Manufacturing Associate jobs at Moderna - 42 jobs

Manufacturing Associate (1st Shift, Systems) - Bothell, WA We have an opportunity for a dedicated team player to be a part of a fast-paced, busy manufacturing environment! Fujifilm, Sonosite, Inc is seeking Manufacturing Associates. This role is a full time opportunity with full benefits, a 401K plan, paid time off, plus more perks that come with being a full time Fujifilm Sonosite employee! As a successful candidate you will exhibit manual dexterity, reliability, basic math and computer skills and an aptitude for learning things quickly. Manufacturing experience is not required but is preferred. Any college level educational experience considered. This position is responsible for performing a variety of tasks associated with manufacturing diagnostic ultrasound transducers. Specific tasks may include some of the following: Weighing and mixing epoxy-based materials. Cleaning and assembling high precision molds. Light mechanical assembly of small components using hand tools and torque drivers. Manual assembly operations including shielding, gluing, and cable preparation. Work with hands under a microscope performing hand soldering of fine pitch cables and flexible circuits. Measurement of thin layers using high precision drop gauges. Use of high-precision tools such as: height gage, calipers, micrometers. Basic equipment skills such as: saws, machine mill, machine lathe. Basic computer skills desired for device history record transactions. Company Overview At FUJIFILM Sonosite, we reinvent how healthcare is delivered with point-of-care ultrasound technology. As the leader in bedside ultrasound systems, our innovations save lives-from premature babies in NICUs to trauma patients in emergency rooms. We're looking for purpose-driven team members ready to build technology that impacts real-world scenarios, including natural disasters and even war zones. By joining FUJIFILM Sonosite, you'll be part of a team that thrives on collaboration, out-of-the-box thinking, and a passion for life-saving innovations. Let's make a difference together. Our headquarters in Bothell, Washington, blends riverside charm with urban amenities, quality schools, and an ever-evolving downtown-all part of the vibrant Seattle metro area. Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: *************************************************** Job Description Essential Job Functions: Follow all required procedures such as Assembly Instruction, Personal Protective Equipment, and Device History Record while performing the job responsibilities. Mixing, casting and curing epoxy-based materials. Perform functions of casting, bonding, shielding, packaging, go-no-go testing, wiring, gluing, hand soldering, component installation, or bonding using tools such as soldering irons, glue dispensers, scales, microscopes, calipers, micrometers, various hand tools, or other precision equipment. Provide training and guidance to other Manufacturing Associates. Provide assistance in other areas of Manufacturing and Operations group as needed and directed. Perform required machine cleaning and maintenance as needed. Participate in projects such as Internal Assessment, Material Management, Yield Improvement, etc. Responsible and accountable for carrying out the requirements of the company's quality system. Knowledge and Experience: High school diploma or equivalent preferred. Experience in high tech manufacturing preferred. Must have excellent hand-eye coordination, manual dexterity. Must have the ability to read and comprehend written instructions. Effective verbal communication skills and written communication skills necessary to complete various manufacturing documentation. Must have excellent attention to detail. Ability to work effectively in a team-oriented environment. Must be familiar with basic math. Must have the ability to work with minimum supervision. Must be able to handle & work with chemicals. Able to lift 25lbs with or without accommodations. Shift Requirements: Shift hours are 5:00am to 3:30pm, Monday - Thursday with an excellent opportunity for overtime on Friday-Saturday Salary and Benefits: Starting wage of $24.00/hr. + $0.50 raise after 6 months of service Insurance: Medical, Dental & Vision Life & Company paid Disability Retirement Plan (401k): 4% automatic Company contribution Fujifilm matches 50 cents for every dollar you contribute, up to 6% of your salary Paid Time Off: You can accrue up to three (3) weeks of PTO in your first year of employment PTO increases based on years of service Employee Choice Holidays: Four (4) additional paid days off, based on date of hire in the calendar year Paid Holidays: Eight (8) paid holidays per year FUJIFILM Sonosite offers a fantastic compensation package, including benefits, and a 401k program. Visit us today to learn more about our exciting technologies and how you can make a difference. To apply and obtain further details regarding key responsibilities and experience requirements, check out our careers page at ******************************* To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid. #CB #LI-MW EEO Information Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc. ADA Information If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (******************** or ***************.

