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Job Description About Forge: Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most. Forge is based in Columbus, Ohio, in a 200,000 square foot facility known affectionately by team members as, the Hearth. The Hearth, is a custom-designed cGMP facility dedicated to AAV manufacturing and hosts scalable, end-to-end manufacturing services. Job Title: Senior Associate Scientist Responsibilities: • Assist with overall maintenance of the production and testing facilities. This includes but may not be limited to performing quality systems checks, buffer preparation, autoclaving of media, packing of biohazard material, monitoring or sanitizing equipment, preparing facility for production campaigns, and periodic cleaning of incubators, centrifuges, FPLCs, biological safety cabinets (BSCs), and other equipment., • Culturing cells, performing transfections and/or infections with seed vectors, harvesting and lysing cells, and purifying vectors using density gradients, FPLC, or other techniques, • Provide support in the receipt and distribution of incoming raw materials for research, preclinical, and clinical manufacturing., • Unpack reagents, maintaining proper cold storage, restock supplies in storerooms or laboratories., • Quarantine and prepare incoming raw materials intended for preclinical or clinical manufacturing for inspection and release., • Assist in maintaining proper inventories of raw materials and consumables., • Prepares formulations and raw materials as specified in protocols without the introduction of contaminants., • Prepare sterile reagents as dictated by procedures or management by filtration or steam autoclaving., • Maintains clean work environment in all work areas., • Reports any discrepancies from protocols/study procedures or any materials preparation problems to management., • Delivering results in a high paced environment, • Bachelor's degree in Biology, Molecular Biology, Virology, Biochemistry or related discipline, • Practical experience with FPLC is required, ideally with lab, pilot, and large-scale systems., • Experience with other aspects of downstream purification (e.g. – clarification/filtration, TFF, etc.), • Experience with purification of vaccines or viral vectors is preferred., • Experience with production of biologics and performing bioassays is preferred., • Must be self-motivating, organized and proactive,, • Strong technical aptitude including demonstrated experience in applying scientific reasoning to solve complex problems., • Ability to work hours necessary to support production and/or product transfer activities. This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Competitive paid time off plan Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Onsite fitness facility Professional & Personal development resources

Job Description About Ohio Dominican University Founded by the Dominican Sisters of Peace in 1911, Ohio Dominican University is the only Catholic university in central Ohio. We are dedicated to academic excellence, teaching and to living out the Gospel supported by the four pillars of Dominican tradition: Prayer, Study, Community, and Service. Our Catholic identity is a call to action and service to all humanity that is faithful to the past and open to the future. About the Role Ohio Dominican University's Division of Mathematics, Computer, and Natural Sciences seeks adjunct faculty members to teach Chemistry Lab. The Division offers undergraduate and graduate programs in Biology, Chemistry, Environmental Science, Exercise Science, and Physician Assistant Studies. Qualified candidates will possess a minimum of a Master's degree in an associated field of biology with Ph.D. preferred. Previous experience teaching in higher education a plus. Ohio Dominican University is continually searching for part-time faculty members to teach in a variety of academic disciplines. We maintain a file of potential candidates that we review when a specific need arises. We contact candidates when we find a match and keep these positions continually posted so that we can maintain an active and up to date pool. Ohio Dominican offers classes in the daytime, at night, and online in a variety of academic disciplines. Successful candidates will display a willingness to support the University's Catholic and Dominican identity and mission. Ohio Dominican University is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees, as we respect and seek to empower each individual and support the various cultures, perspectives, skills and experiences within our workforce. Job Posted by ApplicantPro

Job Description R&D Quality Specialist The R&D Quality Specialist plays a critical role in Process Development (PD) for maintaining quality throughout the product development lifecycle by implementing quality control measures, actively managing documentation and samples, and ensuring compliance with regulations and company guidelines, guaranteeing that process development procedures and products meet established quality standards. About The Role: The R&D Quality Specialist (Process Development and Late-Stage Process Characterization) role focuses on ensuring product quality throughout the development lifecycle by developing training, implementing quality control measures, and collaborating with cross-functional teams while adhering to regulatory standards and company guidelines. This position will be responsible for training the team on process characterization procedures and SOPs while ensuring that activities occur in an efficient and GDP-compliant manner. The R&D Specialist will work with the Quality department and the Process Development department, ensuring cutting-edge technologies are employed to maintain the highest quality standards for gene therapy products. What You'll Do: • Work closely with process development research scientists to ensure adherence to quality standards and regulatory requirements., • Know how to use our electronic lab notebook system, Benchling, documentation and training system, Quality Management System (Veeva), and our equipment management system (Blue Mountain Regulatory Asset Manager)., • Create a phase-appropriate quality plan in collaboration with the process development team, outlining critical quality attributes, acceptance criteria and testing protocols., • Maintain accurate and detailed documentation of all process characterization activities., • Provide compliance oversight by ensuring adherence to relevant regulatory standards (e.g., FDA, GDP) throughout the process development and characterization phase., • Provide training to PD team members on quality standards and procedures. Ensure the PD group is properly trained including but not limited to appropriate SOPs and work instructions., • Ensure that the equipment that PD group uses is properly inspected, calibrated, and maintained to a level of quality appropriate for process characterization, and that equipment readiness is properly scheduled and documented in BMRAM., • Ensure data used for process characterization is accurate and controlled., • Ensure samples used for process characterization are inventoried accurately and controlled., • Ensure that changes in the PD space, equipment, facility, or procedures are properly documented and controlled as appropriate when relevant to process characterization., • Review study protocols, and technical reports and approve documentation associated with in-process, final product, and stability testing., • Provide technical guidance and mentorship to junior team members, promoting their personal growth and skill development., • Compile data with minimal oversight, reviewing reports, and performing the analysis and interpretation of assay results., • Support regulatory and client inspections and internal audits of lab quality systems., • Manage tracking and trending of in-process and final product testing data in the development space. What You'll Bring: • Bachelor's, Master's, or PhD or in a relevant scientific field (e.g., biology, biochemistry, molecular biology). Advanced degree preferred., • SME for quality processes and systems., • Proven ability to perform quality reviews on documentation and processes., • Skilled at organization and managing multiple projects simultaneously., • Strong analytical and data interpretation skills to assess and drive quality improvement through the analysis of quality metrics and performance data., • Robust understanding of regulatory requirements as they pertain to process characterization., • Excellent communication and collaboration skills to work effectively with cross-functional teams., • Experience in leading, mentoring, and guiding junior team members., • Strong understanding and experience in Electronic Quality Management Systems (EQMS), Laboratory Information Management Systems (LIMS), and regulatory requirements relevant to the industry., • Experience with electronic Quality Management Systems (EQMS) and laboratory Information Management Systems (LIMS). Work Environment and Physical Demands This position works in both a laboratory environment and a typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned. Forge Biologics is an equal-opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Competitive paid time off plan Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Onsite fitness facility Professional & Personal development resources

