Chemist jobs in Bethlehem, PA - 26 jobs

At Mindlance, we strive to deliver value through the combination of right people, processes, technologies and program management solutions. Our methods include- applying domain expertise in specific industry segments, utilizing a highly-skilled workforce, leveraging a proven global delivery model, implementing structured and scalable quality processes and methodologies and yet, staying cost-effective All in all, our expertise lies in providing trained and committed minds to help meet your business objectives, irrespective of the stage your business is in. Job DescriptionJob Title: Chemist II Duration: 7 Months+ Location : Spring House, PA Summary: • With Quality as their primary focus, this group strives to provides access and affordability through innovation and strong collaboration with their R&D and Commercial partners to deliver life changing solutions for patients in need. • The successful candidate will join a multi-disciplinary team of scientists and engineers involved in assessing cleaning protocols for consumer and pharmaceutical products. • The candidate will use QCM with dissipation to study residues on manufacturing surfaces. • Prior knowledge of QCM is not required but considered a plus. • The candidate will conduct DOE design experiments using the QCM and conduct supporting experiments with spectroscopy techniques such as FTIR or UV-visible spectrometry. • The position also involves wet lab techniques (preparing solutions); spin coating films onto metallic substrates, and chemical cleaning of substrates. • Familiarity with basic light microscopy also considered a plus. • Qualified candidates must have the ability to work independently and as part of a team. • Written communications in the form of reports and PowerPoint presentations is required. • Good verbal and written communication skills a must. QualificationsEducational Qualification/ Experience Required: • Degree in Chemistry, Physics, Materials Chemistry or related field B.S or engineering degree with 3-6 yrs, M.S. 1-2 yrs industrial experience. • Techniques: Quartz crystal microbalance (QCM) with dissipation, FTIR, UV, coursework in analytical chemistry, physical chemistry, and statistics Additional InformationRegards ___________________________________________________________________________________________________ Pooja Mishra | Team Recruitment | Mindlance, Inc. | Office: 732-243-0715

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • Techniques : FTIR, SEM, foreign matter isolation, coursework in analytical chemistry, physical chemistry, and statistics Global Technical Services, part of the Janssen Supply Chain, is currently looking for a Scientist Advanced Analytics , a global organization responsible for supplying medicines to markets around the world. • With Quality as their primary focus, this group strives to provides access and affordability through innovation and strong collaboration with their R&D and Commercial partners to deliver life changing solutions for patients in need. • The successful candidate will join a multi-disciplinary team of scientists and engineers involved in analytical characterization of pharmaceutical products. • The candidate must be capable of conducting research experiments related to the characterization of conventional pharmaceutical products as well as stem cell or large molecule API formulations by several different analytical methods. • The position involves significant laboratory work involving filtration and isolation of particulate matter from pharmaceutical formulations. • The data will be recorded using electronic laboratory notebooks. • The successful candidate should have a working knowledge of FTIR, SEM, and light microscopy. Opportunities for other experimentation include vibrational spectroscopy such as NIR or Raman, thermal techniques such as DSC or TGA, particle analysis by light obscuration, and powder rheology. • Qualified candidates must have the ability to work independently and as part of a team. Good verbal and written communication skills a must. • Written reports and PowerPoint presentations are examples of communication formats. Qualifications Physical Characterization of Pharmaceutical Products Position Skill Set Degree in Chemistry, Physics, Materials Chemistry or related field B.S with 3-6 yrs, M.S. 2-4 yrs or Ph.D. with 0-3 yrs industrial experience. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Position Summary The Senior Analyst II, Quality Control - Flow Cytometry is to support our Quality Control department. The successful candidate will be responsible for performing routine testing for manufacturing release and stability samples of gene (viral vector) and cell therapy products. In this role, the Senior Analyst II will collaborate closely with Manufacturing and Quality Control Operations teams to ensure all required testing is completed accurately, on time, and in full compliance with established standard operating procedures and testing methods. This position reports to the Technical Lead Manager, Quality Control - Analytical, and is based at our East Norriton, PA facility. Job Responsibilities * Perform routine sample analysis in support of manufacturing release and stability activities. * Sample testing of manufactured products using protein-based assays, molecular methods, and cellular assays. * Participate in method qualification/validation activities, as necessary. * Analyze, document, and report experimental data in accordance with Resilience requirements. * Maintain, calibrate, and operate analytical equipment. * Qualify equipment related to testing. * Serve as owner of QC equipment and complete necessary owner tasks, as assigned by management. * Perform method transfer and qualification activities. * Document work in accordance with cGMPs, established business processes and applicable SOPs. * Review data, identify discrepancies, and escalate issues to management. * Author SOPs, methods, protocols, training materials, and reports in alignment with applicable cGMPs, business standards, and intended use. * Own, author, review/approve, and support QC change controls, deviations, and other quality records for the East Norriton site, as applicable. * Investigate OOS or OOT events and develop/implement preventive and corrective actions. * Mentor, coach and train Quality Control Associates. * Completes qualified program requirements necessary to train other employees. * Acts as liaison with Clients for site-specific Flow Cytometry, as needed. * Other activities as assigned. Minimum Qualifications * Experience in mammalian cell culture. * Knowledge of general analytical methods. * Successful visual acuity test required for this role. * Experience in Flow Cytometry. Preferred Qualifications * BS in relevant discipline (immunology, cell biology, or related field). * 5+ years relevant life science experience. * GMP experience preferred. Other Ideal Personal Characteristics: * Ability to thrive in ambiguous or complex situations. * Highly motivated and self-directed. * Thrives in matrix environment. * Excellent interpersonal, verbal and written communication skills Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $100,000.00 - $137,500.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

