Manufacturing Technician Jobs in Hatfield, PA

$31.75 per hr 6 month extendable CONTRACT to HIRE Shift B-rotation-Confirmed Week 1 Wednesday to Saturday: 6:00PM - 5:30AM Week 2 Thursday to Saturday: 6:00PM - 6:30AM Shift Differential: 15% additional pay on top of hourly rate for night shift The shift differential is 15% - note, they train on day shift for ~12 weeks, when they move to the night shift, the 15% differential kicks in. REQUIRED: 1+ years of GMP biotech, pharma or medical device industry experience Aseptic technique experience OR cell/gene therapy, biologics experience Downstream/cell culture ideal is a plus Essential Functions and Responsibilities: Develop a comprehensive understanding of and execute clients GMP proficiently. cell therapy manufacturing process(es). Complete training sessions and ensure training documentation is maintained. Understand and comply with quality standards and requirements as documented. Provide operational support functions, including materials stocking and transfer, kit preparation, reagent preparation, room readiness, cleaning activities, and equipment maintenance. Perform document review, including executed Batch Records and Logbooks. Support documentation needs, which include a review of SOPs, Batch Records, Deviations, CAPAs, etc. Supports technical transfer and additional research-level testing activities as needed. Perform basic revisions as needed to reflect current procedures accurately. Support departmental projects in a contributor capacity. May support training sessions as a qualified trainer, ensuring training documentation is maintained. Assists with identifying training needs, establishing a feedback loop to ensure continuous improvement. May work on moderately complex assignments, requiring judgment to resolve operational issues without negatively impacting manufacturing efforts. Adhere to Good Manufacturing Practices (GMP) and Standard Operating Procedures (SOPs), including Good Documentation Practices (GDP). Completes recording of data to comply with regulatory requirements. Attend the daily huddle meeting and escalates issues/concerns at that forum to Area Management for further investigation. Ability to work in a team environment and independently as required. Works on routine assignments per written procedures, where the ability to recognize deviation from accepted practice is required. Must adhere to the clients core values, policies, procedures, and business ethics. Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations. Perform miscellaneous duties as assigned.

Avo Photonics is a dynamic contract engineering services company that designs, develops, and manufactures custom opto-electronic products for a large customer base. We seek a diligent, dedicated, and meticulous person who will help further our success and reputation in the industry. The successful candidate will have at least three years of manufacturing experience. Responsibilities: Support Process Engineering team by assembling prototypes and provide critical feedback on process viability for manufacturing Perform directed design of experiments; record structured data against controlled experiments and generate reports on procedure and results Perform documented performance checks, calibrations, and preventative maintenance on equipment including laser welders, seam sealers, die bonders, wire bonders, and more Collect measurements to ensure workstations are meeting ESD and cleanroom standards Review work instructions and provide training on developed processes to Manufacturing team Troubleshoot equipment and optical workstations to quickly resolve authorized production-impacting issues Requirements: A.S. (B.S. preferred) in the Sciences or Engineering 3 years of manufacturing experience 2 years experience in an engineer facing role Excellent communication skills and willingness to learn Avo Photonics offers competitive salaries and a comprehensive benefits package. Avo Photonics is not accepting unsolicited assistance from search firms for this employment opportunity. All resumes submitted by search firms to any employee of Avo Photonics by any method without a valid written contract in place with Avo Photonics will be deemed the sole property of Avo Photonics. No fee will be paid in the event the candidate is hired by Avo Photonics as a result of the referral or through any other means.

Day-to-Day Job Description Our large Manufacturing client is looking for a production operator to join their team. The Production Operator is responsible for the accurate and timely manufacturing of batches. The operator is expected to accurately measure all required materials, correctly add, and effectively operate all pressure kettles and mix tanks, including, but not limited to: scales, pumps, tanks and other manufacturing equipment. The operator is expected to maintain a safe and sanitary work area by ensuring the department and all equipment are cleaned and kept in good working order. Must Haves • Ability to operate in a fast-paced environment, effectively working with other members of the department. • Previous manufacturing experience is preferred. • Must be able to work on weekends when needed to complete customer orders that are scheduled. • Ability to lift 50 lbs without difficulty. • Ability to weigh ingredients accurately utilizing tools such as floor scale and flow meter. Compensation: $19/hour - $21/hour Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Driven by integrity and united by the people-and-pet bond, we find strong purpose in the work we do and an even greater joy in those we get to work alongside. Together, we harness the expertise of our long-standing tradition of excellence to embrace possibility and continuously push to do what's never been done before in pet care. Discover your purpose and fuel your passions when you bring your love of pets to a team that prides itself on the power of togetherness-We are Proudly Connected. Purely Driven. Position Summary Just 65 miles from Center City Philadelphia, Allentown is near many major Northeastern U.S. cities, which makes it an ideal location for manufacturing and distributing consumer goods. We utilize thermal processing and high-speed canning to produce varieties of our Friskies , Beneful and Pro Plan brands-product lines that we have carefully produced, packaged, and shipped since 1958. Together, we contribute to Allentown's identity as a busy industrial city, as well as a beautiful rural environment that we are truly proud to call home. That's why we not only make high quality food for pets but our factory is also doing our part to care for the environment we share, like conserving water, investing in renewable electricity and maintaining zero waste for disposal. The Production Operator positions are a vital piece of the Wet and Pouch Plants. You will be required to meet all Safety, Health, Quality and Environmental standards when performing job duties. The primary responsibilities in these roles include, but are not limited to operating various lines of equipment in production, packaging, moving raw material or finished packaged good with a forklift or other pallet jack, and providing relief for absences or vacations. These roles exist on back shifts and the opportunity for mandatory or voluntary overtime exist on these shifts and weekends, as required. Supply production lines and meat prep stations with adequate supplies to ensure continuous operations. Measure, weigh, blend and add materials to manual or automated systems, adjust speeds, temperatures, as needed. Pull samples and perform quality test, assist on quality trials or deliver test samples to Quality Assurance. Visually inspect ingredients and any substandard pallets or cans and remove any foreign materials from products. Clean and sanitize work areas and equipment ensuring safe practices when mixing cleaning chemicals used in the sanitation process. Safely and efficiently operate, troubleshoot, and make minor repairs on operating equipment and use lock out procedures, as prescribed. Support the factory in continuous improvement initiatives. Performs all other duties as assigned. Requirements High School Diploma and/or GED 1+ years' experience working in a manufacturing, agriculture, warehouse, military, or related environment required. Other Must be willing to work an overnight shift. The approximate hourly pay for this position is $30.18. Please note that the pay range provided is a good faith estimate for the position at the time of posting. Final compensation may vary based on factors including but not limited to background, knowledge, skills, and abilities as well as geographic location of the position. Nestlé offers performance-based incentives and a competitive total rewards package, which includes a 401k with Company match, healthcare coverage and a broad range of other benefits. Incentives and/or benefit packages may vary depending on the position. Learn more at About Us | Nestlé Careers (nestlejobs.com) REQUISITION ID 350761 It is our business imperative to remain a very inclusive workplace. To our veterans and separated service members, you're at the forefront of our minds as we recruit top talent to join Nestlé. The skills you've gained while serving our country, such as flexibility, agility, and leadership, are much like the skills that will make you successful in this role. In addition, with our commitment to an inclusive work environment, we recognize the exceptional engagement and innovation displayed by individuals with disabilities. Nestlé seeks such skilled and qualified individuals to share our mission where you'll join a cohort of others who have chosen to call Nestlé home. The Nestlé Companies are equal employment opportunity employers. All applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status or any other characteristic protected by applicable law. Prior to the next step in the recruiting process, we welcome you to inform us confidentially if you may require any special accommodations in order to participate fully in our recruitment experience. Contact us at accommodations@nestle.com or please dial 711 and provide this number to the operator: **************. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at ***********************************

