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Job Description Symmetrio is seeking multiple Senior Network Engineers to support a major enterprise network transformation initiative for our customer, a large government organization. This role centers on the implementation of Juniper MX960 routers and the transition from MC-LAG to EVPN/VXLAN fabrics. This role will involve leading high-impact cutovers and migrations in a production environment, contributing to both hands-on implementation and network architecture design across a multi-overlay fabric. This is a hybrid position based out of Philadelphia, salary is in the 110-150k range. This is a 12 month contract with the possibility of extension. Responsibilities • Lead the planning, prioritization, and execution of enterprise-scale Juniper router migrations (MX960 platform)., • Design and validate EVPN/VXLAN architectures with multiple overlays to ensure scalability, performance, and redundancy., • Collaborate closely with the customer’s Network Engineering team to achieve seamless integration with minimal disruption during migrations., • Configure, test, and deploy Junos OS across MX and EX platforms in production environments., • Provide expert-level guidance on the migration from MC-LAG to EVPN, including design validation, testing, and troubleshooting., • Develop and maintain detailed documentation for network designs, cutover strategies, and post-migration processes., • Serve as a subject matter expert for Juniper routing, EVPN/VXLAN fabrics, and advanced routing protocols., • Support after-hours cutovers and provide escalation assistance during critical events. Requirements • 7+ years of experience as a Network Engineer in enterprise or large data center environments., • 5+ years of hands-on experience with Juniper MX and EX platforms., • Strong knowledge of core routing protocols, particularly BGP and OSPF., • Proficiency with Junos OS configuration and troubleshooting in production environments., • Demonstrated experience supporting large-scale router replacement or network migration projects., • Familiarity with EVPN design, deployment, and operations., • Strong analytical, troubleshooting, and problem-solving skills., • Juniper certifications (JNCIP, JNCIE, or equivalent)., • Experience with network automation and scripting (Python, Ansible, etc.)., • Knowledge of security best practices in routing and switching., • Health Care Plan (Medical, Dental & Vision), • 401k Retirement Plan (4% match), • Paid Time Off (Vacation, Sick & Public Holidays)

Job Description PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success. The Experience With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn. At PSC Biotech®, it’s about more than just a job—it’s about your career and your future. Your Role We are excited to accept applications for future opportunities. Join our talent pool for future openings by applying now. This is a W2-Temp 6-month role with potential FTE extension. We are hiring experienced validation engineers responsible for the commissioning, qualification, and validation for facilities, utilities, and equipment in the pharmaceutical and biotech industries. Our engineers play a critical role in driving project success, while supporting validation planning, development, documentation, and execution, and ensuring regulatory standards and quality requirements are met. • Develop and execute commissioning, qualification, and validation protocols for required equipment and systems., • Prepare and maintain comprehensive documentation, including validation protocols, plans, reports, and standard operating procedures., • Identify and assess risks associated with CQV activities and develop effective mitigation strategies., • Troubleshoot and resolve issues related to equipment and process performance., • Collaborative with cross-functional teams to ensure alignment on CQV activities and project timelines., • Ensure compliance with regulatory requirements (FDA, EMA, etc.) and industry standards (GMP, GAMP, etc.)., • Additional responsibilities as required to drive successful validation project deliverables. Requirements • Bachelor’s degree in Engineering, Life Sciences, or a related field., • 3-5 years of equipment commissioning, qualification, and validation engineering experience in the pharmaceutical and/or biotech industries., • Strong knowledge of regulatory requirements and industry standards., • Experience with validation lifecycle management and risk-based approaches., • Excellent analytical and technical problem solving skills., • Strong technical writing skills and understanding of full lifecycle documentation (protocols, reports, procedures, risk assessments, specifications and requirements, etc.), • Effective communication and interpersonal skills., • Proactive with strong organization, time management, and project management abilities., • Excellent attention to detail with commitment to quality and compliance., • At PSC Biotech, many of our projects and clients are located in various regions around the country. Therefore, we value candidates who are willing and able to travel as needed for project assignments and client engagements. The ability to adapt to different locations, cultures, and work environments is essential, as it allows our team members to collaborate effectively with clients and colleagues nationally. Equal Opportunity Employment Statement PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law. #LI-RW1 Benefits

Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success. The Experience With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn. At PSC Biotech®, it’s about more than just a job—it’s about your career and your future. Your Role We are excited to accept applications for future opportunities. Join our talent pool for future openings by applying now. This is a W2-Temp 6-month role with potential FTE extension.We are seeking a highly skilled and detail-oriented Quality Assurance Engineer to join our team in the life science sector. The ideal candidate will have a strong background in quality assurance processes, with specialized experience in auditing, ensuring compliance with regulatory standards, and maintaining the highest quality standards in pharmaceutical production. This individual will play a crucial role in the review and assessment of manufacturing practices, quality control systems, and regulatory compliance within a highly regulated environment. • Develop, implement, and maintain quality assurance processes and procedures in alignment with industry standards and regulations., • Ensure all manufacturing processes comply with relevant regulations, including but not limited to FDA, EMA, ICH, and GMP guidelines., • Review batch records, validation documentation, and quality control data to ensure compliance and product quality., • Conduct internal and external audits to assess compliance with Good Manufacturing Practices (GMP), FDA regulations, and other relevant standards., • Collaborate with cross-functional teams to ensure effective implementation of audit findings and continuous improvement initiatives., • Prepare detailed audit reports, CAPA (Corrective and Preventive Actions) reports, and other documentation as required., • Maintain thorough and accurate records of quality assurance activities, audits, and regulatory communications., • Participate in the preparation and review of SOPs, work instructions, and other quality-related documents., • Lead or participate in continuous improvement initiatives, focusing on quality and operational efficiency. Requirements • Bachelor's degree in engineering or related technical field., • Minimum of 5-7 years of experience in quality assurance within the life science industry., • Proven experience in conducting GMP audits, both internal and external, in a pharmaceutical or life sciences environment., • Experience with regulatory bodies such as the FDA, EMA, and other international regulatory agencies., • Familiarity with Quality Management Systems (QMS), CAPA, deviation management, and risk management., • Strong understanding of GMP regulations, FDA guidelines, and other applicable industry standards., • Excellent analytical and problem-solving skills., • Exceptional attention to detail and ability to identify potential areas of risk and non-compliance., • Strong verbal and written communication skills, with the ability to prepare clear and concise reports., • Travel is required. At PSC Biotech, many of our projects and clients are located in various regions around the country. Therefore, we value candidates who are willing and able to travel as needed for project assignments and client engagements. The ability to adapt to different locations, cultures, and work environments is essential, as it allows our team members to collaborate effectively with clients and colleagues nationally. Equal Opportunity Employment Statement PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs, including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law. #LI-RW1

