Quality Control Analyst jobs at Iovance Biotherapeutics

Branch Medical Group, a subsidiary of Globus Medical Inc., manufactures a wide range of implants for spinal and orthopedic applications as well as design the instrumentation cases that house them. Our passion, combined with Globus' world-class engineering, transforms clinical insights into tangible musculoskeletal solutions. We are constantly in pursuit of better patient care and understand that speed is critical because life cannot wait. Position Summary: The Quality Control Inspector is responsible for performing inspections at various stages of production of the product from raw material. This effort includes, but is not limited to, providing QA support, where needed, but not limited to QA Operations. This individual works with other quality control inspectors and engineers to ensure products or assignments align with the companies. Essential Functions: * Carries out inspection activities to ensure the quality of products and raw materials used in the production of products to meet customer or internal standards * Responsible for the correct handling of the corresponding fixtures and equipment * Correct use of quality inspection records following GMP requirements * Ensures the consistency and quality of records by editing and proofreading all documentation prior to handling it to the documentation center for storage * Maintains and archives documents in an organized and retrievable state (manual or electronic) for compliance to procedures, regulations and standards * Safekeeping all quality records of In-Process Inspection * Schedules periodic document reviews to ensure documents are compliant with Globus requirements and processes as well as external regulations * Communicates corrections and improvement opportunities * Ensures timely release of subassemblies and assemblies by executing, reviewing and approving Device History Records (DHRs) and ERP transactions per internal requirements * Responsible for the control of nonconforming material (identification, segregation) * Interfaces with cross functional team to ensure internal and external compliance requirements are followed and implemented per requirements * Labels and segregates components and assemblies * Notifies cross functional departments including Production, Quality and Purchasing on component/assembly dispositions and/or material holds * Manages component/assembly disposition and queries using the QAD system * Supports with External Audits activities when required and as directed * Responsible for the release of subassemblies, assemblies and final assemblies * Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies * Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role * Represents the company in a professional manner and uphold the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions. Qualifications: * Quality Inspector or advanced studies in relevant technical discipline required * No fewer than three (3) years of directly related experience, having experience in a class II or III medical device environment quality inspection is preferred, complaints lab inspection or receiving inspection is also preferred, inspection small components using a microscope is preferred * Experience in the medical device industry and with knowledge performing their function within the Food & Drug Administration (FDA), Quality System Regulations (QSRs), International Organization of Standardization (ISO 13485) is preferred * Experience with QAD preferred * Prior experience working with US companies is a plus * IPC-A-610 certification or knowledge in medical device component welding through resistance welding, spot welding or laser welding is a plus * Handling of electrical components is a plus * Experience with ESD processes is a plus * Ability to read and interpret documents such as job travelers, plans, sketches, diagrams and other procedural materials and documents * Fundamental geometry, fractions, percents, relationships and measurements * Ability to work independently with little supervision, as well as in "team" work * Effective interpersonal skills and dexterity on the job with a culturally diverse employee population * Knowledge of measurement instruments, sample plans is a plus * Experience with inspecting small parts under magnification is a plus * Work environment and physical requirements: * Production area / clean room * Some exposure to noisy equipment * Strong organizational and follow-up skills * Excellent verbal and written communication skills * Attention to detail * Self-starter * Advanced critical thinking and problems-solving skills * Proficiency in using Microsoft Office products Physical Demands: The physical demands listed here are representative of those that must be met by and employee to successfully perform the essential functions of this job. * Required to sit; climb or balance; and stoop, kneel, crouch or crawl * Required to regularly lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds * Required to possess specific visons abilities, including: close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus. Our Values: Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven. * Passionate about Innovation: Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate ab our role in improving the lives of patients by continuously developing better solutions. * Customer Focused: We listen to our customers' needs and respond with a sense of urgency. * Teamwork: Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger. * Driven: We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients. Equal Employment Opportunity: Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees' talents and support an environment that is inclusive and respectful. Other Duties: Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Cook MyoSite, Inc., part of the Cook Group, Inc. family of companies, is on a mission to make regenerative medicine a part of everyday medicine. We're investigating our core technology, autologous muscle-derived cells, for the potential treatment of several muscle-related disorders. We at Cook MyoSite have the potential to make a difference in the lives of countless people around the world, and we also have the potential to make a difference in yours. Joining our team is an opportunity to ignite your passion, grow your potential, and define your purpose. If you're curious, motivated by helping others, and driven by integrity, we invite you to apply. The Quality Control Associate I at Cook MyoSite will aid in the development and maintenance of methods for sampling, testing, evaluating, and approving testing results for products and materials. Responsibilities * Performs quality control sampling and testing of materials and products for identity, strength, quality and purity utilizing assays for, but not limited to, DNA isolation, mycoplasma, endotoxin, myogenic differention, and desmin • Performs lot testing • Assists in the investigation of nonconformance activities with additional testing and evaluation activities as needed • Writes quality plans and reports to QC-related activities • Performs QC projects for validation and evaluation of methods • Recommends and establishes different methods for performing QC tasks • General maintenance of side labs • Aids in activities related to monthly inventories and removal of expired products • Cell culturing for lot testing and research • Supports in maintaining cleanroom environment below alert limits by participating in and following established cleaning practices * Exemplifies Cook MyoSite Core Values • Maintain regular and punctual attendance • Must maintain company quality and safety standards • This position requires an ongoing commitment to upgrading knowledge, job skills and abilities in addition to competency related to all duties and responsibilities listed above. • Ability to work in collaborative and independent work situations and environments with minimal supervision • Maintain composure and competence under stressful situations; demonstrate flexibility and adaptability • Must work and interact effectively and professionally with and for others throughout various levels of the global organization to achieve company goals • Trainability • Must have effective verbal, written and interpersonal skills • Excellent analytical skills with the ability to analyze situations accurately and effectively • Must demonstrate critical thinking and proven problem-solving skills • Must exhibit well developed skills in prioritizing, planning, organization, decision making, and time management • Able to analyze situations or data Qualifications Undergraduate degree any Life Sciences, Engineering field, Microbiology, or Molecular Biology or 6 years direct, relevant experience in analytical testing laboratory to provide a comparable background Minimum of 1-3 years' experience in laboratory testing environment Basic understanding of cGMP, 21 CFR Part 11, and related regulations associated with Bio/Pharmaceutical product manufacturing Ability to learn and support new systems and applications, and the ability to provide technical training to end users. Proficient knowledge of Microsoft Office software, and other general office equipment. Full Time On Site Physical Requirements: * Ability to conduct and hear ordinary conversation and telephone communication.• Must be able to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended work hours and/or extra work hours, sometimes on short notice as required.• Ability to work under specific time constraints.• Must be able to sit at desk, in meetings and/or work on a computer for long or extended periods of time.• Visual and manual acuity for working with computers and equipment.• Ability to spend majority of day standing in laboratory setting or sitting at/working in a biological safety hood with potential (limited) exposure to hazardous chemicals and/or harsh disinfectants while in BioSafety Level II or other labs.• Physically capable of standing, walking, stooping, kneeling, crouching, climbing steps and ladders, reaching, twisting and bending on occasion with or without reasonable accommodations.• Must be able to lift/push/pull up to 50 pounds on an occasional basis with or without reasonable accommodations.• Must be capable of performing PPE gowning procedures on a frequent basis to enter BioSafety Level II including but not limited to safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and shirt), appropriate shoes, and facial mask (if required) on a regular basis. Employee that does not interact with Healthcare ProfessionalsCompliance with all policies of the company including without limitation the Cook Employee Manual, Cook Code of Conduct, Quality System Manual, Cook Electronic Information Policy and HIPAA regulations. At Cook MyoSite, we don't just accept difference - we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. Cook MyoSite is proud to be an equal opportunity workplace.This job description features the essential and critical functions of the position described and is not an exhaustive list of tasks and/or responsibilities. This may be subject to change at any time due to reasonable accommodation or other reasons.

