</li>
<li>Collaborative mindset with a continuous improvement focus</li>
</ul>
Preferred 
<ul>
<li>Experience with Zeiss, Hexagon, Nikon, or similar CT scanning platforms</li>
<li>Experience with vision systems and non-contact metrology</li>
<li>Six Sigma or Quality-related certifications</li>
</ul>

Metrology/Programmer - QA Technician III

<h3>Job Description</h3>
Job Description
We are seeking a hands-on, results-driven Manufacturing Project Engineer to support the seamless transition of new products and equipment from development into full-scale production within our regulated medical injection molding and assembly facility.
This role is critical for driving process excellence, scalable manufacturing, regulatory compliance, and cost-effective operations. The ideal candidate combines strong technical expertise, practical project execution skills, cleanroom experience, and a continuous improvement mindset to manage NPI product launches, equipment transfers, process validations, and cleanroom/building projects.
Key Responsibilities
Project Leadership &amp; Equipment Integration
<ul>
<li>Lead manufacturing engineering activities for new product introductions (NPI), equipment integrations, and production ramp-up from concept through validation.</li>
<li>Plan and coordinate transfer of existing machines or installation of new equipment, including proper setup, qualification, and documentation.</li>
<li>Manage project timelines, deliverables, and risk mitigation strategies to ensure on-time, in-spec, and in-budget launches.</li>
<li>Coordinate cross-functional teams, ensuring design for manufacturability (DFM) and smooth technology/equipment transfers.</li>
<li>Facilitate manufacturing readiness reviews and support customer communications as needed.</li>
</ul>
Process Design &amp; Optimization
<ul>
<li>Develop, optimize, and scale injection molding and downstream assembly processes (e.g., ultrasonic welding, pad printing, packaging) for consistent quality, efficiency, and cost-effectiveness.</li>
<li>Apply Lean principles, root cause analysis (5-Whys, Fishbone), and statistical tools to reduce waste, variability, and operational costs.</li>
<li>Identify and implement process improvements and cost reduction initiatives without compromising quality or compliance.</li>
</ul>
Tooling &amp; Equipment Management
<ul>
<li>Oversee the specification, procurement, installation, setup, validation, and maintenance of molds, jigs, fixtures, and custom equipment.</li>
<li>Collaborate with toolroom personnel and external vendors to manage tooling performance, modifications, and preventative maintenance.</li>
<li>Support mold qualification and equipment performance verification to ensure sustained reliability.</li>
</ul>
Cleanroom &amp; Facility Projects
<ul>
<li>Serve as subject matter expert (SME) for cleanroom and controlled environments.</li>
<li>Lead or support the design, build-out, and qualification of new cleanrooms, molding areas, and assembly areas.</li>
<li>Ensure compliance with cleanroom classifications, gowning practices, material flow, and contamination controls.</li>
<li>Conduct cleanroom qualification/requalification (IQ/OQ/PQ) and maintain environmental monitoring programs (particulates, temperature, humidity, differential pressure).</li>