Are you looking for a job that's both challenging and fun? US Cannalytics is looking for a candidate that seeks a challenging Chemistry Laboratory Technician position in the exciting and ever-evolving medical cannabis industry. The successful candidate will be reliable, exhibit strong attention to detail and thrive in a fast-paced laboratory environment LABORATORY TECHNICIAN QUALIFICATIONS, must: Have a valid driver's license and high school diploma or equivalent. 21+ years old and subject to applicable employment requirements for the state of Pennsylvania for cannabis businesses including criminal background check. 2 years of relevant, professional (non-academic) laboratory experience or 1 year of laboratory experience plus a skills assessment. LABORATORY TECHNICIAN RESPONSIBILITIES: The laboratory technician is responsible and accountable for the testing, quality control, and tracking of cannabis material. The laboratory technician will ensure the safe, accurate, and timely testing of cannabis products. ESSENTIAL DUTIES: Proficiently utilize Microsoft Word and Excel, and other laboratory information management systems. Work in a timely manner, while striving to improve quality and maintain accuracy during all laboratory activities. Follow organizational policies and procedures for laboratory operations and comply with all state-specified rules and regulations for cannabis licenses, cannabis transport and cannabis testing, as applicable. Responsible for accurate measurements and documentation of all cannabis and cannabis materials, including sample weights/volumes, compliant cannabis tracking and destruction, and completion of supporting laboratory documentation. Adhere to Good Documentation Practices (GDP) for the completion of laboratory logs, forms, worksheets, or other documentation. Maintain laboratory reagent and supply inventory, including compliant documentation. Assists with the performance of sample intake and accessioning, and non-analytical test methods (foreign material, water activity, moisture content, etc.), as needed. Participate in and endeavor to complete training and be determined competent for assigned test methodologies including the following steps: a. Sample collection, intake and homogeneity. b. Sample preparation across all applicable matrices. c. Reagent preparation, including safe handling, storage and disposal. d. Sample loading and initial data analysis performed under the technical supervision of a Laboratory Chemist. e. Daily performance checks of applicable analytical equipment and method test parameters. f. Regular instrument cleaning and preventative maintenance for applicable analytical equipment. g. Basic troubleshooting of testing methodologies including all items listed within this sub-section. For test methods the employee has been trained and determined competent for: a. Independently prepare samples using aseptic techniques, including compliant documentation and necessary updates to laboratory workflow. b. Independently prepare reagents, solutions, and substrates for the equipment necessary for testing, including compliant documentation and necessary updates to laboratory workflow. c. Perform initial data analysis under the technical supervision of a Laboratory Chemist or Microbiologist. d. Assist in equipment and method validations or verifications, including compliant documentation and necessary updates to laboratory workflow. e. Successful completion of proficiency testing samples, completed as part of ongoing competency within the test method. Perform all other tasks and duties as assigned by Management, which may include cannabis sampling and transport. WORK ENVIRONMENT: The work environment characteristics described below are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Work is performed in a production laboratory environment and requires use of personal protection equipment to limit exposure to chemicals or other hazards found within a laboratory environment. Work environment is fast-paced and will require frequent pivoting and multitasking, as well as the reprioritization of tasks based on demand/urgency. The work environment may expose employee to fumes or airborne particles, moving mechanical parts and vibration. The noise level in the work environment may be loud. Per state requirements for this industry, the facility is secured by user-specific access and is surveillance by cameras located throughout the laboratory except in restrooms. PHYSICAL DEMANDS: The physical demands described are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Ability to concentrate and consistently produce accurate work. Frequent standing, walking, sitting, and use hands. Occasionally lift and/or move up to 40 pounds. Visual requirements to include close vision, color vision and ability to adjust focus. WORK HOURS: Wednesday - Saturday (training and competency determined on a Monday-Friday schedule) Job Type: Full-time, 10-hour shifts Benefits: Dental insurance Health insurance Paid time off Vision insurance Schedule: Tuesday-Saturday 10 hour shifts Overtime available Work Location: In person Job Type: Full-time Compensation: $20-$22 / hour Expected hours: 40 - 45 per week Education: High school or equivalent (required) BS in a natural science (preferred) Experience: Laboratory: 1 year (required) Analytical chemistry in a high-volume laboratory setting: 2 years (preferred) Laboratory sample extractions: 2 years (preferred) Agilent HPLC and/or GC: 2 years (preferred) Cannabis: 1 year (preferred)

Job Title: Production / Process Chemist Reports To : Director of Quality Control & Product Development Department: Production (Reaction Distillation) Summary: Plans the production, monitors the progress, and troubleshoots the processes associated with the Reaction Distillation area. In conjunction, oversees the process development and small-scale production with support from a Lab Technician. Duties and Responsibilities include the following. Other duties may be assigned. In conjunction with the Planning Department, recommend and in turn schedule the production for all products that are manufactured via chemical Reactions and / or Distillation in the designated equipment. Supported by an analytical and quality team, monitor the progress of the reactions and / or distillation to ensure the process meets the quality and timeliness of the established standards. Utilizing the support of an Established Process Development team, develop processes that will improve on established products and in conjunction with our commercial team, In coordination with the Commercial Team, assists in the development of processes for new products and supervises the progress of these processes with the Process Development Team. Evaluates production batches against established product standards and specifications and modifies as needed. Directs, coordinates, and advises production personnel coordinating all three shifts accordingly in the course of scheduling the production, monitoring the progress of the processes, and making the necessary adjustments conditions as needed. Coordinate's production activities between all three (3) shifts. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Experience in a chemical processing environment including: interacting with production personnel; developing and troubleshooting chemical processes; an awareness of safety protocols while working with chemicals under various conditions (pressure and temperature) Must have the ability to multi-task and work in a fast-paced environment. Education/Experience: Bachelor's degree in Chemistry or related field such as Chemical Engineering from a four-year college or university is required. 5 to 10 years of experience is preferred, however, all candidates with strong mechanical aptitude, a solid background in Chemistry and relevant experience will be considered. Language Ability: Demonstrated ability to make successful presentations to individuals and/or groups at all levels of an organization. Excellent written and verbal communication skills. Ability to deal effectively with a variety of individuals at all organizational levels. Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures or government regulations. Ability to write reports, business correspondence and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public. Math Ability: Candidate must be able to calculate reaction stoichiometric quantities, percent yields and interpret GC plots to determine the reaction status or nature of reaction purity. Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Computer Skills: To perform this job successfully, an individual should have basic computer skills and knowledge of how to use Office 365, develop spreadsheets, and ERP and Planning Systems, , inventory software and contact management systems. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly exposed to fumes or airborne particles. The employee is frequently exposed to work near moving mechanical parts and chemicals pertinent to the processes and may be occasionally exposed to allergens. The noise level in the work environment is usually moderate. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands; reach with hands and arms and talk or hear. The employee is frequently required to stand; walk and sit. The employee is occasionally required to climb stairs balance and stoop, kneel, crouch, or crawl.