Job Title: Manufacturing Associate I - Redmond, WA site, Night Shift. About Us: this is who we are At Just Evotec Biologic., we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: / your challenge, …in our journey We're looking for a passionate and curious Manufacturing Associate I to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a Manufacturing Associate I at Just Evotec Biologic., you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team. Just-Evotec Biologics is seeking a highly motivated Manufacturing Associate that desires a significant opportunity to improve worldwide access to biotherapeutics. This team member will be responsible for the commercial manufacturing of mammalian cell-based biotherapeutics under cGMP conditions. Manufacturing Associates are expected to execute process recipes, monitor equipment and processes, perform basic tasks, including sampling, and routine maintenance of lab equipment. Associates will also assist in media and buffer compounding. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. Just Evotec operates 24 hrs a day using day shift, swing shift, and night shift on the front half and back half of the week. Night shift- back half, Wed Thru, Friday and every other Sat 19:00 - 08:00. Note: Night shift receives a 15% premium above base pay. What You'll Do: Perform and monitor critical processes (i.e., Single use bioreactor operations, perfusion, chromatography, product filtration, and solution preparation) Supporting the introduction of new products and technologies into the facility Initiating non-conformances (NC) Execution of Electronic Batch Records (EBR) using Manufacturing Execution System (MES) Draft and revise Manufacturing Procedures and Standard Operating Procedures, as necessary Support operations of glasswasher and autoclave Perform other duties as assigned Who You Are: Candidate must possess strong focus on right the first time and attention to detail Possess effective task/time management organizational skills Capacity to develop solutions to technical issues of moderate scope Ability to organize, analyze/interpret, and effectively communicate individual results Motivated, self-starter with strong mechanical aptitude Good interpersonal, team, and communication skills are a must Excellent oral and written communication skills Qualification Requirements: Bachelor's degree in Science or Engineering; or Associate's degree in science-related area and relevant experience; or High school diploma or GED and 3+ years of relevant experience in Manufacturing or Pharma. Why Join Us: Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow. Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. This is a site based role. Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged. Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them. Are You Still Curious? If you've read this far, then chances are you've got a curious mind-just like us. So, what are you waiting for? Take the leap and apply today. We can't wait to see where your curiosity leads you-and how it will shape the future of Just Evotec Biologic. Let your curiosity guide your career-#BeCurious and explore the endless possibilities at Just Evotec Biologic.! The base pay range for this non-exempt position at commencement of employment is expected to be $26.00 to $30.00 hourly offered may vary depending on individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment to innovation, patient-centered focus, and scientific excellence drives us to develop groundbreaking treatments including MACI (knee cartilage repair), Epicel and Nexobrid (burn care). Position Summary: The Associate I, Cell Therapy Manufacturing is responsible for the execution of process steps to manufacture commercial cell therapy products meeting internal and regulatory requirements. Schedule: This role will be required to work on-site Sun-Wed or Wed-Sat. Position Scope: Perform manufacturing procedures inside a manufacturing clean room in accordance with established SOPs, cGMPs, and safety regulations. Qualified to perform aseptic manipulations of cell culture operations. Document all operations in Electronic Batch Records and log sheets according to cGMPs and established SOPs. Maintain manufacturing-controlled areas in an inspection ready state. Perform clean room equipment sanitization. Record equipment and facility metrology data to ensure the equipment operates within specifications. Report out of specification readings to production management. Able to work independently upon completion of training. Be receptive to feedback and guidance from manager and other more experienced staff. Ability to organize, plan and manage time to effectively complete daily tasks. The ability to cooperate with others in a team environment will be critical to success. Practice safe work habits and adhere to Vericel's safety procedures and guidelines. Able to make cell-culture decisions based on cell observations and guidelines in written procedures. Assist in reviewing and revising production documents (SOP's and electronic records). Fully trained in at least one unit operation in both product lines. Ability to identify and report deviations and contribute to deviation investigations. In addition to being fully qualified in MACI or Epicel, cross train and qualify in at least one core competency e.g. 3T3, Media Prep, GP, TrackWise, Veeva. Achieve Qualified Trainer status. Other duties as assigned. Qualifications: Bachelor's degree (Life Sciences or related field) with 0 - 2 years of experience working in a cGMP environment in the biotechnology/pharmaceutical industry or Biotechnology certificate with 1 - 2+ years of experience working in a cGMP environment in the biotechnology/pharmaceutical industry or HS diploma/GED with 4 - 6+ years of cGMP experience. Excellent communication skills, written and verbal. Experience with Microsoft Office suite. Experience in small scale tissue culture processing (preferred). Experience working within a regulated environment that is frequently audited by internal and external Agencies, such as the FDA and ISO (preferred). Ability to sit for long periods of time while performing cell culture operations. Ability to lift, carry, push and pull up to 50 lbs. Ability to work 1 weekend day and rotating holiday coverage. Ability to gown and gain entry to manufacturing areas. Why Vericel? Cutting-Edge Science: Work with a leading regenerative medicine product that is transforming patient care. Career Growth: Be a part of a growing organization with opportunities to expand your impact. Collaborative Culture: Work alongside a team of dedicated professionals who are passionate about improving lives. The hourly wage range Vericel reasonably and in good faith expects to pay for this position at the time of this posting is $23.08 to $27.40 per hour. The actual salary offered will be determined based on factors such as the candidate's qualifications, experience, and skills. Bonus, incentive pay, equity and benefits may be provided in addition to the base compensation listed above. In accordance with Massachusetts law, Vericel provides the pay range that it reasonably and in good faith expects to pay for a particular and specific employment position at the time of posting or offer. This range is subject to change based on business needs, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying. Retaliation for making such a request is strictly prohibited. EEO Statement All applicants will receive consideration for employment without regard to their race, color, religion, sex, national origin, sexual orientation, gender identity, or protected veteran status and will receive consideration for employment and will not be discriminated against on the basis of disability. Vericel Corporation is an Equal Opportunity/Affirmative Action Employer. Vericel Corporation is VEVRAA federal contractor and desires priority referrals of protected veterans for job openings at all locations within the state.

Job Title: Manufacturing Associate III - Redmond, WA Dayshift: Sun- Wed 0700-1800 or Swingshift: Sun - Wed 12noon - 23:00 Note: Swingshift receives a 10% premium above base pay. About Us: this is who we are At Just Evotec Biologics, we believe that curiosity is the spark that drives innovation and success. As a forward-thinking team, we thrive on challenging the status quo, learning from each other, and pushing the boundaries of what's possible. We're on a mission to create a place where curiosity isn't just encouraged-it's celebrated. Are you someone who asks questions, seeks answers, and isn't afraid to go deeper? #BeCureious with us and see where your curiosity can take you! The Role: / your challenge, …in our journey We're looking for a passionate and curious Manufacturing Associate III to join our team. If you're excited by new challenges, solving complex problems, and learning every step of the way, you might just be the perfect fit. In this role, you'll have the opportunity to drive impactful projects, collaborate with bright minds, and explore uncharted territories. As a Manufacturing Associate III at Just Evotec Biologics, you'll have the freedom to ask the hard questions, think outside the box, and find creative solutions that push us forward. It's a role where your curiosity will fuel both your personal growth and the success of the team. Manufacturing Associates III are expected to execute process recipes, monitor equipment and processes, perform basic tasks, including sampling, and routine maintenance of lab equipment in support of downstream manufacturing operations. The staff member is expected to comply and follow written procedures for safety requirements, cGMP Practices, Standard Operating Procedures, and manufacturing documentation. Manufacturing Associates III may also assist in media and buffer compounding. What You'll Do: Perform and monitor critical processes (i.e., column packing, capture and polishing chromatography steps, viral inactivation, viral filtration, and UF/DF operations) Support the introduction of new products and technologies into the facility Initiate quality records, including but not limited to non-conformances (NC), Corrective/Preventative Actions (CAPA) and assisting in investigations. Draft and revise Manufacturing Procedures and Standard Operating Procedures, as necessary With minimal supervision set up, operate, and maintain a majority of MFG equipment; collects data, and writes/ updates GMP documentation. With direction from Floor Lead/ Supervisor, propose and test solutions to MFG Operational problems. Be able to identify when a deviation has occurred. Actively participate in departmental teams, NPI. May present run data as applicable. Train Junior level staff Respond to equipment alarms with help of Floor Lead. Effectively communicate with Floor Lead/ Supervisor the status of MFG Operations. Document operational requirements in batch records in accordance with cGMP and company guidelines Develop an understanding of equipment and operations used to manufacture biotherapeutics in cGMP manner. Demonstrate situational leadership within MFG and company responsibilities Perform other duties as assigned Who You Are: Master's degree; or Bachelor's degree and 3 years of Manufacturing & Operations experience; or Associate's degree and 5 years of Manufacturing & Operations experience; or High school diploma / GED and 7 years of Manufacturing & Operations experience Preferred Requirements: Single use technology experience Capacity to develop solutions to technical issues of moderate scope Train other personnel on equipment operation Draft and revise SOPs Proven knowledge of cGMP requirements to ensure compliance Experience in operations required for the manufacture of biotherapeutics Focus on quality and attention to detail Ability to organize, analyze/interpret, and effectively communicate data and results Motivated, self-starter with strong mechanical aptitude Good interpersonal, team, and communication skills Troubleshooting skills on Manufacturing equipment including single use equipment Experience with Delta V/MES Experience with lab equipment/testing Be open to change and manage emotions during periods of organizational change. Why Join Us: Growth Opportunities: We're a company that believes in continuous learning and development. Whether it's professional courses, mentorship, or new projects, we'll help you grow. Flexible Work Environment: We offer flexible work options to help you balance your professional and personal life. Site based role. Inclusive Culture: We're committed to building a diverse and inclusive environment where everyone's voice is valued, and curiosity is encouraged. Innovative Projects: You'll have the chance to work on groundbreaking initiatives and cutting-edge technology in an atmosphere where your curiosity is the key to success. A Place for Big Ideas: We don't just talk about thinking outside the box-we throw the box away. If you've got ideas, we want to hear them. The base pay range for this position at commencement of employment is expected to be $32.56 to $41.46; Base salary offered may vary depending on the individual's skills, experience and competitive market value. Additional total rewards include discretionary annual bonus, comprehensive benefits to include Medical, Dental and Vision, short-term and long-term disability, company paid basic life insurance, 401k company match, flexible work, generous paid time off and paid holiday, wellness and transportation benefits. Evotec (US) Inc. is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, gender, age, disability, genetic information, gender expression, gender identity, national origin, religion, sexual orientation, or veteran status.

Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California. Position Summary Reporting to the Manufacturing Sr Manager, the Manufacturing Associate will perform manufacturing activities associated with LNP GMP manufacturing within a state-of-the-art manufacturing facility at 33 New York Ave in Framingham, MA. A successful candidate will be responsible for the manufacture of LNP therapies for clinical studies and as a commercial product. This role requires clear communication across multiple departments for the execution of daily activities. The ideal candidate will have experience successfully performing formulated LNP Manufacturing within a GMP environment. Responsibilities Perform clinical / commercial product manufacturing for LNP therapies according to cGMP standards and SOPs including Lipid and RNA Prep, T-Mix, and TFF operations Perform aseptic vial filling, visual inspection, cryopreservation, process reagent formulation, and material kitting. Transfer raw material inside cleanroom suite using sanitizing reagents or equipment. Participates in technology transfer from Process Development to the Manufacturing group. Assist in the life cycle development of Standard Operating Procedures (SOPs) for manufacturing in collaboration with PD / MSAT and Quality Systems groups. Ensures all materials and equipment are identified and available in time for manufacturing operations. Execute standard work per manufacturing schedule Participate in Quality investigations and resolutions. Ensure cGMP compliance through consistent execution. Other duties and projects as assigned to meet departmental requirements. Minimum Qualifications Certificate, associate's degree or higher in biological sciences or related fields and 2-5 years of relevant Manufacturing experience or related fields Available to work a flexible schedule as needed. Ability to don cleanroom garments and work within a classified environment (Grade B and C) Knowledge of GMP and industry standards T-Mix and TFF experience preferred Fluency in Windows and Microsoft Office applications Attentive to detail and accuracy Ability to effectively communicate and collaborate with internal stakeholders is essential Ability to work effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view. Ability to execute and follow-through to completion Ability to lift 40 pounds Ability to stand for 6 hours in a clean room environment Self-driven, independently motivated, data driven and excellent problem-solving ability Competencies Collaborative - Openness, One Team Undaunted - Fearless, Can-do attitude Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems. Entrepreneurial Spirit - Proactive. Ownership mindset. Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site. Manufacturing Associate: Base pay range of $35.00 per hour to $42.00 per hour + bonus, equity and benefits. The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities. CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. To view our Privacy Statement, please click the following link: ***********************************************

Perform all production operations in the areas assigned within the facility. Perform production support operations in areas assigned and support start-up, changeovers and tech transfer activities. Duties and Responsibilities Operate glass washers and autoclave Prepare buffers, medias and other solutions, following written procedures and batch records Operate process equipment such as tanks, clean in place skids (CIP/SIP), agitators, filtration devices, autoclaves, glass washers, integrity testing and other small equipment Perform process steps in coordination with other associates asking for help as needed so as not to perform steps without proper training/qualification Adhere to scheduling changes and responds appropriately Communicate with supervisor on issues regarding work orders or shifts in process parameters Give input and make suggestions to improve process Follow all GMP's and EHS procedures Attend and completes all mandatory training Ensure training plan is accurate and up-to-date Complete all necessary documentation per the required GMP practices Participate in presenting the manufacturing areas in a state of audit readiness Perform production operations following written SOP's/BR's in accordance with GMPs Other duties as assigned Regulatory Responsibilities Conduct business in a responsible manner that complies with all state, FDA, OSHA and HIPAA regulations, or otherwise as applicable Supervisory Responsibilities N/A Experience Experience in a GMP environment and in an approved laboratory under minimal supervision preferred Education Associates Degree or High School Diploma with zero (0) to two (2) or more years of directly related experience. Degree in other discipline (or lack of degree) may be considered if sufficient technical depth has been achieved from professional experience Knowledge, Skills & Abilities Understanding of the basic FDA cGMP regulations Verbal and written skills Basic software application skills (Word, Power Point) Able to follow detailed processing instruction Accurately document all necessary documentation Satisfactory audio-visual acuity Ability to read and write English Familiarization with technical issues in the area Ability to work shift that covers a 24/7 operation Ability to work shifts and off hours, as applicable Physical Requirements Ability to sit or stand for prolonged periods of time Ability to lift and carry materials weighing as much as 50lbs