Leidos is seeking and exceptional and motivated Research Chemist interested in pursuing their passion by working side-by-side with world experts through a research appointment at the U.S. Department of Energy's (DOE) National Energy Technology Laboratory (NETL). In this role, you will work as part of DOE's leading engineering Research & Development laboratory team supporting NETL to pursue cutting-edge research on carbon nanomaterials for electronic devices. Specifically, you will work with NETL's carbon materials manufacturing team to develop novel methods to synthesize and functionalize graphene quantum dots and fabricate atomically thin quasi-2D amorphous carbon films for electronic memory devices such as transistors and memristors. In this role, you will engage with world-class carbon materials synthesis researchers and electronic memory device engineers, including leading DOE scientists and external partners to develop world-changing memory technologies that address internet of things and big data era challenges. What this opportunity with Leidos supporting NETL uniquely provides you: + Working on applied, cutting-edge projects with global impact while being mentored by the nation's leading energy scientists and engineers. + Real-world experience supplemented with technical development and discussions that provide unique insight into the broad range of mission critical engineering and scientific disciplines NETL leverages to support national energy research and policy development. + Unique access to world-class, customized facilities specific to high impact energy research, technology generation, and patent development. + Participation in novel fundamental and applied energy technology development with direct economic impact on global carbon management and resource use. Primary Responsibilities: + Synthesize graphene, graphene oxide, graphene quantum dots, and carbon quantum dots with tunable sizes/thicknesses using different domestic carbon feedstocks primarily by wet chemistry methods (including some air-free techniques such as the use of a glove box). + Develop various chemical synthesis strategies/methodologies to functionalize graphene, graphene oxide, graphene quantum dots, and carbon quantum dots to tune physical and/or chemical properties, especially post-synthesis surface modification to achieve tunable dispersibility in organic solvent(s) and consistent thin film fabrication. + Synthesize and characterize carbon thin films made from graphene, graphene oxide, graphene quantum dots, and carbon quantum dots using techniques such as spin-coating, Langmuir-Blodgett, and/or self-assembly methods. + Characterize the chemical, structural, optical, and electronic properties of synthesized carbon materials and thin films using techniques including electron microscopy, atomic force microscopy, FTIR, Raman, UV-Vis spectroscopy, DLS, XPS, and XRD. + Participate and present results in regular team meetings, contribute to progress reports and research proposals, and lead and support scientific manuscript development for publication in peer reviewed journals. Required Qualifications: + Master's degree with 3+ years experience in Chemistry or a relevant discipline (Chemical Engineering, Material Science, or a related engineering discipline). + Considerable knowledge of and experimental expertise in conducting synthesis and functionalization of carbon nanomaterials such as graphenes, graphene oxides, graphene quantum dots, carbon quantum dots for electronic or other applications as demonstrated through publication record. + Experience with common carbon materials characterization techniques such as AFM, SEM, XPS, Raman, FTIR, UV-Vis and photoluminescence spectroscopy, and XRD. + Demonstrated ability to publish high impact research. + Demonstrated ability to work as part of a team to solve problems of scientific and technological interest. + Must be able to meet the requirements for gaining access to work on the NETL campus. Preferred Qualifications: + Ph.D. in Chemistry or a relevant discipline (Chemical Engineering, Material Science, or a related engineering discipline). + Experience with or knowledge of thin film fabrications such as chemical vapor deposition, physical vapor deposition, spin coating, spray coating and Langmuir-Blodgett. + Experience with or knowledge of nano/microfabrication processes. + Experience with or knowledge of two-dimensional nanostructured metal-oxide semiconductors. + Experience with or knowledge of electronic memory devices such as transistors or memristors. If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo - because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 - and moving faster than anyone else dares. **Original Posting:** December 5, 2025 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. **Pay Range:** Pay Range $87,100.00 - $157,450.00 The Leidos pay range for this job level is a general guideline onlyand not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law. **About Leidos** Leidos is an industry and technology leader serving government and commercial customers with smarter, more efficient digital and mission innovations. Headquartered in Reston, Virginia, with 47,000 global employees, Leidos reported annual revenues of approximately $16.7 billion for the fiscal year ended January 3, 2025. For more information, visit ************** . **Pay and Benefits** Pay and benefits are fundamental to any career decision. That's why we craft compensation packages that reflect the importance of the work we do for our customers. Employment benefits include competitive compensation, Health and Wellness programs, Income Protection, Paid Leave and Retirement. More details are available at **************/careers/pay-benefits . **Securing Your Data** Beware of fake employment opportunities using Leidos' name. Leidos will never ask you to provide payment-related information during any part of the employment application process (i.e., ask you for money), nor will Leidos ever advance money as part of the hiring process (i.e., send you a check or money order before doing any work). Further, Leidos will only communicate with you through emails that are generated by the Leidos.com automated system - never from free commercial services (e.g., Gmail, Yahoo, Hotmail) or via WhatsApp, Telegram, etc. If you received an email purporting to be from Leidos that asks for payment-related information or any other personal information (e.g., about you or your previous employer), and you are concerned about its legitimacy, please make us aware immediately by emailing us at ***************************** . If you believe you are the victim of a scam, contact your local law enforcement and report the incident to the U.S. Federal Trade Commission (******************************* . **Commitment to Non-Discrimination** All qualified applicants will receive consideration for employment without regard to sex, race, ethnicity, age, national origin, citizenship, religion, physical or mental disability, medical condition, genetic information, pregnancy, family structure, marital status, ancestry, domestic partner status, sexual orientation, gender identity or expression, veteran or military status, or any other basis prohibited by law. Leidos will also consider for employment qualified applicants with criminal histories consistent with relevant laws. REQNUMBER: R-00171673 All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. Leidos will consider qualified applicants with criminal histories for employment in accordance with relevant Laws. Leidos is an equal opportunity employer/disability/vet.

Leidos is seeking and exceptional and motivated Research Chemist interested in pursuing their passion by working side-by-side with world experts through a research appointment at the U.S. Department of Energy's (DOE) National Energy Technology Laboratory (NETL). In this role, you will work as part of DOE's leading engineering Research & Development laboratory team supporting NETL to pursue cutting-edge research on carbon nanomaterials for electronic devices. Specifically, you will work with NETL's carbon materials manufacturing team to develop novel methods to synthesize and functionalize graphene quantum dots and fabricate atomically thin quasi-2D amorphous carbon films for electronic memory devices such as transistors and memristors. In this role, you will engage with world-class carbon materials synthesis researchers and electronic memory device engineers, including leading DOE scientists and external partners to develop world-changing memory technologies that address internet of things and big data era challenges. What this opportunity with Leidos supporting NETL uniquely provides you: Working on applied, cutting-edge projects with global impact while being mentored by the nation's leading energy scientists and engineers. Real-world experience supplemented with technical development and discussions that provide unique insight into the broad range of mission critical engineering and scientific disciplines NETL leverages to support national energy research and policy development. Unique access to world-class, customized facilities specific to high impact energy research, technology generation, and patent development. Participation in novel fundamental and applied energy technology development with direct economic impact on global carbon management and resource use. Primary Responsibilities: Synthesize graphene, graphene oxide, graphene quantum dots, and carbon quantum dots with tunable sizes/thicknesses using different domestic carbon feedstocks primarily by wet chemistry methods (including some air-free techniques such as the use of a glove box). Develop various chemical synthesis strategies/methodologies to functionalize graphene, graphene oxide, graphene quantum dots, and carbon quantum dots to tune physical and/or chemical properties, especially post-synthesis surface modification to achieve tunable dispersibility in organic solvent(s) and consistent thin film fabrication. Synthesize and characterize carbon thin films made from graphene, graphene oxide, graphene quantum dots, and carbon quantum dots using techniques such as spin-coating, Langmuir-Blodgett, and/or self-assembly methods. Characterize the chemical, structural, optical, and electronic properties of synthesized carbon materials and thin films using techniques including electron microscopy, atomic force microscopy, FTIR, Raman, UV-Vis spectroscopy, DLS, XPS, and XRD. Participate and present results in regular team meetings, contribute to progress reports and research proposals, and lead and support scientific manuscript development for publication in peer reviewed journals. Required Qualifications: Master's degree with 3+ years experience in Chemistry or a relevant discipline (Chemical Engineering, Material Science, or a related engineering discipline). Considerable knowledge of and experimental expertise in conducting synthesis and functionalization of carbon nanomaterials such as graphenes, graphene oxides, graphene quantum dots, carbon quantum dots for electronic or other applications as demonstrated through publication record. Experience with common carbon materials characterization techniques such as AFM, SEM, XPS, Raman, FTIR, UV-Vis and photoluminescence spectroscopy, and XRD. Demonstrated ability to publish high impact research. Demonstrated ability to work as part of a team to solve problems of scientific and technological interest. Must be able to meet the requirements for gaining access to work on the NETL campus. Preferred Qualifications: Ph.D. in Chemistry or a relevant discipline (Chemical Engineering, Material Science, or a related engineering discipline). Experience with or knowledge of thin film fabrications such as chemical vapor deposition, physical vapor deposition, spin coating, spray coating and Langmuir-Blodgett. Experience with or knowledge of nano/microfabrication processes. Experience with or knowledge of two-dimensional nanostructured metal-oxide semiconductors. Experience with or knowledge of electronic memory devices such as transistors or memristors. If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo - because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 - and moving faster than anyone else dares. Original Posting:December 5, 2025 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range:Pay Range $87,100.00 - $157,450.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