Certified Group is committed to delivering expert solutions and quality testing our customers can feel confident in - on time, every time - so the world can trust in what it consumes. As a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services, Certified Group includes Food Safety Net Services (FSNS), FSNS Certification & Audit, Certified Laboratories, EAS Consulting Group, and Labstat International Inc. Certified Group provides analytical testing and regulatory guidance services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, personal care, tobacco, nicotine, cannabis, and hemp industries. We have embarked on an important journey to unify and strengthen our culture by living these core values: Start with the Customer, Drive to Deliver, Commit to Safety and Quality, and Believe in the Team - including believing in you. We are currently looking for a Pathogen Lab Analyst to join our growing team! $1000 HIRING BONUS!!! Job Summary: Perform analytical and microbiological testing of food products, ingredients, and environmentals. The position performs the application and evaluation of approved microbiological techniques and methodologies. Essential Responsibilities: * Accurately perform and read test results and notify Laboratory Management of deviations * Prepare and analyze samples for indicator organisms, pathogens, and chemistries * Apply aseptic/microbiological techniques in daily workload * Report inventory and expendable supplies/materials needed for testing requirements * Provide routine preventive maintenance by daily cleaning, sanitizing, trash disposal, and equipment quality control * Assist in quality duties to by taking incubator temperatures, inoculating control organisms, running media controls, etc. * Pursue an assigned series of processes, procedures, or techniques in accordance with FSNS policies/procedures and customer requirements * Maintain a high degree of technical competence by reading scientific journals, attending professional workshops, and being aware of food industry issues and trends * Perform all activities in a neat, safe, hygienic, and efficient manner * Share information in an open and timely manner * Assisting with managing priorities and schedule such that individual goals as well as team goals are achieved with encouraged participation in the Food Safety Net Services Team * Responsible for the safety of oneself and others working within their area Supervision: * This job does has no supervisory responsibilities. Education & Experience: * Associate degree in Life Science or related field with two or more years of laboratory experience, preferred * Two or more years of experience in a commercial food-testing or analytical laboratory * Or equivalent combination of education and experience * Working knowledge of aseptic sampling technique, automated lab equipment, and acceptable methods and procedures * Familiarity with GLP, OSHA guidelines, FDA, BAM, APHA, ISO, and USP methods and procedures * Broad knowledge of concepts, practices, and procedures of a food testing laboratory * Ability to travel when necessary Physical Demands/Work Environment: * Dexterity of hands and fingers to operate a computer keyboard, mouse and to handle other communications/computer components * Potential exposure to odors, fumes, airborne particles, hazardous chemicals, and microbiological pathogens * Noise level varies from quiet to loud * Temperature varies from hot to cold * Interactive and fast-paced team oriented tasks * Overnight Travel is required at the discretion of management * Occasionally lift and/or move up to 25 pounds * Color vision and depth perception Benefits: * Progressive 401k Retirement Savings Plan * Employer Paid Short- Term and Long-Term Disability, and Life Insurance * Group Medical * Tuition Reimbursement * Flexible Spending Accounts * Dental * Paid Holidays and Time Off Certified Group values diversity in its workforce. The company is firmly committed to a policy of Equal Opportunity and will administer its policies in a manner that treats each employee and applicant for employment on the basis of merit. Certified Group will take affirmative action to seek out qualified applicants without regard to race, color, religion, sex, national origin, age, handicap, or veteran status.

Job DescriptionNeeds to make sure that products being produced meet the expectations of the consumer. They examine jobs to make sure they meet quality expectations then assess the final product after production. Their role is to establish an acceptable variation range for jobs and identify when something fails to meet those requirements. Responsible for monitoring and ensuring that each stage of production is followed by all the necessary procedures and each product coming out of the production process. Document the results of their inspections and make recommendations on how to prevent common errors. Responsible for ensuring the quality control of all printing and sign products as well as packaging and shipment/delivery of all products. Responsible for checking in all vended products and ensuring they are ready for delivery or shipment. Duties and Responsibilities Must have attention to detail on quality and packaging for all outgoing shipments. Must be very organized while maintaining the ability to multitask. Coordinate with shipping companies like FedEx, UPS and others and ensure timely delivery. Work effectively with the center manager and sales team for quality delivery and escalations. The job requires repetitive lifting of sometimes heavy boxes. Must be a team player, dependable and have a good work ethic. Good written and verbal communication skills Excellent problem-solving and analytical skills Keen attention to detail Basic computer and math skills to calibrate and measure specifications Ability to use measuring devices like scales and tape measures In-depth understanding of company standards Understanding of target market and consumer needs Documentation and reporting skills Teamwork and collaboration Comfortable standing or walking for long periods of time Some cross training into bindery or other areas of the company will be required at times if another teammate is out. Experience Entry Level Job Full time Print Smith, Shipleap and Microsoft Office knowledge is a huge plus.