LHH Recruitment Solutions has a 1st shift, 6AM - 2:30PM, CNC Manufacturing Engineering Technician role open for our client in the Westchester, PA region. A qualified candidate MUST HAVE proven CNC setup AND operational experience with CNC machines such as; lathes, mills, and machinery such as Miyano, Haas, Mori, Sharp etc. as well as experience in industrial applications required, for a minimum of 3 years! Additionally, experience in troubleshooting and repairing hydraulic, pneumatic, electrical, and mechanical experience is highly preferred. Setup and operation experience with Swiss Lathes HIGHLY preferred. THIS IS A SETUP/OPERATOR POSITION. Salary range is approximately $90-$100k dependent upon experience and qualifications. Role & Responsibilities Must be able to setup, create and edit CNC programs. Ordering of gages, equipment and specific tooling. SME mentality for technical questions or guidance requested from operators. Exhibit understanding of engineered drawings, blueprints and schematics. Oversee the preparation of tooling, gauges to be machined. Perform machine and equipment installation, relocation, removal and/or salvage measures. Identify and procure any parts and components as needed. Upload prior programs and download oversight of new job programs. Manage and oversee outside services/contractors/vendors personnel. Reporting of any deviations and/or change requests to engineering. Lead by example for safety and quality through discipline to 6S program standards. Aid and assist CNC Operators as needed. Conduct visual inspections for irregularities and collaborate with engineering for inspection. Make adjustments to machines and offset as required. Proven leadership and team management. Problem solving skills and critical thinking utilization. Requirements 3+ years industrial machinery maintenance experience required. Proven ability to read pneumatic, hydraulic, and electrical schematics. Minimum of 3+ years CNC machining repair and troubleshooting experience required. Experience working in a Quality Management System such as ISO9001 or AS9100 highly preferred. Lean Manufacturing/Six Sigma/Process improvement tools experience highly preferred. 3 years' experience programming and setup of Swiss lathes HIGHLY preferred. Expertise in all Microsoft Office applications. Exceptionally strong analytical and problem-solving skills. Excellent organizational, communication, and time management utilization. Ability to work overtime when needed. Willingness and ability to work overtime as needed per production demands required.

The Calibration Technician C will apply knowledge of measurement science, mathematics, physics, and electronics to calibrate inspection, measurement, and test equipment in the Acoustical, Chemical, Dimensional, DC/Low Frequency, RF/Microwave, Fluid, Mechanical, Optical, Thermodynamics, and Time & Frequency disciplines to ensure measurement accuracy. Calibration Technician will identify and utilize appropriate manual and automated measurement procedures. This position will normally receive no instruction on work, applying job skills and company policies and procedures to complete a wide range of difficult tasks, and working on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations. Calibration Technician will perform laboratory housekeeping and may perform some administrative duties. Calibration Technician may be asked to report opinions and interpretations. Responsibilities and Duties Calibrate inspection, measurement, and test equipment (IM&TE) in one or more of the following disciplines - Acoustical, Chemical, Dimensional, DC/Low Frequency, RF/Microwave, Fluid, Mechanical, Optical, Thermodynamics, and Time & Frequency, in order to ensure compliance with published specifications Working with a range of RF-enabled devices including cell phone antennas, amplifiers, two-way radios, satellite systems, and internet access points. Troubleshooting circuits used in RF transmission independently and with site engineers. Identifying and repairing faults in finished assemblies making adjustments as required. Identifying the causes of faults and work with on-site teams to implement preventative measures so that they do not happen again. Model creation, assembly, tuning, and plan development as well as modifying antenna prototypes, parts, and assemblies. Maintaining documentation of test cases. Performing routine antenna capability tests. Maintain primary and/or intrinsic calibration standards Maintain secondary and/or working calibration standards Perform maintenance, troubleshooting and repair of precision equipment Develop calibration procedures and methods, according to detailed specifications, blueprints, drawings, and other technical requirements Collect, compile, measure, summarize, and record data gathered during calibration. Identify IM&TE out-of-tolerance conditions and perform corrective action via adjustments, component replacement, correction factors, etc Identify and correct measurement errors, as applicable Prepare calibration reports and certificates Adapt existing calibration equipment, standards, and techniques to accomplish unique measurements tasks for which they are not principally used Perform uncertainty evaluation and analysis for measurement standards and associated measurement processes Train subordinates in calibration concepts and procedures Interact with other technicians, Customer Service Representatives, Account Managers, and customers Other duties and responsibilities as may be assigned Qualifications Minimum High School diploma or equivalent Must be able to perform general math and algebra functions Understanding of Basic Statistics Must possess good written and oral, communication skills Technical writing ability Intermediate ability to troubleshoot repair, align and optimize precision equipment Intermediate computer skills Proficient in use of MS Word and Excel Minimum three years of calibration experience some of which can be offset with formal metrology training Knowledge of Quality Management system (ISO 9001, ISO 17025 and ANSI Z540) Must have great interpersonal and customer service skills Strong attention to details Must be a self-motivator, work as a team player, and follow written procedures Physical Demands Must be able to lift up to 45 pounds without assistance Occasional standing and bending are required Working Environment Works primarily in a laboratory or manufacturing environment at a SIMCO location and/or customer sites Travel may be required to other domestic and possibly international locations What We Offer Full - Time, non-exempt position Excellent benefits package includes; medical, dental, vision, disability, life insurance, 401(k) with company matching, employee funded pre-tax health, child care spending accounts and tuition reimbursement Vacation, sick and paid holidays SIMCO provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, SIMCO complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, and transfer, leaves of absence, compensation and training.

