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<h3>Job Description</h3>
Job Description
As a global organization, PharmEng Technology has been providing quality services to leading manufacturers of the Pharmaceutical and Biotech industries since 1997. Our employees come from diverse backgrounds where we value unique talents and work together to support our clients. In addition, our consultants have extensive experience obtained from world-class organizations across the globe, and the development of our staff continues to grow PharmEng Technology.
We are seeking an experienced Validation Engineer in Dorado, Puerto Rico. 
Objectives of this Role:
<ul>
<li>Write and execute, Installation Qualification (IQ), and Operational Qualification (OQ) protocols and Summary Reports including thorough resolution of protocol discrepancies.</li>
<li>Assess potential sources of variation in materials, processes, facilities, equipment, products, and packaging processes that may impact consistent performance or product quality; where needed, design studies to characterize impact of identified sources.</li>
<li>Maintain an up-to-date knowledge of validation requirements, practices, and procedures.</li>
<li>Interpret existing Validation Plans and Project Plans and apply concepts to the task at hand.</li>
<li>Working with a team to ensure all aspects of activity within the Process Development and Validation group adhere to required policies and procedures, including safety and training.</li>
<li>Investigate/troubleshoot validation problems, as well as, conduct some statistical analysis of testing results.</li>
</ul>
Skills and Qualifications:
<ul>
<li>• More than 5 years of experience in the industry (preferably with experience in medical devices). • Experience executing semi-automatic equipment validations (Debug, IQ/SQ, Process Characterization, OQ/PQ, etc.). </li>
<li>• Technical knowledge.</li>
<li> • Knowledge of software and/or PLC is an advantage.</li>
<li> • The candidate must be committed to the project and work in person daily. Distance should not represent a risk of abandoning the project early.</li>
<li> • Willing to work overtime or weekends if necessary. </li>
</ul>
Our Benefits:
<ul>
<li>Health, Dental, and Vision Insurance Benefits</li>
<li>Training Opportunities and Career Development</li>
<li>401k plan with Employer Contributions</li>
</ul>
PharmEng Technology is committed to attracting and retaining world-class employees valued for their contributions to achieving business objectives. PharmEng offers continuous career growth, competitive wages, travel opportunities, a team mentality that sets us apart from our competitors, and more!

Validation Engineer

<h3>Job Description</h3>
Job Description
Electromechanical Technician - 1st Shift
Golding is growing! As we continue to expand to meet increasing demand, we’re looking to add talented Electromechanical Technicians to our team. This is an exciting time to join us, with new opportunities emerging across our operations. Currently, we operate on a 5-day schedule; however, please note that a transition to a new schedule format is planned for the 4th quarter to better support our growth and production needs. Under consideration is a standard 2-2-3, 12-hour schedule that will support 24/7 coverage. If you're looking for a stable, forward-moving company where your skills are valued, we’d love to hear from you.
Job Description
Summary: The Electromechanical Technician is responsible for repairing and adjusting equipment as needed to ensure it operates according to manufacturer’s specifications and production requirements. Starting pay is $27+ per hour but may be higher depending on experience.
Primary Tasks/Responsibilities:
<ul>
<li>Services, repairs, adjusts and test various machinery, devices, and equipment related to the manufacturing process.</li>
<li>Ability to learn production equipment processes and operations to aid in machine troubleshooting and operation support.</li>
<li>Perform and document preventative maintenance tasks as necessary.</li>
<li>Timely, effective troubleshooting.</li>
<li>Demonstrate knowledge of minor electrical repairs and troubleshooting on motors, VFDs, PLCs, high and low voltage applications.</li>
<li>Safely work inside electrical panels and understand the function of all components inside.</li>
<li>Read and understand wiring schematics and machine manuals.</li>
<li>Troubleshoot safety switches and safety circuitry.</li>
<li>Welding, use of acetylene torch.</li>
<li>Use of pneumatic controls.</li>
<li>Perform work on hydraulic equipment.</li>
<li>Perform regular maintenance on gear boxes and conveyors.</li>
<li>Maintain a clean, sanitary, and safe work area.</li>
<li>Follow all Good Manufacturing Practices and Standard Operating Procedures.</li>
<li>Adhere to all safety and security policies and procedures.</li>
<li>Follow all food safety and quality system requirements by committing to meet all pertinent regulatory, customer and Safe Quality Foods (SQF) requirements.</li>
</ul>
Qualifications/Knowledge:
<ul>
<li>High School Diploma or GED required; Associate degree preferred</li>
<li>5 years experience as maintenance technician in a manufacturing environment required.</li>
<li>5+ years maintenance experience in manufacturing preferred; automated equipment experience a plus</li>
<li>Skilled in installing and maintaining pumps, bearings, pulleys, belts, chains, gearboxes, bushings, etc.</li>
<li>Proficient with automation, production, and computer systems</li>
<li>Strong attention to detail</li>
<li>Clear communicator with technicians, operators, managers, and plant leadership</li>
<li>Able to work independently or in teams; communicates effectively via radio, phone, and in person</li>
</ul>