The QC Analyst II - Chemistry will provide bioanalytical expertise for the Quality Control (QC) department. Key areas of focus are development and implementation of the quality aspects of late stage or marketed product strategy. This role is involved with performing and assisting with OOS investigation and resolution. Additionally, the Analyst II will have responsibility for coordinating the bioanalytical technology transfer from outside departments and to outside contractors. Responsibilities QC Testing/Safety Testing responsibilities may include RP-HPLC, SEC, KF, FT-IR, SDS-PAGE, and UV-Vis. Adheres to Company safety procedures and guidelines on a daily basis Documentation Adheres to Company safety procedures and guidelines on a daily basis. GMP Compliance Adheres to Company safety procedures and guidelines on a daily basis. Technical Writing & Investigations Assists with preparing new SOPs / test methods or revising of existing documentation. Performs and assists with OOS investigations, deviation response, and resolution. Writes Change Controls, Deviation Investigations (DI's), Laboratory Assessments (LA's), CAPA's, and OOS investigation. Technical Transfer Writes Change Controls, Deviation Investigations (DI's), Laboratory Assessments (LA's), CAPA's, and OOS investigation Other Tasks Writes Change Controls, Deviation Investigations (DI's), Laboratory Assessments (LA's), CAPA's, and OOS investigation. Education & Experience B.S. in a Biological Science or related field with a minimum of 3-5 years' experience in pharmaceutical or biotechnology industry required OR M.S. in a Biological Science or related field with a minimum of 1-3 years' experience in pharmaceutical or biotechnology industry. Knowledge Working knowledge in protein chemistry and standard analytical techniques used in the biopharmaceutical industry (e.g., HPLC, FT-IR, SDS-PAGE, UV-Vis, IEF, Capillary Electrophoresis, ELISA). Working knowledge of cGMP practices, ICH requirements, stability, and validation required. Understanding of basic statistical analysis and familiarity with the use of databases is desirable. Skills & Abilities Strong verbal and communication skills required. Proficient in common software applications. Ability to handle multiple priorities in a fast paced environment. Demonstrates excellent interpersonal skills and flexibility. Advanced writing skills. Proficient in running a great number of methods. Apply acquired biopharmaceutical skills to projects and assignments. Physical Requirements Lifting up to 40 lbs. Able to stand for extended periods of time. Keenova offers employees a Total Rewards package which includes competitive pay and benefits. To learn more about our Total Rewards benefits please visit: Keenova Careers | Serve and Grow with Purpose | Keenova Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Exciting Opportunity to Join Our Legacy of Environmental Leadership! About Us: At Arcwood Environmental, we are more than just a company; we are pioneers in industrial waste management, committed to creating a cleaner, safer world. Since our inception during the environmental movement of the 1970s, we've been at the forefront of solving complex environmental challenges. Headquartered in Indianapolis, Indiana with a dedicated team of 2,000+ employees spread across the United States, we provide innovative and compliant solutions to thousands of clients in diverse industries. Why Arcwood? * Impactful Work: Be part of a team that makes a real difference. Our comprehensive services range from hazardous waste management and emergency response to onsite support and technical solutions, allow us to solve our customers' waste challenges. We are part of the solution. We don't generate any waste ourselves. * Growth Opportunities: At Arcwood, your contribution is valued beyond your job title. We believe in the power of continuous learning and growth, encouraging every employee to expand their skills and take on new challenges. * Safety First: Your health and safety are our top priorities. We foster a culture where every employee is empowered to act safely and ensure the well-being of their colleagues. Our mantra is Safe and Compliant, Always. * Collaborative Environment: Together we can achieve much more. Join a supportive and dynamic team where your ideas and efforts are recognized and rewarded. Our Commitment: We are dedicated to fostering an inclusive and innovative workplace where every employee can thrive. As part of our team, you will have the freedom to contribute your expertise wherever needed, ensuring the success of our mission to protect the environment. Our Vision: Our vision is to be the most trusted partner in the environmental services industry. We put our customers first and deliver agile, sustainable, and innovative solutions. We commit to nurturing top talent and creating lasting value for our customers, shareholders, communities, and the planet. Our Ownership: Arcwood Environmental is backed by the EQT Infrastructure VI fund, enhancing our capabilities, and expanding our reach. EQT is a dynamic global investment powerhouse managing EUR 232 billion in assets (EUR 128 billion fee-generating). With a focus on Private Capital and Real Assets, EQT owns and supports leading companies across Europe, Asia-Pacific, and the Americas, fostering sustainable growth, operational excellence, and market leadership. This exciting ownership positions us for continued impacts and growth in the future. Field Chemist As a Field Chemist you will be responsible for sorting and transporting hazardous and non-hazardous materials and waste, always ensuring compatibility and safety in all processes for each service provided to customers. Essential Functions & Requirements: * Prioritizes health and safety by adhering to policies, processes, and maintaining safe practices at all times * Assists in the segregation of chemicals by hazard class and packs compatible materials in appropriate containers and prepares for transportation; completes necessary paperwork for each job * Determines and loads supplies needed for job completion and travels to various industry, laboratory, and educational sites to perform lab pack services * Assists in characterizing materials at field project sites * Adheres to proper placarding and load segregation requirements when transporting hazardous materials * Develops good customer relations by effectively communicating with site points of contact and others at customer location / site * Appropriately directs Field Technicians / Drivers who are assisting with waste collection * Maintains an introductory knowledge of high-hazard materials management / assessment and cylinder handling * Maintains the ability to travel to support outside locations as needed * Takes on additional duties as assigned to support the team and organization Education: * Bachelor's degree (required), with a focus in environmental science or science (preferred) Experience: * In lieu of degree 2+ years of related experience (required), previous experience in lab packing or environmental waste (preferred) * Valid Driver's License and ability to obtain a Class B CDL with Hazmat endorsement within 6 months of hire date (required) * Ability to pass a Motor Vehicle Record search to Company standards (required) Competencies: * Ability to work in a constant state of alertness and in a safe manner * Ability to develop a working knowledge of all Federal, State, and local laws and regulations pertaining to the Environmental Services industry * Excellent interpersonal skills to effectively communicate with internal and external customers * Regular and predictable attendance to perform the functions and requirements of this role Additional Requirements: * Due to the potential exposure to atmospheres/waste/materials this position requires individuals to be clean shaven at all times in order to don a respirator for protection. Benefits, Compensation, & Workforce Diversity: Arcwood offers competitive pay and bonus incentives. Benefits include choice of medical, dental, and vision plans, flexible spending or health savings accounts, employee and dependent life insurance, short and long-term disability, 401(k) savings plan with 7% company match, and tuition reimbursement. Equal Opportunity Employer - Veterans & Disabilities A post-offer drug screen and background check will be required.

