Senior Automation Engineer jobs at Johnson & Johnson

At IPS, we are global leaders in developing innovative solutions for the consulting, architecture, engineering, project controls, procurement, construction management, and CQV of technically complex facilities, primarily in the life sciences industry. We are looking for a talented Senior CQV Engineer to join our team at our office located in _____________. In this role, you will perform cGMP compliance-based services (commissioning, qualification, validation, consulting, etc.) as developed and defined in project agreements with IPS clients. You will also follow IPS and client standards and requirements, overall good industry practices for C/Q/V services, and regulatory requirements. You may also perform standalone commissioning services for non-FDA-regulated clients. Additional Responsibilities Write C/Q/V documents following established standards and templates, including but not limited to the following: Commissioning Forms C/Q/V Protocols and Summary Reports Standard Operating Procedures Impact Assessments Specifications (URS/FRS/DDS) FATS/SATs Perform field/site activities including, but not limited to, the following: Attend and witness FATs and SATs as a representative of IPS clients. Execution of commissioning forms and witnessing of vendor start-up and testing. Execution of C/Q/V protocols. Walkdown and verification of system drawings (P&IDs, as-builts, etc.) Compile data and prepare reports for completed C/Q/V activities including ETOPs, protocol data packages, etc. Assist in deviation investigation and resolution of problems and issues encountered during field execution activities. Work with the Project Delivery department or CM for start-up and vendor testing. Witness and troubleshoot as required. Primary responsibilities include C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries. Read, understand, and utilize the IPS Best Practices and SOPs for the delivery of compliance services Perform work to meet IPS budget requirements and quality standards. Provide consistent, complete, and timely feedback and reports to IPS project leaders, project managers, or management, of project status and issues, as requested. Come join our dynamic team that creates world-class designs for our clients, and propel your career to new horizons! Qualifications & Requirements Bachelor of Science in Engineering. This is an entry-level position. 7 or more years of relevant experience. Experience in Pharmaceutical, Biotech, Medical Device Design, Construction, Commissioning, Validation, or QA. Preferred Qualifications Experience in writing and execution of PFC, FC, IQ, OQ, and PQ forms/protocols for GMP Utilities, Equipment, Systems, and Software. General exposure and experience in a GMP/Validation discipline with a knowledge and understanding of pharmaceutical Design/Build/Commission/Validation processes and how they relate to regulatory requirements and cGMP regulations within the E.U. and U.S. FDA. Context & Safety This position will have up to 100% travel to the site, or as required by the assigned project. You may be assigned to a client site for an extended period. Overnight travel or staying in the city of the client's location is possible depending on the assignment. Travel will be per the IPS Travel Policy, client-specific travel policy, or project-specific travel plan. You may visit active construction sites and will be required to take site safety training and adhere to site safety rules. This position is a safety-sensitive position. The employee is designated for field work and attends activities at client sites where they work in construction, process, packaging, manufacturing, research, or other "non-administrative" areas. All interviews are conducted either in person or virtually, with video required. About Us IPS, a Berkshire Hathaway company, is a global leader in technical consulting, architecture, engineering, procurement, construction management, commissioning, qualification, and validation services for technically complex facilities. Integration is how we think and work. It requires the ability to unite existing and emerging technologies into a process that reliably delivers products and accelerates speed to market. That end-to-end mindset allows us to be agile and anticipate challenges as we move projects toward operational readiness. IPS applies design and delivery expertise, client-side experience, and supplier-side insight to every project. We infuse our curiosity, our passion, and our commitment to partnership in delivering solutions at any scale. We meet our clients where they are and get them to where they need to go. That's only possible when we care as much as our clients do. Specialties Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV, and Staffing Services. All qualified applicants will receive consideration for employment at IPS without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. IPS is proud to be an affirmative action and equal opportunity employer. Connect With Us! If you do not meet the qualifications for this specific role, but would like to submit your resume for general consideration, please click here!

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone, we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to win in self-care. Description Overview As a Quality Assurance Engineer, you will support and participate in continuous improvement activities in the operations areas. This person will provide primary Quality Assurance review and approval for annual product reviews, deviations, and other cGMP documentation and studies conducted at PMI and ensures that all information and documentation conforms to company policy, cGMP's and all other applicable FDA guidance's. Please note: This role is currently structured as 4 days onsite, 1 day remote. Scope of the Role * Leads/Participates in quality driven initiatives in the continuous support of Quality improvements, using data analysis techniques and other improvement tools. * Responsible for reviewing and approving documents such as deviations, Annual product reports, non-routine batch status change requests, planned deviations, calibration non conformances, etc. * Provides initial risk assessment of Quality events. * Works with operations, laboratory, engineering, and maintenance managers and staff to develop, evaluate and implement action plans which maintain or improve product and process quality. Experience Required * Bachelor's Degree in a scientific discipline or closely aligned field, with a minimum of two years experience working in an FDA regulated industry, preferred. * Demonstrated understanding and application of Continuous Improvement and Root Cause analysis skills. * Demonstrated understanding of and ability to apply cGMPs and US FDA laws and requirements in an FDA regulated industry. * Strong functional knowledge of SAP systems. * Demonstrated ability to organize multiple tasks and change priorities to meet project deadlines. Benefits We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo. Hybrid Working Approach We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo Nearest Major Market: Grand Rapids

