Frontage Laboratories jobs - 46 jobs

Title: Safety Pharm Technologist (Associate Scientist) Reports To: Manger/Supervisor Drug Safety Department Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking an experienced, highly-motivated, and detail-oriented team member to support client‑driven projects on Safety Pharmacology. The successful candidate will assist the study director to conduct in vivo safety pharmacology studies, including but not limited to system set up, data acquisition and data management to support central nerve system, respiratory and cardiovascular studies, all in compliance with appropriate SOPs, Protocols, and Regulatory Agency guidelines. Roles and Responsibilities: Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties. Successfully complete necessary tasks involved in safety pharmacology system set up, data acquisition, and data management, etc. Maintain the laboratory equipment in a clean and safe operating condition and maintain a clean and safe work area. Maintain logs and collect data according to GLP guidelines to a high degree of accuracy. Review study data and coordinate data analysis and interpretation. Other duties as assigned. Education and Requirements: Bachelor's or Associate Degree is preferable. An equivalent amount of education and/or experience may be accepted as a satisfactory substitute for the specific education. Willing to train individual with correlating background, education, or skills. Highly desirable hands-on experience in conducting safety pharmacology studies in appropriate species using relevant equipment and software. Proven ability to successfully work in a team environment. Must be able to work in a laboratory setting with laboratory animals. Advanced computer knowledge (e.g. Microsoft Office), corresponding with essential functions of accurately reading and recording data. Salary and Benefits: Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. Job Description The Quality Assurance Manager oversees assigned laboratories to ensure compliance with company policies and procedures, implementation of a robust and effective Quality System, and employment of continuous improvement activities. This includes identifying or developing quality management tools, assessing risks and leading root cause investigations, evaluating company-wide trends for weaknesses and opportunities to advance the company's leadership position in the environmental industry, and training quality staff in the implementation of Quality Systems, techniques, and tools. Quality Assurance Manager responsibilities include, but are not limited to, the following: * Ensure adherence to highest quality and efficiency standards in laboratory operations * Lead team, schedule, and train employees; ensure coverage and performance; foster morale and teamwork * Lead interventions in laboratories with inadequate Quality Systems or management * Review assigned laboratories' monthly reports to stay current with laboratory issues and achievements * Review audit responses for assigned laboratories as needed * Compile Quality System metrics to monitor the status and performance of assigned laboratories * Monitor laboratory certification activities to ensure no major losses of certifications * Investigate issues raised by clients, QA, sales, and other departments to find root cause, implement corrective action, and document proper response * Perform internal investigations of suspected data integrity related and/or ethics violation issues * Provide review and comments on state, client, TNI, and federal agency programs and requirements * Monitor regulatory and accreditation activities for business opportunities and threats * Research Quality Systems information and stay abreast of new practices to maintain knowledge and provide guidance * Participate in environmental industry committees or organizations to contribute to industry-wide initiatives that can impact the company * Identify and/or develop model Quality System tools, policies, and procedures, and make these available for adoption within the laboratories * Develop and participate in the Quality Management Training for new and prospective quality management staff * Coordinate quality assurance and technical training courses, as applicable * Assist Laboratory Directors/BUMAs in QA personnel decisions including: staffing, hiring, evaluations, and disciplinary actions as requested * Attend meetings to stay current with industry trends and QA programs * Participate in the Laboratory Information Management System (LIMS) oversight and standardization * Assist with internal Quality Systems Audits as needed Qualifications The ideal candidate would possess the following skills and knowledge: * Strong leadership, initiative, and teambuilding skills * Knowledge of environmental laboratory accreditation requirements * Quality Assurance and Quality Control principles * Statistics and the fundamental application in an environmental laboratory * Root cause analysis and corrective action principles * Change management techniques and group dynamics * Knowledge of environmental chemistry, regulatory methods and accreditation requirements, and instrumental techniques * Experience with laboratory operations * Strong analytical, logical, and negotiating skills * Strong interpersonal skills and leadership abilities * Ability to handle multiple priorities * Strong computer, scientific, and organizational skills * Excellent communication (oral and written) skills and attention to detail * Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude * Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Basic Minimum Qualifications: * BS degree in a science, combination of QA experience and knowledge of the environmental testing industry may substitute for a degree. * Minimum 5-10 years of environmental laboratory experience and 5 years QA experience. Advanced degree may substitute for experience. * Authorization to work in the United States indefinitely without restriction or sponsorship * Professional working proficiency in English is required, including the ability to read, write, and speak in English. Additional Information * Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with additional time as needed. * Position is located at our Barberton, Ohio location. * Position Pay Range is $75,000- $85,000 target range but will be reviewed based on experience. As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Plant Operator (Technician II) OLON USA LLC is seeking qualified candidates to operate chemical process equipment in a pilot plant and laboratory environment. These positions are 12 hours shifts and are available across all shifts. **We offer competitive wages, great benefits: 2 medical plans, dental, vision, company-paid life insurance and income continuation plan, supplemental life, 401k with company match** Essential Job Functions: This position will involve the operation of chemical process equipment in support of first-time scale-ups, process optimization and small-lot production of chemical-based materials in compliance with FDA's current Good Manufacturing Practice guidelines. The successful candidate will execute processing activities according to specific procedures, make observations, record data and maintain accurate documentation. Educational Requirements: High school diploma, basic math skills and some knowledge of chemistry Candidates should have mechanical aptitude, demonstrate their strong communication skills and be able to work in a team environment. Must be able to work with and move drum quantities of chemicals. Previous experience, as a chemical plant/pilot plant operator is desirable. Knowledge of chemical hazards, forklift operation and college courses in chemistry considered a plus. We offer competitive wages along with a comprehensive benefit plan and a great workplace! -------------------------------------- Olon USA LLC. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, or protected Veteran status.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Eurofins Medical Device Services is seeking a highly experienced Senior Scientific Advisor with deep expertise in medical device microbiology and sterilization technologies (including ethylene oxide sterilization) to provide scientific leadership and strategic guidance for our testing services. This role is critical in supporting clients with complex regulatory and technical challenges, ensuring compliance with ISO 11737, ISO 11135, and related standards, and advancing Eurofins' position as a trusted partner in the medical device industry. As a senior technical advisor, you will collaborate with clients, internal teams, and regulatory bodies to design scientifically robust testing programs, interpret results, and deliver actionable insights. This position is ideal for professionals who combine advanced scientific knowledge with strong communication and advisory skills. Key Responsibilities: Serve as the subject matter expert in microbiology and sterilization services for medical devices, including EO sterilization and sterility assurance. Actively prospect, engage, and close new client relationships to drive top-line revenue growth and expand market share in the microbiological and sterilization testing space. Collaborate with Sales and Key Account Managers to position Eurofins' microbiology and sterilization services as a best-in-class solution, improving quote-to-win ratios. Lead the development of technical scopes of work and respond to RFQs/RFPs with compelling, scientifically robust proposals. Provide strategic insights to business development and operations leadership to ensure alignment of service offerings with market demands. Represent Eurofins at conferences, trade shows, and industry events to enhance visibility and establish thought leadership. Facilitate seamless handoffs to project management and operations teams, ensuring successful project execution and client satisfaction. Monitor the competitive landscape and market trends to support pricing strategy and service differentiation. Travel 30-50% to meet with clients, attend events, and support on-site collaboration with Eurofins teams. Qualifications Bachelor's degree in Microbiology or a related field is required; advanced degree is strongly preferred. Minimum 7+ years of experience in microbiology ad sterilization within a CRO or medical device environment. In-depth knowledge of the AAMI, ISO, FDA and international regulatory requirements. Strong analytical and problem-solving skills with the ability to interpret complex data sets. Excellent verbal and written communication skills; ability to present technical concepts clearly to diverse audiences. Collaborative mindset with proven ability to influence and guide cross-functional teams. Authorized to work in the U.S. without restriction or sponsorship. Additional Information Full-time, Monday-Friday, 8 a.m.-5 p.m. (flexibility required). Remote position with preference for candidates near a major airport for travel to client sites and industry events. What we offer: Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Barberton, OH, USA Full-time ** Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic, and labelling is accurate. Eurofins is dedicated to delivering testing services that contribute to the health and safety of society and the planet, and to its corporate responsibility to protect the environment and ensure diversity, equity, and inclusion across the entire network of Eurofins companies. **Job Description** **Shipping and Receiving Technician responsibilities include, but are not limited to, the following:** + Prepares outgoing shipments of bottle kits and outgoing coolers of samples for delivery to laboratory. + Utilizes Eurofins LIMS system (TALs) to receive bottle orders from project managers and prepare them in kits as directed + Interacts with Project Managers and clients appropriately and professionally + Communicates effectively with coworkers about the status of orders + Restocks supplies when received so supplies are available to employees when needed. + Verifies the validity and completeness of all bottle orders being delivered. This verification is done prior to leaving for delivery + Maintains the shipping/receiving area to ensure a safe work environment. + Performs all duties as outlined in the SOP for Couriers. + Picks up and delivers samples and bottle orders as needed + Counts the number of samples when receiving them from clients to make sure that the Chain of Custody and samples match. Verifies that samples are not broken or damaged. + Receives and sign the Chain of Custody. + Ensures that client signs, dates, and records time on the Chain of Custody when releasing samples. + Transports samples on ice from client site to the service center, or from our service center to a sub-contracted laboratory. + Unloads samples and inspect for damage or violated hold times to maintain sample integrity.. + Follows directions or use maps to locate client offices/sites as specified in the courier request form.. + Records in the courier log book the time that courier arrives to the site and time leaving from the site for all the pick-ups and deliveries. + Maintains records for the vehicle maintenance and driving miles; turn it in at the end of each month.. + Performs duties in accordance with Section 14 of the Transportation and Fleet Safety of the Corporate Safety Manual. + Complies with the Company's "Driver Evaluation and Qualification Policy".. + Maintains delivery vehicle to keep in proper working order. + May be assigned other sample control duties as identified by the Service Center Manager. **Qualifications** **The ideal candidate would possess:** + Ability to prioritize + Excellent communication (oral and written) and attention to detail + Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude + Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies + Ability to read maps and follow directions + Ability to operate a motor vehicle **Basic Minimum Qualifications:** + High school diploma or equivalent + Valid Driver's License + Authorization to work in the United States indefinitely without restriction or sponsorship **Additional Information** **Position is located in Barberton, OH** **Position is 1st shift, Monday- Friday 8:30 AM- 5:00 PM with OT on Saturdays as needed.** **Postion Range starts at $17.75/hr, based on experience.** Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base salary may vary based upon, but not limited to, relevant experience and skill set, base salary of internal peers, business sector, and geographic location. **We support your development!** Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. **We embrace diversity!** Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. **Sustainability matters to us!** We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** **Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.**

