Manufacturing Technician Jobs in Derry, NH

Our client is an American multinational manufacturer and marketer of chemical products and they are currently looking for an Operator Technician in Derry, NH. Great direct hire opportunity. Job Scope A good match for the Operator Technician position should enjoy working with a close, dedicated team. You should be a versatile and adaptable individual with strong technical ability. Experience with plastics material processing and testing or similar experience. Hands-on position. As the Operator Technician you will: Maintain a safe work environment Actively contribute to the safety core values and culture Daily involvement with all aspects of plastics material development including batch making, processing, extruding, and molding Perform laboratory testing using a wide range of equipment and test methods that characterize the material's physical, chemical, and mechanical properties. Prepare concise reports on material characteristics. Perform calibration and preventative maintenance on lab equipment and processing equipment. Create and review work instructions and procedures that facilitate safe and reliable operation of all equipment. Required Qualifications: You must possess the below minimum qualifications to be initially considered for this position. Preferred qualifications are in addition to the minimum requirements and are considered a plus factor in identifying top candidates. Minimum Qualifications: High School Diploma or equivalent. 2+ years of related experience as either R&D Laboratory or manufacturing. Skills and Knowledge: Working knowledge of Microsoft office suite. Technical and problem-solving ability. Experience working in an ISO 9001-compliant facility. Detail oriented. Working with minimal supervision. Ability to effectively communicate with customers and vendors. 5S and lean manufacturing knowledge. Ability to multitask. Preferred Qualifications: Associate's Degree in a technical field. Plastic material testing, extruding, molding, and testing experience. Forklift experience. Hourly wage: $25-$35 based on experience. Apply now for immediate and confidential consideration! #IND1

