Process Technician jobs at New England Life Care - 253 jobs

Sign-on Bonus Available. Responsibilities: RESPONSIBLE FOR: Performs diagnostic and interventional procedures to include but not limited to: angiography, venography, myelography, nephro-ureteral, and gastrointestinal studies, and modality assisted drainage and biopsies. Completes all post processing functions. Performs related record keeping and patient care functions. Ensures the utilization of established protocols and techniques differentiating for adolescent, adult and geriatric patient population in the performance of diagnostic procedures and functions. Qualifications: MINIMUM EDUCATION REQUIRED: Graduate of an AMA approved Radiologic Technology program or JRCERT accredited hospital-based training program. MINIMUM EXPERIENCE REQUIRED: 1-year of experience. MINIMUM LICENSURE/CERTIFICATION REQUIRED BY LAW: Registered by the American Registry of Radiological Technologists (R) plus Advance Certification by ARRT in Vascular-Interventional Radiographer (VI) or Cardiac-Interventional Radiographer (CI). ADDITIONAL QUALIFICATIONS: BLS Certified Business Unit : Company Name: Piedmont Augusta Hospital

Sign-On Bonus Available. Day shift, 3 twelve-hour shifts Sat, Sun, Mon. No call. Responsibilities: RESPONSIBLE FOR: Operates radiologic equipment to make clinical diagnostic radiographs and performs routine diagnostic procedures according to established standards and practices. Provide patient services using imaging modalities. Provides patient care to all age groups to include neonatal, pediatrics, adult, and geriatrics. Qualifications: MINIMUM EDUCATION REQUIRED: Graduate of an AMA approved Radiologic Technology program or JRCERT accredited hospital-based training program. MINIMUM EXPERIENCE REQUIRED: None MINIMUM LICENSURE/CERTIFICATION REQUIRED BY LAW: Registered by the American Registry of Radiologic Technologists (R). ADDITIONAL QUALIFICATIONS: BLS certified. Business Unit : Company Name: Piedmont Augusta Hospital

The Specimen Processing Technician II processes, distributes, and provides quality assurance for all patient specimens. Supplies accurate information to providers and other clinical staff regarding laboratory testing, test requirements and patient results. The Specimen Processing Technician II participates in training new team members. This position's work location is 100% on-site, part-time on campus at the Chestnut Hill location. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. + Performs pre-analytical specimen processing: Receives patient specimens from within the institute and outside institutions. + Becomes familiar with patient and specimen requirements; stores and transports specimens according to procedures; ensure specimen integrity is preserved at all times. + Unloads and loads the pneumatic tube system and accurately distributes specimens; does routine and stat specimen delivery runs to BWH laboratories; does specimen pickup runs from clinic locations at DFCI + Receives specimens into the Laboratory Information System (LIS) by scanning barcodes or manual entry + Verifies upon receipt that all samples are labeled according to policy and addresses variances according to policies. + Documents in the LIS any specimen or test cancellations per policy; contacts the appropriate provider or reference laboratories with questions regarding discrepancies with test orders or specimen containers. + Processes add on tests according to policy. + Processes tests sent out to reference laboratories; communicates with reference labs as needed + Processes specimens by loading the pre-analytic automation system or via centrifugation, aliquoting, storing, and shipping per test requirements. + Performs various quality checks to ensure all requests are accurate before dispensing the specimens to the appropriate performing lab. + Responds to telephone inquiries to assist providers, nurses and other caregivers with lab test, test requirement and result inquiries. + Performs all duties with accuracy and efficiency to ensure patient care is not compromised. + Utilizes electronic system for faxed tests results from reference laboratories. + Accurately enters reference lab results as needed including transplant test results from Rhode Island Blood Center. + Reviews pending lists as required; addresses and corrects discrepancies or pending test results by contacting the reference lab and the provider as necessary. + Participates in training new team members. + Processes bone marrows orders and specimens. + Processes specimens in the Central Pathology Processing area of the department + Performs other duties as assigned. **Minimum Qualifications** + High School diploma required, AS or BS in a physical science preferred. + 1 year of experience in a healthcare or laboratory setting required. **Knowledge, Skills and Abilities Required:** + Fundamental knowledge to accurately and efficiently ensure all test requests are in the LIS. Understands lab safety policy and procedures and Department of Transportation specimen shipping regulations. + Basic knowledge of specimen processing for all specimen types. + Strong communication and interpersonal skills, including phone etiquette; customer service skills + Basic proficiency in computer skills - able to perform essential tasks such as using a keyboard and mouse, navigating the operating system, managing files and folders, and using basic software applications like word processors and web browsers. + Ability to work well in a heavily team-oriented environment. + Ability to work efficiently and effectively in a fast-paced environment. + Capacity to remain flexible and multitask is key. At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply. Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law. **EEO Poster** . Pay Transparency Statement The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications. For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA). $43,700.00 - $48,200.00