Student employees will support the Theater & Dance department's productions, specifically in the areas of technical production, as required by a specific production's needs. This position will be specialized toward the technology components of the theatrical process (lighting, sound, video, etc.), but will also have crossover with the scenic and carpentry responsibilities as needed. This position will also support the technology needs for campus events taking place in the Kaleidoscope (lectures, dinners, ceremonies, etc.) Work is done in the Kaleidoscope's scene shop, Lenfest Theater, and Blackbox Studio Theater, under the direct supervision of the Theater & Dance department's Technical Director & Production Manager and Performing Arts Technician. Schedule may vary weekly. Some evening and weekend hours will likely be required during a production's load in period and tech weekend, and during campus events taking place in the building. Typical work week may average between 12 and 20 hours. Responsibilities: Learn and practice a variety of skills (depending on the needs of the production) primarily including hanging and focusing lights, setting up microphones and speakers, and (as needed for the production), scenic carpentry, metalworking, scenic painting, and theatrical rigging. Support the technology needs for campus events taking place in the Kaleidoscope (lectures, dinners, ceremonies, etc.) Train on the theaters fly-system and operation along with other specified theatrical equipment. Help with the set-up of both theater spaces for rehearsal and technical rehearsals. Assist in scheduled maintenance and organization of shop and theater gear and equipment. Requirements: Current full-time student at Ursinus College Must learn shop and theater safety requirements and adhere to those protocols during work calls. Must be able to lift 25-50lbs. Must be comfortable with, and/or, willing to, work at heights. Prior experience in technical theater is preferred, but not required. Other Duties: The above statements are intended to describe the general nature and level of work being performed by the individual(s) assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Job responsibilities and activities may be modified or changed at any time with or without notice. Job descriptions will be audited periodically by the Ursinus Human Resources department to ensure they are up-to-date and reflect the essential responsibilities and duties of the job. Ursinus EEO Statement Ursinus is an EEO employer. Ursinus College does not discriminate on grounds of race, color, national origin, gender, sexual orientation, gender identity or expression, religion, age, creed, ancestry, veteran status, marital status, disability, or other classification protected by applicable law in the administration of any of its educational programs or activities or with respect to employment.

**Description:** **WHAT WE'RE DOING** Our most advanced radar systems are designed by our Integrated Warfare System and Solutions \(IWSS\) team and we are looking for highly talented individuals, like yourself, with a passion for technology & manufacturing\. **THE WORK** In this important role, some of your responsibilities will include: - Fabricates or assembles production microelectronics components, modules or equipment such as printed circuit boards, hybrid circuits and integrated semiconductor devices by setting up and using a variety of machines, tools, semi\-automated equipment and automated equipment used in microcircuit fabrication and assembly, works from drawings, oral or written instructions generally supplied by manufacturing engineers and supervision\. - Uses machines and equipment such as presses, punches, cleaners, etchers, printers, pick and place, epoxy dispense, wire bond, seam seal, laser pattering and drilling systems as well as general purpose machines which may be required to construct, trim, screen, solder, print, or clean\. - Uses various hand tools and required to perform tasks such as sanding, grinding, tapping cementing, soldering, touch\-up, screening, and cutting\. - Uses gauges, meters, and thermometers and the like to assure that materials, finished products and production environment meet required specifications standards\. - Sets up equipment by installing tools, fixtures, screens, tapes and setting machine controls\. - Checks work to assure that workmanship is in conformance with instructions and specifications and performs rework/repair of non\-conformances per appropriate written instruction\. - May set up, control and analyze associated chemical process baths and solutions and mix adhesives and chemicals per appropriate written instructions\. - Work in a clean room environment\. - May keep record of work assigned; work in process and work completed as required, including the recording of SPC data collection\. - Works with minimum supervision **Please Note: Both 1st and 2nd shift roles are available\.** **WHO WE ARE** Our customers are world\-wide and so is our reputation for creating innovative solutions with the latest technologies\. Our products keep our customers safe and bring them home to their families at night\. We provide the resources, inspiration, and focus \- if you have the resourcefulness and courage to work hard, then we want to build a better tomorrow with you\. Lockheed Martin: An Award\-Winning Place to Work **WHO YOU ARE** You are skilled and detail\-oriented individual with hands\-on experience in microelectronics manufacturing, possessing the ability to perform precise work with specialized equipment and hand tools\. You will have a strong foundation in microcircuit assembly and repair, with a keen eye for detail and a focus on delivering high\-quality results\. **WHY JOIN US** **Your Health, Your Wealth, Your Life** We may not know what's going to change the world next, but chances are we're already working on it, and you can, too\. As part of our culture of innovation, you'll have outstanding benefits and amenities, ongoing career development and support, rewards and recognition to honor your hard work, and more\. **Basic Qualifications:** - Specialized training in specific aspects of Microelectronics job functions and/or demonstrated ability to perform assigned tasks\. - A high school diploma or GED is required\. - Must meet specified certification requirements required by the customer\. - US Citizenship is required for this role\. **Desired Skills:** - Three \(3\) years of professional experience\. - Use machines such as epoxy jet dispensers, conveyor ovens, high speed ball bonders, wedge bonders, ribbon bonders, plasma etch cleaners, reactive ion etch cleaner, eutectic etch reflow ovens, resistive welding seam sealer, laser seam sealer, laser drill, milling machine, gross and fine leak testers, and wave solder\. - Utilizes microscope to build and review product with ease\. - Performs precision work with equipment and hand tools\. - Qualified candidate has technical school training **Clearance Level:** None **Other Important Information You Should Know** **Expression of Interest:** By applying to this job, you are expressing interest in this position and could be considered for other career opportunities where similar skills and requirements have been identified as a match\. Should this match be identified you may be contacted for this and future openings\. **Ability to Work Remotely:** Onsite Full\-time: The work associated with this position will be performed onsite at a designated Lockheed Martin facility\. **Work Schedules:** Lockheed Martin supports a variety of alternate work schedules that provide additional flexibility to our employees\. Schedules range from standard 40 hours over a five day work week while others may be condensed\. These condensed schedules provide employees with additional time away from the office and are in addition to our Paid Time off benefits\. **Schedule for this Position:** Standard Monday to Friday 40 hour work week **Lockheed Martin is an equal opportunity employer\. Qualified candidates will be considered without regard to legally protected characteristics\.** **The application window will close in 90 days; applicants are encouraged to apply within 5 \- 30 days of the requisition posting date in order to receive optimal consideration\.** At Lockheed Martin, we use our passion for purposeful innovation to help keep people safe and solve the world's most complex challenges\. Our people are some of the greatest minds in the industry and truly make Lockheed Martin a great place to work\. With our employees as our priority, we provide diverse career opportunities designed to propel, develop, and boost agility\. Our flexible schedules, competitive pay, and comprehensive benefits enable our employees to live a healthy, fulfilling life at and outside of work\. We place an emphasis on empowering our employees by fostering an inclusive environment built upon integrity and corporate responsibility\. If this sounds like a culture you connect with, you're invited to apply for this role\. Or, if you are unsure whether your experience aligns with the requirements of this position, we encourage you to search on Lockheed Martin Jobs , and apply for roles that align with your qualifications\. **Experience Level:** Hourly/Non\-Exempt **Business Unit:** RMS **Relocation Available:** No **Career Area:** Manufacturing **Type:** Full\-Time **Shift:** Multiple shifts available