PM Group is currently engaged in the delivery of multiple Life Science projects in the USA. Together we will all be sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group's ongoing expansion in the US. Outsourced Technical Services (OTS) is an integral part of our ability to support clients across the complete project life cycle. We deliver fast, flexible outsourcing solutions for clients worldwide. You will be on-site executing cutting-edge projects for Cell & Gene Therapy, Biologics, and Pharma facilities for both US and international clients. PM Group is an employee owned, international project delivery firm with a team of 3,600+ people. We are world leaders in the pharma, food, biotech, medical technology and mission critical sectors. From our network of offices in Europe, Asia and the US, we work with the world's leading organizations. We are focused on growing a sustainable business centered on our people, our clients and trade partners. Responsibilities Cross functional Team Leadership: Lead within cross functional teams to achieve facility start up and technology transfers. The Manufacturing Technology SME in the cross-functional team plays a critical role in ensuring that the facility fit, and technical transfer is successful, compliant, and efficient, while maintaining a strong focus on collaboration, communication, and quality. Technical SME: The role is responsible to represent the Engineering & Technology as facility fit and technical SME. Ensure appropriate equipment specification and procurement through qualification with the QAV SME. Raw material quality for use in manufacturing working in collaboration with PD and QC SME. Interact with process development teams on process design finalization (and control strategy as applicable) in terms of facility/equipment specifics, manufacturability, capacity and cost analysis, process controllability and robustness. Coordination and Communication: Facilitate effective communication and collaboration between different teams, departments, and stakeholders involved in the technical transfer process. Project Planning: Work with a project manager to develop a detailed project plan outlining timelines, tasks, resources, and milestones. This plan should consider potential risks, contingencies, and strategies to address any challenges that may arise during the transfer. Risk Management: Identify potential risks and challenges associated with the technical transfer process, and work with the team to develop mitigation strategies to minimize these risks. This could involve quality issues, regulatory compliance, equipment compatibility, operability, cost considerations and more. Regulatory Compliance: Ensure that all activities related to the technical transfer comply with relevant regulatory guidelines and standards. Quality Assurance: Collaborate with quality assurance and control teams to ensure that the transferred process or product maintains its quality, safety, and efficacy throughout the transfer process. Documentation: Ensure accurate and comprehensive documentation of all steps in the transfer process. This documentation is crucial for regulatory submissions, troubleshooting, and future improvements. Resource Allocation: Work with the project manager to ensure the necessary resources are allocated, such as personnel, equipment, and materials, to support the successful execution of the technical transfer. Problem Solving: Work proactively to address any issues or roadblocks that arise during the transfer process, working with the cross-functional team to find effective solutions. Execute technical assessments of new equipment, instruments, and single-use technology to identify optimal solutions in a fast-paced environment. Training and Knowledge Transfer: Facilitate the training of personnel involved in the technical transfer, ensuring that the receiving team has the necessary skills and knowledge to continue the process smoothly. Continuous Improvement: Identify real time opportunities for process optimization and improvement during the transfer, with the goal of enhancing efficiency, reducing costs, and maintaining or improving product quality. Conduct risk assessments/FMEA Be able to problem solve using systematic approach to root cause analysis. Owner and author of relevant documents which represent the process for GMP manufacturing including, but not limited to SOPs, process descriptions, master batch records, compounding records, critical raw material lists, bill of materials, part number and specification generation, sample map. Owner and author of process related change controls, deviations and CAPA to ensure events have no impact to process performance and product quality, and recurrence is eliminated. Assess and approve non-process related change controls, deviations and CAPA to ensure events have no impact to delivery of acceptable quality product and recurrence of issues are eliminated. Perform other responsibilities as required. Qualifications Minimum Bachelor of Science degree in Biotechnology area, Biological Sciences, or Chemical Engineering. 7+ years' experience with biotech process development, process scale up, tech transfer or manufacturing in the biopharma/biotech industry. 3+ years' experience with functional or cross functional team leadership Demonstrated expertise with multiple tech transfer and scale up of biologic molecules for GMP clinical or commercial production, specifically in advanced therapies manufacturing example viral vector, RNA, cell processing. Prior direct experience in either design, qualification, start-up, or initial licensure of Biologics Manufacturing facilities preferred. Demonstrated evidence of detailed direct experience with process, equipment, single use technology, automation, validation, and facility fit knowledge. Thorough understanding and demonstrated experience with FMEA, risk analysis, process characterization or process validation. Knowledge of quality systems, cGMP, regulatory and industry standards at all phases of drug development. Understanding of regulations pertaining to cGMP manufacturing and analytical requirements for Raw Materials, Critical Components, Drug Substance and Drug Product and the translation of those regulations into process development work products and GMP manufacturing process design. Experience with statistics in the areas of statistical process control, modeling, and data management. Computer skills (MS Office Suite, statistical software, Visio, LIMS, SAP, etc or equivalent). Ability to solve complex problems, and a proactive preventative mindset to enable flawless manufacturing. Strong interpersonal and communication skills - able to clearly express ideas and point of view both verbally and in writing Show commitment and dedication and strive to be ahead of schedule. Maintain on the floor presence to support oversight of operations in conjunction with Manufacturing Leadership - amount of time on the floor will be relative to the development of manufacturing associates as the organization is established. Practice safety awareness always and consider safety when establishing MBR and implementing changes for manufacturing. Share 24/7 on-call support while the product is being manufactured. Why PM Group? As an employee-owned company, we are inclusive, committed and driven. Corporate Responsibility and Sustainability are the heart of our new 2025 business strategy. Click here to read more in our Corporate Responsibility and Heath, Safety & Well-being Report 2023. Inclusion and Diversity are core to our culture and values. Wherever we work, we commit to a culture of mutual respect and belonging by building a truly inclusive workplace rich in diverse people, talents and ideas. Valuing the contributions of all our people and respecting individual differences will sustain our growth into the future. PM Group is committed to ensuring our hiring process is fair and accessible to all and will provide candidates with disabilities with reasonable accommodations required to participate in the recruitment process. If you require any assistance in this regard, please let us know. RECRUITMENT AGENCIES NEED NOT APPLY