The Specimen Processing Technician II processes, distributes, and provides quality assurance for all patient specimens. Supplies accurate information to providers and other clinical staff regarding laboratory testing, test requirements and patient results. The Specimen Processing Technician II participates in training new team members. Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals. * Performs pre-analytical specimen processing: Receives patient specimens from within the institute and outside institutions. * Becomes familiar with patient and specimen requirements; stores and transports specimens according to procedures; ensure specimen integrity is preserved at all times. * Unloads and loads the pneumatic tube system and accurately distributes specimens; does routine and stat specimen delivery runs to BWH laboratories; does specimen pickup runs from clinic locations at DFCI * Receives specimens into the Laboratory Information System (LIS) by scanning barcodes or manual entry * Verifies upon receipt that all samples are labeled according to policy and addresses variances according to policies. * Documents in the LIS any specimen or test cancellations per policy; contacts the appropriate provider or reference laboratories with questions regarding discrepancies with test orders or specimen containers. * Processes add on tests according to policy. * Processes tests sent out to reference laboratories; communicates with reference labs as needed * Processes specimens by loading the pre-analytic automation system or via centrifugation, aliquoting, storing, and shipping per test requirements. * Performs various quality checks to ensure all requests are accurate before dispensing the specimens to the appropriate performing lab. * Responds to telephone inquiries to assist providers, nurses and other caregivers with lab test, test requirement and result inquiries. * Performs all duties with accuracy and efficiency to ensure patient care is not compromised. * Utilizes electronic system for faxed tests results from reference laboratories. * Accurately enters reference lab results as needed including transplant test results from Rhode Island Blood Center. * Reviews pending lists as required; addresses and corrects discrepancies or pending test results by contacting the reference lab and the provider as necessary. * Participates in training new team members. * Processes bone marrows orders and specimens. * Processes specimens in the Central Pathology Processing area of the department * Performs other duties as assigned. Minimum Qualifications * High School diploma required, AS or BS in a physical science preferred. * 1 year of experience in a healthcare or laboratory setting required. Knowledge, Skills and Abilities Required: * Fundamental knowledge to accurately and efficiently ensure all test requests are in the LIS. Understands lab safety policy and procedures and Department of Transportation specimen shipping regulations. * Basic knowledge of specimen processing for all specimen types. * Strong communication and interpersonal skills, including phone etiquette; customer service skills * Basic proficiency in computer skills - able to perform essential tasks such as using a keyboard and mouse, navigating the operating system, managing files and folders, and using basic software applications like word processors and web browsers. * Ability to work well in a heavily team-oriented environment. * Ability to work efficiently and effectively in a fast-paced environment. * Capacity to remain flexible and multitask is key. At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply. Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law. EEO Poster . Pay Transparency Statement The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate's relevant experience, skills and qualifications. For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA). $43,700.00 - $48,200.00

