Eurofins jobs in Philadelphia, PA - 123 jobs

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 Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised 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 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description The position focuses on identifying how to set up computer systems, how to troubleshoot and writing the script and steps on how to complete. This is an on-site role, 5 days/week. The Spring House site is not connected with a public transportation line (such as a bus route), reliable transportation needed to get to and from site. We are seeking a meticulous and analytical User Acceptance Testing (UAT) Specialist / Technical Writer to join our team, focusing on lab-based testing software solutions. This dual-role position will ensure that our software applications meet the specific needs of laboratory environments while also producing clear and comprehensive documentation (SOPs, User Guides, Process Flows, Execution Resources). The UAT Specialist / Technical Writer will collaborate with laboratory personnel and IT to develop test plans, both write and execute test cases, and create user manuals and other technical documents to ensure high-quality deliverables. * Test Planning, design and drafting * Collaborate with IT and laboratory scientists, project managers, and stakeholders to understand requirements and define acceptance criteria specific to lab workflows * Develop comprehensive UAT test plans and necessary test cases based on laboratory processes, regulatory requirements, and user stories * Write specific test scripts that evidence the successful performance of the acceptance criteria * Communicating all found bugs and defects in a timely fashion during this initial "smoke testing" process * Test Execution * Execute UAT test cases documenting results and identifying defects or issues related to software functionality. Defects and issues should be at a minimum with adequate hands on drafting time * Self Execute test scripts or Facilitate UAT sessions with lab personnel (as needed) to gather feedback and validate software performance in real-world scenarios * Defect Management * Log and track defects using a defect management tool, ensuring timely resolution and effective communication with development teams * Work closely with software developers to communicate issues and verify fixes, ensuring compliance with laboratory standards. * Incorporate fixes into test scripts as needed * Documentation and Reporting * Prepare UAT reports summarizing test results, defect status and metrics surrounding the testing process * Maintain clear and organized documentation of test cases, test results, and user feedback, ensuring traceability to laboratory requirements Technical Writing * Documentation Development * Create and maintain SOPs, user manuals, technical specifications, and other documentation to support software applications used in laboratory settings * Collaborate with subject matter experts to gather information and ensure accuracy in technical documentation * Content Review and Editing * Review and edit documentation for clarity, consistency, and adherence to company standards * Ensure that all documentation is user-friendly and accessible to laboratory personnel with varying levels of technical expertise * Training Materials & Training * Be capable of training users on new system functionality and providing demonstrations to senior management as needed * Develop training materials and guides to assist laboratory staff in using new systems and features effectively * Conduct training sessions as needed to ensure users understand the software and its functionalities Qualifications Minimum Qualifications * Completed Bachelors degree in a scientific concentration * Authorization to work in the United States indefinitely without restrictions or sponsorship * Experience * 2+ years of experience in scientific or related field software testing, with a strong focus on user acceptance testing * Experience in technical writing, particularly in creating user manuals and technical documentation for software applications. * Technical Skills * Familiarity with software development life cycle (SDLC) and testing methodologies, especially in lab-based applications. * Strong written and verbal communication skills * Proficiency in using testing tools (e.g., Xray, JIRA, ALM (HP)) and an understanding of laboratory information management systems (LIMS). * Experience with documentation software and Microsoft application tools is a plus. * Soft Skills * Strong analytical and problem-solving skills, with attention to detail. * Excellent communication and interpersonal skills, particularly in an IT and lab environment. * Ability to work independently and collaboratively within a team Preferred Qualifications * Experience in Agile/Scrum methodologies. * Exposure to regulatory standards relevant to laboratory software. * Certification in software testing (e.g., ISTQB) and/or technical writing is an advantage. Work Environment * This position may require occasional overtime and flexibility to meet project deadlines. * The role may involve working in a laboratory setting, with adherence to safety protocols. Additional Information Position is full-time, Monday - Friday 9:00am - 5:00pm. Candidates currently living within a commutable distance of Spring House, PA are encouraged to apply. 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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Manufacturing Assistant Title: Manufacturing Assistant Reports to: Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada 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. Position/Job Summary: Frontage Laboratories Inc. is hiring Manufacturing Assistant. The position is responsible for supporting Manufacturing and R&D staff in manufacturing and laboratory activities. The ideal candidate will play a crucial role in maintaining cleanliness and hygiene in GMP Pharma cleanrooms, supporting areas and laboratory glassware etc., and ensuring that all cleaning tasks are completed to a high standard. The duties include recording data and maintaining an inspection ready clean environment. Roles & Responsibilities: Perform cleaning tasks such as mopping, vacuuming floors, cleaning, and disinfecting cleanrooms and supporting areas. Clean laboratory glassware and manufacturing equipment machinery, and other equipment Safely handle and dispose of industrial waste materials and hazardous substances according to company and regulatory guidelines. Monitor cleaning supplies and equipment, reporting any shortages or maintenance needs to the supervisor. Ensure proper usage of cleaning chemicals, following instructions and safety data sheets (SDS) for safe handling and storage. Adhere to safety protocols, including the use of personal protective equipment (PPE) in hazardous areas. Participate in Setup of equipment and Monitor and record readings of equipment and systems. Assist Manufacturing Associates and Scientists in pharma drug manufacturing activities Report any maintenance or safety issues to the supervisor or facility manager. Maintain accurate logs of daily cleaning activities and any safety incidents. Other duties assigned by Supervisor/Manager. Education, Experience & Skills Required: Some High School education, High school diploma or equivalent preferred. Working knowledge of computer applications Good verbal and written communication skills. Experience in industrial or commercial cleaning preferred but not required. Knowledge of proper cleaning techniques and chemical handling. Strong attention to detail and commitment to maintaining high cleanliness standards. Ability to work independently and follow instructions accurately. Must be physically capable of lifting heavy objects and performing tasks that require prolonged standing, walking, bending, and reaching. 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 disability .