Job Description Medical Guardian is a fast-growing digital health and safety company on a mission to help people live a life without limits. With 13 consecutive years on the Inc. 5000 list of Fastest Growing Companies, we’re redefining what it means to age confidently and independently. We support over 625,000 members nationwide with life-saving emergency response systems and remote patient monitoring solutions. Trusted by families, healthcare providers, and care managers, our work is powered by a culture of innovation, compassion, and purpose. The Hardware Engineer will serve as a subject matter expert (SME) in Medical Guardian’s Personal Emergency Response Systems (PERS), Remote Patient Monitoring (RPM), and Senior Living hardware solutions. This role is responsible for supporting the full lifecycle of hardware including testing, verification, validation, troubleshooting, and root cause analysis. The Hardware Engineer will ensure optimal field performance of all devices by monitoring KPIs, driving improvements, and serving as the central technical resource for hardware reliability and functionality. The role will also require periodic travel to the Sharon Hill warehouse to support device inspections, testing, and collaboration with fulfillment and quality teams. Key Responsibilities: Hardware Support & Subject Matter Expertise • Act as the in-house SME for all PERS, RPM, and senior living hardware devices., • Provide technical expertise to internal teams, vendors, and partners regarding device functionality, integration, and performance., • Design and execute test plans for new hardware and firmware releases., • Perform verification and validation activities to ensure compliance with technical, quality, and regulatory standards (UL, FCC, FDA if applicable)., • Monitor and analyze device KPIs (failure rates, battery life, connectivity stability, false alarms, repair/replacement rates, etc.) to ensure optimal performance in the field., • Conduct root cause analysis of recurring or high-priority field issues and implement corrective/preventive actions., • Partner with Operations, Customer Support, and Quality to ensure member-reported issues are resolved efficiently., • Work with Product and Engineering teams to support new device development, testing, and launch readiness., • Collaborate with Fulfillment, Quality, and Warehouse teams (including periodic travel to Sharon Hill) to inspect inventory, test returns, and validate corrective actions., • Provide input into the hardware roadmap to align future devices with performance standards and member needs. Qualifications: • Bachelor’s degree in Electrical Engineering, Computer Engineering, or related field (Master’s degree preferred)., • 4+ years of experience in hardware engineering, testing, and support., • Experience with PERS, medical devices, RPM, or healthcare technology hardware, strongly preferred., • Strong knowledge of testing methodologies:, • Electrical/Power (battery life, load, EMC/EMI), • RF/Wireless (Bluetooth, Wi-Fi, LTE performance), • Functional/System validation (firmware/hardware integration), • Environmental & Reliability (thermal, vibration, humidity), • Chemical/Biocompatibility testing for medical device, • Experience with Verification & Validation (V&V) lifecycle, translating requirements into test cases, executing, documenting, and ensuring compliance standards., • Familiarity with compliance standards (IEC60601, ISO 13485, FDA) and regulatory standards (UL, FCC, CE, FDA Class I/II, ISO 13485), • Proficiency in test equipment, diagnostic tools, and engineering software to include:, • Test Equipment: oscilloscopes, logic/spectrum analyzers, power analyzers, signal generators, • Debug/Diagnostic Tools: JTAG/SWD debuggers, protocol analyzers (USB, I2C, SPI, CAN), • Engineering Software: LabVIEW or Python for test automation, MATLAB/Simulink, CAD/EDA tools (Altium/OrCAD), and test management platforms (Jira/Xray, TestRail)., • Ability to periodically travel to Sharon Hill, PA warehouse for hands-on support., • Must be legally authorized to work in the United States without the need for employer sponsorship now or in the future. Key Competencies: • Field Performance Focus – Ensures devices perform optimally for members, guided by KPIs and data., • Analytical & Problem-Solving – Skilled in root cause analysis and implementing long-term solutions., • Collaborative Communicator – Works effectively across engineering, product, quality, operations, and fulfillment., • Detail-Oriented – Accurate in testing, verification, and reporting., • Health Care Plan (Medical, Dental & Vision), • Paid Time Off (Vacation, Sick Time Off & Holidays), • Company Paid Short Term Disability and Life Insurance, • Retirement Plan (401k) with Company Match

Job Description In today's dynamic worksites, seamless collaboration between people and machines is essential. FORT's platform ensures safe, secure, and dynamic control that surpasses legacy systems and next-generation AI capabilities. While autonomous machines offer significant advantages, they also introduce new safety challenges. FORT addresses these concerns by providing solutions such as the Wireless E-Stop, which allows operators to instantly stop any machine from a safe distance, enhancing safety during emergencies. Additionally, FORT's Safe Remote Control enables operators to manage heavy machinery remotely, reducing the risk of accidents and improving visibility. By ensuring communications integrity across any network, FORT empowers customers to protect their most valuable assets—people, data, and machines—ensuring they remain safe and secure. We are seeking a Senior Test Engineer with a strong Electrical Engineering (or related) background who thrives at the intersection of embedded testing, manual validation, automation, and lab infrastructure ownership. This role requires someone comfortable running deep manual test campaigns, skilled enough to automate where it adds value, and motivated to design, build, and maintain Hardware-in-the-Loop (HIL) benches. The ideal candidate will also bring hands-on hardware experience — building custom breakout boards, fixtures, or adapters — to expand test coverage and improve bench reliability. Responsibilities • Develop test methods and procedures to transition products from design into volume manufacturing., • Design and execute manual and automated tests for embedded hardware and firmware validation., • Perform regression, performance, stress, and reliability testing on Fort devices., • Establish and maintain test plans, procedures, and documentation to ensure repeatable and auditable testing., • Build, maintain, and upgrade Hardware-in-the-Loop (HIL) benches for system and device-level validation., • Manage and improve lab infrastructure, including test equipment, fixtures, and assets., • Design and build custom breakout boards, adapters, and fixtures to support testing needs, • Collaborate with hardware and firmware engineering teams to debug and resolve issues., • Contribute to design reviews by defining testability requirements early in development., • Support product engineering in maintaining and improving R&D test environments, • Work with manufacturing partners to create and document production test processes (hardware and software), • Provide technical expertise to support production and program management, including special customer deliveries., • Contribute to re-engineering efforts to improve quality and manufacturability., • Deliver clear, data-driven test reports to stakeholders and mentor junior engineers., • Work directly with customers at customer sites to drive success through hands-on support (10–20% travel) Qualifications • Bachelor's or Master's in Electrical Engineering, Computer Engineering, or related discipline preferred, • 5+ years of experience testing complex embedded products, • Strong manual testing skills with attention to detail, • 2+ years of experience using Python and C/C++ for automation and validation, • Experience with hardware/software validation infrastructures (HIL/SIL), • Familiarity with Linux environments, Docker, CI/CD tools (GitLab, Jenkins), and Git version control, • Skilled in designing custom hardware or software fixtures for embedded system testing, • Proficient with wired (Ethernet, CAN, UART) and wireless (BLE, Wi-Fi, LTE) communication technologies, • Strong debugging and troubleshooting skills using oscilloscopes, logic analyzers, and protocol analyzers, • Ability to manage multiple efforts and communicate effectively with technical and non-technical stakeholders, • Growth mindset with interest in advancing responsibilities within Fort Preferred • Hands-on hardware design experience (custom breakout boards, adapters, test fixtures), • Knowledge of RF testing or safety-critical system validation, • Experience with functional safety standards (IEC 61508, ISO 26262), • Prior experience with Azure pipelines or other CI/CD tools