Job Overview: Production Technician IIThe Allentown operation is a state of the art aseptic bottling and variety packaging facility along with a full beverage distribution center. The site operation will function on the foundational principles of TPM (Total Productive Maintenance); principles of Lean manufacturing and Six Sigma; and the power of High Performance Teams. All associates at the Allentown site will have specific accountability and ownership to the site operations and to their respective functional business operation. The site will run on state of the art enterprise information technology systems and manufacturing execution systems; and with highly automated processing equipment, packaging equipment, and material movement equipment; and very standardized lean processes. Shift & Schedule: Our Allentown site is a 24/7 facility. Our shift patterns follow a 12hr, 2-2-3 schedule. With this schedule you are working a full time job while only working half of the days out of the year! Great work lift balance! We have this position available on our night shift. Night shift: 6:00pm - 6:00am on a 2-2-3 rotating schedule The Production Machine Operator/ Technician II at Keurig Dr Pepper operates, monitors, troubleshoots, and maintains production and packaging equipment to maximize operational efficiency and maintain Keurig Dr Pepper's high standards in safety and quality in a state of the art aseptic manufacturing facility. This includes preventative maintenance, machine changeovers, and making minor adjustments. This role will also be engaged in the improvement of manufacturing processes for the improvement of safety, quality, delivery, cost and culture. There will be a potential for domestic travel during the training period. A Successful Candidate Has Experience With:Troubleshooting equipment Working in a fast pace, high volume environment (Bonus if experience in the Food/Bev/Bottling/Medical Industries) Very familiar with 5S, Lean Manufacturing, TPM principles Similar titles may look like: Machine Operator, Production Technician, Production Machine Operator, etc. ResponsibilitiesPerforms duties with a safety first approach Ensures work areas are clean and organized at all times Set up machinery and replenish production materials as needed. Operate and monitor line for defective materials and perform other related work in accordance with line quality. Troubleshoot and make minor repairs and adjustments as needed. Record all data as required (i. e. charts, necessary process adjustments based on data findings, etc. ). Perform standard work for Autonomous (AM) and Preventative (PM) maintenance activities. Perform machine changeovers and clean and sanitize all equipment Total Rewards: Pay starting at $25. 46 per hour plus a $2. 00 shift differential. The employee will move to a higher rate of $26. 78 per hour in the quarter after their 6-month anniversary. Where Applicable:Benefits eligible day one!!Benefits, subject to eligibility, and collective bargaining agreements (where applicable): Medical, Dental, Vision, Disability, Paid Time Off (including vacation and sick time), 401k with company match, Tuition Reimbursement, and Mileage Reimbursement Requirements:2 years of experience working with and on automated machinery and troubleshooting electrical mechanical equipment1 years prior experience monitoring and performing product quality testing Computer and software skills (Microsoft Office) Basic understanding and application of mathematical skills to make production calculations and perform loss and waste analysis Ability to lift, push, and pull 50 pounds frequently without assistance Ability to frequently kneel, squat, bend, and stoop, twist, and reach overhead with repetitive motion Ability to spend significant time standing on the manufacturing floor with some frequency of computer work Must be available to work extended hours and flexible time in different departments based on business needs Aseptic manufacturing experience preferred Company Overview: Keurig Dr Pepper (NASDAQ: KDP) is a leading beverage company in North America, with a portfolio of more than 125 owned, licensed and partners brands and powerful distribution capabilities to provide a beverage for every need, anytime, anywhere. We operate with a differentiated business model and world-class brand portfolio, powered by a talented and engaged team that is anchored in our values. We work with big, exciting beverage brands and the #1 single-serve coffee brewing system in North America at KDP, and we have fun doing it! Together, we have built a leading beverage company in North America offering hot and cold beverages together at scale. Whatever your area of expertise, at KDP you can be a part of a team that's proud of its brands, partnerships, innovation, and growth. Will you join us? We strive to be an employer of choice, providing a culture and opportunities that empower our team of ~29,000 employees to grow and develop. We offer robust benefits to support your health and wellness as well as your personal and financial well-being. We also provide employee programs designed to enhance your professional growth and development, while ensuring you feel valued, inspired and appreciated at work. Keurig Dr Pepper is an equal opportunity employer and recruits qualified applicants and advances in employment its employees without regard to race, color, religion, gender, sexual orientation, gender identity, gender expression, age, disability or association with a person with a disability, medical condition, genetic information, ethnic or national origin, marital status, veteran status, or any other status protected by law.

Primary Duties & Responsibilities Execute manufacturing or manufacturing-support processes according to standard operating procedures and current curriculum Support schedule adjustments to meet production and shipping requirements, review visual schedule Follow all appropriate Work Instructions, SOPs, Safety procedures and Company Policies while ensuring the safe use and proper care of company equipment Retrieve and analyze trend charts and process data on trained procedures Verify and enter production parameters per SOP and Routings Accurately complete documentation in SOP's, logbooks and other WI documents Maintain equipment and instruments Demonstrate training progression through assigned curriculum Proactively maintain a clean and safe work environment, take necessary action to eliminate safety hazards, and communicate to others any observed unsafe behavior Education & Experience High School Diploma or (GED) or equivalent experience 2 years of experience in a manufacturing environment or a vocational or technical certificate Photolithography or related optics manufacturing experience desired Skills & Other Requirements Basic skills in MS Office Fundamental math skills are required; advanced math skills (algebra, trigonometry) preferred Ability to read instructions and maintain concise written records are required Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals Ability to apply common sense understanding to carry out instructions in furnished written, oral or diagram form Ability to deal with problems involving several concrete variables in standardized situations Physical Requirements Standing.: Particularly for sustained periods of time. (up to 2 hrs) Working with Hand / Fingers: Picking, pinching, typing or otherwise working, primarily with fingers rather than with the whole hand as in handling Lifting: Raising objects from a lower to a higher position or moving objects horizontally from position-to-position. This factor is important if it occurs to a considerable degree and requires substantial use of upper extremities and back muscles (up to 40lbs) Visual acuity requirements including color, depth perception, and field of vision: Requiring close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication parts at distances close to the eyes Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corporate EHS standards. Wears personal protective equipment (PPE) as required, including smocks and other clean room apparel for prolonged periods. May be required to wear a respirator during certain tasks. 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. To conform to U.S. Government export regulations (ITAR), applicant must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8. U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State."

