equipment validation engineer

Software Technology, Inc.

Position: Mechanical Validation Engineer
 
Location: Sunnyvale, CA (Onsite)
 
Exp: 4-10 years
 
What you will do: 
<ul>
<li>Develop and execute detailed mechanical validation test plans for wearables, covering different areas of lifecycle testing.</li>
<li>Define validation scope, objectives, and deliverables for each product phase (from prototype to production).</li>
<li>Set up and maintain test fixtures, equipment, and prototype devices for validation activities.</li>
<li>Work with design, hardware, and manufacturing teams to align on validation requirements and schedules.</li>
<li>Participate in design reviews, provide feedback on mechanical robustness, and suggest design improvements based on test results.</li>
<li>Collect, analyze, and interpret test data to identify failure modes and root causes.</li>
<li>Document and communicate test results, issues, and recommendations to stakeholders.</li>
<li>Maintain comprehensive validation documentation and dashboards (e.g., JIRA, Confluence).</li>
<li>Drive resolution of mechanical issues by collaborating with engineering teams during validation phases.</li>
<li>Proactively unblock teams and adjust focus areas to ensure timely issue closure.</li>
<li>Contribute to process improvements in validation methodologies, test automation, and lab infrastructure.</li>
<li>Stay updated on industry best practices and emerging technologies in mechanical validation for wearables.</li>
</ul>
What You Will Bring: 
<ul>
<li>Bachelor's degree in Mechanical Engineering or related field.</li>
<li>3+ years of hands-on experience in mechanical validation or testing, preferably in consumer electronics or wearables.</li>
<li>Strong knowledge of mechanical test methods (drop, shock, vibration, thermal, humidity, IP, etc.).</li>
<li>Experience with test equipment, data acquisition systems, and failure analysis.</li>
<li>Familiarity with product development cycles (proto to PVT) and cross-functional project execution.</li>
<li>Excellent communication, documentation, and stakeholder management skills.</li>
<li>Experience with risk management and process improvement.</li>
</ul>

Mechanical Validation Engineer - Sunnyvale, CA (Onsite)

Valeo

<div>
 
 He/She defines the product system test strategy based on Customer and Valeo standards specifications and risk analysis (PCA, PHA, DFMEA, Newness analysis).
 
 
 
 
 He/She analyzes system and functional requirements and defines test strategy allocation.
 
 
 
 
 He/she defines functional test plan. And support test bench, scripts specification, tools development required.
 
 
 
 
 Regarding requirements assigned to functional validation scope, he/she executes test cases script on the test bench with DUT.
 
 
 
 
 He/She extends test coverage with some robustness tests and end user test cases.
 
 
 
 
 He/She performs tests, and reports test case results.
 
 
 
 
 He/She secures that functional validation conditions &amp; planning feasibility are within project commitments :
 
 
 
 <ul>
 <li>
 Validation data (technical and system requirements, technical inputs for testing&hellip;) to be supplied by the product architect and metier design leaders
 </li>
 <li>
 Labs means availability (tests equipment, mission profiles, skills, suppliers)
 </li>
 <li>
 State with Validation Leader that test prerequisites checklist deliverables are ok regarding part level and functional features maturity required until SSSR.
 
 
 </li>
 </ul>
 
 
 Nota1 : prototypes, samples and pre-series parts procurements &amp; audit check + purchase admin are not managed by labs.
 
 
 
 
 
 
 Nota 2: Functional test benches setup are developed by Test Bench Engineer.
 
 
 
 
 
 He/she secures reports archiving in PLM.
 
 
 
 
 He/She reports issues at the first level of analysis and progress through SyVSR dashboard (KPIs).
 
 
 
 
 He/She reports project functional validation risks assessment to the Validation leader
 
 
 
 
 He/She contributes to Functional DR Validation metier checklist review
 
 
 
 
 He/She documents and updates IVV Plan &amp; Report
 
 
 
 
 Rights related to the employment relationship, which were defined, e.g. in:
 
 
 
 <ul>
 <li>
 The Labor Code,
 </li>
 <li>
 Work Regulations of VLS Chrzan&oacute;w,
 </li>
 <li>
 Remuneration Regulations of VLS Chrzan&oacute;w,
 </li>
 <li>
 Regulations of the Company Social Benefits Fund.
 