Job Description Job Title: Automation Design Engineer Job Location: Philadelphia Job Type: [Full-Time] Reports To: [VP Engineering] Company Overview: Biomeme is a leading innovator … We are committed to providing high-quality solutions to our customers and are seeking a talented and experienced Automation Design Engineer to join our dynamic engineering team. Position Summary: As an Automation Design Engineer, you will be responsible for designing, developing, and optimizing production line fixtures for the manufacturing of biotech instruments. You will work closely with cross-functional teams to ensure that fixtures are reliable, efficient, and meet the high standards required for precision manufacturing in the biotech industry. Key Responsibilities: • Design and develop innovative fixtures through software and hands-on work for automation production lines, ensuring alignment with product specifications, regulatory standards, and manufacturing requirements., • Collaborate with manufacturing, mechanical, and electrical engineering teams to integrate fixtures seamlessly into automated production lines., • Conduct feasibility studies and simulations to validate fixture design and optimize for cost, efficiency, and scalability., • Review and refine designs using CAD software (e.g., SolidWorks) and ensure designs are manufacturable, functional, and robust., • Develop detailed technical drawings and specifications for fixture manufacturing, ensuring they comply with quality and regulatory standards., • Work closely with the production team to troubleshoot and resolve any fixture-related issues that arise during the production process., • Implement continuous improvements to production line fixtures, ensuring minimal downtime and increased throughput in a fast-paced environment., • Support testing and validation of fixtures to ensure performance under real-world conditions, ensuring they meet the stringent requirements for biotech instrument production., • Provide technical support to manufacturing teams to ensure proper fixture use, maintenance, and troubleshooting., • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related field., • Proven experience (3+ years) in fixture design and automation for high-precision manufacturing, preferably within the biotech, medical device, or automation industries., • Strong proficiency in CAD software (SolidWorks, AutoCAD, or similar)., • Knowledge of manufacturing processes and material selection, particularly in automated production environments., • Familiarity with regulatory standards and quality control processes in the biotech or medical device industries (e.g., ISO 13485, GMP)., • Strong problem-solving skills with a focus on continuous improvement and innovation., • Excellent communication and teamwork skills to collaborate effectively with cross-functional teams., • Detail-oriented with a strong commitment to quality, safety, and operational efficiency., • Experience with the design and integration of automated systems for biotech instrument production., • Familiarity with PLCs, robotics, and control systems used in automated production lines., • Competitive salary and benefits package., • Opportunities for career growth and professional development., • Health, dental, and vision insurance., • Retirement savings plan with company contributions. How to Apply: Please submit your resume, portfolio (if applicable), and a cover letter detailing your experience and qualifications through applying on our website, biomeme.com.