Leidos is seeking and exceptional and motivated Research Chemist interested in pursuing their passion by working side-by-side with world experts through a research appointment at the U.S. Department of Energy's (DOE) National Energy Technology Laboratory (NETL). In this role, you will work as part of DOE's leading engineering Research & Development laboratory team supporting NETL to pursue cutting-edge research on carbon nanomaterials for electronic devices. Specifically, you will work with NETL's carbon materials manufacturing team to develop novel methods to synthesize and functionalize graphene quantum dots and fabricate atomically thin quasi-2D amorphous carbon films for electronic memory devices such as transistors and memristors. In this role, you will engage with world-class carbon materials synthesis researchers and electronic memory device engineers, including leading DOE scientists and external partners to develop world-changing memory technologies that address internet of things and big data era challenges. What this opportunity with Leidos supporting NETL uniquely provides you: * Working on applied, cutting-edge projects with global impact while being mentored by the nation's leading energy scientists and engineers. * Real-world experience supplemented with technical development and discussions that provide unique insight into the broad range of mission critical engineering and scientific disciplines NETL leverages to support national energy research and policy development. * Unique access to world-class, customized facilities specific to high impact energy research, technology generation, and patent development. * Participation in novel fundamental and applied energy technology development with direct economic impact on global carbon management and resource use. Primary Responsibilities: * Synthesize graphene, graphene oxide, graphene quantum dots, and carbon quantum dots with tunable sizes/thicknesses using different domestic carbon feedstocks primarily by wet chemistry methods (including some air-free techniques such as the use of a glove box). * Develop various chemical synthesis strategies/methodologies to functionalize graphene, graphene oxide, graphene quantum dots, and carbon quantum dots to tune physical and/or chemical properties, especially post-synthesis surface modification to achieve tunable dispersibility in organic solvent(s) and consistent thin film fabrication. * Synthesize and characterize carbon thin films made from graphene, graphene oxide, graphene quantum dots, and carbon quantum dots using techniques such as spin-coating, Langmuir-Blodgett, and/or self-assembly methods. * Characterize the chemical, structural, optical, and electronic properties of synthesized carbon materials and thin films using techniques including electron microscopy, atomic force microscopy, FTIR, Raman, UV-Vis spectroscopy, DLS, XPS, and XRD. * Participate and present results in regular team meetings, contribute to progress reports and research proposals, and lead and support scientific manuscript development for publication in peer reviewed journals. Required Qualifications: * Master's degree with 3+ years experience in Chemistry or a relevant discipline (Chemical Engineering, Material Science, or a related engineering discipline). * Considerable knowledge of and experimental expertise in conducting synthesis and functionalization of carbon nanomaterials such as graphenes, graphene oxides, graphene quantum dots, carbon quantum dots for electronic or other applications as demonstrated through publication record. * Experience with common carbon materials characterization techniques such as AFM, SEM, XPS, Raman, FTIR, UV-Vis and photoluminescence spectroscopy, and XRD. * Demonstrated ability to publish high impact research. * Demonstrated ability to work as part of a team to solve problems of scientific and technological interest. * Must be able to meet the requirements for gaining access to work on the NETL campus. Preferred Qualifications: * Ph.D. in Chemistry or a relevant discipline (Chemical Engineering, Material Science, or a related engineering discipline). * Experience with or knowledge of thin film fabrications such as chemical vapor deposition, physical vapor deposition, spin coating, spray coating and Langmuir-Blodgett. * Experience with or knowledge of nano/microfabrication processes. * Experience with or knowledge of two-dimensional nanostructured metal-oxide semiconductors. * Experience with or knowledge of electronic memory devices such as transistors or memristors. If you're looking for comfort, keep scrolling. At Leidos, we outthink, outbuild, and outpace the status quo - because the mission demands it. We're not hiring followers. We're recruiting the ones who disrupt, provoke, and refuse to fail. Step 10 is ancient history. We're already at step 30 - and moving faster than anyone else dares. Original Posting: December 5, 2025 For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above. Pay Range: Pay Range $87,100.00 - $157,450.00 The Leidos pay range for this job level is a general guideline only and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

Branch Medical Group, a subsidiary of Globus Medical Inc., manufactures a wide range of implants for spinal and orthopedic applications as well as design the instrumentation cases that house them. Our passion, combined with Globus' world-class engineering, transforms clinical insights into tangible musculoskeletal solutions. We are constantly in pursuit of better patient care and understand that speed is critical because life cannot wait. **Position Summary:** The Quality Control Inspector is responsible for performing QC inspections and package testing on in-process materials and finished products. The QC inspector will also be responsible for ensuring all policies and procedures in compliance with applicable FDA, state, OSHA, AATB, and ISO regulations and standards. **Essential Functions:** - Performs quality control inspections on manufacturing supplies, labels, in-process materials, and sterile packed finished products. - Performs peel testing of sterile product seals. - Follows verbal and/or written instructions such as production traveler/batch record, work instruction, and process specifications at the direction of supervisor in completing a variety of inspection tasks. - Document non-conformances when found. - Bringing problems/issues to attention of Quality Control Supervisor. - Always Practice Good Manufacturing Practices and Inspection techniques. - Work efficiently to achieve targeted goals as set by the production schedule. - Follow proper safety precautions. - Maintains the quality control lab and work areas in an organized manner. - Verifying inspection equipment, machinery and tools used are calibrated per company policy. - Team player, open to new ideas and teamwork, self-motivated individual, willingness to continually strive to increase personal knowledge and value. - Performing other duties as assigned, to maintain efficiency throughout the company. - Adheres to the letter and spirit of the company Code of Conduct, the AdvaMed Code, MedTech Code, and all other company policies. Ensures Compliance with applicable governmental laws, rules, and regulations, both in the United States and internationally, by completing introductory and annual training and maintaining knowledge of compliance as it applies to your role. - Represents the company in a professional manner and upholds the highest standards of ethical business practices and socially responsible conduct in all interactions with other employees, customers, suppliers, and other third parties. _Reasonable accommodations may be made to enable individuals with disabilities to perform these essential functions._ **Qualifications:** - High School diploma or equivalent required - Minimum one (1) years' experience with quality control inspections is preferred. - Ability to use standard measuring equipment (i.e. Micrometers, Calipers, Height Gages, profilometer, ring, plug and thread, go no/go gages, dial indicator, surface plate, gage blocks and torque wrench) - Excellent verbal and written communication skills - Reliable, self-starter with the ability to work with little or no supervision and is detail oriented. - Required to possess specific visons abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus. - Familiarity with GMP and SOPs to ISO standards a plus. - Strong clerical and math skills. - Must be a flexible team player capable of working in a deadline dictated environment. - Strong organizational, problem solving, and follow-up skills; Ability to work in a fast-paced environment while multi-tasking and maintaining attention to detail. - Proficiency in using Microsoft Office products. **Physical Demands:** The physical demands listed here are representative of those that must be met by an employee to successfully perform the essential functions of this job. - Required to sit; climb or balance; and stoop, kneel, crouch or crawl. - Required to regularly lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. - Required to possess specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception and capacity to adjust focus." **Our Values** **:** Our Life Moves Us philosophy is built on four values: Passionate About Innovation, Customer Focused, Teamwork, and Driven. + **Passionate about Innovation** : Improving patient care by delivering advanced technology to our customers is at the core of what we do. We are passionate ab our role in improving the lives of patients by continuously developing better solutions. + **Customer Focused** : We listen to our customers' needs and respond with a sense of urgency. + **Teamwork** : Working together, anything is possible. We value every person on our team and treat each other with respect. We are accountable to one another and support each other. Together, we make each other stronger. + **Driven** : We pursue our mission with energy and passion. We are nimble, results-oriented and decisive. We overcome obstacles that arise in our quest to deliver solutions that will improve the lives of our customers and patients. **Equal Employment Opportunity** **:** Globus Medical is an equal opportunity employer. All applicants will receive consideration for employment without regard to race, color, religion, gender, sexual orientation, age, disability, marital status, pregnancy, national origin or citizenship. We are committed to a diverse workforce. We value all employees' talents and support an environment that is inclusive and respectful. **Other Duties** **:** Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice.