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job Description Position Responsibilities: • Responsible for product-related operations in cell culture/fermentation and bioreactor operations. Primarily focused on cell culture activities; secondary focus and small scale inoculum preparation. • Operates and maintains production equipment as it relates to cell culture - fermentation. Including, but not limited to: • calibrations, preventative maintenance, initiating work orders, etc. • Performs a variety of complex tasks under general guidance and in accordance with current GMPs. • Experienced with drafting, executing, documenting and reviewing data, and approval of SOP's and batch records according to GMP guidelines. • Maintain records to comply with regulatory requirements and performs daily in-process testing. • Provides detailed observations, analyzes data, and interprets results. • Initiates deviations, assesses product quality impact, and proposes and executes Corrective and Preventative Actions (CAPA). • Change owner for implementation or revision of equipment, documentation, and material specifications. • Maintains daily workload schedule and relevant resource requirements. • Proposes implementation of production procedures to optimize manufacturing processes. Monitor processes and results and suggest methods to ensure process success. • Develops effective working relationships with both internal and external partners. • Provides training to new personnel in a specific technical process. • Assisting in audits from internal or external partners. • Performs other related duties as required. General Responsibilities: • Transparent and adheres to quality standards set by regulations and GMP policies, procedures and mission. • Communicates effectively with managers, colleagues and subordinates. • Ability to participate effectively as a team player in all aspects of GMP's. • Demonstrated administrative leadership with knowledge-based expertise in related areas that can be applied to meeting GMP's strategic goals. • Travels as needed. Qualifications/Skills Required: • Associates degree with a minimum of 5 years' experience in upstream mammalian cell culture or upstream process development. • Knowledge of cell culture process steps including cell banking, thaw and expansion, production, and harvest. • Experienced with manufacturing of bulk drug substance following SOPs and batch records within a cGMP regulated environment. • Knowledge of specific product-related operations in cell culture/fermentation. • Skill leading upstream production in absence of Associate Manager. • Ability to ensure plans and resources (people, facilities, supplies etc.) are efficiently utilized to ensure uninterrupted supply of products produced. • Ability to mentor and train colleagues. • Occasional off shift work and weekend work. • 1st shift and/or possible swing shift, if necessary to meet manufacturing process schedule. • On-call required for acknowledging alarms from equipment during off shift hours. Qualifications/Skills Preferred: • Preferred BS degree in Chemical Engineering, Biotechnology, Biology, Chemistry or related Engineering discipline with 3-5 years mammalian cell culture experience, or MS with at least 2 years' experience in upstream mammalian cell culture and cGMP manufacturing. • Single use bioreactor and single use media preparation experience. • Ability to observe technical issues and directs troubleshooting of process and equipment problems. • Ability to operate with minimal supervision of complex systems and equipment and optimizes their use in manufacturing in accordance with GMP's. • Ability to work on complex assignments of diverse scope and ability to exercise judgment within defined procedures and practices to determine appropriate actions. Qualifications Qualifications/Skills Required: • Associates degree with a minimum of 5 years' experience in upstream mammalian cell culture or upstream process development. • Knowledge of cell culture process steps including cell banking, thaw and expansion, production, and harvest. • Experienced with manufacturing of bulk drug substance following SOPs and batch records within a cGMP regulated environment. • Knowledge of specific product-related operations in cell culture/fermentation. • Skill leading upstream production in absence of Associate Manager. • Ability to ensure plans and resources (people, facilities, supplies etc.) are efficiently utilized to ensure uninterrupted supply of products produced. • Ability to mentor and train colleagues. • Occasional off shift work and weekend work. • 1st shift and/or possible swing shift, if necessary to meet manufacturing process schedule. • On-call required for acknowledging alarms from equipment during off shift hours. Qualifications/Skills Preferred: • Preferred BS degree in Chemical Engineering, Biotechnology, Biology, Chemistry or related Engineering discipline with 3-5 years mammalian cell culture experience, or MS with at least 2 years' experience in upstream mammalian cell culture and cGMP manufacturing. • Single use bioreactor and single use media preparation experience. • Ability to observe technical issues and directs troubleshooting of process and equipment problems. • Ability to operate with minimal supervision of complex systems and equipment and optimizes their use in manufacturing in accordance with GMP's. • Ability to work on complex assignments of diverse scope and ability to exercise judgment within defined procedures and practices to determine appropriate actions. Additional Information All your information will be kept confidential according to EEO guidelines.

About Our Client - Enzene Enzene Inc. is an emerging Contract Development and Manufacturing Organization (CDMO) with a strong operational footprint in India. We are a subsidiary of Enzene Biosciences, a leading biotechnology company. Our mission is to provide high-quality biologics manufacturing services to our clients, contributing to the advancement of the pharmaceutical industry. Website: ************** Position Overview The Manufacturing Associate will be responsible (or lead, depending on level) for the day-to-day operations of upstream processing in a clean room environment. This role includes buffer and media preparation, cell culture, perfusion bioreactors, batch fed bioreactors, harvest operations, filtration, and aseptic processing. Key Responsibilities: · Buffer and Media Preparation: Prepare and maintain buffers and media required for downstream processes. Ensure accurate formulation and timely availability of all solutions. Maintain detailed records of preparation and usage. Cell Culture: Operate and maintain cell cultures in flasks, bioreactors and perfusion reactors. Monitor process parameters and ensure consistent product quality. Troubleshoot and resolve any issues that arise during vial thaw and cell expansion. Aseptic Processing: Perform aseptic processing in a clean room environment. Adhere to strict aseptic techniques to prevent contamination. Ensure compliance with Good Manufacturing Practices (GMP). · Clean Room Operations: Maintain a clean and organized work environment. Follow all clean room protocols and procedures. Participate in regular clean room maintenance and cleaning activities. · Documentation and Compliance: Maintain accurate and detailed records of all manufacturing activities. Ensure compliance with GMP and regulatory requirements. Participate in audits and inspections as needed. · Leadership (as appropriate for level of role): Lead daily manufacturing operations, ensuring production targets are met while maintaining high standards of quality and efficiency. Ensure team adherence to standard operating procedures (SOPs) and Good Manufacturing Practices (GMP) regulatory and safety regulations. Provide training, guidance, and performance feedback to team members. Lead and mentor members within your team, providing guidance, support and feedback to ensure overall effective performance and continuous improvement. Job requirements Qualifications Education and Experience: Bachelor's degree in biotechnology, Biochemistry, Chemical Engineering, or a related field with 0+ years of relevant experience. Individuals with 4+ years of relevant experience required for senior roles (H.S diploma with 4+ years of experience will be considered in lieu of Bachelors Degree). Skills: Ability to follow instructions and procedures. Experience with buffer and media preparation, chromatography, TFF, viral filtration, and aseptic processing a plus. Excellent problem-solving and analytical skills. Effective communication, leadership and teamwork abilities. Strong knowledge and experience working in a biopharmaceutical cGMP- regulated environment. This position requires the ability to stand for extended periods, bend, and lift objects weighing up to 50 pounds. Candidates must be physically capable of performing these tasks safely and effectively. Why Join Enzene? At Enzene, we foster a collaborative and innovative environment where science and business intersect. Our team is dedicated to pushing the boundaries of biosimilar manufacturing, and we are constantly striving to improve processes and patient outcomes. Joining Enzene means being part of a company that values integrity, innovation, and collaboration in pursuit of scientific excellence. We offer an environment of growth, learning, and opportunity in a sector that is driving change in healthcare. Equal Opportunity Employer Enzene is an equal opportunity employer, committed to fostering a diverse and inclusive work environment where all employees can thrive. All done! Your application has been successfully submitted! Other jobs