Vaxess is a NIH and venture-funded company developing a pipeline of next-generation vaccines and therapeutics on the MIMIX platform. With only five minutes of wear-time on the skin, the self-applied MIMIX patch enables up to two weeks of sustained delivery. The platform combines high temperature stability with simplified application to dramatically alter the way that drugs are delivered. Vaxess is committed to enabling products that are not only more effective, but also more accessible to patients around the world. Research & development at Vaxess is cross-disciplinary, integrating mechanical, industrial, biomedical, and chemical engineering with chemistry, biology, and human factors to address important unmet medical needs. We are seeking a skilled, collaborative, and highly motivated technician with expertise in medical device or pharmaceutical manufacturing to join our growing team. This role offers a unique opportunity to build manufacturing capacity from the ground up to bring innovative technology to the global vaccine and therapeutic market. Responsibilities Perform cGMP manufacturing operations according to documented procedures or batch records Operate automated manufacturing equipment and record relevant in-process data. Complete production and testing records following Good Documentation Practices (GDP) Handle, assemble, and visually inspect products, including use of a microscope, automated inspection systems, or other optical systems. Contribute to root cause analysis (RCA) and help contribute to manufacturing investigations Support manufacturing related R&D efforts as needed Perform other assigned duties related to manufacturing, quality control, and/or facility operations. Qualifications 2+ years' relevant experience working in regulated environments in medical device or biopharmaceutical industries; experience working in a clean room is preferred High school diploma minimal, associate's degree or trade certifications preferred Good written and verbal communication skills, attention to detail, and a demonstrated ability to work effectively within a team Ability to stand or sit for a full shift on a manufacturing line Entrepreneurial spirit and drive to positively impact global human health Vaxess is building a team of exceptional people to rapidly advance product development. We work closely as a team and thrive in a dynamic, exciting, and engaging work environment. If you're interested in joining the Vaxess team, please submit your CV/resume to ******************.

Our Client is looking for motivated and ambitious Manufacturing Associates to join their team in Manchester, NH, on a temp-to-hire basis. The ideal candidate will have 1+ years of manufacturing experience and be a true team player. If this sounds like you, please apply today! Location: Manchester, NH Hours: 6 AM - 2:30 PM, Monday - Friday (30-minute lunch) Pay: $18 - $20/hr Temp-to-Hire Duties Include: Assist with various manufacturing operations, including cleaning, assembly, wrapping, packaging, and labeling as needed. Process top-level assemblies to determine whether the product should be sent to finished goods inventory or shipping. Responsible for moving excess parts to temporary bin locations for transfer by stockroom personnel. Track job completion and exceptions using business software for each task. What You'll Need: 1+ years of experience in a manufacturing environment Willing to submit to a drug test and background check Proficiency in calculating figures and amounts related to weights and volumes. Desired Skills and Experience Manufacturing, Assembly, Production All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles' Fair Chance Initiative for Hiring Ordinance, and Los Angeles County Fair Chance Ordinance. For unincorporated Los Angeles county, to the extent our customers require a background check for certain positions, the Company faces a significant risk to its business operations and business reputation unless a review of criminal history is conducted for those specific job positions.

We are looking for a Manufacturing Associate I, where you'll be involved in ELISA manufacturing, including plate coating, buffer preparation, reagent dispensing, and kit assembly. You'll work with automated systems, follow ISO 9001 quality standards, and ensure compliance with batch records and SOPs. Requirements: Experience with ISO 9001/GMP (preferred) Knowledge of aseptic techniques, ERP, and QMS (a plus) Ability to lift 25 lbs regularly Proficiency in Microsoft Excel & Word AS/BS in Science or relevant certificate (0-2+ years experience)

The Manufacturing Operator reports to the Manufacturing Line Lead and assists with various tasks involved in the production of fluid management products. Responsibilities include performing production activities such as kitting parts, cutting tubing and polymer film, interpreting design drawings, applying both basic and advanced assembly techniques, conducting thorough visual inspections, operating both manual and automated machinery, and carrying out packaging and labeling tasks. The ideal candidate will be instrumental in helping the department meet its safety, quality, and production targets. Responsibilities: Execute basic assembly tasks Interpret manufacturing drawings and adhere to standard operating procedures of varying complexity Conduct detailed visual inspections of in-process and finished products Package and label completed products Collaborate with a team in a fast-paced ISO-certified cleanroom environment for 8 hours a day Perform housekeeping duties as assigned Cut tubing and polymer film to precise tolerances using both manual and automated tools Safely operate cleanroom machinery by strictly following standard operating procedures Perform inventory checks and promptly report any discrepancies Complete documentation in accordance with Good Documentation Practices (GDP) Learn the Performance System and contribute to fostering a culture of continuous improvement Qualifications: 0-2 years of relevant experience High School Diploma or equivalent Basic arithmetic skills Strong attention to detail with a focus on maintaining quality standards Ability to use hand tools and equipment, including repetitive forceful gripping, grasping, pushing, and pulling Ability to stand and move during the shift, including actions such as reaching, bending, stooping, and grasping Ability to frequently lift up to 30 pounds and occasionally lift up to 50 pounds Wear Personal Protective Equipment (PPE) and adhere to chemical hygiene protocols Follow all safety procedures Demonstrate R-TEAM Values