 
 </li>
 </ul>
 
 Regardless of the above rights, you have the right
 
 
 
 <ul>
 <li>
 resulting from the powers of attorney and authorizations held,
 </li>
 <li>
 processing of personal data to the extent and for the purpose necessary to perform official duties,
 </li>
 <li>
 refusal to carry out an official order, if this would lead to committing a crime, misdemeanor or risking
 </li>
 <li>
 irreparable losses.
 </li>
 <li>
 Each manager is empowered to contribute to reduce risks to prevent incidents and ergonomics issues into his/her job description.
 </li>
 <li>
 Knowledge and application of EMS policies, procedures and documentation
 </li>
 <li>
 Management of waste materials according to the principles set out in the Environmental Management Systems documentation.
 </li>
 <li>
 Ensuring the efficient use of equipment, materials, time, energy and other resources to optimize costs
 </li>
 <li>
 Education/Training
 </li>
 <ul>
 <li>
 Engineering Degree
 
 </li>
 </ul>
 </ul>
 
 
 Professional
 
 
 Experience
 
 
 
 
 
 Education: Master in engineering (System engineering, general technical engineering knowledge: embedded electronics, software, optical system, mechanics.
 
 
 
 
 Experience
 
 
 
 
 Qualification: First development experience in product/system integration/testing/validation
 
 
 
 
 knowledge: Diag On Can /UDS /Requirements management/Test cases script editing
 
 
 
 
 Confident with tools Doors - VtestStudio - Teststand - LabWindows/CVI..
 
 
 
 
 Confident with CAN / LIN network and associated tools (CANoe, CANdela..)
 
</div>

System Validation Engineer, LIGHT

Bristol Myers Squibb

<div>Working with Us 
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. 
 
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . 
 
PRINCIPAL OBJECTIVE OF THE POSITION:
 
 
The Senior Specialist, Validation Engineer II supports the successful implementation of manufacturing, and laboratory equipment alongside facilities and utilities at multi-use sites through interaction with internal customers and external service providers. The incumbent is tasked with qualifying new equipment, facilities, utilities and maintaining equipment systems in a qualified / validated state according to established policies and procedures. The individual participates in projects and ongoing work activities of low to moderate complexity. With minimum supervision and given general instructions, this individual carries out routine tasks and functions, and uses basic analytical skills to recognize and solve common problems of limited scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization. 
 
MAJOR DUTIES AND RESONSIBILITIES:
<ul><li>Develops and executes validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports</li><li>
Ensure periodic reviews and requalification is being performed in accordance with schedule.</li><li>
Supports equipment qualification and validation activities.</li><li>
Develops qualification protocols, and associated reports while adhering to a change management process.</li><li>
Author and review the Development/Review of SOPs, WPs, test protocols, validation deliverables, plans and policies as needed.</li><li>
Responsibilities include execution of validation lifecycle maintenance that includes establishment of validation document hierarchy, tracking execution work arising from change controls, shutdown/changeover management related to validation, and management of the revalidation and cleaning monitoring programs, if necessary.</li><li>
Execute work arising from change strategy, risk assessment, testing and compliance gaps.
</li><li>Executes portfolio of limited scope and complex validation projects under strict deadlines to ensure stakeholder success and bulk drug supply.</li><li>
Maintains familiarity on BMS directives and industry guidelines on qualification/validation.</li></ul>
Promotes and provides excellent customer service and support<ul><li>
Regularly reviews, prioritizes, and promptly responds to end user equipment qualification and support requests.</li><li>
Provides technical support and guidance on qualification and validations issues. Interfaces with customers to ensure all expectations are being met.</li><li>
Maintain a positive relationship with all team members and site customers while promoting a positive team environment.</li><li>
Contributes to multi-function teams, representing validation.</li></ul>
Regulatory Responsibilities<ul><li>
Ensure alignment with BMS directives and industry guidelines on validation and quality engineering.
</li><li>May be called upon as SME in both internal and regulatory audits.
</li><li>Responsible to contribute to the preparation for regulatory inspection readiness.
</li><li>Performs other duties as assigned.
</li></ul>KNOWLEDGE AND SKILL:
<ul><li>Familiarity of cGMP in the pharmaceutical industry.</li><li>
Direct experience with equipment, facility, sterilization commissioning and qualification, critical utilities validation, and temperature mapping concepts is preferred.</li><li>
Knowledge of distributed control systems and automation (GAMP) validation concepts suggested.</li><li>
Knowledge in designing and implementing quality systems and validation program elements required to manage the validation lifecycle of a fully automated, multi-product, biologics / cell therapy manufacturing facility.</li><li>
Familiarity of regulatory validation requirements including FDA, EMA and all other Worldwide Regulatory requirements (ICH Q7, Q8, and Q9) particularly as it applies to biologics / cell therapy manufacturing.</li><li>
A working understanding of lean principles and six sigma process is preferred.</li><li>
Demonstrated high proficiency in project management, communication, and technical writing skills suggested.</li><li>
Experienced self-motivated individual who can handle multiple priorities to meet project team goals and timelines.</li><li>
Understands business needs and synthesizes solutions across functions.</li><li>
The successful candidate will possess the professionalism and technical competency required to represent the department before our customers, regulatory agencies, and management.</li><li>
Ability to handle difficult and unusual tasks, often using creative problem-solving.</li><li>
Working knowledge of SOPs, cGMPs and compliance requirements and regulatory guidelines (FDA, EU) and the general understanding to work within a regulatory environment. Knowledge must be demonstrated through previous projects of establishing validation philosophies and regulations at a site level.</li><li>
Must have strong interpersonal and communication skills, be a team player and be willing to work in an environment where individual initiative, accountability to the team, and professional maturity are required.Strong level of problem-solving skills, verbal and written communication skills, and the ability to work independently.</li><li>
Understanding of investigations, deviations and CAPA management in a regulated pharmaceutical industry.
</li></ul>QUALIFICATIONS:
<ul><li>Knowledge of engineering generally attained through studies resulting in a Bachelor of Science degree in Chemical Engineering, Mechanical Engineering, related discipline, or its equivalent is required.</li><li>
A minimum of 3+ years relevant experience with process equipment, computer systems, manufacturing process control systems (automation) and laboratory instrumentation in an FDA regulated manufacturing facility.</li><li>
Minimum of 2+ years' experience in equipment, facility, or utility qualification.</li></ul>
If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
 