Full-time Exton, PA Frontage Laboratories: Frontage Laboratories Inc. (Frontage), is a global contract research organization with broad expertise in supporting pre-clinical and clinical drug development. Frontage operates out of several different locations within the USA, Canada, and China. Frontage's core competencies include drug metabolism, pharmokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: The Project Coordinator will support Project Management teams in the management and successful delivery of assigned Projects. Responsible for communicating e-mail and other forms of client communication. The Project Coordinator role is critical to our clients. Focus on professionalism and Customer Service Excellence with project success in mind, executing with efficiency always. Quality, and communication skills are a must to be successful in this role! Position Responsibilities: Under direction from PM team co-ordinate projects from award stage to completion ensuring correct planning timelines are generated, monitored and tracked to ensure successful adherence and completion. Attend and produce minutes and actions for internal and external client meetings/teleconferences/client visits and Audits to support PM team and understand full scope requirements to generate all required project documentation. Be the primary liaison between the Project Management Team and the Lab Operations Team and Sample Management Team. Monitor and track client studies in line with project requirements. Collect and supply relevant information and produce project forecasts to Project Teams to support client management. Support Project Management and Lab Operations team with Invoicing, as necessary. Provide information to Project Manager on specific project requirements and act as back up to Project Managers for specific tasks in the Project Manager's absence Become proficient in understanding timelines and tasks required for biological studies in order to set up projects within tracking systems, track projects in tracking systems and enter data and maintain projects in tracking systems. Become proficient in understanding project financial milestones to support invoicing under the guidance of PM. Assist in the preparation and regular review of Standing Operating Procedures relating to own areas of responsibility. Position Requirements: Minimum of a High School Diploma. Associates Degree strongly preferred. 6 months to 1 year experience in a customer service or appropriate business-related area preferred. Good Time Management/ Organizational skills adopting a committed approach to providing a high level of customer service when managing multiple tasks. Excellent communication skills - written and verbal. The ability to work as part of a team, adopting a right first-time approach ensuring the commitments are met in a timely manner. Demonstrated professionalism including excellent work ethic, positive attitude and experience communicating with external clients. 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 disability.

Job DescriptionScientist, Biologics Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada 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. Responsibilities: Primary responsibilities include, but are not limited to the following: Perform analytical and biological sample testing • Conduct method development and validation studies • Perform immunoassay techniques: (ligand binding assays, ELISA, MSD, and/or RIA applicable to Pharmacokinetic and Immunogenicity studies), with proficiency • Prepare and handle various cell lines, tissue culture media and other reagents for cell-based assays such as Neutralizing Antibody (NAb) assays • Maintenance of instruments, and address technical and instrumental issues • Assist the Principal Investigator with study conduct • Maintain study documentation • Meet regulatory compliance requirements • Maintain a safe work environment Requirements: Bachelor's degree in related scientific discipline or Bachelors degree with relevant experience • At least 2 years working in a laboratory preferred 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 disability.

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominantly performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions. Responsibilities: * Proficient in aseptic technique concepts. * Ability to complete and maintain aseptic gowning qualification, aseptic process qualification, and cleaning & disinfection qualification. * Perform aseptic processing, including media exchanges, vessel passaging, harvest & cryopreservation of cells as required by the daily production schedule. * Perform media and reagent preparation duties as required. * Ability to operate and maintain equipment. * Perform equipment preventative maintenance and cleaning/disinfection as required. * Basic User trained on electronic support systems (i.e. BMRAM, MasterControl, etc.) * Perform, record, and report various inventory tasks (i.e., consumables, media, cryovials, etc.) * Follows, revises, and executes SOPs and WBRs in accordance with cGMPs. * Collects and records scientific and process data per good documentation practices (GDPs). * Participates in quality event investigations by providing accurate information. * Assists with the receipt and organization of materials. * Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. * Manages time well and multitasks to complete all assignments and responsibilities with the supervisor's guidance. * Maintains a safe working environment for self and others, including work area cleanliness. * Monitors resources and enforces SOPs to ensure data integrity and compliance with industry. * Participates in process optimization and continuous improvement opportunities. Computer Skills: * Use of basic Microsoft applications efficiently. * Contribute to SOP/BR generation and revision, quality investigations, Corrective/Preventive Action initiatives, and Change Control procedures. Qualifications Education: * Minimum Bachelor of Science degree in a scientific discipline (or equivalent industry experience) Experience: * 1 year experience in mammalian cell culture in an academic or industrial laboratory * Knowledge of basic laboratory skills (aseptic technique, pipetting, etc.) are required. * Must be comfortable with performing tasks while fully gowned in an aseptic cleanroom environment. * Knowledge of 21CFR Part 11, standard GxP best practices and other industry standards. * Mammalian cell biology experience is considered a plus. * Excellent verbal and written skills. * Good interpersonal communication skills. * Must be willing to work weekends, evenings, and holidays (as needed). Additional Information What to Expect in the Hiring Process: * 10-15 Minute Phone Interview with Region Recruiter * 45-60 Minute Virtual Interview with Manager and/or Group Leader Additional Details: This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to Exton, PA are strongly encouraged to apply. Excellent full-time benefits include: * comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions 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. The Eurofins network of companies believes that it is a global leader in food, environment, pharmaceutical and cosmetic product testing and in discovery pharmacology, forensics, advanced material sciences and agroscience contract research services. It is also one of the market leaders in certain testing and laboratory services for genomics, and in the support of clinical studies, as well as in biopharma contract development and manufacturing. 