Do you want to gain incredible experience with a growing company in an amazing industry? Do you know how often you use conveyor and power transmission belts? Apply your skills in a company that helps bring packages to your doorstep, food to your table, keep you healthy on a treadmill, facilitate automation and so much more! Our organization is highly focused on customers, employees, entrepreneurship, agility and responsibility. Our values and continuous improvement culture build the foundation of strong and sustainable businesses, appreciated by our employees and customers around the world. For our MIR and AMMEGA Production team, we are currently looking for a Conveyor Belt Technician As a Conveyor Belt Technician, you will be responsible for the fabrication and installation of conveyor belts and related industrial products. In this role, you will be based in East Norriton, PA. Hours will be Monday through Friday, 8:00AM - 5:00PM. A day in the life of a Conveyor Belt Technician can look like: Processing orders in a safe and efficient manner and operating light industrial equipment. Communicating with supervisor regarding assigned orders, scheduling, and other production issues. Ensuring timely shipping of belting product; receiving shipments in a timely manner and ensuring delivery to correct recipient. Maintaining shipping/receiving department with needed supplies. Processing and maintaining reports. Traveling to various locations to install products. Occasional overnight travel required. ( We will pay for gas, meals, and hotel while traveling overnight). Providing on-call assistance as required. Recognizing appropriate inventory usage and report low levels to supervisor, maintaining cycle counts log, and participating in once-a-year inventory. We are looking for you to have: A High School diploma. A valid driver's license. Flexibility around scheduling - ability to work occasional nights and/or weekend coverage. Previous industrial or production experience. Strong fundamental math skills. Ability to regularly lift heavy weight materials (75+ pounds on average). Ability to regularly bend, stoop, rotate arms and upper body; ability to frequently push, pull, sit, stand, and reach. Some climbing is required. Leadership acumen. Positive team spirit. Learning agility. Ability to deliver what is promised. Drive for change and innovation. Ability to build relationships through collaboration. What we offer you: The benefits of working at AMMEGA go beyond the daily work. You will join a world class team and have the opportunity to grow through internal advancement, on-the job training, educational support, and access to a global network. Other benefits include: Paid training. Team bonuses and learning incentives. Medical, Dental, and Vision insurance. Life insurance. Employer-paid Short- and Long-Term Disability insurance. 401k with company match. Tuition reimbursement for Undergraduate and Graduate education. Paid time off. AMMEGA is an Equal Opportunity Employer. Employment decisions are made without regard to age, race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, disability, veteran status or other characteristics protected by law. Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Paid time off Referral program Tuition reimbursement Vision insurance Schedule: Monday to Friday

Job Title: Manufacturing Process Technician / Pharma Manufacturing Duration: 06 months contract, extendable up to 24 months Note: Client has the right-to-hire you as a permanent employee at any time during or after the end of contract. You may participate in the company group medical insurance plan which includes dental and vision. Position Title: Temporary Biotechnician (Scientific Process Operator) Reports to (Title): Manufacturing Supervisor Department: Technical Operations Site: Malvern Position Summary: This position is responsible for performing manufacturing procedures and the execution of scheduled tasks within a CGMP environment in Downstream Manufacturing. This position is responsible for quality and maintaining the highest standards in compliance within company policies, procedures and all applicable regulations. Essential Functions: Executes manufacturing processes according to Technical Operations and Operational Services standard operating procedures § Verifies and enters production parameters per SOP and Batch Record on trained procedures § Retrieves and analyze trend charts and process data on trained procedures § Accurately completes documentation in SOP's, logbooks and other GMP documents § Demonstrate training progression through assigned curriculum § Accountable for adherence to compliance policies and regulations § Wear the appropriate PPE when working in manufacturing and other hazardous working environments § Takes necessary action to eliminate safety hazards and communicate to others any observed unsafe behaviors § Additional Responsibilities/Duties: Carries out duties in compliance with all state and federal regulations and guidelines including FDA, EPA and OSHA. Adheres to the Safety Code of Conduct and attend all required EHS training Support the ongoing production schedule by: Report to work on-time and according to the shift schedule Be available for other duties as assigned Attend departmental and other scheduled meetings Good interpersonal and communication skills Demonstrates positive team-oriented attitude in the daily execution of procedures Promote and work within a team environment Continue professional development through learning new skills, procedures, processes and seminars This is not an exhaustive or comprehensive listing of job functions. May perform other duties as assigned. Essential Functions Per Job Level: Autonomy and Complexity Basic Technical Knowledge within functional area § Introduced to troubleshooting of routine manufacturing processes § Needs direction to perform daily tasks § May offer suggestions for process improvements § Basic GMP understanding § Attend PE awareness classes and may participate PE projects § Education And/Or Experience: College degree or HS Diploma with +5 years industrial experience § Experience must be Biotech/Pharmaceutical industry or relevant experience working with Standard Operating Procedures (SOP's) where formal documentation is required § Previous experience with MES would be an advantage § Knowledge of routine and non-routine testing and sampling methods, techniques and related equipment would be an advantage § Computer Ability: Computer literate Working knowledge of MS Office, MS Word, MS Excel, Windows or equivalent is required Ability to learn and operate a range of industry systems including SAP Production, Werum MES, Compliance-Kaplan Wire and others § Language Skills: Read and interpret documents such as safety rules, operating instructions and logbooks Review and provide feedback for SOP and Batch Record revisions. Reasoning Ability: Interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Follows both verbal and written instructions (100% adherence to SOPs) § Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists § Work with high level of concentration Accept and adapt to procedural changes Mathematical Skills: Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations. § Other Skills, Abilities Or Qualifications: Knowledge and ability to operate manufacturing equipment and hand tools § Physical Demands: While performing the duties of this job, the employee: Needs to be mobile and able to independently transport themselves between various sites/locations, as dictated by the essential functions and responsibilities of the position. § Is frequently required to talk or hear. § While performing the duties of this job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; climb, bend and stoop; and reach with hands and arms § Ability to lift 20 lbs § Additional Information Anuj Mehta ************