At UC Health, we're proud to have the best and brightest teams and clinicians collaborating toward our common purpose: to advance healing and reduce suffering. As the region's adult academic health system, we strive for innovation and provide world-class care for not only our community, but patients from all over the world. Join our team and you'll be able to develop your skills, grow your career, build relationships with your peers and patients, and help us be a source of hope for our friends and neighbors. UC Health is an EEO employer. Performs all activities associated with decontamination, clean prep, tray assembly, sterilization, distribution and acquiring of instruments and supplies for the OR and L/D Departments Minimum Required: Graduate of CRCST program or graduate of Surgical Technology program. | CRCST required along with annual maintenance for non-Surgical Technology graduates. | 1 year sterile processing experience preferred. Perform all level I tech duties and responsibilities Train and precept new staff Responsible for oversight of processing department equipment Identify specialty instruments and supplies Complete all paperwork associated with sterilization processes for patient safety and accreditation purposes Attention to detail in performing job duties and responsibilities Maintain and recognize sterility of supplies and trays Deliver and interpret requested supplies/items Must be able to prioritize and respond appropriately to a variety of situations Able to perform and organize high volume cases

At UC Health, we're proud to have the best and brightest teams and clinicians collaborating toward our common purpose: to advance healing and reduce suffering. As the region's adult academic health system, we strive for innovation and provide world-class care for not only our community, but patients from all over the world. Join our team and you'll be able to develop your skills, grow your career, build relationships with your peers and patients, and help us be a source of hope for our friends and neighbors. UC Health is an EEO employer. Performs all activities associated with decontamination, clean prep, tray assembly, sterilization, distribution and acquiring of instruments and supplies for the OR and L/D Departments Minimum Required: Graduate of CRCST program or graduate of Surgical Technology program. | CRCST required along with annual maintenance for non-Surgical Technology graduates. | 1 year sterile processing experience preferred. Perform all level I tech duties and responsibilities Train and precept new staff Responsible for oversight of processing department equipment Identify specialty instruments and supplies Complete all paperwork associated with sterilization processes for patient safety and accreditation purposes Attention to detail in performing job duties and responsibilities Maintain and recognize sterility of supplies and trays Deliver and interpret requested supplies/items Must be able to prioritize and respond appropriately to a variety of situations Able to perform and organize high volume cases

Department: Sterile Processing Hours: Full-Time, 40 Hours/Week Shift: Second, 3p-1130p Instrument Processing Technician, Full Time, Second Shift UC Health is hiring an Instrument Processing Technician to join our Sterile Processing Department on second shift. The Instrument Processing Technician provides cleaning, decontamination, assembly processing and sterilization of instruments, trays and endoscopes. Also assembles case carts with needed surgical supplies. Minimum Required: High School diploma or GED required; Associate's degree preferred. Upon 1 year of hire, obtain certification: CRST. Maintain a current registration as a CRST. 1 year minimum SPD experience; prefer 3 years SPD experience. Join our team to BE UC Health. Be Extraordinary. Be Supported. Be Hope. Apply Today! About UC Health UC Health is an integrated academic health system serving Greater Cincinnati and Northern Kentucky. In partnership with the University of Cincinnati, UC Health combines clinical expertise and compassion with research and teaching-a combination that provides patients with options for even the most complex situations. Members of UC Health include: UC Medical Center, West Chester Hospital, University of Cincinnati Physicians and UC Health Ambulatory Services (with more than 900 board-certified clinicians and surgeons), Lindner Center of HOPE and several specialized institutes including: UC Gardner Neuroscience Institute and the University of Cincinnati Cancer Center. Many UC Health locations have received national recognition for outstanding quality and patient satisfaction. Learn more at uchealth.com. At UC Health, we're proud to have the best and brightest teams and clinicians collaborating toward our common purpose: to advance healing and reduce suffering. As the region's adult academic health system, we strive for innovation and provide world-class care for not only our community, but patients from all over the world. Join our team and you'll be able to develop your skills, grow your career, build relationships with your peers and patients, and help us be a source of hope for our friends and neighbors. UC Health is an EEO employer. Performs decontamination functions: Disassembles, cleans and disinfects instruments and equipment used for patient care utilizing correct manual and mechanical processes. Operates equipment used in decontamination process, i.e. sonic washer, cart washers, washer sterilizers, and decontaminators. Unloads case carts containing soiled instruments and places in designated area. Performs cleaning tasks in work area as assigned. Used universal precautions when working in decontamination area, i.e. gloves, face shield, protective gown Utilizes computer system to track instruments and case cart. Assembles instrument trays and packs: Unloads instruments from washer sterilizers and distributes to appropriate workstations. Assembles instrument trays and packs utilizing written instructions and proper protocol. Applies sterilization wrappers properly to maintain integrity of the contents. Utilizes heat sealer on packs as needed. Each item is identified correctly on the outside packaging of each item. Transports trays to sterilization area. Consistent use of the barcode technology to track productivity. Use of computerized instrument tracking system to validate tray production against online list/error proofing systems to ensure accuracy of assembly. Operates sterilizers, documents loads, and returns stock to appropriate area: Loads trays, packs, and basins onto sterilizer loading rack, utilizing correct procedures. Able to operate each type of sterilizer (e.g. Steam, Plasma, Steris) per manufacture's instructions and departmental guidelines and polices. Accurately documents all sterilization information. Biological monitoring is completed per departmental policy. Sterile supplies are handled properly and restocked in sterile storage area. Rotates sterile supplies and inventories for expiration dates as required. Maintain assigned work area and equipment in a clean and organized condition to maintain required safety standards for handling sterilized and clean materials and to maintain a safe work environment. Assembles case carts per departmental procedures: Produce pick sheets from computer. Able to pull instruments and sterile supplies per pick sheet accurately and completely. Other duties as assigned: Active participant in QA activities. Assists with training of other associates. Attends departmental in-services and mandatory meetings. Acts as a liaison between Sterile Processing and all customers and communicates in a courteous manner. Makes effective use of time and is able to distinguish between low and high priority activities. Delivers equipment and supplies to various departments as needed. Able to fulfill on-call requirements.

