Trabajos Science en MI

Job Description Day Shift-- Vehicle Emissions Lab. Chemist The Chemist will perform liquid chromatograph analysis (carbonyl analysis from vehicle exhaust) and perform gas chromatograph analysis (hydrocarbon speciation, fuel dilution in engine oil, etc.). The Chemists responsibilities include but are not limited to: • Conducting various fuel analysis (fuel composition, heating value, distillation points), • Managing fuel inventory and fuel ordering, • Perform maintenance and calibration on various instruments (all kinds of instruments in emissions lab, not limited to chemical instruments), • Support testing operation and trouble shoot instrument problems, • Bachelor's degree in Chemistry, • Minimum 3-5 years' experience in chemistry analysis with liquid chromatograph and gas chromatograph, • General understanding of vehicle powertrain and exhaust after treatment, • Experience with vehicle emissions testing and with conventional emission analyzers (HC, CO, CO2, NOx and CH4), • Team player with good communication skills, • Dedicated and well organized, • Master's degree in Chemistry

Job DescriptionGeneral Description The Senior Quality Control Chemist is responsible for assisting with the daily oversight and management of the Biovire laboratory. The Senior Quality Control Chemist excels at understanding, implementing, and improving current and future Quality Control workflows to ensure timely completion of Quality Control deliverables. The Senior Quality Control Chemist drives collaboration within the Quality Control department as well as interdepartmentally. The Senior Quality Control Chemist has experience with a wide array of laboratory instrumentation techniques including, but not limited to, High Performance Liquid Chromatography, Gas Chromatography, Mass Spectroscopy, Karl Fisher Analysis, Total Organic Carbon Analysis, Viscosity Analysis, and Titrimetric Analysis. DUTIES AND RESPONSIBILITIES Essential Duties and Responsibilities: 1. Perform laboratory testing in compliance with regulatory requirements and internal procedures., 2. Support root cause analysis determinations for deviations and laboratory investigations., 3. Assist with training and mentorship of Quality Control personnel., 4. Learn, create, and implement new systems and programs as business, industry, and regulatory expectations grow and evolve., 5. Assist with raw material and stability programs., 6. Practice appropriate safety and analytical standards of excellence within the shared Biovire laboratory., 7. Practice applicable laboratory inventory and housekeeping programs within the shared Biovire laboratory., 8. Assist with equipment onboarding, calibration, and preventative maintenance programs., 9. Perform peer review of laboratory data., 10. Support Business Development, as necessary., 11. Adhere to all Biovire policies including, but not limited to, Quality, Human Resources, and Environmental Health and Safety., 12. Other duties as required or assigned by management. Behavioral Expectations: 1. Strong work ethic and ability to accomplish tasks without supervision., 2. Demonstrate leadership both by words and leading by example to foster Biovire One Team culture., 3. Adhere to and follow all Company Policies and Procedures., 4. Excellent interpersonal skills with the ability to cooperate with others in a high-performance setting., 5. Basic computer skills (proficient in Microsoft Office applications)., 6. Strong mathematical and organizational skills., 7. Excellent English communication skills, both written and verbal., 8. Must possess honesty, integrity, and a commitment to the highest legal and ethical standards., 9. Ability to treat every person with courtesy and respect., 10. Demonstrate ownership and accountability to production schedule without compromising product quality., 11. Knowledge of fundamental cGMP and regulatory principles such as deviations and CAPA. Physical Expectations: 1. Frequent lifting, bending, stooping, squatting, pushing, and pulling., 2. Long periods of sitting and walking. Minimum of 6 years of experience using HPLC in a laboratory environment. Four-year degree in Chemistry, Biology, or a related Life Science. 2-4 years of method development experience is preferred. Working knowledge of standard software applications such as Chromatography Data Systems, Microsoft Office, and ERP. Working knowledge of Agilent OpenLab CDS or Agilent ChemStation is a plus. Employment at Bryllan (Biovire) is contingent upon a successful Background check.