Job Description About Forge Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most. Forge is based in Columbus, Ohio, in a 200,000 square foot facility known affectionately by team members as, the Hearth. The Hearth, is a custom-designed cGMP facility dedicated to AAV manufacturing and hosts scalable, end-to-end manufacturing services. About the role: The Laboratory Coordinator, QC Analytical Testing is responsible for day-to-day coordination of laboratory operations to ensure that QC spaces are well-maintained, and compliant with GMP expectations. Key responsibilities include oversight of laboratory cleaning and 5S activities, support for equipment calibration and preventive maintenance (PM), pipette verifications, and sample shipment for external testing. This role will work closely with the Laboratory Manager and QC staff to support smooth laboratory operations and execution of GMP testing. What you'll do: • Assist with scheduling for release and stability testing across all client programs for AAV, plasmids, and cell banks, • Coordinate and/or perform pipette verifications, equipment calibrations, and equipment preventive maintenance with internal teams and external vendors., • Maintain logs and records of completed PM and calibration events in compliance with GMP documentation requirements., • Coordinate with QC analysts to ship samples for external contract laboratory testing, • Support implementation and enforcement of 5S and cleanliness standards across all QC lab spaces., • Perform routine walkthroughs to support the AOP program, ensuring labs are organized, stocked, and audit ready., • Facilitate material ordering to maintain appropriate warehouse stock for lab materials, • Coordinate general lab cleaning schedules and liaise with facilities or janitorial staff as needed., • Partner with QC staff to ensure proper sample receipt, labeling, storage, and documentation of samples and reagents., • Support organization of stability and release samples in monitored cold storage units., • Coordinate logistics for QC lab training, including scheduling, tracking completions, and maintaining training files., • Partner with the Laboratory Manager and other QC leaders to support onboarding of new analysts., • Assist with maintaining laboratory notebooks, equipment binders, and tracking logs., • Collaborate with Supply Chain, Facilities, and EHS to ensure timely support of laboratory needs., • Serve as a liaison for basic lab operations issues and escalate concerns to the Laboratory Manager as appropriate. What you'll bring: • Bachelor's degree in scientific discipline (Biology, Chemistry, or related field) or equivalent experience., • 1–3 years of experience in a GMP laboratory or QC environment preferred., • Working knowledge of laboratory equipment, maintenance practices, and GMP documentation., • Familiarity with calibration, PM procedures, or pipette verification is a plus., • Strong organizational and time management skills with attention to detail., • Proficient in Microsoft Office (Excel, Outlook, Word); experience with LIMS, ELN, or QMS systems is a plus., • Effective verbal and written communication skills. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Competitive paid time off plan Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Onsite fitness facility Professional & Personal development resources

Job Description About Forge At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from idea into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins. Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen — you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases. About The Role The Lead, GMP Manufacturing Support plays a critical role in maintaining and supporting GMP-compliant cleanroom environments (ISO 5–8 / Grade A–D) essential for the production of viral vector products. This role is responsible for overseeing contamination control strategies, coordinating day-to-day operations, and leading a team of personnel responsible for cleaning and GMP support activities. The ideal candidate brings a strong understanding of aseptic practices, contamination control, and GMP regulations, along with the leadership skills to promote a high standard of compliance, safety, and operational excellence. What You'll Do: • Lead the cleanroom cleaning team to perform routine and non-routine cleaning operations per SOPs and GMP requirements., • Oversee cleaning of aseptic fill areas, upstream/downstream suites, airlocks, corridors, and equipment in accordance with validated procedures., • Perform verification of cleaning and sanitization activities and ensure accurate documentation; perform the manufacturing review of logbooks and associated documents; and resolve out-of-trend situations promptly., • Act as SME for cleanroom behaviors, gowning, and contamination control best practices., • Support deviation investigations, root cause analysis, and CAPA development related to cleaning issues or contamination events., • Plan and assign daily tasks for effective resource utilization, collaborating with planning, and maintaining schedules., • Train and coach new and existing staff on cleaning techniques, gowning, aseptic behavior, and cleanroom discipline., • Collaborate with Manufacturing, Quality Assurance, Quality Control, Environmental Monitoring, and Facilities & Engineering to resolve issues and drive continuous improvement., • Support cleaning validation and requalification activities for classified spaces and equipment., • Manage cleanroom inventory to ensure availability of common-use items and uninterrupted operations., • Oversee consumable expiration tracking and storage, implementing rotation protocols and guiding technicians to meet operational and regulatory standards., • Other responsibilities may include supporting tubing sets preparation, process improvement initiatives and collaborating with cross-functional teams to ensure the efficient production of gene therapy products., • Associate's or Bachelor's degree in a relevant scientific field (e.g., Biology, Chemistry, Engineering) or equivalent experience., • Minimum 5 years of experience in a GMP manufacturing environment, preferably in biologics, gene therapy, or sterile manufacturing., • Demonstrated leadership skills with experience overseeing or mentoring team members., • Strong understanding of cleanroom classifications, contamination control principles, and GMP regulations., • Experience working within a Quality Management System (QMS)., • Proven experience overseeing manufacturing support functions (e.g., cleaning and sanitization, tube set building and setup)., • Excellent communication, organization, and problem-solving skills., • Exceptional computer skills, prior experience with a manufacturing software (e.g., MRP or ERP System), and ability to use data analytics to drive process improvements and results., • Flexibility to work in shifts, including weekends and holidays, as required by manufacturing production schedules., • Ability to work in classified cleanroom environments (ISO 5–8 / Grade A–D) for extended periods while fully gowned in aseptic/sterile PPE attire. Physical Requirements: This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed such as cleanroom gowning. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Forge Your Future with Us What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together. At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us. If you're ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. • Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents, • Competitive PTO (plus 14 paid company holidays), • Annual bonus for all full-time employees, • 401(K) company match, • Fully-stocked kitchen with free food/drinks, • Onsite gym, • 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care, • Employee Assistance Program, • Wellness benefits (financial planning services, mental health counseling, employer paid disability), • Professional & Personal development resources