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

This hands-on role leads complex troubleshooting, system integration, and automation projects while mentoring other technicians, ensuring compliance, and partnering with Engineering, Quality, and IT to enhance efficiency and product performance. Key Responsibilities Drive process automation and MES workflow optimization. Configure and troubleshoot MES and reporting tools. Lead cross-functional projects with Engineering, Quality, and IT. Ensure compliance with ISO/FDA and internal standards. Train and mentor Technicians I-III. Lead testing, troubleshooting, and equipment repair activities. Support design changes and provide technical assistance to operations. Qualifications Associate's or Bachelor's in a technical field preferred. 6-8+ years progressive technician experience. Expert MES configuration and electromechanical troubleshooting skills. Fixture/jig design experience; project leadership a plus. Familiarity with ISO or FDA environments preferred. Must be legally authorized to work in the U.S. without sponsorship. What We Offer: We appreciate that our employees work diligently to contribute to our success as an organization. We also recognize the importance of work-life balance and therefore developed a competitive total rewards package including programs that offer employees flexibility to balance their work and life including: 9/80 work schedule - enjoy every other Friday off! Comprehensive benefits including medical, dental, vision, life insurance and disability plans. HRA (for PPO plan participants) / HSA (Health Savings Account for high deductible plan participants) contribution 401K with company match and immediate vesting Continuous Education Assistance Supportive culture that values innovation, collaboration, and excellence On-site Fitness Center & Café

Salary Range:$55,000.00 To $65,000.00 Annually The Aseptic Manufacturing Technician II has primary responsible for the activities and procedures required for the manufacture and filling of Aseptic products. 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 aseptic fills (transfer, set-up, sanitization, autoclaving, process simulation, etc.,) * 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 Aseptic 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. 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.