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods. We are seeking a detail-oriented QA Engineer to join our Pharmaceutical Quality Assurance. In this role, the Quality Assurance Engineer plays a key role in maintaining FDA and cGMP compliance for OTC pharmaceutical manufacturing operations. This position supports quality systems, investigations, and process improvements to ensure consistent product quality. Work Schedule: Monday - Friday 8:00 AM - 4:30 PM JOB QUALIFICATIONS: Bachelor's degree in Pharmaceutical Sciences, Chemistry, Biology, Engineering, or a related field 2-5+ years of experience in Quality Assurance within pharmaceutical or OTC manufacturing Strong knowledge of cGMP, FDA regulations, and quality systems Experience with deviation investigations, CAPA management, and change control Familiarity with OTC drug manufacturing and labeling requirements Excellent written and verbal communication skills Strong attention to detail and documentation skills Ability to work cross-functionally in a regulated environment POSITION RESPONSIBILITIES: Ensure compliance with FDA regulations (21 CFR Parts 210, 211), cGMPs, and company quality systems Review and approve batch records, deviations, investigations, CAPAs, and change controls Provide quality oversight for manufacturing, packaging, labeling, and testing operations Investigate nonconformances, deviations, and complaints, and lead root cause analyses Support internal audits, FDA inspections, and third-party regulatory audits Review and approve SOPs, protocols, validation documents, and quality records Collaborate with Manufacturing, QC, Regulatory, and Engineering teams to resolve quality issues Ensure proper implementation of process validation, cleaning validation, and equipment qualification Monitor quality metrics and support continuous improvement initiatives Provide QA guidance and training to manufacturing and support staff Support product releases and ensure documentation accuracy and completeness PHYSICAL REQUIREMENTS: Work safely and follow all OSHA regulations and company safety policies and procedures Works frequently in a lab environment, handling of chemicals. Employees are required to wear eye protection and lab coats while in the lab area. Ability to frequently lift and/or move up to 25 lbs. Ability to occasionally lift and/or move up to 35 lbs. Ability to regularly stand, sit, and walk to perform tasks BENEFITS: PLD is a proud employer offering many corporate benefits, including: Medical and Dental Benefits Vision 401K with employer match Group Life Insurance Flex Spending Accounts Paid Time Off and Paid Holidays Tuition Assistance Corporate Discount Program Opportunities to Flourish Within the Company PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Duration of Contract: Long term , Starts Immediate , runs through March 2027, with possible extension Responsibilities Implement capital automation projects using industry best practices and company business processes. Support the scope, deliverables, schedule, and project team for capital expenditure (CapEx) of automation projects. Participate in the development and evaluation of RFP and bidder/vendor analysis for General contracting and engineering services when design build method used. Works directly with project controls to prepare and update project status, schedule, resource, and cost reports within Oracle based tools (OPPM & P6) for the use of numerous BMRN departments. Identify and oversee system integrations. Ensure consultants & contractors working on any automation related projects maintain compliance with all GMP requirements (including training), EHS&S and security requirements, including completion and review of Job Hazard Assessments and company policies. Coordinate/support engineering and automation design, commissioning, qualification, and the QA Validation groups as appropriate. Proactively look for and recommend improvements in site processes and procedures. Represent the Capital Project Automation group with good communication and presentationskills. Provide status reports on Projects to Automation Management as required. RequirementsRequirements Minimum 10 years of automation engineering experience preferably in the biotech or pharmaceutical organization. Experience with Emerson DeltaV Process Control System (PCS) Ability to work with minimal direct supervision: meet deadlines, prioritize assignments, provide recommendations and effectively communicate updates. Experienced with communicating with in supporting Executive Management as well as providing direction support for multiple projects simultaneously. Must be very organized and possess strong verbal and written communications skills. Must be proficient with Internet navigation, Microsoft Office (Outlook, Word, PowerPoint, Excel, Project, Teams, Sharepoint), Adobe Acrobat Should be flexible to working outside the core business hours (occasionally on short notice, and a limited basis) as needed. Proven ability to manage multiple and fast -moving priorities. Ability to work well in a fast -paced collaborative team environment within a rapidly evolving business environment. Skilled at solving multi -dimensional problems with both quantitative and qualitative variables. Ability to lead and influence others in support of company objectives. Excellent decision making and cross functional team building skills. Solid understanding of GMP, GLP, and non -GMP project requirements Able to read and understand engineering plans and specifications. BS degree from an accredited university in a construction or engineering related field. Could be a combination of AS degree and industry experience.

SummaryJob Description We are the makers of possible BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it's no small feat. It takes the imagination and passion of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products per year-to look at the impossible and find transformative solutions that turn dreams into possibilities. We believe that the human element, across our global teams, is what allows us to continually evolve. Join us and discover an environment in which you'll be supported to learn, grow and become your best self. Become a maker of possible with us. Senior Automation Engineer- Innovative Core Solutions Systems Engineer JOB SUMMARY This is a critical role within the Research and Development based Innovative Core Solutions Team. The successful candidate will be responsible for driving automation solutions for Quality Control testing of flow cytometry antibody reagents specifically as the Automation Workcell owner for this testing segment. With a focus on bench science, this individual will work cross-functionally and be primarily responsible for implementing, optimizing, and maintaining robust and creative automation solutions. The position requires hands-on experience with automation (e.g., Hamilton or other liquid handlers) and assay development as well as a familiarity or interest in biological sciences. This laboratory-based position will ensure workflow coordination for method development and method support functions within the Lab Automation segment of the Innovative Core Solutions Team for consistent solutions across all deployed Automation Workcells. This position also requires an ability to think proactively and spearhead process improvements while also seeking and evaluating new technologies to apply to current work streams. Responsibilities: Manage automation workcells comprehensively, including robot teaching, coordinating field service engineers for calibrations/preventive maintenance, and overseeing all equipment components through regular cleaning, lubrication, and performance checks. Collaborate with scientists to understand laboratory protocols and translate them into automated workflows, while applying automation expertise to improve processes, troubleshoot procedures, and lead programming of new methods to expand throughput. Identify operational bottlenecks, evaluate new technologies, and work cross-functionally to scale in vitro assays by multiple orders of magnitude, including vendor coordination for hardware integration and collaboration with software developers. Develop and maintain comprehensive documentation including training guides and verification reports, while providing ad hoc instrument troubleshooting, error recovery, and end-user training through detailed work instructions. Manage equipment scheduling calendars, track critical metrics (uptime, downtime, usage), and provide regular performance reports to leadership to ensure optimal laboratory automation operations. Minimum Requirements: Bachelor's or Master's degree in Engineering, Life Sciences, or Computer Science (preferably Biomedical Engineering, Robotics, Biology, Chemistry), or PhD with 2+ years of relevant Lab Automation experience. Non-PhD candidates require minimum 6 years of relevant experience. Minimum 2 years of supervisory experience in a lab setting, with demonstrated ability to lead without authority, coordinate small teams to achieve program goals, and work cross-functionally with strong communication skills. Proven experience implementing and maintaining automation solutions, troubleshooting liquid handling equipment and laboratory automation systems, and ability to generate, evaluate, and understand scientific data from robotic platforms. Self-motivated with strong analytical and problem-solving abilities, capable of effectively prioritizing tasks and multitasking to achieve goals while maintaining focus on customer deliverables. Self-motivated with strong analytical and problem-solving abilities, capable of effectively prioritizing tasks and multitasking to achieve goals while maintaining focus on customer deliverables. Preferred Requirements: Previous experience programming Hamilton Robotics instrumentation (Venus software) is preferable. 3D printing experience preferred. Ability to program in languages such as R or Python preferred. Experience with integrated robotic system schedulers (e.g. Cellario, Biosero). Knowledge of basic scientific principles in biology and chemistry and/or experience working closely with scientists to automate biological or chemical processes. At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry. For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting. For certain roles at BD, employment is contingent upon the Company's receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required. Consistent with BD's Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law. Why Join Us? A career at BD means being part of a team that values your opinions and contributions and that encourages you to bring your authentic self to work. It's also a place where we help each other be great, we do what's right, we hold each other accountable, and learn and improve every day. To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you'll discover a culture in which you can learn, grow, and thrive. And find satisfaction in doing your part to make the world a better place. To learn more about BD visit ********************** Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics. Required Skills Optional Skills . Primary Work LocationUSA CA - San Diego (BDB) Additional LocationsWork Shift At BD, we are strongly committed to investing in our associates-their well-being and development, and in providing rewards and recognition opportunities that promote a performance-based culture. We demonstrate this commitment by offering a valuable, competitive package of compensation and benefits programs which you can learn more about on our Careers Site under Our Commitment to You. Salary or hourly rate ranges have been implemented to reward associates fairly and competitively, as well as to support recognition of associates' progress, ranging from entry level to experts in their field, and talent mobility. There are many factors, such as location, that contribute to the range displayed. The salary or hourly rate offered to a successful candidate is based on experience, education, skills, and any step rate pay system of the actual work location, as applicable to the role or position. Salary or hourly pay ranges may vary for Field-based and Remote roles. Salary Range Information