The Medical Science Liaison (MSL) for Amneal's Central Territory (CO, MO, KS, NE, UT, WY, ID, MT) is a field-based professional with scientific, clinical, and therapeutic area expertise. This role is responsible for providing medical and scientific support for Amneal's marketed products, new indications for current products, and compounds in development. The incumbent engages in scientific exchange with medical and scientific experts, including healthcare professionals and managed markets customers across the assigned states. Essential Functions: Develops peer-level relationships with medical and scientific experts, including healthcare professionals and managed markets customers. Delivers appropriate clinical and scientific information that clinically differentiates Amneal products; provides clinical support and delivers data presentations regionally and nationally. Provides actionable information that enhances the value and appropriate use of Amneal products to internal stakeholders. Responds to customer inquiries to ensure focused and balanced clinical and scientific information that supports the appropriate use of Amneal's products and services. Trains and mentors within therapeutic area, providing performance guidance and coaching. Additional Responsibilities: Adheres to internal standard processes and complies with regulatory and compliance requirements. Sustains expertise in disease state management, emerging therapies, and the competitive landscape. Demonstrates project leadership and management in and across field team and therapeutic area. Education: Doctorate Degree Advanced degree (PhD, PharmD, MD) in biological sciences (neuroscience preferred), pharmacology, Pharmacy or medicine. - Required Experience: 5 years or more in Experience in Biological Sciences, Pharmacology, Medicine or the equivalent Industry experience focused on Parkinson's Disease (preferred) Skills: Demonstrated expertise in discussing scientific content and context to multiple audiences. - Intermediate Excellent project management ability. - Intermediate Excellent oral and written communication and interpersonal skills. - Intermediate Strong leadership capabilities. - Intermediate Experience in pharmaceutical industry. - Intermediate Specialized Knowledge: Knowledgeable on using resources for accessing scientific and clinical information. Knowledgeable on using Microsoft Office Programs (Word, Excel, Outlook and PowerPoint) Location/Travel: Remote Work with Frequent Travel required 60-70% Field Work: Travel to meet HCPs, attend conferences, or support clinical sites. 20-30% Remote Work: Virtual meetings, data analysis, content review. The base salary for this position ranges from $160,000 to $180,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description As a Senior Field Engineer you will conduct on-site Field Evaluations of electrical equipment for compliance to regulatory product safety standards (UL, NFPA, CSA, ANSI, etc.). Perform construction and engineering review of electrical equipment in a multitude of industries (manufacturing, laboratory, medical, commercial, retail, food service, etc.). 100% travel both domestic and internationally, though majority of travel will be within the lower 48 (must possess or be able to obtain a passport). Territory: San Francisco, CA; Los Angeles, CA; Las Vegas, NV; Phoenix, AZ. RESPONSIBILITIES The Senior Field Engineers' duties and responsibilities include, but are not limited to: * Perform Field Evaluations under the Eurofins E&E North America/MET Labs Field Labeling program * Review scope of work and identify all necessary items prior to arranging travel * Responsible for coordinating all travel arrangements * Communicate with client, AHJ, contractors, and other relevant parties * Identify applicability of national codes and standards * Review manuals, schematics, BOMs, site procedures, data sheets and more * Document construction details and any non-conformances during the inspection * Assess compliance to the relevant UL, NFPA, CSA, or ANSI standards * Determine eligibility of equipment for labeling and issue all final reports * Submit all expenses and necessary documentation for billing * Meet or exceed minimum billing goals while meeting project deadlines * Grow relationships with clients and promote our company and the various services we offer Qualifications The ideal candidate will demonstrate the following experience, skills, and personal attributes: * Electrical Engineering Bachelor's Degree preferred and/or equivalent experience. * MUST have direct Field Engineering experience with a Nationally Recognized Testing Laboratory (NRTL) or Field Evaluation Body (FEB) using product safety standards. * Experience as a Follow-Up Inspector is not relevant unless there is experience performing multiple UL 508A training seminars. * Conversant with UL 508A, UL 61010-1, UL 73, NFPA 70, & NFPA 79. * Though not required, experience with Hazardous Location and CSA standards is desired. * Must have strong technical writing skills and experience with Microsoft Office Suite. * This position requires strong verbal and written communication skills and excellent interpersonal skills as the candidate will interact with customers on many different levels. * Must be able to work in elevated and/or confined spaces. Must be able to lift 30+ pounds. * This position requires a strong electrical background and understanding of electrical systems. * Must possess sound problem-solving skills. * Skillful ability to work independently. * Demonstrated ability working with diverse populations and communities. Work Remotely * Position is entirely remote. Must be near a major airport. Additional Information Salary Range: * $110,000 - $150,000/yr. What we offer: * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Title: Pathologist/Senior Pathologist Full-time Who we are and what we do: Frontage Laboratories Inc. is an award winning, full-service, Contract Research Organization (CRO) operating over 25 state-of-the-art laboratories across the US, Canada, Europe, and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Our