Quality Control Analyst jobs at Cambridge Isotope Laboratories - 25 jobs

Job DescriptionDescriptionPerforms routine chemical productions and process developments based on provided work instructions and training in a safe and high-quality manner. Works collaboratively with internal laboratory production colleagues, R&D, operations, and quality during directed development efforts. Key Responsibilities Performs and completes routine chemical production based on written procedures or direct instruction within expected timelines. Ability to set up all required equipment for production of products and other related activities. Evaluates his/her projects/production (e.g. in process parameters and quality control measures) and offers suggestions for improvements. Capable of running routine in-process control tests based upon written and direct instructions. Responsible for maintaining a clear and detailed lab notebook and production records. Responsible for maintaining neat, clean and safe work area. Performs other duties of similar complexity as directed. Skills, Knowledge and ExpertiseMinimum Qualifications: Associate degree in chemistry or engineering with 5+ years of relevant experience. Proficiency in general inorganic and organic chemistry. Demonstrated experience in laboratory chemical processes and techniques. Experience working with products that may pose special hazards, such as air-sensitive, moisture-sensitive, pyrophoric, high-energy, toxic, high-potency, etc., as well as synthetic organic, organometallic, or inorganic chemistries and associated equipment and techniques (e.g., glove boxes, Schlenk techniques). Strong organizational, problem-solving, and analytical skills. Self-starter with the ability to manage priorities and workflow. Capacity to work independently and handle multiple projects while meeting deadlines. Strong interpersonal skills. Proficient in collaboration tools such as Teams, Salesforce, SharePoint, and Electronic notebooks. Preferred Qualifications: Bachelor's degree in chemistry or engineering with 0-2+ years of relevant experience. Benefits Medical, Dental, Vision - effective day one of employment. 401(k) with company match with immediate vesting - effective first of the month, following date of hire. First 3% is matched dollar-for-dollar. Second 3% is matched at 70 cents on the dollar. 3 Weeks' Vacation. 12 Paid Holidays. Basic Life, AD&D, STD, and LTD provided at no cost to employee.

Application Deadline February 27, 2026 Department Operations Employment Type Full Time Location Newburyport, MA Workplace type Onsite Reporting To Laboratory Production Manager Key Responsibilities Skills, Knowledge and Expertise Benefits About Ascensus Specialties We partner with companies of all kinds to develop chemical solutions that improve everyday products and processes to enhance people's lives. Ascensus Specialties, LLC, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Job Description About Us Stellar Industries is a rapidly growing industry leader in manufacturing metalized ceramics. We are a major supplier of innovative, high-quality parts to the Aerospace, Photonics, Telecommunications, and Commercial industries. The company was acquired by TRUMPF Photonics in 2019 and has significant growth goals. About the Role The Quality Control Inspector Level II maintains quality standards by inspecting incoming materials from outside suppliers, in-process production, and finished products in accordance with the quality standards and operating procedures set forth by the Head of Quality Control/Quality Assurance. What You Get to Do Works independently with minimal supervision. Maintain an organized and clean work area. Uses Hand tools, including but not limited to tweezers, calipers, and micrometers. Confirms specifications by conducting visual and measurement tests. Works with a variety of blueprints and technical drawings; must be able to interpret changing requirements as products and builds vary. Completes a General Inspection Report by documenting inspection findings regarding product dimensions, quantity of parts accepted/rejected, and basis of rejection. Uses Vision Systems and documents results into the computer. Follow all safety protocols. Cross-train as requested in other areas of the company. About You Minimum of 3 years of quality control experience. Must be able to work in a sitting position for up to 10 hours. Must be able to wear a lab coat, spittle mask, and gloves while working. The position requires working with measuring devices and microscopes. Individuals must have previous experience working in a similar environment. Must be able to work independently and demonstrate extremely high levels of precision and accuracy. line, High-Temperature BTU Furnaces, as well as various facility-related items, including air handlers, air compressors, air filtration units, etc. What We Offer Competitive pay A generous benefits package that includes medical, dental, 401K plan, and PTO Employer-paid vision plan, Employer paid Basic Life and AD&D Insurance, and Employer Paid Disability Insurance Tuition Reimbursement 4-Day workweek, Monday-Thursday 12 pm-10:30 pm Monday-Thursday 12:00 pm - 10:30 pm