Eurofins Scientific is a network of independent companies 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 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. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients-including DoD, DOE, and municipalities-through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing is seeking a Senior Analyst to join our team! The Senior Analyst will have previous experience with HR/MS instrumentation in a production, laboratory setting. The Senior Analyst prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins' Quality Assurance programs and SOP's. The Senior Analyst is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diagnosing complex problems and offering solutions with a high degree of independence; suggesting and implementing improvements to maximize quality and productivity; acting as technical resource for internal problems and projects; assisting in “brainstorming” client problems and projects; training new employees in all aspects of instrumentation; researching new and emerging technologies. Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrates and promotes the company vision Regular attendance and punctuality Perform routine and advanced maintenance on the instrumentation Tune and calibrate instrumentation Analyze samples and associated QC Review, work up, and assemble all supporting data Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department Perform additional responsibilities (i.e., audit, verification, etc.) with minimal supervision Evaluate current analytical system performance and recommend corrective action to enhance efficiency and productivity Train other departmental analysts in procedures related to operations listed in the above Search technical literature for scientific information relative to improving analytical or operational performance Understand and use LIMS Make working calibration standards Use word processor on PC Monitor and change gas cylinders Review and amend departmental methods when required, either as part of yearly review or when an analytical change to the method is made Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Basic Minimum Qualifications 5+ year HR/MS experience in a production laboratory At least 5 years experience related to performing extractions and/or instrumental chromatographic analyses utilizing wet chemical and chromatographic techniques) in a wide variety of matrices encountered in environmental testing. Bachelor's degree in chemistry, biology, physics or related degree concentration 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 Skills and Abilities Exceptional technical skills, including logical thinking and deductive reasoning; good work habits (e.g., cleanliness, efficiency, carefulness, effective organizational skills); High accuracy in recording and transcribing data; Personal maturity and sense of responsibility; Good written and oral communication skills; Ability to learn new methods and techniques; Willingness to follow instructions and comply with company policies; Consciousness of, and a positive attitude toward, quality control and safety procedures; Good understanding of chemical principles; Accurate management of numbers, both by hand and using a calculator; Set up and perform nonroutine standardized tests with minimal supervision; Demonstrated versatility, flexibility, and efficiency; Effective use of time while managing multiple priorities; Above satisfactory reasoning ability; Self-motivated to improve technical skills and operations; Superior leadership, organizational, and communication skills; Lead a project to a satisfactory conclusion on time; Consult with clients on work performed for them; Problem solving skills; Function under high stress levels; multitask; See cause-and-effect relationships; Retain large amounts of information Additional Information Compensation Range: $80,000 - $120,000 per year depending on level of experience and qualifications. Position is full-time, and exempt from overtime pay. Candidates must be available to work the following shift: Monday - Friday, 8:00am to 5:00pm and any additional hours needed 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 offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** 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 6.151 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is a network of independent companies 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 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. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients-including DoD, DOE, and municipalities-through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing is seeking a Senior Analyst to join our team! The Senior Analyst will have previous experience with HR/MS instrumentation in a production, laboratory setting. The Senior Analyst prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins' Quality Assurance programs and SOP's. The Senior Analyst is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diagnosing complex problems and offering solutions with a high degree of independence; suggesting and implementing improvements to maximize quality and productivity; acting as technical resource for internal problems and projects; assisting in "brainstorming" client problems and projects; training new employees in all aspects of instrumentation; researching new and emerging technologies. Essential Duties and Responsibilities: * Applies GMP/GLP in all areas of responsibility, as appropriate * Demonstrates and promotes the company vision * Regular attendance and punctuality * Perform routine and advanced maintenance on the instrumentation * Tune and calibrate instrumentation * Analyze samples and associated QC * Review, work up, and assemble all supporting data * Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department * Perform additional responsibilities (i.e., audit, verification, etc.) with minimal supervision * Evaluate current analytical system performance and recommend corrective action to enhance efficiency and productivity * Train other departmental analysts in procedures related to operations listed in the above * Search technical literature for scientific information relative to improving analytical or operational performance * Understand and use LIMS * Make working calibration standards * Use word processor on PC * Monitor and change gas cylinders * Review and amend departmental methods when required, either as part of yearly review or when an analytical change to the method is made * Conducts all activities in a safe and efficient manner * Performs other duties as assigned Qualifications Basic Minimum Qualifications * 5+ year HR/MS experience in a production laboratory * At least 5 years experience related to performing extractions and/or instrumental chromatographic analyses utilizing wet chemical and chromatographic techniques) in a wide variety of matrices encountered in environmental testing. * Bachelor's degree in chemistry, biology, physics or related degree concentration * 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 Skills and Abilities * Exceptional technical skills, including logical thinking and deductive reasoning; good work habits (e.g., cleanliness, efficiency, carefulness, effective organizational skills); * High accuracy in recording and transcribing data; * Personal maturity and sense of responsibility; * Good written and oral communication skills; * Ability to learn new methods and techniques; * Willingness to follow instructions and comply with company