Frontage Laboratories jobs

Job Description 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.

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.

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.

Responsibilities: Support the overall effort of Quality Assurance and the Product Development & Manufacturing team to develop new products in collaboration with external clients Facilitate root cause analysis as part of exception investigations and incorporate the results into investigation documentation Write, review and edit technical documentation (batch records, material specifications, etc.) in collaboration with PD&M personnel to assist in the development and qualification of commercial and clinical products Work collaboratively with engineers project teams as needed to develop manufacturing work instructions, product specifications and validation documents Track document review and approval routings, accurately track the status of multiple documents simultaneously Prepare and route documents for approval ensuring compliance with Good Documentation Practices (GDP) and FDA requirements Interface with multiple internal disciplines including manufacturing, analytical, supply chain etc. Occasionally interface with external suppliers and customers Assist in the execution of project plans to satisfy required actions, milestones and deadlines Provide training to other team members as needed Adhere to and ensure compliance with Quality System Standard Operating Procedures (SOP's), Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and FDA requirements Requirements: Working knowledge of regulated manufacturing environments Experience conducting / facilitating root cause analysis using standardized tools Ability to create a variety of manufacturing and engineering documents including production batch records, specifications and test plans Strong command of English language including editing and proofreading skills, spelling, grammer and punctuation Great attention to detail and the ability to communicate well across functions and organizational levels Capable of organizing information into a clear and concise written form Ability to multitask and work in a deadline driven environment Ability to work independently as well as with a team Excellent command of Microsoft Office Suite, especially Word and Excel Bachelor's Degree in a technical discipline (preferred) or equivalent combination of education and professional experience

Job DescriptionDirector 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. 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.