Other Skills and relevant considerations:
<ul>
<li>Ability to work well with others in fast paced, dynamic environment.</li>
<li>Ability to be respectful, approachable and team oriented while building strong working relationships and a positive work environment.</li>
<li>Must be able to read, write, perform basic mathematical calculations, and accurately record data required.</li>
<li>Must be willing to work weekends, holidays, and varying shifts, as required.</li>
<li>Must be able to frequently stand, walk, kneel, reach, climb, pull, and bend with full range of body motion. </li>
<li>Must be able to work independently and/or on a team in a fast-paced environment.</li>
<li>Must be able to work in a wet and/or humid environment. Occasional exposure to fumes or airborne particles; toxic or caustic chemicals will occur. Exposure to nut allergens.</li>
</ul>
Physical Requirements / Other Pertinent Job Information:
<ul>
<li>May work 12-hour shifts on a fixed schedule rotation, including holidays</li>
<li>Must lift up to 50 lbs.; requires walking, bending, squatting, and climbing ladders/stairs</li>
</ul>
 Currently: 7:00 Am - 3:30 PM Please note that in the 4th Quarter we will be transitioning to a 2-2-3, 12 hour schedule.

Electromechanical Technician

<h3>Job Description</h3>
Job Description
At Cadence, we improve product performance by building solution-oriented partnerships with our customers and delivering highly technical, measurable outcomes across medical, life sciences, automotive, and other advanced industries.
We’re an engineering company at heart—with over 75 engineers across our organization—and have built a legacy of over three decades of manufacturing excellence by doing what others consider impossible.
Position Overview: We are seeking a highly motivated Validation Engineer onsite at Cranberry Twp., Sturgeon, WI or Cranston, RI sites, to lead and support validation activities across multiple projects at our facility. This role is critical in ensuring compliance with regulatory standards (FDA, ISO 13485, 21 CFR Part 820), working closely with engineering, QA, and manufacturing teams. 
Key Responsibilities:
<ul>
<li>Develop and execute validation protocols. (IQ, OQ, PQ, TMV)</li>
<li>Maintain detailed validation documentation. (VMPs, reports, SOPs)</li>
<li>Conduct risk assessments and manage change controls.</li>
<li>Ensure regulatory compliance. (GMP, GLP, CSV, data integrity)</li>
<li>Collaborate cross-functionally to support validation strategy and training.</li>
<li>Monitor system performance and lead requalification activities.</li>
<li>Qualify suppliers and vendors.</li>
<li>Contribute to process improvements and continuous improvement initiatives.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s in Engineering, Life Sciences, or related field.</li>
<li>3+ years' experience in validation or quality in a regulated industry.</li>
<li>Knowledge of FDA, ISO 13485, 21 CFR Part 820 standards.</li>
<li>Proficiency in Microsoft Suite; experience with validation software.</li>
<li>Strong communication, documentation, and analytical skills.</li>
<li>Preferred: Lean/Six Sigma certification; experience with LMS systems.</li>
</ul>
Work Environment: Split between office and production floor. Requires clear communication, computer use, and occasional physical movement around facility.
We are not offering sponsorship at this time for this position.

