Process engineer jobs in Delaware

Selectek is partnering with a firm in Georgetown, Delaware to hire a Process Engineer on a direct hire basis. Ideal candidates have worked in an Injection Plastic Molding facility for minimum of 3-5 years and can handle supervisory duties. Expected Pay Range: $75,000 - $125,000 base salary Location: Georgetown, DE Schedule: Monday-Friday, 8:00a - 5:00p Essential Duties & Responsibilities: Responsible for supervision of tool room, process techs, trainees and material handlers, process engineers and maintenance Be a liaison between manufacturing and engineering Responsible for training of technical resources Use Lean/Six Sigma methodologies for process development and problem solving Responsible for building and maintaining a high performance team Maintain associated metrics for respective area Responsible for optimizing cycle times, reducing scrap, and reducing downtime Participate on teams that require technical expertise Responsible for creating and maintaining associated department procedures Maintain a high level of professionalism Monitor processes and ensure accurate execution f defined processes Responsible for level of quality produced by the department Promote a high level of communication between departments to execute customer orders Promote and participate actively in continuous improvement Develop growth and development plans for personnel Maintain working relationships with other department managers and personnel Assess equipment and personnel requirements for department and make/implement necessary changes Perform other tasks as directed by manager Additional responsibilities as assigned Supervisory Responsibilities: Responsible for supervision of personnel Responsible for ensuring a safe work environment Responsible for accurately assessing labor needs and making appropriate schedule adjustments Responsible for maintenance of timecards Responsible for vacation request and approvals for personnel Responsible for maintenance of personnel training records Responsible for discipline of personnel Required: Proficient with injection molding processing Experience with Engineered and high-temp resins Ability to interpret part prints, quality plans, work instructions, and apply the knowledge appropriately Ability to develop and write work procedures and train personnel Proficient in use of Office Software, including work processing and spreadsheets Must possess excellent written, verbal, and interpersonal communication skills to interact with all levels of the organization Working knowledge of CAD/Solid works and Mold flow Demonstrated experience in formalized problem solving Ability to program robots and exchange end-of-arm tooling Working knowledge of ISO 900-2008 and TS-16949-2009 Preferred: Lean/Six Sigma training/certification preferred Certificate of supervisory training preferred Six Sigma Green Belt or Black Belt training preferred In addition to these requirements, candidates must be eligible to work in the United States as Selectek is unable to provide sponsorship or work visa documentation. To be considered for this position, apply via the link, or if email is more convenient, send an up-to-date resume to jfairbanks@selectek.net and reference this job posting. Call 470.203.9530 to reach Joey Fairbanks from Selectek for more information.

Newark, DE, United States **Why join Hologic:** You will have the opportunity to get in on the ground floor at a high growth world class manufacturing facility working on life-saving medical devices with potential for future growth. This is a great opportunity to enhance your manufacturing operation skills and knowledge to further your career. **What to expect:** Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is the fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. **What we expect:** + Performs complex experiments that may require support and coordination of other engineers or technicians. + Active participant in R&D projects, providing design input and ensuring projects can be translated into cost-effective production. Supports R&D in marking cost estimated for equipment, tools, and components. + Responsible for the manufacture and performance of assigned product line (s). + Responsible for setting up fabrication and assembly procedures to manufacture products. Establishes methods and tooling needed for new and existing processes. Assists in the design of tooling and fixtures. + Initiates and/or approves necessary changes in design, drafting, tooling, methods, processes, and documentation that affects the manufacturing process. + Oversee the creation and revision of standard operation procedures, organizational standards, directives pertaining to scheduling, cost control and production performance evaluation. Develop, verifies and validate processes for manufacturing. + Responsible for the maintenance of production equipment and works with Facilities on the implementation of predictive maintenance of manufacturing equipment. + Responsible for identifying, diagnosing, prioritizing, and correcting technical issues that may arise in standard manufacturing. Works in conjunction with other departments where appropriate. + Evaluate and develop process control data for trending analysis. Analyzes defects, provides feedback, and implements process improvements. + Participates in design reviews, working with R&D and manufacturing to resolve all issues, particularly those arising from the violation of design standards or changes from existing manufacturing procedures. + Actively supports and adheres to the Quality Policy and Quality System procedures. + Identify and lead complex projects that drive meaningful improvements positively impacting product quality and manufacturing efficiency and costs. + Establish collaborative relationships with all stakeholders within the site and create links with experts within the Hologic network. + Maintains professional and technical knowledge by attending educational workshops. + Manage one project without supervision. + Train and mentor Manufacturing Engineer 1 + Be a change agent driving improvement on a daily basis. **Education & Experience:** + Preferred Minimum Non-Technical Degree: College Degree + Preferred Minimum Technical/Advanced Degree: Technical Bachelor's Degree + Preferred Minimum Non-Technical Degree: 5-8 Years + Preferred Minimum Technical/Advanced Degree: 2-5 Years with Technical Bachelor's Degree, 1-3 Years with Master's Degree, 0-1 Years with PhD + Automation experience, such as implementation of an automated cell/line is beneficial. + Experience in rapid scale up of new products or operations is beneficial. The annualized base salary range for this role is $97,500 to $152,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.. **Agency and Third Party Recruiter Notice:** Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. **_Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans._** **_\#LI-PR1_** **_Must follow all applicable FDA regulations and ISO requirements._** **_Hologic is an equal opportunity employer inclusive of female, minority, disabled and veterans, (F/M/D/V)_**