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 Role The Production Technician is responsible for manicuring and packaging plant material and infused products. In this role, maintaining accuracy in weighing product, fulfilling product, labelling, and inventory is paramount. The Production Technician is also responsible for maintaining a perpetually clean workspace to provide a sterile environment for production of medical products. This person will also have some responsibility for tracking product electronically on the company MRP system to ensure compliance with state laws and program regulations. The ideal candidate has a relentlessly positive attitude, a strong work ethic, competitive and team-oriented spirit, and great attention to detail. Responsibilities Breakdown cured batches and extracted oil from the lab into multiple different weight increments (3.5 g, 7 g, ½ g and 1 g etc.) and package them accordingly Keep a precise count of all packaged product and weight(s) of product used for an accurate end of day reconciliation of packaged inventory and remaining inventory Package infused and plant material into proper containers with proper labeling to ensure compliance with state regulations Electronically convert packaged products in the state traceability system Exhibit competency in basic organizational skills, communication skills and windows based operating software Manage time efficiently in order to meet goals while consistently producing quality product Sanitation & cleanup of all processing areas throughout the day Other duties as assigned Qualifications High School Education or GED required 1+ years working in production environment required Experience processing medical cannabis or other botanicals highly desirable Must work well in a group and independently; demonstrate self-motivation and initiative Must be able to adapt quickly to changes in policy, procedure and technique Employee must exhibit personal hygiene and follow the health guidelines set forth by Green Thumb and the state while processing patient medicine Ability to listen well and communicate effectively with various audiences, especially with the direct supervisors and co-workers Ability to perform a monotonous task with great efficiency over 8-hour work periods without losing quality Employee must be able to follow basic instructions as well as be able to take constructive criticism from their managers so they can help maintain quality standards and production goals Must understand and comply with the rules, regulations, policies, and procedures of Green Thumb Must have a solid understanding of the Cannabis laws, rules and regulations and passion to further their understanding and knowledge of the industry and the laws. Additional Requirements Must pass any and all required background checks Must be and remain compliant with all legal or company regulations for working in the industry Must possess valid driver's license or state ID card Must be a minimum of 21 years of age Must be approved by state badging agency to work in cannabis industry Working Conditions While performing the duties of this job, the employee is regularly required to perform reaching, grasping, bending, stooping, talking, hearing, seeing and repetitive motions Must be able to sit and/or stand for extended periods of time while maintaining focus PHYSICAL DEMANDS: Must be able to lift, carry and balance up to 50 pounds (100 pounds with assistance) AND must be able to do so with extreme care and caution when working with plants and product The pay range is competitive and based on experience, qualifications, and/or location of the role. Positions may be eligible for a discretionary annual incentive program driven by organization and individual performance. Green Thumb Pay Range$18.50-$19 USD