Job Description Company Overview At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from idea into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you're driven by purpose and excited to make a tangible impact, this is where your journey begins. Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won't just watch innovation happen — you'll be part of it. Whether you're scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you'll play a key role in bringing hope to patients with genetic diseases. About the Role As a Technical Writer, you will play a key role in developing clear, accurate, and well-organized documentation to support the Technical Operations teams at our Columbus facility. In this cross-functional role, you'll partner with subject matter experts and fellow technical writers to create critical procedural documents that are both effective and compliant—ensuring alignment with Good Manufacturing Practices (GMP), regulatory standards (e.g., FDA), and internal quality requirements. What You'll Do • Write, edit, and maintain a variety of technical documents, including standard operating procedures (SOPs), work instructions (WIs), and batch records., • Organize and streamline written procedures and forms to improve usability and comprehension., • Collaborate with scientists, engineers, and subject matter experts (SMEs) to gather detailed technical information through interviews and hands-on observation., • Translate complex technical concepts into clear, accessible content tailored to specific audiences and applications., • Partner with cross-functional teams to gain a comprehensive understanding of the company's manufacturing processes, technologies, and products., • Review and revise documents for grammatical accuracy, technical precision, regulatory compliance, and consistency with internal quality standards., • Maintain consistent formatting, structure, terminology, and tone across all document types in accordance with established templates and style guidelines., • Identify redundancies, content gaps, and inconsistencies in documentation—proposing improvements based on research and SME input., • Enhance documentation with visual aids, such as photographs, diagrams, process flows, charts, maps, and other illustrations, to clarify complex procedures., • Track documentation throughout its lifecycle, facilitating collaboration among applicable departments regarding ongoing document projects., • Study and interpret drawings, specifications, mockups, and product samples to accurately develop procedures for relevant production methods and technologies., • Extract key information from manufacturer manuals, trade catalogs, and other resources to support operational and maintenance documentation for onsite equipment., • Bachelor's degree in a relevant writing, scientific, or technical field (e.g., English, Biology, Chemistry, Engineering, Pharmaceutical Science), or equivalent experience., • 0–2 years of experience in technical writing or a related role, with demonstrated skills in writing, copy editing, and formatting documents—particularly with scientific or technical content., • Strong written and verbal communication skills, with the ability to engage effectively with both technical and non-technical audiences., • Ability to translate complex technical concepts into clear, concise, and user-friendly content., • Self-driven and highly motivated, capable of working independently while effectively collaborating with cross-functional teams., • Ability to manage multiple projects in a fast-paced, dynamic environment—adapting quickly to evolving priorities and timelines., • Excellent organizational and time-management skills, with the ability to balance immediate demands with long-term project goals., • Strong attention to detail paired with an inquisitive, knowledge-seeking mindset., • Proficiency in Microsoft Office Suite (Outlook, Excel, Word, PowerPoint), with the ability to quickly learn new software and tools., • Familiarity with document management systems, such as Veeva Vault, is a plus., • Experience with photo-editing software and diagramming tools is desirable but not required. This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Forge Your Future with Us What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together. At Forge, your growth matters. We're committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we're proud to see team members grow with us. If you're ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. • Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents, • Competitive PTO (plus 14 paid company holidays), • Annual bonus for all full-time employees, • 401(K) company match, • Fully-stocked kitchen with free food/drinks, • Onsite gym, • 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care, • Employee Assistance Program, • Wellness benefits (financial planning services, mental health counseling, employer paid disability), • Professional & Personal development resources

Job Description Job Summary: We are seeking a motivated and detail-oriented Quality Intern to join our team for the spring semester. The ideal candidate will assist in ensuring that our products/services meet or exceed industry standards and customer expectations. Under the guidance of our experienced quality professionals, the Quality Intern will gain hands-on experience in quality assurance and quality control. Duties/Responsibilities: • Support investigations into deviations, out-of-specification results, and non-conformances by collecting data, conducting root cause analysis, and assisting in the development of corrective and preventive actions (CAPAs), • Participate in the review and approval of manufacturing and testing documentation, including batch records, protocols, specifications, and standard operating procedures (SOPs), to ensure compliance with regulatory requirements and internal quality standards., • Collaborate with cross-functional teams, including manufacturing, research and development, and regulatory affairs, to address quality-related issues and implement process improvements., • Support cGMP training initiatives by participating in training sessions and assisting in the development of training materials for employees across various departments., • Create and maintain log books and documentation systems in compliance with cGMP requirements, ensuring accurate and timely recording of critical manufacturing, testing, and quality control data., • Regularly review and verify entries in log books to ensure completeness, accuracy, and compliance with established procedures and regulatory requirements., • Coordinate the archival and retention of log books and documentation records according to cGMP guidelines and company policies, facilitating efficient retrieval and audit trails. Required Skills/Abilities: • Strong attention to detail and commitment to upholding the highest standards of product quality and regulatory compliance., • Willingness to learn and develop new skills in pharmaceutical quality assurance, cGMP compliance, and related areas., • Value patient safety and demonstrate a commitment to upholding the highest standards of product quality and regulatory compliance., • Ability to complete a project that contributes to the understanding of pharmaceutical quality assurance, cGMP compliance, or related topics, which can also fulfill academic requirements for the intern's school program. Education and Experience: • Currently enrolled in a relevant field (e.g., quality management, pharmacy, pharmaceutical sciences, chemistry, biology, biochemistry, biomedical, or related disciplines)., • Sophomore, Junior, Senior, or graduate level., • Excellent oral communication and technical writing skills., • Microsoft word and excel experience. Physical Requirements: • Prolonged periods of sitting at a desk and working on a computer., • Must be able to lift up to 50 pounds at a time.