Job Description Analytical Chemist – TSL For over 80 years, LECO has been a leader in the development and production of world class laboratory instruments delivering state of the art products nationwide and across the globe. Located in St. Joseph, Michigan, LECO continues to be a family-owned company that understands the value of shared interests, long-term stability, loyalty, and trust. Schedule: Full Time: 8:00am – 5:00pm, Monday – Friday Position Summary: Analytical chemist performing analysis on a wide variety of samples using LECO instrumentation. Chemist will also provide support to existing customers as well as to the LECO sales team working with new and prospective customers. Position Responsibilities: The responsibilities and authority of this position may vary, as functions are delegated by the Laboratory Direction. The specific duties include: • Log, print, and file sales and customer service reports as required, • Review reports for compliance with department requirements, • Data entry and effective input to the Laboratory Information Management System (LIMS), • Follow company procedures; recommend solutions to quality problems through supervisor, • Operate, calibrate, and maintain a variety of analytical instruments as needed, • Develop and write Application Notes for LECO instruments, • Compile and review analytical data, • Develop analytical procedures and documents, • Prepare detailed sample analysis reports, • Perform quality control analysis as needed, • Analyze a variety of sample materials for various elements following the procedures outlined in the department manual as required, • Present scientific work to a broad audience in a variety of formats including webinars and scientific conferences/meetings, • Assist customers with application related questions and basic troubleshooting, • Evaluate new LECO products and provide feedback to Research & Development, • Maintain a laboratory notebook, • Provide hands on training to new employees and the LECO sales team Position Requirements: • Ability to work with a variety of software programs including MS Office, LECO Instrumentation software and the LIMS system, • Willingness to work in a team environment and multitask various job responsibilities, • Must possess excellent written and verbal communication skills Education/Certifications: • Bachelor’s Degree in Chemistry EOE M/F/VET/Disability

Location: Auburn Hills, MI Pay: $37/hr Day Shift-- Vehicle Emissions Lab. Chemist The Chemist will perform liquid chromatograph analysis (carbonyl analysis from vehicle exhaust) and perform gas chromatograph analysis (hydrocarbon speciation, fuel dilution in engine oil, etc.). The Chemists responsibilities include but are not limited to: • Conducting various fuel analysis (fuel composition, heating value, distillation points), • Managing fuel inventory and fuel ordering, • Perform maintenance and calibration on various instruments (all kinds of instruments in emissions lab, not limited to chemical instruments), • Support testing operation and trouble shoot instrument problems, • Develop new chemical analysis when there are new emissions testing needs Requirements: • Bachelor's degree in Chemistry, • Minimum 3-5 years' experience in chemistry analysis with liquid chromatograph and gas chromatograph, • General understanding of vehicle powertrain and exhaust after treatment, • Experience with vehicle emissions testing and with conventional emission analyzers (HC, CO, CO2, NOx and CH4), • Team player with good communication skills, • Dedicated and well organized Preferred Requirements: • Master's degree in Chemistry