Safety & Toxicology facilities are located in the US (Ohio and Illinois), Canada (Toronto) and China (Suzhou) and are growing rapidly. Our Concord, OH and Chicago, IL sites provide toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products. Position Summary We are currently looking for a Senior Pathologist/Pathologist to be located on-site at our Concord, OH toxicology facility. Pathologists at Frontage Laboratories serve as technical experts and consultants in pathology and related fields, working in a collaborative environment on projects throughout the discovery and development continuum and have a passion for science and quality. The ideal candidate will have knowledge of toxicological pathology across multiple laboratory species. Experience in regulatory toxicology/pathology and familiarity with Good Laboratory Practices (GLPs) and drug development is desirable. Roles & Responsibilities * Attend necropsies as requested and be available for expert oversight of necropsies as needed. * Interpret and report pathology findings in exploratory and regulatory studies including correlating microscopic findings to macroscopic observations, organ weight changes, and clinical pathology data. * Maintain accurate records of all procedures according to FDA GLP regulations and applicable SOPs. * Conduct pathology peer reviews, depending on experience. * Maintain current knowledge of pathology literature, best practices, and industry directions. * Function as a key member of the pathology team interacting daily with members located in Chicago or off-site locations. * Provide pathology expertise for regulatory submissions and regulatory responses. * Support business development initiatives through client interactions and expert guidance. * Support necropsy either through supervision or training. * Demonstrate scientific leadership through participation in professional organizations, presentations, and publications. * Work closely and collaboratively with other Pathologists and Toxicology Study Directors. * Perform additional duties and tasks assigned by Management. Qualifications/Requirements: * DVM and Diplomate of ACVP (anatomic pathology) or equivalent certification. * Preferably (3+ years) experience in interpreting and reporting pathology findings in a CRO, pharmaceutical, or biotechnology setting; however, qualified candidates with other relevant experience are encouraged to apply. * Experience in immuno- and/or neuropath desirable, with potential growth to set up in-house specialty service offerings, including IHC. * Strong, effective written and oral communication skills, including the ability to organize and clearly present complex data and concepts. * Ability to work in a fast-paced environment, manage multiple projects, demonstrate consistent productivity, and meet project timelines. * Ability to work independently and collaboratively. Salary and Benefits * Frontage Laboratories offer competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, short and long‑term disability insurance, life insurance etc. * Concord, Ohio is a township about 30 miles east of Cleveland. The housing is more affordable than many areas close to major cities and is nestled in a rural setting, yet with good restaurants, shopping, and schools within the township. We consider the lifestyle and proximity to attractions in Cleveland to be a hidden benefit of living and working in Concord. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2024, Eurofins generated total revenues of EUR € 6,515 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Eurofins is seeking a self-motivated and enthusiastic IT Field Service Technician, which is a Second Level / Tier 2 position where you will be responsible for a combination of remote desktop support for local and nationwide support tickets, in-person support and act as fill in for occasional overflow of Service Desk calls. * Support one or more localized laboratories to provide in-person, on-site support, 2-4 days per week. * Provide remote support to laboratories across North America. * Troubleshoot and resolve customer hardware, software and general network connectivity issues. * Break highly technical concepts down into non-technical language and communicate them to people of all IT skill levels. * Must be open-minded and considered a change agent. * Provide hands on/onsite support for various technical challenges. Qualifications Skills and Relevant Experience: * Minimum 3 years of Desktop Support w/increasing responsibilities * 1 yr. minimum of Help Desk Support (or equivalent) * 1 yr. minimum of Knowledge Management * 1 yr. minimum ServiceNow (or equivalent ITIL Incident tracking) * Intermediate troubleshooting and repair of Windows OS's (Win10 and Win11) * Intermediate troubleshooting and repair of hardware, UPS's, installing workstations, onboarding new users, off boarding users, etc. * Intermediate troubleshooting and repair of on premise and cloud based Microsoft products including MS Office 2016, O365, SCCM, Azure, Exchange, Server 2008-2021, Windows 7 - 11, etc. * Basic knowledge of Active Directory, DNS, DHCP, Group Policy as well as support for such things as setting up or repairing access to network folder and file shares, setting up network printing, scan to email configurations, etc. * Intermediate support for VPN and remote access, Citrix, thin clients, VMWare or equivalent * Support for Citrix FileShare, Bomgar, Remote Desktop, Symantec VIP/Microsoft Authenticator, Cisco IP Communicator, Cisco WebEx, SentinalOne, Remote and On-Prem imaging PC's and laptops and so much more. * Intermediate troubleshooting and providing HOW TO support for MS Office O365, MS Teams, OneDrive, SharePoint and more. * Familiarity with network connectivity, TCI/IP, Firewalls, Vlan's, Ethernet, etc. * Have basic understanding of ITIL concepts: Incident, Major Incident, Problem Record, Knowledge Article, Asset Management, Change Request, Service Portal, etc. * Provide timely, first contact resolution (FCR) to technical support issues while following company standards and procedures * Provide occasional on-call support * Develop Knowledge Based Articles (KBA) for publication and support. Other Qualifications Considered: * HDI Support Customer Service Representative Certification (or equivalent) * HDI Support Center Analyst Certification (or equivalent) * HDI Desktop Support Technician Certification (or equivalent) * HDI Technical Support Professional Certification (or equivalent) * ITIL Foundations Certification V3 or V4 * A+, Network+, Security+ * Microsoft MCP * Apple Certified Technician Additional information * Authorization to work in the United States indefinitely without restriction or sponsorship * Travel up to 50% required Additional Information Position is full-time, working Monday - Friday 8:00am - 5:00pm, with overtime as needed. This is a field-based position, requiring candidates to reside in New Jersey and travel up to 50% of the time. * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Position