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 you Dow's Coating Materials Plant Support team has an exciting opportunity for a Sr. Analytical Technician in Collegeville, PA. In this role, you will contribute to advancing innovation and operational excellence in product development and quality assurance and provide specialized analytical expertise to support manufacturing and technical service activities. Additionally, you will spent time working closely with cross-functional teams, ensuring precision and reliability in laboratory processes, leveraging advanced instrumentation-including HPLC, GC, and particle size analyzers. You will play a key role in method validation, troubleshooting, and continuous improvement initiatives within a dynamic, safety-focused environment. Key ResponsibilitiesAnalytical Testing & Instrumentation Perform analytical testing using HPLC, GC, particle size analyzers, titrators, pH meters, viscometers, densitometers, and centrifuges. Troubleshoot and resolve issues with analytical instrumentation to maintain accuracy and reliability. Method Validation & QC Support Execute test methods to support production and validate analytical methods for manufacturing quality control. Conduct emulsion preservation testing and document results accurately. Maintenance & Inventory Own calibration and routine maintenance of laboratory instruments; initiate repairs as needed. Maintain inventory of chemicals, consumables, and supplies to ensure uninterrupted operations. Safety & Compliance Adhere to EH&S protocols and ensure safe handling and disposal of materials. Collaboration & Communication Communicate technical findings promptly to project leaders and participate in team meetings focused on safety, process improvement, and problem-solving. Competencies: Strong communication and data documentation skills. Self-motivated, able to work independently with minimal supervision, and thrive in an empowered team environment. Open to learning, adopting, and co-creating digital solutions to improve workflows and drive innovation. Qualifications A minimum of an Associates degree in a science related discipline/Military Degree Equivalency (MDE) and 3 years of relevant work experience OR a high school diploma/GED and 5 years of relevant work experience Proficiency in Microsoft Office. 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. Preferred qualifications Hands-on experience with laboratory instruments such as HPLC, GC, particle size analyzers, titrators, pH meters, viscometers, densitometers, and centrifuges. Demonstrate strong interpersonal skills to communicate technical findings to diverse audiences, including internal stakeholders. Skilled in documenting experimental data accurately and reliably, with proficiency in Microsoft Office and laboratory data management systems. Strong understanding of EH&S protocols and laboratory operations. Collaborative mindset with cross-functional networking ability. 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.

Job Details Division: Nucor Rebar Fabrication Northeast Other Available Locations: N/A Welcome to Nucor, where our unique culture sets us apart. Joining Nucor means becoming part of North America's largest steel and steel products manufacturer, offering unmatched career opportunities and stability. We are known for our innovative sustainability practices and are the continent's largest recycler. Our vibrant culture, built on personal connections and teamwork, empowers every team member with the freedom to innovate and contribute to our collective success. Experience a workplace where safety, efficiency, and meaningful personal connections define every day, enriching both our teammates and the communities we serve. Nucor supports its teammates with top-tier benefits like Medical, Dental, Vision, and Disability Insurance, 401K and Roth accounts, Profit sharing, Pay-for-performance bonuses, Paid parental leave, Tuition reimbursement, Stock program, Scholarships and more. Basic Job Functions: * Must adhere to Nucor's safety programs and standards. * Demonstrate conduct consistent with Nucor's vision and values. * Perform and document all tests required (per the Quality Manual) during a production shift. * Participate in non-conformance root cause analysis. * Report and document any non-conformance to the Quality Manual requirements. * Report and document any non-conformance to tests performed. * Perform other tasks and duties as assigned Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times.Minimum Requirements: * Legally authorized to work in the United States without company sponsorship now or in the future. * High school diploma, GED or state/local equivalent Preferences: * Knowledge of CRSI quality standards * Proficiency in MS Office, including strong Excel and Word.Physical Demands: * Some heavy lifting may be necessary * Working conditions can be noisy, dusty, hot, cold Special Demands: * Must be able to work overtime when required * Some travel may be required * Must be able to work any shift * Must be familiar with and adhere to shop safety policies and procedures * Communication with various DOT customers * Communication with CRSI * Maintain and update CRIS QM as needed * Maintain DOT certifications with all states as needed * Understanding of ASTM coating and fabrication standards Nucor is an Equal Opportunity/Affirmative Action Employer - M/F/Disabled/Vets - and a drug - free workplace