Job Description As a member of the Analytics/Gene Therapy group, this position will be responsible for performing analytical assays supporting the evaluation of early-stage production processes for the AAV vector research pipeline and supporting AAV product testing. The individual may collaborate with Process Development and additional internal and external stakeholders to ensure the development and transfer of robust analytical methods. The Opportunity to Make a Difference · Perform analytical assays to support production, purification, and comparability of AAV gene therapy products using qPCR, ddPCR, BLI, DLS, ELISA, and other general laboratory techniques • Work seamlessly with cross functional stakeholders to help advance the AAV vector production portfolios, • Participate in project related teams and other internal/external collaborations, • Ensure that scientific and technical challenges are resolved in a timely manner, • Maintain all appropriate laboratory records, • Perform routine data analysis for use in presentations, publications, and internal reports, • Contribute to a safe, efficient, and effective environment with personal accountability, • Perform other related duties as required More about You • Degree in Biology, Biotechnology, Molecular Biology, Virology, or a related field, • BS degree (or equivalent) with at least 1-2 years of relevant experience preferred, • Working experience in gene therapy and/or viral vector biology is preferred, • Experience with at least 2 techniques – qPCR, ddPCR, BLI, DLS, and ELISA is desirable, • Attention to details is a must, • Strong organizational skillsCompany DescriptionBeacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations. Beacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting & Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S. Whether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.Beacon Hill Life Sciences, a part of BHSG, a specialty division, is a national staffing organization that provides contract, direct (permanent), FSP/outsourcing and consulting to pharmaceutical, medical device, biotech and contract research organizations.\r\n\r\nBeacon Hill Life Sciences places contractors in all 50 states by seamlessly coordinating recruiting resources in local and regional markets with Beacon Hill Life Sciences National Recruiting & Delivery, a dedicated national recruiting team that focuses exclusively on national accounts, supporting regional recruiting operations and delivering contractors to all markets in the U.S.\r\n\r\nWhether start-ups or the Fortune 500, the public or private sector, Beacon Hill Life Sciences matches world class talent with exceptional opportunities.

Job Description Summary: We are currently seeking an Associate Scientist II, Process Development - Downstream to join the Forge Biologics team. This is an exciting opportunity to assist in the execution of laboratory experiments and protocols for downstream process development efforts. The candidate will assist in process development protocols/studies to optimize procedures for unique viral vector platform process and to assist in the transfer of client programs. The Associate Scientist will work to meet production goals, notify management of any potential delays in the schedule, and make recommendations to resolve the issues. What You'll Do: • Assist with overall maintenance of the production and testing facilities. This includes but may not be limited to performing quality systems checks, buffer preparation, autoclaving of media, packing of biohazard material, monitoring or sanitizing equipment, preparing facility for production campaigns, and periodic cleaning of incubators, centrifuges, FPLCs, biological safety cabinets (BSCs), and other equipment., • Culturing cells, performing transfections and/or infections with seed vectors, harvesting and lysing cells, and purifying vectors using density gradients, FPLC, or other techniques, • Provide receipt and distribution of incoming raw materials for research, preclinical, and clinical manufacturing., • Unpack reagents, maintaining proper cold storage, restock supplies in storerooms or laboratories., • Quarantine and prepare incoming raw materials intended for preclinical or clinical manufacturing for inspection and release., • Maintain proper inventories of raw materials and consumables., • Prepare formulations and raw materials as specified in protocols without the introduction of contaminants., • Prepare sterile reagents as dictated by procedures or management by filtration or steam autoclaving., • Report any discrepancies from protocols/study procedures or any materials preparation problems to management., • Package and ship finished product to clients in accordance with procedures and regulations., • Bachelor's Degree in Biology, Molecular Biology, Virology, Biochemistry or related discipline, • Practical experience with FPLC or other chromatography systems., • Must be self-motivating, organized, and proactive., • Strong technical aptitude including demonstrated experience in applying scientific reasoning to solve complex problems., • Ability to work hours necessary to support production and/or product transfer activities., • Master's Degree in Biology, Molecular Biology, Virology, Biochemistry, or related discipline., • Experience with pilot and large-scale FPLC systems This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Competitive paid time off plan Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Onsite fitness facility Professional & Personal development resources