Site Name: USA - Pennsylvania - King of Prussia GSK is currently looking for an Manufacturing Specialist to join our team in Upper Merion, PA. The Associate Manufacturing Specialist will be part of a high performing team responsible for delivering the supply of GSK products to the One Biopharm supply chain. They will demonstrate GSK Values (Patient Focus, Transparency, Respect, & Integrity) and Expectations (Courage, Accountability, Development, & Teamwork) on a daily basis by engaging positively with team members and production support groups. The associate manufacturing specialist, with support from team leads and supervisors, will perform a mix of tasks ranging from operation of GMP equipment, to leading pieces of work associated with supporting new product introduction and/or improvement of existing processes. The work this role will support will follow the lifecycle of new products, more specifically: Equipment/Facility Design, Technology Transfer, Commissioning & Qualification, Start-up & Engineering Batch manufacture, Process Performance Qualification batch manufacture, Clinical Supply, Commercial Supply, Changeover, Process Improvement. KEY RESPONSIBILITIES * Demonstrate GSK Values - Our culture of Ambitious for patients, Accountable for Impact and Do the right thing are the foundations for how, together, we'll deliver for our patients, shareholders and GSK people. * Adhere to safety procedures and training requirements in accordance with site, GSK, and federal regulations including the proper use of controls, personal protection equipment, and waste handling practices. Escalate equipment and processing issues that pose a safety or compliance risk. * Understand production equipment systems in use and P&ID diagrams of production equipment. Serve as technical experts for the production process and owners of production equipment. * Follow ALCOA (Attributable, Legible, Contemporaneous, Original, Accurate) principles for all documentation of performed tasks. Own Commissioning/Qualification/Validation protocols, deviation investigations, writeups, and management of corrective and preventative actions. * Support delivery of key product lifecycle deliverables from various functional groups (Production, Engineering, Technical, Validation, etc.) for new, or changes to existing, equipment and processes. Draft, review and/or execute documents and protocols (i.e. component/system assessments, specifications, equipment testing, ERP data collection, SOPs, batch documents, equipment or process qualification). Own and manage Deviations, CAPAs, and AL1/AL2 change controls. * Schedule and track activities which (directly or indirectly) impact the schedule of manufacturing and/or required documentation. Manage inventory of raw materials and single-use components, execute Batch Document revisions, and perform the role of Lead Investigator through the use of Enterprise Resource Planning (ERP) systems at site. * During Engineering, PPQ, Clinical or Commercial manufacturing campaigns: train on and perform GMP operations in the seed lab (aseptic processing), cell culture, media and buffer prep, equipment prep, purification, and final fill (aseptic processing) production areas based on standard operating procedures (SOPs) and digitalized technologies. Expectation is that during manufacturing campaigns, this role spends up to 80% of time in the production suite, supporting operations directly as needed. * Identify and implement process improvements (i.e. reduce material waste, improve productivity) and required documentation updates, within the controlled systems of the site. Own production area metrics as part of the GSK Production System. * The associate manufacturing specialist may be responsible for availability as on-call personnel, remotely monitoring, and working occasional weekend or night coverage as needed. Why you? Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: * BS/BA degree * 2+ year of GMP experience in biopharma/pharma manufacturing Preferred Qualifications: If you have the following characteristics, it would be a plus: * Strong DeltaV, SAP, Syncade and Aspen IP21 * Knowledge of cGMPs and their relationship to statistical methods. * Strong communications skills. * Project and priority management. #LI-GSK Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology). Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at ************** (US Toll Free) or *************** (outside US). GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at *********************************

Vibrantz Technologies (“Vibrantz” or “Company”) is a leading global provider of specialty chemicals and materials solutions whose purpose is to bring color, performance and vibrancy to life. Every day, our employees, the products we make, and our valued customer partnerships are inspired by this purpose. Serving customers globally, our innovations are trusted in a variety of advanced materials, color solutions and performance coatings applications to enhance the hue, functionality, safety and environmental footprint of everyday consumer products. Our key competencies in particle engineering, glass and ceramic science and color technology enable benefits like more durable vehicles and batteries, easier-to-clean appliances, energy efficient roof tiles and bricks, stronger and more decorative glass, and eco-friendly paints. Headquartered in Houston, Texas, Vibrantz has over 60 manufacturing facilities and sales offices on six continents and employs roughly 4,000 individuals. We are building a strong, shared culture that is rooted strongly in our six core values that focus on safety, our people, customers, excellence in all we do, environmental stewardship, and integrity, ethics, and trust. And we are intent upon fostering a workplace that engages employees' heads, hands and - uniquely - their hearts. Vibrantz is owned by American Securities, a leading U.S. private equity firm that invests in market-leading North American companies with annual revenue generally ranging from $200 million to $2 billion and/or $50 million to $200 million of EBITDA. American Securities and its affiliates have approximately $23 billion under management and are based in New York with an office in Shanghai. For more information, please visit **************** and **************************** Job Description Essential Responsibilities: Follows all safety policies and ensures compliance of other associates in all work areas. This includes room and process policies for PPE and security. Observe all safety and security regulations pertaining to personnel, chemicals, equipment, and building. On time for shift start, scheduled training, and meetings. Maintains high level of organization and cleanliness in all work areas. Demonstrates Values and accompanying Behaviors that guide how we work at Ferro: Customer Focus; Accountability for Performance; Innovative Thinking; Teamwork and Collaboration. Attention to detail. Ability to learn and perform job functions to quality and time standards. Able to follow instructions and communicate difficulties immediately. Able to work independently and multi-task. Trained, proficient, and performing all of the process functions and operating all equipment pertaining to the manufacture of paste products. (Scales, mixers, 3-roll mills, etc.) Ensures timely, accurate, and complete recording all required transactional data. Actively participates in Quality System activities and participates in continuous improvement in Paste Manufacturing. Participate in plant wide improvement efforts and project assignments as requested. Participates in scheduled physical counts of inventory. Excellent communication skills. Must be able to read, speak, write and understand English. Other temporary assignments, duties, or projects as required. Required Qualifications: High School Diploma or equivalent as minimum. Experience in a manufacturing environment also preferred. Basic math skills. Able to perform simple math formulas and percentage calculations. Basic computer use. Proficient in all required business software including systems used for inventory control (example: SAP, Excel) and communications (example: Outlook, Word, Workday). Preferred Qualifications: Some college with science emphasis preferred. Experience with SAP or other ERP computer system Travel Requirements: None Competencies/Job Skills: Job Knowledge: Understands duties and responsibilities, knows products and use, keeps knowledge current. Technical Skills: Knows specialty equipment and test methods, follows standards. Sense of Urgency: Prioritizes work to meet deadlines, raises issues early, and uses time productively. Decision Making/Judgment: Systematically gathers data, communicates in a timely manner, seeks input as needed. Computer Skills: Uses computer to compile data and write short summaries. For Plant Locations Only: Physical Demands: Must stand or walk on hard surface 5 - 6 hours per workday. Required to occasionally lift up to fifty pounds. Safely operates material handling equipment. Required to move wheeled containers, pallets, and or drums using manual jacks, powered lifts, or assistance of other operators. Must have ability to perform repetitive arm and hand motions for 1-2 hours that are typically not continuous. Environmental, Health & Safety Requirements: This job shall maintain compliance with all applicable Environmental, Health & Safety Regulations at all times. The employee in this job shall maintain compliance with all Ferro Safety Standards as well as EHS rules/requirements of the site at all times. Location King of Prussia, PA Vibrantz is committed to protecting your privacy. We provide a Website Privacy Policy located on our Vibrantz.com site to explain the type of information we collect and to inform you of the specific practices and guidelines that protect the security and confidentiality of your personal data. Please read that policy carefully. If any term in the policy is unacceptable to you, please do not use the Website or provide any personal data. This policy may change from time to time (see Revisions to Our Privacy Policy on Vibrantz.com). Vibrantz Technologies Inc. (“Vibrantz”) is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. Vibrantz strictly prohibits and does not tolerate discrimination against employees, applicants, or any other covered persons because of race, color, religion, creed, national origin or ancestry, ethnicity, sex, gender, age, physical or mental disability, genetic information, sexual orientation, or any other characteristic protected under applicable federal, state, or local law.