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 ca. 63,000 staff across a decentralised and entrepreneurial network of more than 950 laboratories in 60 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 million, and has been among the best performing stocks in Europe over the past 20 years. Job Description Eurofins' corporate development team leads the execution of the company's strategic business and financial goals through merger and acquisition activity across all business lines. Our inorganic growth is a key component of Eurofins' overall strategy. The company has historically completed several dozen transactions annually on a global basis. The Associate will manage a complete pipeline of M&A targets in United States that generates $10MM to $50MM new revenues annually with an appropriate return in line with Eurofins' financial objectives. This is a highly visible role in the organization with direct exposure to, and interaction with, business and corporate leadership. The ideal candidate will have 4-6 years of experience in corporate development, transaction advisory, investment banking or private equity. Job Duties and Responsibilities: 1. Prospection: · Market analysis and identification (through lists of accreditations as well as market rumors and internal inputs) of potential acquisition targets · Select targets together with business leaders based on strategic relevance and likelihood of success (long list) · Coordinate information flow between the targets, Business Unit, and Eurofins via log-file (long list) and active project list (short list) · Approach potential targets, check with owner compatibility of interest/objectives and sell them the Eurofins concept 2. Acquisitions: · Negotiate confidentiality agreements and gather and analyze preliminary data such as confidential information memoranda, management presentations, financial statements, shareholding and leadership details · Evaluate targets in conjunction with Business Unit leader and members of the corporate development team based on their business and financial condition and outlook and recommend deal structure · In conjunction with members of the corporate development team, advise on the transaction process and tactics, in particular interfacing with the potential targets, shareholders or advisors and assist the business leaders in preparing negotiation documents required to progress a transaction towards completion including term sheets, heads of agreements, indicative offer letters or exclusivity agreements as required · Coordinate the due diligence and coordinate the activities of other external advisors (e.g. legal counsel, auditors) as required by the company · Assist negotiations and related strategy, attend meetings and give comments on sale and purchase documentation until signing/closing as required by the company · Validate the acquisition contracts, e.g., representations and warranties … · Create and manage attachments and exhibits for contract · Prepare recommendations to the investment committee · Coordinate of the closing of the deal, including financial statements 3. Integration of the acquired companies: · Assist in setting up reporting and quality of communication between the acquired companies and the general management of Eurofins · Support a potential legal reorganization of some companies, fiscal and financial optimization · Follow-up any post-closing obligation resulting from the acquisition (earn-outs, closing balance sheet adjustments, escrow releases, etc…) · Assist internal counsel with preparation of shareholder resolutions Qualifications EDUCATION and/or EXPERIENCE: · Bachelor's Degree in Business or Finance o MBA or CPA is preferred o Science background or interest preferred · Outstanding technical / conceptual understanding of finance & valuations · Minimum 4-6 years of M&A experience in Audit (big 4) / Consulting, M&A (industry or boutique), Investment Banking or Private Equity; preferably experience in executing M+A strategy for an acquisitive corporation · Previous exposure and solid understanding of the M&A process (NDA, LOI, DD, SPA) · Fluency in English. Fluency in Spanish is a plus · Excellent knowledge of MS Office tools (Excel, PowerPoint) OTHER SKILLS and ABILITIES: · Strong analytical and conceptual skills, good strategic thinking and business acumen · High energy level, drive and a passion to succeed; eager to learn and to grow · Strong interpersonal skills, including listening and communication skills (verbal and written) · Excellent interpersonal, communication & team leadership skills · Self-starter, ownership and natural leadership & drive to get things done · Pragmatic and "roll up sleeves" mentality, can do attitude, result driven, strong work ethics · Courage and self-confidence to take initiatives; autonomy · Ability to work with people from different cultural backgrounds · Thinking big picture, yet understanding details · Consistent exercise of independent judgment and discretion in significant matters · Comfortable to work in a very dynamic, fast growing environment and entrepreneurial, de-centralized organizations · Perform comprehensive peer reviews of team member transactions and support, in relation to the workload, similar activities in other lines of business / countries · Ability to manage multiple projects concurrently and work during nights and/or weekends as necessary · Domestic travel is required - 15%-20% Additional Information Why Eurofins? Eurofins is a global leader in analytical testing, with 62,000+ employees across 900 labs. Our New Orleans site plays a critical role in food safety and botanical testing. You'll join a mission-driven team that values integrity, innovation, and impact-and you'll have real ownership to grow the business. Ready to Lead? Apply now to take charge of a thriving lab and help shape the future of contaminant chemistry at Eurofins. Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. All your information will be kept confidential according to EEO guidelines.

Full Time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada 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. Position/Job Summary The lab assistant position entails calibrations and maintenance of various laboratory equipment for our 760 Exton location located on Pennsylvania Drive. Primarily calibrating freezers, incubators, automation platforms and various other smaller lab equipment's. The position requires an individual to be flexible at the requests of laboratory scientists including buffer prep and various instrument flushing. General laboratory housekeeping is also included. Roles and Responsibilities Ability to read and position various calibration instruments. Ability to keep documentation in a neat and orderly fashion. Ability to lift to 50lbs. Ability to follow safety procedures. Ability to work as a team. Ability to work independently with little supervision. Ability to work the 9am to 5:30pm shift. An 8 hour work shift everyday M-F. Education Requirements: High school diploma or higher. Experience and Skills Prior experience working in a laboratory, particularly with sample preparation, equipment operation, and data recording is preferred. Familiarity with common laboratory equipment and instruments, such as centrifuges, microscopes, pH meters, etc. Knowledge of preparing buffers, media, and other common laboratory reagents. Capable of recording experimental data and using computer software (e.g., Excel, SPSS) for data processing and analysis. Able to manage time and prioritize tasks effectively in a fast-paced work environment. Strong learning ability. 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 disability.