**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. The Integrated Operations Process Safety Management (PSM) team within Qnity Electronics is seeking a Principal Engineer - Process Safety Management to strengthen and advance our corporate process safety system, with a focus on leading the Training and Performance element. This role is pivotal in enhancing the effectiveness of the corporate training program, including content development, delivery, and competency testing to help ensure site personnel fully understand corporate and regulatory Process Safety requirements and are proficient in using corporate tools to meet those standards. The successful candidate will serve as the corporate process owner for Training and Performance, providing technical expertise, leadership, and strategic direction to reduce risk to people, assets, and the environment. Hazards of concern include toxicity, flammability, explosion risks, and reactive chemical behavior involving liquids, gases, combustible dusts, and other high-hazard materials. **Key Responsibilities** + Serve as the corporate process owner for the Training and Performance element of Process Safety Management. + Develop and maintain corporate training programs aligned with regulatory and internal PSM requirements. + Oversee training delivery methods, competency assessments, and performance tracking across global sites. + Establish and monitor key performance indicators (KPIs) to assess and improve the global T&P program. + Facilitate PHA, LOPA (Layers of Protection Analysis), and DHA (Dust Hazard Analysis) for both cyclic reviews and capital projects. + Provide technical guidance and subject matter expertise to ensure effective implementation of PSM standards. + Collaborate with site leadership, engineering, and EHS teams to drive continuous improvement in process safety performance. + Lead strategic initiatives to enhance risk reduction related to high-hazard materials and processes. + Support audits, compliance reviews, and incident investigations as needed. **Required Capabilities & Qualifications** + Bachelor's degree in Chemical Engineering, Mechanical Engineering, or a related technical discipline + 10+ years of experience in Process Safety Management within a high hazard manufacturing or chemical processing environment. + Strong knowledge of OSHA PSM, EPA RMP, and relevant international process safety standards. + Proven experience in developing and implementing corporate training programs for technical and operational personnel. + Strong understanding of hazards such as toxicity, flammability, explosion risks, and reactive chemical behavior. + Demonstrated ability to lead cross-functional teams and influence at all organizational levels. + Excellent communication, facilitation, and project management skills. + Experience with risk assessment methodologies (HAZOP, LOPA, etc.) and process and dust hazard analysis. + Strong background in PSM auditing and compliance assurance. + Proven ability to lead change, influence stakeholders, and drive performance improvements. + Excellent communication skills-both written and verbal-with the ability to engage across all levels of the organization and with external agencies. + Ability to travel domestically and internationally as required. **Additional Attributes** + Strong interest in project engineering and technical advisement. + High emotional intelligence and interpersonal skills to navigate diverse, global teams. + Ability to work independently, manage multiple priorities, and deliver results in a fast-paced environment. + Certified Process Safety Professional (CCPS) or equivalent preferred. + Training and Development Certification (e.g., ATD or similar) is a plus. Join our Talent Community (*************************************************************** to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** .

Reference ID: 41290 Are you interested in high-quality, natural, and tasty nutrition? We are! It's our ambition to shape the future of nutrition. Döhler is a leading global producer of natural ingredients and solutions for the food, beverage, lifestyle and nutrition industries. We use innovative technology to process plant-based raw materials and enrich products such as lifestyle drinks, cereals, dairy, and confectionery goods for almost every well-known brand. Close to 10.000 dedicated employees in more than 70 countries share one common goal - to ensure that millions of people around the world enjoy the products created by us. We strive to inspire and empower our employees in everything we do, and we invite you to join our team - together WE BRING IDEAS TO LIFE. Your role: * You support global production sites in all matters relating to manufacturing technologies * You develop global standards for process technology * End-to-end implementation and support of technical and technological projects is part of your responsibilities. These projects can also be carried out in collaboration with related departments, such as R&D, Technology Development, and Production. * You support the optimization of plant availability by further developing current plant and process technology, taking occupational safety, quality, and environmental aspects into account. * With your support, continuous improvement processes will be driven forward with regard to plants, systems, methodologies, processes, and competencies. * You are looking for solutions to increase productivity and improve process stability Your profile: * Completed degree in food process engineering, biotechnology, bioprocess engineering, engineering, food technology, dairy, brewery, or mechanical engineering * At least 5 years of experience in plant processes/production, experience in plant or equipment engineering, ideally in food or biotechnology. * In-depth knowledge of a wide range of process engineering processes * Experience in optimization/analysis processes and tools. * Working language is German and English (spoken and written) Your Benefits * Culture: Friendly and informal atmosphere, family-owned company, flat hierarchies, short communication channels, and helpful colleagues * Impact: You are an integral part of our business success and make an important contribution to the future of nutrition * Empowerment: You can fully unleash your potential and have the opportunity to take on responsibilities * Digitalization: We maintain excellent partnerships with market-leading innovators, allowing you to access and work with state-of-the-art technologies * Anniversary and special payments * Employee referral bonuses * Additional benefits: Christmas parties, events, financial benefits, and online shop discounts (e.g., IT leasing, mobile phone contracts, shopping, and travel discounts, etc.) * Optional Benefits * Welcome@Döhler: Onboarding event for all new colleagues, as well as several weeks of individual training (DA only) * Döhler Academy: You have the opportunity to continuously develop your education further through internal and external training programs * Food is taken care of: On-site cafeteria with regional and varied cuisine and complimentary drinks (location-specific) * Stay fit: Take advantage of local sports offerings at reduced prices (DA only) * Mobility: Subsidized Germany ticket or JobRad (DA only; also in DA: cooperation partners for all things related to cars) * Insurance benefits such as company pension plans and accident insurance (DA only) * Global growth trajectory: Challenging and internationally oriented work at our headquarters in Darmstadt (DA / Global; Comm., CF, SC Group Func.) * Attractive location in Darmstadt: Easily accessible by train, bus, on foot, or by car (free parking) (DA / Supply Chain) Equal opportunities for all We welcome applicants, who are just as diverse as we are - regardless of age, ancestry, disability, ethnic origin, gender, nationality, religion, sexual orientation, social background or any other characteristic protected by applicable laws, regulations and ordinances. Become a part of our team and apply online trough our career portal to the attention of Anika Werner-Sencandan. Please note that we are unable to consider or return application documents sent by mail.