Summary: The core responsibility of the Consumer Products Assurance Social Compliance Lead Auditor will be to execute assigned social compliance audits for Eurofins' clients - primarily in the US. As a lead auditor, the role will involve managing and developing social compliance auditors - in addition to leading audit executions. Objectives: Audit Execution Lead auditor will support the operating results of the business through the execution of audit services - with approximately 14 billable days per month. In audit execution, the lead auditor will be responsible to for supporting the training and development of junior auditors - participating in audits as a team member. Technical Support and Governance As a member of the audit team, the lead auditor will contribute technical input and perspective to the development of operating procedures and methodologies to ensure audit service delivery capabilities support client service delivery objectives - enhancing satisfaction among clients. Customer Service Provide customer support as the audit service stream program managers for selected large global accounts and collaborative programs. Roles and Responsibilities: Audit Execution and Reporting * Perform audits consistent with Eurofins' client and program instructions in accordance with established protocols * Prepare audit reports in a complete, accurate and timely manner for submission to the Eurofins ARCC * Respond timely to any post audit queries from ARCC to close and finalize audit report Technical Support and Governance * Ensure the integrity and consistency of the delivery of CPA audit services though support for the continuous improvement of operating procedures and methodologies to ensure service delivery capabilities support client service delivery objectives on a global basis. * Provide subject matter support for the effective and timely resolution of issues and problems with audits related in other key sourcing markets. Qualifications * Bachelors or advanced degree in Business, Finance or a related field of study. * At least 5 years' experience in professional services and/or auditing. * At least 3years' experience managing teams of professionals. * APSCA CSCA certificate/license Key Skills Subject Matter * Significant knowledge of audit subject matter - particularly social audits, service delivery methodologies for audit services and the demonstrated ability to implement them * General knowledge of risk management, auditing, and process management consulting concepts and the demonstrated ability to implement them Client interaction * Demonstrated ability to work with clients and facilities to be audited, understand their requirements, define and assist in solving problems, and generally ensure client's total satisfaction with Eurofins Management/Leadership * Effective oral and written communications skills including professional English presentation * Strong skills as a team leader and ability to work well with peers. * Highly developed organizational and interpersonal skills. * Ability to interpret regulations and standards. * Technical aptitude, the ability to quickly assimilate and assess new information and develop plans to capitalize or react to it Additional Information Schedule: * 40 hours per week What we offer: * Excellent full time benefits including comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Eurofins USA Consumer Product Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Fairfield, OH, USA Full-time ** DNA Diagnostics Center is the world leader in DNA relationship testing, processing over one million DNA samples from customers all over the world. Our broad portfolio of products includes our Paternity, Immigration, and other DNA Relationship services for consumers, government agencies, healthcare providers, and legal professionals; PeekabooTM Early Gender DNA Test for expecting mothers; SpermCheck fertility and vasectomy test; and Pets & Vets DNA testing for breeders and pet enthusiasts. Our corporate headquarters, including our DNA testing laboratory, is based in Fairfield, OH in the greater Cincinnati Area. DDC is part of Eurofins, a global scientific company with over 950 laboratories in 60 countries and more than 65,000 employees. **Job Description** Are you a rising leader with a passion for process excellence, customer experience, and transformational change? DDC is seeking a Client Services Supervisor who thrives on improving operations, engaging teams, and driving meaningful impact - not just maintaining the status quo. This is not your typical call center leadership role. We're looking for someone business-savvy, customer-obsessed, and process-driven - someone who's excited to learn a new industry, lead a tenured team, and elevate our service operations. Background in contact center operations is not required. What You'll Do + Lead and inspire a remote Client Services team across multiple channels (phone, chat, email). + Drive continuous improvement in workflows, policies, and performance metrics. + Champion data-driven decision-making and develop tools to monitor trends and KPIs. + Collaborate cross-functionally to enhance customer experience and operational efficiency. + Recruit, coach, and develop team members with a focus on accountability and empowerment. + Identify opportunities for innovation and challenge legacy processes with fresh thinking. + Represent the voice of the customer and advocate for quality at every touchpoint. Why Join Us? + Be part of a mission-driven company making a real difference in people's lives. + Work with a passionate, experienced remote team eager for strong leadership. + Lead transformation in a supportive, high-performance culture. + Enjoy opportunities for professional development and cross-functional collaboration. Ready to lead with purpose and drive change? Apply now and help us shape the future of client services at DDC. **Qualifications** + Bachelor's degree in business, operations, or a related field preferred. + 5+ years in a leadership role, preferably in a healthcare service environment. + A track record of managing people and improving processes - not necessarily in a call center. + Strong analytical skills and comfort with data, dashboards, and performance metrics. + Excellent communication, collaboration, and change management abilities. + A mindset for growth, curiosity, and accountability. + Proficiency in Microsoft Office tools (Word, Excel, PowerPoint). **Physical Requirements** + Prolonged periods of sitting at a desk and working on a computer. + Must be able to lift up to 15 pounds at times. + Communicating with others to exchange information. + Ability to travel, as needed. **Additional Information** **Schedule:** + Monday - Friday, 8:00am to 6:00pm **What we offer:** + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.**