Job Description Position Summary Delva Tool & Machine (DTM) is seeking a Quality Engineer for our Cinnaminson, NJ location. The Quality Engineer will ensure the products and all associated documentation are per requirements and standards as defined by our customers and our internal quality system. They will also perform timely and thorough inspections of products and documentation as required. If you are looking for an organization and career that will match your strong work ethic and passion for success, Delva Tool & Machine is a great place to start! This position works a schedule of Monday thru Friday from 7:30am-4:00pm. The pay range for this role is between $75,000 - $85,000 per year depending on experience* Essential Duties and Responsibilities • Assist with managing the Quality Management System., • Creates and revises manufacturing documents, specifications, standard operating procedures (SOP's), safety instructions, validation protocols, risk assessment, and procedures and other technical documents to ensure compliant, efficient, and safe procedures., • Investigate customer complaints/returns., • Initiates and leads to resolution of quality incidents and CAPA., • Manage CAR/PAR log., • Bachelor's degree in manufacturing or something similar is required., • Minimum 4+ years' experience in a production engineering role is required., • Familiarity with general inspection equipment such as mics, calipers, gages, comparator or vision systems., • Ability to read and understand blueprints with knowledge of GD&T., • ISO9001 or AS9100 standards highly preferred., • Aerospace and defense industry experience preferred., • Six Sigma greenbelt or above preferred. Our comprehensive benefits package includes, but is not limited to, a competitive pay rate, accrued vacation time, sick time, paid holidays, 401(k) with company match, health, dental, and vision insurance as well as Short-Term Disability, Long-Term Disability, and life/AD&D insurance. We are a drug-free workplace / Equal Opportunity Employer and Prohibit Discrimination and Harassment of Any Kind: We are committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions are based on business needs, job requirements, and individual experience and qualifications, without regard to a person's sexual orientation, gender identity, gender expression, religion, disability, race, creed, color, sex, age, national origin or ancestry, or any other status protected by the laws or regulations in the locations where we operate. Powered by JazzHR xgRlGTRwVK

Job DescriptionCareer Renew is recruiting for one of its clients a Client Platform Engineer - Fintech - this is a fully remote role for candidates based in the US or LATAM regions. Implement and operate the company’s client platform with a focus on macOS. Administer Google Workspace, manage a 100–200 device macOS fleet with Kandji and zero-touch enrollment via Apple Business Manager (ABM), and enforce security baselines defined in partnership with Security. Execute procurement for US and international employees, drive automation in Bash, handle access requests, and deliver predictable onboarding/off boarding. What you’ll do Endpoint management and automation * Implement and maintain macOS configuration baselines in Kandji (blueprints, profiles, scripts) derived from security-defined standards. * Run ABM-based zero-touch enrollment; ensure devices are supervised, compliant, and land in correct configurations on first boot. * Package and deploy software and OS updates; use ringed deployments (test > pilot > production) with rollback plans. * Automate repetitive tasks in Bash (inventory reconciliation, compliance checks, reporting). Python is a plus. * Monitor device health: patch levels, EDR coverage, and compliance drift; execute remediations within defined SLAs. Security and compliance * Implement FileVault, Firewall, Gatekeeper, password/SSO policies, and PPPC/TCC controls per Security’s baselines. * Operate and monitor CrowdStrike on macOS (agent deployment, policy assignment, health checks) and coordinate incident handoffs. * Maintain exceptions and remediation timelines; produce compliance reports and dashboards. Google Workspace administration * Manage users, groups, org units, and policies with least-privilege patterns. * Execute lifecycle standards for account creation, deprovisioning, and data retention. * Manage device trust policies for browsers and endpoints as applicable. Employee lifecycle and access * Deliver predictable onboarding/offboarding: accounts, licenses, device provisioning/returns, and secure wipes. * Handle access requests with auditable workflows and defined SLAs; maintain accurate entitlements. Procurement and asset lifecycle (US and international) * Execute purchasing against standard kits and budget guidelines; maintain buffer stock based on hiring plans. * Coordinate international logistics (customs/imports, power/keyboard variants, regional warranty). * Track assets end-to-end: tagging, inventory accuracy, RMAs, and secure end-of-life disposal. Reliability, documentation, and support * Author and maintain SOPs, runbooks, and user guides; keep them version-controlled. * Act as Tier-1 escalation for endpoint issues; drive root cause analysis and preventative fixes. * Track and report KPIs: deployment success, compliance, MTTR, ticket types/volumes, and device health. How you’ll work * Treat configuration as code (profiles, scripts, blueprints) with change control and reviews. * Use ringed deployments with automated validation and fast rollback. * Standardize device configurations to minimize drift; manage exceptions explicitly. * Automate first; eliminate manual steps in provisioning, access, and reporting. * Partner tightly with Security: co-own baselines, telemetry, and incident response interfaces. Tools you’ll use * Google Workspace Admin * Kandji (MDM) * Apple Business Manager (ABM) for Automated Device Enrollment * CrowdStrike (EDR) * Bash/shell; Python a plus * Version control and ticketing systems Minimum qualifications * 3 - 5 years in client platforms, IT engineering, or similar role managing primarily macOS fleets at 100–200 device scale. * Hands-on Google Workspace administration (users, groups, org units, policies). * Proven Kandji administration with ABM zero-touch enrollment. * Experience operating CrowdStrike EDR on macOS. * Fluency in Bash/shell and Git-based workflows. * Strong understanding of macOS management primitives: configuration profiles, PPPC/TCC, FileVault, launchd, software packaging, and update channels. * Experience delivering onboarding/offboarding, access management, and asset lifecycle with clear SLAs. * Exposure to US and international procurement and logistics. Compensation & Package Health Stipend Office Stipend Laptop Unlimited Leave Options