Job Description Duties and Responsibilities Primary Job Functions: · Prepare human tissue for microscopic examination and diagnosis by a Pathologist. · Perform technical skills that may include accessioning, grossing, processing, embedding, microtomy, staining, special staining, and coverslipping. · Ensure proper specimen handling and specimen transfer. · Package slides for review by a Pathologist. · File, retrieve, and distribute blocks, slides, and pathology reports. · Responsible for maintaining lab equipment and QC/QM documents. · Perform lab tasks that aide in the day to day operation of lab. · Inform supervisor when lab supplies are getting low. · Responsible for maintaining a safe environment according to the proper regulations. Secondary Job Functions: · Act as a leader and mentor to other laboratory personnel. · Act as a liaison and resource between lab, centers, and pathology group in regards to patient specimens. · Adhere to CLIA, HIPAA, Safety, OSHA and state regulations. · Any other tasks as requested by the pathologist, physician & human resource manager2. Knowledge, Skills, and Abilities · Thorough knowledge of tissue processing principles and functionality of processing instruments. · In depth knowledge of the principles of embedding, cutting, staining & the functionality of related instruments. · Ability to work within a strict deadline (works well under pressure). · Ability to perform detailed & accurate work. · Good communication skills, both in writing & speaking. · Knowledge of medical terminology. · Knowledge of modern office procedures and methods including telephone communications, office systems, and record keeping. · Knowledge of modern business communication, including style and format of letters, memoranda, minutes, and reports. · Skill to use a personal computer and various software packages. · Ability to establish priorities, work independently, and proceed with objectives with little supervision. · Ability to handle and resolve problems. · Fluent in English. · Ability to maintain a neat appearance and professional demeanor. Credentials and Experience · Associate degree or higher (with a minimum of 60 semester hours and 24 semester hours in chemistry and biology) in a chemical, physical, biological or clinical laboratory science, or in medical technology - preferred · May have completed a clinical laboratory training program approved or accredited by the NAACLS or the ABHES, or other organization approved by HHS - preferred · HT or HTL, ASCP certification (American Society of Clinical Pathologists) - preferred · At least 3 years’ experience working in the medical field (office, clinical, or hospital) - preferred Special Requirements · Must have good precision, hand-eye coordination & manual dexterity · Flexibility in working hours; willingness to work occasional over time when needed · Willingness to learn new tasks, be flexible with work load, assist others when needed Physical Demands · Must be able to sit (frequently), stand (frequently), walk (frequently), stoop (frequently), bend over (frequently) · Must be able to independently lift 25 pounds (occasionally) · Applies the principles of body mechanics in lifting or moving equipment (occasionally) Work Environment · Medical office and lab · Will work with chemicals Ohio Gastroenterology Group offers a nice life/work balance and a great benefits package that includes: • Medical, dental and vision coverage- benefits are effective the first of the month following 30 days of employment, • Company paid life insurance and short term disability, • Generous paid time off plans (vacation, sick and personal), • 7 paid holidays, • Two retirements plans:, • 401(k) plan that offers a 3% safe harbor contribution with immediate vesting as well as annual profit sharing contributions., • Cash balance pension plan – company contributes 2.5% and offers full vesting after 3 years of employment., • Tuition reimbursement programs, • Employee appreciation programs, • Uniform reimbursement programs, • Growth opportunities, • Learning and development training Apply now to join a great company!

Job Description Job Title: QC Analyst II (Environmental Monitoring)Position Summary: Forge Biologics is seeking a Quality Control Analyst II (Environmental Monitoring) to join our growing team. This role is a key contributor to the Environmental Monitoring (EM) program, supporting the aseptic manufacturing environment and ensuring compliance with GMP standards. The QC Analyst II will lead EM initiatives, mentor junior analysts, and drive continuous improvement in EM practices and systems. This position requires a strong technical background, leadership capabilities, and a proactive approach to problem-solving in a fast-paced GMP environment. Key Responsibilities: • Lead and coordinate EM sampling activities, ensuring adherence to GMP principles and regulatory requirements., • Perform advanced environmental monitoring including viable and non-viable air, surface, and personnel monitoring in classified cleanroom areas., • Analyze and trend EM data using statistical software (e.g., JMP, LIMS) and generate reports for internal and regulatory use., • Lead and support complex investigations, including root cause analysis for OOS and deviations, and implement CAPAs., • Mentor and train junior QC Analysts in EM techniques, aseptic behavior, and GMP documentation practices., • Support and lead EM-related activities during Media Fills/Process Simulations and EMPQ., • Collaborate with cross-functional teams including Manufacturing, QA, and Facilities to ensure environmental control and compliance., • Author and review SOPs, protocols, and technical reports related to EM., • Participate in audits and inspections, providing subject matter expertise on EM practices and data., • Drive continuous improvement initiatives within the EM program, including implementation of new technologies and process optimizations.Qualifications:, • Bachelor's degree in Microbiology, Biology, or a related scientific field required., • 2+ of experience in a GMP-regulated QC or EM environment., • Demonstrated expertise in aseptic technique and cleanroom behavior., • Strong understanding of FDA, EMA, and ICH regulations related to environmental monitoring and GMP compliance., • Proficiency in data analysis tools (e.g., JMP, LIMS) and Microsoft Office Suite., • Excellent communication, organizational, and leadership skills., • Ability to work independently and manage multiple priorities in a dynamic environment., • Willingness to work flexible hours to support production schedules and EM requirements., • Ability to work in cleanroom environments with appropriate PPE and gowning.Preferred Skills:, • Experience leading EM programs or projects., • Prior involvement in regulatory inspections or audits., • Familiarity with risk assessment tools and quality systems.

Job Description Summary: We are currently seeking a Quality Control (QC) Analyst I, Analytical Testing, to join the Forge Biologics team. This role will perform characterization and release testing QC for AAV vectors, plasmids, and cell banks, while maintaining meticulous records and ensuring the accuracy of data for all products. This position is responsible for routine test method execution, assisting in method qualification and validation, instrumentation troubleshooting, and data analysis. The ideal candidate will be skilled in technical problem-solving and laboratory techniques to support our growth in the Gene Therapy sector. The Analyst I role offers an excellent opportunity to gain hands-on experience in the field of gene therapy. Shift Requirement: This position is intended for Second Shift. However, to ensure a successful onboarding experience, the selected candidate will begin on First Shift for the initial training period, which is expected to last several months. After training is complete, the role will transition to its regular Second Shift schedule. Responsibilities: • Performs in process and release testing for our most advanced AAV-based (viral vector) therapeutic candidates generated from the PD, research, and GMP laboratories, • Performs raw materials testing to ensure they conform to manufacturer specifications, • Provides Biochemistry and/or Molecular Biological expertise for the Forge GMP facility, • Executes the procedures designed to demonstrate safety efficacy, and purity of the drug products under evaluations, • Performs technical writing, routine testing, and all other associated activities., • Responsible for training, sampling, routine testing, method qualification/validations, and investigations., • Adheres to all GMP requirements, maintains a solid understanding of FDA/EMEA regulations, and interacts/communicates with Quality Management., • Supports the QC management team for activities related to interviewing and training of employees, compliance with GMP, and identifying and implementing corrective and preventive actions., • May be responsible for upstream (cell culture and virus production) and downstream (harvest and purification) testing activities to support a singular "platform" process for the entire AAV program portfolio Requirements: • Bachelor's degree in biology, molecular biology, virology, biochemistry or related discipline with 0-4 years of related experience, • Experience in qPCR, ELISA, Western Blot, Cell Culture, and immunoassays is preferred, • Proficiency with Microsoft Office, • Excellent verbal and written communication skills, • Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members, • Ability to work with a high attention to detail, • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area. Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. Life at Forge We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge's core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by. HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge's vision, mission and goals. We've Got You Covered We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents Competitive paid time off plan Annual bonus for all full-time employees 401(K) company match Fully-stocked kitchen with free food/drinks 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care Employee Assistance Program Wellness benefits (financial planning services, mental health counseling, employer paid disability) Onsite fitness facility Professional & Personal development resources