Being on medication is tough enough. We want to make getting it the easy part. Getting prescriptions to patients has become increasingly complex. When things get messy along the prescription journey, pharmaceutical manufacturers rely on us to untangle the process and create a clear path-allowing patients to build trusting relationships with their medication brands. We're not only committed to taking the pain out of the prescription process, but we're also devoted to bringing the brightest minds together under one roof. We bring together diverse voices-engineers, pharmacists, customer service veterans, developers, program strategists and more-all with one vision. Each perspective and experience makes ConnectiveRx better than the sum of its parts. The Operations Quality Assurance Associate I will evaluate work completed by Operations agents against program SOPs, WINs, business rules, and other program-related documents for adherence to expectations outlined in the documents. The QA Associate I must be able to use objective decision-making and critical thinking skills to determine whether audited work meets internal and external expectations. The Operations Quality Assurance Associate I will be a subject matter expert for their respective assigned business unit(s) and will utilize analytical skills to analyze data, processes, and workflows to provide insightful, actionable coaching for the Operations Agents. Responsibilities What you will do: Coach Operations agents (peer to peer) on areas of opportunity for improvement found during evaluations, collaborate with training for Operations agents (i.e., new hire, refresher, and nesting training) Performs and documents results of all quality assurance evaluations on all operational products and services, including (but not limited to) benefit verification cases, patient assistance cases, software support calls/emails, inbound calls from patients or health care providers, data entry, etc. Participates in internal, vendor, or client calibration meetings as required to address quality initiatives but does not lead them Identifies and escalates critical quality issues appropriately to senior management Assists with other QA-related functions and responsibilities as needed to meet department and company goals Availability to work occasional evening and/or weekend hours to meet company and departmental goals as the business need arises Auditing work completed by Operations agents Sending feedback to Operations leadership on agent performance Attending meetings, helping with data analysis, and other duties as assigned Qualifications What we need from you: Highschool or relevant experience 1 - 3 years as a Case Manager, Benefit Verification Specialist, or Contact Center agent at ConnectiveRx, or equivalent experience in a similar role in another company, or 1 - 3 years of prior quality control experience Moderate Excel ability (data validation, data entry, tables, simple formulas) Experience with technical writing (e.g., SOPs, User Manuals, Work Instructions), typing, and PowerPoint ability. Knowledge Solid working knowledge of quality-orientated services such as accuracy management, performance metrics, customer experience/satisfaction, healthcare benefits, and SOP execution. Health Care Experience is required, specifically claim processing, contact center, benefit verification, or similar industry experience. Call Center and/or Claim Processing experience is a plus. Problem-solving, results-oriented, active listening, and high attention to detail. Monitor telephone calls and communications between The Customer and The Customer Care Center. A strong understanding of empathy across the Customer Care Center is required in all patient interactions. Ensure provision of exceptional customer service required in customer care case management engagement. Work in a matrix environment requiring strong collaboration skills. Compensation & Benefits: This position offers opportunities for a bonus (or commissions), with total compensation varying based on factors such as location, relevant skills, experience, and capabilities. Employees at ConnectiveRx can access comprehensive benefits, including medical, dental, vision, life, and disability insurance. The company regularly reviews and updates its health, welfare, and fringe benefit policies to ensure competitive offerings. Employees may also participate in the company's 401(k) plan, with employer contributions where applicable. Time-Off & Holidays: ConnectiveRx provides a flexible paid time off (PTO) policy for exempt employees, covering sick days, personal days, and vacations. PTO is determined based on an employee's first year of service. Employees also receive eight standard company holidays and three floating holidays annually, with prorations applied in the first year. The company remains committed to providing competitive benefits and reserves the right to modify employee offerings, including PTO, STO, and holiday policies, in accordance with applicable laws and regulations. Posted Salary Range USD $18.96 - USD $25.10 /Hr.

Cook MyoSite, Inc., part of the Cook Group, Inc. family of companies, is on a mission to make regenerative medicine a part of everyday medicine. We're investigating our core technology, autologous muscle-derived cells, for the potential treatment of several muscle-related disorders. We at Cook MyoSite have the potential to make a difference in the lives of countless people around the world, and we also have the potential to make a difference in yours. Joining our team is an opportunity to ignite your passion, grow your potential, and define your purpose. If you're curious, motivated by helping others, and driven by integrity, we invite you to apply. The Quality Control Associate I at Cook MyoSite will aid in the development and maintenance of methods for sampling, testing, evaluating, and approving testing results for products and materials. Responsibilities • Performs quality control sampling and testing of materials and products for identity, strength, quality and purity utilizing assays for, but not limited to, DNA isolation, mycoplasma, endotoxin, myogenic differention, and desmin • Performs lot testing • Assists in the investigation of nonconformance activities with additional testing and evaluation activities as needed • Writes quality plans and reports to QC-related activities • Performs QC projects for validation and evaluation of methods • Recommends and establishes different methods for performing QC tasks • General maintenance of side labs • Aids in activities related to monthly inventories and removal of expired products • Cell culturing for lot testing and research • Supports in maintaining cleanroom environment below alert limits by participating in and following established cleaning practices • Exemplifies Cook MyoSite Core Values • Maintain regular and punctual attendance • Must maintain company quality and safety standards • This position requires an ongoing commitment to upgrading knowledge, job skills and abilities in addition to competency related to all duties and responsibilities listed above. • Ability to work in collaborative and independent work situations and environments with minimal supervision • Maintain composure and competence under stressful situations; demonstrate flexibility and adaptability • Must work and interact effectively and professionally with and for others throughout various levels of the global organization to achieve company goals • Trainability • Must have effective verbal, written and interpersonal skills • Excellent analytical skills with the ability to analyze situations accurately and effectively • Must demonstrate critical thinking and proven problem-solving skills • Must exhibit well developed skills in prioritizing, planning, organization, decision making, and time management • Able to analyze situations or data Qualifications Undergraduate degree any Life Sciences, Engineering field, Microbiology, or Molecular Biology or 6 years direct, relevant experience in analytical testing laboratory to provide a comparable background Minimum of 1-3 years' experience in laboratory testing environment Basic understanding of cGMP, 21 CFR Part 11, and related regulations associated with Bio/Pharmaceutical product manufacturing Ability to learn and support new systems and applications, and the ability to provide technical training to end users. Proficient knowledge of Microsoft Office software, and other general office equipment. Full Time On Site Physical Requirements: • Ability to conduct and hear ordinary conversation and telephone communication. • Must be able to work extended hours beyond normal work schedule to include, but not limited to, evenings, weekends, extended work hours and/or extra work hours, sometimes on short notice as required. • Ability to work under specific time constraints. • Must be able to sit at desk, in meetings and/or work on a computer for long or extended periods of time. • Visual and manual acuity for working with computers and equipment. • Ability to spend majority of day standing in laboratory setting or sitting at/working in a biological safety hood with potential (limited) exposure to hazardous chemicals and/or harsh disinfectants while in BioSafety Level II or other labs. • Physically capable of standing, walking, stooping, kneeling, crouching, climbing steps and ladders, reaching, twisting and bending on occasion with or without reasonable accommodations. • Must be able to lift/push/pull up to 50 pounds on an occasional basis with or without reasonable accommodations. • Must be capable of performing PPE gowning procedures on a frequent basis to enter BioSafety Level II including but not limited to safety glasses, lab coat, gloves, specialized clothing including laboratory scrubs (pants and shirt), appropriate shoes, and facial mask (if required) on a regular basis. Employee that does not interact with Healthcare Professionals Compliance with all policies of the company including without limitation the Cook Employee Manual, Cook Code of Conduct, Quality System Manual, Cook Electronic Information Policy and HIPAA regulations. At Cook MyoSite, we don't just accept difference - we celebrate it, we support it, and we thrive on it for the benefit of our employees, our products, and our community. Cook MyoSite is proud to be an equal opportunity workplace. This job description features the essential and critical functions of the position described and is not an exhaustive list of tasks and/or responsibilities. This may be subject to change at any time due to reasonable accommodation or other reasons.

Job DescriptionCertified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! $1000 HIRING BONUS!!! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: Accurately perform and read test results and notify Laboratory Management of deviations Prepare and analyze samples for indicator organisms, pathogens, and chemistries Apply aseptic/microbiological techniques in daily workload Report inventory and expendable supplies/materials needed for testing requirements Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends Perform all activities in a neat, safe, hygienic, and efficient manner Share information in an open and timely manner Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team Responsible for the safety of oneself and others working within their area Supervision: This job does has no supervisory responsibilities. Education & Experience: Associate degree in Life Science or related field with two or more years of laboratory experience, preferred Two or more years of experience in a commercial food-testing or analytical laboratory Or equivalent combination of education and experience Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures Broad knowledge of concepts, practices, and procedures of a food testing laboratory Ability to travel when necessary Physical Demands/Work Environment: Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens Noise level varies from quiet to loud Temperature varies from hot to cold Interactive and fast-paced team oriented tasks Overnight Travel is required at the discretion of management Occasionally lift and/or move up to 25 pounds Color vision and depth perception Benefits: Progressive 401k Retirement Savings Plan Employer Paid Short- Term and Long-Term Disability, and Life Insurance Group Medical Tuition Reimbursement Flexible Spending Accounts Dental Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