Exton, PA, USA Full-time ** The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. **If you're looking for a rewarding career, a place to call home, apply with us today!** **Job Description** **General Responsibilities:** Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominately performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions. **Responsibilities:** + Proficient in aseptic processing including media exchanges, vessel passaging, harvest & cryopreservation of cells as required by the daily production schedule. + Ability to complete and maintains aseptic gowning qualification, aseptic process qualification and cleaning & disinfection qualification. + Perform media and reagent preparation duties as required. + Ability to operate and maintain equipment. + Perform equipment preventative maintenance, cleaning/disinfection, and basic troubleshooting, as required. + Perform, record and report various inventory tasks (i.e. consumables, media, cryovial, etc. + Ability to train others on support tasks, basic SOPs, equipment, and process operations. + Achieves PowerUser status on supporting electronic systems (i.e. MasterControl). + Follows, revises, executes, and authors SOPs and MBRs in accordance with cGMPs. + Ability to open and review documentation and MBR's at a high level. + Ability to author and close quality items. + Ability to initiate simple change controls and manage tasks required. + Assists with material procurement and receipt. + Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. + Manages time well and multi-tasks to complete all assignments and responsibilities with supervisor's guidance. + Maintains a safe working environment for self and others, including work area cleanliness. + Monitors resources and enforces SOPs to ensure data integrity and compliance with industry. + Participates in process optimization and continuous improvement opportunities. + Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. **Computer Skills:** + Use of basic Microsoft applications efficiently. + Contribute to SOP/BR generation and revision, quality investigations, Corrective/Preventative Action initiatives, and Change Control procedures. **Qualifications** **Education:** + Minimum Bachelor of Science degree in a scientific discipline (or equivalent industry experience) **Experience:** + 2+ years of experience in mammalian cell culture in an academic or industrial laboratory + Knowledge of basic laboratory skills (aseptic technique, pipetting, etc.) are required + Must be comfortable with performing tasks while fully gowned in a cleanroom environment. + Proficient in Manufacturing Process. + Knowledge of 21CFR Part 11, standard GxP best practices and other industry standards. + Proficient in Mammalian cell biology + Excellent verbal and written skills + Good interpersonal communication skills + Must be willing to work weekends, evenings, and holidays (as needed). **Additional Information** **What to Expect in the Hiring Process:** + 10-15 Minute Phone Interview with Region Recruiter + 45-60 Minute Virtual Interview with Manager and/or Group Leader **Additional Details:** This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to Exton, PA are strongly encouraged to apply. **Excellent full-time benefits include:** + comprehensive medical coverage, dental, and vision options + Life and disability insurance + 401(k) with company match + Paid vacation and holidays **_Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day._** **Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

Job Description Associate Project Manager- Bioanalytical & Biologics Services Reports to: Group Leader, BioA Project Management Full-time Frontage Laboratories: Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada 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. Bioanalytical & Biologics Services: At Frontage, we believe that we deliver high quality services through our focus on technical excellence, which enables us to understand and solve complex drug development challenges. Our deep scientific expertise in method development, transfer and validation allows us to provide clients with complex solutions for challenging studies including oncology clinical trials, rare disease assay development and specialty assays Position Summary: -Manage and monitor project progress and timelines to ensure successful completion from start up to end of study. -Participate and communicate effectively in project meetings with clients on a regular basis as well as with cross-functional teams to ensure projects are met with quality and within the applicable scope and budget. -Collaborate with the financial sector throughout various stages of projects (monthly invoices, revenue recognition, and budget final reconciliation). -Support Management and BD team for new business opportunities. -Onsite is required as needed. Position Responsibilities: -Minimizes risks on projects by working closely with the lab operations and lab support teams, PIs, and sponsors to ensure project progress is met for each milestone in accordance with project scope per requested timelines by the sponsor. -Creates, updates and tracks projects in project management tool (QuickBase) daily and generating project trackers and reports as requested. -Leads/participate in project meetings with sponsors on a regular basis or on as needed basis and prepare meeting minutes to ensure alignment of deliverables. -Serves as a liaison between internal departments (scientific staff, QC/TW, QA, SM, etc.) to ensure project timelines are met with quality. -Proactively communicate with clients on project timelines, issues, and updates via phone, e-mails, or TC as necessary. -Requests and reviews invoices per milestone on a rolling basis that are tracked in QuickBase and respond to client's questions related to invoices or finance aspects or assists finance team on those issues as needed (i.e. revenue recognition per month and final budget reconciliation. -Facilitate internal and external communication and activities on data transfer specification (DTS) development and complete data transfers to data management vendors/sponsors. -Participate in onsite client visits and assist internally in preparation as necessary. Position Requirements: Bachelor's degree or higher in biological sciences, chemistry, or related discipline. In-depth knowledge of bioanalytical and/or biologics assays. Minimum 1-2 years of project management experience in GLP, Pharmaceutical or CRO environment. Excellent communication and strong client relationship management skills. Proficient with Excel, Word, PowerPoint and other computer skills. Good Time Management/ Organizational skills adopting a committed approach to providing a high level of customer service when managing multiple tasks. Demonstrated professionalism including excellent work ethic, positive attitude and experience communicating with external clients. Salary and Benefits: Frontage Laboratories offer 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 disability.

Title: Project Manager Assistant- Central Lab Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada 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. Position Summary: Assisting project managers in compiling information from the different protocols, ie. Counting how many types of samples and how many of each type. Onsite only. Position Responsibilities: * Making edits to lab manuals which will be reviewed by project managers * Entering in tracking data from samples into the different tracking sheets. * Create PPT slides, word, and excel documents based on existing templates (including formatting) * Inventory management and restocking office supplies * Label printing and creation of label packets * QC eManifest timepoints, PIF, label excel, label barcode, supply orders * Schedule meetings and take meeting minutes * Other duties as assigned Position Requirements: * Associate's Degree or higher * Has excellent communication skills * Proficient with Excel, Word, PowerPoint, Microsoft Teams, and other computer skills * High level of accountability with self and others * Hands-on approach with a desire to teach others * Track record of challenging the status quo * Team and action-oriented * Problem-solving * Priority setting 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 disability.