Johnson Controls is a global diversified technology and multi industrial leader serving a wide range of customers in more than 150 countries. Our 117,000 employees create intelligent buildings, efficient energy solutions, integrated infrastructure and next generation transportation systems that work seamlessly together to deliver on the promise of smart cities and communities. Our commitment to sustainability dates back to our roots in 1885, with the invention of the first electric room thermostat. We are committed to helping our customers win and creating greater value for all of our stakeholders through strategic focus on our buildings and energy growth platforms. For additional information, please visit *********************** or follow us @johnsoncontrols on Twitter. WD**********7 Process Launch Engineer - DE - Middletown Job Description: Process Launch Engineer Johnson Controls is a global diversified technology and industrial leader serving customers in more than 150 countries. Our 170,000 employees create quality products, services and solutions to optimize energy and operational efficiencies of buildings; lead-acid automotive batteries and advanced batteries for hybrid and electric vehicles; and interior systems for automobiles. Johnson Controls, Inc. is an equal employment opportunity and affirmative action employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, protected veteran status, sexual orientation, gender identity, status as a qualified individual with a disability or any other characteristic protected by law. The Process Launch Engineer position is a corporate position for a candidate that will be located at a battery assembly plant location in the U.S. The candidate will report directly to corporate Manufacturing Engineering but will work closely with the plant manufacturing team in the facility they are located. The position will require the candidate to travel to other assembly plant locations in the U.S. and possibly Mexico that have defined capacity expansion projects. The Process Launch Engineer participates as a team member in projects of varying complexity and duration in the Mfg. Eng. Assembly area. The primary task assignment of the position is to provide assistance for the installation and start-up of equipment in the battery assembly area. The candidate will also assist in performing equipment checkout and acceptance at supplier facilities. The candidate will provide equipment design and PLC software support for the assigned projects. The candidate will assist in developing process specifications, Work instructions and other process documentation as assigned. Duties: Participates as an Electrical Engineer team member in cross-functional teams assigned to startup new equipment and to develop changes to existing equipment as required. Acts as manufacturing engineering lead in smaller projects that improves the battery assembly process capability. Prepares and presents project progress reports with team members and plant personnel. Seeks out and secures team members input and participation on projects. Identifies barriers to project success and leads efforts to eliminate the barriers. Collaborates with Safety, Environmental, and Quality Assurance Dept. personnel to ensure that battery assembly process and equipment are capable of producing a product that meets all Safety, Environmental, Quality and Engineering standards. Interactions with plant manufacturing employees, plant maintenance employees and plant leadership in understanding the plant focus and the barriers to production performance. Performs other tasks as assigned. Qualifications Job Qualifications: Requirements: A Bachelor of Science degree in Electrical Engineering. AutoCAD drafting experience; ability to design and generate electrical schematics adhering to NFPA standards is required. Demonstrable ability to fluently communicate in the English language. Required Skill set: Allen-Bradley PLC and HMI Programming (RS-View, Panel builder, RS Logix500, RS Logix5000) Siemens (TI) PLC ProgrammingRobot Programming, Servo and motion control systems AutoCAD, Microsoft Office, Other beneficial skills:Minitab, Six Sigma Additional requirements: Travel to various battery assembly plants throughout the US and Mexico is to be expected. Travel away from the assigned assembly plant location can reach or exceed 50% during peak expansion project implementation phases. Working hours in the battery plants during expansion project implementation may require working shifts other than 1st and working days on the weekend as needed; compensated work days that occur on the weekend will be provided. Additional Information Organization: Power Solutions Primary Location: United States-Middletown, DE ******************************************************************************** EEO/AA/Female/Minority/Veteran/Disability Employer We welcome diversity in our workplace and encourage applications from all qualified women and men,

This role will design, develop, optimize, and support GMP drug product manufacturing and packaging process, including equipment, facilities, and control systems at our Middletown, Delaware site. This may include support of CQV programs for manufacturing/packaging equipment, instruments, utilities, and processes. The Engineer is also responsible for ensuring external and internal quality standards are applied and followed. **Responsibilities** + Implementing and maintaining manufacturing process automation and control systems. + Participate as a member of cross functional teams in completion of system impact evaluations and system risk assessments in a multi-product facility. Performs gap assessments and remediates new risks as new equipment and/or products are introduced. + Assists with the preparation and maintenance of User Requirements Specifications. + Ensuring compliance with regulatory requirements (FDA, EMA, cGMP), quality standards, and safety regulations. + Conducting risk assessments and supporting equipment/utilities qualification activities. + Hands-on experience with troubleshooting and resolving process equipment-related issues during production. + Experience managing equipment, Preventive Maintenance, Calibration, and reliability programs independently with minimum supervision. + Experience with OSD equipment but not limited to Wet Granulation systems, Bin Blenders, Encapsulation, Tablet Presses, Tablet Coaters, Roller Compactors, etc. is a must. + Experience in packaging equipment like bottle packaging, blister packaging, and powder packaging. + Collaborating with cross-functional teams, including R&D, Quality Assurance, Production, and Regulatory Affairs. + Experience in writing Change Controls, Investigation reports, Work Orders, CAPA, Standard Operating Procedures (SOP), and risk assessments. + Analyzing process data and driving continuous improvement initiatives to enhance efficiency, reduce costs, and improve product quality. + Providing technical support and training to production staff on new processes, equipment, and safety protocols. + Identifies and proposes process improvement ideas and collaborates with cross-functional teams to meet project deliverables and timelines, including scheduling, testing, and deviation resolution. + Performs other related duties as assigned. **Qualifications** + 3 - 5 years of experience in a Process or Equipment engineering role, preferably in the pharmaceutical drug products manufacturing industry. + Ability to read and understand engineering drawings such as P&IDs, equipment/facility layout drawings, electrical/pneumatic drawings, and functional specifications. + Thorough understanding of cGMP and FDA requirements + Strong communication and documentation skills + Proven project management skills + Experience with equipment qualification following ISPE and ASTM guidelines. + Proficient with Microsoft Office Suite, Maximo, Calibration program software, MES, etc. + Preferred Qualifications: + Prior experience as an equipment or process engineer with process control systems and troubleshooting of pharmaceutical manufacturing processes and packaging equipment. + Familiarity with Sterile F/F equipment qualification is a plus. + Familiarity with the IOQ/PQ process/packaging equipment for the pharmaceutical industry. + Familiarity with Maximo or equivalent Regulatory Asset Manager software. **Experience / Education:** + Bachelor's degree in engineering (Mechanical, Electrical, Industrial) or a related field. + 3-5 years of maintenance experience in a pharmaceutical, biotechnology, life science, or FDA-regulated manufacturing environment. **Knowledge / Skills / Abilities:** + Technical: Strong understanding of engineering principles, process design and optimization, quality control, pharmaceutical manufacturing technologies, equipment, and relevant software. Knowledge of cGMP guidelines and regulatory compliance is essential. + Analytical & Problem-Solving: Ability to analyze complex processes and data, identify bottlenecks, troubleshoot issues, and develop effective solutions. + Soft Skills: Excellent communication (written and verbal), teamwork, leadership, project management, organizational abilities, time management, adaptability, attention to detail, critical thinking, and negotiation skills.Industry Specific: Familiarity with FDA regulations, cGMP guidelines, Lean Manufacturing, and risk assessment techniques (HAZOP, FMEA). An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. **Need help finding the right job?** We can recommend jobs specifically for you! An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability (************************************************************************************************** **Job Locations** _US-DE-Middletown_ **Job ID** _2025-13789_

Join Kistler - A Global Leader in Measurement Technology! At Kistler, we're revolutionizing industries with our cutting-edge dynamic measurement technology, helping customers optimize products and processes. From automobile development to smart factories, our Swiss-designed sensor solutions are driving the future of electrified drive technology, industrial automation, and emission reduction. Why Kistler? At Kistler, we value your expertise and offer opportunities for professional growth in a global environment. Our competitive benefits package includes: * Medical, dental, vision, life, and disability coverage * 401(k) plan with a 4% company match * Generous personal and vacation time Join a team that's shaping the future of measurement technology. We look forward to meeting you! Kistler Instrument Corporation is an Equal Opportunity Employer.