Needs to make sure that products being produced meet the expectations of the consumer. They examine jobs to make sure they meet quality expectations then assess the final product after production. Their role is to establish an acceptable variation range for jobs and identify when something fails to meet those requirements. Responsible for monitoring and ensuring that each stage of production is followed by all the necessary procedures and each product coming out of the production process. Document the results of their inspections and make recommendations on how to prevent common errors. Responsible for ensuring the quality control of all printing and sign products as well as packaging and shipment/delivery of all products. Responsible for checking in all vended products and ensuring they are ready for delivery or shipment. Duties and Responsibilities ● Must have attention to detail on quality and packaging for all outgoing shipments. ● Must be very organized while maintaining the ability to multitask. ● Coordinate with shipping companies like FedEx, UPS and others and ensure timely delivery. ● Work effectively with the center manager and sales team for quality delivery and escalations. ● The job requires repetitive lifting of sometimes heavy boxes. ● Must be a team player, dependable and have a good work ethic. ● Good written and verbal communication skills ● Excellent problem-solving and analytical skills ● Keen attention to detail ● Basic computer and math skills to calibrate and measure specifications ● Ability to use measuring devices like scales and tape measures ● In-depth understanding of company standards ● Understanding of target market and consumer needs ● Documentation and reporting skills ● Teamwork and collaboration ● Comfortable standing or walking for long periods of time Some cross training into bindery or other areas of the company will be required at times if another teammate is out. Experience Entry Level Job Full time Print Smith, Shipleap and Microsoft Office knowledge is a huge plus. Compensation: $15.00 per hour At AlphaGraphics, we offer careers for everyone! Whether you are just starting out, looking for that next great growth opportunity, or seeking a change, we have exciting roles to suit you. We pride ourselves on our training programs in management, sales, operations, print, signs, design, and marketing. Join us with or without experience, and we will succeed together as a team! We invite EVERYONE to apply! *AlphaGraphics centers (locations) are independently owned and operated. The posted positions are offered by individual franchisees who interview, hire, manage and pay the employees hired for positions in a specific local location (center) through their specific business.

Manufacturing Clinton , NJ, US + Added - 30/04/2025 Apply for Job Our Client, a Fortune 100 energy company who specializes in pioneering new research and pursuing new technologies to create more efficient forms of energy, is seeking a Chemical Technician to join their growing team. Pay: $25-28/hr 1st shift M-F **Summary:** + Maintaining the safety and security of the work area + Chemical handling requiring physical labor + Following detailed instructions to create lab and pilot scale lubricant blends + Preparing samples for evaluation and analysis + Maintaining supplies, files, and chemical inventory + Detailed data management + Performing safety inspections and general housekeeping duties **Qualifications:** + 2+ years of experience compounding, mixing, blending materials + Experience handling chemicals or other manufacturing material + Strong communication skills + Minimum of a HS Diploma or GED required This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you! We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Quality Control Intake AssociateJob Description The Quality Control Intake Associate is responsible for physically inspecting and evaluating products from our revolving inventory of over 15,000 antique and estate items including furniture, art, and home decor, and entering that information into our internal database. The details to enter will include measuring the physical dimensions of products, estimating weight, noting condition, defects, and repair needs, as well as, manufacturer, and artist details. The Quality Control Intake Associate will work closely with Photography Team Members to ensure inspected items are readily available to photograph and is responsible to ensure that the queue of products to be photographed is sufficient and that there are no downtimes of Photographers needing products to photograph. The Quality Control Intake Associate will also work closely with Warehouse/Moving Team Members to ensure the “product flow” of items physically moving into the Photography areas to the Photography Booths then removal of the processed items from the Photography Booths to their next showroom or warehouse location. The ideal candidate will be computer/tablet savvy and a fast typist with a keen eye for detail. Knowledge of antiques, art, and collectibles is a plus, but high attention to detail and the ability to effectively document your observations is the most important skill required. Responsibilities Safely receive antique and estate items including furniture, art, and home decor from internal warehouse personnel and organize the areas where the received products are waiting to be processed. Perform the intake of these items including accurately documenting measurements, weight, product attributes, condition, and repairs needed. Type in data directly into computer, tablet, and phone applications. Assist Photographers moving products in and out of photo booths. Assist Warehouse/Moving Staff moving products in and out of photo staging areas. Sort and organize paperwork after entering data to ensure it is not lost Communicate continually with Photography, Warehouse, and Repair teams to convey findings and request assistance. Comprehend and effectively demonstrate that the goal of the QC Intake role is to gather and document the required product details while ensuring that physical product flow is uninterrupted. Provide general assistance to other internal departments as needed. Skills Great attention to detail Excellent descriptive writing Fast typing skills Excellent command of English both oral and written and customer service skills Ability to lift 40 lbs High school degree or equivalent Salary and Schedule $18.00 - $22.00 per hour Monday - Saturday shifts 8:00 to 4:00. Full Time or Part Time is available depending on your availability. At least bi-weekly rotating Saturday shifts required for Full Time. Benefits IRA/401(k) with matching contributions Paid Maternity/Paternity leave Education reimbursement Healthcare plan

