Research and development technician jobs in Reading, PA

Universal Ingredients, Inc. is a premier manufacturer of vanilla extracts, other extracts, natural and artificial flavors, food colors, syrups, and sauces. Shank's quality products are widely distributed to industrial, private-label, and grocery customers worldwide. We have an immediate opening for an R&D Laboratory Technologist Available Immediately Upon Hire: Medical, Dental, Vision, FSA, HSA, EAP, ID Theft, 401K, and PTO. Disclaimer: Shank's Extracts manufactures various products that identify as major food allergens (milk, eggs, tree nuts, wheat, and soybeans) as well as several other food ingredients. We cannot guarantee you will not be exposed to skin and/or odor contact with these various ingredients. Your health and safety are our number one priority, and we will do our best to accommodate within reason. ESSENTIAL FUNCTION: Prepares bench top and pilot lab flavor/food/beverage prototypes to showcase Universal Ingredients' portfolio & technologies under supervision as required. DUTIES AND RESPONSIBILITIES: * Compounds flavor formulas for active project work as instructed by the flavorist. * Prepares application samples for ongoing development projects, including scaling, heat treatment, and packaging. * Utilizes basic mathematical procedures to calculate flavor adjustment percentages and create chemical solutions. * Adjust flavor formulas as instructed by the flavorist and records changes in Excel formulas. * Doses finished flavors at tasting strength and prepares flavor and application tastings for flavorist and team. * Completes chemical analyses of flavor and application products for commercialization. * Maintains raw material inventory through warehouse sampling and proper labeling. * Contacts raw material suppliers for samples of ingredients not maintained in warehouse inventory. * Fulfills open sample requests in a timely manner by preparing samples, providing copies of necessary documentation, and coordinating shipping. * Maintains laboratory equipment and space in a clean, orderly, and safe manner daily. * Follows appropriate safety, laboratory, and GMP procedures. * Performs other duties as assigned. ESSENTIAL/SKILLS NEEDED: * Must have a positive attitude, be self-motivated, detail-oriented and organized. * Must work well in a team environment. * Ability to work in a fast-paced environment and adapt to constant change in a positive manner. * Ability to understand instructions and execute in an efficient and effective manner. * Capable of handling multiple projects in a limited time frame. * Familiar with food industry practices and procedures, and basic knowledge of GMP's and HACCP. * Ability to read and interpret various formula sheets. * Ability to use basic lab equipment such as scales, pipettes, pH meters, blenders, mixers, and hot plates/stirrers. * Proficient in Microsoft Office and able to learn new software systems quickly. * Excellent hand-eye coordination. * English comprehension including speaking, reading, and writing is required for our business's necessity to ensure a safe and effective work environment. EDUCATION AND EXPERIENCE * High school diploma required. * Associate degree in the Sciences preferred. * 1-2 years of experience working in a laboratory setting preferred. * ERP Experience preferred. * Experience in a food manufacturing company preferred. PHYSICAL REQUIREMENTS: * Requires standing for an entire shift. * Requires frequent lifting and/or carrying objects weighing up to ten (10) pounds. * Requires pushing, pulling, bending, twisting, squatting, and lifting close to the body. * Require frequent repetitive motion. * Ability to work in a consistent area for an entire shift. * Must be able to work in various indoor temperatures including elevated heat and humidity. * Exposure to elevated noise levels which occur below OSHA thresholds. * Infrequent exposure to machine sanitation solutions and detergents. * Requires frequent visual quality control observations which may include turning and bending of the neck and head area. * Exposure to various odors throughout a work shift. * Required to wear Personal Protective Equipment [PPE] * Required to follow Good Manufacturing Practices [GMPs] * Exposure to food allergens such as, but not limited to, milk, eggs, tree nuts, wheat, and soybeans will occur. Conduct, Quality, Integrity, and Culture Conduct: We will conduct every aspect of our business with honesty, integrity, and openness, respecting human rights and the interests of our employees, customers, and third parties. Quality: Shank's is committed to food safety and product quality. We employ extensive food safety programs and controls at all levels. Our quality standards and food safety procedures are thoroughly being evaluated internally and externally. We continuously strive to improve our performance. Integrity: Shank's and its employees will not offer, give, seek or receive, either directly or indirectly, improper inducements for business or financial gain. Where information is confidential, that confidentiality must be protected. Culture: Shank's respects the cultural values of our employees, contractors, and customers. We also promote a balanced work-life environment. We recognize and celebrate our employees for their hard work and the contributions they make to our company. Shanks Core Values: ASPIRATION: Share a vision for achievement ACCOUNTABILITY: Support company reputation ADAPTABILITY: Evolve to meet business needs * Competitive compensation and benefits package* Shank's Extracts, LLC d/b/a Universal Ingredients - Shank's is an Equal Employment Opportunity/Affirmative Action (EEO/AA) Employer.