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. Regulatory Affairs Specialist Working at Abbott Our nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to: • Career development with an international company where you can grow the career you dream of., • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year., • An excellent retirement savings plan with a high employer contribution, • Tuition reimbursement, the ___ student debt program, and ___ education benefit - an affordable and convenient path to getting a bachelor’s degree., • A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune., • A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists. The Opportunity Our location in Columbus, OH or Abbott Park, IL currently has an opportunity for a Regulatory Affairs Specialist. WHAT YOU’LL DO Primary Function/Primary Goals/Objectives: • Provide support for the regulatory department to ensure efficient and compliant business processes and environment., • Execute regulatory tasks and exercise influence generally at the middle management level., • Responsible for compliance with applicable Corporate and Divisional Policies and procedures and Regulatory SOPs., • Support maintenance of Regulatory Affairs quality system documentation, • Provide regulatory input to product lifecycle planning., • Assist in the development of regulatory strategy and update strategy based upon regulatory changes., • Interpret and apply regulatory requirements., • Understand the business environment and relate extensive knowledge of internal and external activities to trends; Determine trade issues to anticipate regulatory obstacles., • Participate in risk-benefit analysis for regulatory compliance., • Plan and organize project assignments of substantial variety and complexity; initiate and/or maintain schedule for projects and project milestones., • Maintain regulatory data in electronic systems., • Depending on specific role, the Regulatory Affairs Specialist may be involved in various regulatory activities (review of documentation; regulatory submissions and follow-up; evaluation of product and manufacturing changes for regulatory implications; maintaining annual licenses, registrations, listings with regulatory IT systems management and data analytics. Influence/Impact/Leadership: • May provide direction and guidance to exempt and/or skilled non-exempt levels of employees;, • Participate in the development of less experienced staff by setting an example, providing guidance, and offering counsel., • Interface with a variety of management levels on significant matters, often requiring the coordination of activity across organizational units., • Perform work under minimal supervision and may independently determine and develop approach to solutions. Required Qualifications Required • Bachelor's degree (or equivalent) is required - preferred area of focus in science (biology, chemistry, nutrition, dietetics, microbiology, immunology, medical technology, pharmacy, and pharmacology), math, engineering, or medical fields. Preferred • 2-3 years of experience in a regulated industry (e.g., nutritionals, medical products). Regulatory area is preferred, but may consider quality assurance, research and development/support, scientific affairs, operations, or related area., • Note: Higher education may compensate for years of experience or vice versa., • This position does not require previous regulatory experience. Principles and requirements of regulatory submissions, advertising/promotion, and labeling. • Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Accountability/Scope: • Execute and manage regulatory activities., • Ability to work independently and prioritize work to meet deadlines, • Resourceful, ability to use resources to solve problems, • May lead a departmental project team. MISC: • This is an on-site role - not a remote role., • There’s no relocation assistance available for this role., • Sponsorship: we will not provide sponsorship of any kind for this role (including OPT). Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: ___ Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity. Connect with us at ___, on Facebook at ___ and on Twitter @AbbottNews and @AbbottGlobal. The base pay for this position is $60,000.00 – $120,000.00. In specific locations, the pay range may vary from the range posted.