$10,000.00 SIGN-ON BONUS ELIGIBLE The Laboratory Technologist will demonstrate multiple analytical and judgment skills and knowledge of clinical laboratory science to provide accurate, timely results. The incumbent uses high complexity methods and instrumentation and will work independently in multiple areas of the laboratory. Essential Job Functions Procure, prepare and process specimen using various approved techniques and procedures. Perform phlebotomy in accordance with established procedures and in a manner consistent with customer service needs and expectations. Receive specimens into the LIS, verifies orders, understands priorities and communicates all pertinent information. Validate test orders, appropriateness of specimen and ensure required documentation is present. Process and organize specimens using standard precautions, maintaining specimen integrity and identity. Recognize, resolve and document specimen tracking and integrity issues. Utilize specimen rejection and irretrievable specimen policies to document specimen issues. Validate and research unusual reference test orders, arrange proper specimen collection, and ensure that documentation is complete and information effectively communicated. Package specimens for transport according to regulations and established protocol. Prepare appropriate quantity of reagents and consumables in accordance with section guidelines; maintains reagents to maximize stability and shelf-life. Perform preventative and corrective maintenance; anticipate problem situations and take preventative action to avoid delay of patient care. Maintain supplies at adequate levels to support operations, monitoring utilization and reporting unusual situations to supervisor. Perform low, moderate and high complexity technical assays, evaluate and interpret results forming conclusions requiring a high level of judgment. Determine and validate appropriate instrument settings and making adjustments as needed. Demonstrate competency on all instrumentation and methods in assigned work areas. Perform laboratory tests in assigned area, using established protocols and with an awareness of accuracy, method sensitivity, specificity, and turn-around-time and cost management. Assess test methods for procedural validity and testing accuracy, re-evaluating patient data for validity when instrument or methodology malfunctions are suspected. Perform and document all quality control, maintenance and variances. Maintain an in-depth knowledge of the test methods and procedures in two or more laboratory sections, and show an understanding of the correlation of patient results to the overall clinical picture. Identify, investigate and resolve questionable test orders and/or results through correlation of disease state/diagnosis and patient history. Assess specimen integrity, validity and identification; recognize abnormal, unusual, or problem situations, and correlate patient laboratory results when specimens are suboptimal. Correlate patient data with other clinical information to assess the possibility of inconsistent orders or results. Participate in a quality management system to include quality control and assurance of laboratory testing, competency assessment and appropriate utilization of laboratory services. Compose correlation studies, QC reports, and maintain monthly logs. Evaluate quality control data to assist the supervisor in the assessment of accuracy, reproducibility and validity of methods. Participate in section readiness to meet CAP, JCAHO, OSHA and DOH compliance. Utilize HIS as needed for patient or test order information, and to process supply or work orders. Utilize functions of LIS to accession, receive, result and monitor functions related to patient testing. Participate in initial and monthly validation of LIS and instrument interfaces. Evaluate laboratory data to assess the need for recollection of the specimen. Correlate patient laboratory results to suspect pathological state, and recognizes the need for follow-up or reflex testing. Redirect testing to appropriate backup or secondary test methods and seeks to resolve primary testing issues. Interact with healthcare providers to interpret laboratory results within the framework of medical technology. Answer inquiries from other healthcare providers concerning test appropriateness, quality, accuracy and procedural requirements. Assist in the evaluation and development of new methods/instruments. Recommend process improvements to workflow and assist in implementation of changes to improve operation. Report and document critical values and read back verifications according to policy. Adhere to laboratory and section specific Environmental Control Plan. When appropriate, enter reflex testing codes into LIS to generate billing. Retain records of instrument printouts and specimens according to policy. Other duties as assigned. Competency and Experience [Knowledge, Skills and Abilities] Required Qualifications/Experience Associate of Science or higher-level degree from an accredited institution in chemical, physical, biological or clinical laboratory science, or medical technology, OR, Equivalent laboratory training and experience meeting the requirements defined by CLIA 88 for individuals performing high complexity testing. Knowledge of Medical terminology and laboratory information system. Functional skills in Microsoft Office applications, including Outlook. Strong leadership ability, good organizational skills, independent and critical thinking skills, sound judgment, and knowledge of legal aspects and liability of nursing practice. Strong ability to communicate complex and/or controversial topics and concepts to a wide and diverse audience. Preferred Qualifications/Experience Prior experience within a clinical laboratory. License, Certification & Clearances ASCP preferred. Act 33 clearance with renewal. Act 34 clearance with renewal. Act 73 FBI Clearance with renewal. Position Type/Expected Hours of Work Incumbent will be scheduled based on operational need (rotate shifts, standby, on-call, etc.). Travel may be expected locally between System locations. Equal Employment Opportunity Independence Health and its affiliated companies are Equal Opportunity Employers. It is their policy to prohibit discrimination of any type and to afford equal employment opportunities to employees and applicants without regard to race, color, religion, sex, sexual orientation, national origin, age, marital status, disability, veteran status, or genetic information, or any other classification protected by law. Independence Health and its affiliated companies will comply with all applicable laws and regulations. Disclaimer This job description is not designed to contain a comprehensive listing of all activities, duties or responsibilities that are required of the employee. Moreover, duties, responsibilities and activities may change or new ones may be assigned at any time with or without notice. Work EnvironmentEffective March 2020 or during pandemic: goggles, face shield and mask are required according to CDC guidelines When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Extreme Heat X X Extreme Cold X X Heights X X Confined Spaces X X Extreme Noise(>85dB) X X Mechanical Hazards X X Use of Vibrating Tools X X Operates Vehicle X Operates Heavy Equipment X Use of Lifting/Transfer Devices X Rotates All Shifts X X 8 Hours Shifts X X 10-12 Hours Shifts X X On-Call X Overtime(+8/hrs/shift; 40/hrs/wk) X X Travel Between Sites X X Direct Patient Care X X Respirator Protective Equipment X X Eye Protection X X Head Protection (hard hat) X Hearing Protection X X Hand Protection X X Feet, Toe Protection X Body Protection X X Latex Exposure X X Solvent Exposure X X Paint (direct use) Exposure X Dust (sanding) Exposure X Ethylene Oxide Exposure X Cytotoxic (Chemo) Exposure X Blood/Body Fluid Exposure X X Chemicals (direct use) Exposure X X Mist Exposure X Wax Stripper (direct use) X Non-Ionizing Radiation Exposure X Ionizing Radiation Exposure X Laser Exposure X X Physical Demands When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required. Essential - Absolute Necessity. Marginal - Minimal Necessity. Constantly - 5.5 to 8 hours or more or 200 reps/shift. Frequently - 2.5 to 5.5 hours or more or 32-200 reps/shift. Occasionally - 0.25 to 2.5 hours or 2-32 reps/shift. Rarely - Less than 0.25 hours or less than 2 reps/shift. Physical Condition Essential Marginal Constantly Frequently Occasionally Rarely Never Bending (Stooping) X X Sitting X X Walking X X Climbing Stairs X X Climbing Ladders X X Standing X X Kneeling X X Squatting (Crouching) X X Twisting/Turning X X Keyboard/Computer Operation X X Gross Grasp X X Fine Finger Manipulation X X Hand/Arm Coordination X X Pushing/Pulling(lbs. of force) X X Carry X X Transfer/Push/Pull Patients X Seeing Near w/Acuity X X Feeling (Sensation) X X Color Vision X X Hearing Clearly X X Pulling/Pushing Objects Overhead X X Reaching Above Shoulder Level X X Reaching Forward X X Lifting Floor to Knuckle X 25# Lifting Seat Pan to Knuckle X 10# Lifting Knuckle to Shoulder X 10# Lifting Shoulder to Overhead X 10# When lift requirement is in excess of 50#, lift assistance (2 person) and/or transfer device is required.

Job Description Join a Team That Makes a Difference! At Noble, the work you do matters. We manufacture innovative products that support the military, advance the medical field, and improve everyday life. Whether it's enhancing safety, enabling critical care, or solving real-world challenges, our solutions help people when it matters most. Be part of a purpose-driven team where your skills contribute to meaningful change. Noble Biomaterials, Inc is currently seeking a Chemical Lab Analyst for our 1st shift. The Chemical Lab Analyst performs laboratory testing on raw materials, in-process samples, and finished products to ensure quality and compliance. This role includes running various test methods, entering and verifying data, and maintaining lab equipment while following Good Documentation Practices (GDP) and Good Laboratory Practices (GLP). What You'll Get: Starting Pay: $18.00/hour Weekly Pay - Get Paid Every Thursday! Full Benefits Starting the 1st of the Month After Hire! Medical, Dental, Vision $2,000-$4,000 Health Reimbursement Account (HRA) An account that is funded by the company to cover a portion of the in-network deductible for you and your family. (debit card) Company-Paid Life, Short & Long-Term Disability FSA, Voluntary Insurance Options 401(k) + Company Match (after 6 months) 11 Paid Holidays + PTO What You'll Do: Perform routine and non-routine testing on raw materials, in-process samples, and finished goods Prepare and analyze samples using methods such as: Titration ASE extraction Atomic Absorption (AA) ICP-OES FTIR Conduct simulated at-home laundering on fabrics Record and interpret test results Enter and verify all testing data Maintain and troubleshoot basic lab equipment Assist with investigations and reporting when issues arise Communicate and collaborate with cross-functional teams Report out-of-specification or questionable results Perform other tasks as assigned by management Job Flexibility Employees in this position may be assigned to different work areas or job duties based on production demands. Applicants should be comfortable learning new tasks and adapting to changing priorities. The Skills You'll Need: Strong analytical and problem-solving skills High attention to detail and commitment to quality Reliable attendance and time management Team-oriented with strong communication skills Commitment to safety, ethics, and inclusive workplace practices Work in varied indoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE) What We're Looking For: Associate degree in a related science field required 3-6 months of quality related experience in a manufacturing setting preferred. Proficiency with Excel, Word, and Outlook preferred Age 18+ with reliable transportation Ready to Join a Team That Invests in You? Apply today and take the next step in your manufacturing career with a company that values its employees and offers weekly pay and benefits that start right away! Equal Opportunity Employer/Veterans/Disabled