Job Description The Plant Manufacturing Engineer II - Equipment is responsible for manufacturing related projects in areas that include, but are not limited to, equipment assessment and improvement, process improvements, safety and environmental issues, information systems and lean practices. This position will also initiate, lead, and execute cost out projects that may include the preparation of Capital Expenditure Requests, with financial justification, for equipment repair, new technology, and/or processes. The individual shall demonstrate BAC's values of Earning Trust, Embracing Responsibility, Showing Courage, and Driving Innovation. The purpose for every position at BAC, regardless of department or level, can be summed up as doing the right thing in the right way. PRINCIPAL ACCOUNTABILITIES Lead the identification and initiation of safety, quality and productivity cost out projects. Develop detailed project plans and improvement projections to recommend a course of action to the Department Manager and Plant Leadership Team. Benchmark, research, evaluate and specify technology and/or equipment for process improvement projects. Implement new technology, equipment, or processes while tracking completion against the project plan. Identify and lead, while partnering with the maintenance department, equipment refurbishment and upgrade projects, to improve reliability, throughput, OEE (Overall Equipment Effectiveness) and MTBF (Mean Time Between Failures). Partner with the engineering, maintenance and operations teams to improve Preventive Maintenance programs effectiveness, driving a sustainable TPM culture. Analyze significant equipment and process failures to determine the root cause and create action plans to mitigate future risk. Support commissioning activities for all upgrade, renovation, and construction projects which may include, but are not limited to, operating procedures, repair procedures, energy isolation procedures, PM tasks and critical spare parts lists. Support, train and mentor maintenance mechanics and machine operators on optimal machine function, and service techniques. Develop control plans for equipment. Audit existing processes for conformance to standards. Design and implement complex fixtures and tooling, when necessary, to support consistent and safe manufacturing processes. Prepares Capital Expenditure Requests for equipment and process improvements. Maintains accurate cost out performance for the project. Acts locally while thinking regionally by sharing and adopting best practices in manufacturing technology and processes. Develop a deep understanding of manufacturing equipment. Demonstrated commitment to safety and adherence to safety polices. NATURE & SCOPE The Plant Manufacturing Engineer II will report to the Manufacturing Engineering Manager. This role is based in Milford, DE. This position does not have direct reports. KNOWLEDGE & SKILLS Education and Experience: Bachelor of Science in an Engineering discipline; Manufacturing, Industrial or Mechanical preferred Minimum 5 years' experience with metal fabrication equipment and process improvement Demonstrated hands-on and leadership experience executing projects Systems Experience: Excellent skills in MS Office Suite, specifically Excel, Word and PowerPoint Demonstrated strong engineering skills, including 2D/3D CAD design and GD&T experience Office365 experience and low coding strongly preferred CMMS experience preferred Project Management Experience: Demonstrated project management skills and sound technical judgment Strong internal/external customer focus to drive successful project results Demonstrated leadership, communication, and collaboration skills Ability to influence, negotiate, and build consensus in order to make decisions to move projects forward Experience with change management methodologies preferred Technical Experience: Knowledge/experience of electrical, pneumatic, and hydraulic systems preferred Knowledge of manufacturing technologies including sheet metal fabrication, steel tube fabrication/bending, welding, coatings, thermoforming, controls, automation and IoT preferred Hands on fabrication and/or operations experience preferred (Mills, Lathes, Grinders, CNCs, Welding, etc.) Demonstrated proficiency leading and executing actions to correct machinery deficiencies yielding throughput and OEE (Overall Equipment Effectiveness) improvements Experience identifying and implementing opportunities using the Five Lean Principles, 5S and the Eight Wastes Demonstrated competency with Root Cause Analysis and Problem-Solving techniques such as 5Y, Fish Bone and A3 Experience with the FMEA process to eliminate and mitigate risk Experience with identifying and implementing cost outs for labor, materials and overhead Demonstrated proficiency for data collection, analysis, presentation, and decision making Communication Experience: Effective written and oral communication skills Strong interpersonal skills Ability to work on a wide variety of projects and communicate effectively with key stakeholders WORKING CONDITIONS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the job. While performing this job, the employee is regularly required to stand and walk up to 60% of the time. Physical work is required up to 25% of the time. This position requires occasional lifting up to 50 pounds and travel up to 10% of the time.

Graver Technologies LLC As a part of the global industrial organization Marmon Holdings-which is backed by Berkshire Hathaway-you'll be doing things that matter, leading at every level, and winning a better way. We're committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone's empowered to be their best. Under broad supervision, responsible for product and/or business services sales in order to reach the project profitability and billing levels so that clients are satisfied. Develops proposals, assesses customer needs in order to recommend appropriate products/services. May customize product in order to meet client requirements. Provides technical support to clients after the sale of the product, troubleshoots technical problems. May visit clients in order to present company's products/services. Has working technical knowledge of all phases of the activity. Role typically requires between 3 and 5 years of experience. We are seeking a technically skilled and customer-focused Applications Engineer to join our inside sales team. In this role, you will serve as the technical liaison between our customers and the engineering team, providing expert consultation on our liquid process filtration and crossflow membrane technologies. You will be responsible for understanding customer requirements, recommending appropriate filtration solutions, and providing technical support throughout the sales process. Key Responsibilities * Provide technical expertise and application support for our liquid process filtration and crossflow membrane product lines * Analyze customer requirements and process conditions to recommend optimal filtration solutions * Collaborate with field sales representatives to develop technical proposals and quotations * Conduct technical presentations and product demonstrations for customers and prospects * Assist in troubleshooting customer applications and resolving technical issues * Support product trials and pilot testing at customer facilities * Participate in technical trade shows and industry events * Document and communicate application successes and challenges to R&D and product management * Stay current on industry trends, competitive offerings, and emerging technologies * Contribute to the development of technical literature, application notes, and case studies Qualifications * Bachelor's degree in Chemical Engineering, Mechanical Engineering, or related technical field * 2+ years of experience in liquid filtration, separation processes, or related industries * Strong understanding of fluid dynamics, filtration theory, and membrane separation principles * Knowledge of industrial manufacturing processes and equipment * Excellent problem-solving skills and technical aptitude * Strong communication skills, with the ability to explain complex technical concepts clearly * Customer-focused mindset with consultative sales approach * Proficiency with CRM systems and MS Office applications * Experience with filter sizing calculations and system design (preferred) * Knowledge of regulatory requirements in regulated industries like food, beverage, or pharmaceuticals (preferred) Specific Technical Knowledge Areas * Knowledge of depth filtration and surface filtration principles * Experience with crossflow membrane technologies (microfiltration, ultrafiltration, nanofiltration) * Understanding of filter media types and performance characteristics and filtration system components and operation * Knowledge of filter testing methodologies and performance evaluation * Understanding of common contaminants and separation challenges * Familiarity with industrial process flow diagrams and P&IDs Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law. We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to ******************, and please be sure to include the title and the location of the position for which you are applying.