At Dow, we believe in putting people first and we're passionate about delivering integrity, respect and safety to our customers, our employees and the planet. Our people are at the heart of our solutions. They reflect the communities we live in and the world where we do business. Their diversity is our strength. We're a community of relentless problem solvers that offers the daily opportunity to contribute with your perspective, transform industries and shape the future. Our purpose is simple - to deliver a sustainable future for the world through science and collaboration. If you're looking for a challenge and meaningful role, you're in the right place. Dow (NYSE: DOW) is one of the world's leading materials science companies, serving customers in high-growth markets such as packaging, infrastructure, mobility and consumer applications. Our global breadth, asset integration and scale, focused innovation, leading business positions and commitment to sustainability enable us to achieve profitable growth and help deliver a sustainable future. We operate manufacturing sites in 30 countries and employ approximately 36,000 people. Dow delivered sales of approximately $43 billion in 2024. References to Dow or the Company mean Dow Inc. and its subsidiaries. Learn more about us and our ambition to be the most innovative, customer-centric, inclusive and sustainable materials science company in the world by visiting ************ About this role Dow has an exciting opportunity for a Senior Research & Development/Technical Service & Development Technician located in Collegeville, PA. This role: Provides technical support to Lead Scientists and Technologist Leaders in the preparation and execution of experimental activities and studies. Acts as primary focal point for technical support of a process, program, product, or application within the work group and occasionally for internal/external clients and customers. Provides technical support for product development, application development, technical service, and/or product or process research. This role requires that you gain proficiency through on-the-job training and experience. You will develop either deep skills in architectural coatings or knowledge of a range of processes, procedures, and systems. You will develop a broad understanding of the job and understand how to apply your knowledge and skills to complete the assigned tasks. You should understand how your team works with others to accomplish objectives and be able to exchange detailed, complicated information with other team members. It is your responsibility to evaluate analytical or scientific problems in high-pressure situations and select solutions based on established procedures. You will serve as an informal resource on operational, administrative, data organization, or coordination tasks for less experienced team members with no direct supervisory responsibilities. Your performance will impact the quality, timeliness, and effectiveness of your own work and your team's work. You should be able to suggest modifications to work practices and processes to achieve results and/or improve efficiency. Responsibilities - Duties, projects, tasks, and activities you would be responsible for in this role Works as part of a team in a laboratory supporting chemists and engineers in developing, screening and commercializing new products and processes in the architectural coatings space. Manages and then safely executes laboratory work requests, maintaining and running relevant laboratory apparatus and testing equipment and documenting data. Develops experimental plans for review/approval by Lead Scientist or Technology Leader, and executes approved plans by performing routine and non-standard tasks or procedures of higher complexity. Achieves project goals using technical, role-specific skills and experience, and introduces new procedures for new instrument methods, equipment changes, or new equipment. Develops a specific expertise within the department and laboratory work group in specific procedures, equipment, or instruments. Acts responsible for calibration, safe operation and routine maintenance of simple and complex instruments, machinery, and system components, including production equipment. Updates personal knowledge for proper use of equipment via manuals and job aids, logs maintenance activities and calibration results as required. Communicates scientific observations to project team or principle investigator, and organizes and prepares data tables and charts for inclusion in supported studies. Qualifications A minimum of a High School Diploma/GED and 5 years of relevant working experience OR a minimum of an Associates degree in a science related discipline/Military Degree Equivalency (MDE) A minimum requirement for this U.S. based position is the ability to work legally in the United States. No visa sponsorship/support is available for this position, including for any type of U.S. permanent residency (green card) process. Your Skills Laboratory Instrumentation: Ability to operate, calibrate, and maintain laboratory instruments and equipment, ensuring accurate measurements and reliable performance. Laboratory Safety: Knowledge and application of safety protocols, hazard identification, and compliance with regulatory standards to maintain a safe working environment. Analytical Thinking: Capacity to evaluate complex problems, interpret data, and select solutions based on established procedures and scientific reasoning. Technical Communication: Ability to clearly convey technical information, observations, and data through reports, charts, and verbal updates to scientists and team members. Organizing, Planning, and Prioritizing Work: Skill in structuring tasks, managing time, and prioritizing activities to meet project goals efficiently. Note: This role does not offer relocation assistance. Benefits - What Dow offers you We invest in you. Dow invests in total rewards programs to help you manage all aspects of you: your pay, your health, your life, your future, and your career. You bring your background, talent, and perspective to work every day. Dow rewards that commitment by investing in your total wellbeing. Here are just a few highlights of what you would be offered as a Dow employee: Equitable and market-competitive base pay and bonus opportunity across our global markets, along with locally relevant incentives. Benefits and programs to support your physical, mental, financial, and social well-being, to help you get the care you need...when you need it. Competitive retirement program that may include company-provided benefits, savings opportunities, financial planning, and educational resources to help you achieve your long term financial-goals. Employee stock purchase programs (availability varies depending on location). Student Debt Retirement Savings Match Program (U.S. only). Dow will take the value of monthly student debt payments and apply them as if they are contributions to the Employees' Savings Plan (401(k)), helping employees reach the Company match. Robust medical and life insurance packages that offer a variety of coverage options to meet your individual needs. Travel insurance is also available in certain countries/locations. Opportunities to learn and grow through training and mentoring, work experiences, community involvement and team building. Workplace culture empowering role-based flexibility to maximize personal productivity and balance personal needs. Competitive yearly vacation allowance. Paid time off for new parents (birthing and non-birthing, including adoptive and foster parents). Paid time off to care for family members who are sick or injured. Paid time off to support volunteering and Employee Resource Group's (ERG) participation. Wellbeing Portal for all Dow employees, our one-stop shop to promote wellbeing, empowering employees to take ownership of their entire wellbeing journey. On-site fitness facilities to help stay healthy and active (availability varies depending on location). Employee discounts for online shopping, cinema tickets, gym memberships and more. Additionally, some of our locations might offer: Transportation allowance (availability varies depending on location) Meal subsidiaries/vouchers (availability varies depending on location) Carbon-neutral transportation incentives e.g. bike to work (availability varies depending on location) Join our team, we can make a difference together. About Dow Dow (NYSE: DOW) is one of the world's leading materials science companies, serving customers in high-growth markets such as packaging, infrastructure, mobility and consumer applications. Our global breadth, asset integration and scale, focused innovation, leading business positions and commitment to sustainability enable us to achieve profitable growth and help deliver a sustainable future. We operate manufacturing sites in 30 countries and employ approximately 36,000 people. Dow delivered sales of approximately $43 billion in 2024. References to Dow or the Company mean Dow Inc. and its subsidiaries. Learn more about us and our ambition to be the most innovative, customer-centric, inclusive and sustainable materials science company in the world by visiting ************ As part of our dedication to inclusion, Dow is committed to equal opportunities in employment. We encourage every employee to bring their whole self to work each day to not only deliver more value, but also have a more fulfilling career. Further information regarding Dow's equal opportunities is available on ************ Dow is an Equal Employment Opportunity employer and is committed to providing opportunities without regard for race, color, religion, sex, including pregnancy, sexual orientation, or gender identity, national origin, age, disability and genetic information, including family medical history. We are also committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, you may call us at 1-833-My Dow HR ************** and select option 8.

**Company:** Teleflex **Expected Travel** : None **Requisition ID** :13117 Incorporated** As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rüsch, UroLift and Weck - trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com. **Vascular Access -** Built on a history of innovation, our Arrow brand of technically advanced vascular access devices are renowned throughout the world. Many of our vascular access products have antimicrobial and antithrombogenic protection designed to reduce vascular-related complications and include long and short dwell central venous catheters (CVC), sheath introducers, arterial lines, peripherally inserted central catheters (PICC), as well as specialty devices and an advanced vascular positioning system to facilitate precise placement of a PICC or CVC near the heart. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives. **Position Summary** The Scientist is responsible for conducting microbiological and biological testing, optimizing methods, and supporting new test method development for the evaluation of medical devices. This role requires a solid foundation in microbiology and biology theory, proven competency in laboratory practices, and the ability to troubleshoot, analyze, and interpret experimental results with minimal supervision. The Scientist contributes to project deliverables, supports regulatory and design control activities, and provides technical expertise to cross-functional teams. The position also involves mentoring junior staff, reviewing documentation, and participating in innovative initiatives that enhance laboratory efficiency and quality. **Principal Responsibilities** - Conduct microbiology and biology testing in support of R&D, method development, and medical device evaluation, ensuring compliance with protocols, quality systems, and regulatory requirements. - Prepare, optimize, and perform biological assays and laboratory procedures, including aseptic techniques, media preparation, and device-related testing. - Troubleshoot instrumentation, methods, and results; provide initial corrective action proposals, escalating as needed. - Document all experimental work using good documentation practices (GDP), ensuring accuracy, completeness, and regulatory compliance. - Summarize and communicate data clearly in reports, presentations, and cross-functional discussions; review and approve junior team members' laboratory notebooks and reports. - Assist in test method design, optimization, and validation to improve efficiency, accuracy, and compliance. - Apply biological and microbiological principles to interpret results, make connections across steps, and explain reasoning behind test protocols. - Contribute to design control deliverables (e.g., IMHs, VERs, LRs), supporting regulatory submissions and quality system compliance. - Support lab quality initiatives, including nonconformance (NC) resolution, CAPAs, and internal audit readiness. - Take ownership of small-scale projects, managing timelines, resources, and reporting while supporting senior scientists on larger initiatives. - Train and mentor junior staff in laboratory techniques, documentation, and safety practices. - Actively contribute to innovation by identifying process improvements and collaborating with cross-functional stakeholders. - Represent R&D in cross-functional meetings, aligning project objectives with company goals and contributing to strategic discussions. - Uphold Teleflex's Code of Ethics, maintain a safe laboratory environment, and model professional and ethical conduct. **Education / Experience Requirements** - Bachelor's or Master's degree in Microbiology, Biology, Biomedical Sciences, or related field. - 2-4 years of relevant laboratory experience (medical device, microbiology, or related industry preferred). - Demonstrated competency in aseptic techniques, microbial culture preparation, serial dilutions, and biology/microbiology test methods. - Experience with documentation, method optimization, and cross-functional collaboration. - Familiarity with regulatory and quality frameworks (e.g., FDA 21 CFR Part 820, ISO 13485, ISO 17025) preferred. **Specialized Skills / Other Requirements** - Proficiency in laboratory practices, including aseptic techniques, solution/media preparation, and instrumentation use and maintenance. - Strong technical writing and communication skills, with the ability to prepare reports, protocols, and technical documentation for diverse audiences. - Ability to review and approve data and reports generated by junior staff, ensuring accuracy and compliance. - Foundational knowledge of root cause analysis tools (Fishbone, 5 Whys, Six Sigma, CAPA) with ability to contribute to problem-solving efforts. - Understanding of microbiology and biology principles relevant to medical devices (biofilm formation, pathogenicity, molecular biology, cellular response). - Familiarity with medical devices, their clinical use (PICC, CVC, AHDC, etc.), and associated complications such as infection and thrombosis. - Working knowledge of design control principles and agile documentation systems. - Awareness of regulatory requirements for medical device testing and development. - Effective time and project management skills with the ability to manage multiple assignments, track progress, and meet deadlines. - Strong accountability, ownership, and initiative in managing tasks and small projects. - Ability to influence cross-functional teams through clear, data-driven communication. - Collaborative, inclusive, and adaptable mindset, fostering teamwork and continuous improvement. - Commitment to ethical standards, safety, and compliance in all laboratory and project activities. \#LI-EB1 **Working Conditions / Physical Demands** TRAVEL REQUIRED: 0 % WORKING ENVIRONMENT: ☒ Office/Professional ☐ Plant/Manufacturing ☐ Remote/Field ☒ Laboratory _At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front._ _Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: ************ or *******************._ _Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rüsch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries._ _© 2025 Teleflex Incorporated. All rights reserved._