Director of Business Development - Drug Safety, Toxicology, and Preclinical Services Reports to: Vice President, Business Development Full -Time Company Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing and expanding rapidly. Our core competencies cover all aspects of drug discovery and development, including medicinal chemistry, discovery biology, DMPK, safety and toxicology, CMC and API manufacture, laboratory testing services and early clinical trials. Position Summary The Director of Business Development role involves the creation of long-term valued business relationships for the Company from both existing and new customers, with primary emphasis on new account development. The focus of the role is new business development for pre-clinical / non-clinical toxicology and drug safety services in pharmaceutical drug development, plus related services including DMPK and related bioanalytical. The primary target market is small-to-mid biotech and pharma in the ‘small molecule' space. Some activity in ‘Big Pharma' and in large-molecule (proteins / antibodies) is expected as the Company's services continue to expand. This is an outside sales position working from home serving markets in the Southeast/Mid-Atlantic region to support our aggressive growth objectives. Roles & Responsibilities Meet or exceed sales objectives for assigned region Solicit and develop new business opportunities through direct calling efforts, referral sources, industry trade shows and conferences, and meetings; as well as any other appropriate means Visit existing and former customers periodically to reaffirm satisfaction and identify new and expanding opportunities for deeper client engagement. Develop new business plans for existing customers as well as potential new customers Respond to new business development leads promptly and coordinate / follow up with internal support team to ensure same Qualify, pursue, and close new opportunities. Identify decision-makers and areas of need. Negotiate and close Keep accurate records of calls, meetings and other activities (call reports) in CRM Maintain an up-to-date pipeline of new business opportunities Assist with preparing proposals, quotes, and customer contracts Develop a comprehensive understanding of all services offered Other duties as assigned by management. Education, Experience and Skills Required Minimum of three years of demonstrated success in outside sales / business development in a scientific field or similar / related experience in customer-facing role. Proven sales experience with a documented history of sustainable growth is a must. Familiarity with GLP regulatory process. Prior experience in a GLP CRO is a plus. Familiarity with drug development biology to include toxicology, metabolism, and pharmacokinetics. Excellent organizational and planning skills Ability to operate in an independent, self-directed manner Strong English language communication skills, including persuasive interpersonal communication and sales techniques to include presentation skills, sales interview skills, and closing skills. Working knowledge of business office software (Word, Excel, PowerPoint, Outlook) Working knowledge of CRM (Salesforce, Microsoft Dynamics, Zoho, or other) BA or BS required - biology, chemistry, or related Must have a functional home office setup. Must have reliable means of transportation as needed. Frontage will reimburse business mileage for use of personal vehicle. If personal vehicle is to be used for company business, the employee must have a valid driver license and a late-model automobile which is in good repair and suitable appearance. Salary and Benefits: Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with a disability.

Fairfield, OH, USA Full-time ** DNA Diagnostics Center is the world leader in DNA relationship testing, processing over one million DNA samples from customers all over the world. Our broad portfolio of products includes our Paternity, Immigration, and other DNA Relationship services for consumers, government agencies, healthcare providers, and legal professionals; PeekabooTM Early Gender DNA Test for expecting mothers; SpermCheck fertility and vasectomy test; and Pets & Vets DNA testing for breeders and pet enthusiasts. Our corporate headquarters, including our DNA testing laboratory, is based in Fairfield, OH in the greater Cincinnati Area. DDC is part of Eurofins, a global scientific company with over 950 laboratories in 60 countries and more than 65,000 employees. **Job Description** The Contact Center Supervisor is a dynamic leader passionate about maximizing employee potential to improve client outcomes. Providing leadership and guidance over process and training within the contact center, the Contact Center Supervisor advances impactful process improvements. They remove barriers for the Client Service team and set the tone for a high-performance culture that emphasizes quality and efficiency. Operating with accuracy and integrity, they anticipate and meet strategic customer and employee needs proactively. They work in conjunction with Client Service Representatives to ensure the successful delivery of services. **Essential Duties & Responsibilities** + Own the resolution of escalated client concerns in the form of calls, emails, faxes and chats. + Oversee and support assignment of daily work volume and re-allocation of resources to meet SLAs + Identify process bottlenecks and workflow inefficiencies, championing solutions that are approved by internal stakeholders and that are compliant with external regulations and requirements. + Establish subject matter expertise regarding roles/responsibilities of the Client Services team and intersections with other functional teams. + Maintain extensive and accurate product and process knowledge by regularly communicating to understand needs and explain products. + Partner with other supervisors to achieve KPIs through managing staffing, productivity, and efficiency. + Create and implement strategy around process communication, creating a culture of awareness, transparency, and continuous process improvement + Identify trends and assess department needs for training and standard operating procedures + Develop and maintain a strategy for contact center training, including delivery, content, and schedule for new hires and current employees requiring remedial training + Lead piloting of new channel, product, or systems initiatives while overseeing documentation of workflow and adoption within the contact center. + Provide recommendations on how to maximize efficiency within the contact center. + Engage in the interview and selection process and oversee new hire onboarding and assimilation. + Provide effective feedback during annual appraisals, counseling and discipline, and recognition. + Other duties as assigned or become evident **Qualifications** + Bachelor's degree in business or related field preferred + Minimum of five (5) years leadership role required + Strong will to drive impactful change and continuously challenge the status quo + Excellent interpersonal skills, creating a supportive work culture while compelling others to achieve. + Strong conflict resolution skills, including identifying issues and advancing practical solutions + Strong analytical skills, evaluating KPIs to form actionable insights and provide recommendations. + Strong decision-making skills, evaluating competing priorities and setting a course of action. + Demonstrated ability to interact with and effectively present to senior leadership + Excellent project management skills, managing multiple priorities and meeting established deadlines + Demonstrated ability to build a collaborative culture and relationships with strategic partners + Highly proficient in Microsoft Office and other computer software programs **Physical Requirements** + Prolonged periods of sitting at a desk and working on a computer. + Must be able to lift up to 15 pounds at times. + Communicating with others to exchange information. + Ability to travel, as needed. **Additional Information** **Schedule:** + Monday - Friday, 8:00am to 6:00pm **What we offer:** + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal Employment Opportunity employer.**