Title: Engineering - Bio Process Associate - 2nd Shift Primary Recruiter: Jane Bautista Pay Rate:: $38/Hour # of Openings: 4 initial 6 months contract possible extension Schedule: Shift rotation: Shift: 5p- 5a 3 days on (Sat, Sun, Mon), 2 days off (Tues, Wed), 2 days on (Thurs, Fri), 3 days off (Sat to Mon). Job responsibilities: Operates control systems and processes in Biotechnology Pilot Plants as assigned. Prepares process buffers and reagents. Cleans equipment and maintain area in clean and orderly fashion. Recognizes and reports safety, maintenance and operational variances to area management. Communicates status of voperations to area management in a timely manner. Follows detailed SOP's and batch records. Ensures compliance with cGMP and safety requirements. Maintains files, records and equipment. Records data, logs activities and monitors processes. Achieves and maintains proficiency through training. Education/skills: The successful candidate will have a high school diploma with a minimum of 5 years process operations experience, A.A.S. or B.S. degree is preferred. Prior job related experience required along with demonstrated mechanical aptitude. Familiarity with general chemistry, mathematics, microbiology and cGMP clean room operations is a plus. Keen attention to detail. Prior experience following and documenting written instructions is required. Committed team player prepared to work in and embrace a team based culture. Shift work and overtime required. ADDITIONAL INFORMATION: Work in a cGMP laboratory and/or manufacturing environment following techniques which require one to maintain a high attention to detail. Properly use Personal Protective Equipment (PPE), gowning for restricted areas, aseptic processing, handling chemicals, and work in a general office environment. Contingent Workers whose jobs involve the operation of a vehicle or machinery, or physical presence in a laboratory, research, drug development, or manufacturing facility are prohibited from having any amount of alcohol or illicit drugs in their body while in the workplace or performing their job functions. Suppliers and the Contingent Worker are responsible for insuring they are fit for all the duties of the job.

Education and Experience: · A strong mechanical aptitude. · Experience with hand tools such as ratchets, wrenches, battery and pneumatic operated tools. · Ability to stand for long periods of time, safely lift up to 20 pounds on a regular basis and ability to safely lift up to 50 pounds (with assistance if required). · Basic computer skills - email, work instructions. · Attention to detail. · Good command of the English language, both written and verbal.

Title: Manufacturing Technician 2nd shift Status: 12-contract 2nd shift from 3:30 pm to 11 pm EST Compensation: $33-$35 per hour DOE The Manufacturing Technician is responsible for manufacturing oral dosage products to support clinical through commercial needs. The manufacturing team is responsible for manufacturing clinical trial supplies and process development, scale-up, and transfer to commercial production. This successful candidate will work closely with other manufacturing Technicians/Operators, Quality, Development, EHS, Supply Chain, the Quality Control Lab, and a diverse set of colleagues to support company manufacturing goals. We are seeking people with exceptional people skills who want to work in a supportive fast-paced environment. Day to day responsibilities: Manufacturing and production support of novel extended-release drug delivery technology including GMP operation of manufacturing equipment Polymer drying, blending and extrusion Automated and manual assembly of polymer-based dosage forms using plastic welding techniques Powder blend granulation and capsule coating Required Experience: Bachelor's Degree in a technical field related to polymers, chemical or mechanical production or, Associate's degree and 1-3+ years in a technical field related to polymers, chemical or mechanical production (biotech or pharmaceutical manufacturing experience preferred) or, HS diploma (or GED) and 7+ years in mechanical production or manufacturing experience (biotech or pharmaceutical manufacturing experience preferred) Hands-on manufacturing operations skills required GMP experience is a plus, ISO-8 or higher clean room experience is a plus