Veterinarian - Full time (onsite) Concord, Unit of Frontage Laboratories: A global pharmaceutical development organization advancing drug discovery and development through integrated laboratory and clinical services. We are more than just a CRO - we are drug developers assisting clients in advancing therapeutics through development to commercial launch in global markets. Location: Concord, Ohio Role Join our team as Staff veterinarian and make a meaningful impact in a dynamic and fast-paced laboratory animal environment. At our Concord, Ohio facility, you will play a crucial role in upholding the highest standards of animal welfare working under the guidance of our Attending Veterinarian. In this vital position you will be responsible for the clinical, preventative and surgical care of our research animals, ensuring their well-being and health. Your contributions will be instrumental in providing veterinary guidance and expertise to groundbreaking research projects, consulting and collaborating with investigators and assisting with facility management. Moreover, you will be a key player in ensuring compliance with federal regulations and international standards, contributing to our commitment to excellence. Your role will also involve providing essential training to our staff, fostering a culture of continuous learning and improvement. If you are passionate about animal welfare and eager to contribute to innovative research, we invite you to join our team and help us achieve our mission of advancing scientific discovery while maintaining the highest ethical standards Key Responsibilities * Clinical Care: providing comprehensive clinical, preventative, surgical care and ensuring the overall well-being of the animals. * Assist composition and refinement of living documents applicable to Animal Care and Use Program. * Compliance: Ensuring compliance with federal regulations and international standards/guidelines related to animal welfare. * Maintaining compliance with Good Laboratory Practices (GLP) and departmental Standard Operating Procedures (SOPs). * Assist with preparation and submission of all reports to proper agencies to maintain compliance with the law and keep current accreditation status. * Provide technical and scientific expertise to departmental scientists and technicians. * Maintain Personal Documentation Record (curriculum vitae, job description, training record). * Participation in Institutional Animal Care and Use Committee (IACUC). * Review of proposal and protocol design for management and IACUC. * Communication: Maintaining effective communication throughout the establishment regarding animal welfare and associated concerns. Including fostering an environment where staff feel confident to communicate animal welfare concerns and ensuring that communication is open and transparent. * Maintain and facilitate communication with the Attending Veterinarian, Study Directors, Sponsors, and management as to the status of studies. * Adhere to corporate and departmental Environmental and Occupational Safety policies. * Facilitate cooperation between Drug Safety and other Frontage operating units. * Other responsibilities/duties as assigned. Education, skills, and experience * Requires a D.V.M. or V.M.D. degree with 3 years of related experience preferably in a laboratory animal environment * Surgical experience: highly desirable. * Experience with husbandry practices and environmental enrichment plans for small and large research animals * Research experience with broad knowledge of animal models: preferred * Experience with GLP regulations and compliance: desirable. * Excellent communication, interpersonal, collaborative communication style, and professional writing. * Knowledge with Good Laboratory Practices (GLP) and compliance * Knowledge of Microsoft Word, Excel and Adobe Systems is desirable. * Maintain professional competence through continuing education. Who we are & what we offer * Frontage is publicly traded and an award winning CRO with over 20 locations across North America and Asia and growing. We offer competitive compensation (base salary, bonus, and equity) and benefits, great place and teams to work with and state of the art facilities. Learn more about us at ******************* * Concord is a unit of Frontage Laboratories. This site provides toxicology testing and research laboratory services and specialized pre-clinical studies in support of pharmaceutical and biotechnology products. 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: 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 saftey pharmacology stdudies 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 Position Summary: The Credit Administrative Assistant performs a variety of clerical responsibilities under minimal supervision. Responsible for processing new and updated credit applications, forwarding credit packets and/or reviews to the business for approval of terms and credit. Other duties include recording and entering customer data into electronic databases (LIMS), along with updating client names and addresses. Responsible for maintaining the client files in the electronic folder. Essential Duties and Responsibilities: * Obtain credit applications from clients based on received request forms or email from facility. Perform credit checks from trade references and obtains credit report. * Obtain credit line approval from the business. Follow up by notifying requestor of new client code number, line of credit and terms. Send credit notification letter to client informing them of their account information. * Generate new client codes for new locations for Eurofins clients. * Maintain address book in LIMS to ensure the legal name and address are accurate to send invoices and statements. Updates client name and address when requested. * All other projects assigned. This role will train onsite at the Barberton lab. Once trained, the work will be remote. Candidate must live within a commutable distance of Barberton, OH. Qualifications Basic Minimum Qualifications (BMQ): Education/Experience (BMQ): * High school diploma or equivalent * General office experience Ability and/or Skills (BMQ): * Time management skills * Requires working knowledge of technical language and terms specific to field of work * Strong customer service skills * Organization skills * Problem solving skills * Ability to communicate effectively at all levels of the organization with internal and external contacts * Analyze problems and effect solutions * Work independently with minimal supervision Additional Information Requirements: * Authorization to work in the United States indefinitely without restriction or sponsorship * Professional working proficiency in English is a requirement, including the ability to read, write and speak in English Position is full-time Monday - Friday 7:00 am - 3:30 pm. Candidates currently living within a commutable distance of Barberton, OH are encouraged to apply. Pay rate: $17/hr 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. 