<h3>Job Description</h3>
Job Description
ABOUT INSPIRE MEDICAL SYSTEMS
Inspire is the first of its kind medical device designed to make a difference in the lives of those living with Obstructive Sleep Apnea (OSA). We are revolutionizing the sleep industry with our FDA-approved medical device, designed to reduce OSA severity for those who cannot tolerate or get consistent benefit from CPAP. Inspire Medical Systems is committed to enhancing patients' lives through sleep innovation. We are steadfast in our commitment to prioritize patient outcomes, act with integrity and lead with respect. With positive persistence at our core, we are committed to all those we serve.
WHY JOIN OUR FAST-GROWING TEAM
At Inspire, we value people – your diverse experiences, backgrounds, and thoughts. We elevate voices and encourage learning opportunities to build a professional network that grows into community. We embrace a people-first culture by offering excellent benefits, 401k matching, ESPP, flexible time off (FTO), and tuition reimbursement. 
If you're passionate about making a difference in people's lives and want to work with innovative technology, come be a part of our great team! 
ABOUT THIS POSITION 
This position must provide expertise and leadership in the areas of finished medical device manufacturing, product inspection/test, manufacturing process monitoring and control implementation, sterilization, labeling, supplier development, audit and supplier management. This person is responsible for performing tasks that will assure a high level of product reliability along with regulatory compliance. This position will work with Development, Operations, Manufacturing, Regulatory and other Quality functional areas to ensure work is completed in accordance with Inspire procedures and geographic regulations. In addition, this role must be flexible for changing priorities and able to work without direct supervision. 
OPPORTUNITIES YOU WILL HAVE IN THIS ROLE 
<ul>
<li>Partner with Inspire manufacturing team to lead/support quality engineering activities with contract manufacturers (e.g., IQ, OQ and PQ support, non-conformance resolution, temporary authorities, labeling validations, and deviations, etc.)</li>
<li>Manage non-conformance, deviation, and temporary authorization processes for both contract manufacturers and Inspire. </li>
<li>Manage, lead, and coach cross-functional teams with contract manufacturers to resolve quality issues and navigate the CAPA process. </li>
<li>Coach Inspire personnel and contract manufacturers on GMP and QMS requirements for medical device manufacturers. </li>
<li>Conduct first article inspections (FAIs) on finished medical products. </li>
<li>Provide expertise on finished device specifications as well as generating and approving ECOs.</li>
<li>Generate and approve design history file documents, device master record documents and supplier change request records.</li>
<li>Lead IP development processes for warehouse inspections of new products and revise existing IPs for contract manufacturers as needed.</li>
<li>Lead contract manufacturer (supplier) audits.</li>
<li>Support manufacturing risk management activities (i.e., pFMEAs) at suppliers.</li>
<li>Lead special projects (e.g., dual sourcing, metrics, etc.) along with supplier product improvement processes at the direction of quality management. </li>
<li>Participate in product performance reviews and emerging quality reviews; support any resulting corrective/preventive actions.</li>
<li>Support QMS audits with both internal and external auditors.</li>
<li>Ability to work efficiently and effectively in both a paper-based and electronic QMS.</li>
<li>Recommend process improvements, driving both efficiency and compliance.</li>
</ul>
Required Qualifications
<ul>
<li>Bachelor's degree in a technical or scientific field, preferably an engineering discipline</li>
</ul>
<ul>
<li>5 years minimum experience in medical device </li>