 
Compensation Overview: 
 
Devens - MA - US: $92,540 - $112,136 
 
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
 
 
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
 
 
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
<ul><li>Health Coverage: Medical, pharmacy, dental, and vision care.</li><li>
Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
</li><li>Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.
</li></ul>Work-life benefits include:
 
 
Paid Time Off
<ul><li>US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
</li><li>Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays
</li></ul>Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
 
 
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. 
 
<ul><li>Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
</li></ul> 
Uniquely Interesting Work, Life-changing Careers 
With a single vision as inspiring as Transforming patients' lives through science&trade; , every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. 
 
On-site Protocol 
 
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
 
 
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
 
 
Supporting People with Disabilities 
 
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com . Visit careers.bms.com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.
 
 
Candidate Rights 
 
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
 
 
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
 
 
Data Protection 
 
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection . 
 
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. 
 
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com . Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
 
 
R1601122 : Senior Specialist, Validation Engineer II</div>

Senior Specialist, Validation Engineer II

Lennox International

<div><div>Lennox (NYSE: LII) Driven by 130 years of legacy, HVAC and refrigeration success, Lennox provides our residential and commercial customers with industry-leading climate-control solutions. At Lennox, we win as a team, aiming for excellence and delivering innovative, sustainable products and services. Our culture guides us and creates a workplace where all employees feel heard and welcomed. Lennox is a global community that values each team member&rsquo;s contributions and offers a supportive environment for career development. Come, stay, and grow with us.</div> 
Innovate your career. 
When you choose Lennox, you're getting the best. 
When you work at Lennox, you&rsquo;re among the best.
Lennox is seeking a highly skilled and experienced Software Systems Validation Engineer to join our team in Carrollton, TX. This role focuses on the validation of embedded controllers that power innovative HVAC solutions for commercial applications. 
As a key member of the validation team, the selected candidate will be responsible for ensuring the quality, reliability, and robustness of embedded HVAC controller systems. The role involves validating complex system interactions across hardware, firmware, and communication layers. It requires a proactive, hands-on engineer with the ability to thrive in fast-paced environments, adapt to dynamic project requirements, and deliver results under constrained timelines. 
DUTIES INCLUDE BUT ARE NOT LIMITED TO: 
<ul><li>
Design and develop comprehensive validation strategies tailored for embedded controllers in the HVAC domain.</li><li>
Create and maintain test deliverables, including:
</li><li><ul><li>Test plans aligned with project requirements and functional specifications.</li><li>
Test content such as manual and automated test cases for validating system functionality, performance, and reliability.</li><li>
Test execution schedules, ensuring all test activities are performed on time.</li><li>
Bug reports with detailed root cause analysis and actionable feedback for development teams.</li><li>
Test reports summarizing results, coverage, and overall system quality.</li></ul></li><li>
Execute validation activities across all stages of the Software Testing Life Cycle (STLC), ensuring system compliance with functional, performance, and reliability requirements.</li><li>
Collaborate with cross-functional teams, including software developers, system architects, hardware engineers, and product managers, to define test requirements, align on deliverables, and resolve issues.</li><li>
Develop and maintain automated test solutions to enhance coverage, efficiency, and repeatability of validation processes.</li><li>
Debug and troubleshoot complex interactions between hardware and software, utilizing tools like oscilloscopes, logic analyzers, and protocol analyzers.</li><li>
Contribute to continuous improvement efforts in validation methodologies, tools, and processes to elevate quality standards.</li><li>
Ensure alignment with project schedules, consistently meeting deadlines with minimal supervision while maintaining high-quality standards.</li></ul><div>
#LI-onsite #LI-JM1</div> 
Required:<ul><li>
Bachelor&rsquo;s or Master&rsquo;s degree in Electronics Engineering, Computer Science, or a related field.</li><li>
Minimum 5 years of professional experience in system-level validation, ideally in embedded systems.</li><li>
Strong understanding of embedded systems, including microcontrollers, real-time operating systems (RTOS), and firmware development.</li><li>
Proficiency in debugging and troubleshooting hardware/software interfaces.</li><li>
Expertise in validation tools, automation frameworks, and scripting languages (Python preferred).</li><li>
Familiarity with communication protocols such as UART, I2C, SPI, CAN, BLE.</li></ul>
Preferred:<ul><li>
Familiarity with programming languages such as C, C++, C#, and scripting languages like Python, bash, Rust.</li><li>
Experience validating systems in industries such as HVAC, automotive, aerospace, medical, industrial controls, or related fields.</li><li>
Hands-on experience with test management tools, Azure DevOps preferred.</li><li>
Expertise with Version control tools, preferably Git, and knowledge of CI/CD pipelines for continuous integration and deployment is a plus.</li></ul>
Soft Skills and Working Style:<ul><li>
Capable of working independently with minimal supervision, taking initiative to identify and address challenges.</li><li>
Thrives in fast-paced environments with tight deadlines and evolving project priorities.</li><li>
Flexible and adaptable to last-minute changes in project scope or timelines.</li><li>
Strong problem-solving skills with a methodical approach to debugging and root cause analysis.</li><li>
Excellent communication and collaboration skills, able to convey complex technical concepts to diverse audiences.</li><li>
Passionate about innovation and continuous improvement, contributing creative ideas to improve validation processes.</li></ul></div>