Shift: Full-Time; Monday - Friday; 8am-5pm EST **ONSITE/HYBRID:** This is a fully onsite role based at our customer's site in **_(Boston, MA)._** We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner. Within our Analytical Services team, we have a functional service provider solution, which is a unique partnership that allows our customers to leverage the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. **Key responsibilities:** + Perform technical and quality reviews of internal and external documents, including raw data, stability protocols/reports, CoAs/stability data reports, risk assessments, sampling plans, shelf-life reports and etc. + Enter and trend stability data in SLIM system and generate stability timepoint summary reports. + Establish/extend DS and DP shelf lives and generate shelf-life reports based on stability data. + Plan, manage and communicate stability pulls and ensure stability testing occurs within specified testing windows. **Education and Experience:** + Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar + **Sr. Scientist:** Previous experience that provides the knowledge, skills, and abilities to perform the job **(comparable to 4+ years')** + OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job **(comparable to 2+ years')** + OR **PhD** In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. **Knowledge, Skills and Abilities:** + Proven Experience with stability studies, stability protocols/reports, CoAs/stability data reports, risk assessments, sampling plans, shelf-life reports, including raw data and external documents. + Stability data in SLIM system and generate stability timepoint summary reports. + DS and DP shelf lives and generate shelf-life reports based on stability data. + Plan, manage and communicate stability pulls and ensure stability testing occurs within specified testing windows. + Attention to detail and ability to multitask, review tons of data. **Working Environment:** Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. **Benefits** We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! **Compensation and Benefits** The salary range estimated for this position based in Massachusetts is $90,000.00-$110,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: + A choice of national medical and dental plans, and a national vision plan, including health incentive programs + Employee assistance and family support programs, including commuter benefits and tuition reimbursement + At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy + Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan + Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: ***************************************************** Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Sr. Scientist - FSP - Quality Control Shift: Full-Time; Monday - Friday; 8am-5pm EST ONSITE: This is a fully onsite role based at our customer's site in (Boston, MA). We welcome applicants from all locations within the US. Please note that relocation assistance is not provided for this position, and any relocation costs will be the responsibility of the candidate. Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Thermo Fisher's clinical research business is a leading global contract research organization and world leader in serving science. We are passionate, deliberate, and driven by our mission - to enable our customers to make the world healthier, safer, and cleaner. Our Laboratories Functional Service Partnership (FSP) team plays a direct role in advancing drug development by creating sustained groups of talent within our customers' organizations to provide long-term support. Through this collaborative approach, our professionals bring their commitment to excellence, industry knowledge, and operational strength directly into customer environments, helping to enhance capabilities and advance the delivery of life-changing therapies. Key responsibilities: * Perform in-process, release, and stability testing and/or review independently following established methodology, procedures and SOPs * Maintain accurate testing records and adhere to cGMP/GDP expectations * May participate in executing method validations and/or method transfers * Assist in troubleshooting of analytical methods with the assistance of manager when necessary * May participates in author and review of data, SOPs, analytical methods, protocols and reports * May participate in compliance related teams working towards the goal of continuous improvement. * Report OOT/OOS results and other deviations to area management. * Perform other laboratory duties as assigned. Education and Experience: * Bachelor's degree in lab sciences such as Chemistry, Biochemistry, Material Science, Immunology, Biology, Molecular Biology or similar * Sr. Scientist: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 4+ years') * OR Masters degree and previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years') * OR PhD In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: * Understands cGMP concepts and general practices * Knowledge and experience in chromatography, dissolution, and Karl Fisher * Knowledge of various complex laboratory equipment including HPLC, GC, KF, dissolution, TOC, UV, IR, pH meter, and balance * Strong attention to detail * Demonstrate good communication skills both oral and written. * A minimum of a Bachelor Degree in science or related discipline is required. * Typically requires 4 years of experience in GMP pharmaceutical/biopharmaceutical industry Working Environment: Below is listed the working environment/requirements for this role: Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner. Able to work upright and stationary and/or standing for typical working hours. Able to lift and move objects up to 25 pounds Able to work in non-traditional work environments. Able to use and learn standard office equipment and technology with proficiency. May have exposure to potentially hazardous elements, including infectious agents, typically found in healthcare or laboratory environments. Able to perform successfully under pressure while prioritizing and handling multiple projects or activities. Benefits We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Compensation and Benefits The salary range estimated for this position based in Massachusetts is $95,000.00-$110,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: * A choice of national medical and dental plans, and a national vision plan, including health incentive programs * Employee assistance and family support programs, including commuter benefits and tuition reimbursement * At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy * Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan * Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: *****************************************************

Whirlpool is currently seeking qualified candidates for a Quality Control Technician. This role is for our Fall River, MA site. The role of the 1st Shift Quality Tech is to help solve quality problems on dryers by taking measurements, doing testing and effecting repairs. Additionally, will assist in certifying materials or machines to reduce the End of line (EOL) testing and field failures. Areas can be main line or medium large assembly or fabrication as required by the problems. Tasks will vary day by day based on the needs of Quality and production. Flexibility in work hours as needed. Reports to Metrology/Fabrication Engineer. Pay Rate $27.05 an hour Your responsibilities will include * Working with test booth operators to understand and aid in the problems * Understanding of the EOL inspections and helping to improve in line inspection to reduce failures at EOL and in the field. * Inspecting and taking measurements on dryers in the line * Performing inspections of materials required to run the next day (in line, fabrication, incoming material from suppliers). * Performing repairs or some assembly operations on the Line to stage the line for success the next day. * Run dryers through the Main Line Customer Assurance Lab (CAL) test as required when it is installed. * Performing process audits as required on the off shift. * Will need to have the ability to plan and perform work and the making of decisions involving the use of considerable judgment and initiative. * Lead problem solving using World Class Manufacturing (WCM) tools. * Learn new skills as needed * Follow all Whirlpool Safety policies when working in the plant. * Will add, subtract, divide and multiply decimals and fractions, use measuring devices, read simple drawings, and interpret production schedules and inspection reports. * Will be lifting parts and doing assembly operations in a safe manner. * Support cost and quality projects by providing data and evaluation. * Evaluate parts and products for Non-conformances * Report issues with accuracy of BOMs * Track/Understand CN's * Understand and support the APQP and QMS process as needed. * Communicate directly with suppliers & operations concerning APQP issues * Perform fit / function evaluations * Uses all designated safety equipment, observes all safety rules, and follows recognized rules of safe practice. Performs duties of a similar or lesser skill to facilitate the flow of work in the department. Minimum requirements * High School Diploma / GED * 6+months of experience doing manufacturing quality inspections and running tests. * Lift 40+ pounds * Be able to be Preferred skills and experiences * Attention to detail. * Ability to operate complicated equipment safely including electrical and gas hookups. * Self motivated and able to work on their own. This role in summary [ACTION REQUIRED - DO NOT POST AS IS]In 1-2 sentences, provide an overview of the purpose, priorities, deliverables and expected outcomes of the role. Your responsibilities will include [ACTION REQUIRED - DO NOT POST AS IS] Describe the main responsibilities of this position. We recommend up to 8 bullet points, preferably starting each statement with a verb. Minimum requirements [ACTION REQUIRED - DO NOT POST AS IS]Describe what is absolutely required for the role, meaning that the candidate cannot be hired if they do not have these requirements. We recommend no more than 3 items and suggest prioritizing:Years of experience Education (majors, minimum degree, etc.) Language skills CertificationsSystems/Technical knowledge Preferred skills and experiences [ACTION REQUIRED - DO NOT POST AS IS]Describe the desirable background and experiences which will be a plus if the candidate possesses them. We recommend no more than 5 items, and suggest including:Years of experience Education (majors, minimum degree, etc.) Language skills CertificationsSystems/Technical knowledge We strongly recommend NOT including behavioral traits in this section. Why should you apply? [ACTION REQUIRED - DO NOT POST AS IS]Describe the benefits and/or advantages of working in that particular location, such as core benefits, vacation days, home office days, on-site daycare, work environment, etc Additional information [ACTION REQUIRED - DO NOT POST AS IS]Use this section to include any other information that was not mentioned in the previous sections. If there is nothing to add, this section should be deleted. Whirlpool Corporation (NYSE: WHR) is the number one major appliance manufacturer in the world, with approximately $21 billion in annual sales, 97,000 employees and 70 manufacturing and technology research centers. The company markets Whirlpool, KitchenAid, Maytag, Consul, Brastemp, Amana, Bauknecht, Jenn-Air, Indesit and other major brand names in nearly every country throughout the world. We stay true to our philosophy that says good business begins by not following but leading. Our brands and products help people make the most of time so they can focus on making the most of moments that matter. At Whirlpool Corporation, we believe that all people matter. Celebrating diversity and including thousands of perspectives empower us to create products that blend into every concept of home. Whirlpool Corporation is committed to equal employment opportunities regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Additional information about our company can be found at ***************************** Follow us on LinkedIn or join the conversation @ HYPERLINK "********************************** HYPERLINK "********************************** HYPERLINK "*********************************