Join a Team That Makes a Difference! At Noble, the work you do matters. We manufacture innovative products that support the military, advance the medical field, and improve everyday life. Whether it's enhancing safety, enabling critical care, or solving real-world challenges, our solutions help people when it matters most. Be part of a purpose-driven team where your skills contribute to meaningful change. Noble Biomaterials, Inc is currently seeking a Chemical Lab Analyst for our 1st shift. The Chemical Lab Analyst performs laboratory testing on raw materials, in-process samples, and finished products to ensure quality and compliance. This role includes running various test methods, entering and verifying data, and maintaining lab equipment while following Good Documentation Practices (GDP) and Good Laboratory Practices (GLP). What You'll Get: Starting Pay: $18.00/hour Weekly Pay - Get Paid Every Thursday! Full Benefits Starting the 1st of the Month After Hire! Medical, Dental, Vision $2,000-$4,000 Health Reimbursement Account (HRA) An account that is funded by the company to cover a portion of the in-network deductible for you and your family. (debit card) Company-Paid Life, Short & Long-Term Disability FSA, Voluntary Insurance Options 401(k) + Company Match (after 6 months) 11 Paid Holidays + PTO What You'll Do: Perform routine and non-routine testing on raw materials, in-process samples, and finished goods Prepare and analyze samples using methods such as: Titration ASE extraction Atomic Absorption (AA) ICP-OES FTIR Conduct simulated at-home laundering on fabrics Record and interpret test results Enter and verify all testing data Maintain and troubleshoot basic lab equipment Assist with investigations and reporting when issues arise Communicate and collaborate with cross-functional teams Report out-of-specification or questionable results Perform other tasks as assigned by management Job Flexibility Employees in this position may be assigned to different work areas or job duties based on production demands. Applicants should be comfortable learning new tasks and adapting to changing priorities. The Skills You'll Need: Strong analytical and problem-solving skills High attention to detail and commitment to quality Reliable attendance and time management Team-oriented with strong communication skills Commitment to safety, ethics, and inclusive workplace practices Work in varied indoor conditions which may include heat, cold, dust, loud noise, etc., with the use of personal protective equipment (PPE) What We're Looking For: Associate degree in a related science field required 3-6 months of quality related experience in a manufacturing setting preferred. Proficiency with Excel, Word, and Outlook preferred Age 18+ with reliable transportation Ready to Join a Team That Invests in You? Apply today and take the next step in your manufacturing career with a company that values its employees and offers weekly pay and benefits that start right away! Equal Opportunity Employer/Veterans/Disabled

Title: QC Specialist Department: Quality Control Job Type: Regular Full-Time Shift: 2nd Schedule: Monday-Friday, 2:00pm to 10:30pm NMS Labs has developed an extensive menu of more than 2,500 tests to support clients in forensic, criminalistic, public health and clinical fields. For over 50 years, our clients have relied on NMS Labs for unique testing solutions that demonstrate our company core values of Quality, Integrity, Service, Innovation and Engagement. As we work to increase the company's positive impact on public health and public safety, we are seeking talented professionals to join us for the journey! We invite you to learn more about our company by visiting NMSLabs.com. Job Description: We are seeking a QC Specialist to work in our Quality Control department. The QC Specialist will be responsible for the proper and timely preparations of reagents and quality control/standard material for NMS Labs, as well as maintaining direct communication with laboratory departments regarding preparations. Major duties and responsibilities include: * Label, aliquot, and package Quality Control samples and/or reagents. * File or scan associated paperwork appropriately * Maintain inventory of manufactured drug standard solutions and NMS prepared solutions and/or chemicals and supplies and order as needed. * Receive and log stock standards into drug database. * Monitor the incoming requests from the laboratory * Gather appropriate materials needed to complete requests * Accurately generate QC preparation worksheets * Accurately prepare quality control and standard reference material or reagents and other materials for the lab * Accurately perform calculations needed for any of the following: * to prepare stock standards including but not limited to compensation for salts, moisture and waters of hydration dilutions to target concentrations * to account for volume variations of requested reagents * Verify prepared standards by UV-Vis Spectrophotometry or other appropriate means * Review any of the following for accuracy and relevance: * Testing department's methods * Reagent preparation instructions * Assist with scheduling the pending requests to assure timely delivery to the laboratory * Track expiration of materials in QC department, and accordingly discard or re-evaluate the material when expired * Dispose of chemicals properly. Requirements: * Associate degree or higher, and 0-1year relevant laboratory experience * Ability to perform calculations needed to prepare standards, including but not limited to compensation for salts, moisture, waters of hydration, and dilutions to target concentrations * Experience with the following preferred: * Pipettes and/or syringes * Chemicals, pH meter, and metric balance Physical Demands: * Ability to hear * Vision (with correction) including color, distance, peripheral vision, depth perception, and the ability to adjust focus * Standing, reaching with hands and arms, and using hands and fingers to manipulate instrument or equipment controls, computer keyboard, office equipment, objects or tools * Movement from one work location to another * Sitting and standing, sometimes for extended periods of time * Lifting objects up to 20 lbs. * Exposure to intermittent or constant sounds generated by equipment * Exposure to fumes, noxious odors and dust * Handling of biological material and blood-borne pathogens * Handling of toxic or caustic chemicals * Proximity to moving parts Offers of employment are made contingent upon a nationwide background investigation and urine drug screen with results satisfactory to standards of employment at NMS. * We are an equal opportunity employer and will not discriminate against any employee or applicant for employment because of race, creed, sexual orientation, color, religion, gender, sex, sex identity, gender identity, national origin, age, marital status, citizenship

Philadelphia, PA Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on developing and launching the first curative targeted cell therapies designed specifically for patients with autoimmune diseases. The CABA™ platform encompasses two complementary strategies which aim to advance the discovery and development of engineered T cell therapies with the potential to become deep and durable, perhaps curative, treatments for a broad range of autoimmune diseases. The lead CARTA (Chimeric Antigen Receptor T cells for Autoimmunity) strategy is prioritizing the development of rese-cel, a 4-1BB-containing fully human CD19-CAR T cell investigational therapy. Rese-cel is currently being evaluated in the RESET™ (REstoring SElf-Tolerance) clinical development program spanning multiple therapeutic areas, including rheumatology, neurology and dermatology. Cabaletta Bio's headquarters and labs are located in Philadelphia, PA. For more information, please visit ******************** and connect with us on LinkedIn. Uniquely Differentiated. Rapid. Elegant. At Cabaletta, we are driven by the shared mission of developing cures, where a patients' own cells are used to fight disease. We are building a culture grounded in the knowledge that successful cures can be achieved for patients if every member of the Cabaletta is focused on the success of the team. To nurture this, we make an active commitment to the well-being and continuous growth of each employee who joins the team. In this way, we are not only working to improve the lives of patients, but of everyone involved. #CabalettaCrew. We're proud to be a Great Place to Work-Certified™ company! #GPTWcertified Check out what our employees say makes working here so great: Working at Cabaletta Bio Inc | Great Place to Work Position Description: This role can be hybrid or based in our Philadelphia, PA headquarters. Reporting to the Director, QA Operations, the GMP QC Specialist, CMC, will be responsible for ensuring the compliance of generated QC data with Good Manufacturing Practices (GMP) both within the organization and generated by third parties. The individual will be involved in developing, implementing, and maintaining Quality Control review processes to uphold the highest standards in internal and external laboratory activities. The role will work closely with cross-functional teams to assess, monitor, and enhance quality systems, ensuring that all GMP data adhere to relevant internal and regulatory requirements. Our ideal candidate will have strong experience with microbiological assays, including compendial methods (sterility, endotoxin, mycoplasma assays, APS, APV and Environmental Monitoring). Responsibilities: GMP Compliance: Ensure that all internal laboratory activities are maintained in accordance with internal data integrity practices and standards. Ensure that external laboratory activities comply with GMP regulations and guidelines. Stay current with regulatory requirements and industry standards related to GMP. Batch Review / Release: Perform full batch record review of all types of investigations; perform appropriate quality control review of all QC data generated by third parties; draft, review, and approve CoA (internal/external). Investigations: Identify issues of non-compliance and work directly with the third party to resolve prior to batch release. Review and approve any out-of-specification investigations in a timely manner. Quality Control Procedures: Develop, implement, and maintain quality control procedures to monitor and assess internal laboratory processes, as well as the processes employed by external laboratories used to generate QC data. Conduct regular reviews to identify areas for improvement and initiate corrective action(s) as needed. Audits and Inspections: Assist in the planning and conducting of internal audits to assess compliance with data integrity standards and approved procedures (e.g. SOPs, test methods). Support audits of external laboratories as needed. Assay Qualification / Validation: Review and approve assay development, qualification and validation plans, data generated and reports. Provide primary QC support for all activities. Documentation Management: Oversee the creation, review, and approval of laboratory documentation, including SOPs, test methods, protocols, and reports. Ensure that the documentation is accurate, complete, and in compliance with GMP requirements. Ensure all Process Development (Analytical Development and Manufacturing Sciences & Technology) related documentation and data are reviewed and archived in a timely and accurate manner. Training and Education: Assist in providing training and guidance to Process Development personnel on GMP principles, procedures, and compliance requirements. Ensure that all team members are informed and adhere to quality control measures. Risk Management: Identify and assess potential risks related to GMP compliance. Develop and implement risk mitigation strategies to minimize the likelihood of compliance issues. Continuous Improvement: Drive continuous improvement initiatives within the quality control function. Collaborate with relevant stakeholders to implement changes that enhance overall laboratory efficiency and quality. Communication: Effectively communicate with cross-functional teams, management, and regulatory agencies regarding quality control matters. Provide regular updates on compliance status, issues, and improvements to Quality Management. Qualifications: Bachelor's degree in scientific discipline; Advanced degree preferred. Minimum of 5 years' hands-on experience in biopharmaceutical technical operations, QC operations and/or quality operations. Minimum of 2 years' hands-on experience in GMP laboratory environment, with specific familiarity with cell and gene therapy release assay development, performance, and qualification. Specific experience performing or reviewing microbiological assays, including compendial methods (sterility, endotoxin, mycoplasma assays, APS, APV and Environmental Monitoring) Experience interacting with external testing laboratories preferred. Working knowledge of GMP and ICH guidance and both US and international regulatory requirements. Highly organized, effective, and proactive communicator verbally and in writing. Able to work independently to appropriately prioritize work. Strong team orientation and passion for continuous self-development. Experience in industry or in a startup industrial setting is preferred. Our name - Cabaletta - is derived from the operatic term that represents a rapid, repetitive, and technically challenging section of an operatic aria, designed to showcase the skills of the lead singer. Analogously, Cabaletta Bio strives to achieve rapid and repetitive product development, building on our indication prioritization and biologic platform that targets the driver of specific autoimmune diseases without the need for long-term immunosuppression. For more information, please visit https://********************/join-our-crew Our most important asset is our people, and we offer competitive benefits, PTO, and stock option plans. Cabaletta Bio is an equal opportunity employer. We do not discriminate on the basis of race, color, gender, gender identity, sexual orientation, age, religion, national or ethnic origin, disability, protected veteran status or any other basis protected by applicable law. Cabaletta Bio, Inc. does not accept unsolicited resumes from recruiters, employment agencies, or staffing firms. To conduct business with Cabaletta, a Master Services Agreement (MSA) must be executed and confirmed prior to submitting any information relating to a potential candidate. Without a signed MSA, Cabaletta shall not be responsible to any individual or entity for any payment relating to any form of fee or compensation. And, if a resume or candidate is submitted by a recruiter, an employment agency, or a staffing firm without a fully executed MSA, Cabaletta has the unrestricted right to pursue and hire any of those candidate(s) without any legal or financial responsibility to the recruiter, agency, and/or firm. #LI-ONSITE