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us. Click on the link below to learn what our employees have to say about Evonik: ************************************************** RESPONSIBILITIES Be able to perform routine analytical measurements with guidance on chromatographic methods (for example, GC, HPLC, GPC etc.) Run other routine analytical measurements with guidance, such as ICP-OES, titration, physical measurements, thermal analysis, particle characterization and NMR etc. Maintain analytical instruments (including initial and regular calibration and qualification, maintenance), participate in general lab activities, such as 5S, and trash disposal etc. Be responsible for all ESH and legal related issues in the lab, including but not limited to: 1) compliant with all company policies; 2) train the related employees; 3) incident/near miss reporting and investigation etc. 4) chemical inventory, yearly reconciliation and waste disposal. Implement improvements and provide feedback on them. Use change management systems and protocols to provide routine supportive services. Support others by carrying out a range of product development and engineering activities such as analyzing client situations or interpreting data. Collect and prepare standard data related to ongoing issues. Support others by carrying out routine policy-related tasks. Support project managers by performing simple tasks. Involves following established procedures. Assess compliance with established standards and protocols. Organize own work schedule in order to get the job done, coordinating with support services and assigning short-term tasks to others if necessary. REQUIREMENTS BS in Chemistry or Chemical Engineering with 5 - 8 years of experience working in laboratory environment, or a MS in Chemistry or Chemical Engineering with a minimum of 3 years of experience working in a laboratory environment Good organizational skills r equired, react flexibly to varous assignments and different clients; Efficient use of resources (instruments, time, materials). Good communication skills required in dealing with direct colleagues, internal clients, and German technical experts; Team working experience Entrepreneurship and self-determination Good oral and written English skills Practical experience in analytical methods essential. The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at *************************** Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Wenda Cenexant [C] Company is Evonik Corporation

New Product Development Lab Technician - 1st Shift Hours are 8:00am - 5:00pm Monday thru Friday The NPD Lab Technician plays a key role in bringing packaging concepts to life by operating sample lab thermoforming equipment consisting of, a semi-automated vacuum former, swing arm clicker trim press, 3D printer, and other various equipment to produce high-quality prototypes. Along with these duties, this employee will also maintain the lab's inventory of supplies and cleanliness. The NPD Lab Technician will collaborate closely with engineers and designers to support prototyping, testing, and sample production across multiple projects. Employee may perform other related duties as required to meet the ongoing needs of the organization. Essential Responsibilities: Set up, run, and monitor 3D printer; manage the print queue based on project priorities and deadlines. Maintain adequate supplies and materials for 3D printing and lab operations; place orders or flag shortages as needed. Perform basic 3D printer maintenance and troubleshoot printing issues. Operate thermoforming and vacuum forming lab equipment to produce sample parts. Trim sample parts with clicker press or other hand methods. Inspect prototype parts for visual quality, dimensional accuracy, and overall performance. Record process parameters and measurements during prototyping to support repeatability and documentation. Maintain a clean, organized, lab space with well-labeled materials, parts, and tools. Support the Design Engineering team by assembling mockups, running tests, or preparing materials. Assist with fixture building, and other hands-on tasks. Crosstrain to support QA as needed. Participate in process improvement efforts and provide feedback on prototype functionality. Follow all lab safety procedures and ensure compliance with operational best practices Essential Skills: High school diploma or equivalent required; technical coursework or associate degree preferred. 1-3 years of experience in a manufacturing, prototyping, or lab setting preferred. Mechanical aptitude with the ability to work hands-on with equipment, tools, and materials. Experience operating or maintaining 3D printers (FDM preferred) is a strong plus. Familiarity with thermoforming, vacuum forming, or plastics manufacturing is highly desirable. Ability to read and interpret basic engineering drawings or part specifications. Comfortable using measurement tools (e.g., calipers, rulers, gauges) for quality checks. Strong organizational skills and the ability to manage multiple projects simultaneously. Basic computer skills, including file management and use of standard office software Brentwood offers professional growth potential, pleasant work environment, and an excellent wage and benefits package including 401K w/employer match. Brentwood Industries, Inc., provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, or genetics. At Brentwood, we have a passion for both our products and our people. Our goal as an employer is to help you excel as an individual and as part of a team by providing you with a satisfying, motivating and stimulating work experience. The varied nature of the environment at Brentwood allows you to work alongside industry professionals on a wide range of projects, contributing your knowledge and strengths to develop innovative, market-driven solutions. To begin the application process, please click the "Apply" button.

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. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. 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, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing. In 2019, Eurofins generated total revenues of EUR € 4.56 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description As an HPLC Biochemist, you'll be at the forefront of analytical excellence, developing and validating robust methods to ensure the safety and efficacy of our products. You'll work in a collaborative lab environment where your expertise will directly impact global health. Key Responsibilities Design, develop, and validate HPLC methods for complex biologics and biosimilars Analyze and interpret chromatographic data using Empower software Collaborate with cross-functional teams to support product release and stability testing Troubleshoot and optimize analytical methods for improved performance Author technical protocols, reports, and regulatory documentation Qualifications The Ideal Candidate would possess: Experience with Protein Sciences, mainly protein and glycoprotein characterization. Experience in High Resolution Mass Spectrometry. Experience in HPLC ( at least 1+ year applied) Experience with other Biochemistry techniques (e.g Amino Acid Analysis, Glycosylation profiling) Strong computer, scientific, and organizational skill Theoretical understanding of large molecule biochemistry Excellent communication (oral and written) and attention to detail Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies Minimum Qualifications: Minimum 2 years of relevant experience, either post-doctoral or in the bio/pharmaceutical industry Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, Monday - Friday 8:00am - 4:00pm. Candidates currently living within a commutable distance of Lancaster, 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 is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. #LIAD1 Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer. #LI-EB1 Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Job DescriptionAssociate Scientist, Pharmaceutical Analysis-Small Molecule 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: Performs routine sample analysis and a variety of tasks to support product development, ensuring agreed timelines Assists method development Performs method validation under supervision Reports and resolves any unexpected issues under supervision Complies with all relevant cGMP and/or GLP regulatory requirements while carrying out assigned studies Requirements: B.S. in Chemistry or related discipline 1-2 years of related industry experience preferred Hands-on experience with HPLC, UPLC, GC, LC/MS, IC and Dissolution Testing Excellent oral and written communications skills Capable of setting priorities based on a fast-paced, changing environment Good team player to work with Formulators and QA CRO experience 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.

Responsibilities: • Experience with lab instrumentation/equipment such as pH, viscometer, FTIR, Near-IR, AA preferred. • Hands on set-up and troubleshooting experience with HPLC and GC required. • Experience with sample preparation required. • Experience with a chromatographic data acquisition system required. • Experience with Compendia USP and preferred experience with NF, EP and/or FCC required. • Computer skills with utilization of Microsoft Office (Outlook, Word, and Excel) required. • Problem solving skills required, preferred experience with laboratory investigations. • Ability to work individually as well as in a team. • Self-motivated. Job Description Experience: A minimum of 1 years of analytical laboratory experience within the pharmaceutical or consumer healthcare industry. Qualifications Education: Bachelor Degree in Chemistry, related science or the equivalent. Additional Information Contact me at 732-549-5307