STC Biologics is a boutique biologics contract development and manufacturing organization (CDMO). Our commitment to innovation, quality, and customer service sets us apart in the biopharmaceutical landscape. We are seeking a highly motivated, detail oriented, and experienced Supervisor of Biologics Manufacturing to join our dynamic team. The ideal candidate will oversee day-to-day operations in the biologics manufacturing department, draft and review GMP batch records, ensuring compliance with cGMP standards and based on STC's Quality Manual and SOPs, quality regulations, and safety protocols. This role is crucial to maintaining production efficiency and fostering a productive work environment. **Key Responsibilities:** - Supervise and lead a team of manufacturing personnel in the production of biologic products. -Technical expert in GMP biologics production able to draft and review batch records - Ensure compliance with all cGMP and safety regulations, conducting regular audits and inspections. - Develop and implement standard operating procedures (SOPs) to enhance manufacturing processes. - Collaborate with quality assurance and other departments to resolve production issues and deviations. - Monitor production schedules, resource allocation, equipment and inventory management to meet project timelines. - Train, mentor, and evaluate team members, fostering a culture of continuous improvement and professional development. - Participate in process optimization to improve production efficiency. - Prepare reports and documentation related to manufacturing activities and performance metrics -Expert either in Upstream or Downstream Process execution **Qualifications:** - Bachelor's degree in Biotechnology, Biological Sciences, or a related field (Master's preferred). - Minimum of 7 years of experience in biologics manufacturing, with at least 2 years in a supervisory role. - Strong knowledge of cGMP regulations and biologics production processes. - Excellent leadership, communication, and interpersonal skills. - Ability to work in a fast-paced environment and manage multiple priorities. - Proficiency in data analysis and problem-solving.

Garuda Therapeutics is seeking a motivated Manufacturing Associate/Sr. Manufacturing Associate to support routine GMP Manufacturing operations. This includes day-to-day operational tasks including but not limited to Cell Culture in a clean room environment, GMP Materials Logistics, and Environmental Monitoring within Garuda's GMP manufacturing space. This is an on-site role, primarily in Watertown, MA with occasional work in Cambridge MA. Some travel between sites is required. ROLE AND RESPONSIBILITIES • Perform, verify, and support GMP Cell Culture manufacturing activities in a cleanroom environment • Complete applicable GMP Manufacturing Batch Records, Forms, and associated documentation • Support GMP materials release and labeling • Transfer materials into the GMP cleanroom suites following proper wipe down procedures. • Follow Personnel, Material, and Waste flow procedures related to GMP manufacturing of Cell Therapy products • Restock cleanroom manufacturing areas as needed. • Perform environmental monitoring sampling when needed. • Support deviation investigations and CAPA activities • Other related duties as needed QUALIFICATIONS AND EDUCATION REQUIREMENTS • Associates degree is required (in a science-related discipline preferred) BA/BS degree preferred • Minimum of 1 year of professional experience working on a cell-based therapeutic product is required • Strong interpersonal skills & attention to detail • Strong commitment to teamwork, collaboration, and professionalism • Proficiency in working with MS Office Suite • Able to handle a dynamic workload, multi-task, and perform effectively under tight deadlines • Must be able to lift 30 lbs.

Job Title: Biotechnologist Associate/Manufacturing Technician Duration : 12 months (possibility of extension) Shift: Night Shift 7pm -7am OR Day Shift - 07AM -07PM (3days on 2 days off and 2 days on 3 days off) Job Description : The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials. Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate. Attain qualification for all assigned tasks and maintain individual training plan. Perform material movements, transfer raw materials, chemicals into, out of, across the production areas. Maintain facility and equipment through routine cleaning and sanitization, support 6S programs. Must be willing to gown and work in a "clean room " environment. Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects. Perform other duties as assigned. CANDIDATES WITH THE FOLLOWING BACKGROUNDS HAVE HAD SUCCESS IN MANUFACTURING AT *** COMBINED WITH SCIENTIFIC DEGREE, MANUFACTURING EXPERIENCE OR COURSES/INTERESTS IN SCIENCE are also welcome