Malvern, PA, 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. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised 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 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. **Job Description** **This isn't just a testing role, it's a chance to contribute directly to breakthroughs that improve patient lives in a collaborative, fast-paced environment.** Role focuses on routine cGMP testing of samples for biopharmaceutical clients in a BSL-2 laboratory which may include HPLC, SEC, CE-SDS, cIEF, MDI/MFI, GC, UV-VIS spectroscopy (A280 and SoloVPE), oligosacharride mapping, turbidity, and/or osmolality + Conduct analysis and reporting of data in accordance with requirements set forth by the department in electronic notebooks. + Apply GMP/GLP in all areas of responsibility, as appropriate + Provide training for other analysts + Demonstrate strong client service skills, teamwork, and collaboration + Meet all quality and productivity metrics and demonstrates strong teamwork and collaboration + Troubleshoot assay or instrumentation problems **Qualifications** + Bachelor's or Master's degree in a related science (chemistry, pharmacy or equivalent sciences degree) + Prior work experience in a **GMP laboratory** + **Must** **have prior experience** with separations techniques **including chromatography or capillary electrophoresis** + Authorization to work in the United States indefinitely without restriction or sponsorship **Additional Information** **Position is full-time, Monday - Friday 9:00am - 5:00pm** . Candidates currently living within a commutable distance of **Malvern, PA** are encouraged to apply. 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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

Horsham, PA, USA Full-time ** Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA. Group's key figures are approx. 6.95 billion Euros turnover, over 950 laboratories across 60 countries and about 63,000 staff. **Job Description** Eurofins Environmental Testing Philadelphia is a full-service environmental laboratory that has provided analytical chemistry and microbiological services to a diverse range of clients since 1943. Eurofins ETP's analytical product array is focused on providing testing services that enable clients to meet their regulatory and monitoring requirements. Analytical data is produced within a quality system framework that provides clients with an accurate and representative portrayal of a sample's constituents. This data empowers them to make informed, confident decisions regarding future actions related to regulatory compliance requirements. Eurofins is searching for a Field Technician located in the Horsham, PA region. Schedule is Mon-Fri 8:00am- 5:00pm +/- overtime as needed. Compensation range - $17-20/hour based on field experience. Full Benefits. This position is outside the majority of the time and will also drive the company vehicle. **MUST have a valid Drivers license.** + 2-4 years' experience in environmental and monitoring well sampling **preferred but not necessary - will train** **Field Technician responsibilities include, but are not limited to, the following:** + Collect field samples in assigned area of responsibility from assigned clients. + Plan and complete daily assigned route in accordance with priorities. Notify supervisor of any changes to plan. + Prepare and deliver sample containers/materials to various clients in support of their account. + Regularly transport, set up, utilize, troubleshoot and break down sample collection/monitoring equipment in support of assigned projects/customer accounts. + Communicate directly with customers providing clear and accurate information concerning their sample collection timeline and access requirements. + Communicate with supervisor and main laboratory, routinely sending timeline and sample/project updates throughout assigned daily route. + Perform miscellaneous on-site testing when required, record all data, and complete/submit all required sample documents. + Transport samples from the field back to the laboratory, maintaining accurate sample custody documentation, occasionally link up with other technicians mid-route to facilitate sample transport and supply exchanges. + Drive safely and observe all traffic laws. Maintain assigned vehicle according to company expectations for cleanliness and maintenance. + Observe all OSHA safety requirements while adhering to the company health and safety policies; do not enter any confined space(s) without direct approval from upper management. + Fill out and maintain documentation/records related to field sampling activity. Document all data as required by the method performed and maintain logbook records in a complete and ethical manner + Work assigned shift/hours in support of business needs maintaining flexibility to work overtime, weekends and/or holidays when requested. **The ideal candidate would possess:** + A working knowledge on the use and maintenance of monitoring well equipment including but not limited to, ready flow pumps, peristaltic pumps, and proactive pumps. + Must be able to navigate using vehicle GPS, roadmaps, and written directions. + Strong computer, scientific, and organizational skills. Able to work with Laboratory Information Management System. + Strong communication and interpersonal skills, customer service oriented; internal and external customers. + Must be able to sit or stand for long periods of time as well as be able to lift a 25-pound object from the floor to a shelf five feet high. + Strong time management skills. Able to adapt and shift priorities as needs of the business evolve. + Ability to work independently and as part of a team with limited supervision, maintaining a positive attitude and a self-motivated/goal oriented mindset. + Detail oriented with ability to learn new techniques, multi-task, keep accurate records, follow instructions, and comply with company standard operating policies. + Experience with technical field equipment including, but not limited to, field measurement meters, well pumps, auto samplers, and tablets/software programs. **Qualifications** **Basic Minimum Qualifications:** + 2-4 years' experience in environmental and monitoring well sampling **preferred but not necessary - will train** + High school diploma or equivalent with degree in environmental sciences, biology, chemistry, or earth sciences + Must have a valid driver's license and possess a clean driving record + Ability to lift up to 50 pounds. Samples will be in coolers packed in ice + 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. + Perform other duties as assigned **The company will provide all required training and a vehicle for use during work hours.** "All offers of employment are contingent upon a successful completion of a pre-employment drug screen and background check." This position description is written as a guideline to inform employees of what is generally expected of them at each job level. The description is not intended to be all encompassing or limiting in any manner; rather, it is hoped it will add understanding and better reflect the work performed at all levels of employment. Duties and responsibilities other than those listed may be included as needed within the work group or the company as a whole. **Additional Information** **_We do not offer Visa Sponsorship for this role._** Eurofins Environment Testing (USA) provides a compensation range for informational purposes, the actual base Compensation may vary based upon, but not limited to, relevant experience and skill set, base compensation 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: ******************************* 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 :40 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 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. 