Position Overview: Lead Chemist We are seeking an experienced Lead Chemist to join our laboratory team. This position is critical within our cGMP manufacturing facility, where you will play a key role in ensuring the quality and reliability of our pharmaceutical products. The Lead Chemist will not only conduct advanced analytical testing but will also lead method development and validation efforts, as well as oversee laboratory operations to maintain compliance with regulatory standards. In this role, you will have the opportunity to implement and uphold best practices in analytical chemistry, contribute to continuous improvement initiatives, and mentor junior laboratory staff. As a leader within the laboratory, you will be expected to collaborate closely with other departments, including production and quality assurance, to forecast analytical needs and ensure timely delivery of results that meet both production schedules and regulatory requirements. Qualifications: ● Minimum of a Bachelor’s Degree in Chemistry or a closely related discipline. ● 5+ years of experience in a cGMP/cGLP environment. Important Skills and Competencies: ● Analytical Proficiency • Extensive experience with chromatographic techniques such as High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC)., • Strong understanding of spectroscopic techniques, including Ultraviolet (UV) and Infrared (IR) spectroscopy., • Ability to perform Total Organic Carbon (TOC) analysis, particularly in the context of cleaning validation. ● Method Development and Validation • Expertise in developing robust analytical methods tailored to specific product requirements., • Proven experience in validating analytical methods in accordance with regulatory guidelines to ensure accuracy, precision, and reproducibility., • Knowledge of statistical analysis tools for data interpretation and method optimization. ● Instrumentation Skills • Familiarity with a range of laboratory instrumentation, including troubleshooting, calibration, and routine maintenance., • Ability to assess and improve instrument performance, ensuring adherence to operational standards. ● Regulatory Knowledge • In-depth understanding of cGMP and cGLP regulations as they pertain to laboratory operations., • Experience with regulatory audits and the ability to maintain compliance documentation. ● Problem Solving and Critical Thinking • Strong analytical and problem-solving skills to identify root causes of issues, particularly during Out Of Specification (OOS) and Non-Conforming Material Reports (NCMR)., • Capability to devise and implement corrective and preventive actions based on investigation outcomes. ● Leadership and Team Collaboration • Proven leadership skills to effectively manage and mentor laboratory personnel, fostering a culture of continuous learning and improvement. - Ability to communicate clearly and effectively across departments to ensure alignment on analytical needs and priorities. ● Project Management • Strong organizational skills to prioritize multiple laboratory analyses, balancing production demands with regulatory requirements., • Experience in project management principles to oversee method validation and laboratory initiatives. ● Interpersonal Skills: • Excellent communication skills to convey complex scientific information to both technical and non-technical stakeholders., • Ability to foster a collaborative team environment that emphasizes mutual respect and accountability. ● Continuous Improvement Mindset: • A proactive approach to identifying areas for improvement within laboratory processes and methodologies., • Commitment to staying current with advancements in analytical chemistry techniques and regulatory changes. Full-Time Benefits: ● Comprehensive Dental, Health, and Vision Insurance. ● Paid Time Off and Holidays. ● 401(k) Plan with limited matching.

Why Endo? We want the best and brightest people at Endo to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life. Job Description Summary The Chemist III, under minimal supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability & finished products, and testing to support process validation. Has demonstrated competence in conducting all types of physical & chemical analyses (including complex analyses) using all equipment. Detects, conducts, and reports on OOS/OOT/NOE and other investigations. Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing. Participates in troubleshooting analyses and instrumentation. Trains less senior staff. Job Description Scope of Authority - span of control (work unit, site, department, division, etc.), monetary value of budget/spend authority ( capital, operating, etc.), P&L responsibility, etc. Typically supports one Par business, at a single site Key Accountabilities - key outcomes/deliverables, the major responsibilities, and % of time Accountability Responsibilities % of Time Analysis & Testing • Conducts laboratory analyses according to approved test methods: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing. Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Uses laboratory software for analyses, • Reviews and approves laboratory test data and documentation for completeness and compliance, • Is alert to and detects abnormalities during performances of tests and reviews. Elevates abnormalities to Supervisor Lab Equipment • Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping, • Cleans lab working surfaces and dispose of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals Investigations • Detects, conducts and reports on OOS/OOT/NOE and other investigations, • Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor and recommends a course of action Training • Maintains assigned training records current and in-compliance Compliance • Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting, • Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs Safety • Follows EH&S procedures to ensure a safe work environment Total 100% Qualifications Education & Experience Minimal acceptable level of education, work experience and certifications required for the job • Bachelor of Science Degree in chemistry, chemical engineering or related field with 4+ years’ relevant analytical laboratory experience OR, • Master’s Degree in above disciplines with 2+ years’ relevant analytical lab experience Knowledge Proficiency in a body of information required for the job e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. • Has strong knowledge of laboratory software and has expanded knowledge of chromatographic software (e.g. Waters Empower, Agilent ChemStation and Sotax WinSotax), using custom fields, custom calculations and custom reports, • Full proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc., • Thorough knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS, • Has demonstrated competence in conducting chemical analyses, • Strong knowledge of wet chemistry techniques & Abilities Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc. • Ability to critically review, analyze data, interpret information, and draw conclusions from relevant or missing information, • Ability to display and analyze data in a logical manner, • Strong verbal and written communication skills as well as good computer skills, • Strong attention to details and accurate record keeping, • Establish and maintain cooperative working relationships with others, • Solid organizational skills, • Ability to coach less senior staff and develop laboratory skills and ability Physical & mental requirements e.g. lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc. • Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals, • Must occasionally lift and/or move up to 15-25 lbs., • Ability to wear personal protective equipment, including respirators, gloves, etc., • Specific visions abilities are required by this job include close vision and color vision, • Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods 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. EEO Statement: At Endo, we firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.