Infinite Cooling's mission is to mitigate water scarcity and reduce emissions around the world by making industrial cooling more efficient. Industrial cooling systems are the largest users of water after agriculture and major users of energy. We help industrial plants reduce their water consumption and energy usage by optimizing the operation of their cooling systems. We are a vibrant startup based in the Boston area, and we are on a mission to be a global leader in cooling for industrial applications. Infinite Cooling is venture-backed and has raised over $16M of capital and was awarded over $3M of prizes and grants. We are seeking a proactive, detail-oriented, and experienced Engineering Technician to join our team. This role offers the opportunity to engage in all facets of product design and production, supporting the development and manufacturing of cutting-edge technologies. The ideal candidate will possess strong communication skills, adaptability, and a willingness to "wear many hats" in a fast-paced environment. What you will do: Assemble Mechanical Systems: Support the production of the WaterPanel™ product line. Electrical Assembly & Wiring: Assemble and wire electrical components for the TowerPulse™ product line. Inventory Management: Track and maintain inventory levels for all BOM components. R&D Testing: Develop and conduct tests of electromechanical assemblies. Troubleshooting: Diagnose and resolve technical issues with products. Documentation: Record findings and provide recommendations to improve products and standard operating procedures (SOPs). SOP Creation: Develop and maintain clear, concise SOPs for assembly and testing operations. Packaging & Shipping Coordination: Oversee product packaging and shipping logistics. Preferred skills and experience: Experience with mechanical or electrical assembly. Ability to maintain a clean, organized workspace. Proficiency with MS Office Suite. Physical capability to lift 50 pounds unassisted. Commitment to a safety-first approach. Familiarity with engineering and electrical documentation. Ability to work both independently and within small teams with minimal supervision. Proficiency with shop tools (e.g., drills, saws, grinders, welding equipment). Experience conducting product testing.

This position reports to the Branch Manager and is responsible for performing inspections, installations, selling, and servicing a variety of kitchen fire suppression systems in a professional and timely manner. The Kitchen Suppression Technician will be expected to meet weekly service and productivity goals. The Technician is also responsible for maintaining a clean, well-organized vehicle and ensuring a safe environment for his/herself, co-workers and customers. Responsibilities include • Manage their time to complete the maximum amount of service, inspection, and installation calls while maintaining a high level of quality. • Achieve any weekly productivity goals assigned by the Suppression Manager. • Learn applicable fire protection codes and obtain any licensing and certification required by National, State and Local codes. • Protect and maintain company equipment. • Work in a safe manner as outlined by company safety procedures including the driving, personal protective equipment, and lockout/tag-out policies. • Maintain their vehicle in accordance with company procedures and ensure it is clean and organized. • Protect the Company’s assets. • Perform any other tasks assigned by the Suppression Manager. Qualifications include • Minimum of 1 year inspection experience; kitchen fire suppression systems background or a basic level of comfort and knowledge with pipe fitting, electrical work, and commercial kitchen appliances • Ability to perform physical activities outlined in the accompanying physical requirements checklist. • A strong work ethic and professional appearance. • Excellent selling, communications, and customer service skills. • Ability to fit in with our culture of teamwork. • Ability to adhere to, implement, and follow safety guidelines and procedures at all times. • Possess a valid driver’s license and driving record that meets company requirements. Preferred Qualifications • Applicable experience either in the fire protection industry or the commercial customer service business in some capacity. • An ability to provide services across multiple product lines. • Residence in close proximity to one of our locations. • Working habits and personal appearance which are both neat and well organized.

Qualifications: AS in Electronics Ideal candidates would come from a Telecommunications industry 5 + years' experience working with electronics, electro-mechanical systems in a test Must be very comfortable using an oscilloscope Able to use Allegro Viewer a big plus Understands and is familiar with electrical circuits, soldering, making mechanical connections and electrical/electronic troubleshooting down to component level Able to understand test methods, test setups, test procedures and test plans Experience using electronic test and measurement tools such as Oscilloscopes, Voltmeters, Digital Multimeters (DMM), Digital Voltmeter (DVM), Digital/Analog Power Supplies Ability to read and interpret electrical schematics, mechanical drawings Strong interpersonal and communications skills Responsibilities: Support Test Engineers to set up and execute test plans as directed Develop and document test processes for electronic equipment. Perform minor soldering and electronic repair. Design and document minor electronics and cable assemblies. Utilize various electronic test equipment, such as meters, oscilloscopes and power supplies. Support engineering and manufacturing tasks as needed