<li>Provide training for operators and staff on cleanroom procedures, contamination control, and safe operation practices.</li>
</ul>
Documentation &amp; Training
<ul>
<li>Create and maintain process flow diagrams, work instructions, SOPs, validation protocols, and project documentation.</li>
<li>Lead operator training and knowledge transfer for new or revised manufacturing processes.</li>
<li>Ensure all documentation meets regulatory, customer, and quality system requirements.</li>
</ul>
Compliance &amp; Validation
<ul>
<li>Develop and execute process validation protocols (IQ/OQ/PQ) in alignment with FDA, ISO 13485, GMP, and internal quality standards.</li>
<li>Ensure all processes and equipment are audit-ready and meet regulatory compliance requirements.</li>
</ul>
Cross-Functional Collaboration
<ul>
<li>Partner with Program Management, Quality, Operations, Supply Chain, and Tooling to ensure smooth product launches, equipment transfers, and process readiness.</li>
<li>Collaborate during design reviews, DFM assessments, and risk analyses.</li>
<li>Support customer communications and technical discussions related to manufacturability, validation, and production readiness.</li>
</ul>
Continuous Improvement
<ul>
<li>Drive Kaizen and Lean initiatives, leading root cause investigations and implementing sustainable Corrective and Preventive Actions (CAPA).</li>
<li>Utilize statistical tools and data-driven decision-making to improve process capability, reduce scrap, and enhance efficiency.</li>
<li>Contribute to a culture of accountability, problem-solving, and innovation across the manufacturing floor.</li>
</ul>
Qualifications
Education
<ul>
<li>Bachelor's degree in Manufacturing, Mechanical, Industrial, or related Engineering discipline.</li>
</ul>
Experience
<ul>
<li>3-7 years in manufacturing engineering, process development, or project engineering in medical device, injection molding, or other regulated industries.</li>
<li>Demonstrated experience in NPI, equipment/machine transfers, process validation, and cleanroom/facility projects.</li>
</ul>
Technical Proficiency
<ul>
<li>Strong understanding of injection molding processes, mold qualification, and downstream assembly operations.</li>
<li>Hands-on experience with tooling design, equipment procurement, machine setup, and transfers.</li>
<li>Proficient in process validation methodologies (IQ/OQ/PQ) and statistical analysis tools (e.g., Minitab, GainSeeker).</li>
<li>CAD experience required; simulation tools a plus.</li>
<li>In-depth knowledge of ISO 13485, ISO 9001, FDA, GMP, and medical device standards.</li>
</ul>
Soft Skills
<ul>
<li>Strong project management and organizational abilities.</li>
<li>Excellent problem-solving and analytical thinking.</li>
<li>Effective communicator across functions and levels; customer-facing experience a plus.</li>
<li>High sense of urgency, ownership, and adaptability in fast-paced environments.</li>
</ul>
Work Environment &amp; Physical Requirements
<ul>
<li>Work performed in both office, production, and cleanroom environments.</li>
<li>Must be able to stand, walk, and interact with manufacturing equipment daily.</li>
<li>Ability to lift up to 25 lbs.</li>
<li>Must adhere to cleanroom and safety protocols.</li>
<li>Travel: up to 30% domestic for equipment transfers, validations, and site support.</li>
</ul>