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Analyst I as part of the Quality team based in Raritan, NJ. Role Overview The QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment. Key Responsibilities Be responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations. Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories. Perform peer review/approval of laboratory data. Utilize electronic systems (LIMS) for execution and documentation of testing. Create, review and approve relevant QC documents, SOP's and WI's. Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements. Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development. Job duties performed require routine exposure to and handling of biological materials and hazardous chemicals. Requirements Bachelor's Degree in Science, Engineering or equivalent technical discipline is required. Minimum of 1 year relevant work experience, preferably within a biological and/or pharmaceutical industry is required. Experience in a Quality Control setting is preferred. Experience with processing samples in biosafety cabinets utilizing aseptic technique is strongly preferred. Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is strongly preferred. Knowledge of Good Tissue Practices is required. Knowledge of CAR-T QC test methods and related equipment is preferred. Excellent written and oral communication skill are required. Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process. Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice. The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision. Comfortable with speaking and interacting with regulatory inspectors. This position may require occasional travel to partner sites in NJ or PA as business demands. This position may require up to 5% domestic or international travel as business demands. Ownership and Commitment Takes responsibility for one's results and deliverables; sets and achieves goals to support organizational priorities. Takes initiative; willing to take unpopular positions/actions when necessary; courageous and assertive. Works effectively in the face of ambiguity, shifting priorities, and rapid change; maintains a positive outlook in difficult situations; a change agent. Agility and Prioritization Identifies and focuses on activities of highest value and impact; makes informed decisions quickly. Results oriented; defines goals, metrics and actionable plans and manages work to deliver desired outcomes; has a sense of urgency. Considers resources, alternatives, constraints and desired outcomes to make effective decisions. Employs good project management principles to appropriately align time, resources, and budgets. Teamwork and Communication Appreciates diverse perspectives and is actively inclusive of others' input and ideas; treats others with respect. Articulates ideas clearly and succinctly in a variety of settings and styles; can get messages across that have the desired effect. Leverages personal credibility and interpersonal skills to help others make better decisions and positively impact outcomes; able to develop/maintain effective working relationships internally and externally Employs a global mindset in decision-making and errs on the side of over-communicating to create organizational transparency, trust and alignment. Continuous Improvement Takes initiative, actively shares knowledge, builds skills, promotes new ideas and embraces change. Generates new solutions to problems by challenging the status quo and conventional thinking. #Li-BG1 #Li-Onsite The anticipated base pay range is$61,454-$80,656 USD Benefits We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles, we offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes 15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, and 3 floating holidays. Additional benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs - demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work. EEO Statement Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend's policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by applicable law. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions. Legend Biotech maintains a drug-free workplace.

Annual Compensation Range: $57,000-$62,000 Surmodics Services & Technologies ("SST") (formerly Biocoat) is committed to providing the best in developing, manufacturing, and applying coatings on medical devices. We are looking for a Quality Control Associate to be part of a positive team-oriented environment. Responsibilities: Responsibilities include, but are not limited to: Establish, execute, review, evaluate, and optimize laboratory procedures and policies • Perform, record and report quality control inspections and testing • Troubleshoot and participate in resolution of administrative or technical problems • Review batch records and supporting documents for production activities and release of product • Initiate, facilitate, assist, and review investigations and associated work for NCPs, CAPAs, ECOs, and failures for laboratory-related events • Assist with purchase, use, storage, and management of laboratory inventory/supplies. • Investigate customer complaints • Coordinate Material Review Board (MRB) meetings and facilitate material and documentation dispositions, as needed • Author and review quality procedures, templates, forms, and reports • Communicate deficiencies, safety and/or compliance issues • Compile data and report QMS metrics as required (e.g., special projects, product study, Management Review) • Support audit preparation and performance audit activities Skills & Requirements: Bachelor's degree in chemistry, biology, biomedical engineering, or similar Life Science field required • Experience in regulated manufacturing lab setting a plus • Prior experience with ISO 9001 or ISO 13485, and/or experience with QMS documentation and Good Document Practices highly desirable • Ability to report, evaluate and interpret scientific data to be successful in this role • Excellent math skills to adequately perform and interpret calculations and test parameters needed • Analytical approach to problem solving; critical thinker; uses data to substantiate decision making • Excellent technical writing skills with great proficiency in spelling, grammar, formatting, and completeness of documentation with extreme detail required • Proficiency with Microsoft Word, Excel, and Outlook; Prior experience with eQMS or ERP systems highly desired • Ability to complete assigned tasks in a timely manner with minimal day-to-day direction while meeting deadlines • Strong interpersonal and communication skills (verbal/written) • Ability to follow and adhere to all Safety guidelines and processes including wearing appropriate lab gowning and other PPE as required. The conditions herein are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. Work Environment: Office environment with occasional manufacturing and warehouse area exposure. Physical requirements are those that could be reasonably anticipated given the job duties and work environment. Exposure to hazardous chemicals in certain areas of the office. Must wear required personal protective equipment while demonstrating safe working practices. Physical Requirements Physical Demands: Stooping, turning, bending, squatting, kneeling and the ability to lift up to 30 pounds; constant/repetitive standing; requires normal, correctable vision and hearing, and the ability to accurately discern color as necessary to perform job functions. This position requires regular and sustained laboratory time around chemicals which may be hazardous. All personnel are required to follow all safety and chemical handling processes as outlined in various SOPs and Biocoat's Chemical Hygiene Plan. This position works within a Class 7 cleanroom for periods of time. All personnel are required to follow Biocoat's requirements for gowning and conduct while working within this environment. What SST Offers: Competitive salary, eligible for a discretionary bonus Benefits (medical with HSA component, dental, vision, critical illness, and accident insurance) Life insurance, short- and long-term disability paid by the company Flexible Spending Accounts (FSAs) 401(k) plan with an immediate company match Paid time off Education Assistance Program Rewards and Recognition Program Parental Leave Employee Assistance Program Additional benefits such as the opportunity to leave early on Friday's, business casual dress, friendly work environment, and fun company events. SST is an is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, status as a qualified individual with disability, or any other protected characteristic under law. SST Human Resources leads recruitment and employment for SST. Unsolicited resumes sent to SST from recruiters do not constitute any type of relationship between the recruiter and SST and do not obligate SST to pay fees should we hire from those resumes. We ask those external recruiters and/or agencies not contact or present candidates directly to our hiring managers or employees.