policies; * Consciousness of, and a positive attitude toward, quality control and safety procedures; * Good understanding of chemical principles; * Accurate management of numbers, both by hand and using a calculator; * Set up and perform nonroutine standardized tests with minimal supervision; * Demonstrated versatility, flexibility, and efficiency; * Effective use of time while managing multiple priorities; * Above satisfactory reasoning ability; * Self-motivated to improve technical skills and operations; * Superior leadership, organizational, and communication skills; * Lead a project to a satisfactory conclusion on time; * Consult with clients on work performed for them; * Problem solving skills; * Function under high stress levels; multitask; * See cause-and-effect relationships; * Retain large amounts of information Additional Information Compensation Range: $80,000 - $120,000 per year depending on level of experience and qualifications. Position is full-time, and exempt from overtime pay. Candidates must be available to work the following shift: * Monday - Friday, 8:00am to 5:00pm and any additional hours needed 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 offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** 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 6.151 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is a network of independent companies 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 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. With over 50 laboratories and more than 40 service centers nationwide, Eurofins Environment Testing provides full-service environmental analysis across all 50 states. Our network supports public and private clients-including DoD, DOE, and municipalities-through robust logistics and continuous investment in people, technology, and infrastructure. We offer comprehensive testing for air, water, soil, sediment, tissue, and waste, covering a wide range of analytes including PFAS, metals, VOCs/SVOCs, dioxins/furans, radiochemicals, and more. Job Description Eurofins Environment Testing is seeking a Senior Analyst to join our team! The Senior Analyst will have previous experience with HR/MS instrumentation in a production, laboratory setting. The Senior Analyst prepares and analyzes environmental samples using standard analytical techniques according to scientific and EPA methodology in compliance with Eurofins' Quality Assurance programs and SOP's. The Senior Analyst is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diagnosing complex problems and offering solutions with a high degree of independence; suggesting and implementing improvements to maximize quality and productivity; acting as technical resource for internal problems and projects; assisting in “brainstorming” client problems and projects; training new employees in all aspects of instrumentation; researching new and emerging technologies. Essential Duties and Responsibilities: Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrates and promotes the company vision Regular attendance and punctuality Perform routine and advanced maintenance on the instrumentation Tune and calibrate instrumentation Analyze samples and associated QC Review, work up, and assemble all supporting data Read, understand, and carry out SOPs required by EPA or company methods, governing agencies, clients, and our internal QC department Perform additional responsibilities (i.e., audit, verification, etc.) with minimal supervision Evaluate current analytical system performance and recommend corrective action to enhance efficiency and productivity Train other departmental analysts in procedures related to operations listed in the above Search technical literature for scientific information relative to improving analytical or operational performance Understand and use LIMS Make working calibration standards Use word processor on PC Monitor and change gas cylinders Review and amend departmental methods when required, either as part of yearly review or when an analytical change to the method is made Conducts all activities in a safe and efficient manner Performs other duties as assigned Qualifications Basic Minimum Qualifications 5+ year HR/MS experience in a production laboratory At least 5 years experience related to performing extractions and/or instrumental chromatographic analyses utilizing wet chemical and chromatographic techniques) in a wide variety of matrices encountered in environmental testing. Bachelor's degree in chemistry, biology, physics or related degree concentration 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 Skills and Abilities Exceptional technical skills, including logical thinking and deductive reasoning; good work habits (e.g., cleanliness, efficiency, carefulness, effective organizational skills); High accuracy in recording and transcribing data; Personal maturity and sense of responsibility; Good written and oral communication skills; Ability to learn new methods and techniques; Willingness to follow instructions and comply with company policies; Consciousness of, and a positive attitude toward, quality control and safety procedures; Good understanding of chemical principles; Accurate management of numbers, both by hand and using a calculator; Set up and perform nonroutine standardized tests with minimal supervision; Demonstrated versatility, flexibility, and efficiency; Effective use of time while managing multiple priorities; Above satisfactory reasoning ability; Self-motivated to improve technical skills and operations; Superior leadership, organizational, and communication skills; Lead a project to a satisfactory conclusion on time; Consult with clients on work performed for them; Problem solving skills; Function under high stress levels; multitask; See cause-and-effect relationships; Retain large amounts of information Additional Information Compensation Range: $80,000 - $120,000 per year depending on level of experience and qualifications. Position is full-time, and exempt from overtime pay. Candidates must be available to work the following shift: Monday - Friday, 8:00am to 5:00pm and any additional hours needed 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 offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options. We support your development! Do you feel you don't match 100% of the requirements? Don't hesitate to apply anyway! Eurofins companies are committed to supporting your career development. We embrace diversity! Eurofins network of companies believe in strength and innovation through diversity, being an Equal Opportunity Employer. We prohibit discrimination against employees or applications based on gender identity and/or expression, race, nationality, age, religion, sexual orientation, disability, and everything else that makes employees of Eurofins companies unique. Sustainability matters to us! We are well on our way to achieving our objective of carbon neutrality by 2025, through a combination of emission reduction and compensation initiatives. We encourage our laboratory leaders to make sustainable changes at their local level, and in addition to their initiatives we also count on our dedicated carbon reduction team to help us to achieve this goal! Find out more in our career page: ***************************** 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 6.151 billion, and has been among the best performing stocks in Europe over the past 20 years. Eurofins USA Environment Testing is a Disabled and Veteran Equal Employment Opportunity employer.