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. **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 Business Unit Manager (BUMa) is responsible for maintaining positive operating margin at the laboratory level and for meeting and exceeding the annual budget. Supervises all laboratory personnel and provides leadership and direction as needed. Responsible for ensuring compliance and integration of facility operation with corporate and regulatory policies and procedures. The Business Unit Manager will serve as a liaison with corporate business partners and will champion Company policies, vision, and mission. Business Unit Manager responsibilities include, but are not limited to, the following: · Lead team, schedule, and train employees · Ensure adherence to highest quality and efficiency standards in laboratory operations · Ensure coverage and performance · Foster morale and teamwork · Demonstrates and promotes the company vision · Regular attendance and punctuality · Manage the technical conduct, quality control, and related record keeping of all analytical evaluations performed · Responsible for the supervision, organization, and coordination of all technical activities of personnel within the principles of sound scientific endeavors, business economy, and the professional development of subordinate employees. · Provide the necessary planning, organization, direction, and control to meet the goals of the company. · Ensure that all pertinent company health, safety, and environmental programs are adhered to and documentation is maintained. · Establish and maintain professional business relationships with clients, industry officials, and peers. · Assist in the generation of marketing strategies, prepare comprehensive technical work proposals, and maintain an influential position in establishing business expansion plans. · Provide input toward the financial growth and development of the company. · Coordinate business activities with the Business Unit Managers from the other locations to ensure customer expectations are met without duplication of testing activities. · Responsible for the overall operational success of the laboratory, which includes, but is not limited to: budgeting, making decisions on capital expenses, managing senior staff, attending to major client needs, revenue & profit growth, and cost control. · Oversee daily operations including: laboratory, quality, logistic, and managerial duties. · Represent the laboratory in technical meetings. · Participate with the Sales/Marketing team in the preparation and quotation of major technical studies. · Propose major investments to company executives. · Ensure that the laboratory expenses are on track with the annual budget. · Approve major expenses and control the costs of the laboratory within established company guidelines. · Analyze monthly laboratory indicators (operating and labor costs, turnaround time, productivity, etc.). · Verify that company employment policies and procedures are followed correctly. · Perform annual performance reviews for direct reporting personnel. Coordinate and review annual reviews of other lab personnel. · Handle employee relation issues as per company guidelines and with the support of Human Resources. · Coordinate the interaction between the different laboratory departments. · Understand and follow each Quality System document relevant to employment responsibilities, e.g., methods, SOPs, etc. Propose changes to documents and approve documents when required · Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Education: · Bachelor's degree in biology, chemistry, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major) Experience: · At least 10 years of supervisory experience · At least 10 years professional experience in laboratory operations with a minimum of 5 years of laboratory operations or large/multi-department/team leadership with profit/loss accountability - $5M+ Net Sales or equivalent size operation. Demonstrated success in improving operational, profit, quality and safety performance. · Familiarity with laboratory operations and services · Familiarity with EPA, DOT, OSHA, and DOL regulations · Excellent verbal and written skills · Strong customer relations skills · Ability to manage a business at a profit/loss responsibility level · Ability to control operating budgets · Ability to develop and enforce policies and operating practices · Ability to prioritize and delegate responsibilities · Ability to successfully handle contract and other negotiations · Strong decision-making abilities · Problem-solving abilities Professional working proficiency in English is a requirement, including the ability to read, write and speak in English. Additional Information 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 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 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. We do not offer Visa Sponsorship for this role. 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. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description General Responsibilities: Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominately performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions. Responsibilities: * Proficient in aseptic processing including media exchanges, vessel passaging, harvest & cryopreservation of cells as required by the daily production schedule. * Ability to complete and maintains aseptic gowning qualification, aseptic process qualification and cleaning & disinfection qualification. * Perform media and reagent preparation duties as required. * Ability to operate and maintain equipment. * Perform equipment preventative maintenance, cleaning/disinfection, and basic troubleshooting, as required. * Perform, record and report various inventory tasks (i.e. consumables, media, cryovial, etc. * Ability to train others on support tasks, basic SOPs, equipment, and process operations. * Achieves PowerUser status on supporting electronic systems (i.e. MasterControl). * Follows, revises, executes, and authors SOPs and MBRs in accordance with cGMPs. * Ability to open and review documentation and MBR's at a high level. * Ability to author and close quality items. * Ability to initiate simple change controls and manage tasks required. * Assists with material procurement and receipt. * Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. * Manages time well and multi-tasks to complete all assignments and responsibilities with supervisor's guidance. * Maintains a safe working environment for self and others, including work area cleanliness. * Monitors resources and enforces SOPs to ensure data integrity and compliance with industry. * Participates in process optimization and continuous improvement opportunities. * Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. * Supervise a team including task assignments and performance management Qualifications Education: * Minimum Bachelor of Science degree in a scientific discipline (or equivalent industry experience) Experience: * 3+ years of experience in a cGMP setting * Hands on experience with cell therapy manufacturing and mammalian cell culture * Experience in a leadership role * Knowledge of basic laboratory skills (aseptic technique, pipetting, etc.) are required * Must be comfortable with performing tasks while fully gowned in a cleanroom environment. * Proficient in Manufacturing Process. * Knowledge of 21CFR Part 11, standard GxP best practices and other industry standards. * Proficient in Mammalian cell biology * Excellent verbal and written skills * Good interpersonal communication skills * Must be willing to work weekends, evenings, and holidays (as needed). Additional Information What to Expect in the Hiring Process: * 10-15 Minute Phone Interview with Region Recruiter * 45-60 Minute Virtual Interview with Manager and/or Group Leader Additional Details: This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to Exton, PA are strongly encouraged to apply. Excellent full-time benefits include: * comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Philadelphia, PA, USA Part-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 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.** **In 2020, Eurofins generated total revenues of EUR 5.4 billion, and has been among the best performing stocks in Europe over the past 20 years.