Primary Duties & Responsibilities * Product focused materials R&D: Optimize existing materials, develop new materials, productionize of successful development projects * Lead materials characterization activities for Delaware site * Participate in prototyping activities in line with 5-year plan, including planning and scheduling, documentation, customer interface, supplier interface, and hands-on activities * Participate in Lean/Kaizen events with goals of increasing efficiency, enhancing quality and improving output * Participate in ISO activities for R&D group * Maintain a focus outside of Coherent to keep track of innovations in the field (e.g., external literature, external conferences, use of AI searches) Education & Experience * PhD degree in Materials Engineering or related fields with 5+ years of industrial experience highly preferred. Combination of schooling and relevant experience can be considered. * Demonstrated experience with publishing technical papers, presenting at technical conferences and/or patent preparation a strong plus. * Interact with customers to set acceptable material requirements and characterization standards. Skills * Strong background in materials R&D field, with focus on ceramics, metals, and coatings * Experience with materials manufacturing equipment, including vacuum furnaces, alternate atmosphere kilns, mixers, presses, alloy melters, and molders * Experience with materials characterization equipment, including optical microscopes, SEMs, X-ray diffraction, ICP, GDMS, universal testing machines, etc. * Experience with powder characterization equipment, including particle size analyzers and tap pack density machines * Working knowledge of data analysis tools (SPC, MiniTab and DoE) * Experience with problem solving and resolution (8D, fishbone, etc.) * Demonstrated ability to work as part of a team and leading lower level engineers and technicians * Hands-on and very direct approach to problem solving * Excellent interpersonal and communication skills * Experience with networked PC based computer system (MS Office, spreadsheets, data bases, graphics, Email, etc.) Working Conditions Office and Shopfloor Physical Requirements * Ability to occasionally lift/push/pull up to 20 lbs * Able to sit, stand, bend, squat and walk about the facility * Walk of uneven and slippery surfaces Safety Requirements All employees are required to attend scheduled training, follow the site EHS procedures and Corporate EHS standards. This includes the use of proper protective equipment (PPE) as required by the job responsibilities. Managers will ensure that all safety and environmental procedures are followed consistently. They will ensure that risk assessments are performed, proper training, work instructions, required PPE is available, and will monitor compliance. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Textile Materials Engineer BH Job ID: 3295 SF Job Req ID: 15727 Ingersoll Rand is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. Job Title: Textile Materials Engineer Location : Frederica, DE (Onsite with travel) About Us Imagine a company with technology leadership of over 160 years, yet it operates with the energy of a startup. Ingersoll Rand has dedicated itself to Making Life Better for its employees, customers, shareholders, and planets. We produce innovative and mission-critical flow creation and life science technologies - from compressors to precision handling of liquids, gasses, and powers - to increase industrial productivity, efficiency, and sustainability. Supported by over 80+ brands, our products are used in various end-markets including life sciences, food and beverage, clean energy, industrial manufacturing, infrastructure, and more. Across the globe, we're driving growth with an entrepreneurial spirit and ownership mindset. Learn more at irco.com and join us to own your future. Job Overview: We're looking for a Textile Materials Engineer to ensure advanced materials meet the rigorous demands of human spaceflight. As part of ILC Dover, an Ingersoll Rand Business, you'll join the team behind the only proven and flown spacesuits for NASA; a legacy of innovation that has protected astronauts for generations. As a Textile Materials Engineer , you'll be at the forefront, developing and qualifying advanced textile -based materials that make human spaceflight possible. This is not a typical engineering role. It's high-stakes and hands-on, where every decision matters. You'll identify, test, and qualify technical fabrics and composite materials for spaceflight hardware, collaborating directly with textile manufacturers to ensure every material meets mission-critical performance demands. Your work will also involve developing and maintaining engineering documentation aligned with NASA's strict Materials & Processes standards. Beyond documentation, this role puts you on the production floor, solving real-time materials challenges during suit fabrication, and your expertise will help shape the integrity of suits destined for orbit and beyond. You'll also play a key role in configuration management and change control through MasterControl , ensuring precision at every stage. The engineers who thrive here are those who bring experience with technical textiles (technical fabrics), PPE , military gear, fire-resistant fabrics, and / or inflatable systems. They are curious, collaborative problem solvers who want their work to mean something, something bigger than Earth itself. Are you ready to engineer the future of space exploration? Suit up, build what astronauts trust with their lives, and your work could walk on the Moon. Responsibilities: * Employ established science and engineering principles in the research, design and development of materials and processes for space flight hardware. * Maintain a detailed knowledge and understanding of softgood materials, their testing, and manufacturing processes, specifically for space flight applications. * Generate and maintain engineering and material control documents to ensure compliance with space flight hardware requirements including material drawings, Material Identification and Usage Lists, flight or material waivers (including Material Usage Agreements and Material Review Board waivers ), and other program documentation related to material/product definition and control. * Identify, evaluate, and define material requirements and generate specifications. * Perform materials testing/analysis and generate testing/analysis documentation. * Effectively present materials engineering information to team members as well as cross-functional partners and external clients/ customers as necessary. Requirements: * Bachelor of Science Degree in Textile Engineering , or related field of study; or equivalent combination of education and experience * 4+ years of experience performing Technical Fabric / Textile Engineering tasks or similar experience with NASA M&P ( materials & processes) * Must work effectively cross-functionally with peers and departmental teams to deliver on time for internal and external customers, perform under pressure, and meet tight deadlines. * Must have strong proficiency in word processing, spreadsheet software, intermediate CAD , and basic 3D modeling , along with the ability to communicate clearly and concisely, both verbally and in writing. * Proven in following work instructions, blueprints, and other technical documents, while always adhering to safety protocols, including proper use of personal protective equipment ( PPE ). * Requires U.S. Citizenship or lawful Permanent Resident due to access to shared databases and systems that support government programs. * The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Communicate with team members on a regular basis in writing and speech; use of hands to handle, control, or feel objects, tools, or controls; wear common protective or safety equipment; standing for long periods of time. The employee is frequently stooping, crawling, climbing, and performing repetitive motion with arms. The employee occasionally sits. The employee frequently lifts up to 50 Lbs. and occasionally will lift up to 75 lbs. Core Competencies: * Textile Materials Expertise - Expertly test, analyze, and qualify advanced textiles and composites that make spaceflight possible. * Documentation & Compliance - Create and manage critical engineering documents to ensure every material meets NASA standards. * Hands-On Problem Solving - Address materials challenges on the production floor and deliver solutions that impact real-time operations. * Cross-Functional Collaboration - Work seamlessly across teams and with external partners to achieve precise, mission-critical results. * Performance Under Pressure - Interpret complex instructions, meet tight deadlines, and maintain focus in high-stakes situations. Travel & Work Arrangements * Work is fully onsite with required travel to local worksites as needed. * Anticipated travel is less than 20% as might be needed for supplier and customer visit. * U.S. Citizenship or lawful Permanent Resident due to government contracts * Position is eligible for relocation assistance What We Offer At Ingersoll Rand, we embrace a culture of personal ownership - taking responsibility for our company, our communities, and our environment, as well as our individual health and well-being. Our comprehensive benefits package is designed to empower you with the tools and support necessary to take charge of your health, ensuring that together, we can continue to make life better. Our range of benefits includes health care options like medical and prescription plans, dental and vision coverage, as well as wellness programs. Additionally, we provide life insurance, a robust 401(k) plan, paid time off, and even an employee stock grant, among other offerings. These benefits are our commitment to you, so you can be your best at work and beyond. Ingersoll Rand Inc. (NYSE:IR), driven by an entrepreneurial spirit and ownership mindset, is dedicated to helping make life better for our employees, customers and communities. Customers lean on us for our technology-driven excellence in mission-critical flow creation and industrial solutions across 40+ respected brands where our products and services excel in the most complex and harsh conditions. Our employees develop customers for life through their daily commitment to expertise, productivity and efficiency. For more information, visit *************