Job Description What we are looking for: The Quality Control Technician conducts inspection and testing activities at various manufacturing states including incoming, in process, and final release. 2nd Shift: Monday-Friday 3:00pm-11:00pm What you will do: Performs first article, in process, and final release testing for raw materials, as well as textile-based products. Utilizes a variety of testing equipment, including tensile testing machines, microscopes, and vision systems. Records and communicates test results manually and/or electronically. Inspects product for defects and contamination, according to Work Instructions (WI), Visual Inspection Criteria, SOP's, and internal specifications. Conducts extensive data collection to support the identification of trends to increase yields through process improvement. Enters visual inspections results as well as physical testing results into the applicable tracking databases. Packages and labels components in preparation for release. Generates certification documentation to accompany shipments. Enters information and uses ERP system to report quantities. Other duties as assigned Who you are: High School diploma or equivalent required. 0-1-year related experience preferred. Strong attention to detail. Intermediate computer skills. Proficiency in MS Word and MS Excel. Basic understanding of GMP and working within regulated industries. Demonstrated ability to communicate effectively with peers and management. Ability to multi-task change direction with shifting priorities. What we offer: Paid Breaks Generous Paid Time off and Holiday Pay Annual Bonuses Health Insurance: Medical with Rx plan / Dental / Vision 401k (retirement savings) with excellent company match Company Paid Short-Term and Long-Term Disability

Job Description The Quality Assurance Associate, under the direction of the Chief Compliance & Quality Officer and working in cooperation with the Lead Quality Assurance Associate, utilizes a combination of excellent customer service, administrative, and analytical skills to ensure the agency can deliver high-quality client care services. This role is focused on investigating, managing, and resolving incidents that affect quality care. ESSENTIAL DUTIES AND RESPONSIBILITIES: 1. Conducts investigations for both the Personal Care and Developmental Care service lines. These investigations involve obtaining witness statements and interviews, securing evidence, retrieving information from electronic surveillance, reviewing staff schedules, compiling information from the agency's EHR system, and developing a chronological summary of factual findings from occurrence to closure. Depending on the incident, investigations may require traveling into the field to client homes to conduct investigations. (Coverage area: Philadelphia, Bucks, Montgomery, Delaware and Chester counties) 2. Completes and maintains Certified Investigator credential status from the PA Office of Development Program (ODP). Conducts investigations in accordance with ODP regulations. 3. Complies with required incident management reporting timeframes, ensuring investigations are filed, finalized or extended according to the timelines set forth by regulatory and agency standards to maintain speed, objectivity, and thoroughness. 4. Attends to all reportable data entry in the PA Enterprise Incident Management (EIM) System and documents all case activity for internal records. 5. Investigates potential fraud events and complaints involving client or caregiver safety. Makes recommendations for resolution, documents actions taken, and analyzes issues to prevent recurrence. 6. Provides education, guidance, and training to employees regarding incidents, complaints, and potential fraud events. 7. Engages in Administrative Reviews and Certified Investigation Peer Reviews to ensure processes meet regulatory standards. 8. Establishes rapport with staff, caregivers, clients, providers, families, and outside agencies to coordinate investigations. 9. Compiles, trends and reports quality data to analyze why incidents occur and how recurrences can be prevented. 10. Assists the Director of Quality & Clinical Management in the administration of the agency's quality improvement plans, infection control program, and accreditation standards. 11. Assists the Compliance Officer in monitoring the agency's compliance with regulatory mandates. Assists with the preparation of plans of correction for state surveys and auditing bodies. 12. Performs other duties as assigned by the Chief Compliance Officer. COMPLIANCE AS REQUIREMENT OF PERFORMANCE: Compliance with AmeriBest policies and procedures is a responsibility of all AmeriBest associates. It is a part of each associate's performance to follow these requirements: All associates are expected to participate in any investigatory activities All associates are expected to report any violation of AmeriBest policies and procedures All associates are expected to conduct themselves in an ethical manner consistent with the AmeriBest mission statement and Standards of Conduct All associates are expected to protect the privacy of protected records and must conduct themselves consistent with all applicable laws and policies regarding privacy protection, including HIPAA and state specific privacy laws COMPETENCIES/SKILLS: Planning/Organizing - Prioritizes and plans work activities; Uses time efficiently. Process Building - seeks to develop better efficiencies in agency processes. Actively engages in the use of technology to automate and enhance day-to-day workflows. Problem solving - effective at identifying root causes and creative solutions to issues. Analytical - strong quantitative and analytical skills. Apply critical thinking to make informed, data driven decisions. Teamwork - ability to work effectively as part of a team Communication - Communicates effectively and concisely; Strong ability to create effective visual summations of data. Customer focused - strong customer service skills, able to deal with people in a polite and caring manner. Strong Computer Proficiency- Uses Microsoft 365 applications with proficiency. Intermediate to advanced skillset preferred in Word, Excel, Forms, and PowerPoint, Familiarity with EMR and data repository systems. Some Clinical Knowledge- Knowledge of medical terminology, familiarity with medical notes and discharge reports, and common chronic illnesses. Attention to Detail with Quality Focus. Deadline Oriented EDUCATION AND/OR EXPERIENCE: A bachelor's degree in social work, behavior sciences, human services, or a related field. At least one (1) years' experience in home care, social work, case management, or hospital discharge planning. PREFERRED EXPERIENCE: Associates Degree Prior experience working for a Home Health Care Agency One (1) year of experience in a healthcare organization ADDITIONAL REQUIREMENTS: Must have and maintain a valid Driver's License, a good driving record, maintain automobile insurance coverage, and have access to a reliable automobile. Ability to work occasional evenings and weekends to conduct investigations in client homes. Currently hold a PA-Office of Development Program (ODP) Certified Investigator certificate or must successfully complete this certification within 12 months of hire. PHYSICAL DEMANDS: Regular requirement to sit; use hands to touch, handle or feel. Regular requirement to stand; kneel, squat, walk and reach with hands and arms. Occasional requirement to lift and/or move up to 10 pounds. Vision abilities include close vision, peripheral vision, depth perception and the ability to adjust focus. Able to travel throughout Philadelphia and surrounding counties and enter clients' homes. WORK ENVIRONMENT: Location: In-office position (Philadelphia office) Business Office Environment The noise level is usually moderate Local travel to client homes in the five county Philadelphia area Benefits: PTO Medical, Dental, and Vision Insurance 401(k) and HSA AmeriBest Home Care is an equal opportunity employer. We value and encourage diversity in our workforce and provide equal employment opportunities to all individuals protected by applicable laws.