Job Description Reporting to the Sr. Director of Engineering and Facilities, this position will support an Aseptic Fill Finish manufacturing facility by designing, operating and maintaining the automation systems at Pyramid Labs. The filling lines include semi-automatic operations as well as fully automatic/ robotic filling. All automated systems are in scope of responsibility including building automation, SCADA, data management and standalone equipment. PRINCIPAL DUTIES: Process Equipment and Utilities Troubleshooting CC/ CAPA/ SOP ownership Controls/ Automation design, upgrades and specification development Automation Project Management PCS, BAS, Vaisala Ownership and administration Partner with IT for networking and data management Specification/ URS generation Own DI assessment from an Automation/Validation perspective Impact and Risk assessment Vaisala, Wonderware, SQL, Alan Bradley experience is a plus QUALIFICATIONS AND EXPERIENCE: Automation Validation 21CFR, part 11 Bachelor's Degree in Automation related discipline or 8+ years' experience as an Automation Engineer Network Integration and configuration

Fulltime opportunity Concord in Charlotte, NC Annual base pay of $126k/yr plus benefit • Primarily supporting STH (Syringe Tub Handling) platforms • Secondary support for LLRS (literature loading) and BACS (Bin assembly and Collapsing system) platforms Project Delivery Support - o Provide automation/mechanical technical support for troubleshooting during the commissioning and qualification phase. o Perform &/or support the execution of commissioning and qualification testing on the equipment. o Provide technical support for integration of the line with site automation systems and other ancillary equipment (ie: MES) o Perform source code review and code management for associated manufacturing equipment o Update technical design documentation with respect to project delivery change management processes. o Support site engineering initiatives including but not limited to training/development of site staff, drafting technical procedures, troubleshooting guides • Knowledge sharing - o Serve as a key resource to support site engineering groups. o Communicate continuous improvement solutions to respective GR platform stewards, and gain support for ideas on issue resolution. o Hands -on resource to help troubleshoot issues but also be primary point of contact for GR personnel when trying to resolve items. Requirements Basic Requirements • Bachelor's degree in an Engineering discipline or equivalent experience in pharmaceutical parenteral manufacturing. • Experience working with and programming automated equipment including vision systems, high -speed mechanical assembly lines, Fanuc robotics. • Minimum of three (3) years' experience with pharmaceutical manufacturing, additional benefit if direct experience with: o high -speed device assembly, o packaging manufacturing equipment, o parenteral manufacturing equipment (filling/inspection lines) o Automated Storage Retrieval Systems (ASRS) o Automated Guided Vehicles (AGV) • Knowledge on Documentation management, and ability to execute Test Cases, Checklists and capture a pending point list with appropriate responsible and resolution • Ability to program Rockwell PLC, FactoryTalk HMI/SCADA systems with hands -on troubleshooting experience. • Experience working hands -on with mechanical assembly machines, pneumatics, instrumentation, electrical drawings, etc. • Experience working with vendors/OEM personnel • Strong communicator, as individual will be attending many remote meetings with Global Robotics personnel via Teams. Strong ability to escalate and work cross -functionally.

Fulltime role at Indianapolis, IN Annual base pay of $126k/yr plus benefit • Primarily supporting CTH (Cartridge Tray Handling) and STH (Syringe Tray Handling) platforms Project Delivery Support - o Provide automation/mechanical technical support for troubleshooting during the commissioning and qualification phase. o Perform &/or support the execution of commissioning and qualification testing on the equipment. o Provide technical support for integration of the line with site automation systems and other ancillary equipment (ie: MES) o Perform source code review and code management for associated manufacturing equipment o Update technical design documentation with respect to project delivery change management processes. o Support site engineering initiatives including but not limited to training/development of site staff, drafting technical procedures, troubleshooting guides • Knowledge sharing - o Serve as a key resource to support site engineering groups. o Communicate continuous improvement solutions to respective GR platform stewards, and gain support for ideas on issue resolution. o Hands -on resource to help troubleshoot issues but also be primary point of contact for GR personnel when trying to resolve items. Requirements Basic Requirements • Bachelor's degree in an Engineering discipline or equivalent experience in pharmaceutical parenteral manufacturing. • Experience working with and programming automated equipment including vision systems, high -speed mechanical assembly lines, Fanuc robotics. • Minimum of three (3) years' experience with pharmaceutical manufacturing, additional benefit if direct experience with: o high -speed device assembly, o packaging manufacturing equipment, o parenteral manufacturing equipment (filling/inspection lines) o Automated Storage Retrieval Systems (ASRS) o Automated Guided Vehicles (AGV) • Knowledge on Documentation management, and ability to execute Test Cases, Checklists and capture a pending point list with appropriate responsible and resolution • Ability to program Rockwell PLC, FactoryTalk HMI/SCADA systems with hands -on troubleshooting experience. • Experience working hands -on with mechanical assembly machines, pneumatics, instrumentation, electrical drawings, etc. • Experience working with vendors/OEM personnel • Strong communicator, as individual will be attending many remote meetings with Global Robotics personnel via Teams. Strong ability to escalate and work cross -functionally.

onsite - Norwood,MA 3 months contract with extension possible Requirements 1. Support staff - on site resource 2. Setup and troubleshooting activities 3. MES Responsibilities 1. Set up master data (BOMs, BOPs, etc.) 2. Syncade administrative settings 3. Testing MES integrations - simulating commands, etc. 4. Set up printers - configuration and testing 5. Set up scales - configuration and testing 6. Set up barcode scanners - configuration and testing

Job SummaryResponsible for specifying, procuring and installing new equipment for an aseptic manufacturing facility. Responsible for reviewing designs of new equipment and making modifications to existing equipment. Must manage equipment and facilities projects from conception through completion, determine change control requirements and follow through on pre-approval requirements and support the execution of validation protocols. Excellent written and verbal communication skills. Excellent project management, including experience using MS Project. Experienced in PLC and HMI programming. Must maintain cGMP and EU compliance. Salary Range: $73,614 - $103,528 Position is eligible to participate in a bonus plan with a target of 6% of the base salary. Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities. Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.Responsibilities Develops and manages site projects by employing past experience, research, design and concept sketches, layouts, drawings, vendor interaction, preparation of specifications, discussions with appropriate management and site personnel. Prepares, writes and executes Risk Analysis (FMEA, Fishbone Diagrams) and Critical Change Requests. Prepares and executes User Requirement Specifications, Functional Requirement Specifications, Design Specifications/Qualifications, Factory and Site Acceptance Tests, Machinability Studies and Standard Operating Procedures as necessary for new and modified equipment. Prepares funding requests per corporate guidelines, including detailed project descriptions, backgrounds, sketches, alternatives, financial data, justifications, quotations, estimates and schedules. Manages and supervises the installation of equipment and/or facility modifications or additions. Includes vendor selection, procurement of equipment or services, scheduling, vendor coordination, rigging, set-up, start-up, troubleshooting, de-bugging, training and budgeting. Assists Operations and Maintenance with solving problems, improving processes and reducing costs. Maintain Regulatory, Fresenius Kabi and customer compliance. Additional Information We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program. Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