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

Why join Hologic: You will have the opportunity to get in on the ground floor at a high growth world class manufacturing facility working on life-saving medical devices with potential for future growth. This is a great opportunity to enhance your manufacturing operation skills and knowledge to further your career. What to expect: Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing cost determines time standards and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. A seasoned, experienced professional with a full understanding of area of specialization; resolves a wide range of issues in creative ways. This job is the fully qualified, career-oriented, journey-level position. Normally receives little instruction on day-to-day work, general instructions on new assignments. Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. Demonstrates good judgment in selecting methods and techniques for obtaining solutions. Networks with senior internal and external personnel in own area of expertise. What we expect: Performs complex experiments that may require support and coordination of other engineers or technicians. Active participant in R&D projects, providing design input and ensuring projects can be translated into cost-effective production. Supports R&D in marking cost estimated for equipment, tools, and components. Responsible for the manufacture and performance of assigned product line (s). Responsible for setting up fabrication and assembly procedures to manufacture products. Establishes methods and tooling needed for new and existing processes. Assists in the design of tooling and fixtures. Initiates and/or approves necessary changes in design, drafting, tooling, methods, processes, and documentation that affects the manufacturing process. Oversee the creation and revision of standard operation procedures, organizational standards, directives pertaining to scheduling, cost control and production performance evaluation. Develop, verifies and validate processes for manufacturing. Responsible for the maintenance of production equipment and works with Facilities on the implementation of predictive maintenance of manufacturing equipment. Responsible for identifying, diagnosing, prioritizing, and correcting technical issues that may arise in standard manufacturing. Works in conjunction with other departments where appropriate. Evaluate and develop process control data for trending analysis. Analyzes defects, provides feedback, and implements process improvements. Participates in design reviews, working with R&D and manufacturing to resolve all issues, particularly those arising from the violation of design standards or changes from existing manufacturing procedures. Actively supports and adheres to the Quality Policy and Quality System procedures. Identify and lead complex projects that drive meaningful improvements positively impacting product quality and manufacturing efficiency and costs. Establish collaborative relationships with all stakeholders within the site and create links with experts within the Hologic network. Maintains professional and technical knowledge by attending educational workshops. Manage one project without supervision. Train and mentor Manufacturing Engineer 1 Be a change agent driving improvement on a daily basis. Education & Experience: Preferred Minimum Non-Technical Degree: College Degree Preferred Minimum Technical/Advanced Degree: Technical Bachelor's Degree Preferred Minimum Non-Technical Degree: 5-8 Years Preferred Minimum Technical/Advanced Degree: 2-5 Years with Technical Bachelor's Degree, 1-3 Years with Master's Degree, 0-1 Years with PhD Automation experience, such as implementation of an automated cell/line is beneficial. Experience in rapid scale up of new products or operations is beneficial. The annualized base salary range for this role is $97,500 to $152,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.. Agency and Third Party Recruiter Notice: Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans. #LI-PR1 Must follow all applicable FDA regulations and ISO requirements. Hologic is an equal opportunity employer inclusive of female, minority, disabled and veterans, (F/M/D/V)

About the Role Selectek is seeking a Process Engineer with strong injection molding expertise to drive process optimization, new mold introduction, and continuous improvement for a growing manufacturer serving aerospace, pharma, automotive, medical, and other industries. This is a hands-on role with direct impact on cycle times, scrap reduction, uptime, and quality. The environment is collaborative and relaxed-great for someone who enjoys solving technical problems without high corporate pressure. Key Responsibilities Own molding process development for new molds, including trials, DOE, and parameter optimization. Partner with customers on mold modifications and manufacturability decisions. Improve existing lines: optimize cycle time, reduce scrap and downtime, and raise first-pass yield. Create, update, and maintain standard work, work instructions, and department procedures. Conduct/oversee Arc Flash relevance to process equipment as needed (coordination with EHS/maintenance). Perform root cause analysis and lead corrective actions using formal problem-solving and Lean/Six Sigma methods. Support daily start-ups/restarts/shutdowns when development work is light. Mentor process technicians; contribute to skills growth and cross-training. Track and report area KPIs/metrics (scrap, OEE, downtime drivers, throughput). Collaborate closely with manufacturing, tool room, maintenance, quality, and engineering to meet customer demand and quality targets. Ensure ISO procedures and quality plans are followed; promote a strong safety culture. Team scope today: No direct reports initially; mentorship of techs is expected. As the site grows, leadership scope may increase. Required Qualifications Proven proficiency with injection molding processing. Experience with engineered and high-temperature resins. Ability to interpret part prints, quality plans, and work instructions and apply them at the press. Demonstrated use of formal problem-solving (e.g., 8D, PDCA, fishbone, Five Whys). Ability to program robots and exchange end-of-arm tooling. Working knowledge of CAD/SolidWorks and Moldflow (or equivalent). Familiarity with ISO 9001:2008 and TS 16949:2009 (IATF 16949 exposure a plus). Proficient with Microsoft Office (Word, Excel) for documentation and analysis. Excellent written, verbal, and interpersonal communication skills. Preferred Qualifications Lean/Six Sigma training/certification (Green Belt or Black Belt). Supervisory/lead experience in a manufacturing setting. Formal supervisory training. What You'll Love Impact: Direct ownership of molding performance and new product/mold launches. Growth: Company has doubled in size over the last three years; advancement opportunities as the team scales. Culture: Relaxed, low-stress environment focused on practical results and continuous improvement. Benefits: Negotiable package including 2-3 weeks PTO, 401(k), and relocation assistance. Hiring Process & Requirements Interviews: Local candidates typically 2 rounds; non-local: initial Teams, then onsite. Assessments: Possible personality and/or CAD exercise. Screens: Background check (7 years) and drug screen conducted by the employer. Location: Georgetown, DE 19947 Schedule: Monday-Friday, ~8:00 AM - 5:00 PM (may vary) Employment Type: Direct Hire Compensation: $75,000-$90,000 (DOE) | Relocation Assistance Available Work Setup: Onsite (not remote) | Travel: No Apply Now If you're interested in this opportunity, contact: Jaie Rogers - Selectek ? jrogers@selectek.com |? 678-802-6632