Controls Software Validation Engineer

CSI Global

<div><h1 class="jobSectionHeader">Job Title: Commissioning ELV Engineer</h1>
<h1 class="jobSectionHeader">Location: Riyadh / KSA</h1>
<h1 class="jobSectionHeader">Employment Type: Full-Time | On-Site</h1>
<h2 class="jobSectionHeader">About CSI Global:</h2>
At CSI Global, we specialize in delivering advanced electromechanical, testing, and commissioning services across the GCC and Globally. We power infrastructure through technical excellence and engineering innovation. Join a team committed to shaping the future of transmission and energy systems in the region.
<h2 class="jobSectionHeader">Position Overview:</h2>
We are seeking Commissioning ELV Engineer who will execute commissioning of ELV / ICT / BMS / SAS / Fire &amp; Life Safety systems on complex projects to achieve safe, SBC-Compliant, on-schedule handover with complete and auditable records.
<h2 class="jobSectionHeader">Key Responsibilities:</h2>
<ul><li>Perform tests per approved Method Statements / ITPs / Test Packs (pre-functional &amp; functional), record measurements and results precisely.</li><li>
Fire Alarm &amp; PAVA/Voice Evac: device addressing/labels, loop/line tests, cause-and-effect, audibility/intelligibility, battery/autonomy.</li><li>
Security (Access/CCTV/Intrusion): device I/O, events/alarms, storage &amp; retention, basic analytics scenarios.</li><li>
Emergency Lighting &amp; Lighting Control: auto-test/DT, spot lux checks, scenarios/overrides, BMS/FA interlocks.</li><li>
ICT/Structured Cabling &amp; Fiber: OTDR, end-to-end loss, copper certification (Fluke classes), rack/patch management.</li><li>
IBS/DAS &amp; Wi-Fi: basic sweep/coverage spot checks and operator/vendor integration readiness.</li><li>
SMATV/IPTV, Intercom, Parking/ANPR: functional scenarios and BMS/FA interface tests.</li><li>
Participate in IST with BMS/FA/Electrical; execute scripted steps, capture logs, report deviations.</li><li>
Verify installation against drawings/specs/codes; raise and track RFI/NCR to closure with evidence.</li><li>
Produce test results, update cause-and-effect matrices, red-line/as-built inputs; support O&amp;M/training packages.</li><li>
Authority/third-party prep (KSA): assemble labels, logs, and evidence for Saudi Civil Defense inspections and House of Expertise engagements; align with SBC + NFPA/IEC/TIA/BICSI.</li><li>
Submit weekly progress updates to the Commissioning Manager; escalate risks early.</li></ul>
<h2 class="jobSectionHeader">Required Qualifications:</h2>
<ul><li>3&ndash;5 years ELV testing &amp; commissioning on building/complex facilities.</li><li>
Hands-on with FAT/SAT/FPT, ITP/Test Packs, and IST participation.</li><li>
Practical experience across FAS/PAVA, Access/CCTV, Emergency Lighting, Lighting Control, and Structured Cabling/Fiber.</li><li>
Standards literacy: SBC, NFPA 72/101, IEC/BS EN, TIA/BICSI.</li><li>
Competent with ELV test gear (addressing/programming tools, sound level/intelligibility meters, lux meters, OTDR, copper certifiers).</li><li>
HSE awareness (PTW/LOTO), clear technical reporting, and drawing/spec literacy.</li></ul>
<h2 class="jobSectionHeader">Preferred Qualifications:</h2>
<ul><li>Commissioning on healthcare, airports, data centers, rail, or high-rise.</li><li>
Vendor familiarity (e.g., Honeywell/JCI/Siemens/BMS; ACS/CCTV/Access; PAVA; structured cabling).</li><li>
Experience with third-party certifications/Authority approvals (e.g., Civil Defense/House of Expertise).</li></ul></div>

Commissioning ELV Engineer

Ole Mexican Foods

<div>At Ole, our mission is to produce the finest Authentic Mexican inspired products with an unwavering commitment to quality and freshness. We believe that holding a seat at your dinner table is the ultimate compliment, and we strive to help families create wholesome, fun, and authentic eating experiences.