Job Description Demo Applications Chemist – Separation Science For over 85 years, LECO has been a leader in the development and production of world class laboratory instruments delivering state of the art products nationwide and across the globe. Located in St. Joseph, Michigan, LECO continues to be a family-owned company that understands the value of shared interests, long-term stability, loyalty, and trust. Schedule: This full-time demo applications chemist position is located at LECO headquarters in St. Joseph, MI. This position requires relocation due to the requirement to be onsite daily. Full Time: 8:00am – 5:00pm, Monday - Friday Position Summary: This role reports directly to the Domestic Separation Science Applications Director. The role of the separation science demo applications chemist includes, but is not limited to: providing instrumentation demos for prospective customers across LECO’s GC and GCxGC product lines, assisting applications team by generating data for developing new applications for these product lines, and providing technical support to the separation science sales team. Position Responsibilities: This role reports directly to the Domestic Separation Science Applications Director and will work closely with the USA separation science sales and applications teams. Specific responsibilities will include: • Providing sales-related product demonstrations for prospective customers of LECO GC-MS, GCxGC-FID, and GCxGC-MS instrumentation. This involves working closely with sales to determine customer needs prior to quotation/sale of the instrument and will also typically involve analysis of customer samples to demonstrate instrument performance., • Working closely with the USA applications team to develop a working knowledge of our core markets (petrochemical, flavors/aroma, environmental, metabolomics, food safety, and pharmaceuticals)., • Assist applications team with creation of content to support core markets., • Hands-on experience with GCxGC, and/or High Resolution Mass Spectrometry a plus, • Strong written, verbal communication, and presentation skills are a must., • Experience with direct customer interaction, • Desire to function in a customer-service oriented, team environment, • Desire for continuous learning through team interactions as well as independent self-education on diverse scientific instrumentation-related topics, • BS Degree in chemistry or related field

Job Description Summary The Field Service Chemist is responsible for ensuring the safe pick- up and transport of waste to and from customer facilities. Utilizing education and experience, this position serves as a subject matter expert with regard to profiling and packaging of chemical waste according to standard categories. Essential Duties and Responsibilities include the following. Other duties may be assigned. • Drives straight truck to and from customer locations., • Prepares driving log according to state and federal regulations., • Sorts and identifies hazardous and nonhazardous waste according to waste profiles., • Packages, labels and manifests waste., • Performs computer entry and inventory management., • Maintains telephone or radio contact with supervisor to receive pick up instructions., • Loads and transfers containers of hazardous and nonhazardous waste on and off truck., • Inspects truck equipment and supplies such as tires, lights, brakes, gas, oil, and water., • Secures waste for transit., • Assists in training new Field Service Chemists, • Some overnight travel