**Are you looking to power the next leap** in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. Join our Talent Community (*************************************************************** to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** .

This role will design, develop, optimize, and support GMP drug product manufacturing and packaging process, including equipment, facilities, and control systems at our Middletown, Delaware site. This may include support of CQV programs for manufacturing/packaging equipment, instruments, utilities, and processes. The Engineer is also responsible for ensuring external and internal quality standards are applied and followed. Responsibilities Implementing and maintaining manufacturing process automation and control systems. Participate as a member of cross functional teams in completion of system impact evaluations and system risk assessments in a multi-product facility. Performs gap assessments and remediates new risks as new equipment and/or products are introduced. Assists with the preparation and maintenance of User Requirements Specifications. Ensuring compliance with regulatory requirements (FDA, EMA, cGMP), quality standards, and safety regulations. Conducting risk assessments and supporting equipment/utilities qualification activities. Hands-on experience with troubleshooting and resolving process equipment-related issues during production. Experience managing equipment, Preventive Maintenance, Calibration, and reliability programs independently with minimum supervision. Experience with OSD equipment but not limited to Wet Granulation systems, Bin Blenders, Encapsulation, Tablet Presses, Tablet Coaters, Roller Compactors, etc. is a must. Experience in packaging equipment like bottle packaging, blister packaging, and powder packaging. Collaborating with cross-functional teams, including R&D, Quality Assurance, Production, and Regulatory Affairs. Experience in writing Change Controls, Investigation reports, Work Orders, CAPA, Standard Operating Procedures (SOP), and risk assessments. Analyzing process data and driving continuous improvement initiatives to enhance efficiency, reduce costs, and improve product quality. Providing technical support and training to production staff on new processes, equipment, and safety protocols. Identifies and proposes process improvement ideas and collaborates with cross-functional teams to meet project deliverables and timelines, including scheduling, testing, and deviation resolution. Performs other related duties as assigned. Qualifications 3 - 5 years of experience in a Process or Equipment engineering role, preferably in the pharmaceutical drug products manufacturing industry. Ability to read and understand engineering drawings such as P&IDs, equipment/facility layout drawings, electrical/pneumatic drawings, and functional specifications. Thorough understanding of cGMP and FDA requirements Strong communication and documentation skills Proven project management skills Experience with equipment qualification following ISPE and ASTM guidelines. Proficient with Microsoft Office Suite, Maximo, Calibration program software, MES, etc. Preferred Qualifications: Prior experience as an equipment or process engineer with process control systems and troubleshooting of pharmaceutical manufacturing processes and packaging equipment. Familiarity with Sterile F/F equipment qualification is a plus. Familiarity with the IOQ/PQ process/packaging equipment for the pharmaceutical industry. Familiarity with Maximo or equivalent Regulatory Asset Manager software. Experience / Education: Bachelor's degree in engineering (Mechanical, Electrical, Industrial) or a related field. 3-5 years of maintenance experience in a pharmaceutical, biotechnology, life science, or FDA-regulated manufacturing environment. Knowledge / Skills / Abilities: Technical: Strong understanding of engineering principles, process design and optimization, quality control, pharmaceutical manufacturing technologies, equipment, and relevant software. Knowledge of cGMP guidelines and regulatory compliance is essential. Analytical & Problem-Solving: Ability to analyze complex processes and data, identify bottlenecks, troubleshoot issues, and develop effective solutions. Soft Skills: Excellent communication (written and verbal), teamwork, leadership, project management, organizational abilities, time management, adaptability, attention to detail, critical thinking, and negotiation skills. Industry Specific: Familiarity with FDA regulations, cGMP guidelines, Lean Manufacturing, and risk assessment techniques (HAZOP, FMEA). An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

Primary Duties & Responsibilities Product focused materials R&D: Optimize existing materials, develop new materials, productionize of successful development projects Lead materials characterization activities for Delaware site Participate in prototyping activities in line with 5-year plan, including planning and scheduling, documentation, customer interface, supplier interface, and hands-on activities Participate in Lean/Kaizen events with goals of increasing efficiency, enhancing quality and improving output Participate in ISO activities for R&D group Maintain a focus outside of Coherent to keep track of innovations in the field (e.g., external literature, external conferences, use of AI searches) Education & Experience PhD degree in Materials Engineering or related fields with 5+ years of industrial experience highly preferred. Combination of schooling and relevant experience can be considered. Demonstrated experience with publishing technical papers, presenting at technical conferences and/or patent preparation a strong plus. Interact with customers to set acceptable material requirements and characterization standards. Skills Strong background in materials R&D field, with focus on ceramics, metals, and coatings Experience with materials manufacturing equipment, including vacuum furnaces, alternate atmosphere kilns, mixers, presses, alloy melters, and molders Experience with materials characterization equipment, including optical microscopes, SEMs, X-ray diffraction, ICP, GDMS, universal testing machines, etc. Experience with powder characterization equipment, including particle size analyzers and tap pack density machines Working knowledge of data analysis tools (SPC, MiniTab and DoE) Experience with problem solving and resolution (8D, fishbone, etc.) Demonstrated ability to work as part of a team and leading lower level engineers and technicians Hands-on and very direct approach to problem solving Excellent interpersonal and communication skills Experience with networked PC based computer system (MS Office, spreadsheets, data bases, graphics, Email, etc.) Working Conditions Office and Shopfloor Physical Requirements Ability to occasionally lift/push/pull up to 20 lbs Able to sit, stand, bend, squat and walk about the facility Walk of uneven and slippery surfaces Safety Requirements All employees are required to attend scheduled training, follow the site EHS procedures and Corporate EHS standards. This includes the use of proper protective equipment (PPE) as required by the job responsibilities. Managers will ensure that all safety and environmental procedures are followed consistently. They will ensure that risk assessments are performed, proper training, work instructions, required PPE is available, and will monitor compliance. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ****************************** .