The Manufacturing Technician position is responsible for the manufacture, inspection, and final product packaging and sterilization of Conformis implants and components. 2 nd Shift - Mon - Fri, 3:00pm - 11:30pm Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across Conformis. Understand the objectives, responsibilities, and mission of the Production department and work towards those goals. Prioritize and plan work activities; adapt for changing conditions. Execute daily maintenance and start-up activities. Perform machine set-ups. Perform inspection of components and assembly as required. Perform cleaning, pouching/sealing, labeling, and sterilization operations. Strict adherence to Good Documentation Practices when executing all assignments. Perform timely and accurate transactions of workflow in ERP system. Participate in inventory cycle counts, variance investigation, and reconciliation. Assist in performing required process capability studies, equipment installation qualifications, and process validation. Assist in the investigation and implementation of corrective actions on product and process failures. Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions, and Good Manufacturing Procedures. Interface with vendors to seek solutions for equipment repairs and refurbishment. Responsible for upkeep of manufacturing areas and provide a clean and safe work environment. Review all manufacturing documentation, assembly, inspection, test, and packaging procedures, and provide feedback. Other duties as assigned. Qualifications: High School diploma or equivalent; Technical education preferred. 2+ years' work experience in a medical device and/or regulated environment. Familiarity with Oracle (or equivalent) ERP systems and Microsoft Office Applications. Familiar with ISO Standards and Good Manufacturing Practices. Excellent verbal and written communication. Demonstrated English reading and writing skills. Ability to understand and follow comprehensive work instructions and guidance documents. Shipping/receiving/stockroom experience a plus. Skills, Abilities, Competencies Required: Excellent written and verbal communication skills. Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail. Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness. Strong organizational, analytical, and time-management skills. Able to self-motivate and work both independently and as part of a team. Manual dexterity to handle tools, inspection gauges, and equipment of different sizes. Demonstrated organizational skills. Ability to work in a fast-paced environment and multitask. Comfortable with change. Flexible to work overtime, extended hours, and weekends as business demands. Ability to work as part of a team as well as independently. Working conditions: Ability to lift, pull, and push up to 40 lbs. Ability to stand for prolonged periods of time. Ability to work in a Class 10,000 or ISO class VII clean room environment for prolonged periods of time. Capable of working in material blending area with necessary personal safety equipment (eye protection, dust masks). Busy work environment with frequent interruptions. Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies. Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, dust, etc.). Conformis is an Equal Opportunity Employer

The Manufacturing Technician position is responsible for the manufacture, inspection, and final product packaging and sterilization of restor3d implants and components. 2 nd Shift - Mon - Fri, 3:00pm - 11:30pm Essential Duties and Responsibilities: Develop and maintain strong internal working relationships across restor3d. Understand the objectives, responsibilities, and mission of the Production department and work towards those goals. Prioritize and plan work activities; adapt for changing conditions. Execute daily maintenance and start-up activities. Perform machine set-ups. Perform inspection of components and assembly as required. Perform cleaning, pouching/sealing, labeling, and sterilization operations. Strict adherence to Good Documentation Practices when executing all assignments. Perform timely and accurate transactions of workflow in ERP system. Participate in inventory cycle counts, variance investigation, and reconciliation. Assist in performing required process capability studies, equipment installation qualifications, and process validation. Assist in the investigation and implementation of corrective actions on product and process failures. Comply with all company policies and procedures including safety regulations, personal protective equipment requirements, Standard Operating Procedures, Work Instructions, and Good Manufacturing Procedures. Interface with vendors to seek solutions for equipment repairs and refurbishment. Responsible for upkeep of manufacturing areas and provide a clean and safe work environment. Review all manufacturing documentation, assembly, inspection, test, and packaging procedures, and provide feedback. Other duties as assigned. Qualifications: High School diploma or equivalent; Technical education preferred. 2+ years' work experience in a medical device and/or regulated environment. Familiarity with Oracle (or equivalent) ERP systems and Microsoft Office Applications. Familiar with ISO Standards and Good Manufacturing Practices. Excellent verbal and written communication. Demonstrated English reading and writing skills. Ability to understand and follow comprehensive work instructions and guidance documents. Shipping/receiving/stockroom experience a plus. Skills, Abilities, Competencies Required: Excellent written and verbal communication skills. Able to work accurately in a fast-paced, hectic, ever-changing environment with strong attention to detail. Demonstrated ability to monitor own work to ensure quality, accuracy, and thoroughness. Strong organizational, analytical, and time-management skills. Able to self-motivate and work both independently and as part of a team. Manual dexterity to handle tools, inspection gauges, and equipment of different sizes. Demonstrated organizational skills. Ability to work in a fast-paced environment and multitask. Comfortable with change. Flexible to work overtime, extended hours, and weekends as business demands. Ability to work as part of a team as well as independently. Working conditions: Ability to lift, pull, and push up to 40 lbs. Ability to stand for prolonged periods of time. Ability to work in a Class 10,000 or ISO class VII clean room environment for prolonged periods of time. Capable of working in material blending area with necessary personal safety equipment (eye protection, dust masks). Busy work environment with frequent interruptions. Must be aware of hazards within the company; adhere to quality and safety standards established by FDA and other regulatory agencies. Able to work in changing environments (reduced lighting, increased noise, temperature variances, unpleasant odors, dust, etc.). restor3d is an Equal Opportunity Employer