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 benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays, paid time off, and dental and vision options. * The benefits package offered will vary based on the employee's full-time or part-time regular status. To learn more about Eurofins, please explore our website ******************* 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: ***************************** Company description: 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 discovery pharmacology, forensics, advanced material sciences and Eurofins Scientific 2/2 March 2023 agroscience contract research 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 Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 35 years, Eurofins has grown from one laboratory in Nantes, France to 61,000 staff across a decentralised and entrepreneurial network of ca. 900 laboratories in 61 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 2022, Eurofins generated total revenues of EUR 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing 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 Schedule: * Monday-Friday 8:00pm-5:00pm 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 SUMMARY: To travel to offsite locations throughout the coverage area to perform visual inspection and analysis of grain to determine a grade in accordance with Eurofins Grain Inspection SOPs and USDA grain standards on multiple classes of grain or commodities; to perform mycotoxin and other testing procedures on a variety of commodities. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. * Ability to work varying schedules; notifications can be on short notice; workday can vary in the number of hours required to complete an assignment. Overnight stays at the company's expense may be necessary on occasion. * Inspect and grade grain samples accurately and in a timely manner. * Perform tests in accordance with accepted industry practice. Test samples of grain using visual procedures and computerized equipment; test sample for weight, moisture, foreign material, and damage; including mycotoxin and falling number. * Process necessary paperwork required by the Client Company and Eurofins Grain Inspection Manager. Complete appropriate record keeping accurately and legibly. * Responsible for accuracy in reporting results; record test results and provide information to client in the form of a Grain Inspection Certificate. Responsible for timely reporting of billing information to the Rail Inspection Manager in the form of a Rail Report. * Demonstrate good verbal and written communication skills. Maintain regular communication with administrative staff regarding job status, progress, problems, etc. Relay information to the Rail Inspection Manager for proper action. * Maintain grain sampling equipment properly and ensures it is in good working order. * Represent Eurofins Grain Inspection to Client Company by acting as a liaison between facility and Eurofins Grain Inspection. Exhibit excellent interpersonal and communication skills to establish and maintain effective working relationships with subordinates, peers, management, and customers. * Must be able to follow work instructions in a safe, accurate, and timely manner. * Demonstrate proven time management skills and strong attention to detail. * Ability to work well under pressure. * Demonstrate the ability to exercise discretion and independent judgment when necessary. * Exhibit a positive team mindset. * Display the ability to adhere to internal standards, policies, and procedures and the clients. * Assist in training incoming Rail Inspectors in all aspects of grain inspection and all types of grain. Assist in evaluating ability and readiness of new Rail Inspectors to assume responsibility for testing. * Other duties as assigned. Qualifications To perform this job successfully, Rail Inspector must be able to work well independently and with others, have a valid driver's license, and have proof of up-to-date auto insurance. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. EDUCATION and/or EXPERIENCE: * High school diploma and 1-2 years related experience; or equivalent combination of education and experience. DRIVING RECORD: * Position requires a clean driving record within last 3 years, a motor vehicle check is required * Have two years of verifiable driving experience OTHER SKILLS and ABILITIES: * Ability to work autonomously. * Excellent interpersonal and organizational skills. * Excellent communication skills. * Computer skills: Knowledge of Microsoft Office; Word, Outlook, Excel, and Teams. * Attendance and reliability will be mandatory. * Responsive problem solver and action oriented. * Responsive to clients' safety and PPE requirements. PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand, sit and communicate effectively. The employee is required to use different types of equipment and maintain/transfer a mobile lab on wheels for onsite mycotoxin testing. The employee must occasionally lift and/or move up to 15 pounds. Specific vision abilities required by this job include close vision and distance vision. WORK ENVIRONMENT: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Noise level in the work environment is usually moderate. * Allergens present. * Dust Present. Additional Information Pay Range: $16.50/Hr.- $18.50/Hr. Schedule: * Monday-Friday 8:00pm-5:00pm 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 Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Olon USA is a contract manufacturing organization focused on making active pharmaceutical ingredients (API). The primary area of specialization is first time scale up of complex organic chemistry reactions and corresponding purification processes to achieve successful pilot plant production. The company is comprised of highly technical staff with about 75% of all employees being in a technical role. Significant interaction occurs between Chemical Engineers, Organic Chemists, and Analytical Chemists for each pilot plant project that is executed. Essential Responsibilities The ability to interact with chemists to learn new chemical processes, translate these processes into executable instructions, and guide operators through production. Be willing to learn how to scale up production processes from the lab to the pilot plant. Be adaptable when processes do not scale as expected and be able to work closely with production operators in providing instructions. 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. Two or more years of relevant chemical processing experience is preferred. B.S. or M.S. in Chemistry with two or more years of plant experience also considered. Experience in a cGMP environment is a plus. Specific Skill and Requirements Works effectively in a multi-disciplinary team environment Effective time management Able to pay close attention to detail Effective oral and written communication skills Exhibits good judgement, makes sound decisions, seeks guidance as appropriate Development troubleshooting and problem solving skills