Gorton's is seeking a passionate and technically skilled Associate Food Technologist to join our Innovation Team, supporting the development of next-generation frozen seafood products. This role will contribute to product ideation, formulation, and commercialization, with a focus on innovation while upholding our commitment to quality, sustainability, and consumer satisfaction. What You'll Do: - Support and potentially lead the creation of new frozen seafood products and improvements to existing products. - Conduct bench-top formulation, prototype development, and plant trials. - Develop and optimize cooking instructions and recipes for consumer use. - Support multiple projects simultaneously and prioritize tasks for robust development plans. - Maintain detailed records of formulations, testing protocols, and ingredient specifications. - Ensure all products meet Gorton's quality standards, regulatory requirements (FDA, CFIA), and shelf-life expectations. - Apply scientific principles and analytical thinking to solve problems and improve products. - Demonstrate understanding of manufacturing systems, processes, and policies. - Support production facility tests and process scale-up development. - Contribute to ingredient optimization, cost savings, and sustainable sourcing initiatives. - Continuously seek process and product improvements, challenging the status quo appropriately. - Collaborate with cross-functional teams (marketing, operations, procurement, supply chain, finance, sales) to execute initiatives. - Organize, facilitate, and lead product evaluation sessions, including cuttings and sensory panels, to assess internal prototypes and benchmark competitive products. - Communicate project status, findings, and recommendations clearly to managers and cross-functional teams. - Partner with Quality Assurance and Regulatory teams to ensure compliance with food safety standards. - Conduct product presentations at sales and management meetings. - Keep up with new technologies, ingredients, regulations, and industry trends. - Leverage internal and external data to meet consumer needs and guide decisions. - Support proper ingredients inventory of the lab for tests and experiments. - Perform lab management tasks such as cleaning, sorting, and storing lab equipment. What You'll Need: - Bachelor's degree in Food Science, Chemistry, Microbiology, Biology, or related field with >2 years of relevant lab experience in food product development or manufacturing. - Excellent oral and written communication abilities; able to translate technical concepts for diverse audiences. - Ability to work independently and collaboratively with minimal supervision. - Strong quantitative, analytical, and project management skills. - Demonstrated ability to tackle new and unfamiliar tasks with minimal assistance. - Basic culinary skills for creative recipe development and comfort in a product development kitchen. - Good interpersonal skills and ability to work well on teams. - Experience with experimental design and statistical analysis are a plus. - Flexibility for early plant tests and willingness to travel (up to 30%). - Proficiency in Microsoft Office, formulation software, and data analysis tools. - Willingness to taste fish and shellfish prototypes and discriminate subtle flavor differences. - Ability to lift up to 50 lbs. Pay Range: $60,632 - $71,240/Annual