We welcome you to join our team! Cascade Dafo is currently hiring full-time Production Workers at our Ferndale facility. The shift we are hiring for is Monday-Friday, 6:00am-2:30pm or 8:30am-5:00pm, and requires some overtime. Production Workers at Cascade Dafo start off by learning a set of core jobs; these core jobs will be the foundation for all other positions in the production departments. We find that successful applicants have these skills and abilities: Able to understand a priority work system Able to hold, firmly grasp, and maneuver product constantly using hand-eye coordination Able to use a variety of hand and electric tools; including safely starting up, troubleshooting and shutting down power equipment Able to clean our braces with solvent as necessary Able to stay current with product and process changes Is committed to following all safety guidelines, protecting themselves and their co-workers Able to lift, reach, and maneuver tubs up to 5 pounds and occasionally up to 10 pounds Able to stand or sit for long periods of time Is punctual and flexible, with the ability to work overtime as needed Has a strong attention to detail with a devotion to produce a high-quality product Is committed to working effectively and respectfully with all coworkers Able to read and understand English; including anatomy terms, colors, and identifying pictures Here's a little bit about us: Cascade Dafo is a manufacturing company that specializes in making ankle foot orthosis (AFO's) for children with mobility challenges. We are proud to report our braces are the best in the industry; we are PROUDER to share that the reason we are the best is because of our team members. Cascade Dafo is a dedicated, caring, hardworking team of people that create, customize, and care for our patients from the moment an order arrives at our facility to long after our braces have been fit on a patient. We know our team members make us successful; therefore, we do our best to show our appreciation to them. Our benefit package includes: Competitive Wages: Our starting wage is $19.50/hour. We provide opportunities for growth by inviting our team members to apply to learn more jobs within our production departments. The more jobs you learn; the higher wage you can earn. We provide career path options and support you on your journey. Profit Sharing: Cascade team members are awarded profit sharing bonuses each quarter. By sharing in the profits, our team members feel a sense of ownership; they reap the benefits of their hard work. In 2025, profit sharing added an average of $1.80- $2.20 more per hour to our new team member's compensation. Healthcare Benefits: We provide medical, dental, and vision insurance to our full-time team members. We offer a QHDHP with employer HSA contribution or a traditional PPO plan; with two different medical plans to choose from, our team members find a plan that best fits their needs. Because healthcare is so important, Cascade will share the cost of your family's medical benefits with you. Time Off: We believe our teams need time off to spend with friends and family; we know team member engagement requires time off to refresh yourself. From your first day of work you'll be earning PTO. PTO hours earned increase with seniority. Our holidays schedule allows for rest time as well; we have a minimum of 10 paid holidays allowing you to relax and make memories with your friends and family. 401(k): Cascade offers a traditional and a ROTH 401k plan to you after 90 days of employment. We fund a company match (up to 4%) per payroll and a 401(k) end of year profit sharing contribution. Additional Benefits: We provide our team members with short/long term disability and life insurance. Work Balance: We are very supportive of your life away from Cascade. Our schedules are posted early so you never have to wonder what time you'll be off work. A Great Atmosphere: When you join our team, you'll find yourself in a caring, fun atmosphere. Our leadership is here to support and guide you; we want you to feel welcome, acknowledged, and appreciated. As for fun, we may spontaneously host a pancake breakfast or holiday themed party. We also love to celebrate birthdays and honor our team members' service to the company, both with cash prizes! If you can picture yourself working here, we invite you to apply today! We will reach out to qualified applicants to scheduled interviews. What is involved with an interview at Cascade Dafo? We want you to feel comfortable and ready when you meet us. We will start with an in-person conversation, giving us a chance to get to know each other. The next step is to tour our production plant, meet some of our leadership team, and “try out” some of our jobs. Don't forget to bring questions you may have about Cascade or the job-we love to share what we do here! Our team provides all the training you'll need to be successful. Thank you for considering working with us at Cascade Dafo, we are excited to meet you!

Salary Range:$45,000.00 To $55,000.00 Annually The Aseptic Manufacturing Technician has primary responsible for the activities and procedures required for the manufacture and filling of Aseptic products. The position works under close supervision and follows established procedures in the execution of daily activities. Specific Tactical Responsibilities: * Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedure (OPM) * Executes all procedures associated with aseptic fills (transfer, set-up, sanitization, autoclaving, process simulation, etc.,) * Adheres to written work instructions to perform solvent recovery, clean out of place, clean in place of complex equipment and components * Assists with troubleshooting and resolution of process related issues * Records data into Batch Records, log books and OPM's * Documents all work activities according to Good Documentation Practices * Reports procedural deviations and nonconformance to management * Maintains current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Job Complexity: The position works on assignments that are routine in nature where cGMP experience is required to perform work activities. The Aseptic Manufacturing Technician I normally receives detailed instruction on routine work and training on new assignments. Supervisory Responsibilities: None Required Qualifications: * High school diploma, GED or equivalent experience * 0 - 1+ years related experience in a manufacturing environment * Ability to work flexible hours to complete work activities * Must possess good written and verbal communication skills * Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas; ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes * Ability to lift, pull or push equipment requiring up to 25-50 lbs; ability to stand for 6 hours in a production suite * Ability to climb ladders and work platforms * Ability to work around chemicals (alcohols, acids & bases) * Ability to work flexible hours to complete work activities Desired Experience, Knowledge, and Skills: * Manufacturing experience in a medical device industry * Experience working in a clean room or using aseptic technique * Experience using commercial scale automated equipment * Ability to perform computerized transactions and maintain spreadsheets are a plus The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law. submit your resume We are an equal opportunity employer, and we do not tolerate discrimination based on characteristics such as age, gender, gender identity and expression, genetic status, sexual orientation, race, ethnicity, national origin, religion, disability, military status, family status, or any other protected category under federal, state, or local law.

How will you make an impact? You will be responsible for the following: Perform kitting operations (measure out components or raw materials) Ability to perform activities under a microscope Prepare components and build device assemblies Prepare bulk drug formulations Perform filing, capping, and crimping operations Perform packaging and labeling operations Perform sampling Perform visual inspections Perform documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements. Additional tasks as required How will you get here? - High School Diploma Required - 4-6 years of related experience in the medical device, pharmaceutical, and/or biotechnology industries, or a AA with less 2-4 years of experience or a bachelor's degree with 0-2 years of experience. Required - It is highly desirable to have experience working in and maintaining a cleanroom in accordance with GDP and cGMPs standards. Required #GKOSUS What will you do? Maintain proper cleanroom environment (including gowning, room cleaning, and supplies) Follow, execute, and adhere to documentation in accordance with cGMP, QMS, and GDP requirements: protocols, specifications, work instructions (WIs), standard operating procedures (SOPs), batch records (BRs), device history records (DHRs), and engineering batches. Perform basic calculation and data entry Ability to assemble, disassemble, and clean process equipment Ability to clean, etch, passivate, assemble, and inspect components Process and assemble components in accordance with documented specifications and procedures Prepare bulk drug formulation operations Perform filling, capping and crimping operations Perform packaging and labeling operations Perform in-process inspection of assemblies and finished products in accordance with specification criteria Organize and clean the work areas Ability to perform validation and qualification activities (IQ/OQ/PQ/PV)

How will you make an impact? You will be responsible for the following: Perform kitting operations (measure out components or raw materials) Ability to perform activities under a microscope Prepare components and build device assemblies Prepare bulk drug formulations Perform filing, capping, and crimping operations Perform packaging and labeling operations Perform sampling Perform visual inspections Perform documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Perform all activities with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality management system (QMS) medical device good manufacturing practices (GMP) requirements. Additional tasks as required