Job DescriptionCompany Description Clean Earth is a leading provider of environmental services in the United States providing remediation, disposal, recycling, and beneficial reuse solutions for hazardous and non-hazardous waste, contaminated soil, and dredged material. Our vast portfolio of technologies and services touches nearly every industry that generates waste including energy, infrastructure, commercial, industrial, retail, and healthcare markets. Every day our teams across the country take a hands-on, dedicated approach to recycling and beneficially reusing waste that would otherwise go into landfills. We value our employees as our most important asset, and this is reflected in many areas across our company including recently being named a 2024 Most Loved Workplace ®. We are committed to creating a positive work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, we also offer: • Health benefits available Day 1, • 401k available Day 1, • 10+ paid holidays/year, • Free HAZWOPER training and certification, • Overtime opportunities, • Ability to be cross-trained into different roles Job Description Performs various assigned tasks and physical labor to ensure proper off-site treatment and disposal of customers’ hazardous waste materials in accordance with environmentally responsible and cost-effective practices and Clean Earth policies, practices, and procedures. The ability to oversee a small project/job with supervision of personnel. Primary Responsibilities (Essential Functions): • Handles hazardous materials including inventorying, identifying, segregating, and packaging waste material in accordance with Lab Pack policies, procedures and practices and all applicable regulations., • Perform onsite services which may include waste collection, consolidation (i.e., bulking, repackaging), sampling, safety/compliance inspections, and other related activities required by the customer/contract., • Assists other business groups, i.e., Depack, Retail and HHW, for both internally and onsite as needed., • Preparing shipment of packaged waste by inspecting, labeling, marking, and loading into the transport vehicle, • Properly completes documentation including shipping papers, Land Disposal Restrictions (LDR’s), evaluations/certifications and other required documentation in accordance with appropriate regulations and procedures., • Maintain a Commercial Driver’s License (CDL) with Hazmat Endorsement to legally operate Clean Earth vehicles necessary for transporting personnel and waste to and from customers’ job locations., • Follows, understands, and promotes by example, all Health & Safety /Job Safety Analysis (JSA’s) procedures including development of on-site Health &Safety plans/JSA’s as outlined in the procedures and policies., • Perform unknown field testing for classification and packaging for transportation and disposal., • Mentor and assist new employees in field work duties., • Complete site walks to inventory and assess requirements for potential and awarded work., • Assist sales in creating estimates for lab pack work., • Performs other duties as assigned., • Associate College degree in area of General Science or equivalent experience, • Commercial Driver’s License (CDL) with Hazardous Material endorsement and a clear record, • Moderate to extensive travel with 20% overnight travel, • Physical ability to lift and move material of various weights frequently exceeding 55 lbs., • Basic understanding of chemistry through general chemistry or biology, • Advanced knowledge of EPA and DOT, • Minimum one (1) year lab pack experience  40-hour OSHA HAZWOPER (29 CFR 1910.120), • 40 hours Depack Experience, • 8 hours DOT Training, • PPE Training which includes Respirators Preferred Qualifications: EDUCATION/CREDENTIALS: • BS/BA in science related field. MEASURES OF PERFORMANCE:  Completion of the following curriculum: • Clean Earth Lab Pack I Training – (24 hours), • RCRA/DOT refresher course, • Department of Transportation, • Lab Pack definitions and procedures, • Lab pack Field Program, • Introduction to High Hazardous Cylinder Assessment course, • Customer Interactions, • Waste Management Methods, • On-Site Expectations, • Manifest/ LDR Completion • Health & Safety course(s), • Customer Approach • Forklift Training, • Local Facility Capabilities, • CPR/First Aid/Blood-borne Pathogen training, • State regulations (if applicable), • All required local training DEMONSTRATED KNOWLEDGE, SKILLS, AND ABILITIES: • Strong communication skills to interact with customer to provide information, explanations, and/or instructions, • Team Player • Attention to detail, • Ability to work independently using initiative and effective communication to solve challenges., • Demonstrate proficiency to operate a computer with Windows based programs (i.e., Microsoft excel and word), • Demonstrates extensive Lab Pack knowledge (i.e., US EPA, DOT, and chemical properties) WORKING ENVIRONMENT: • Customer sites, plant, labs, • Indoor/Outdoor and associated weather conditions Additional Information Clean Earth offers competitive benefits including health, dental, vision, life, and disability insurance plans starting on the first day of employment; paid time off, wellness benefits, employee discount program, tuition assistance, and a 401k with company matching. We provide equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, veteran status, gender identity, or genetics. 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. If you have a difficulty applying for any job posted on Harsco Clean Earth’s website because a disability prevents you from using the online system, Clean Earth offers the following alternate application procedure: Call toll free (833) 209-2659 and leave your name, phone number, city and state of residence. Clean Earth will arrange for an alternate method of applying and will consider your application together with all other applications received for the job. This line is dedicated to disability applications only. No other inquiries will receive a response.