Bay State Milling Job Description Job Title: R&D Technician Department: Research and Development FLSA Status: Non-Exempt (hourly, overtime eligible) Pay Range: $55,000 - $70,000 per year, dependent on experience SUMMARY This R&D Technician supports technical activities associated with the research and development of new plant-based ingredients and applications at Bay State Milling and aligns with BSMC's Strategic Intent of being the leading supplier of plant-based ingredients for the next generation of foods in North America. This role will align directly with the initiatives of our Business Units (Milling & Ingredient Solutions, Oat Milling, Varietal Solutions). ESSENTIAL DUTIES AND RESPONSIBILITIES include, but are not limited to the following. Other duties may be assigned. Conduct testing on grains, flours, food ingredients, and finished foods to aid research and development of new ingredients. This may include research on new grain cultivars, or research that may help us understand our ingredients better. Common analyses include testing % moisture, protein, ash, viscosity, dough rheology, water absorption, texture analysis, and starch pasting. Provide support on R&D projects which may include formula scaleup, ingredient sourcing, and maintaining ingredient databases. Be a trained member of our Sensory Team. Bake lab flour and ingredient inventory management. Data management and report-outs. Collaborate with other R&D members. Maintain a safe workspace and abide by the Innovation Center lab manual to help us all maintain a state of the art innovation center, team, and culture. 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. EDUCATION and EXPERIENCE B.S degree in food science or related science from an accredited university Experience in a lab setting running routine analyses for accuracy and precision. OTHER SKILLS & ABILITIES Ability to touch and taste grains, flours, and grain-based foods. Ability to accurately input data via computer screens and programs Proficiency in Microsoft Office programs Comfort with using mechanical equipment (mills, mixers, ovens, etc), handling chemicals, and using various analytical instruments (training will be provided) Ability to understand and follow through with detailed spoken and/or written instructions. Ability to communicate information both verbally and in writing in a clear and concise manner 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 this job, this employee is required to be on her/his feet during part or all of the day. This employee must be able to run analytical equipment in a safe manner. Must be able to lift and carry 50 pounds occasionally. Should not be allergic to wheat, soy and/or associated dusts. 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. Usually will work in analytical laboratory & food product development lab. LANGUAGE SKILLS Must speak fluent English as the primary language. Must have the ability to read, analyze, and interpret memos, general business communications, technical procedures, and governmental regulations and/or labels. Must have the ability to write in English and complete reports. MATHEMATICAL SKILLS Must possess the ability to work with mathematical concepts and apply concepts such as addition, subtraction, multiplication, division, fractions, percentages, ratios, and proportions to analytical situations. REASONING ABILITY Must possess the ability to define problems, collect data, establish facts, and draw valid conclusions. Must have the ability to interpret technical instruction in mathematical or diagram form and deal with multiple tests operating at any given time. SAFETY While performing the essential job functions, the employee is expected to work in a safe manner and to follow company policies regarding safety. It is the expectation and responsibility of the employee to report any and all injuries immediately to the Vice President of Corporate Quality Assurance and to resolve any safety situation that is substandard and poses a risk for employee injury, property damage or loss. FOOD SAFETY/SECURITY REQUIREMENTS The Company is committed to producing and delivering defect-free products. To ensure this, all employees are required to be trained on and adhere to the Good Manufacturing Policies set forth by the Company as they pertain to personnel practices, equipment, and facilities. It is also vital that all employees be aware of their work environment and prevent any accidental or intentional adulteration of products produced at this facility.

Job Description The Quality Control Technician is responsible for testing seafood products and materials used during the manufacturing process to verify the products meet predefined criteria and conform to all applicable laws and company standards. They will test products across three stages of production (before, in-process, and final) to ensure that the final product is safe to release for sale or distribution and report findings back to management. The QC Technician will participate in the inspection and grading of Grade-A products, perform moisture analysis, produce written reports, verify inventory, quality, and usability of products. This position reports to the Quality Control Supervisor or Manager. DUTIES AND RESPONSIBILITES Serve as the primary contact between the production staff and the Quality department for all Quality, Food Safety and Regulatory issues Responsible for filling out assigned HACCP compliance documents Conducts internal audits of plant and paperwork in conjunction with the QC supervisor Test and record measurements of seafood product attributes Communicate quality or compliance concerns with urgency to QA leadership Performs other related duties as assigned Performs analytical and organoleptic product quality inspection of fresh and frozen seafoods, ensuring products are produces to specification standards Requirements 1+ years, experience in inspection and/or production 1+ years, practical experience with Microbiology method verification and routine testing practices, EM Monitoring and basic knowledge of method/equipment validation principle 1+ years, experience in food manufacturing; seafood or meat processing a plus Excellent verbal and written skills Excellent customer service skills Strong working knowledge of various mathematical concepts Strong analytical and problem-solving skills Strong project management and organizational skills; able to prioritize and manage multiple tasks and projects on time Exceptional interpersonal skills: able to navigate organizations to build relationships and garner support Able to maintain an environment that drives performance and a safe workplace Drive an environment of teamwork and open communication OTHER REQUIREMENTS Must be able to lift 30-50 pounds Work up to a 10-hour workday: standing/walking most of the day Hand use: single grasping, fine manipulation, pushing and pulling Work requires the following motions: bending, twisting, squatting and reaching Exposure to FDA approved cleaning chemicals Exposure to temperatures: Ability to work in wet and dry conditions Ability to work Monday-Friday, weekends when needed Ability to use tools and equipment, including knives Specific vision abilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus, required North Coast Seafoods is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status. Benefits At North Coast, employees are considered part of a family where everyone works together to ensure the founding mission and values of the company are upheld every day. We offer an inclusive work environment spearheaded by an approachable leadership team who believes in the idea that it is not just about the work we do, it's about what the work allows us to do for our loved ones. We foster the opportunity for real growth and long-term employment. Most members of our leadership team started out on the floor and through mentorship advanced into their current roles. We are currently looking to build the next generation of leaders. We offer competitive compensation packages including comprehensive health care coverage, vacation and 401(k) to all full-time benefit-eligible employees. Employees also have access to the highest quality seafood at cost. This is a full-time, non-exempt position.