Job Summary: The Package Engineer is an experienced technical professional who leads packaging projects involving varying degrees of complexity from manufacturer quality concerns to continuous improvement to ground-up product development across all product lines involving legacy and sister companies. The Senior Package Engineer employs innovative problem-solving to provide technical options with cost-effective solutions. Collaboration with and education of all levels across all functions within the organization is a daily occurrence. The Senior Package Engineer role focuses heavily on project management, advanced technical problem-solving and cross-functional leadership to ensure packaging materials meet exacting quality, regulatory and supply chain requirements. This role requires advanced knowledge of packaging materials, package format manufacturing, packaging component filling machinery as well as validation protocols with focus on total cost optimization, compliance and sustainability.
 Location: Onsite in Norcross, GA 
Job Duties and Responsibilities:
Project Management &amp; Technical Execution<ul><li>
Lead package development projects from conceptualization and design through validation and commercialization.</li><li>
Design, develop and test primary, secondary and tertiary package systems to ensure product integrity and protection from manufacturing through the supply chain to consumer use.</li><li>
Perform advanced analysis and validation to include compatibility with filling equipment, compatibility with the designated product and distribution testing.</li><li>
Create and manage detailed material specifications to include technical drawings, material standards and palletization patterns for transit.</li><li>
Provide packaging Bill of Materials to documentation specialists.</li></ul>
Optimization &amp; Performance<ul><li>
Identify and implement innovative, sustainable and cost-saving packaging solutions with a focus on material reduction, recyclability, and supply chain efficiency.</li></ul><ul><li>
Drive cost-saving and efficiency initiatives by identifying opportunities to optimize packaging materials, design, and processes.</li><li>
Identify and implement sustainable packaging solutions and support the environmental goals of the company and their customers.</li><li>
Ensure package materials and designs comply with all relevant industry regulations.</li><li>
Conduct root cause analysis and implement corrective and preventive actions for recurring packaging failures or line performance issues.</li></ul>
Cross-Functional Collaboration &amp; Education<ul><li>
Provide technical support and education to Sales &amp; Marketing, Research &amp; Development, Quality Assurance, Operations and Supply Chain teams.</li><li>
Collaborate with suppliers to qualify new materials, tooling and packing equipment, managing technical trials and approval processes.</li><li>
Collaborate with potential suppliers to qualify their versions of existing materials.</li></ul> 
Qualifications:
Education and Experience<ul><li>
Education: Bachelor's degree in Package Engineering or other closely related technical field.</li><li>
Experience: 3+ years of experience in package engineering, development or manufacturing.</li></ul>
Technical Expertise<ul><li>
Strong knowledge of packaging materials science and related manufacturing, converting and printing/labeling processes of flexible films, rigid polymers, paperboard and corrugated paperboard.</li><li>
Extensive practical experience with package testing standards and validation protocols.</li><li>
Proficiency in palletization software.</li><li>
Demonstrated experience with packing equipment capabilities and manufacturing line efficiencies.</li><li>
Understanding of Good Manufacturing Practices and relevant industry-specific regulations.</li></ul>
Abilities<ul><li>
Proven ability to manage multiple complex projects simultaneously, delivering results on time and within budget.</li><li>
Exceptional analytical and problem-solving skills for tackling high-impact technical challenges.</li><li>
Excellent verbal and written communication skills to explain complex technical information to non-technical personnel.</li></ul> 
Job Type: Full-time - Onsite
Benefits:<ul><li>
401(k)</li><li>
401(k) matching</li><li>
Dental insurance</li><li>
Health insurance</li><li>
Life insurance</li><li>
Paid time off</li><li>
Vision insurance</li></ul></div>