APPLICATION INSTRUCTIONS: * CURRENT PENN STATE EMPLOYEE (faculty, staff, technical service, or student), please login to Workday to complete the internal application process. Please do not apply here, apply internally through Workday. * CURRENT PENN STATE STUDENT (not employed previously at the university) and seeking employment with Penn State, please login to Workday to complete the student application process. Please do not apply here, apply internally through Workday. * If you are NOT a current employee or student, please click "Apply" and complete the application process for external applicants. JOB DESCRIPTION AND POSITION REQUIREMENTS: We are seeking a motivated, experienced, and driven Systems Research and Development Engineer to join the Strategic Systems Operations Division in the Applied Research Laboratory (ARL) at Penn State. This position will be working with senior technical staff to research, design, develop, integrate, and test advanced communications systems. If you are interested in collaborating and learning with a team of brilliant fellow researchers to develop the next generation communications and signal processing software and hardware solutions, this is for you! ARL fosters and develops some of the greatest minds that the Department of Defense (DoD) has to offer. ARL is an authorized DoD SkillBridge partner and welcomes all transitioning military members to apply. You will: * Organize and direct a multi-disciplinary, strong, and diverse engineering team * Balance team members, activities, and priorities with the process to achieve a final product * Provide technical leadership within the CSP Division projects * Plan and direct research projects related to communications * Guide programs of national or international significance; identify future problems, research trends, and opportunities * Interact and collaborate regularly with the engineering team, principal investigator, sponsors, and other stakeholders This position can be filled at multiple levels depending on your education and work experience. Minimally requires a Bachelor's degree in an engineering or science discipline plus five years' related experience. Additional education and/or experience required for higher level positions. A Master's degree in Electrical Engineering is preferred. Required skills/experience areas to include: * Advanced understanding of electrical engineering principles associated with communications * Collection and processing architectures for RF signals in general, with emphasis on the impact of propagation effects in the HF and below bands as well as UHF through Ku bands * AoA and TDOA/FDOA geolocation techniques * Communications protocols - OSI stack, UDP/TCP/IP * Familiarity with wireless specifications such as cellular(4G/5G)/WiFi (802.11) * Capable of creating testable system level performance requirements from sponsor defined use cases or user stories * Capable of taking high level system requirements and performing a first order decomposition into hardware and software functions * Capable of generating test plans/procedures to validate system level performance Preferred skills/experience areas to include: * TS/SCI Clearance * Communication, Analytical, and Organizational skills * Detail-oriented thinking with the ability to see the "big picture" * Troubleshooting experience * Conflict resolution experience * FFRDC or UARC experience The position will be located in State College, PA, Reston, VA, or Annapolis Junction, MD. This position requires in-office work, but may allow for hybrid work when contract permits. Questions related to flexible work should be directed to the hiring manager during the interview process. This position will require occasional travel to CONUS and possibly OCONUS locations. Candidate selected will be subject to a government security investigation. You must be a U.S. citizen to apply. Employment with the Applied Research Laboratory will require successful completion of a pre-employment drug screen. FOR FURTHER INFORMATION on ARL, visit our web site at **************** The proposed salary range may be impacted by geographic differential. The salary range for this position, including all possible grades is: $109,300.00 - $191,000.00 Salary Structure - additional information on Penn State's job and salary structure. CAMPUS SECURITY CRIME STATISTICS: Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act and the Pennsylvania Act of 1988, Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR). The ASR includes crime statistics and institutional policies concerning campus security, such as those concerning alcohol and drug use, crime prevention, the reporting of crimes, sexual assault, and other matters. The ASR is available for review here. Employment with the University will require successful completion of background check(s) in accordance with University policies. EEO IS THE LAW Penn State is an equal opportunity employer and is committed to providing employment opportunities to all qualified applicants without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you are unable to use our online application process due to an impairment or disability, please contact ************. Federal Contractors Labor Law Poster PA State Labor Law Poster Penn State Policies Copyright Information Hotlines University Park, PA

Full-time Description Experience Fulfilling Work with our Purpose-Driven Laboratory We're seeking a talented, detail-oriented Chemist to join our Metals laboratory team in Reading, PA. In this role, you'll perform analytical testing, method development, and data validation that ensure the accuracy and quality our clients depend on for regulatory compliance and decision-making. Working alongside experienced professionals, you'll gain exposure to advanced laboratory instrumentation, contribute to continuous improvement initiatives, and help deliver precise, defensible results that make a measurable impact. If you're curious, focused, and eager to enhance your skills in a fast-paced laboratory setting, we'd love to hear from you! Why You'll Love This Role Play a hands-on role in transforming data into decisions that make a real-world impact; Work with state-of-the-art laboratory instrumentation and analytical techniques across diverse projects; Build your expertise in method development, data validation, and quality control in a collaborative, learning-focused environment; Contribute to work that supports client success, regulatory compliance, and SPL's mission of turning science into impact. What You'll Do Prepare, analyze, and document client and quality control samples using approved methods and Standard Operating Procedures (SOPs); Operate, calibrate, and maintain analytical instruments to ensure accuracy and reliability of results; Record, validate, and manage analytical data within the Laboratory Information Management System (LIMS) while ensuring traceability and compliance with quality standards; Participate in method development, validation, and troubleshooting activities to enhance analytical performance and efficiency; Support quality assurance initiatives, including audits, corrective actions, and continuous improvement projects; Collaborate with peers and supervisors to meet deadlines, maintain safety protocols, and uphold SPL's commitment to data integrity; Contribute to team training, mentorship, and the continuous improvement of laboratory practices; Perform other duties as assigned. Requirements What Makes You a Great Fit Bachelor's degree in Chemistry, Science, or a related field required; Minimum of two (2) years of analytical laboratory experience required; Experience with ion chromatography (IC), flow injection analysis (FIA), segmented flow analysis (SFA), spectrophotometry, biochemical oxygen demand (BOD), gravimetric analyses, mercury analysis, turbidity, or hardness testing strongly preferred; Experience with ICP, ICP-MS, and EPA methods 200.7, 200.8, 6010, and 6020 strongly preferred; Ability to manage and process high volumes of samples efficiently; Proficiency with Microsoft Office tools (Word, Excel, Outlook) and Adobe Acrobat. The Perks of Being Part of Our Team Grow Your Future: 401(k) plan with company matching to boost your retirement savings; Health & Wellness Covered: Comprehensive dental, vision, and health insurance plans; Spend Smart, Live Well: Flexible HSA and FSA accounts to help manage healthcare costs; Safety Net On Us: Employer-paid short-term and long-term disability coverage; Celebrate & Recharge: 9 paid holidays plus a generous PTO plan to balance work and life; Extra Protection: Employer-paid voluntary life and AD&D insurance; Family First: Paid parental leave available for both parents; Support When You Need It: Employee Assistance Program (EAP) for personal and professional help; Exclusive Perks: Discounts on products, services, and experiences just for you. Your Schedule and The Fine Print Full-time position working Monday through Friday from 9 AM to 5:30 PM; Ability to work overtime and outside of scheduled hours, including evenings or weekends, as required to meet operational or workload needs. Our Commitment to Diversity and Inclusion At SPL, we believe that a diverse team is a strong team. We are proud to be an equal opportunity employer, committed to creating an inclusive environment where all employees can thrive. We make all employment decisions based on qualifications, merit, and business needs, without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, age, disability, veteran status, or any other legally protected characteristic. We are also committed to providing reasonable accommodations to applicants and employees with disabilities or for sincerely held religious beliefs, in accordance with applicable laws. If you need assistance or an accommodation during the application process, please let us know. Visa Sponsorship At this time, SPL is not able to offer visa sponsorship for this position. We sincerely appreciate your interest and understanding, and we encourage you to explore other opportunities with us that may be a fit in the future.