The QC Inspector will perform incoming, in process and final inspection of products and components used in NRC/FDA regulated environment. Primary Responsibilities * Mechanical inspection * Tensile and hardness testing * Weld Inspection in accordance with ASNT/AWS * Perform radiation profiling of devices * Work with engineering to define appropriate inspection and acceptance criteria * Assists with testing of product to demonstrate regulatory compliance * Assist with investigating problems and recommending / implementing solutions * Perform inspections of components at various stages of assembly to applicable written procedures. * Inspect soldered assemblies to in-house and industry standards. * Maintain documentation and databases to support inspection activities * Verify test data * Other related duties as assigned Job Requirements * High school diploma required, with specialized training. * Must have experience in Mechanical inspection including experience with typical QC inspection equipment / tools. * Proficient with MSOffice applications. * A plus but is not required is experience in an electronic device atmosphere with printed circuit board and electronic soldering inspection. Physical and Visual Activities * Reading and comprehending written instructions. * Capable of communicating clearly with relevant personnel. Physical demands; Able to lift 55 lbs. Compensation Information: 25 - 35 hourly ITW is an equal opportunity employer. We value our colleagues' unique perspectives, experiences and ideas and create workplaces where everyone can develop their careers and perform to their full potential. As an equal employment opportunity employer, ITW is committed to equal employment opportunity and fair treatment for employees, beginning with the hiring process and continuing through all aspects of the employment relationship. All qualified applicants will receive consideration for employment without regard to race, color, sex, gender identity, sexual orientation, religion, national origin, age, disability, protected Veteran status or any other characteristic protected by applicable federal, state, or local laws.

The QC Inspector will perform incoming, in process and final inspection of products and components used in NRC/FDA regulated environment. Primary Responsibilities Mechanical inspection Tensile and hardness testing Weld Inspection in accordance with ASNT/AWS Perform radiation profiling of devices Work with engineering to define appropriate inspection and acceptance criteria Assists with testing of product to demonstrate regulatory compliance Assist with investigating problems and recommending / implementing solutions Perform inspections of components at various stages of assembly to applicable written procedures. Inspect soldered assemblies to in-house and industry standards. Maintain documentation and databases to support inspection activities Verify test data Other related duties as assigned Job Requirements High school diploma required, with specialized training. Must have experience in Mechanical inspection including experience with typical QC inspection equipment / tools. Proficient with MSOffice applications. A plus but is not required is experience in an electronic device atmosphere with printed circuit board and electronic soldering inspection. Physical and Visual Activities Reading and comprehending written instructions. Capable of communicating clearly with relevant personnel. Physical demands; Able to lift 55 lbs. Compensation Information: 25 - 35 hourly

Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful and usable solutions. From military defense and space exploration to biomedical engineering, lives often depend on the solutions we provide. Our multidisciplinary teams of engineers and scientists work in a collaborative environment that inspires the cross-fertilization of ideas necessary for true innovation. For more information about Draper, visit *************** Summary: Engineering Students (interns) support the manufacturing of electronic systems or may assist in sustaining and improving the quality processes across the full engineering and manufacturing life cycle. Students will contribute to projects in various engineering disciplines and have the opportunity to collaborate with engineers or technicians to build and test systems, hardware, or components on various projects. Students may also be involved in ensuring quality products are produced and quality procedures are upheld. : Duties/Responsibilities * Design, develop, and enhancement engineering solutions for challenging problems. * Implement, test, perform analysis, and provide documentation support. * Generate and present test reports including plots, tables, evaluation criteria, and conclusions from data collected and analyzed throughout the test process. * Complete assignments designed to develop a practical knowledge of processes, procedures, equipment, facilities, and systems as well as their interrelationships within engineering disciplines. * Performs other duties as assigned. Program Requirements * Enrolled in an accredited full-time undergraduate or graduate degree program required. * There is flexibility regarding hours and program duration based on applicant's school schedule and availability. Skills/Abilities * Excellent written and oral communication skills. * Excellent work ethic with the ability to work independently or in a team environment. * Ability to adapt to ever-changing environments, risks, and vulnerabilities. * Strong computer skills including MS Word, PowerPoint and Excel. Additional Job Description: Duties/Responsibilities * Support Quality Engineers in day-to-day activities pertaining to assigned projects. This may include the following: * Performance of Inspections: Receiving, Touch Labor, Shipping, First Article Inspections (FAI) etc. * Development and verification of work instructions and their implementation in the Manufacturing Execution System (MES) * Performance of End Item Acceptances * Performance of Audits: Physical Configuration Audit (PCA), Functional Configuration Audit (FCA), Process, Infrastructure * Development and verification of governing and implementing documents * Nonconformance review and management * Continuous Process Improvements (CPI) * Risk and Opportunity Management * Interfacing with suppliers * Technology Readiness Level (TRL) and Manufacturing Readiness Level (MRL) assessments * Perform data analysis of project trends * Perform other related duties as assigned. Program Requirements * Enrolled in an accredited full-time undergraduate or graduate degree program required. Students pursuing the following degrees are encouraged to apply: Mechanical, Aerospace, Electrical, and Industrial Engineering. * Ability to commit to being on site at Cambridge full-time. Note: There is flexibility regarding hours, and program duration based on applicant's school schedule and availability. Connect With Draper for Future Opportunities! If you don't find the right posting in our Career Opportunities, you may submit your resume for future consideration. Job Location - City: Cambridge Job Location - State: Massachusetts Job Location - Postal Code: 02139-3563 The US base salary range for this full-time position is $15.00 - $225.00 Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Union ranges will be in compliance with the collective bargaining agreement's approved rates by location and role. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Please note that the compensation details listed in US role postings reflect the base salary only, and does not include bonuses or benefits. Our work is very important to us, but so is our life outside of work. Draper supports many programs to improve work-life balance including workplace flexibility, employee clubs ranging from photography to yoga, health and finance workshops, off site social events and discounts to local museums and cultural activities. If this specific job opportunity and the chance to work at a nationally renowned R&D innovation company appeals to you, apply now *********************** Draper is committed to creating an inclusive environment. We understand the value of inclusivity and its impact on a high-performance culture. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, disability, age, sexual orientation, national origin, veteran status, or genetic information. Draper is committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, its services, programs, and activities. To request reasonable accommodation, please contact *************.