Now Hiring!! Company: Acero Precision Salary Information: $20.00 - $26.00 Full-Time | On-site | Some Weekend Availability Why Join the Acero Precision Team? Acero Precision, located in West Chester, PA is an industry leading Medical Device contract manufacturer producing the very best in precision engineered components. To succeed in today's manufacturing industry- with its demands to serve customers in a truly global environment- we rely on three vital resources: the newest engineering technologies, quality systems, and most importantly highly-skilled people. We invite you to become a member of an organization that has established an outstanding reputation for quality and excellence. Highly competitive wages, a state-of-the-art-facility, an emphasis on work/life balance, career advancement, a team-centered workplace culture, and the opportunity to be your best is waiting for you at Acero Precision. Why You'll Love Working Here * We offer defined career advancement opportunities for employees seeking long-term growth within our organization * Competitive premium pay for 1st shift * Overtime hours available * Weekend premiums available * Multiple health insurance plans, including a no-cost HSA health plan for eligible employees. * Affordable Dental, and Vision benefits * 100% Paid Uniforms * 401k with employer match * Paid training on advanced CNC programming software * This role offers 100 hours of PTO in the first year, with PTO increasing at defined service milestones. * 7 paid holidays every year * State-of-the-art, climate-controlled facility with 5-axis and Swiss turning * Employee Assistance Program (EAP) offering free confidential support services to employees and their families. * Access to our Wellness Coach Program Be the eyes of precision. Join a team where quality is more than a goal-it's a way of life. Are you a detail-oriented quality professional with a passion for excellence in manufacturing? Acero Precision is seeking a dedicated Quality Control Roving Inspector to uphold and elevate our industry-leading standards. What You'll Do As a Quality Control Roving Inspector, you'll be the frontline advocate for our customers-ensuring every part meets our rigorous quality standards. Your day-to-day will include: * Conducting in-process and final inspections across multiple machines and cells. * Collaborating with machinists, production team leads, and quality controllers to identify and resolve non-conformances. * Maintaining ISO 9001 and ISO 13485 compliance. * Coaching Final Inspectors and training production staff on inspection tools and quality processes. * Leading by example in inspection practices and quality improvement. Your Impact * Ensure product accuracy and compliance using the Monitor Report and Sponge Data System. * Maintain inspection equipment and accurate calibration records. * Act as a quality "help desk" for operators and a mentor for new team members. * Support continuous improvement by generating NCRs and developing corrective actions. What You Bring * Bachelor's degree in Engineering or a related field, or equivalent experience. * 5+ years of quality experience in a precision machining environment. * Working knowledge of ISO 9001 and 13485 standards. * Proficiency with inspection tools: calipers, micrometers, comparators, etc. * Strong communication, problem-solving, and organizational skills. * Willingness to work 50+ hours weekly, including occasional weekends. Bonus Points CNC/Swiss machining experience Quality certifications (e.g., CQT, CQI, Six Sigma) Acero Precision is proud to be an Equal Opportunity Employer. Acero Precision does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need. * Principals only. Recruiters please do not apply on behalf of your candidates to Acero Precision job posts. All applications and/or contact information submitted are kept on file and are the property of Acero Precision. Please note recruiting fees will not be honored with candidate applications submitted by recruiters. Make Our Mission Your Mission!

Job Description Now Hiring!! Company: Acero Precision Salary Information: $20.00 - $26.00 ???? Full-Time | On-site | Some Weekend Availability Why Join the Acero Precision Team? Acero Precision, located in West Chester, PA is an industry leading Medical Device contract manufacturer producing the very best in precision engineered components. To succeed in today's manufacturing industry- with its demands to serve customers in a truly global environment- we rely on three vital resources: the newest engineering technologies, quality systems, and most importantly highly-skilled people. We invite you to become a member of an organization that has established an outstanding reputation for quality and excellence. Highly competitive wages, a state-of-the-art-facility, an emphasis on work/life balance, career advancement, a team-centered workplace culture, and the opportunity to be your best is waiting for you at Acero Precision. Why You'll Love Working Here We offer defined career advancement opportunities for employees seeking long-term growth within our organization Competitive premium pay for 1st shift Overtime hours available Weekend premiums available Multiple health insurance plans, including a no-cost HSA health plan for eligible employees. Affordable Dental, and Vision benefits 100% Paid Uniforms 401k with employer match Paid training on advanced CNC programming software This role offers 100 hours of PTO in the first year, with PTO increasing at defined service milestones. 7 paid holidays every year State-of-the-art, climate-controlled facility with 5-axis and Swiss turning Employee Assistance Program (EAP) offering free confidential support services to employees and their families. Access to our Wellness Coach Program Be the eyes of precision. Join a team where quality is more than a goal-it's a way of life. Are you a detail-oriented quality professional with a passion for excellence in manufacturing? Acero Precision is seeking a dedicated Quality Control Roving Inspector to uphold and elevate our industry-leading standards. What You'll Do As a Quality Control Roving Inspector, you'll be the frontline advocate for our customers-ensuring every part meets our rigorous quality standards. Your day-to-day will include: Conducting in-process and final inspections across multiple machines and cells. Collaborating with machinists, production team leads, and quality controllers to identify and resolve non-conformances. Maintaining ISO 9001 and ISO 13485 compliance. Coaching Final Inspectors and training production staff on inspection tools and quality processes. Leading by example in inspection practices and quality improvement. Your Impact Ensure product accuracy and compliance using the Monitor Report and Sponge Data System. Maintain inspection equipment and accurate calibration records. Act as a quality “help desk” for operators and a mentor for new team members. Support continuous improvement by generating NCRs and developing corrective actions. What You Bring Bachelor's degree in Engineering or a related field, or equivalent experience. 5+ years of quality experience in a precision machining environment. Working knowledge of ISO 9001 and 13485 standards. Proficiency with inspection tools: calipers, micrometers, comparators, etc. Strong communication, problem-solving, and organizational skills. Willingness to work 50+ hours weekly, including occasional weekends. Bonus Points CNC/Swiss machining experience Quality certifications (e.g., CQT, CQI, Six Sigma) Acero Precision is proud to be an Equal Opportunity Employer. Acero Precision does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need. *Principals only. Recruiters please do not apply on behalf of your candidates to Acero Precision job posts. All applications and/or contact information submitted are kept on file and are the property of Acero Precision. Please note recruiting fees will not be honored with candidate applications submitted by recruiters. Make Our Mission Your Mission!

Now Hiring!! Company: Acero Precision Salary Information: $20.00 - $26.00 🕒 Full-Time | On-site | Some Weekend Availability Why Join the Acero Precision Team? Acero Precision, located in West Chester, PA is an industry leading Medical Device contract manufacturer producing the very best in precision engineered components. To succeed in today's manufacturing industry- with its demands to serve customers in a truly global environment- we rely on three vital resources: the newest engineering technologies, quality systems, and most importantly highly-skilled people. We invite you to become a member of an organization that has established an outstanding reputation for quality and excellence. Highly competitive wages, a state-of-the-art-facility, an emphasis on work/life balance, career advancement, a team-centered workplace culture, and the opportunity to be your best is waiting for you at Acero Precision. Why You'll Love Working Here We offer defined career advancement opportunities for employees seeking long-term growth within our organization Competitive premium pay for 1st shift Overtime hours available Weekend premiums available Multiple health insurance plans, including a no-cost HSA health plan for eligible employees. Affordable Dental, and Vision benefits 100% Paid Uniforms 401k with employer match Paid training on advanced CNC programming software This role offers 100 hours of PTO in the first year, with PTO increasing at defined service milestones. 7 paid holidays every year State-of-the-art, climate-controlled facility with 5-axis and Swiss turning Employee Assistance Program (EAP) offering free confidential support services to employees and their families. Access to our Wellness Coach Program Be the eyes of precision. Join a team where quality is more than a goal-it's a way of life. Are you a detail-oriented quality professional with a passion for excellence in manufacturing? Acero Precision is seeking a dedicated Quality Control Roving Inspector to uphold and elevate our industry-leading standards. What You'll Do As a Quality Control Roving Inspector, you'll be the frontline advocate for our customers-ensuring every part meets our rigorous quality standards. Your day-to-day will include: Conducting in-process and final inspections across multiple machines and cells. Collaborating with machinists, production team leads, and quality controllers to identify and resolve non-conformances. Maintaining ISO 9001 and ISO 13485 compliance. Coaching Final Inspectors and training production staff on inspection tools and quality processes. Leading by example in inspection practices and quality improvement. Your Impact Ensure product accuracy and compliance using the Monitor Report and Sponge Data System. Maintain inspection equipment and accurate calibration records. Act as a quality “help desk” for operators and a mentor for new team members. Support continuous improvement by generating NCRs and developing corrective actions. What You Bring Bachelor's degree in Engineering or a related field, or equivalent experience. 5+ years of quality experience in a precision machining environment. Working knowledge of ISO 9001 and 13485 standards. Proficiency with inspection tools: calipers, micrometers, comparators, etc. Strong communication, problem-solving, and organizational skills. Willingness to work 50+ hours weekly, including occasional weekends. Bonus Points CNC/Swiss machining experience Quality certifications (e.g., CQT, CQI, Six Sigma) Acero Precision is proud to be an Equal Opportunity Employer. Acero Precision does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status, or any basis covered by appropriate law. All employment is decided on the basis of qualifications, merit and business need. *Principals only. Recruiters please do not apply on behalf of your candidates to Acero Precision job posts. All applications and/or contact information submitted are kept on file and are the property of Acero Precision. Please note recruiting fees will not be honored with candidate applications submitted by recruiters. Make Our Mission Your Mission!