Package Engineer

ISPA Technology

<div><div>Position Title: Hardware &amp; Software Test Engineer</div>
<div>Location: Panama City Beach, FL 
Clearance: Top Secret (preferred) or Secret (required)</div>
<div></div><div>Position Overview</div>
 <div>ISPA Technology is looking for a Hardware &amp; Software Test Engineer to perform hands-on testing of integrated hardware and software systems. This role is for the engineer who enjoys the moment where design meets reality: setup, execution, anomalies, retest, and evidence. You will support technical test planning and execution, work with multidisciplinary teams to isolate failures, and help ensure that delivered systems behave as intended across functional and integration scenarios.</div>
<div>What You Will Do</div>
<ul><li>Execute hands-on hardware and software tests, including setup, instrumentation, operation, observation, and result capture.</li>
<li>Develop and refine test procedures, acceptance criteria, discrepancy documentation, and result summaries.</li>
<li>Troubleshoot failures and coordinate with developers, systems engineers, and network personnel to isolate root causes.</li>
<li>Support repeat testing, regression validation, and configuration-controlled test events.</li>
<li>Maintain lab discipline, test records, and technical evidence that support engineering and release decisions.</li>
<li>Contribute to process improvements that make test execution safer, faster, clearer, and more repeatable.</li>
</ul><div>Technical Environment</div>
<ul><li>Integrated hardware/software test execution</li>
<li>Procedure-driven validation and discrepancy tracking</li>
<li>System troubleshooting and root cause isolation</li>
<li>Configuration-controlled test environments</li>
<li>Technical result reporting and collaboration across engineering teams</li>
</ul><div>Required Qualifications</div>
<ul><li>Experience in hardware test, software test, systems integration, or verification and validation environments.</li>
<li>Ability to execute detailed technical procedures and document results accurately.</li>
<li>Strong troubleshooting skills and engineering curiosity.</li>
<li>Comfort working hands-on with physical equipment and software under test.</li>
<li>Ability to communicate clearly with multidisciplinary technical teams.</li>
</ul><div>Preferred Qualifications</div>
<ul><li>Experience with automated testing, scripting, or lab instrumentation.</li>
<li>Familiarity with networked systems, cyber-conscious environments, or controlled test labs.</li>
<li>Background in mission-support or defense engineering programs.</li>
</ul><div>Why ISPA Technology</div>
<ul><li>Work on meaningful defense and mission-support engineering problems with experienced technical teams.</li>
<li>Contribute across automation, cyber, platforms, networking, integration, and test&mdash;not just one narrow lane.</li>
<li>Join a culture that values ownership, technical depth, curiosity, and practical execution.</li>
<li>Live and work in Panama City Beach, Florida, with direct access to a growing technical mission hub.</li>
</ul><div>We are looking for engineers who combine technical depth with practical execution&mdash;people who can turn complexity into clarity, and design into dependable results.</div></div>

Hardware & Software Test Engineer

Search 10000+ Equipment validation engineer jobs near you this April. New roles added regularly across leading industries. Apply today.