One of our large clients in the pharmaceutical industry in Spring House, PA is seeking a highly skilled and detail-oriented GxP Validation Engineer to support validation activities for CAR T-cell therapy manufacturing equipment and systems. Collaborate with cross-functional teams to ensure validatio

Examples of our core services within the life science space, include: Capital Project Management (including Project Controls and Scheduling); Facility Management & Builds; Tech Transfers; Validation Life Cycle (including Commissioning and Qualification, Process Validation, Computer System Validation

Bachelor’s degree in civil engineering or relevant field from an accredited four-year college or university.

Our client is searching for a Global Capacity Center (GCC) Project Manager for a remote position.All candidates must have experience managing Global Capacity Center construction projects internationally.This includes planning, building, and implementing GCC's internationally***.This work focuses on

Bachelor’s degree in civil engineering or relevant field from an accredited four-year college or university.

Bachelor’s degree in civil engineering or relevant field from an accredited four-year college or university.

Bachelor's degree in construction management, engineering, or a similar field plus.

Bachelor’s degree in civil engineering or relevant field from an accredited four-year college or university.

Headquartered in Farmington Hills, Michigan, RHP Properties ( is the nation's largest private owner and operator of manufactured home communities.With over 370 communities throughout 30 states, we continue to expand our footprint to provide accessible and affordable housing across the country.All of

Degree in Mechanical Engineering, Manufacturing Engineering, or related field preferred. Senior CNC Manufacturing Engineer. Collaborate with engineering, production, and R&D to optimize machining strategies.

Bachelor’s degree in construction management, engineering, or a similar field plus.

Bachelor’s degree in Construction Management, Civil Engineering, or a related field preferred.

Bachelor's degree in either Industrial or Mechanical Engineering. At least 6+ years' of engineering experience.

The Project Manager reports directly to the Construction Operations Manager.The PM is the direct supervisor of assigned estimator(s).The PM is responsible for the solicitation of project documents and information, ensures that all information is put into the hands of hub estimators, support team mem

Project Manager | Data Centers | Travelling.Philadelphia, PA | 💼 Full-Time - Travel.Senior Project Managers in overseeing day-to-day operations for fast-paced, MEP-intensive Data Center construction project.Based on site in Philadelphia, PA.This is a travelling position, you will be required to b

Per Se Group has an outstanding and unique full-time job opportunity for a Project Architect to work with our premier developer client in New Jersey.In this role, you will help support commercial construction and design projects.Examples of the type of projects you will work on include medical offic

Our client is seeking a Project Manager III who has a solid background in project management with experience in healthcare, business and systems projects, leading from inception to close.Manages projects of high complexity and risk or to manage application module installations.Exhibits advanced skil

Bachelor's Degree in electrical Engineering or a related field. Experience in electrical engineering, applications, or project management. Coordinating with other engineers, architects, and contractors to ensure the seamless integration of electrical systems.

Heavy Civil Project Manager – Philadelphia, PA.This is more than just another PM role—it’s a fast-track opportunity with a clear succession plan, unrivalled compensation, and the chance to help drive the company’s continued growth across Eastern Pennsylvania.Why This Opportunity Stands Out:.