<li>5 years minimum experience in a product, manufacturing quality (process), material or component quality engineering position</li>
<li>Knowledge of ISO and FDA Quality System Requirements (e.g., ISO 13485; FDA 21 CFR Part 820)</li>
<li>Demonstrated team leadership skills and ability to prioritize, execute and report on projects</li>
<li>Experience with engineering tools such as; dFMEA, pFMEA, SPC, etc.</li>
<li>Working knowledge of process improvement techniques such as Six Sigma, Lean Sigma, Proof of Station, etc.</li>
<li>Strong project and time management skills</li>
<li>Demonstrated creative and effective problem solving and original thinking for compliance solutions</li>
<li>Ability to work on multiple tasks concurrently with changing priorities</li>
<li>Proficient with of MS Word, Excel and PowerPoint</li>
</ul>
Preferred Qualifications
<ul>
<li>Master's degree in a technical or scientific field</li>
</ul>
<ul>
<li>Experience in component, manufacturing quality (process) and product quality assurance functions</li>
<li>Experience in design assurance or quality systems functions.</li>
<li>Experience with 21 CFR 820, ISO 13485, ISO 14971, European Directives and European Regulations</li>
<li>Experience with SPC software tools</li>
<li>Experience with engineering tools such as; DOE, FTA, GHTF requirements for process validations, etc.</li>
<li>ISO 13485 certified auditor or RAB auditor</li>
<li>ASQ certifications; CRE, CQM, CQE, CQA etc.</li>
<li>ISO 14971 training</li>
</ul>
#LI-Onsite
The salary for this position will be offered at a level consistent with the experience and qualifications of the candidate. This information reflects the anticipated salary range for this position at the time of posting. The salary range may be modified in the future and actual compensation may vary from the posting based on various factors such as geographic location, work experience, education and/or skill level.
Salary$105,000—$157,600 USD
BENEFITS AND OTHER COMPENSATION
Inspire offers a highly competitive benefits package including (general description of the benefits and other compensation offered):
<ul>
<li>Multiple health insurance plan options.</li>
<li>Employer contributions to Health Savings Account.</li>
<li>Dental, Vision, Life and Disability benefits.</li>
<li>401k plan + employer match.</li>
<li>Identity Protection.</li>
<li>Flexible time off.</li>
<li>Tuition Reimbursement.</li>
<li>Employee Assistance program.</li>
<li>All employees have the opportunity to participate in the ownership and success of Inspire. Employees at all levels can participate through equity awards and the Employee Stock Purchase Program.</li>
</ul>
Inspire Medical Systems provides equal employment opportunity (EEO) to all employees and applicants without regard to race, color, religion, creed, sex, national origin, age, disability, marital status, familial status, sexual orientation, status regarding public assistance, membership or activity in a local commission, military or veteran status, genetic information, pregnancy or childbirth, or any other status protected by applicable federal, state, and local laws. This policy applies to all aspects of the employment relationship, including recruitment, hiring, compensation, promotion, transfer, disciplinary action, layoff, return from layoff, training, and social and recreational programs. Inspire Medical Systems complies with applicable laws governing non-discrimination in employment in every location in which Inspire Medical Systems has facilities. All such employment decisions will be made without unlawfully discriminating on any prohibited basis. Inspire Medical Systems is an equal opportunity employer with recruitment efforts focused on ensuring a diverse workforce. Applicants with a disability that need accommodation to complete the Inspire Medical Systems application process should contact Human Resources at 844-672-4357 or email careers@inspiresleep(dot)com Inspire Medical Systems participates in E-Verify.