Manufacturing Engineer

<h3>Job Description</h3>
Job Description
Aptyx Torrington is seeking a hands-on, results-driven Quality Engineer to support medical plastic injection molding and assembly operations. This role is responsible for ensuring the quality, validation, and regulatory compliance of new and existing medical products, processes, and equipment.
The position also serves as the Cleanroom Subject Matter Expert (SME), supporting cleanroom build-outs, environmental monitoring, and adherence to contamination control standards. The ideal candidate will have experience in process validation, NPI, product/equipment transfers, and cleanroom operations within a regulated medical device environment.
Key Responsibilities
Quality Engineering &amp; Assurance
<ul>
<li>Develop, implement, and maintain quality assurance practices, policies, and documentation, including Control Plans, pFMEAs, Inspection Plans, SOPs, and Validation Reports.</li>
<li>Conduct audits of raw materials, in-process components, and finished goods to ensure compliance with quality standards.</li>
<li>Schedule and coordinate inspection and quality resources to support projects, NPI, and validation activities.</li>
</ul>
Process Validation &amp; Product/Equipment Transfer
<ul>
<li>Lead and execute process and equipment validations (IQ/OQ/PQ) for new, transferred, or modified products, molds, and manufacturing equipment.</li>
<li>Support machine, mold, and product transfers between lines or facilities, ensuring validation scope, documentation, and regulatory compliance.</li>
<li>Coordinate validation testing, data collection, statistical analysis, and final reporting.</li>
<li>Partner with Manufacturing, Engineering, Tooling, and Program Management to ensure production readiness and long-term process capability.</li>
</ul>
Cleanroom SME &amp; Environmental Compliance
<ul>
<li>Serve as Cleanroom Subject Matter Expert (SME) for quality, compliance, and regulatory requirements.</li>
<li>Support cleanroom design, build-out, and qualification, ensuring alignment with product and process requirements.</li>
<li>Lead cleanroom qualification and requalification activities (IQ/OQ/PQ) and establish environmental monitoring programs (particulates, temperature, humidity, differential pressure).</li>
<li>Review and trend environmental monitoring data; initiate investigations and CAPAs as needed.</li>
<li>Develop and maintain cleanroom documentation, including SOPs, gowning procedures, monitoring plans, and risk assessments.</li>
<li>Provide training on cleanroom behavior, contamination control, and gowning procedures to operators and staff.</li>
</ul>
Regulatory Compliance &amp; Audits
<ul>
<li>Ensure compliance with ISO 13485, FDA 21 CFR Part 820, GMP, and customer-specific requirements.</li>
<li>Support internal, customer, and regulatory audits, maintaining traceable documentation for product launches and equipment integration.</li>
<li>Participate in drawing reviews, DFM assessments, and design transfer to ensure quality requirements are achievable and measurable.</li>
</ul>
Problem Solving &amp; Continuous Improvement
<ul>
<li>Lead root cause investigations, CAPAs, and nonconformance resolution related to processes, products, and validation activities.</li>
<li>Monitor production processes and quality data to identify trends and improvement opportunities.</li>
<li>Drive continuous improvement initiatives to enhance process capability, product quality, and QMS effectiveness.</li>
<li>Review process and product changes for potential QMS and validation impact.</li>
</ul>
Supplier &amp; Customer Quality Support
<ul>
<li>Support supplier qualification, audits, performance monitoring, and corrective actions.</li>
<li>Participate in new supplier evaluations and maintain the Approved Supplier List (ASL).</li>
<li>Manage customer quality interactions including complaints, RMAs, corrective actions, and routine status updates.</li>
</ul>
Cross-Functional Collaboration &amp; Training
<ul>
<li>Collaborate with Manufacturing Project Engineers and cross-functional teams to ensure seamless execution of product and equipment transfers.</li>
<li>Provide quality input during design reviews, process development, and risk assessments.</li>
<li>Mentor junior quality engineers and technicians, and support operator training on quality and validated processes.</li>
</ul>
 
Qualifications
Education
<ul>
<li>Bachelor's degree in Engineering (Mechanical, Industrial, Plastics, or related discipline).</li>
</ul>
Experience
<ul>
<li>3-5+ years of experience in Quality Engineering within medical device manufacturing, preferably injection molding, NPI, and equipment integration.</li>
<li>Experience supporting regulated environments, cleanroom operations, and process validation.</li>
</ul>
Knowledge &amp; Skills
<ul>
<li>Strong understanding of process validation (IQ/OQ/PQ), risk management, and design transfer requirements.</li>
<li>Familiarity with ISO 13485, FDA QSR, GMP, and other medical device standards.</li>
<li>Knowledge of statistical tools (SPC, MSA, DOE) and quality management systems.</li>
<li>Experience with injection molding processes and equipment.</li>
<li>Excellent documentation, technical writing, analytical, and project coordination skills.</li>
<li>Strong verbal and written communication to collaborate across functions.</li>
</ul>
Certifications (Preferred)
<ul>
<li>ASQ Certified Quality Engineer (CQE) or equivalent.</li>
<li>Cleanroom or contamination control training/certifications are a plus.</li>
</ul>
Work Environment &amp; Physical Requirements
<ul>
<li>Combination of office and manufacturing floor environment.</li>
<li>Exposure to machinery noise, moderate heat, and typical plant conditions.</li>
<li>Ability to stand or walk for extended periods; occasional lifting up to 25 lbs.</li>
<li>Fast-paced, deadline-driven, collaborative environment.</li>
<li>Up to 30% domestic travel for equipment integration, validation, or supplier support.</li>
<li>Flexible hours may be required during validation execution, launches, or critical project phases.</li>
</ul>

7,762 Manufacturing Jobs in Pickens County