The Crosslink Technician II has primary responsible for the activities and procedures required for cross linked hyaluronic acid product production. The position follows established procedures in the execution of daily activities and receives instructions on new assignments. Specific Tactical Responsibilities: Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedure (OPM) Executes all procedures associated with cross linked hyaluronic acid product production Adheres strictly to written work instructions to perform solvent recovery, clean out of place, clean in place of complex equipment and components Performs scheduled cleanings and sterilization of equipment Supports change over activities Troubleshoots and resolves process related issues Records data into Batch Records, log books and OPM's Reviews Logbook and Forms Documents all work activities according to Good Documentation Practices Reports procedural deviations and nonconformance to management Maintains current training on all assigned procedures to include read & understood, skills development and classroom training activities as required. Job Complexity: The position works on assignments that are routine in nature where cGMP experience is required to perform work activities. The Crosslink Manufacturing Technician II normally follows procedures on routine work, requires instruction and training on new assignments. Supervisory Responsibilities: None Required Qualifications: High school diploma, GED or equivalent experience 2-4 years related experience in a cGMP manufacturing environment Ability to work flexible hours to complete work activities Must possess written and verbal communication skills Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas; ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes Ability to lift, pull or push equipment requiring up to 25-50 lbs; ability to stand for 6 hours in a production suite Ability to climb ladders and work platforms Ability to work around chemicals (alcohols, acids & bases) Ability to work flexible hours to complete work activities Desired Experience, Knowledge, and Skills: Manufacturing experience in a medical device industry Experience working in a clean room or using aseptic technique Experience using commercial scale automated equipment Ability to perform computerized transactions and maintain spreadsheets are a plus The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

The Aseptic Manufacturing Technician has primary responsible for the activities and procedures required for the manufacture and filling of Aseptic products. The position works under close supervision and follows established procedures in the execution of daily activities. Specific Tactical Responsibilities: Operates production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedure (OPM) Executes all procedures associated with aseptic fills (transfer, set-up, sanitization, autoclaving, process simulation, etc.,) Adheres to written work instructions to perform solvent recovery, clean out of place, clean in place of complex equipment and components Assists with troubleshooting and resolution of process related issues Records data into Batch Records, log books and OPM's Documents all work activities according to Good Documentation Practices Reports procedural deviations and nonconformance to management Maintains current training on all assigned procedures to include read & understood, skills development and classroom training activities as required Job Complexity: The position works on assignments that are routine in nature where cGMP experience is required to perform work activities. The Aseptic Manufacturing Technician I normally receives detailed instruction on routine work and training on new assignments. Supervisory Responsibilities: None Required Qualifications: High school diploma, GED or equivalent experience 0 - 1+ years related experience in a manufacturing environment Ability to work flexible hours to complete work activities Must possess good written and verbal communication skills Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas; ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes Ability to lift, pull or push equipment requiring up to 25-50 lbs; ability to stand for 6 hours in a production suite Ability to climb ladders and work platforms Ability to work around chemicals (alcohols, acids & bases) Ability to work flexible hours to complete work activities Desired Experience, Knowledge, and Skills: Manufacturing experience in a medical device industry Experience working in a clean room or using aseptic technique Experience using commercial scale automated equipment Ability to perform computerized transactions and maintain spreadsheets are a plus The salary range provided is based on the Company's reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life. The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Company Overview Hamilton Storage provides automation solutions to customers in life science and clinical research. The company develops modular, scalable systems that automate sample storage, management, and processing. Hamilton provides all the benefits of advanced automation without the complexity associated with installing, operating, and maintaining large-scale custom systems. Acquired in 2007, Hamilton Storage is headquartered in Franklin, Massachusetts, USA with R&D facilities co-existing in both Franklin, MA and Bonaduz, Switzerland. The decentralized R&D organization benefits both production and marketing and allows Hamilton to stay close to the local markets and respond quickly to market needs. Responsibilities Perform a wide variety of mechanical and electromechanical assemblies from engineering drawings, verbal and written procedures. Other responsibilities include: Conduct documented tests at the subassembly level to assess performance and validate unit functions according to specifications. Troubleshoot subassemblies and perform corrections and repairs as directed. Test functional performance of systems, subassemblies, and parts under specified conditions (e.g. cold temperature). Work with senior technicians and engineering to make process and functional improvement suggestions. Ability to use and configure PC's in a Windows environment is necessary. Qualifications Ability to read electrical and mechanical schematics. Must have the ability to manage tasks, meet schedule commitments, and possess basic troubleshooting skills. Education/Experience High school diploma or general education degree (GED) required. Three (3) or more years of experience in the assembly and testing of electromechanical assemblies required. Experience with capital/process equipment, automation, and motion control systems is a plus. Attention to detail, strong documentation and record keeping skills, is required. Must be able to lift 50lbs. The ability to use Microsoft Office is a plus. About Hamilton Diverse portfolio of exciting and innovative design projects. Tremendous opportunities for professional growth. Commitment to sustainable design. Competitive compensation. Excellent benefit package includes medical, dental, vision insurance, paid vacation time, paid sick time, disability insurance, 401k, tuition reimbursement and more. Must pass drug and background screens. May be required to wear Personal Protective Equipment (provided by employer). EEO - It is the policy of this organization to provide equal employment opportunities to all qualified applicants without regard to race, creed, color, national origin, sex, age 40 and over, disability, marital status, sexual orientation, gender identity, genetic information, citizenship status, religious preference, or veteran status in all phases of the employment process and in compliance with applicable federal, state, and local laws and regulations.