Newark, DE, United States **Why join Hologic:** You will have the opportunity to get in on the ground floor at a high growth world class manufacturing facility working on life-saving medical devices with potential for future growth. This is a great opportunity to enhance your manufacturing operation skills and knowledge to further your career. **What to expect:** Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. Interfaces with design engineering in coordinating the release of new products. Estimates manufacturing costs, determines time standards, and makes recommendations for tooling and process requirements of new or existing product lines. Maintains records and reporting systems for coordination of manufacturing operations. Learns to use professional concepts. Applies company policies and procedures to resolve routine issues. Normally receives detailed instructions on all work. Works on problems of limited scope. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained. Builds stable working relationships internally. **What we expect:** + Perform experiments of limited scope and collect data. + Participate in the transfer of design changes from design engineering to manufacturing. + Define and develop assembly and test methods for assigned product line. + Specify and provide all necessary tools, equipment, fixtures, and facilities required for assigned product line. + Assure that work instructions and drawings are created and updated when necessary. + Assists in maintaining existing mechanical and electrical test fixtures. + Assist in developing, verifying, and validating processes for manufacturing. + Monitor quality reports and field performance of assigned product line, identify trends, investigate problems, perform root cause analysis, and recommend and implement corrective actions. + Actively supports and adheres to the Quality Policy and Quality System procedures. + Support projects that drive meaningful improvements positively impacting product quality and manufacturing efficiency and costs + Establish collaborative relationships with all stakeholders within the site. + Maintains professional and technical knowledge by attending educational workshops. + Manage one project at a time under a more senior Engineer supervision. **Education & Experience:** + Preferred Minimum Non-Technical Degree: College Degree + Preferred Minimum Technical/Advanced Degree: Technical Bachelor's Degree + Preferred Minimum Non-Technical Degree: 0-2 Years + Preferred Minimum Technical/Advanced Degree: 0-1 Years **Skills:** + Proficient in MS Office + Detail oriented + Ability to work well within a team environment + Ability to read and interpret mechanical drawings + Ability to understand, troubleshoot and resolve issues with equipment & processes + Strong written, verbal, and interpersonal communication skills + Strong organizational and time management skills + Ability to work independently + Takes initiative + Training or certification in Six Sigma, SPC and/or other statistical process control methods is beneficial + SolidWorks and AutoCAD is beneficial + Understanding of Lean Manufacturing principles is beneficial + Understanding of Root Cause and Root Cause Failure Analysis Methodologies is beneficial The annualized base salary range for this role is $65,000 to $102,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, geography, education, business needs and market demand.. **Agency and Third Party Recruiter Notice:** Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered. **_Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans._** **_\#LI-PR1_** **_Must follow all applicable FDA regulations and ISO requirements._** **_Hologic is an equal opportunity employer inclusive of female, minority, disabled and veterans, (F/M/D/V)_**

This role will design, develop, optimize, and support GMP drug product manufacturing and packaging process, including equipment, facilities, and control systems at our Middletown, Delaware site. This may include support of CQV programs for manufacturing/packaging equipment, instruments, utilities, and processes. The Engineer is also responsible for ensuring external and internal quality standards are applied and followed. Responsibilities Implementing and maintaining manufacturing process automation and control systems. Participate as a member of cross functional teams in completion of system impact evaluations and system risk assessments in a multi-product facility. Performs gap assessments and remediates new risks as new equipment and/or products are introduced. Assists with the preparation and maintenance of User Requirements Specifications. Ensuring compliance with regulatory requirements (FDA, EMA, cGMP), quality standards, and safety regulations. Conducting risk assessments and supporting equipment/utilities qualification activities. Hands-on experience with troubleshooting and resolving process equipment-related issues during production. Experience managing equipment, Preventive Maintenance, Calibration, and reliability programs independently with minimum supervision. Experience with OSD equipment but not limited to Wet Granulation systems, Bin Blenders, Encapsulation, Tablet Presses, Tablet Coaters, Roller Compactors, etc. is a must. Experience in packaging equipment like bottle packaging, blister packaging, and powder packaging. Collaborating with cross-functional teams, including R&D, Quality Assurance, Production, and Regulatory Affairs. Experience in writing Change Controls, Investigation reports, Work Orders, CAPA, Standard Operating Procedures (SOP), and risk assessments. Analyzing process data and driving continuous improvement initiatives to enhance efficiency, reduce costs, and improve product quality. Providing technical support and training to production staff on new processes, equipment, and safety protocols. Identifies and proposes process improvement ideas and collaborates with cross-functional teams to meet project deliverables and timelines, including scheduling, testing, and deviation resolution. Performs other related duties as assigned. Qualifications 3 - 5 years of experience in a Process or Equipment engineering role, preferably in the pharmaceutical drug products manufacturing industry. Ability to read and understand engineering drawings such as P&IDs, equipment/facility layout drawings, electrical/pneumatic drawings, and functional specifications. Thorough understanding of cGMP and FDA requirements Strong communication and documentation skills Proven project management skills Experience with equipment qualification following ISPE and ASTM guidelines. Proficient with Microsoft Office Suite, Maximo, Calibration program software, MES, etc. Preferred Qualifications: Prior experience as an equipment or process engineer with process control systems and troubleshooting of pharmaceutical manufacturing processes and packaging equipment. Familiarity with Sterile F/F equipment qualification is a plus. Familiarity with the IOQ/PQ process/packaging equipment for the pharmaceutical industry. Familiarity with Maximo or equivalent Regulatory Asset Manager software. Experience / Education: Bachelor's degree in engineering (Mechanical, Electrical, Industrial) or a related field. 3-5 years of maintenance experience in a pharmaceutical, biotechnology, life science, or FDA-regulated manufacturing environment. Knowledge / Skills / Abilities: Technical: Strong understanding of engineering principles, process design and optimization, quality control, pharmaceutical manufacturing technologies, equipment, and relevant software. Knowledge of cGMP guidelines and regulatory compliance is essential. Analytical & Problem-Solving: Ability to analyze complex processes and data, identify bottlenecks, troubleshoot issues, and develop effective solutions. Soft Skills: Excellent communication (written and verbal), teamwork, leadership, project management, organizational abilities, time management, adaptability, attention to detail, critical thinking, and negotiation skills. Industry Specific: Familiarity with FDA regulations, cGMP guidelines, Lean Manufacturing, and risk assessment techniques (HAZOP, FMEA). An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. We can recommend jobs specifically for you! An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability Click here to get started.