Job Description 2024 was a Record Sales Year. Our Largest Sales Growth in Decades. 2025 is trending to be even better. Water Treatment Sales Support Service Technician—Columbus, Ohio Garratt-Callahan () is family friendly, profitable, stable, and fiercely private. No layoffs in 120 years. No ownership changes in 120 years. 80 straight years of profitability. We have operations in every state in the USA. Technical Sales Support Service Technicians are responsible for maintaining the existing customer base in the greater Columbus area, and for performing water treatment tests at the existing customers. With the freedom of working from your home, you can work and train in a territory alongside veteran Territory Managers. The best place to live is in Central Ohio near or in Columbus. The career track for a Technical Sales Support/Service Technician is to train to become a Territory Manager. Territory Managers are eligible for unlimited commission and a year-end bonus. As a Technical Sales Support/Service Technician, you will receive an industry competitive salary, expenses, benefits, and a $675 per month car allowance. In addition, ample technical support is provided along with continuous training. Paperwork is kept to a minimum. Compensation is based upon experience and the ability to succeed. $65,000 to $75,000 first year base for a qualified candidate. We hire with a focus that favors the committed employee both in terms of overall compensation and growth opportunities. We have designed our compensation package accordingly. Benefits include a corporate 401k, health, dental, vision, and life insurance. Job Responsibilities: • Solve customers' water problems., • Treat industrial boilers and cooling towers to keep them energy efficient and environmentally friendly., • Perform detailed water testing & analyses at industrial sites such as food processing plants, hospitals, manufacturing plants, commercial buildings, and data centers., • Help sell Garratt-Callahan's proprietary chemical blends, equipment, & monitoring technology., • Passivation of stainless steel in industrial water treatment systems., • Help sell corrosion & scale inhibitors, coagulants, flocculants, biocides, bio-augmentation, feed & monitoring equipment, water management plans, reverse osmosis products., • Help sell Water Safety Programs., • Keep our existing customers happy., • Help bring on new industrial customers. About Garratt-Callahan: Garratt-Callahan is a US based private 120-year-old, nationwide water treatment chemical company. Garratt-Callahan treats industrial boilers and cooling towers to keep them energy efficient and environmentally friendly with one of the most advanced product lines in the industry. We are registered to ISO 9001:2015 and sell an industry leading line of “green" solutions, G-C GreenTech. We are headquartered in Burlingame, California. G-C is family owned, profitable, and expanding. We have five chemical plants in the USA, technical salespeople in every state, and the Caribbean. Benefits: • We offer a competitive benefit package which includes medical, dental, vision, AD&D, LT, and 401k. A monthly car allowance and travel expenses are provided., • First year compensation is $65,000 to $75,000 depending on experience., • Advanced training, and a clear career path., • Family friendly, flexible hours., • A huge benefit of working for Garratt-Callahan is our stability and low turnover., • No Layoffs in our 120-year history, • G-C is a profitable company. The last year that G-C did not turn a profit was during World War 2., • 2024 was a record sales year, and 2025 sales are trending to be even better. To Apply, please log on to: Thank you for considering Garratt-Callahan Company. Garratt-Callahan is an EEO/AAE employer. Minorities, women, veterans and individuals with disabilities are encouraged to apply. Requirements: You will be a successful applicant if you have a technical degree such as Chemistry, Chemical Engineering, Biology, Mechanical Engineering, Paper Science, or Water Resources. You must have a 4-year science degree to qualify for this position. You must be a capable Chemist. One-year technical sales, or an internship related to water treatment chemicals is preferred, but we are willing to train and mentor. Outside industrial sales experience is a plus. You must live in the greater Columbus area and be familiar with the industrial marketplace of Central Ohio. NOTE: Garratt-Callahan does not sponsor work visas. No recruiters please. If you have a disability, and need assistance during the application and selection process as a result, please contact the Garratt-Callahan Human Resources department at 650.697.5811. Arrangements can be made to provide an accommodation in order to assist you in applying for an open position using our on-line system, completing any other related paperwork, interviewing, or any other portion of the employment process. When requesting an accommodation, please provide your name, phone, email address, or any other means of contacting you. Provide a brief description of the nature of the requested accommodation. A member of the Human Resources team will then contact you to discuss your request. A request for an accommodation will not affect your opportunities for employment with Garratt-Callahan. Garratt-Callahan values differing experiences, backgrounds and perspectives among our employees, and see them as a competitive advantage. Garratt-Callahan is committed to the fair and equal treatment of all associates and applicants. Garratt-Callahan is an equal opportunity employer that evaluates qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law. Key Words: Chemistry, chemicals, scientific, science, salesperson, salesman, saleswoman, outside sales, technical sales, account representative, account executive, territory sales, territory manager, district sales, district manager, field engineer, field service, AE, sales engineer, data center, chemical engineer, chemist, mechanical engineer, biologist, biology, microbiology, nalco, ecolab, us water, Suez, ge water, chemtreat, industrial water engineering, solenis, chem-aqua, kurita, evoqua, fremont, water treatment, boilers, cooling towers, waste water, pumps, equipment, chillers, polymers, biocides, Columbus, Ohio.

Starkville, Mississippi (USDA ARS Corn Host Plant Resistance Research Unit, Mississippi State). Questions about the research: contact mentor. Engage with literature and meetings to advance research.

OSUCareers/job/Columbus-Campus/Assistant-Professor_R136799-1. The Ohio State University, Department of Microbiology in the College of Arts and Sciences, invites applications for a tenure-track Assistant Professor position in the area of microbial cell biology.

We are seeking a postdoc with strong bioinformatics/computational biology skills to join the Harari Lab. The Postdoc will work with large scale genomic and genetics data, including Next Generation Sequencing (NGS), GWAS chip data, Single Cell Transcriptomics (scRNA-seq, single cell ATAC-seq and spat

Supervises and trains junior research staff, post doctoral researchers, residents, and undergraduate & graduate students. Writes and submits grant proposals of original research in the area of tumor cell biology and oncogenic viruses as co-investigator or collaborator to obtain funding in suppor

The role involves developing and implementing goals and objectives of studies; designing and executing complex laboratory experiments; performing advanced molecular and cellular techniques; collecting, analyzing and interpreting research data; assisting with development and implementation of new and

The Research Associate designs, executes, and manages research projects investigating immunology, cancer biology, and neuroscience and experimental therapeutic techniques for the treatment of various cancers in the Liang lab in the Department of Radiation Oncology. Develops and implements new and/or

Job Description Job Title: Medical Device Sports Medicine Representative Location: Columbus and Athens Ohio Company: Arthrex Columbus Job Description: We are seeking a motivated and experienced Medical Device Sports Medicine Representative to join our team. The ideal candidate will be responsible for promoting and selling our sports medicine products to healthcare professionals in the assigned territory. This role requires building and maintaining strong relationships with orthopedic surgeons, sports medicine physicians, and other healthcare providers. Responsibilities: 1. Promote and sell sports medicine products to healthcare professionals and facilities within the assigned territory., 2. Build and maintain strong relationships with orthopedic surgeons, sports medicine physicians, and other key decision-makers., 3. Provide product demonstrations and training to healthcare professionals., 4. Attend and organize educational events, workshops, and conferences to promote the company's products., 5. Keep abreast of industry trends, competitive products, and market developments., 6. Collaborate with the sales and marketing teams to develop and implement sales strategies., 7. Provide exceptional customer service and support to healthcare professionals., 8. Undertakes additional duties in alignment with role requirements. Requirements: 1. Bachelor's degree in a related field (e.g., business, biology, kinesiology) preferred., 2. Proven track record of sales success in the medical device or pharmaceutical industry, preferably within the sports medicine or orthopedic space., 3. Strong understanding of anatomy, physiology, and medical terminology., 4. Excellent communication, presentation, and negotiation skills., 5. Ability to travel within the assigned territory., 6. Valid driver's license and clean driving record. We offer a competitive compensation package, including base salary, commission, benefits, and opportunities for career advancement. If you are passionate about sports medicine and have a strong sales background in the medical device industry, we would love to hear from you. Please submit your resume and cover letter detailing your relevant experience.