Hamilton Storage provides automation solutions to customers in life science and clinical research. The company develops modular, scalable systems that automate sample storage, management, and processing. Hamilton provides all the benefits of advanced automation without the complexity associated with installing, operating, and maintaining large-scale custom systems. Acquired in 2007, Hamilton Storage is headquartered in Franklin, Massachusetts, USA with R&D facilities co-existing in both Franklin, MA and Bonaduz, Switzerland. The decentralized R&D organization benefits both production and marketing and allows Hamilton to stay close to the local markets and respond quickly to market needs. Responsibilities Perform a wide variety of mechanical and electromechanical assemblies from engineering drawings, verbal and written procedures. Other responsibilities include: * Conduct documented tests at the subassembly level to assess performance and validate unit functions according to specifications. * Troubleshoot subassemblies and perform corrections and repairs as directed. * Test functional performance of systems, subassemblies, and parts under specified conditions (e.g. cold temperature). * Work with senior technicians and engineering to make process and functional improvement suggestions. * Ability to use and configure PC's in a Windows environment is necessary. Qualifications * Ability to read electrical and mechanical schematics. * Must have the ability to manage tasks, meet schedule commitments, and possess basic troubleshooting skills. Education/Experience * High school diploma or general education degree (GED) required. * Three (3) or more years of experience in the assembly and testing of electromechanical assemblies required. * Experience with capital/process equipment, automation, and motion control systems is a plus. * Attention to detail, strong documentation and record keeping skills, is required. * Must be able to lift 50lbs. * The ability to use Microsoft Office is a plus. About Hamilton * Diverse portfolio of exciting and innovative design projects. * Tremendous opportunities for professional growth. * Commitment to sustainable design. * Competitive compensation. * Excellent benefit package includes medical, dental, vision insurance, paid vacation time, paid sick time, disability insurance, 401k, tuition reimbursement and more. * Must pass drug and background screens. * May be required to wear Personal Protective Equipment (provided by employer). EEO - It is the policy of this organization to provide equal employment opportunities to all qualified applicants without regard to race, creed, color, national origin, sex, age 40 and over, disability, marital status, sexual orientation, gender identity, genetic information, citizenship status, religious preference, or veteran status in all phases of the employment process and in compliance with applicable federal, state, and local laws and regulations. Mid Salary

This is an evening weekend shift. Working hours are 6:00 pm - 6:30 am, Friday - Sunday. This position is eligible for additional shift differential compensation. The Associate Manufacturing Technician will be a critical contributor in a mission that truly represents a once-in-a-lifetime opportunity to join a company that is making significant investments in establishing US manufacturing, expanding internationally, and delivering a consistent cadence of product innovations to the market and investing in its people. The successful candidate will be responsible for operating and maintaining highly automated and advanced manufacturing equipment necessary to produce our signature product. This individual will be trained and cross-trained to both operate and repair issues across a variety of technologies including: heat staking, laser welding, mechanical swaging, printed circuit board (PCB) handling and testing, robotic automation, metal stamping and bending, form/fill/seal medical packaging, and high-speed discrete component assembly. In addition to equipment operation and maintenance, this individual will be responsible for the product quality performance of the equipment and basic machine troubleshooting in the event of faults and machine stops. This position requires mechanical aptitude, technical ability, machine troubleshooting and problem-solving skills, and the willingness to work in a fast-paced manufacturing environment. Responsibilities: • Perform equipment operation, basic repair, and minor daily/weekly preventative maintenance tasks to meet all standards for safety, quality and efficiency. These tasks must be completed under minimal supervision. • Maintain machine raw material feeds, perform any fault clearing and clear stoppages on automated equipment. • Utilize human machine interfaces (HMIs) to identify and correct shifts in process control. • Ensures adequate raw material is prepared correctly and jobs are run in a timely manner to ensure on-time delivery. • Executes equipment inspections and generates emergency, corrective, and/or preventative work orders as needed. • Troubleshoot and identify potential solutions for minor mechanical errors, safety issues or general operating inefficiencies within the production processes. • Able to utilize computer systems to support in the material inventory and quality management processes. • Participates in manufacturing processes to support new product design transfer, process development, equipment validations, and process validations. • Investigates and resolves process issues within their equipment cells. • Perform routine cleaning/inspection/lubrication of machinery. • Works from specifications, work orders, and general instructions from Production Supervisor/Team Lead. • Safely follow standard operating procedures including but not limited to material handling, record keeping, packaging, and shipment preparation. Must follow all Good Manufacturing Practices (GMPs). • Notifies Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained . • Excellent attention to detail, good organization, and capable of working independently with minimal instruction from production supervisor. • Able to work in small groups and cross functional teams to troubleshoot issues, identify and implement collective corrective actions. • Maintain a clean work environment suitable for medical device manufacturing and cleanroom production. • Performs other duties as required Education and Experience: Minimum Requirements: • High School Diploma or GED Preferred Skills and Competencies: • Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment. • Must be proficient in English language to be able to read documentation, communicate, and write. • Ideal candidate will have keen eye for quality, is dependable, and will work collaboratively within a team, and possess a positive attitude. • Previous experience working in a clean room environment. • Previous experience with debugging and optimizing assembly processes. • Experience in a start-up production environment is a plus. • Manufacturing experience in a regulated industry is a plus. • Mechanical Aptitude - Knowledge of and experience with industrial machines and tools, including design, uses, repair, and maintenance. • Production & Processing - Knowledge of raw materials, measurement instruments, production processes, quality control, and other techniques for the manufacture and distribution of goods. • Mathematics - Knowledge of basic arithmetic. • Problem Solving - Recognizes problems and understands root cause analysis techniques/concepts. Physical Requirements (if applicable): • Required to stand for at least 75% of working time per shift, with walking at least 50% of working time per shift. • Required to reach above shoulder frequently and below waist occasionally. • Required to push and pull. • Ability to lift up to 20lbs occasionally, 5-20lbs frequently. NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite Additional Information: Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com. We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it! At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. (Know Your Rights)