7,000 Diseases - 500 Treatments - 1 Rare Pharmacy PANTHERx is the nation's largest rare disease pharmacy, and we put the patient experience at the top of everything that we do. If you are looking for a career in the healthcare field that embraces authentic dedication to patient care, you don't need to look beyond PANTHERx. In every line of service, in every position and area of expertise, PANTHERx associates are driven to provide the highest quality outcomes for our patients. We are seeking team members who: Are inspired and compassionate problem solvers; Produce high quality work; Thrive in the excitement of the ever-challenging environment of modern medicine; and Are committed to achieving superior health outcomes for people living with rare and devastating diseases. At PANTHERx, we know our employees are the driving force in what we do. We cultivate talent and encourage growth within PANTHERx so that our associates can continue to explore their interests and expand their careers. Guided by our mission to provide uncompromising quality every day, we continue our strategic growth to further reach those affected by rare diseases. Join the PANTHERx team, and define your own RxARE future in healthcare! Location: Pittsburgh, PA (Hybrid) Classification: Exempt Status: Full-Time Reports to: Manager, Quality Assurance Business Purpose As a member of our IT Quality Assurance team, the QA Engineer will design and execute test plans to ensure the highest quality software products for our specialty pharmacy customers, relying on a strong technical knowledge of software quality assurance and emerging AI-driven testing methodologies. This role requires excellent communication and problem-solving skills with the ability to think critically to evaluate and analyze software applications. This position will be responsible for evangelizing and executing QA policies and procedures, adhering to QA standards, and monitoring the QA process to ensure a high quality of deliverables. Responsibilities Develops test plans and executes test cases based on business requirements. Tests across multiple platforms and applications on mobile and desktop. Monitors the QA process to ensure the highest quality of deliverables. Follows comprehensive QA processes and procedures. Analyzes and evaluates QA results. Provides a voice during team meetings and scrum ceremonies. Writes SQL queries to set up and validate test data. Communicates QA results to stakeholders. Develops and implements automated testing. Ability to leverage AI-powered testing tools and frameworks to enhance test coverage and efficiency. Implements machine learning models for predictive defect analysis and risk-based testing. Utilizes AI-driven test case generation and optimization techniques. Required Qualifications Bachelor's degree in computer science, Information Technology, or a related field. Minimum of two (2) years of experience in software quality assurance. Knowledge of software testing processes and methodology. Excellent problem-solving and troubleshooting skills. Excellent verbal and written communication skills. Basic understanding of AI concepts and their application in software testing. Familiarity with AI-driven software tools (e.g., Claude, Copilot). Preferred Qualifications Two (2) years of experience in a software QA role. Two (2) years of experience testing mobile applications. Experience testing SMS. Experience in the pharmacy industry Experience using proprietary project and issue tracking software (Azure DevOps, JIRA, etc.). Experience using test management systems (Azure Test Plans, TestRail, etc.) Experience in developing and implementing automated testing using a scripting language (C# preferred) and Selenium. Experience with AI-based visual testing and intelligent defect prediction tools. Work Environment This position operates in a home or professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines. Physical Demands While performing the duties of this job, the employee is regularly required to sit, see, talk, or hear. The employee frequently is required to stand; walk; use hands and fingers to handle or feel; and reach with hands and arms. Visual acuity is necessary for tasks such as reading, or working with various forms of data on a screen for extended periods. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. Benefits: Hybrid, remote and flexible on-site work schedules are available, based on the position. PANTHERx Rare Pharmacy also affords an excellent benefit package, including but not limited to medical, dental, vision, health savings and flexible spending accounts, 401K with employer matching, employer-paid life insurance and short/long term disability coverage, and an Employee Assistance Program! Generous paid time off is also available to all full-time employees, as well as limited paid time off for part-time employees. Of course we offer paid holidays too! Equal Opportunity: PANTHERx Rare Pharmacy is an equal opportunity employer, and does not discriminate in recruiting, hiring, promotions or any term or condition of employment based on race, age, religion, gender, ethnicity, sexual orientation, gender identity, disability, protected veteran's status, or any other characteristic protected by federal, state or local laws.

7,000 Diseases - 500 Treatments - 1 Rare Pharmacy PANTHERx is the nation's largest rare disease pharmacy, and we put the patient experience at the top of everything that we do. If you are looking for a career in the healthcare field that embraces authentic dedication to patient care, you don't need to look beyond PANTHERx. In every line of service, in every position and area of expertise, PANTHERx associates are driven to provide the highest quality outcomes for our patients. We are seeking team members who: Are inspired and compassionate problem solvers; Produce high quality work; Thrive in the excitement of the ever-challenging environment of modern medicine; and Are committed to achieving superior health outcomes for people living with rare and devastating diseases. At PANTHERx, we know our employees are the driving force in what we do. We cultivate talent and encourage growth within PANTHERx so that our associates can continue to explore their interests and expand their careers. Guided by our mission to provide uncompromising quality every day, we continue our strategic growth to further reach those affected by rare diseases. Join the PANTHERx team, and define your own RxARE future in healthcare! Location: Pittsburgh, PA (Hybrid) Classification: Exempt Status: Full-Time Reports to: Manager, IT Quality Assurance (QA) Purpose The Data Quality Assurance Engineer must possess strong technical knowledge and experience in data quality assurance. This role requires excellent communication and problem-solving skills and must be able to think critically to evaluate and analyze reports, dashboards and exports. This position will be responsible for advancing and executing data QA policies and procedures, adhering to company standards, and monitoring the process to ensure a high quality of deliverables. Responsibilities Collaborates with teams across the organization to understand the business requirements and creates testing documentation. Develops test strategies, test approaches and test documentation to support the business needs. Creates data profiling and data mapping documents to support testing requirements. Contributes to testing frameworks using PySpark and validates data, reports, and dashboards with various checks. Monitors and reports defects and contributes to the defect triage calls. Designs test data to validate the accuracy of transformation and logic between layers. Spearheads dashboard and ETL Result testing and verification. Establishes data quality rules & checks based on data completeness & data transformation logic. Required Qualifications Bachelor's degree in Computer Science, Information Technology, or a related field. Knowledge of data testing processes and methodology. Minimum of two (2) years experience in data quality testing, design and implementation of mixed Cloud/on-prem solution. Minimum of two (2) years experience in creating data profiling, data mapping & SQL. Minimum of two (2) years experience using management systems (Azure DevOps, ADF Orchestration, etc.), Azure Cloud Data Services (ADLS Gen 2, ADF) and Microsoft Azure DataBricks. Experience in Test Automation using Python (Pandas, Pyspark, Pytest,), Github API testing, and Jenkins. Strong experience in ETL (cleansing and normalizing source data, transformation, and loading) reports and dashboard testing. Excellent experience in executing data pipeline and testing. Understanding of DWH concepts, Dimensional modeling. Experience in business requirements participation and documentation of data quality requirements, data analysis and validation. Preferred Qualifications Minimum of two (2) years experience in a data QA role Experience in BI Tools like MS Power BI and Tableau. Excellent problem-solving and troubleshooting skills. Excellent verbal and written communication skills. Work Environment This position operates in a home and professional office environment. When in-office this role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines, and communications via MS Teams. Physical Demands While performing the duties of this job, the employee is regularly required to sit, see, talk, or hear. The employee frequently is required to sit; stand; walk; use hands and fingers to handle or feel; and reach with hands and arms. Visual acuity is necessary for tasks such as reading, observing surroundings, and working with various forms of data. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. Benefits: Hybrid, remote and flexible on-site work schedules are available, based on the position. PANTHERx Rare Pharmacy also affords an excellent benefit package, including but not limited to medical, dental, vision, health savings and flexible spending accounts, 401K with employer matching, employer-paid life insurance and short/long term disability coverage, and an Employee Assistance Program! Generous paid time off is also available to all full-time employees, as well as limited paid time off for part-time employees. Of course we offer paid holidays too! Equal Opportunity: PANTHERx Rare Pharmacy is an equal opportunity employer, and does not discriminate in recruiting, hiring, promotions or any term or condition of employment based on race, age, religion, gender, ethnicity, sexual orientation, gender identity, disability, protected veteran's status, or any other characteristic protected by federal, state or local laws.