Job DescriptionThe Chemist will perform liquid chromatograph analysis (carbonyl analysis from vehicle exhaust) and perform gas chromatograph analysis (hydrocarbon speciation, fuel dilution in engine oil, etc.). The Chemists' responsibilities include but are not limited to: • Conducting various fuel analysis (fuel composition, heating value, distillation points), • Managing fuel inventory and fuel ordering, • Perform maintenance and calibration on various instruments (all kinds of instruments in emissions lab, not limited to chemical instruments), • Support testing operation and trouble shoot instrument problems, • Develop new chemical analysis when there are new emissions testing needs * Requirements * Requirements: -Bachelor's degree in Chemistry -Minimum three years' lab experience -General understanding of vehicle powertrain and exhaust after treatment -Experience with vehicle emissions testing and with conventional emission analyzers (HC, CO, CO2, NOx and CH4) -Team player with good communication skills Dedicated and well organized * * Preferred Requirements: -Master's degree in Chemistr

Job Description Position Overview: The Senior Vinyl Chemist is responsible for developing, formulating, and testing materials used in the manufacture of self-adhesive cast vinyl products targeting various applications, such as signage, vehicle wraps, and specialized coatings. This role involves designing and optimizing vinyl formulations, adhesives and coatings to meet performance, durability, and aesthetic requirements while ensuring compliance with industry standards and environmental regulations. The successful candidate will be a proactive leader that collaborates with cross-functional teams, including production, quality control, and sales/marketing, to innovate and optimize product performance. Key Responsibilities: • Formulation Development: Design and develop cast vinyl formulations, including polymers, plasticizers, stabilizers, and additives, to achieve desired properties such as flexibility, adhesion, UV resistance, and color stability., • Testing and Analysis: Conduct laboratory tests to evaluate the physical, chemical, and mechanical properties of vinyl materials, including tensile strength, elongation, and weatherability., • Process Optimization: Collaborate with manufacturing teams to optimize casting processes, ensuring consistent product quality and scalability., • Quality Control: Develop and implement quality assurance protocols to ensure products meet customer specifications and industry standards (e.g., ASTM, ISO)., • Research and Innovation: Stay updated on advancements in polymer chemistry and vinyl technology to innovate new products or improve existing formulations., • Regulatory Compliance: Ensure formulations comply with environmental, health, and safety regulations, such as REACH, RoHS, and Environmental standards., • Troubleshooting: Investigate and resolve issues related to product performance, manufacturing defects, or customer complaints., • Documentation: Maintain detailed records of formulations, test results, and process parameters; prepare technical reports and presentations for internal and external stakeholders., • Collaboration: Work with cross-functional teams, including product managers, engineers, and sales teams, to align formulations with market needs and customer requirements. Qualifications: Education: Bachelor’s or master’s degree in chemistry, Polymer Science, or a related field. Experience: 5+ years of experience in polymer chemistry, preferably with vinyl or related materials. Experience with cast vinyl production is a plus. Skills: • Strong knowledge of polymer chemistry, formulation techniques (DOE), material science and statistical analysis of experimental metrics., • Proficiency in physical testing and analytical techniques., • Familiarity with casting processes and equipment., • Problem-solving skills and attention to detail. Software: Proficiency in laboratory information management systems (LIMS) and data analysis tools (e.g., Excel, Minitab). Work Environment: Primarily laboratory-based with occasional work in manufacturing facilities. May require handling of chemicals and adherence to safety protocols. Full-time position with occasional travel for supplier meetings or customer support.