The Operations Quality 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 ensuring our manufacturing site produces and distributes products which meet or exceed all established quality standards and will be responsible for ensuring our processes and procedures are compliant with corporate policies and federal law. The individual will be trained in performing Incoming, In-process inspections in the cleanroom, or assessing the final product's efficacy prior to market release. In addition to those activities, this position may also be required to support production operations, metrology, microbiology, or other manufacturing functions as business needs arise. This position requires a strong attention to detail, problem solving skills, and willingness to work in a fast-paced manufacturing environment. Responsibilities: • Inspect and record results of work on Incoming raw material, In-process, or Lot Qualification at various stages of the production process, distribution process to determine and maintain the quality and reliability of our product. • Assess and complete inspection reports and records including the entry of data into various electronic systems. (For example - Word, Excel, SAP, Electronic DHR systems, Oracle Agile, and others). • Generate, review, and maintain quality records in support of the Quality System. (For example - device history records and training records) • Ensure the equipment calibration status is within the timeframe of use. • Assist the Quality Manager in notified body and regulatory authority audits and inspections. • Works from specifications, work plans, procedures, and general instructions from either Quality Engineers, Quality Supervisor, or the Quality Manager. • Required to maintain and enforce cGMPs. • Safely follow standard operating procedures including but not limited to quality standards, material handling, and record keeping. Must follow all Good Manufacturing Practices (GMPs), Good Documentation Practices (GDPs), and Good Laboratory Practices (GLPs). • Notifies Quality or Operations Leadership of any discrepancies to ensure quality standards and safety of operations are maintained at all times. • 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 Required Core Competencies: • Excels at the organization and maintenance records accurately. • 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. • Mathematics - Basic mathematics skills (adding, subtracting, multiplying, dividing) • Autonomy - Capable of working independently with minimal instruction from their supervisor. • Familiarity with measurement instrumentation such as micrometers, calipers, tensile testers, video microscopes, and optical gauging products preferred, not required. • Experience working in a lab setting environment in the medical device industry preferred, but not required. • The ability to use stereoscopes and varying microscope setups preferred, but not required. Physical Requirements: • 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 50lbs occasionally, 5-20lbs frequently. • Vision capability to inspect small parts/components/labeling (Corrective lenses allowed) *Would like to add a test component to ensure that candidates can successfully utilize the microscopes from a vision perspective. NOTE: This position requires on-site working (requires on-site office/plant/lab work). #LI-Onsite Additional Information: Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $19.00 - $28.00 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: • Medical, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) • And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education. 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 Plant Operations Technician position is responsible to perform work as assigned by the Facilities Supervisor and/or Director to maintain the hospital's property and equipment in safe, efficient, operating condition, and assist others, as needed. This includes basic installation, cleaning, repairing, removal, and disposal of equipment, and property. Performs other duties as assigned on an “as needed” basis, including snow removal, as applicable. Essential Duties and Responsibilities Supports and promotes the mission and values of Covenant Health Ministry. Ensures Plant provides heat and A/C to maintain appropriate temperatures, and humidity levels throughout the hospital Maintains logs, completes scheduled tours Follows Environment of Care and Life Safety Standards as identified in DNV plans for working in the Physical Environment Other duties as consistent with this role. Job Requirements Job Knowledge and Skills Computer skills required. Knowledge of hand tools, and power tools, used to assist/complete carpentry, mechanical, electrical, and plumbing required, both within the Powerhouse and the hospital as possible Education and Experience Valid Driver's License required. High School Diploma and/or equivalent educational knowledge preferred. Relevant Technical School, Certifications, and Health Care experience preferred. An equivalent combination of education and experience which provides proficiency in the areas of responsibility listed above may be substituted for the above education and experience requirements. Working Conditions/Physical Demands Must possess the physical and mental abilities to perform the tasks normally associated with this position that involves a combination of sitting, standing, walking, bending, stooping, and reaching. Occasional lifting/carrying up to 25 lbs. Some stress related to high level of responsibility for quality care. Americans with Disabilities Statement Must be able to perform all essential functions of this position with reasonable accommodation if disabled. The above statements are intended to describe the general nature and level of work being performed. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of personnel so classified. Covenant Health reserves the right to modify position duties at any time, to reflect process improvements and business necessity. Standard of Business Conduct Every St Joseph Hospital employee is required to abide by the Standards of Conduct and to report any activity that appears to violate the Standards of Conduct. Covenant Health Mission Statement We are a Catholic health ministry, providing healing and care for the whole person, in service to all in our communities. Our Core Values: •Compassion We show respect, caring and sensitivity towards all, honoring the dignity of each person, especially the poor, vulnerable and suffering. •Integrity We promote justice and ethical behavior, and responsibly steward our human, financial and environmental resources. •Collaboration We work in partnership, dialogue and shared purpose to create healthy communities. •Excellence We deliver all services with the highest level of quality, while seeking creative innovation. Applicants, employees and former employees are protected from employment discrimination based on race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age (40 or older), disability, and genetic information (including family medical history). Comp Range: $21.55 - $29.68 Rate of pay displayed reflects the beginning of the pay scale. At the time of an offer, determination of your offer will reflect your skills and experience as it relates to the position. Our people make the difference. See firsthand what makes our employees and culture shine!

To provide safe and effective care and technical assistance to patients in the Emergency Department under the direction of a Registered Nurse or Physician, consistent with the Hospital's mission statement, policies and procedures and based on standards of patient care. Scope of patient care services provided encompasses age groups ranging from pediatric patients to adults including geriatric and psychiatric patients. Accountabilities include: assisting patients in moving as rapidly, uneventfully, safely and effectively as possible through the Emergency Department.