** **Job Description** The Laboratory Technician Shall: + Responsible for pre-analytical processes within the life cycle of the laboratory specimen collection, packaging, shipping, receiving, processing, tracking, test adds/cancellations, create and resolve specimen service requests, specimen archiving, and archive returns to customers. + Technician will not perform any work related to patient testing (i.e. specimen dilutions, assay set-up, placing patient specimens on instrumentations, etc.); this work is to be performed solely by licensed CLS employees. + Perform cleaning duties, equipment maintenance (daily/PM, as needed) + Perform filing, scanning and archiving of quality and testing records + Work closely and communicate with other lab staff to complete daily activities efficiently, contribute to team effort + Interfaces with Eurofins DPT clients to resolve specimen issues + Recommends changes in services, processes, and policies that enhance pre-analytical efficiencies. + Contributes to team effort by accomplishing related results as needed + Other duties as assigned + Performs duties in compliance with all applicable regulatory and accrediting agencies + Supports Eurofins DPT's business philosophy, leadership values, and ethics + Meets basic expectations of Eurofins DPT's quality management system, including, but not limited to good workmanship, adherence to standard operational procedures, training, good documentation practices, accurate recordkeeping so the company may meet its stated quality policy and objectives The essential physical and mental requirements described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. **Qualifications** **MINIMUM EDUCATIONAL REQUIREMENTS** + High School diploma or GED equivalent **WORK EXPERIENCE REQUIREMENTS** + 0-2 years of experience + Specimen management experience (preferred, but not mandatory) + Effective time management, organizational skills, and the ability to multi-task and prioritize with minimal assistance + Ability to partner effectively with management and laboratory teams + Strong written and oral communication skills, inter-personal, and negotiation skills + Intermediate Excel, Word, PowerPoint, Outlook, and other systems + Ability to work in a controlled environment and within Quality Systems under regulatory requirements **Additional Information** **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.**

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 Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised 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 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Responsibilities include, but are not limited to, the following: * Execute assay runs and maintenance activities to support the development, qualification, and clinical testing for various immunological techniques (ELISA, MSD, Luminex, and cell based assays) * General laboratory upkeep, maintenance, and ordering of supplies * Use LIMS and/or Excel workbooks to analyze run data * Work according to established Standard Operating Procedures (SOPs) and regulatory guidance * Maintain accurate records in adherence with documentation standards * Collaborate and communicate within and across the work group * Work in a structured environment under direct to moderate supervision * The position requires work with infectious agents and/or pathogens. The site is not connected or nearby to public transportation options (bus/train etc.) Qualifications Basic Minimum Qualifications: * B.S./B.A. in Molecular Biology, Immunology, Cell Biology, Biology, Biochemistry, Biology, or related biological science discipline. * Experience and knowledge of cell-based assays, pipetting, aseptic technique * Authorization to work in the United States indefinitely without restriction or sponsorship. The ideal candidate would possess: * Strong computer, scientific, and organizational skills * Familiarity with Laboratory Information Management System (LIMS) * 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 and real time records, follow instructions, and comply with company policies * High sense of responsibility, accountability, and professional integrity * Previous working experience in a regulated environment (GxP) * Experience with immunological techniques (ELISA, MSD, Luminex, and/or cell based assays) is also desirable Additional Information This position is Full-Time, Monday through Friday, 8a.m. to 5 p.m with overtime as needed. Candidates currently living within a commutable distance of Spring House, PA are encouraged to apply. 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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Spring House, PA, 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. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation 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 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised 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 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. **Job Description** **_The position focuses on identifying how to set up computer systems, how to troubleshoot and writing the script and steps on how to complete._** **_This is an on-site role, 5 days/week. The Spring House site is not connected with a public transportation line (such as a bus route), reliable transportation needed to get to and from site._** We are seeking a meticulous and analytical User Acceptance Testing (UAT) Specialist / Technical Writer to join our team, focusing on lab-based testing software solutions. This dual-role position will ensure that our software applications meet the specific needs of laboratory environments while also producing clear and comprehensive documentation (SOPs, User Guides, Process Flows, Execution Resources). The UAT Specialist / Technical Writer will collaborate with laboratory personnel and IT to develop test plans, both write and execute test cases, and create user manuals and other technical documents to ensure high-quality deliverables. + **Test Planning, design and drafting** + Collaborate with IT and laboratory scientists, project managers, and stakeholders to understand requirements and define acceptance criteria specific to lab workflows + Develop comprehensive UAT test plans and necessary test cases based on laboratory processes, regulatory requirements, and user stories + Write specific test scripts that evidence the successful performance of the acceptance criteria + Communicating all found bugs and defects in a timely fashion during this initial "smoke testing" process + **Test Execution** + Execute UAT test cases documenting results and identifying defects or issues related to software functionality. Defects and issues should be at a minimum with adequate hands on drafting time + Self Execute test scripts or Facilitate UAT sessions with lab personnel (as needed) to gather feedback and validate software performance in real-world scenarios + **Defect Management** + Log and track defects using a defect management tool, ensuring timely resolution and effective communication with development teams + Work closely with software developers to communicate issues and verify fixes, ensuring compliance with laboratory standards. + Incorporate fixes into test scripts as needed + **Documentation and Reporting** + Prepare UAT reports summarizing test results, defect status and metrics surrounding the testing process + Maintain clear and organized documentation of test cases, test results, and user feedback, ensuring traceability to laboratory requirements **Technical Writing** + **Documentation Development** + Create and maintain SOPs, user manuals, technical specifications, and other documentation to support software applications used in laboratory settings + Collaborate with subject matter experts to gather information and ensure accuracy in technical documentation + **Content Review and Editing** + Review and edit documentation for clarity, consistency, and adherence to company standards + Ensure that all documentation is user-friendly and accessible to laboratory personnel with varying levels of technical expertise + **Training Materials & Training** + Be capable of training users on new system functionality and providing demonstrations to senior management as needed + Develop training materials and guides to assist laboratory staff in using new systems and features effectively + Conduct training sessions as needed to ensure users understand the software and its functionalities **Qualifications** **Minimum Qualifications** + Completed Bachelors degree in a scientific concentration + Authorization to work in the United States indefinitely without restrictions or sponsorship + **Experience** + 2+ years of experience in scientific or related field software testing, with a strong focus on user acceptance testing + Experience in technical writing, particularly in creating user manuals and technical documentation for software applications. + **Technical Skills** + Familiarity with software development life cycle (SDLC) and testing methodologies, especially in lab-based applications. + Strong written and verbal communication skills + Proficiency in using testing tools (e.g., Xray, JIRA, ALM (HP)) and an understanding of laboratory information management systems (LIMS). + Experience with documentation software and Microsoft application tools is a plus. + **Soft Skills** + Strong analytical and problem-solving skills, with attention to detail. + Excellent communication and interpersonal skills, particularly in an IT and lab environment. + Ability to work independently and collaboratively within a team **Preferred Qualifications** + Experience in Agile/Scrum methodologies. + Exposure to regulatory standards relevant to laboratory software. + Certification in software testing (e.g., ISTQB) and/or technical writing is an advantage. **Work Environment** + This position may require occasional overtime and flexibility to meet project deadlines. + The role may involve working in a laboratory setting, with adherence to safety protocols. **Additional Information** **Position is full-time, Monday - Friday 9:00am - 5:00pm** . Candidates currently living within a commutable distance of **Spring House, PA** are encouraged to apply. 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 PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.**