Job Description The Methods Development Chemist ensures the establishment and continual improvement of analytical test methods required to verify the quality, safety, and efficacy of all products produced by Tower Laboratories. The position directly supports all Quality Control equipment and personnel by providing technical expertise in the acquisition, troubleshooting, and proper use of all instrumentation and analytical apparatus, through the establishment and review of Standard Operating Procedures. The position supports Quality Assurance in the investigation and resolution of quality concerns related to Quality Control testing identified from internal and external audits, or non-conformances. Ideal candidate will be proficient in developing and validating new analytical methods with minimal supervision, as well as performing all phases of chemical testing of raw materials, in-process samples, and finished products for full integration and support of Tower Laboratories’ business and operations. This position may be based either in our Centerbrook, CT or Montague, MI facilities. Essential Functions: • In collaboration with the QC department, Develop and conduct validation studies for all test methods for all products as applicable., • Support the implementation of new testing strategies and methods to improve accuracy, cost-effectiveness, and productivity., • Adhere to the Method validation master plan when developing new validation studies., • Report all observations and data promptly, meeting specified deadlines., • Adhere to cGMP, Good Laboratory Practices, and all quality and safety requirements while maintaining an orderly working environment., • Support and assist in investigations, audits, and customer concerns regarding analytical data as needed., • Assist in the creation, review, and approval of Tower’s various QC and technical documents regarding SOPs, validations, operations, and other QC/R&D studies as needed., • Minimum 3 yrs. of proven success in developing and writing procedures and methodology and performing methods development and validation., • Experience/knowledge in identifying, sourcing, and coordinating implementation of appropriate analytical instrumentation as part of the method development process., • Excellent analytical and wet chemical techniques in support of chemical and manufacturing operations;, • Demonstrated proficiency with HPLC, • Demonstrated self-starter and independent worker with strong commitment to Quality and Compliance., • Strong writing skills, • Good interpersonal skills; ability to communicate effectively with all levels of plant personnel., • Strong team player, demonstrated team attitude and behaviors. This medium sized company offers a friendly, dynamic working environment with a competitive benefit package including 401(k) with company match. Tower Labs is a Socially Responsible employer and a great place to work! Apply and start the conversation today!

Job DescriptionJob Title: Analytical Chemist Job Description We are seeking an analytical chemist to lead client projects, develop testing methods, and guide a team in executing these methods. The role involves working with Chromatography, Mass-Spectrometry, and ICP-MS technologies, primarily focusing on method development rather than conducting tests. You will present methods to both the team and clients, and occasionally to the quality team, to justify the chosen approaches. While not directly managing other chemists, you will provide them with tasks and have opportunities for training and development. Responsibilities • Qualify projects with clients and develop testing methods., • Guide the team in executing developed methods., • Present methods to the team and clients, and justify them to the quality team., • Write work instructions from a method level on client projects., • Communicate complex technical information to non-technical stakeholders.Essential Skills, • Strong background in analytical chemistry., • Proficiency in Chromatography, Mass-Spectrometry, and ICP-MS., • Experience with method validation and development., • Minimum of a BS in Chemistry., • Ability to follow GMP processes., • Five years of experience in a QA or QC lab., • Excellent communication skills with clients and team members.Additional Skills & Qualifications, • Experience with lab equipment maintenance or validation is advantageous., • Advanced degrees such as a Master's or PhD are considered but not required., • Strong report writing skills.Work Environment The role is based in a cGMP site, though not within a Quality Control Lab. The analytical team consists of 6-8 chemists working in a stand-alone building. The position follows a standard Monday to Friday first-shift schedule with flexible hours. The environment encourages innovation and offers the chance to work on new pharmaceutical products. Pay and Benefits The pay range for this position is $30.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision, • Critical Illness, Accident, and Hospital, • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available, • Life Insurance (Voluntary Life & AD&D for the employee and dependents), • Short and long-term disability, • Health Spending Account (HSA), • Transportation benefits, • Employee Assistance Program, • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in South Haven,MI. Application Deadline This position is anticipated to close on Sep 25, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.