Job Description Title: Necropsy Technician, Histology and Necropsy Reports To: Team Leader, Histology and Necropsy Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a highly-motivated, detail-oriented team member to support client-driven projects using necropsy and histology techniques. The successful candidate will perform necropsy laboratory procedures, including but not limited to tissue collection/preservation, tissue trimming and weighing, and data entry, all in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines. In support of Histology, team member may also trim, embed, cut, and stain collected tissues, all in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines. Roles and Responsibilities: Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties. Observe all safety procedures and working methods by making proper use of protective clothing and equipment and by reading, understanding, and following all safety documents. Successfully complete necessary tasks involved in animal necropsy and tissue trimming: proper dissection and collection of samples, organ weights and verification, laboratory preparation, and preparation of laboratory solutions. Provide support in the histology lab in trimming, processing, embedding, cutting, and staining collected tissues. Maintain the laboratory equipment in a clean and safe operating condition and maintain a clean and safe work area. Maintain logs and collect data according to GLP guidelines to a high degree of accuracy. Education and Requirements: Bachelor's Degree in Life Sciences, or Associate Degree/Certification in Histology, Laboratory Animal Technology, or Veterinary Technology (or related) is preferable, but not required. An equivalent amount of education and/or experience may be accepted as a satisfactory substitute for the specific education. Willing to train individual with correlating background, education, or skills. Highly desirable to have experience with necropsy procedures and/or working in a histology laboratory, preferably with multiple species. Proven ability to successfully work in a team environment. Excellent oral and written communication skills. Must be able to work in a laboratory setting with laboratory animals and chemicals. Basic computer knowledge (e.g. Microsoft Office), corresponding with essential functions of accurately reading and recording data. Must be able to stand or sit for extended periods of time. Must be able to lift up to 30 pounds regularly and 50 pounds on occasion. Must be able to tolerate strong odors. Salary and Benefits: Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Job Description Title: Animal Technician Reports To: Manger/Supervisor Drug Safety Department Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a highly-motivated, detail-oriented team member to support client-driven projects. The successful candidate will perform animal care procedures, including but not limited to room and cage cleaning, dosing, observations, and data entry, all in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines. In support of Drug Safety, team member must be able to work in compliance with appropriate SOP, Protocol, and Regulatory Agency guidelines. Roles and Responsibilities: Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties. Observe all safety procedures and working methods by making proper use of protective clothing and equipment and by reading, understanding, and following all safety documents. Successfully complete necessary tasks involved in animal care and related activities: room cleaning, cage cleaning, animal observations, animal dosing, etc. Maintain the laboratory equipment in a clean and safe operating condition and maintain a clean and safe work area. Maintain logs and collect data according to GLP guidelines to a high degree of accuracy. Education and Requirements: Bachelor's Degree in Life Sciences, or Associate Degree, Laboratory Animal Technology, or Veterinary Technology (or related) is preferable, but not required. An equivalent amount of education and/or experience may be accepted as a satisfactory substitute for the specific education. Willing to train individual with correlating background, education, or skills. Highly desirable to have experience with animals, preferably with multiple species. Proven ability to successfully work in a team environment. Excellent oral and written communication skills. Must be able to work in a laboratory setting with laboratory animals. Basic computer knowledge (e.g. Microsoft Office), corresponding with essential functions of accurately reading and recording data. Must be able to stand or sit for extended periods of time with frequent bending/lifting. Must be able to lift up to 30 pounds regularly and 50 pounds on occasion. Must be able to tolerate strong odors. Salary and Benefits: Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Essential Job Functions: This position will involve the operation of chemical process equipment in support of first-time scale-ups in compliance with FDA's current Good Manufacturing Practice guidelines. Given the challenges faced when scaling up new production processes, each day requires challenges to be addressed with close cooperation required between operators, engineers, and chemists. The successful candidate will execute processing activities according to specific procedures, make observations, record data, and maintain accurate documentation. Position Requirements: High school diploma, basic math skills, mechanical aptitude, basic knowledge of chemical hazards, communication, and teamwork abilities. The position is an 8 hour, 5 days a week schedule on day shift. Need to be able to move drum quantities of solvents and wear respirators as required. Careful attention to documentation is required. Previous experience as a chemical plant/pilot plant operator is desirable. Experience working with hazardous chemicals, forklifts, and/or in a cGMP or ISO certified company is also considered a plus.