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.

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.

Title: Scientist, Genetic Toxicology 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 seeking a detail-oriented and highly collaborative person for a Scientist role to support client‑driven projects using Genetic Toxicology techniques. The successful candidate will work hands‑on in the lab to develop and validate new genetic toxicology assays to meet growing business needs, effectively communicate with internal teams and clients. Responsibilities: Validate unique genetic toxicology assays, trouble shooting for the existing assays, if and when needed Perform experimental phases of GLP and non-GLP studies. Act as Study Director, if and when needed, to conduct GLP and non-GLP studies. Simultaneously handle new assay development and conducting client studies. Ability to work on multiple projects at the same time. Coordinate with department and site management. Write reports for the validation studies and study reports for the assigned client studies while working as Study Director by maintaining the proper level of regulatory compliance and addressing QA audit findings. Maintain tools, computer programs, and SOPs required for studies. Research literature and external sources and identify new techniques and procedures that strengthen Frontage's capabilities. Help with training and/or mentoring of junior scientific staff. Ensure that GLP regulations and SOPs are followed in all service activities. Set-up, utilize, and maintain complex instrumentation Follow safety precautions. Education and Requirements: Understanding of genetic toxicology assays and OECD and ICH guidelines. Experience with flow cytometry. Proven ability to successfully work in a team environment. Excellent oral and written communication skills. PhD with 3 years or MS with 5 years of hand-on working experience in GeneTox labs. Previous working experience in GLP setup is a plus. 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 Data Entry Assistant performs a variety of clerical tasks under minimal supervision. Duties include data entry, electronic reporting, uploading to state web portals and updating database information. Will be cross trained as backup to other team members. This role will train onsite at the Barberton lab. Candidate must live within a commutable distance of Barberton, OH. Essential Duties and Responsibilities: * Basic computer knowledge including prior use of the MS Office Suite (Outlook, Word, Excel) * Basic data entry * Creating and updating simple Excel spreadsheets * Electronic filing of completed work Essential skills: * MS Office skills * Time management * Problem solving * Communicate effectively via email to internal and external accounts * Work through difficult situations with a professional approach * Prioritize workload * Work independently with minimal supervision Qualifications Basic Minimum Qualifications: * Education: High school diploma * Experience: general MS Office experience Ability and/or Skills: * Proficiency in MS Office (Outlook, Excel, Word) * Customer service skills * Communication skills * Ability to prioritize workload and manage interruptions * Time management and organizational skills * Ability to work independently with minimal supervision * Operate standard office equipment Additional Information Position is located, onsite, in Barberton, Ohio. Position will be looking to offer a starting rate of $17.75/hr. Position is full-time, Monday- Friday 8 AM- 5 PM 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.

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 Eurofins Environment Testing North Central LLC in Barberton, OH is seeking to hire a Sample Receiving Technician. Sample Receiving is the first step in our testing process. Every sample you log, store, and route correctly ensures accurate, timely results for clients who depend on our testing-environmental agencies, manufacturers, engineering firms, and more. If you enjoy staying active, keeping things organized, and working as part of a close-knit team, this is a great entry point into the environmental science and laboratory field. This position operates in a fast-moving laboratory intake area. Responsibilities include, but are not limited to, the following: * Unpacking and preparing environmental samples for processing * Logging sample information accurately into the LIMS system * Delivering samples to the correct testing departments * Maintaining sample storage (shelving, refrigerators, and coolers) * Restocking, disposal prep, and general workspace organization * Following strict quality and safety standards * Supporting the entire Receiving team during high-volume periods Qualifications Basic Minimum Qualifications: * HS Diploma * Ability to lift up to 50 lbs. on a repeated basis. * Standing for the majority of the shift. Constant bending, twisting and moving * Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. * Authorization to work in the United States indefinitely without restriction or sponsorship The ideal candidate would possess: * Like active, hands-on work (standing, lifting, moving throughout shift) * Want stable hours with predictable seasonal patterns * Enjoy teamwork and communication throughout the day * Learn best by doing and improving processes over time * Looking for a first step into environmental science or laboratory work * Demonstrates strong organizational skills * Pays close attention to detail * Possesses basic math and computer skills * Demonstrates solid problem-solving skills * Demonstrates awareness of safety procedures * Previous exposure to chemistry, environment science or lab operations Additional Information Schedule: Tuesday-Saturday, 9:00 AM - 5:00 PM (with seasonal overtime) Starting Pay: $17.75/hr. Location: Barberton, OH What we Offer: * Clear training and pathways for advancement * Opportunities to learn other lab areas over time * Overtime pay during peak workload * A supportive, diverse, safety-focused workplace * The ability to contribute to real environmental and public health outcomes * Development opportunities across the Eurofins network 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.

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.

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.

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: 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.