The North America Specialty Reserving Lead is responsible for managing the day-to-day workflow of up to 4 analysts with the responsibility of coordinating and reviewing the North America Specialty reserving process.Managing the Monthly and Quarterly AvE process, reviewing the outputs and communicati

A National General Contractor specializing in commercial projects, from full build outs and renovations to large scale projects is seeking a talented Assistant Project Manager to help assist with new and existing construction.This position is based out of their office in Union County, NJ.Benefits +

You’re an experienced civil engineer ready to lead projects, guide teams, and take ownership of client success. Civil Engineering Project Manager. Mentor junior engineers and contribute to a culture of collaboration and growth.

An engineering/architectural background is preferred. The APM will have the opportunity to gain varied and in-depth technical knowledge in Façade Project Management, Production Management, Scheduling, Engineering, and Site Installation. The APM must coordinate work with other departments, including

Per Se Group has an outstanding and unique full-time job opportunity for a Project Architect to work with our premier developer client in New Jersey.In this role, you will help support commercial construction and design projects.Examples of the type of projects you will work on include medical offic

Bachelors degree in construction management, engineering, or a similar field plus.

The North America Specialty Reserving Lead is responsible for managing the day-to-day workflow of up to 4 analysts with the responsibility of coordinating and reviewing the North America Specialty reserving process.Managing the Monthly and Quarterly AvE process, reviewing the outputs and communicati

Project Manager | Data Centers | Travelling.Philadelphia, PA | 💼 Full-Time - Travel.Senior Project Managers in overseeing day-to-day operations for fast-paced, MEP-intensive Data Center construction project.Based on site in Philadelphia, PA.This is a travelling position, you will be required to b

The Project Manager reports directly to the Construction Operations Manager.The PM is the direct supervisor of assigned estimator(s).The PM is responsible for the solicitation of project documents and information, ensures that all information is put into the hands of hub estimators, support team mem

Our client is seeking a Project Manager III who has a solid background in project management with experience in healthcare, business and systems projects, leading from inception to close.Manages projects of high complexity and risk or to manage application module installations.Exhibits advanced skil

The APM will have the opportunity to gain varied and in-depth technical knowledge in Faade Project Management, Production Management, Scheduling, Engineering, and Site Installation. The APM must coordinate work with other departments, including procurement, manufacturing, construction teams, externa

Headquartered in Farmington Hills, Michigan, RHP Properties ( over 370 communities throughout 30 states, we continue to expand our footprint to provide accessible and affordable housing across the country.All of this would not be possible without the energy and drive of our talented team mem

Coordinating with other engineers, architects, and contractors to ensure the seamless integration of electrical systems. Performing quality control checks and system validations to ensure the functionality and safety of electrical installations. Bachelor's Degree in electrical Engineering or a relat

Bachelors degree in Construction Management, Civil Engineering, or a related field preferred.

Mentor junior engineers and contribute to a culture of collaboration and growth. Bachelors degree in Civil Engineering. Project Manager Civil Engineering | Philadelphia, PA.

A National General Contractor specializing in commercial projects, from full build outs and renovations to large scale projects is seeking a talented Assistant Project Manager to help assist with new and existing construction.This position is based out of their office in Union County, NJ.Benefits +

Heavy Civil Project Manager Philadelphia, PA.This is more than just another PM roleits a fast-track opportunity with a clear succession plan, unrivalled compensation, and the chance to help drive the companys continued growth across Eastern Pennsylvania.Why This Opportunity Stands Out:.Market-leadi

Degree in Mechanical Engineering, Manufacturing Engineering, or related field preferred. Senior CNC Manufacturing Engineer. Collaborate with engineering, production, and R&D to optimize machining strategies.

Civil Engineering Project Manager – Transportation Location: Hybrid | Multiple Office Locations Salary Range: $95,000 – $130,000 (commensurate with experience and qualifications) A leading multidisciplinary design firm is seeking a skilled Civil Engineering Project Manager to oversee transportat

This individual will play a pivotal role in elevating ASC Engineered Solutions' presence in key marketsparticularly within the data center and semiconductor sectorsby targeting, engaging, and influencing owners, engineers, and other critical project stakeholders. ASC Engineered Solutions is looking

Join our dynamic Planning and Site Design Department, where you will play a pivotal role as a Project Manager (Civil Engineer). Preferred: Professional Engineer (PE) license in Pennsylvania. Required: Engineer in Training (EIT) certification.