Sr Product Quality Engineer

<h3>Job Description</h3>
Job DescriptionSuperior Skilled Trades is seeking Shop Welders/Fabricators for an immediate start in New Britain, PA! WEEKLY PAY -- LONG TERM &amp; FULL TIME! 
<ul>
<li>PAY: $23-$26/hour (based upon experience)</li>
<li>HOURS: Shifts will be 8-hour workdays, 5 days per week (40 hours/week)</li>
<li>SCHEDULE: Workdays will be Monday-Friday; 6:00am – 3:00pm</li>
<li>START DATE: ASAP</li>
<li>DURATION: Temp-to-Hire</li>
</ul>
 Job Description:We are seeking a skilled and detail-oriented Shop Welder/Fabricator to join our manufacturing team. In this role, you will be responsible for the fabrication and operational testing of custom equipment and machines. You will work with a variety of tools, machinery, and welding processes to produce high-quality components that meet engineering specifications. This position requires strong mechanical aptitude, the ability to read blueprints, and a commitment to precision and safety. Key Responsibilities:
<ul>
<li>Fabricate and perform operational testing of machines and equipment</li>
<li>Operate tools and machinery including grinders, band saws, plasma cutters, mag drills, hand drills, levels, squares, welders, shearing machines, and sheet metal break machines</li>
<li>Perform tasks from blueprints and drawings, such as drilling, tapping, and welding</li>
<li>Repair and retrofit used equipment according to engineering specifications</li>
<li>Apply paint using rollers and spray guns as needed</li>
<li>Operate lift equipment and perform rigging tasks when required</li>
<li>Maintain a safe and organized work environment, following all safety procedures</li>
<li>Perform other duties as assigned to support shop operations</li>
</ul>
 Requirements:
<ul>
<li>Mechanical aptitude and problem-solving skills</li>
<li>Ability to read and work from blueprints and technical drawings</li>
<li>Knowledge of MIG and TIG welding setup and operation</li>
<li>Experience using hand tools, measuring devices, and machine shop equipment</li>
<li>Strong mathematical skills for precise measurements and layout</li>
<li>Ability to work independently and as part of a team</li>
<li>Capable of managing multiple tasks and meeting deadlines</li>
<li>Able to stand for extended periods and lift a minimum of 50 lbs without assistance</li>
<li>Willingness to obtain welding certification if required</li>
<li>Clear verbal and written communication skills in English</li>
</ul>
 Preferred Education &amp; Experience:
<ul>
<li>High school diploma or equivalent</li>
<li>3–5 years of machine fabrication experience or equivalent combination of education and experience</li>
<li>Experience working with sheet metal</li>
<li>Welding certification preferred</li>
</ul>
 Additional Requirements:
<ul>
<li>Must be eligible to work in the United States</li>
<li>Must have reliable transportation to the job site</li>
<li>Pre-employment drug screen and background check are required</li>
</ul>
 WE ARE AN EQUAL OPPORTUNITY EMPLOYER!

Shop Welder

<h3>Job Description</h3>
Job Description🚀 We're Hiring: Production Control Coordinator
📍Midland, Texas| Contract-to-Hire | Climate-Controlled Production Environment
Are you detail-oriented, organized, and passionate about keeping production running smoothly? Join our team as a Production Control Coordinator and play a key role in ensuring our manufacturing operations stay efficient, timely, and well-supported.
🔧What You'll Do
As a Production Control Coordinator, you’ll be the backbone of our production process—ensuring materials, work orders, and equipment are where they need to be, when they need to be there. Your responsibilities will include:
<ul>
<li>Coordinating daily manufacturing activities to meet production goals</li>
<li>Collaborating with management to align schedules and priorities</li>
<li>Creating and managing work orders</li>
<li>Delivering equipment to designated departments</li>
<li>Entering and maintaining accurate data for supervisor access</li>
<li>Supporting smooth and efficient production flow</li>
</ul>
🧠What You Bring
<ul>
<li>Strong experince in inventory management and production coordination</li>
<li>Advanced Excel skills and order entry experience</li>
<li>Familiarity with supply chain processes and the ability to expedite materials</li>
<li>Preferred experience with ERP systems like SAP, NetSuite, QAD, JDE, or MES</li>
<li>High school diploma or GED - must show upon offer</li>
<li>Successful completion of an Excel proficiency test</li>
</ul>
💡Why You'll Love Working Here
<ul>
<li>Monthly stipend offered upon transition to direct employment</li>
<li>A company culture focused on efficiency, productivity, and growth</li>
<li>A dynamic, active work environment where you're on your feet and engaged</li>
<li>Climate-controlled facility for year-round comfort</li>
</ul>
Ready to take the next step in your career? Apply now and help us build something great—one product at a time.
 Pay and Benefits
The pay range for this position is $22.00 - $26.40/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Midland,TX.
Application Deadline
This position is anticipated to close on Aug 22, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Production Control Coordinator - APPLY SOON

<h3>Job Description</h3>
Job Description
Position Summary:
We are seeking a CAPA Engineer (Technical Writer) to support our Quality Control Department, with a focus on the Corrective and Preventive Action (CAPA) process. The selected candidate will manage all phases of the CAPA lifecycle—including initiation, investigation, implementation, and closure—in alignment with FDA, ISO, and global regulatory standards. This role requires collaboration with cross-functional teams to address deviations, non-conformances, and audit findings using a structured, traceable, and well-documented approach. Strong technical writing skills and a solid understanding of medical device regulatory requirements are essential.
Location: Eastern Region, Puerto Rico 

Key Responsibilities:

 CAPA Initiation &amp; Writing
<ul>
<li>Draft and initiate CAPAs per internal procedures and regulatory requirements</li>
<li>Define scope, issue, risk impact, and acceptance criteria</li>
</ul>

CAPA Investigation
<ul>
<li>Conduct root cause analyses using tools like 5 Whys, Fishbone, FMEA</li>
<li>Collect and document supporting evidence; conduct technical interviews</li>
</ul>

 Action Planning &amp; Implementation
<ul>
<li>Develop effective, timely action plans with responsible parties</li>
<li>Coordinate implementation across functions: engineering, validation, microbiology, etc.</li>
<li>Define and document effectiveness checks</li>
</ul>

CAPA Closure
<ul>
<li>Verify and document completion and effectiveness of actions</li>
<li>Ensure all documentation is audit-ready and compliant with QMS</li>
</ul>

Documentation &amp; Quality Systems
<ul>
<li>Use electronic CAPA platforms (Track Wise, Master Control, EtQ Reliance, etc.)</li>
<li>Ensure compliance with Good Documentation Practices (GDP)</li>
<li>Participate in CAPA boards and quality review meetings</li>
</ul>
Regulatory &amp; Technical Expertise:

<ul>
<li>Deep understanding of medical device regulations:
<ol>
<li>21 CFR Part 820, ISO 13485, ISO 14971, MDR 2017/745, ICH Q9/Q10</li>
</ol>
</li>
<li>Experience with FDA inspections and Notified Body audits</li>
<li>Strong grasp of CAPA systems and identifying systemic issues</li>
</ul>

Education &amp; Experience Requirements:
<ul>
<li>Bachelor’s degree in Electric Engineering or Mechanical Engineering is required. </li>
<li>3+ years of experience managing CAPAs in the medical device industry</li>
<li>Regulatory audit experience (FDA, ISO, EU)</li>
<li>Quality certifications (CQE, CAPA Specialist, Lean Six Sigma) – a plus</li>
</ul>

Technical &amp; Process Knowledge:
<ul>
<li>Familiarity with medical device manufacturing processes</li>
<li>Understanding of validation protocols (IQ, OQ, PQ)</li>
<li>Experience with statistical tools (e.g., Minitab, advanced Excel)</li>
</ul>

Key Skills &amp; Competencies:
<ul>
<li>Excellent technical writing in English and Spanish</li>
<li>High attention to detail with a strong compliance mindset</li>
<li>Strong communication and project coordination skills</li>
<li>Ability to manage multiple priorities under strict deadlines</li>
<li>Team-oriented with initiative and independence</li>
</ul>

Join us in contributing to the advancement of safe, effective medical devices by ensuring quality system integrity through expert CAPA process execution.

CAPA Engineer

<h3>Job Description</h3>
Job Description
Rockville Technology, LLC. is a family owned, fast-paced machining services and fabrication company focused on creation nonferrous machine parts primarily for the US Aerospace and Defense Industry. We're looking to bring on a Quality Engineer at our location in Vernon, CT. 
 
Why Work with Us: 
<ul>
<li>Competitive salary between $85,000-$135,000 depending on experience </li>
<li>A solid benefits package including Health &amp; Dental </li>
<li>401k Plan with 50% company match on your contributions up to 8% of your pay with no vesting period </li>
<li>Bonus Plan based on personal performance and annual profits </li>
<li>Paid Time Off and Sick Time </li>
<li>A clean working environment with a great company culture </li>
<li>Small company environment where you can have a significant impact on the future of the organization </li>
</ul>
 
 
The Position: 
This position will support Rockville’s quality system and customers. The Quality Engineer role is critical to Rockville’s business continuity and facilities routine customer audits, supports the maintenance of the quality system and the key licenses and certifications (NADCAP, ISO, AS9100) required to do business in aerospace and defense. The Quality Engineer works directly with customers understanding their specific quality requirements and ensuring delivery of the expected parts and accompanying documentation and quality data. This role must understand the critical customer needs and be able to communicate clearly through direct communication as well as completing any necessary supporting documentation and required notifications. 
 