RAYUS now offers DailyPay! Work today, get paid today! RAYUS Radiology is looking for an MRI Technologist to join our team. We are challenging the status quo by shining light on radiology and making it a critical first step in diagnosis and proper treatment. Come join us and shine brighter together! As an MRI Technologist, you will operate your assigned scanner(s) to produce images of the patient's body for diagnostic purposes. Taking a patient centered approach, you will provide MRI services within professional standards and with excellent customer service. Each patient comes to our centers looking for answers. You will guide patients through this sometimes difficult process by kindly talking them through the steps and answering their questions and concerns regarding exam procedures and process. This is a full-time position working 2:00 PM to 10:00 PM Monday - Friday. ESSENTIAL DUTIES AND RESPONSIBILITIES: (90%) Patient MRI Imaging Screens patient before exam for any precautions or contradictions pertaining to examination, using two patient identifiers to ensure correct patient and procedure Explains and prepares patients for MRI procedures that will be performed, explaining the procedure, positioning patients so that the parts of the body can be appropriately Performs routine and advanced MRI procedures on designated portions of the body for use by physicians in the diagnosing and treating of patient illness and/or injury with minimal amount of supervision or repeats scanned, while providing patient support by talking to patients throughout procedure Adjusts MRI scan parameters correctly and as needed Maintains positive attitude and working relationships with radiologist, referring customers and other associates and peers Follows physicians' orders precisely and conforms to safety regulations to protect yourself, your patients, and coworkers Accurately maintains patient records within Radiology Information System (RIS) Maintains an orderly and clean work area promoting good safety habits for patients and co-workers Maintains ACR toolkit and accreditation requirements Maintains equipment in good working order; cleans and disinfects equipment after each use Ensures compliance with all HIPAA guidelines (5%) MRI Department Support Assists with maintaining an updated imaging protocol manual and software upgrades Monitors medical supply inventory and requests supplies as necessary Assists with training of new associates, providing resource and technical expertise, as applicable (5%) Completes other tasks as assigned

Job Type: Fulltime Experience: 6+years Experience Required: Datacenter Operations Management Service Now knowledge Vendor Management JIRA/Confluence Tape Management Hands on support experience of data center IT equipment and processes such as networking, server racking cable management and installs. Roles & Responsibilities: 6-8 years of experience in a large Data center support environment Install and remove IT equipment as needed. Read and review patch sheets, label and run cables per specs and SOP's. Power readings and reporting. Tape operation Install and extend circuits as needed. Review new projects needs and help determine location, power, and network capacities. Set up distribute/ship equipment for remote sites. Applies technical knowledge to ensure that CPU's, tape units, disk storage, and other peripherals are working properly. Recognizes and analyzes problem conditions and determines root cause whether hardware, software, network, or media. Applies technical knowledge to determine remedies and/or work arounds for abnormal conditions. Must be able to determine when vendor assistance and other technical support is required. Identifies the need for documentation and job aids and follows through to ensure completion and dissemination. Learns new technologies that will be implemented in the data center and trains other associates. Ensures physical security for the data center and systems hardware. Analyzes existing methods and workflows and optimizes to increase operations and production efficiency. Recognizes and identifies potential areas where existing policies and procedures require change, and where new ones need to be developed to accommodate business expansion. Maintain service level agreements with the various user departments and enterprise business units. Performs at or above the enterprise's Information Technology performance standards. Require vendor onsite support and IS assistance when necessary 24 hours per day Fulfills departmental requirements in terms of providing work coverage and administrative notification during periods of illness, vacation, or education Understating of ITIL processes [Incident, Change & Problem] Understanding of monitoring tools Co-Ordinate with Service providers, third parties to fix the issues. #LI-RJ2 Salary Range - $60,000-$73,000 a year