Essential Responsibilities The ability to interact with chemists to help guide the development of new chemical processes, translate these processes into executable instructions, and guide operators through production. Provide guidance in scaling up production processes from the lab to the pilot plant. Be able to provide flexible solutions when processes do not scale as expected and be able to work closely with production operators in providing instructions. Able to assist other engineers with difficult scale up situations. Provide supporting documentations (batch records, specifications, hazard sheets, safety review packages, air emissions, processing reports) necessary to support processing in the plant. Conduct safety meetings, oversee execution of processing, participate on the floor as appropriate and review executed batch records. Interact closely with our chemistry and quality departments throughout the production process. External interactions include meeting with clients, vendors and contractors. Engineering support of pilot plant infrastructure. Ability to multi-task and work with supervisor to establish priorities. Required Educational & Industrial Qualifications B.S. or M.S. in Chemical Engineering or Chemistry with ten or more years of experience in scale-up/preparation of pharmaceutical and specialty chemicals Specific Skill and Requirements Works effectively in a multi-disciplinary team environment Strong problem-solving capabilities Experience in first time scale-up and preparation Demonstrate success in prior positions Experience with pilot plant and kilo scale process equipment Knowledgeable in process/cleaning validation and equipment commissioning/qualification Good trouble shooting and problem-solving skills Highly motivated team player with excellent written and oral communication

Title: Scientist/Senior Scientist Reports To: Study Director Manager Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary We are currently looking for a scientist/senior scientist to be located on-site at our Concord, OH toxicology facility to develop in vitro toxicology assays and new approach methodologies (NAMs). Scientists at Frontage Laboratories serve as technical experts and consultants in in vitro toxicology and related fields, working in a collaborative environment on projects throughout the discovery and development continuum and have a passion for science and quality. The ideal candidate will have knowledge of New Approach Methodologies (NAMs) to replace or reduce the use of animals in drug development and to refine the use of animals to achieve better results.in vitro toxicology. Experience in regulatory toxicology and familiarity with Good Laboratory Practices (GLPs) and drug development is preferred but not required. Roles & Responsibilities * Knowledge and Experience: Full knowledge of New Approach Methodologies (NAMs) for use in toxicological research and implement NAMs in drug development processes. * Method Development & Validation: Hands-on experience in developing, optimizing, and validating novel in vitro toxicology platforms (i.e., cell cultures, organoids, or high-throughput systems). * Laboratory Execution: Performing experiments using modern instruments including but not limited to flow cytometry and plate readers, etc. * Data Interpretation & Reporting: Interpreting and reporting experimental data; familiarity with computational modeling and statistical analysis. * Scientific and Regulatory Compliance: Ensuring all experimental activities adhere to guidelines and supporting regulatory submissions by providing data that can waive or reduce the need for animal testing. * Collaboration and Communication: Working closely with collaborators; Demonstrating scientific leadership through participation in professional organizations, presentations, and publications. * Additional Responsibilities: Performing additional duties and tasks assigned by the Management. Qualifications/Requirements: * Master or PhD in cell biological sciences or related fields. * Preferably (3+ years) experience of in vitro toxicology in a CRO, pharmaceutical, or biotechnology setting; however, qualified candidates with other relevant experience are encouraged to apply. * Proficiency in techniques such as cell culture, molecular biology, and biomarker development. * Knowledge of NAMs and AI tools in drug discovery and development. * Strong, effective written and oral communication skills, including the ability to organize and clearly present complex data and concepts. * Ability to work in a fast-paced environment, manage multiple projects, demonstrate consistent productivity, and meet project timelines. * Ability to work independently and collaboratively. Salary and Benefits * Frontage Laboratories offer a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, short and long‑term disability insurance, life insurance etc. * Concord, Ohio is a township about 30 miles east of Cleveland. The housing is more affordable than many areas close to major cities and is nestled in a rural setting, yet with good restaurants, shopping, and schools within the township. We consider the lifestyle and proximity to attractions in Cleveland to be a hidden benefit of living and working in Concord. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

Title: Archivist/ Receptionist, Laboratory Operations Reports To: Director, Laboratory Operations Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada, and China, growing significant YoY growth. Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a detail-oriented and highly collaborative support person to aid in duties of the Receptionist as the first point of contact for our company, greeting visitors, and answering phones to provide information and direct inquiries as well as being the archivist relating to the receipt, processing, storage, transfer, and retrieval of study and non-study specific materials. Responsibilities: ESSENTIAL FUNCTIONS: * Greet visitors and aids with meetings and supplies * Perform 5S of lobby and conference rooms as well as keeping the first aid cabinet, visitor supplies, and breakroom supplies stocked * Assist in the creation of employee badges, parking passes and phone list. * Receive, organize, index, and process study and non-study specific (NSS) materials per governing SOPs. * Assign study and NSS document numbers requested by personnel or request them as designee in the archive database in response to emails issuing new protocols. * Issue notebooks and logbooks to study personnel. * Maintain an understanding of federal agency regulations which relate archived materials and maintain records of archival information for all materials received in the Archives using the archive database system. * Maintain on-site Interim Archives * Arrange for transfer to client or client archives, re-archive, or destruction of study materials per request by client, per client response to disposition request, or authorization obtained by Study Director or Principal Investigator. * Interact with personnel at off-site commercial archive facilities for the transfer, storage, disposal and/or retrieval of archived materials. * Perform queries, pull records for audits, viewing, or reproducing as requested. * Review and revise archive SOPs and associated forms as needed. Maintain historical SOP and Test Method Manuals. Education and Requirements: * High School Diploma with 1-2 years experience or Bachelor's Degree with no experience * Strong attention to details Salary and Benefits: Frontage Laboratories offers a competitive compensation and generous benefits package including health and dental insurance, a 401(k) plan, health insurance, short and long-term disability insurance, life insurance etc. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.