This is a weekend days shift. Working hours are 6:00 am - 6:30 pm, Friday - Sunday. The Associate Manufacturing Technician will be a critical contributor in a mission that truly represents a once-in-a-lifetime opportunity to join a company that is making significant investments in establishing US manufacturing, expanding internationally, and delivering a consistent cadence of product innovations to the market and investing in its people. The successful candidate will be responsible for operating and maintaining highly automated and advanced manufacturing equipment necessary to produce our signature product. This individual will be trained and cross-trained to both operate and repair issues across a variety of technologies including: heat staking, laser welding, mechanical swaging, printed circuit board (PCB) handling and testing, robotic automation, metal stamping and bending, form/fill/seal medical packaging, and high-speed discrete component assembly. In addition to equipment operation and maintenance, this individual will be responsible for the product quality performance of the equipment and basic machine troubleshooting in the event of faults and machine stops. This position requires mechanical aptitude, technical ability, machine troubleshooting and problem-solving skills, and the willingness to work in a fast-paced manufacturing environment. Responsibilities: * Perform equipment operation, basic repair, and minor daily/weekly preventative maintenance tasks to meet all standards for safety, quality and efficiency. These tasks must be completed under minimal supervision. * Maintain machine raw material feeds, perform any fault clearing and clear stoppages on automated equipment. * Utilize human machine interfaces (HMIs) to identify and correct shifts in process control. * Ensures adequate raw material is prepared correctly and jobs are run in a timely manner to ensure on-time delivery. * Executes equipment inspections and generates emergency, corrective, and/or preventative work orders as needed. * Troubleshoot and identify potential solutions for minor mechanical errors, safety issues or general operating inefficiencies within the production processes. * Able to utilize computer systems to support in the material inventory and quality management processes. * Participates in manufacturing processes to support new product design transfer, process development, equipment validations, and process validations. * Investigates and resolves process issues within their equipment cells. * Perform routine cleaning/inspection/lubrication of machinery. * Works from specifications, work orders, and general instructions from Production Supervisor/Team Lead. * Safely follow standard operating procedures including but not limited to material handling, record keeping, packaging, and shipment preparation. Must follow all Good Manufacturing Practices (GMPs). * Notifies Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained . * Excellent attention to detail, good organization, and capable of working independently with minimal instruction from production supervisor. * Able to work in small groups and cross functional teams to troubleshoot issues, identify and implement collective corrective actions. * Maintain a clean work environment suitable for medical device manufacturing and cleanroom production. * Performs other duties as required Education and Experience: Minimum Requirements: * High School Diploma or GED Preferred Skills and Competencies: * Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment. * Must be proficient in English language to be able to read documentation, communicate, and write. * Ideal candidate will have keen eye for quality, is dependable, and will work collaboratively within a team, and possess a positive attitude. * Previous experience working in a clean room environment. * Previous experience with debugging and optimizing assembly processes. * Experience in a start-up production environment is a plus. * Manufacturing experience in a regulated industry is a plus. * Mechanical Aptitude - Knowledge of and experience with industrial machines and tools, including design, uses, repair, and maintenance. * Production & Processing - Knowledge of raw materials, measurement instruments, production processes, quality control, and other techniques for the manufacture and distribution of goods. * Mathematics - Knowledge of basic arithmetic. * Problem Solving - Recognizes problems and understands root cause analysis techniques/concepts. Physical Requirements (if applicable): * Required to stand for at least 75% of working time per shift, with walking at least 50% of working time per shift. * Required to reach above shoulder frequently and below waist occasionally. * Required to push and pull. * Ability to lift up to 20lbs occasionally, 5-20lbs frequently. NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite Additional Information: Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com. We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it! At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. (Know Your Rights)

The Associate Manufacturing Technician will be a critical contributor in a mission that truly represents a once-in-a-lifetime opportunity to join a company that is making significant investments in establishing US manufacturing, expanding internationally, and delivering a consistent cadence of product innovations to the market and investing in its people. This is a 12-hour weeknight shift. Working hours are 6:00 pm - 6:30 am, Monday - Thursday. The successful candidate will be responsible for operating and maintaining highly automated and advanced manufacturing equipment necessary to produce our signature product. This individual will be trained and cross-trained to both operate and repair issues across a variety of technologies including: heat staking, laser welding, mechanical swaging, printed circuit board (PCB) handling and testing, robotic automation, metal stamping and bending, form/fill/seal medical packaging, and high-speed discrete component assembly. In addition to equipment operation and maintenance, this individual will be responsible for the product quality performance of the equipment and basic machine troubleshooting in the event of faults and machine stops. This position requires mechanical aptitude, technical ability, machine troubleshooting and problem-solving skills, and the willingness to work in a fast-paced manufacturing environment. Responsibilities: • Perform equipment operation, basic repair, and minor daily/weekly preventative maintenance tasks to meet all standards for safety, quality and efficiency. These tasks must be completed under minimal supervision. • Maintain machine raw material feeds, perform any fault clearing and clear stoppages on automated equipment. • Utilize human machine interfaces (HMIs) to identify and correct shifts in process control. • Ensures adequate raw material is prepared correctly and jobs are run in a timely manner to ensure on-time delivery. • Executes equipment inspections and generates emergency, corrective, and/or preventative work orders as needed. • Troubleshoot and identify potential solutions for minor mechanical errors, safety issues or general operating inefficiencies within the production processes. • Able to utilize computer systems to support in the material inventory and quality management processes. • Participates in manufacturing processes to support new product design transfer, process development, equipment validations, and process validations. • Investigates and resolves process issues within their equipment cells. • Perform routine cleaning/inspection/lubrication of machinery. • Works from specifications, work orders, and general instructions from Production Supervisor/Team Lead. • Safely follow standard operating procedures including but not limited to material handling, record keeping, packaging, and shipment preparation. Must follow all Good Manufacturing Practices (GMPs). • Notifies Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained . • Excellent attention to detail, good organization, and capable of working independently with minimal instruction from production supervisor. • Able to work in small groups and cross functional teams to troubleshoot issues, identify and implement collective corrective actions. • Maintain a clean work environment suitable for medical device manufacturing and cleanroom production. • Performs other duties as required Education and Experience: Minimum Requirements: • High School Diploma or GED Preferred Skills and Competencies: • Self-starter capable of dealing with a variety of tasks in a fast paced, multi-tasking environment. • Must be proficient in English language to be able to read documentation, communicate, and write. • Ideal candidate will have keen eye for quality, is dependable, and will work collaboratively within a team, and possess a positive attitude. • Previous experience working in a clean room environment. • Previous experience with debugging and optimizing assembly processes. • Experience in a start-up production environment is a plus. • Manufacturing experience in a regulated industry is a plus. • Mechanical Aptitude - Knowledge of and experience with industrial machines and tools, including design, uses, repair, and maintenance. • Production & Processing - Knowledge of raw materials, measurement instruments, production processes, quality control, and other techniques for the manufacture and distribution of goods. • Mathematics - Knowledge of basic arithmetic. • Problem Solving - Recognizes problems and understands root cause analysis techniques/concepts. Physical Requirements (if applicable): • Required to stand for at least 75% of working time per shift, with walking at least 50% of working time per shift. • Required to reach above shoulder frequently and below waist occasionally. • Required to push and pull. • Ability to lift up to 20lbs occasionally, 5-20lbs frequently. NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite Additional Information: Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet's flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com. We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it! At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. (Know Your Rights)