Start here, end here. There is a reason why we have so many employees with 20+ years with the company-Pace offers careers. Join us in becoming the premier die casting manufacturer and engineering solutions supplier worldwide. Quality Control Inspector: Perform inspections and tests on in-process and finished product as defined in procedures and work instructions to ensure that quality standards and process controls are being met throughout the manufacturing process. Generate the appropriate documentation, records and reports. Support quality, engineering and manufacturing as needed. Compensation range: $21.00-$28.25 What Pace Offers You: * Comprehensive Benefits: Medical, Dental, Vision, Life Insurance, and more! * Secure Future: 401K with company match * Work-Life Balance: PTO and 11 Paid Company Holidays * Invest in Your Growth: Tuition Reimbursement and Paid Company Training * Opportunities to Advance Your Career Duties and Responsibilities: * Must have numeracy skills to calibrate and measure specifications. * Must be a self-starter taking initiative without direction. * Dedicated to Department/Company Objectives. * Detail Oriented: Must spot issues and monitor products or parts that do not meet compliance. * Follows instructions provided by supervisors & inspectors for visual inspection of parts at incoming and outgoing. Also performs mechanical inspections of the castings. * Reads and understands inspection reports, provides feedback to supervisor and production floor. * Inspect and pack shipments daily. * Inspects and records all parts at specified frequencies, with specified lot size, in accordance with approved Quality Control procedures with calibrated gauges and measuring devices. * Performs audits as necessary to ascertain quality. * Make sure all suspect parts have been properly tagged and sent to the designated holding area. * Capable and willing to work overtime. * Works in a safe manner, so not to endanger self or co-workers. * Reports on unsafe conditions. * Wears required personal protective equipment. * Participates in training programs deemed necessary by the company. * Performs other associated duties, functions or work needed or assigned to continue the productive operation of the company. * Must follow all safety rules and policies as set forth by OSHA guidelines and pace Industries policies and procedures as outlined in the employee manual. * Reports to Quality Manager. Has the authority and responsibility for controlling quality as delegated by management. Please note that the duties and requirements described herein are intended to represent general contents of this job. This is not to be construed as an exhaustive statement of duties and responsibilities. Position Requirements: A high school diploma or prior quality inspection background is required. On the job training will be provided for candidates with limited experience in quality control. Physical Requirements: * Must be able to perform moderately heavy lifting up to 30 pounds. * Must have dexterity to be able to access/remove sample parts or products during the manufacturing process. * Must be able to sit, stand for long periods, bend, stoop, walk, ascend and descend stairs. * Technical skills - to understand technical documents, manuals, and blueprints to ensure that products meet the correct standards Pace is a career destination for engaged, passionate and talented people who are driven to seek the innovation, growth and opportunity that only we offer.

About Us: SMC, Ltd. is a globally recognized premium supplier to the medical market with locations throughout the world. People committed to speed, technology, and exceptional performance are the cornerstone of our organization. Comprised of dedicated people and decades of manufacturing experience, we have continued to experience strong growth and currently have outstanding career opportunities for equally dedicated people. We currently have an immediate need to bring on two QC Analysts for a contract role within our Metrology Department in Devens, MA. One opening is 8pm-8am (12 hour shifts rotating schedule) and the other opening is for 4pm - 12:00am. These openings are long-term, open-ended contracts with benefits with the possibility to go permanent. Job Summary: This position has primary responsibilities which include accurate part and assembly inspections and tests performed to customer specifications, operating computerized inspection systems, such as coordinate measurement machines and vision inspection equipment. Essential Job Duties and Responsibilities: Takes instruction, training and guidance from senior level metrologists. Works closely with other quality, manufacturing and engineering personnel, performs special and on-going projects to improve the reliability of products and processes. Participates in MSA (Measurement Systems Analysis) i.e.: GR&Rs (Gage Repeatability and Reproducibility) Assist Quality personnel with in-process inspections (WIP) Prioritizes workload to meet project deadlines and interim due dates Reads, understands and executes inspections per documented Metrology Requests, drawings and specifications and verbal communication Performs first piece inspections under guidance Performs Process Capability studies (Variable Data) Performs Attribute Analysis (Visual Data) Other duties as assigned. Regular attendance Essential Qualifications: High School Diploma or equivalent required Minimum 2 years experience in the quality field Basic Knowledge of IQMS Good written and verbal communication skills Measurement System Analysis experience preferred Basic knowledge of 3-axis coordinate measuring equipment Must have working knowledge of Statistical Process Control and understand basic statistical concepts Must be able to use Microsoft Excel and Word proficiently Analyze data using statistical operations Basic interpretation of engineering drawings and specifications Ability to read, write and communicate in English ADA Requirements: Office II Typically sits, grasps items and performs keyboarding for frequent operation of a computer Stand, walk, bend, reach or otherwise move about occasionally Lift, move or otherwise transfer items up to 30 lbs. occasionally Occasional exposure to typical machine shop physical hazards Travel by air or car occasionally At SMC Ltd. we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful worktherefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process. SMC Ltd. is an equal opportunity employer. M/F/D/V; this organization uses E-Verify. Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.