In this role you will: 
 
<ul>
<li>Assist with performing and monitoring of internal audits </li>
<li>Generate, perform, and monitor supplier audits </li>
<li>Assist with customer quality audits and answer corrective action requests as assigned </li>
<li>Develop and Perform SPC </li>
<li>Oversee inspections and audits and Inspection Department as assigned by Quality Manager </li>
<li>Prepare First Article’s and Inspection methods sheets as assigned by Quality Manager </li>
<li>Investigate product quality problems and recommends changes or improvements </li>
<li>Work directly with customers, suppliers, and internal personnel to establish consistent inspection techniques and resolve issues </li>
<li>Assist with overseeing the companies Cause and Corrective Action and Preventive Action systems </li>
</ul>
 
 
About You: 
 
<ul>
<li>Degree in quality, industrial, mechanical engineering or equivalent </li>
<li>10+ years of experience in quality engineering, quality assurance, or a similar role </li>
<li>ASQ certification and ISO Internal Auditor certification preferred </li>
<li>Demonstrated execution of PPAP management </li>
<li>Experience coding and using QA software tools and processes </li>
<li>Strong communication, interpersonal, analytical, and problem-solving, and project management skills </li>
<li>Able to work efficiently in a team environment and maintain high confidentiality </li>
<li>Excellent organizational and time-management skills </li>
<li>Proficiency with Microsoft Office, particularly Excel </li>
<li>Must be a US Citizen. Must comply with EAR regulations and site SSA requirements. </li>
</ul>
 
 
If you’re a hard-working, team-oriented, and reliable individual who would like to join a stable and growing organization, we want to hear from you! Learn more about us at <a href="https://rockvilletechnology.com/" target="_blank">https://rockvilletechnology.com/</a>. 
 IND1

Quality Engineer

<h3>Job Description</h3>
Job DescriptionQuality Inspector - 2nd shift 
Responsibilities:
<ul>
<li>Read blueprints and drawings to understand specifications and tolerances for parts.</li>
<li>Inspect and measure machined component parts and incoming materials using hard gauges, hand tools, and other equipment to ensure compliance with specifications.</li>
<li>Perform inspections in receiving, in-process, and final stages.</li>
<li>Complete and submit required inspection documentation, labels, and electronic transactions.</li>
<li>Suggest improvements to inspection processes and methods.</li>
<li>Collaborate with cross-functional teams to communicate quality standards and expectations.</li>
<li>Assist in meeting goals related to quality, cost, and delivery.</li>
<li>Operate in compliance with safety and quality standards.</li>
<li>Uphold the organization's quality policy and commitment to customer satisfaction.</li>
<li>Perform other duties as required.</li>
</ul>
Qualifications:
<ul>
<li>Experience with inspection tools such as calipers, micrometers, and CMM.</li>
<li>Ability to read and interpret blueprints and technical drawings.</li>
<li>Strong attention to detail and problem-solving skills.</li>
<li>Excellent communication and teamwork abilities.</li>
<li>Commitment to safety and quality standards.</li>
</ul>
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Pay and Benefits
The pay range for this position is $52000.00 - $72800.00/yr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Maple Grove,MN.
Application Deadline
This position is anticipated to close on Aug 25, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Quality Inspector

<h3>Job Description</h3>
Job Description
Validation &amp; Engineering Group, Inc. (V&amp;EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
<ul>
<li>Validation Specialist</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's Degree in Engineering.</li>
<li>Minimum of 3 years of experience in direct pharmaceutical, medical device or biotechnology industries.</li>
<li>Experience in direct process / manufacturing areas.</li>
<li>Must be fully bilingual (English / Spanish) with excellent oral skills.</li>
<li>Must be proficient using MS Windows and Microsoft Office applications.</li>
<li>Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.</li>
<li>Experience in Design Documentation (URS, DS), IQ, OQ, PQ protocols development and execution, deviations and reports generation.</li>
<li>SDLC, Risk Assessment, Data Integrity, Factory Acceptance Test (FAT) &amp; Site Acceptance Test (SAT).</li>
<li>Strong knowledge in medical devices equipment preferred.</li>
<li>Technical Writing skills and investigations processes.</li>
<li>Available to work extended hours, possibility of weekends and holidays.</li>
</ul>

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