Job Description 7,000 Diseases - 500 Treatments - 1 Rare Pharmacy PANTHERx is the nation's largest rare disease pharmacy, and we put the patient experience at the top of everything that we do. If you are looking for a career in the healthcare field that embraces authentic dedication to patient care, you don't need to look beyond PANTHERx. In every line of service, in every position and area of expertise, PANTHERx associates are driven to provide the highest quality outcomes for our patients. We are seeking team members who: Are inspired and compassionate problem solvers; Produce high quality work; Thrive in the excitement of the ever-challenging environment of modern medicine; and Are committed to achieving superior health outcomes for people living with rare and devastating diseases. At PANTHERx, we know our employees are the driving force in what we do. We cultivate talent and encourage growth within PANTHERx so that our associates can continue to explore their interests and expand their careers. Guided by our mission to provide uncompromising quality every day, we continue our strategic growth to further reach those affected by rare diseases. Join the PANTHERx team, and define your own RxARE future in healthcare! Location: Pittsburgh, PA (Hybrid) Classification: Exempt Status: Full-Time Reports to: Manager, IT Quality Assurance (QA) Purpose The Data Quality Assurance Engineer must possess strong technical knowledge and experience in data quality assurance. This role requires excellent communication and problem-solving skills and must be able to think critically to evaluate and analyze reports, dashboards and exports. This position will be responsible for advancing and executing data QA policies and procedures, adhering to company standards, and monitoring the process to ensure a high quality of deliverables. Responsibilities Collaborates with teams across the organization to understand the business requirements and creates testing documentation. Develops test strategies, test approaches and test documentation to support the business needs. Creates data profiling and data mapping documents to support testing requirements. Contributes to testing frameworks using PySpark and validates data, reports, and dashboards with various checks. Monitors and reports defects and contributes to the defect triage calls. Designs test data to validate the accuracy of transformation and logic between layers. Spearheads dashboard and ETL Result testing and verification. Establishes data quality rules & checks based on data completeness & data transformation logic. Required Qualifications Bachelor's degree in Computer Science, Information Technology, or a related field. Knowledge of data testing processes and methodology. Minimum of two (2) years experience in data quality testing, design and implementation of mixed Cloud/on-prem solution. Minimum of two (2) years experience in creating data profiling, data mapping & SQL. Minimum of two (2) years experience using management systems (Azure DevOps, ADF Orchestration, etc.), Azure Cloud Data Services (ADLS Gen 2, ADF) and Microsoft Azure DataBricks. Experience in Test Automation using Python (Pandas, Pyspark, Pytest,), Github API testing, and Jenkins. Strong experience in ETL (cleansing and normalizing source data, transformation, and loading) reports and dashboard testing. Excellent experience in executing data pipeline and testing. Understanding of DWH concepts, Dimensional modeling. Experience in business requirements participation and documentation of data quality requirements, data analysis and validation. Preferred Qualifications Minimum of two (2) years experience in a data QA role Experience in BI Tools like MS Power BI and Tableau. Excellent problem-solving and troubleshooting skills. Excellent verbal and written communication skills. Work Environment This position operates in a home and professional office environment. When in-office this role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines, and communications via MS Teams. Physical Demands While performing the duties of this job, the employee is regularly required to sit, see, talk, or hear. The employee frequently is required to sit; stand; walk; use hands and fingers to handle or feel; and reach with hands and arms. Visual acuity is necessary for tasks such as reading, observing surroundings, and working with various forms of data. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job. Benefits: Hybrid, remote and flexible on-site work schedules are available, based on the position. PANTHERx Rare Pharmacy also affords an excellent benefit package, including but not limited to medical, dental, vision, health savings and flexible spending accounts, 401K with employer matching, employer-paid life insurance and short/long term disability coverage, and an Employee Assistance Program! Generous paid time off is also available to all full-time employees, as well as limited paid time off for part-time employees. Of course we offer paid holidays too! Equal Opportunity: PANTHERx Rare Pharmacy is an equal opportunity employer, and does not discriminate in recruiting, hiring, promotions or any term or condition of employment based on race, age, religion, gender, ethnicity, sexual orientation, gender identity, disability, protected veteran's status, or any other characteristic protected by federal, state or local laws.

Test Lead Duration: 12 months + Physical Supply Chain Test Lead We are seeking an experienced Test Lead to lead the testing for a crucial project in our Physical Supply Chain space. We will be consolidating our technology stack with one of our key partners, moving order management and fulfillment to a central Order Management and Warehouse Management solution set across business lines. This project is a mix of internally supported and SaaS technology and our testing plan needs to account for the end -to -end processes and flow between all impacted business processes and systems. As a Test Lead you will participate in all aspects of testing lifecycle which includes test strategy, test readiness, SIT, UAT (including day in the life), regression and smoke testing. As part of the team you will work with business stakeholders, business analysts, developers and SaaS providers translating business requirements and technical solutions needs into actionable test strategy and test collateral as well as supporting test delivery. What You'll Do • Test Planning and Strategy: Collaborate with technical and business stakeholders to develop comprehensive test plans for the project, identify necessary resources (people and tools) ensuring coverage of functional and non -functional requirements including both positive and negative test cases. • Test environment and Data strategy: Align on our test environment and test data strategy and ensure both are ready ahead of test execution. • Test Documentation: Create/maintain clear, concise, detail -oriented comprehensive test documentation, including test plans, test cases, test scripts, and test reports. • Test Case Development: Design and develop test scenarios, test cases, and test scripts based on business requirements, system specifications, and industry best practices including enhancing user stories with acceptance criteria where needed. • Test reporting: Weekly reporting on testing and defect status, with move to daily during critical test phases. • Test Execution: Execute test cases and document test results, ensuring the system's compliance with functional and non -functional requirements. • Regression Testing: Perform regression testing to ensure that system changes and enhancements do not adversely impact existing module functionalities. • Analyze and reports defects and verify defect fixes • Proactively communicates with Product Manager, Business Analysts, and Developers on open issues and test status RequirementsRequired Skills and Experience • 8+ years of experience developing test plans, test cases, test strategies for functional, integration, and end -to -end user testing • 5+ years of experience working on supply chain systems including Warehouse Management and Order Management solutions • Experience working on large, cross system projects and complex business applications including multiple SaaS partners • Solid grounding in different levels of testing: Web services/API testing (using Postman/Insomnia), functional testing (both desktop and mobile), regression testing, performance testing • Experience with test automation is a major plus • Experience working with waterfall and Agile methodologies is preferred. • Strong self -driving force and quick learning ability • Excellent critical analysis skills • Superior organizational and communication skills (proactive communicator) • Ability to work independently, prioritize tasks based on priority, and meet deadlines in a fast -paced