We are a growing manufacturing company looking for an individual to assist or lead our quality control department Requirements A qualified individual would: Be able to read and interpret drawings. Understand GD&T. Understand a variety of sampling plans. Utilize best practice inspection methods to ensure product conforms to customer and drawing specifications. Be familiar with and able to use a variety of inspection tooling (micrometers, calipers, CMM, indicators, optical comparator, etc). Have good computer skills (Microsoft Office, Outlook, be able to learn a robust ERP system). Be familiar with completing first article inspections per AS9102 and complete utilizing specialized software. Have a good organizational skill set as each customer has a different set of requirements that are critical to product acceptance. Be familiar with the requirements of ISO9001. Attention to detail is critical. FULL TIME EMPLOYEE BENEFITS: Competitive compensation based on experience BCBS Medical, Altus Dental and Vision, Disability and Life Insurance - 100% Company Paid. Paid personal and vacation time (PTO) 10+ Paid holidays 401K plan Potential for Growth OT based on business conditions COMPANY: Bendon Gear is a precision machine and gear company doing business for over 40 years, with a stable set of excellent customers. We are a good, solid company, and we wish to build a team of good people who are motivated, flexible, and capable. Job Types: Full-time, Part-time Salary: $18.00 - $27.00 per hour Benefits: 401(k) Dental insurance Health insurance Life insurance Paid time off Professional development assistance Vision insurance Schedule: 10 hour shift 8 hour shift Monday to Friday Salary Description $18 - 27.00 / Hr

Essential Duties & Responsibilities: Evaluate setup and components submitted for 1st Piece approval using Component Process Specification (CPS) requirements Perform periodic inspection at the LRT (In-line Auditing) Provide feedback to operators and technicians on product acceptance or rejection Provide feedback to Production and Process Engineering regarding processing issues Inspections performed at processing workstations. Other inspection duties as assigned Requirements: Knowledge of Micross processes and component handling Familiar with inspection equipment such as microscopes, measurement tools Be detail oriented to ensure customer requirements have been met Ability to follow work instructions Maintain proper documentation on traveler and electronic data entry Good communication skills Customer focus Benefits: Medical, Dental, and Vision 401k Company Paid Basic Life Insurance, STD, and LTD Vacation Time Sick Time Holidays Tuition Reimbursement Pet Insurance Legal Insurance offered through Allstate Critical Illness, Hospitalization and Accident Insurance offered through Allstate

Job Description As a Quality Control Associate, you will test, weigh, measure, and inspect products for defects and deviations from stated specifications. You must be a quick learner and possess a proven ability to work in a fast-paced environment. Essential Functions: Able to read instructions or specifications and perform basic mathematical calculations accurately perform time-sensitive duties utilizing a pH meter, thermometer, viscometer, and moisture analyzer Perform all product testing and verification with accuracy including Net Content, Metal Detectors, Check-Weigher Systems, Goodway, Vacuum Leaker, Residual Gas, etc. in accordance with SOPs Adhere to all GMP, PPE, safety procedures, and protocols Complete and verify all records with accuracy and timeliness Possess strong communication skills, able to: communicate, understand, and follow written and verbal directions in English Exhibit good judgment and possess the ability to make quick decisions frequently. Taste food products which may include, nuts, soy, wheat, and other allergens to ensure quality meets product specifications occasionally Other duties as assigned Report to work as scheduled Essential Functions: Able to work in variable temperatures between 34 - 55OF throughout the shift Exposure to water/dampness, moving vehicles and machinery, and noise throughout the shift Able to lift and carry up to 10 pounds frequently Able to stand and/or walk continuously throughout shift on the concrete floor Able to ascend and descend stairs, ladders, and platforms occasionally Able to bend, twist, raise and lower arms, grasp frequently Able to distinguish and identify colors accurately Have close visual acuity to perform close activities such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; inspection involving small product defects and print; using measurement devices at distances close to the eyes. Education and Experience Associated degree preferred or equivalent experience Quality inspection, auditing, and testing experience Experience with the implementation of corrective action programs Strong computer skills Knowledge of tools, concepts, and methodologies of QA Knowledge of relevant regulatory requirements THIS POSITION DESCRIPTION IS INTENDED TO BE A SUMMARY ONLY AND IS NOT AN EXHAUSTIVE LIST OF ALL RESPONSIBILITIES, SKILLS, OR EFFORTS. Cedar's Foods, Cedar's Distribution, and International Bakers Company is an Equal Opportunity employer M/F/Veteran/Disability. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, disability, protected veteran status, or any other category protected under federal, state, or local laws.