Piper Companies is seeking a Quality Control Analytical Scientist (qPCR) to join a growing biopharmaceutical organization pioneering gene therapies for rare genetic disorders. This onsite position in Exton, PA provides the opportunity to perform advanced molecular testing and DNA-based assays that directly support GMP manufacturing and product quality operations. Responsibilities of the Quality Control Analytical Scientist (qPCR): * Perform GMP-compliant qPCR testing to support bulk, drug substance, and final product analysis. * Conduct DNA extraction and assays including Vector Copy Number (VCN) and VSVG testing. * Support complementary methods such as cell culture, ELISA, and flow cytometry. * Review data for accuracy, integrity, and compliance with GMP and documentation standards. * Execute OOS investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, calibration schedules, and audit readiness. Qualifications of the Quality Control Analytical Scientist (qPCR): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong proficiency in qPCR methodology, DNA extraction, and molecular analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiarity with analytical platforms such as ELISA and flow cytometry. * Excellent attention to detail, communication, and documentation skills. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (qPCR): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 11/17/2025 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, qPCR, Vector Copy Number, VCN, DNA Extraction, VSVG, GMP, Biologics, Gene Therapy, Molecular Testing, Analytical Methods, Cell Culture, ELISA, Flow Cytometry, CAPA, SOP, Data Integrity, Aseptic Technique, ALCOA, Good Documentation Practices, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

At Viwinco, Inc, we design and manufacture high-performance custom vinyl windows and patio doors with a focus on quality, innovation, and craftsmanship. As a family-owned company, we take pride in fostering a collaborative culture where every employee contributes to our continued growth and success. Our team is driven by innovation and a commitment to excellence-both in the products we make and the people who make them. We are in search of an experienced Research and Development Engineer to play a key role in supporting the R&D department through the design, testing, improvement, and implementation of window systems and related equipment. This position will also collaborate closely with production teams to develop tools and fixtures that enhance efficiency and improve manufacturing processes. The ideal candidate is detail-oriented, organized, and thrives in a hands-on, manufacturing-focused environment. Key Responsibilities Assist in the development, testing, and certification of new components, products, and processes to ensure compliance with quality, safety, and industry performance standards. Create, update, and maintain bills of materials (BOMs) for product offerings. Organize and maintain comprehensive documentation of designs, prototypes, and modifications. Collaborate with the R&D team to create and revise part drawings, assembly drawings, and technical specifications for window systems and related equipment. Design and prototype tools, fixtures, carts, and other equipment to improve production processes and operator efficiency. Troubleshoot and resolve issues related to part designs, mechanical systems, or equipment in R&D and production settings. Work cross-functionally with design, engineering, and production teams to ensure smooth implementation of new products and processes. Qualifications Bachelor's degree in Mechanical Engineering, Industrial Engineering, or a related field. At least 3 years of experience in an engineering or R&D role within a manufacturing environment. Familiarity with steel welding, metal fabrication, and pneumatic systems. Proficiency in 3D CAD software (Fusion, SolidWorks, or similar); experience with 2D drafting is a plus. Experience creating detailed technical drawings and assembly instructions. Hands-on approach and comfort working in production or manufacturing environments. Strong organizational skills with attention to detail and the ability to prioritize multiple tasks. Excellent problem-solving and communication skills, both written and verbal. Preferred Qualifications Experience in window manufacturing or related industries (e.g., construction materials, architecture). Knowledge of lean manufacturing or process improvement methodologies. Familiarity with quality control processes and industrial safety standards. Experience applying project management principles to achieve business objectives. Why Join Viwinco? Competitive pay and comprehensive benefits package 401(k) with company match Paid time off and holidays Opportunities for career growth and professional development Family-oriented culture with a strong commitment to employee success Interested? Join a company that values innovation, craftsmanship, and continuous improvement. Apply today to become part of the Viwinco team!

At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong emphasis on research and development. Our history includes the development of many innovative medicines, notably the discovery of the world's most widely-used treatment for Alzheimer's disease. As we continue to expand, we are seeking highly-motivated individuals who want to work in a fast-paced environment and make a difference. If this is your profile, we want to hear from you. The person will have demonstrated expertise in the analytical sciences and will be expected to provide guidance to methods development, supervise release and stability testing activities; direct product characterization and assay validation. The individual may be required to perform hands-on testing in the lab and will be expected to be a resource for resolving technical issues at CMOs and CROs. The individual will have demonstrated expertise in such procedures and techniques as compendial methods, HPLC, ELISA, LC-MS, qPCR, UV spectrophotometry, CE-SDS, SDS-PAGE, and their use, singly or in combination with other techniques, to test and characterize protein-based biopharmaceuticals. The person will author protocols; reports; author and revise SOPs and lead investigations into assay failures, OOS/OOT events; direct the implementation of CAPAs and evaluate their effectiveness. This position primarily oversees analytical testing and characterization at external laboratories and will be expected to effectively manage the alliance with the CROs/CDMOs to meet project timelines. The ability to function in a fast-paced, highly technical environment, and ability to communicate effectively are essential. Job Summary The person will have demonstrated expertise in the analytical sciences and will be expected to provide guidance to methods development, supervise release and stability testing activities; direct product characterization and assay validation. The individual may be required to perform hands-on testing in the lab and will be expected to be a resource for resolving technical issues at CMOs and CROs. The individual will have demonstrated expertise in such procedures and techniques as compendial methods, HPLC, ELISA, LC-MS, qPCR, UV spectrophotometry, CE-SDS, SDS-PAGE, and their use, singly or in combination with other techniques, to test and characterize protein-based biopharmaceuticals. The person will author protocols; reports; author and revise SOPs and lead investigations into assay failures, OOS/OOT events; direct the implementation of CAPAs and evaluate their effectiveness. This position primarily oversees analytical testing and characterization at external laboratories and will be expected to effectively manage the alliance with the CROs/CDMOs to meet project timelines. The ability to function in a fast-paced, highly technical environment, and ability to communicate effectively are essential. Job Functions Provide technical expertise and direction to the development and validation of phase-appropriate analytical methods to support current and future programs. Lead development of product specifications. Proficiency in the use of statistical tools is essential. Prioritize, schedule, and monitor analytical projects, ensuring timely completion. Review and approve stability protocols relating to method development, product release and characterization, assessment of stability, validation of assays, and- when appropriate- personally performing the assays and techniques Negotiate service contracts with external providers. Assess and document CMO/CRO analytical proficiencies and readiness to perform various types of assays. Support analytical method transfers by co-leading vendor due diligence activities as well as review and/or author all method transfers related documents. Review laboratory data to support product release, characterization, stability assessment, assay validation, and process development, while serving as a primary technical resource for internal teams and CMO/CRO analysts in troubleshooting and resolving analytical issues. Work with CMOs in investigating and documenting assay failures and OOS/OOT events. Help in identifying and implementing CAPAs. Help in the administration of external stability programs, ensuring regulatory compliance, adherence to protocol requirements and timely completion of results at each time point. Author and maintain SOPs, forms, protocols and other controlled documents. Draft regulatory documents to support IND/IMPD/BLA/MAA filings. Present assay/stability study results and related findings to relevant project stakeholders. Required Qualifications & Skills Academic/PhD in relevant scientific discipline with minimum 2 years of post-doctoral experience in relevant technical field (industry or academia) (OR) Combination of equivalent education & experience in an earlier role/ comparable role along with demonstrated skills listed below. Exhibits a complete understanding of principles, concepts, practices and standards in GMP testing of biopharmaceuticals, including a thorough understanding of industry practices. Extensive hands-on experience in HPLC, capillary electrophoresis, ELISA, gel-based assays and other relevant assay technologies used for the analysis of recombinant proteins. Demonstrated knowledge of biopharmaceutical development through all clinical phases and post-commercialization. Strong familiarity with cGMP/ICH/FDA/EMA regulations and guidelines. Ability to communicate effectively within own team and cross-functionally and presents insightful assessments of analytical data. Ability to work closely and influence external partners/CMOs/CROs. Ability to independently identify and investigate assay-related issues and formulate hypotheses and/or experimental design to support effective solutions. Ability to identify and implement improvements to methods/assays and processes. Demonstrated knowledge of plate-based and other potency assays is a must. Eisai Salary Transparency Language: The base salary range for the Scientist II, Analytical Outsource & Stability is from :113,400-148,900Under current guidelines, this position is eligible to participate in : Eisai Inc. Annual Incentive Plan. Final pay determinations will depend on various factors including but not limited to experience level, education, knowledge, and skills. Employees are eligible to participate in Company employee benefit programs. For additional information on Company employee benefits programs, visit *********************************************** Certain other benefits may be available for this position, please discuss any questions with your recruiter. Eisai is an equal opportunity employer and as such, is committed in policy and in practice to recruit, hire, train, and promote in all job qualifications without regard to race, color, religion, gender, age, national origin, citizenship status, marital status, sexual orientation, gender identity, disability or veteran status. Similarly, considering the need for reasonable accommodations, Eisai prohibits discrimination against persons because of disability, including disabled veterans. Eisai Inc. participates in E-Verify. E-Verify is an Internet based system operated by the Department of Homeland Security in partnership with the Social Security Administration that allows participating employers to electronically verify the employment eligibility of all new hires in the United States. Please click on the following link for more information: Right To Work E-Verify Participation