We are seeking a 3rd shift Ceramics Manufacturing Technician in our Philadelphia, PA facility where we develop, produce and process specialized coatings and materials, primarily for the defense market. This role performs a variety of manufacturing processes and operates sophisticated manufacturing equipment. Our 3rd shift will run Monday - Friday from 11:00 pm to 7:00 am. Initial training will take place on 1st shift for around 2 months. Primary Duties & Responsibilities * Follow detailed manufacturing instructions to complete daily tasks in an effective and timely manner * Operate advanced custom robotic equipment to achieve specified results * Ensure product maintains conformance to process standards and tolerances through measurement analysis * Daily detailed data capturing to maintain appropriate records * Operate advanced custom robotic equipment to achieve specified results * Measure, mill, and mix materials following standardized recipes and procedures * Perform routine maintenance and cleaning of equipment; replaces critical/consumable components on scheduled interval * Perform basic troubleshooting of equipment when necessary * Maintain manufacturing supplies to ensure continuous workflow * Maintain clean workspace, including shared work areas, utilizing 6S practices Education & Experience * High School diploma or GED or equivalent experience required * Minimum of 2 years of related experience * College or vocational training in physical science, mathematics, and or engineering preferred Skills * Attention to detail * High discipline * Ability to follow detailed work instructions * Aptitude for maintaining detailed records * Computer literacy (Microsoft Office suite) * Good communication skills * Team Player Working Conditions Temperature/humidity-controlled manufacturing environment First shift focus core hours (8am-5pm) Flexibility to shift to off core hours when necessary Physical Requirements * Standing (4hours per day) * Lifting (50lbs.) * Pushing/Pulling (20lbs.) * Sitting (2hours per day Safety Requirements All employees are required to follow the site EHS procedures and Coherent Corp. Corporate EHS standards. 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. To conform to U.S. Government export regulations (ITAR), applicant must be a U.S. citizen, lawful permanent resident of the U.S., protected individual as defined by 8. U.S.C. 1324b(a)(3), or eligible to obtain the required authorizations from the U.S. Department of State."

Day to day operations of secondary manufacturing workflows while continuously using ERP system (Epicor). Must also understand general maintenance and housekeeping of manufacturing space. A great opportunity to break into the Manufacturing field. Requirements GED or high school equivalency Basic understanding of Manufacturing Basic computer skills Ability to stand for prolonged periods of time Ability to lift a minimum of 20 lbs. Communication skills both written and verbal Attention to detail Duties include the operation of the following secondary work stations: Ice Blasting/Vapor Degreasing Anodizing/Passivation/Laser Marking Sodium Bicarbonate Blasting/Manual Deburring Tantalum Pin Placement/Epoxy Paint QC Inspection/Packaging and Labelling

Do you want to gain incredible experience with a growing company in an amazing industry? Do you know how often you use conveyor and power transmission belts? Apply your skills in a company that helps bring packages to your doorstep, food to your table, keep you healthy on a treadmill, facilitate automation and so much more! Our organization is highly focused on customers, employees, entrepreneurship, agility and responsibility. Our values and continuous improvement culture build the foundation of strong and sustainable businesses, appreciated by our employees and customers around the world. For our MIR and AMMEGA Production team, we are currently looking for a Conveyor Belt Technician As a Conveyor Belt Technician, you will be responsible for the fabrication and installation of conveyor belts and related industrial products. In this role, you will be based in East Norriton, PA. Hours will be Monday through Friday, 8:00AM - 5:00PM. A day in the life of a Conveyor Belt Technician can look like: * Processing orders in a safe and efficient manner and operating light industrial equipment. * Communicating with supervisor regarding assigned orders, scheduling, and other production issues. * Ensuring timely shipping of belting product; receiving shipments in a timely manner and ensuring delivery to correct recipient. * Maintaining shipping/receiving department with needed supplies. * Processing and maintaining reports. * Traveling to various locations to install products. Occasional overnight travel required. (We will pay for gas, meals, and hotel while traveling overnight). * Providing on-call assistance as required. * Recognizing appropriate inventory usage and report low levels to supervisor, maintaining cycle counts log, and participating in once-a-year inventory. We are looking for you to have: * A High School diploma. * A valid driver's license. * Flexibility around scheduling - ability to work occasional nights and/or weekend coverage. * Previous industrial or production experience. * Strong fundamental math skills. * Ability to regularly lift heavy weight materials (75+ pounds on average). * Ability to regularly bend, stoop, rotate arms and upper body; ability to frequently push, pull, sit, stand, and reach. Some climbing is required. * Leadership acumen. * Positive team spirit. * Learning agility. * Ability to deliver what is promised. * Drive for change and innovation. * Ability to build relationships through collaboration. What we offer you: The benefits of working at AMMEGA go beyond the daily work. You will join a world class team and have the opportunity to grow through internal advancement, on-the job training, educational support, and access to a global network. Other benefits include: * Paid training. * Team bonuses and learning incentives. * Medical, Dental, and Vision insurance. * Life insurance. * Employer-paid Short- and Long-Term Disability insurance. * 401k with company match. * Tuition reimbursement for Undergraduate and Graduate education. * Paid time off. AMMEGA is an Equal Opportunity Employer. Employment decisions are made without regard to age, race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, disability, veteran status or other characteristics protected by law. Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Referral program * Tuition reimbursement * Vision insurance Schedule: * Monday to Friday