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package. 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 believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies. If you're looking for a rewarding career, a place to call home, apply with us today! Job Description General Responsibilities: Responsible for performing a variety of tasks in support of the daily production of sterile cell therapy products. Tasks are predominately performed within a cleanroom environment under current Good Manufacturing Practices (cGMP) conditions. Responsibilities: * Proficient in aseptic processing including media exchanges, vessel passaging, harvest & cryopreservation of cells as required by the daily production schedule. * Ability to complete and maintains aseptic gowning qualification, aseptic process qualification and cleaning & disinfection qualification. * Perform media and reagent preparation duties as required. * Ability to operate and maintain equipment. * Perform equipment preventative maintenance, cleaning/disinfection, and basic troubleshooting, as required. * Perform, record and report various inventory tasks (i.e. consumables, media, cryovial, etc. * Ability to train others on support tasks, basic SOPs, equipment, and process operations. * Achieves PowerUser status on supporting electronic systems (i.e. MasterControl). * Follows, revises, executes, and authors SOPs and MBRs in accordance with cGMPs. * Ability to open and review documentation and MBR's at a high level. * Ability to author and close quality items. * Ability to initiate simple change controls and manage tasks required. * Assists with material procurement and receipt. * Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. * Manages time well and multi-tasks to complete all assignments and responsibilities with supervisor's guidance. * Maintains a safe working environment for self and others, including work area cleanliness. * Monitors resources and enforces SOPs to ensure data integrity and compliance with industry. * Participates in process optimization and continuous improvement opportunities. * Maintains orderly and timely records of samples and data, in accordance with company policy and legal requirements. Computer Skills: * Use of basic Microsoft applications efficiently. * Contribute to SOP/BR generation and revision, quality investigations, Corrective/Preventative Action initiatives, and Change Control procedures. Qualifications Education: * Minimum Bachelor of Science degree in a scientific discipline (or equivalent industry experience) Experience: * 2+ years of experience in mammalian cell culture in an academic or industrial laboratory * Knowledge of basic laboratory skills (aseptic technique, pipetting, etc.) are required * Must be comfortable with performing tasks while fully gowned in a cleanroom environment. * Proficient in Manufacturing Process. * Knowledge of 21CFR Part 11, standard GxP best practices and other industry standards. * Proficient in Mammalian cell biology * Excellent verbal and written skills * Good interpersonal communication skills * Must be willing to work weekends, evenings, and holidays (as needed). Additional Information What to Expect in the Hiring Process: * 10-15 Minute Phone Interview with Region Recruiter * 45-60 Minute Virtual Interview with Manager and/or Group Leader Additional Details: This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 8:00am to 5:00pm), with overtime required as needed. Candidates located within a commutable distance to Exton, PA are strongly encouraged to apply. Excellent full-time benefits include: * comprehensive medical coverage, dental, and vision options * Life and disability insurance * 401(k) with company match * Paid vacation and holidays Ready to take the next step in your career? Apply today and join a team that's making a difference in science every day. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Manufacturing Manager Title: Manager, Manufacturing Operations Reports to: Vice President, PD & Manufacturing Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada 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. Position/Job Summary: The Manager Manufacturing Operations position is responsible for all aspects of Clinical Trial Material manufacturing for the company. Accountabilities include manufacturing staff supervision, facility and equipment qualification, technology transfer, scheduling, and management of manufacturing projects. Manufacturing projects span multiple disciplines including, but not limited to material sourcing, process development, analytical testing, and business development. Develop and implement technically sound batch records, SOPs, specifications, protocols, and reports as required, while adhering to CGMP and GDP. Manage manufacturing activities and interaction/compliance with clients and appropriate regulatory authorities as needed. Roles & Responsibilities: Manage the manufacturing and supply of clinical trial materials (CTM), for Oral Solid Doses and Sterile drug product for clinical studies from development till post-marketing. Manage a team of manufacturing technologists, operators, and warehouse coordinators. Interface with product development team for transfer of knowledge and processes for CTM Batch Manufacturing Collaborate with other teams including but not limited to product development, procurement, supply chain, analytical testing, quality assurance and business development to ensure proper project execution. Develop and implement technically sound clinical Manufacturing batch records, SOPs, protocols, and specifications as required. Manage review quality control records, Change Controls, CAPAs and other GMP related documents and support on-time closure of deviations and CAPAs. Partner with CMC project management for alignment on and prioritization within manufacturing timelines to deliver CTM. Write, review and approve SOP's, qualification protocols, and other GMP documentation. Develop and maintain strategic partnerships with technical and operational colleagues to optimally collaborate with other departments and clients. Implements site initiatives in production operation as advised by site management. Ensures manufacturing, testing and CTM labeling/shipping/packaging is done according to guidelines and specifications. Execution and overseeing of facility and equipment qualification/validation which includes authoring specification, protocols, and writing reports. Responsible for compliance monitoring of area operations. Participates in regulatory and customer audits/inspections. Collaborates with functional departments to resolve issues. Process and analyze manufacturing results, data and provide status updates to the management. Establish and maintain positive relationships with project stakeholders. Education, Experience & Skills Required: Bachelor's Degree in Pharmaceuticals, Engineering or Sciences 8+ years in the pharmaceutical industry. Strong experience in tech transfer, process development, facility & equipment validation/qualification, and pharmaceutical manufacturing. 5+ years of people management experience. Experience with cGMP guidelines and regulations. Strong knowledge of FDA, EMEA & ISO regulations. Strong oral and written communication and interpersonal skills. Ability to work well in a team environment, eager, adaptable. Ability to perform frequent physical tasks with strength and mobility. Experience in microbiology and sterile manufacturing is a plus. 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 disability.