We Are:At Synopsys, we drive the innovations that shape the way we live and connect. Our technology is central to the Era of Pervasive Intelligence, from self-driving cars to learning machines. We lead in chip design, verification, and IP integration, empowering the creation of high-performance silicon chips and software content. Join us to transform the future through continuous technological innovation. Ansys Government Initiatives (AGI), part of Synopsys, is at the forefront of Digital Mission Engineering (DME) for space systems. Our team builds and supports ODTK (Orbit Determination Tool Kit), a powerful product enabling highly accurate orbit estimation from real or simulated tracking data. ODTK is trusted by engineers and mission planners throughout the mission lifecycle-from design to operations-making critical impacts in aerospace, defense, and research sectors. This position is based in Exton, PA and it is not eligible for immigration sponsorship. You Are: You are a passionate and driven software developer eager to make a real-world impact in the field of space systems and digital engineering. Your curiosity pushes you to explore the intricacies of orbital mechanics and trajectory optimization, and your commitment to excellence ensures the creation of robust, reliable, and innovative software solutions. With a background in computer science, engineering, or a related discipline, you thrive in collaborative, high-performing teams where your ideas and expertise help shape mission-critical products. You are motivated by the opportunity to solve challenging problems, working alongside subject matter experts and leveraging modern development tools. You bring a growth mindset, continuously seeking to expand your knowledge in both domain-specific areas and software engineering best practices. Your adaptability and eagerness to learn make you a valuable contributor to an agile team, and you take pride in writing clean, efficient code that stands up to rigorous testing and real-world applications. You communicate effectively, value diverse perspectives, and foster an inclusive environment where everyone is empowered to innovate. Above all, you desire to play a key role in advancing the future of space exploration and digital mission engineering. What You'll Be Doing: * Design, develop, test, and document new features for the ODTK product, enhancing its capabilities for mission planning and operations. * Collaborate with a multidisciplinary team to integrate advanced algorithms and optimize software performance. * Investigate and resolve issues identified by QA or product support, delivering timely and effective solutions. * Apply and promote best practices in commercial software development, including code reviews, version control, and continuous integration. * Contribute to backlog reduction by addressing existing bugs and implementing architecture improvements. * Engage with PhD-level experts to understand complex requirements and translate them into robust software implementations. * Participate in agile development cycles, providing feedback and ideas to continually improve team processes and product quality. The Impact You Will Have: * Directly enhance the accuracy and reliability of orbit determination for critical space missions. * Enable engineers and mission planners to make informed decisions using advanced modeling and simulation tools. * Accelerate the development of innovative features that support both government and commercial customers in the aerospace sector. * Contribute to the reduction of technical debt, improving the long-term stability and scalability of our software products. * Foster a culture of excellence and continuous improvement within the team and broader organization. * Drive adoption of modern engineering practices, raising the bar for software quality and maintainability. * Support the success of high-profile space missions by delivering reliable tools used throughout the mission lifecycle. What You'll Need: * BS in Aerospace Engineering, Mathematics, Physics, Computer Science or related field with 2 years' experience, or MS degree. * Strong proficiency in software development, with hands-on experience in C++, C#, and Visual Studio. * Understanding of commercial software development lifecycle, including agile methodologies. * Knowledge of one or more domain areas such as trajectory optimization, optimal control, attitude control & determination, or orbit determination. * Experience in troubleshooting and resolving technical issues in complex software systems. * Ability to document code and technical solutions for future reference and team collaboration. Who You Are: * Collaborative team player who thrives in fast-paced, innovative environments. * Excellent communicator with strong interpersonal skills. * Quick learner who adapts to new technologies and domain-specific challenges. * Detail-oriented problem solver, able to analyze complex issues and deliver effective solutions. * Inclusive and open-minded, valuing diverse perspectives and fostering a welcoming team culture. * Proactive contributor who takes ownership of tasks and follows through to completion. The Team You'll Be A Part Of: You'll join the Digital Mission Engineering Space Products Development Team, a diverse and dynamic group of engineers and scientists passionate about advancing space systems technology. The team collaborates closely with subject matter experts, product managers, and QA professionals to deliver best-in-class solutions for orbit determination and mission analysis. Together, we support the full lifecycle of space missions, driving innovation and excellence in everything we do. Rewards and Benefits: We offer a comprehensive range of health, wellness, and financial benefits to cater to your needs. Our total rewards include both monetary and non-monetary offerings. Your recruiter will provide more details about the salary range and benefits during the hiring process. At Synopsys, we want talented people of every background to feel valued and supported to do their best work. Synopsys considers all applicants for employment without regard to race, color, religion, national origin, gender, sexual orientation, age, military veteran status, or disability. In addition to the base salary, this role may be eligible for an annual bonus, equity, and other discretionary bonuses. Synopsys offers comprehensive health, wellness, and financial benefits as part of a competitive total rewards package. The actual compensation offered will be based on a number of job-related factors, including location, skills, experience, and education. Your recruiter can share more specific details on the total rewards package upon request. The base salary range for this role is across the U.S. Apply Now Save

For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we'll help you build a career that you can feel passionate about. Job Summary We are seeking an experienced Research Study Technician II to join our Insourcing Solutions team, located in Philadelphia, PA. As the Research Study Technician II you will facilitate the goals of drug discovery projects through hands-on conduct of in vivo experiments in rodents. Additional responsibilities include: * Reviews and complies with all policies, guidelines and operating procedures pertaining to the animal care and research program. * May coordinate (or assist) or manage schedules of other team members; resolves schedule conflicts * Assemble, set up, operate and maintain any necessary experimental equipment to conduct in-vivo studies. * Conduct laboratory procedures in compliance with established protocols/plans and with regulatory and laboratory requirements. * Document experimental data in technical notebooks or approved electronic files including activities undertaken, existing conditions, observed results and variation from expected data patterns. * Record, prepare, and analyze data for inclusion in project reports. * Able to perform the following techniques in rodents: * PO, IV, SQ, IP, IM, and IN dosing and/or inoculation techniques * Blood collection from multiple vessels or cardiac, and perfusions * Tumor measurements, body weights, IBD and EAE scoring, behavioral monitoring, etc * Rodent telemetry and physiological recordings * Necropsy, tissue and fluid collections * Rodent euthanasia using CO2, anesthesia, and/or approved physical methods. * Experience in generating/supporting/conducting patient derived mouse models will be an added advantage * Support study set-up, take downs, ex-vivo assays * Aseptic tissue culture experience with human cancer cell lines * Interact with other personnel within the department, multiple research groups, to develop a network of resources to facilitate completion of assignments. * Perform animal care and husbandry as needed, including receipt, stocking, and maintenance of research supplies. Job Qualifications To qualify for this role candidates must have one of the following combinations of education/experience: * B.S./B.A. degree in Biological Sciences or related field, or Associate's degree in veterinary technology or equivalent college level program and 4 years of previous laboratory animal research experience, using the skills listed above. OR * High School Diploma and at least 6 years of previous laboratory animal research experience, with 3 years using skills listed above. Certification/Licensure: AALAS certification preferred but not required. The pay range for this position is $37.50 to $39.00 USD per hour. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, and location. About Insourcing Solutions Charles River Insourcing Solutions℠ can streamline research by delivering operational and cost efficiencies through the strategic insourcing of GMP, GLP and non-GLP research services from discovery through safety assessment. Insourcing Solutions℠ provides you with the ability to maintain control of your facility and expertise while leveraging available space. About Charles River Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years. We're committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility. Equal Employment Opportunity Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws. It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_**********. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications. For more information, please visit *************** 231144