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description The Quality Assurance (QA) Engineer will be responsible for bridging technical operations and quality assurance. Valuable in high throughput, regulated labs, and are key to preventing quality failures through proactive risk and process management. This role involves monitoring lab processes, conducting audits, analyzing data to identify potential issues, and driving continuous improvement initiatives to minimize errors and ensure data integrity. Key Responsibilities & Duties * Quality Management System (QMS): Participate in the maintenance and improvement of the QMS. Help ensure that procedures are compliance with regulatory standards (e.g. CLIA, CAP, FDA, ISO 15189). Identify and investigate non-conformances. Assist in developing technical SOPs and work instructions. * Auditing and Compliance: Provide technical documentation for audits and inspections. Ensure all validation and qualification documentation is complete and audit ready. Plan and conduct internal audits of laboratory operations, processes, and systems to assess compliance with established quality standards and regulations. Support external audits and inspections from regulatory agencies. * Corrective and Preventive Actions (CAPA): Conduct technical root cause analyses for system-related failures or deviations. Help develop and implement Action Plans. * Process Improvement: Identify areas for process improvement and lead continuous improvement activities. Utilize Lean Six Sigma or other quality tools to identify inefficiencies. Develop and maintain process maps, value stream maps and other visual tools to identify bottlenecks and opportunities. Collaborate with lab operations and IT to improve workflows and reduce errors. Develop and use statistical analysis and quality control charts to monitor trends and recommend solutions for enhanced quality and efficiency. Assist in the development and refinement of quality metrics and dashboards. * Training: Assist in the development and delivery of quality assurance training programs for laboratory staff to ensure adherence to quality protocols and procedures. * Collaboration: Work closely with lab management, technical directors, and other cross-functional teams to integrate process improvements and quality requirements into daily operations and new process development. Contribute to the evolution of a proactive quality culture, aligned with our service vision and mission Qualifications * Education: Bachelor's degree in a chemical, biological, physical, laboratory science or related science or engineering field. * Experience: 3+ years of experience in a Quality Engineering or Process Improvement preferable in a regulated laboratory or healthcare setting. * Regulatory Knowledge: Thorough understanding of industry-specific quality standards and regulations (e.g., ISO 15189, CAP, CLIA, FDA, etc.). * Technical Skills: Proficiency with Laboratory Information Management Systems (LIMS), statistical analysis software, and Microsoft Office (especially Excel for data analysis). Experience with Lean Six Sigma, Statistical Process Control, Value Stream Mapping, Root Cause Analysis, CAPA, etc. is key toward process improvement role. * Problem-Solving: Strong analytical and problem-solving abilities with experience in root cause analysis. * Communication: Excellent written and verbal communication skills, with the ability to present data and reports to diverse stakeholders. * Attention to Detail: Meticulous attention to detail and a high level of accuracy in all documentation and processes. * Work Environment: Ability to work independently and collaboratively in a fast-paced, deadline-driven laboratory environment, which may involve working with potential biohazards or wearing personal protective equipment (PPE). Additional Information Compensation: * $90,000-$110,000 per year Schedule: * Monday - Friday 8:00am-4:30pm 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.

Full-time Description At SpectraWAVE, our mission is bold yet simple: to provide unrivaled optical and computational insights to improve the treatment and outcomes for patients with coronary artery disease (CAD) the leading cause of death worldwide. Our FDA-cleared HyperVue™ Imaging System integrates DeepOCT™, near-infrared spectroscopy (NIRS), and advanced machine learning to give interventional cardiologists real-time clarity inside the artery, where it matters most. SpectraWAVE recently received FDA 510(k) clearance for X1-FFR, an AI-enabled, wire free, drug-free, single angiogram physiology solution that delivers powerful insights without disrupting workflow. Together, HyperVue™ and X1-FFR represent a new era of precision and simplicity in coronary imaging and physiology. Backed by Johnson & Johnson Innovation - JJDC, Inc. and other leading MedTech investors, SpectraWAVE recently completed a $50M Series B funding round to accelerate commercialization and product innovation. We're a fast-growing, collaborative team united by the belief that technology can save lives. If you're inspired by innovation, energized by challenge, and ready to make a measurable impact on patient outcomes, we'd love to meet you. We are seeking a highly motivated and detail-oriented Software Quality Assurance (SQA) Engineer to join our growing team. In this role, you will contribute to ensuring the safety and reliability of our medical device software through rigorous testing and documentation. This position offers an excellent opportunity to learn and grow within the medical device industry, gaining valuable experience in a regulated environment. You will work closely with experienced engineers and cross-functional teams to deliver high-quality software that meets stringent regulatory requirements. Key Responsibilities: Participate in all aspects of software quality assurance for medical device software including Requirements management Test protocol development and execution Test report creation Automated test development and execution Adhere to all applicable regulatory requirements and company quality standards Collaborate with software developers, product managers, and other team members to ensure effective communication and problem-solving Requirements Minimum Qualifications: Bachelor's degree in computer science, engineering, or related field Basic understanding of software testing concepts and methodologies 2 - 5 years' experience working in a product or component test capacity Excellent written and verbal communication skills Eagerness and ability to learn on the job Results oriented Desired Qualifications: Familiarity with Python or similar scripting language Familiarity with automated software test Familiarity with IEC 62304 Familiarity with medical device development Familiarity with bug tracking systems (i.e. JIRA) Familiarity with requirements management systems like JAMA Ability and Desire to develop and support Python based utilities used by Manufacturing and Field Service Ability and Desire to develop proficiency with cybersecurity risk analysis and mitigation per applicable regulatory requirements Salary Description $70,000 - $130,000