Biocytogen is a comprehensive research and discovery service provider for the biotech and pharmaceutical industries and academic institutions. Its service platform integrates preclinical studies with innovative animal models, CRISPR-based gene editing, and animal supplies, with a current focus on immuno-oncology and oncology. We are seeking a detail-oriented and compassionate Husbandry Technician to oversee and maintain the health and well-being of our research animal colonies. The successful candidate will be responsible for daily husbandry, colony management, and accurate record-keeping to support research and breeding activities. Job Responsibilities: Monitor and assess the health and well-being of mice and identify and report any signs of illness or distress. Provide daily care and husbandry for the breeding colony, including feeding, cage changing, food/water refilling, checking for pregnancy and new litter, and following established protocols and schedules. Ensure proper cleaning and maintenance of cages, equipment, and workspaces according to standard operating procedures (SOPs). Work collaboratively with research associates or scientists to meet project needs and animal welfare standards. Monitor environmental conditions (e.g., temperature, humidity) to ensure compliance with facility guidelines. Adhere to all institutional and regulatory guidelines and ethical standards regarding animal care and use. Required Skills and Experience: Associate of Bachelor's degree in biology, animal science, veterinary technology, or related field preferred. Previous experience with lab rodents is not required but should be able to work with lab rodents comfortably. Demonstrate ability for quality execution, attention to detail, and proficiency in multi-tasking in a fast-paced environment. Collaborative team player. Effective communication and interpersonal skills, with the ability to work collaboratively in a team environment. Willingness to work flexible hours, including weekends and holidays, as needed. Employee Benefits Medical Insurance Dental Insurance Vision Insurance Health Reimbursement Accounts Life and AD&D Insurance Short and Long Term Disability 401(k) with Company Match Paid Time off Paid Sick Days Paid Holidays BIOCYTOGEN is an Equal Opportunity Employer. Employment opportunities at BIOCYTOGEN BOSTON CORP are based upon one's qualifications and capabilities to perform the essential functions of a particular job. All employment opportunities are provided without regard to race, color religion, sex, national origin, ancestry, age, sexual orientation, gender identity and expression, veteran status, military status, disability, mental illness, genetic information, or any other characteristic protected by law. This Equal Employment Opportunity policy governs all aspects of employment, including, but not limited to, recruitment, hiring, selection, job assignment, promotions, transfers, compensation, discipline, termination, layoff, access to benefits and training, and all other conditions and privileges of employment.

We are seeking a detail-oriented Cathode Technician to join our battery cathode production team. In this role, you will assist with the synthesis of cathode active material (CAM) and cathode electrode fabrication by following standard operating procedures (SOPs) and maintaining a safe, efficient work environment. Key Responsibilities: Follow established SOPs to operate equipment used in CAM synthesis, including hydrothermal reactors, membrane filtration systems, and calcination furnaces Follow established SOPs to operate equipment used in CAM electrode fabrication in batch and roll-to-roll system designs Carefully measure and mix precursor materials according to specified ratios Monitor and adjust synthesis parameters such as temperature, pressure, and reaction time Collect samples at designated intervals for quality control testing Perform basic analytical tests to verify CAM and electrode properties meet specifications Properly handle, label, and store raw materials and finished CAM and electrode products Maintain detailed records and equipment logs Clean and maintain laboratory equipment and work areas Adhere to all safety protocols and wear appropriate personal protective equipment Requirements: Associate's degree in chemistry, materials science, or related field 1-2 years of experience in a laboratory or manufacturing environment Ability to follow detailed technical procedures with high accuracy Proficiency with common laboratory equipment and analytical instruments Strong attention to detail and record-keeping skills Ability to work in a team environment and communicate effectively Physical Requirements: Ability to stand for extended periods and lift up to 25 lbs Manual dexterity to handle small samples and operate laboratory equipment Vision to read instrument displays and detect color changes Must be able to wear a respirator as required by the job, including passing a fit test and following all safety protocols related to respirator use About Pure Lithium: A fast-paced Boston-based start-up, Pure Lithium provides the foundation for lithium metal to supplant lithium-ion as the predominant battery technology. Our mission is to enable the mass adoption of lithium metal batteries by getting lithium from the ground into the battery as quickly, sustainably, and inexpensively as possible. Our integrated supply chain development approach solves many pain points for the battery industry. Pure Lithium is led by a world-class team of executives and scientists with extensive experience inventing and commercializing battery and energy technologies. It established its laboratory in Charlestown, Massachusetts, in January 2021, where it produces lithium metal, polymer electrolytes, and batteries daily. Benefits: Fully covered health and dental Generous vacation time Weekly company Grubhub allowance MBTA pre-tax commuter benefit Ability to grow Vibrant and supportive team We seek applicants from all backgrounds, communities, and industries. We are committed to having a team made up of diverse skills, experience, and abilities. How to Apply: If you are a driven and organized professional ready to take on a challenging role in a fast-paced startup environment, we want to hear from you. Please submit your resume, along with a brief cover letter highlighting your relevant experience and explaining why you are the ideal candidate for this position. Interested candidates should apply via LinkedIn. Applications will be reviewed on a rolling basis. Pure Lithium is an equal opportunity employer committed to unlocking innovation and achieving its mission with diverse backgrounds, perspectives, and experiences. Please see our website, ****************** for more information.