Quality Inspector I Full-time RegularHourlyDevens, MA, US11 days ago Requisition ID: 3701Apply About Us: SMC, Ltd. is a globally recognized premium supplier to the medical market with locations throughout the world. People committed to speed, technology, and exceptional performance are the cornerstone of our organization. Comprised of dedicated people and decades of manufacturing experience, we have continued to experience strong growth and currently have outstanding career opportunities for equally dedicated people. Job Summary: Monitors the daily in-process production by performing visual, dimensional and functional inspections. Essential Job Duties and Responsibilities: Perform visual, dimensional and functional inspections in accordance with In-Process inspection procedures and documents in Control plan as required Dimensionally inspect product utilizing various measuring devices, such as calipers, micrometers, vision systems Document inspection data on appropriate records. Utilize computer to record statistical data Able to use day to day gaging used in QA Lab Able to recognize defects on the molded/assembled parts Able to read and follow requirements on a control plan Regular attendance, punctuality and professionalism Essential Qualifications: Follow procedures for retaining samples Notify Supervisor/Lead of any non-conformances. Follow procedures for product rejections Maintain cleanliness of work areas and Quality Control equipment Generate Labels for daily production retains/tailgates at the start of each shift Responsible for supervising the rework of nonconforming product in the hold area and performing final inspection on reworked product if instructed Maintain quality areas clean, neat and organized Other duties as assigned Ability to read, write and communicate in English Minimum 1-3 years prior experience in Quality Control Recommended 1-year experience in Plastic Injection Molding Environment Experience with precision measuring equipment Blueprint Interpretation skills. Must have computer skills and familiarity with Word and Excel programs Knowledge of SPC and ISO 9001 & 13485 system requirements Ability to pay close attention to detail Ability to work well with others and independently. Ability to read, write and communicate in English ADA Requirements: Stand, walk, bend, squat, twist, reach or otherwise move frequently Occasional repetitive motion and grasping Occasional climbing to reach areas on machines or racks Lift, move or otherwise transfer up to 50 lbs. occasionally, >20 lbs. frequently Typically sits, grasps items or performs keyboarding for occasional operation of a computer Exposure to typical machine shop physical hazards which may require respiratory protection At SMC Ltd. we recognize that people come with a wealth of experience and talent beyond just the technical requirements of a job. If your experience is close to what you see listed here, please still consider applying. We know that our differences often can bring about innovation, excellence and meaningful worktherefore, people from all backgrounds are encouraged to apply to our positions. Please let us know if you require reasonable accommodations during the interview process. SMC Ltd. is an equal opportunity employer. M/F/D/V; this organization uses E-Verify. Applicants may be subject to pre-employment screening which may include drug screening, reference checks, employment verifications, background screening and/or skills assessments.

SES AI Corp. (NYSE: SES) is dedicated to accelerating the world's energy transition through groundbreaking material discovery and advanced battery management. We are at the forefront of revolutionizing battery creation, pioneering the integration of cutting-edge machine learning into our research and development. Our AI-enhanced, high-energy-density and high-power-density Li-Metal and Li-ion batteries are unique; they are the first in the world to utilize electrolyte materials discovered by AI. This powerful combination of "AI for science" and material engineering enables batteries that can be used across various applications, including transportation (land and air), energy storage, robotics, and drones. To learn more about us, please visit: ********** What We Offer: A highly competitive salary and robust benefits package, including comprehensive health coverage and an attractive equity/stock options program within our NYSE-listed company. The opportunity to contribute directly to a meaningful scientific project-accelerating the global energy transition-with a clear and broad public impact. Work in a dynamic, collaborative, and innovative environment at the intersection of AI and material science, driving the next generation of battery technology. Significant opportunities for professional growth and career development as you work alongside leading experts in AI, R&D, and engineering. Access to state-of-the-art facilities and proprietary technologies are used to discover and deploy AI-enhanced battery solutions. What we Need: The SES AI Prometheus team is seeking an exceptional Computational Materials & Molecular-Modeling Scientist to specialize in physics-based simulation, utilizing reactive force-field development and MD/DFT coupling. This role is critical for generating validated atomistic and mesoscale data that directly feeds our AI-driven materials discovery workflows. As a key scientist, you will bridge physics-based simulation with advanced AI methods, driving materials discovery through computational rigor. Essential Duties and Responsibilities: Advanced Simulation & Modeling Develop and apply advanced simulation techniques, specializing in Reactive Force Fields (ReaxFF) and MD/DFT coupling, to model complex materials phenomena. Conduct and analyze multi-scale computation projects, covering atomistic simulation up to mesoscale modeling. Utilize and maintain advanced simulation tools, including VASP, LAMMPS, GROMACS, and CP2K, for high-fidelity simulations. Perform rigorous physics-based validation on all simulation outputs to ensure accuracy and reliability. AI Data & Workflow Development Generate and validate high-quality atomistic and mesoscale datasets used for training ML potential and other scientific AI models. Develop advanced simulation workflows and contribute to the creation of ML potentials and AI-driven materials discovery tools. Coding & Collaboration Apply strong coding skills (e.g., Python, C++, FORTRAN) to automate complex simulation workflows and enhance computational efficiency. Maintain a solid understanding of battery chemistry modeling and collaborate effectively across computational and experimental teams. Education and/or Experience: Education: Ph.D. in Computational Chemistry of Energy Materials, Materials Science, or Computational Physics. Core Simulation Expertise: Deep, demonstrated expertise in advanced physics-based simulation, including proficiency with DFT, MD, and Quantum Mechanics (QM) simulation tools. Reactive Potentials: Proven experience with Reactive Force Fields (ReaxFF) and methods for MD/DFT coupling. Coding & Tools: Strong coding ability in languages such as Python, C++, or FORTRAN, and deep practical experience with simulation codes like VASP, LAMMPS, GROMACS, or CP2K. Domain Focus: Solid understanding of battery chemistry modeling and experience in generating and validating atomistic and mesoscale data. Preferred Qualifications: Machine Learning Integration: Experience with Neural Networks and Deep Learning, particularly in applying them to develop ML potential. Familiarity with geometric deep learning libraries like PyTorch Geometric is a plus. Multiscale Methods: Experience with specialized methods like the Materials-Point Method. Hybrid Literacy: Experience with experimental literacy, understanding characterization methods such as SEM, TEM, XPS, Raman, EIS, NMR, DSC, or TGA. Background: Previous experience at advanced simulation labs, battery multiscale modeling groups, or in the computational chemistry of energy materials.