Basic Job Functions: Responsible for weighing raw materials to specific amounts that conform to the customer's formula in a manner that complies with Accupac's Standard Operating Procedures and the FDA's Good Manufacturing Practice regulations. Essential Functions of the Job: · Read, comprehend, and interpret written instructions in order to obtain raw materials in quantities that conform to customer specifications · Requisition raw materials to be weighed from the warehouse · Make standard computations as required in customer specifications · Verify accuracy of raw material information and corresponding documentation · Communicate any variances, deviations or nonconformance issues to appropriate personnel · Follow all applicable SOP's, cGMP's, customer specifications and safety guidelines · Work with careful attention to detail · Assist in maintaining the cleanliness of the chem weigh equipment and area · Create documentation for relative activities in respective logbooks · Conduct routine inspections of scales · Work extended hours as required to meet project deadlines · Work closely with other departments to ensure accuracy and timeliness · Perform all other duties as assigned Minimum Requirements of the Job: · Able to read, write, speak, and understand the English language · Able to perform basic math skills (add, subtract, multiply and divide) with both whole numbers and fractions · Able to operate a forklift or pallet mover safely · Able to perform tasks without constant supervision · Possess a basic working knowledge of how to operate a computer or terminal · Able to operate a pallet jack · Able to wear a tight-fitted negative pressure air-purifying respirator. Employees must be clean shaven with no facial hair to be able to daily use this type of respirator. Physical Requirements: · Able to sustain strenuous activity for a minimum of one (1) hour · Able to lift items up to 50 lbs. from floor to waist level · Able to carry a container weighing up to 50 lbs · Able to perform repetitive movements · Able to push and/or pull items 75 to 100+ pounds · Possess peripheral and color vision · Able to stand and/or walk on cement floors for 90% of the workday · Able to pass PFT test and physical examination. Supervisory Responsibilities: No Travel: None Education and/or Experience: Must have a high school diploma or GED. Prefer previous experience handling chemicals, operating a computer, understanding the Metric System, and forklift experience. #INDOTHER2025

Our large pharmaceutical client is seeking an Associate Scientist to join their growing Biophysics & Molecular Attributes Group in Spring House, PA. The Biophysics & Molecular Attributes Group within Biologics Discovery uses innovative biophysical, biochemical, and mass spectrometry based analytical tools to help select best therapeutic candidates for clinical development. You will be a critical member of the Higher Order Structure (HOS) team that characterizes developability attributes like thermal stability, chemical stability, solubility, and aggregation on a broad range of biologics platforms including monoclonal antibodies, multi-specific antibodies, antibody drug conjugates, antibody radio conjugates, and other therapeutic proteins. You will design and perform experiments using a variety of technologies like HPLC, DSF, DSC, cIEF, GXII, DLS, and more. Key Responsibilities: Execute automated methods for biophysical and structural characterization of antibody therapeutics. Integrate robotic liquid handling systems (e.g., Hamilton, Tecan) with analytical platforms to improve efficiency, consistency, and sample throughput. Execute analytical analysis of biologics candidates using a wide variety of technologies such as size-exclusion HPLC, plate-based HIC/Heparin binding, DSF. Evaluate results to deliver scientifically supported conclusions and recommendations that are documented in appropriate technical reports. Maintain lab and equipment. Collaborate with colleagues in the global organization to support discovery projects. Assist in developing recommendations for improving standard procedures. Required Skills & Experience Master's or Bachelor's degree in a relevant scientific field 2 years of experience in protein characterization (biologics/large molecules) Hands-on expertise in using and troubleshooting analytical techniques such as HPLC, DSF, DSC, cIEF, GXII, and DLS for protein and antibody analysis Nice to Have Skills & Experience Protein purification Salary: $67,000 - $75,000 (can be flexible based off experience) Hours: Monday-Friday, 8:00am-5:00pm Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year PTO: 10 PTO days, 6 paid sick days & paid Holidays Benefits: Medical, Dental, Vision and 401K plans available Exact compensation may vary based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.

Job Title: Production / Process Chemist Reports To: Director of Quality Control & Product Development Department: Production (Reaction Distillation) Summary: Plans the production, monitors the progress, and troubleshoots the processes associated with the Reaction Distillation area. In conjunction, oversees the process development and small-scale production with support from a Lab Technician. Duties and Responsibilities include the following. Other duties may be assigned. In conjunction with the Planning Department, recommend and in turn schedule the production for all products that are manufactured via chemical Reactions and / or Distillation in the designated equipment. Supported by an analytical and quality team, monitor the progress of the reactions and / or distillation to ensure the process meets the quality and timeliness of the established standards. Utilizing the support of an Established Process Development team, develop processes that will improve on established products and in conjunction with our commercial team, In coordination with the Commercial Team, assists in the development of processes for new products and supervises the progress of these processes with the Process Development Team. Evaluates production batches against established product standards and specifications and modifies as needed. Directs, coordinates, and advises production personnel coordinating all three shifts accordingly in the course of scheduling the production, monitoring the progress of the processes, and making the necessary adjustments conditions as needed. Coordinate's production activities between all three (3) shifts. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Experience in a chemical processing environment including: interacting with production personnel; developing and troubleshooting chemical processes; an awareness of safety protocols while working with chemicals under various conditions (pressure and temperature) Must have the ability to multi-task and work in a fast-paced environment. Education/Experience: Bachelor's degree in Chemistry or related field such as Chemical Engineering from a four-year college or university is required. 5 to 10 years of experience is preferred, however, all candidates with strong mechanical aptitude, a solid background in Chemistry and relevant experience will be considered. Language Ability: Demonstrated ability to make successful presentations to individuals and/or groups at all levels of an organization. Excellent written and verbal communication skills. Ability to deal effectively with a variety of individuals at all organizational levels. Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures or government regulations. Ability to write reports, business correspondence and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public. Math Ability: Candidate must be able to calculate reaction stoichiometric quantities, percent yields and interpret GC plots to determine the reaction status or nature of reaction purity. Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Computer Skills: To perform this job successfully, an individual should have basic computer skills and knowledge of how to use Office 365, develop spreadsheets, and ERP and Planning Systems, , inventory software and contact management systems. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly exposed to fumes or airborne particles. The employee is frequently exposed to work near moving mechanical parts and chemicals pertinent to the processes and may be occasionally exposed to allergens. The noise level in the work environment is usually moderate. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands; reach with hands and arms and talk or hear. The employee is frequently required to stand; walk and sit. The employee is occasionally required to climb stairs balance and stoop, kneel, crouch, or crawl.