Reliable Nurse Staffing is seeking a travel Cath Lab Technologist for a travel job in Canton, Ohio.Job Description & Requirements Specialty: Cath Lab Technologist Discipline: Allied Health Professional Start Date: 11/03/2025 Duration: 13 weeks 40 hours per week Shift: 10 hours, days Employment Type:

Unique opportunity to break into the Clinical Research space!.Work with a company that truly cares about their employees and patients.Consistent schedule, no overnights or weekends, Early Fridays, flex holidays, and more!.We can only consider local candidates at this time, no relocation candidates.O

This is a contract to hire and hybrid 3 days a week onsite in Columbus, OH.No sponsorship provided at this time.We are seeking a dynamic and detail-oriented.Project Manager / Business Analyst (PM/BA).Information Technology team in the.This hybrid role is responsible for leading IT projects from init

Home Building Construction Project Manager - Columbus.As the driving force behind our custom homebuilding projects, you’ll ensure every detail is executed to the highest standard—delivered on time and with precision.This role is hands-on, requiring strong organizational skills, a sharp eye for d

Manage workflow by assigning tasks to other administrative employees daily, ensuring that deadlines are met and work is completed correctly.Assist in onboarding new hires.Implement and monitor programs as directed by management, and see the programs through to completion.Generate memos, emails and r

Performance Contracting Group is a national employee-owned specialty contractor that offers quality services and products to the commercial, industrial, and non-residential construction markets.We are committed to recruiting, developing, and advancing employees from a diversity of backgrounds and ex

COTA needs a temporary Project Manager.This role will be a hybrid position with the work location at COTA's downtown office.COTA is looking to fill this position for about a year.The role would be responsible for the annual strategic planning for the VoC program, aligning research needs across COTA

Start Date: January 2026 We are seeking a detail-oriented and motivated Junior Data Analyst to join our Banking Client's dynamic team.In this role, you will be responsible for analyzing data sets, generating reports, and providing insights that drive business decisions.The ideal candidate will have

Build a Career That Builds Your Future with PulteGroup!.Welcome to PulteGroup where we believe in building more than just homeswe believe in building inspired employees, meaningful careers, and a legacy of excellence.If you're looking for work that moves you, a team that values your ideas, and a co

Performs moderately complex administrative duties for one or more individuals within the department.Provides excellent service to both internal and external customers by applying best practices and standard operating procedures.Prepares correspondence, documents, reports and other materials which ma

Project Manager - Multifamily Construction.Lead high-profile multifamily projects with a top developer-builder.Enjoy excellent benefits, a supportive team culture, and long-term career growth.Our client is a mid-sized, privately held developer-builder with a strong reputation for delivering high-qua

Screen reader users may encounter difficulty with this site.For assistance with applying, please contact.If you have questions while submitting an application, please review these.Current Employees and Students:.If you are currently employed or enrolled as a student at The Ohio State University, ple

Project Manager Healthcare Or Light Industrial Construction.Work on impactful healthcare or light industrial projects with a respected GC.Enjoy top-tier benefits, career development, and long-term job security.As a Project Manager, you'll be responsible for overseeing all phases of construction proj

Project Manager For Mission Critical Data Center Projects.Strong communities don't just happen.They're thoughtfully planned and future-ready.We bring life to urban downtowns, suburban hubs, small towns, and rural areas through master-planned communities, mixed-use developments, parks, and recreation

We welcome candidates from diverse technical backgrounds, including geology, environmental science, chemistry, biology, and engineering.

This is a full-time on-site role for a Sr.Project Manager will be responsible for managing projects from start to finish.This will include tasks such as project planning, execution, monitoring, and closing.Project Manager will work closely with the project team to ensure that projects are completed

StructureCare, an industry leader in parking garage engineering and restoration solutions is hiring for a Project Manager! The Project Manager will be responsible for all aspects of sales support and project management for StructureCare working in the Ohio market.The position plans, develops, and di

Must be eligible to work in the United States, unable to provide sponsorship at this time.Degree in Engineering, Construction Management, or related field preferred.Strong organizational skills and ability to manage multiple priorities.Familiarity with design/build projects and industrial equipment

Project Manager - Construction Columbus OH.Turner & Townsend carefully considers multiple factors to determine compensation, including a candidate's education, training, and experience.The minimum salary for this position is $110,000 annually and the maximum salary for this position is $120,000 annu

US Citizen, Green card, GC EAD and H4 EAD accepted.Job description This role would focus on strong Sr Project Manager with Agile / SCRUM / Kanban.Agile, Scrum/Kanban experience The candidate must have managed app development project.

Central Ohio Transit Authority.McKinley Ave Columbus, OH-Ohio 43222.

Pasadena Villa Outpatient Administrative Assistant.At Pasadena Villa Outpatient, we are a dynamic, dedicated, and growing team of professionals deeply passionate about providing evidence-based and personalized clinical care for behavioral health conditions.Our team's foundation is client centered ca

KNK Recruiting, LLC is seeking a.Pay varies depending on experience, education, and skills.Possibility of being extended after 90 days.Our client is a heartfelt home healthcare company serving the Cincinnati and Dayton, Ohio, communities.Born from personal experiences, their mission is to offer comp

Screen reader users may encounter difficulty with this site.For assistance with applying, please contact.If you have questions while submitting an application, please review these.Current Employees and Students:.If you are currently employed or enrolled as a student at The Ohio State University, ple

Executive Administrative Assistant.Responsible for the performance of varied administrative duties and designated administrative functions for assigned Executive.Maintain a close and highly responsive relationship with the day-to-day work activities within assigned function.Work independently under

Provides administrative support to the Center for Real Estate programs and events by relieving the Executive Director of routine and non-routine administrative duties.Acts as a contact and resource for event attendees, center members, directors, and the general public.In consultation with the Execut