KOMAN Government Solutions, LLC (KGS), a wholly-owned 8(a) subsidiary of the Natives of Kodiak, is an Alaska Native Corporation, providing environmental investigation, remediation, munitions and explosives of concern support, operations and maintenance, long-term monitoring, and construction services to our clients. We have an immediate need for a **Senior Environmental Project Chemist** to support our diverse portfolio of DoD, USEPA, other federal agencies, and private sector projects. This position can be full or part-time depending on the candidate's availability. This is a hybrid position reporting to either our Marlborough, MA or Exton, PA office locations. However, remote candidates will also be considered. In this leadership role, you'll serve as principal contact to internal and external customers for all chemistry-related activities and will manage and direct all internal requests for chemistry support. You will be responsible for mentoring and oversight to our part-time data validator and to additional chemistry and data validation staff as we grow the business. You will assign work and review chemistry and data validation work products for completion and accuracy prior to client submittal. You will be responsible for managing laboratory products and determining which validation assignments may need to be subcontracted, as well as monitoring laboratory and validation subcontracts to ensure they are compliant with the project requirements. **Why Work Here?** + Competitive salary with Paid Time Off and Holidays + Benefits selected start first of month after hire. + Robust benefit options: medical, vision, dental, additional life insurance, critical illness, additional hospitalization coverage, pet insurance, and identity theft offerings. + Company paid 1X salary life insurance, short term disability and long-term disability insurance. + Company match up to 4% on 401K **Typical work assignments include:** + Proposal support: identify preferred environmental analytical laboratories, create requests for price proposals, and obtain competitive pricing. + UFP-QAPP and work plan support: prepare chemistry portion of UFP-QAPPs. Ensure that all work plans prepared by junior staff correctly identify analytical methods, preservation requirements, bottleware, and number and frequency of required QA/QC samples. + Resolve chemistry-related client or regulatory comments on plans and reports. + Laboratory procurement and coordination: Support preparation of analytical laboratory scopes of work; procurement of those laboratories; and coordination with laboratories prior to, and following, sampling events. + Auditing laboratory operations when needed. + Laboratory data report review: ensure reports meet criteria for completeness, correctness, sensitivity, and conformance with requirements. Ensure data received meets the requirements of the UFP-QAPP. + Data validation: follow established DoD and USEPA guidelines to determine the analytical quality of laboratory data. Ensure data validation meets the requirements of the UFP-QAPP. Review all data validation reports prepared by junior staff. + Database management: Follow established procedures for management of analytical data in NIRIS, various USACE chemistry databases (including FUDSChem, ERPIMS, and EDMS), and state-specific databases. + Implementation and monitoring of corrective action, as needed. **Required qualifications:** + Bachelor of Science degree (Master's preferred) in Chemistry or Environmental Chemistry. + Minimum 10 years of experience supporting federal projects. + Expertise in chemical data quality management of environmental analytical data, including working knowledge of industry-standard procedures for environmental data verification and data validation. + Working knowledge of Microsoft Office Suite and Adobe. + Excellent communication skills, both verbal and written. **The ideal candidate will have:** + Commercial environmental analytical laboratory experience. + Experience with validation of data using current DoD QSM requirements for various methods including explosives, perchlorate, PFAS, PCBs, in addition to more common environmental analytical methods. + Experience working on DoD, USEPA, and other federal agency projects and/or state environmental/department of health agencies. + Experience directing and mentoring junior staff/chemists. _As a Federal Contract Employer, KOMAN Families of Companies follows Federal Laws as it pertains to drug testing. All candidates who receive a written offer of employment will be required to undergo drug testing for commonly abused controlled substances in accordance with Federal Law. It is important to note although a State may have legalized a controlled substance, if the controlled substance is illegal per Federal Law, it is then considered to be illegal. KOMAN Families of Companies is a Drug-Free Workplace. Successful completion of a background and DMV record check also must be completed prior to hire._ _Preference will be given to Natives of Kodiak, Inc. Shareholders and Descendants of Shareholders in accordance with Title 43 U.S. Code 1626(g) and Title 42 U.S. Code 2000e - 2(i)_ _KGS is an Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities_

KOMAN Government Solutions, LLC (KGS), a wholly-owned 8(a) subsidiary of the Natives of Kodiak, is an Alaska Native Corporation, providing environmental investigation, remediation, munitions and explosives of concern support, operations and maintenance, long-term monitoring, and construction services to our clients. We have an immediate need for a Senior Environmental Project Chemist to support our diverse portfolio of DoD, USEPA, other federal agencies, and private sector projects. This position can be full or part-time depending on the candidates availability. This is a hybrid position reporting to either our Marlborough, MA or Exton, PA office locations. However, remote candidates will also be considered. In this leadership role, youll serve as principal contact to internal and external customers for all chemistry-related activities and will manage and direct all internal requests for chemistry support. You will be responsible for mentoring and oversight to our part-time data validator and to additional chemistry and data validation staff as we grow the business. You will assign work and review chemistry and data validation work products for completion and accuracy prior to client submittal. You will be responsible for managing laboratory products and determining which validation assignments may need to be subcontracted, as well as monitoring laboratory and validation subcontracts to ensure they are compliant with the project requirements. Why Work Here? * Competitive salary with Paid Time Off and Holidays * Benefits selected start first of month after hire. * Robust benefit options: medical, vision, dental, additional life insurance, critical illness, additional hospitalization coverage, pet insurance, and identity theft offerings. * Company paid 1X salary life insurance, short term disability and long-term disability insurance. * Company match up to 4% on 401K Typical work assignments include: * Proposal support: identify preferred environmental analytical laboratories, create requests for price proposals, and obtain competitive pricing. * UFP-QAPP and work plan support: prepare chemistry portion of UFP-QAPPs. Ensure that all work plans prepared by junior staff correctly identify analytical methods, preservation requirements, bottleware, and number and frequency of required QA/QC samples. * Resolve chemistry-related client or regulatory comments on plans and reports. * Laboratory procurement and coordination: Support preparation of analytical laboratory scopes of work; procurement of those laboratories; and coordination with laboratories prior to, and following, sampling events. * Auditing laboratory operations when needed. * Laboratory data report review: ensure reports meet criteria for completeness, correctness, sensitivity, and conformance with requirements. Ensure data received meets the requirements of the UFP-QAPP. * Data validation: follow established DoD and USEPA guidelines to determine the analytical quality of laboratory data. Ensure data validation meets the requirements of the UFP-QAPP. Review all data validation reports prepared by junior staff. * Database management: Follow established procedures for management of analytical data in NIRIS, various USACE chemistry databases (including FUDSChem, ERPIMS, and EDMS), and state-specific databases. * Implementation and monitoring of corrective action, as needed. Required qualifications: * Bachelor of Science degree (Masters preferred) in Chemistry or Environmental Chemistry. * Minimum 10 years of experience supporting federal projects. * Expertise in chemical data quality management of environmental analytical data, including working knowledge of industry-standard procedures for environmental data verification and data validation. * Working knowledge of Microsoft Office Suite and Adobe. * Excellent communication skills, both verbal and written. The ideal candidate will have: * Commercial environmental analytical laboratory experience. * Experience with validation of data using current DoD QSM requirements for various methods including explosives, perchlorate, PFAS, PCBs, in addition to more common environmental analytical methods. * Experience working on DoD, USEPA, and other federal agency projects and/or state environmental/department of health agencies. * Experience directing and mentoring junior staff/chemists. As a Federal Contract Employer, KOMAN Families of Companies follows Federal Laws as it pertains to drug testing. All candidates who receive a written offer of employment will be required to undergo drug testing for commonly abused controlled substances in accordance with Federal Law. It is important to note although a State may have legalized a controlled substance, if the controlled substance is illegal per Federal Law, it is then considered to be illegal. KOMAN Families of Companies is a Drug-Free Workplace. Successful completion of a background and DMV record check also must be completed prior to hire. Preference will be given to Natives of Kodiak, Inc. Shareholders and Descendants of Shareholders in accordance with Title 43 U.S. Code 1626(g) and Title 42 U.S. Code 2000e - 2(i) KGS is an Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities

Senior Environmental Chemist - Exton, PA Location: Exton, PA Company Name: KOMAN Government Solutions, LLC START YOUR APPLICATION KOMAN Government Solutions, LLC (KGS), a wholly-owned 8(a) subsidiary of the Natives of Kodiak, is an Alaska Native Corporation, providing environmental investigation, remediation, munitions and explosives of concern support, operations and maintenance, long-term monitoring, and construction services to our clients. We have an immediate need for a Senior Environmental Project Chemist to support our diverse portfolio of DoD, USEPA, other federal agencies, and private sector projects. This position can be full or part-time depending on the candidates availability. This is a hybrid position reporting to either our Marlborough, MA or Exton, PA office locations. However, remote candidates will also be considered. In this leadership role, youll serve as principal contact to internal and external customers for all chemistry-related activities and will manage and direct all internal requests for chemistry support. You will be responsible for mentoring and oversight to our part-time data validator and to additional chemistry and data validation staff as we grow the business. You will assign work and review chemistry and data validation work products for completion and accuracy prior to client submittal. You will be responsible for managing laboratory products and determining which validation assignments may need to be subcontracted, as well as monitoring laboratory and validation subcontracts to ensure they are compliant with the project requirements. Why Work Here? * Competitive salary with Paid Time Off and Holidays * Benefits selected start first of month after hire. * Robust benefit options: medical, vision, dental, additional life insurance, critical illness, additional hospitalization coverage, pet insurance, and identity theft offerings. * Company paid 1X salary life insurance, short term disability and long-term disability insurance. * Company match up to 4% on 401K Typical work assignments include: * Proposal support: identify preferred environmental analytical laboratories, create requests for price proposals, and obtain competitive pricing. * UFP-QAPP and work plan support: prepare chemistry portion of UFP-QAPPs. Ensure that all work plans prepared by junior staff correctly identify analytical methods, preservation requirements, bottleware, and number and frequency of required QA/QC samples. * Resolve chemistry-related client or regulatory comments on plans and reports. * Laboratory procurement and coordination: Support preparation of analytical laboratory scopes of work; procurement of those laboratories; and coordination with laboratories prior to, and following, sampling events. * Auditing laboratory operations when needed. * Laboratory data report review: ensure reports meet criteria for completeness, correctness, sensitivity, and conformance with requirements. Ensure data received meets the requirements of the UFP-QAPP. * Data validation: follow established DoD and USEPA guidelines to determine the analytical quality of laboratory data. Ensure data validation meets the requirements of the UFP-QAPP. Review all data validation reports prepared by junior staff. * Database management: Follow established procedures for management of analytical data in NIRIS, various USACE chemistry databases (including FUDSChem, ERPIMS, and EDMS), and state-specific databases. * Implementation and monitoring of corrective action, as needed. Required qualifications: * Bachelor of Science degree (Masters preferred) in Chemistry or Environmental Chemistry. * Minimum 10 years of experience supporting federal projects. * Expertise in chemical data quality management of environmental analytical data, including working knowledge of industry-standard procedures for environmental data verification and data validation. * Working knowledge of Microsoft Office Suite and Adobe. * Excellent communication skills, both verbal and written. The ideal candidate will have: * Commercial environmental analytical laboratory experience. * Experience with validation of data using current DoD QSM requirements for various methods including explosives, perchlorate, PFAS, PCBs, in addition to more common environmental analytical methods. * Experience working on DoD, USEPA, and other federal agency projects and/or state environmental/department of health agencies. * Experience directing and mentoring junior staff/chemists. As a Federal Contract Employer, KOMAN Families of Companies follows Federal Laws as it pertains to drug testing. All candidates who receive a written offer of employment will be required to undergo drug testing for commonly abused controlled substances in accordance with Federal Law. It is important to note although a State may have legalized a controlled substance, if the controlled substance is illegal per Federal Law, it is then considered to be illegal. KOMAN Families of Companies is a Drug-Free Workplace. Successful completion of a background and DMV record check also must be completed prior to hire. Preference will be given to Natives of Kodiak, Inc. Shareholders and Descendants of Shareholders in accordance with Title 43 U.S. Code 1626(g) and Title 42 U.S. Code 2000e - 2(i) KGS is an Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities START YOUR APPLICATION

US Tech Solutions is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit our website ********************************** are constantly on the lookout for professionals to fulfill the staffing needs of our clients, and we currently have a job opening that may interest you Job Description Title: Quality control chemist- 2nd shift Duration: 12 Months Location: Myerstown, PA 17067 Description: The Raw Material testing team is responsible for Quality Control testing of APIs and excipients used in the manufacture of pharmaceutical and nutritional products. This is a fast-paced, energetic team that works together across two shifts to meet aggressive throughput times to support a lean manufacturing operation. Position Summary: In this position, the incumbent will be expected to draw upon previous analytical experience, as well as continuously learn Quality Control systems and effectively engage in relationships with peers in the laboratories, Manufacturing/Production, and personnel in other departments as needed. The incumbent will perform analysis on raw materials following prescribed procedures to provide the information base leading to material disposition, as well as assist in troubleshooting and problem solving as directed. Once the incumbent is assigned specific materials on which to perform the quality control tests, or provide development or troubleshooting, the incumbent will have considerable impact on results from his/her work. Material can be rejected and manufacturing procedures can be altered significantly either in schedule changes or in process itself. Position Duties & Responsibilities : Perform standard qualitative and quantitative analysis: • Utilize standard analytical chemistry techniques: wet analytical methods, HPLC, UV, GC, AA, polarimeter, FT-IR, NIR, RAMAN, etc.) to test raw materials in accordance with approved testing procedures, including those from company, the National Formulary (NF), the United States Pharmacopoeia (USP), the European Pharmacopoeia (EP), and the FDA. • Properly document and maintain records of all analysis information of assigned materials on data sheets and laboratory notebooks for permanent file. • Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with Supervisor and recommend additional testing if necessary. • Communicate to supervision in a timely manner all non-compliance situations, and assist in investigations. • Assist with troubleshooting analytical methodology and instrumentation malfunctions. • Perform special assignments as directed by supervisor, for example, revise existing analytical testing monographs to comply with compendia changes or other specific needs. • Accurate, complete and timely fulfillment of the job responsibilities will, in part, ensure GMP compliance as outlined in various Bayer and U.S. government rules and regulations. Documentation Review: • Review testing documentation performed by other analysts for compliance with BAYER, FDA, National Formulary (NF), United States Pharmacopoeia (USP), and European Pharmacopoeia (EP) procedures. Safety: • Adhere to the pertinent aspects of Corporate and plant safety programs and adhering to GMP's, ISO standards or other regulations. Qualifications Requirements/Preferences: • Bachelor's degree in Chemistry, Biology, Pharmacy, or related 4 year science degree required. Chemistry degree is preferred. • At least 1-3 years of experience in a GMP laboratory environment. Master's degree in a related field with 1 year of experience may be considered. • Knowledge, practical application, and understanding of analytical chemistry is required to perform the functions of this position. • Basic experience with Personal Computer (PC). • Demonstrated capability for communicating ideas, concepts, and work results effectively to colleagues and supervision. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Must demonstrate initiative and a willingness to learn. • Good working knowledge of advanced laboratory instrumentation and personal computer skills are required. • Good working knowledge of advanced laboratory instrumentation and computers are required; This is defined as strong troubleshooting skills for assigned area such as HPLC, GC, AA, UV, TOC, NIR and/or dissolution and low error rates with microbiology or chemistry techniques for defined area • A working knowledge of organic chemistry, statistics, data processing and good manufacturing practices is required • Demonstrated ability to clearly communicate technical information in writing required. • Demonstrated ability to manage key projects and display area of expertise; i.e. clear/consistent notebook skills and function as an independent worker. • Demonstrated ability to be self-motivated as well as to work collaboratively in a team-based environment is required. • Demonstrated ability to take initiative and display a willingness to learn required. • A thorough understanding of National Formulary (NF); United States Pharmacopeia (USP); and European Pharmacopeia (EP) testing procedures, as well as, US Pharmaceutical Industry Good Manufacturing Practices (GMP's), quality control methods and procedures is required. • Competencies required: analytical problem solving, alertness, work within established policies and procedures, commitment to task, decisiveness, effective written and interpretive communication skills, and organization and planning skills. • Enter here Travel Requirements: None Thanks & Regards, Mayank Gupta, (M. Pharmacy) (Lead Pharma Technical Recruiter) Additional Information All your information will be kept confidential according to EEO guidelines.