Quality control analyst jobs in Jackson, TN

Who are we? At Scalian, we are a leading multinational engineering consulting firm with 5,500 specialists and over 30 years of experience. We are specialized in Industrial Performance (Quality Assurance, Supply Chain, and Project Management) and Digital Systems (IT & Software and Systems Engineering). Our expertise serves various technological sectors such as the aerospace, defense, rail, and energy industries while providing distinctive support to their development and operations. Are you an experienced Quality Controller? If your answer is yes, it's your lucky day as we are looking for a dynamic and talented person to join our team in the US! What will your role be? As a Quality Controller, you'll play a vital role in ensuring products, components, and processes conform to established quality and regulatory standards. This position is heavily focused on hands-on product control work, documentation accuracy, and clear communication across teams. You will be responsible for ensuring detailed inspections, identifying nonconformities, issuing corrective action reports, and ensuring compliance with technical requirements. Activities: Identify, document, and classify nonconformities; generate Nonconformance Reports (NCRs) with clear, detailed descriptions Create and issue Corrective Action Requests (CARs), ensuring problem statements are accurate and actionable Collaborate with internal teams to support root cause analysis and ensure corrective actions are implemented effectively Maintain accurate inspection records, traceability documentation, and quality logs Communicate inspection results, quality issues, and required corrective actions clearly to production, engineering, and supplier teams Verify compliance with customer specifications, regulatory requirements, and internal quality procedures Support audits and process verification activities as needed Escalate significant quality risks promptly and participate in establishing containment measures Be adaptable to additional inspection-related tasks or changes driven by business needs What skills and qualifications are we looking for? Associate degree or certification required, preferably in Quality Assurance, Manufacturing, or a technical field Inspection Authorization (IA) holder strongly preferred Minimum of 3 years' experience in Quality in a manufacturing, aerospace, or similar regulated industry Strong understanding of inspection methods, measurement tools, and quality documentation practices Ability to write clear, accurate NCRs and corrective action documentation Excellent communication skills with the ability to convey inspection findings and requirements effectively Flexibility, strong attention to detail, and initiative to drive effective quality solutions Work environment typically quiet with occasional moderate noise levels Why join us? To acquire experience in different critical industries and projects while working for the same company; To have a competitive salary and a great benefits package To access trainings that focus on expanding your knowledge while staying up to date with cutting edge technologies and best practices; To have a clear career development plan that suits your goals; To have the possibility of working abroad through our mobility program thanks to our international presence; To join a dynamic, specialized and fast-growing group where communication is key and where every team member is valued. To be part of a team where having fun is essential.

Randstad (Recruiting for a Top Global Client) | Thompsons' Station, TN (Onsite) Role Details Job Title: Microbiology Analyst Duration: 6-month contract (Temp, with potential for full-time conversion Pay: 27.00 per hour Schedule: Must be able to work the required schedule: Tuesday-Saturday, 8:30 AM-5:00 PM. Inability to work weekends is a deal breaker. The Opportunity: What You'll Do You will be a key member of a 10-person lab team, contributing to critical product hold and release testing. Your main focus in the first 90 days will be completing training on sample preparation and petrifilm methods. Perform critical testing to ensure product quality and compliance. Work closely with other analysts and the line manager. Be a reliable, positive, and collaborative team player. Required Qualifications (Deal Breakers) Candidates who cannot meet these mandatory requirements will be automatically disqualified: Education: Associate of Science or Bachelor of Science in Biology, Chemistry, or a related field. Experience: 1-2 years in a laboratory environment. Physical: Must be able to lift 30 lbs. Preferred Skills That Will Make You Stand Out We're looking for someone with practical and theoretical knowledge of lab science: Microbiology Expertise: Experienced in PCR technologies, cultural plating methods, petrifilm use, and anaerobic plating methods. Quality Systems: Practical and theoretical knowledge of ISO 17025. Lab Operations: Knowledge of aseptic technique and cross-contamination management/mitigation in laboratories. Technical Tools: Experience and skill in using computers, spreadsheets (Excel), Word, ELN, and laboratory information management systems (LIMS). Soft Skills: Must be a strong communicator, detail oriented, a self-starter, and comfortable with ambiguity and change.

Work Your Magic with us! Start your next chapter and join MilliporeSigma. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role At MilliporeSigma, the Associate Production Scientist - Night Shift at our 3300 South Second/Cherokee site will be responsible for the large-scale manufacturing of Life Science products. This role involves utilizing standard organic chemistry processes to ensure the efficient and effective production of high-quality products. Job duties include: * Production shifts consist of 12-hour shifts (6 PM - 6:30 AM) with a two-week rotation: Week 1 (Monday, Tuesday, Friday, Saturday) and Week 2 (Sunday, Wednesday, Thursday) * Take the necessary action to maintain a safe working environment. * Carry out production operations and communicate status to Manufacturing Supervision. * Provide technical leadership during the manufacturing process. * Ensure cleaning protocols are followed and recorded. * Prepare production areas, chemicals, and equipment for operations. * Conduct analytical tests and assess results during production. * Advise chemical processors on key in-process decisions based on test results. * Write and revise Master Manufacturing Procedures. * Prepare and review Operating Procedures to ensure compliance. * Participate in quality audits. * Provide complete and accurate records consistent with quality guidelines. * Provide technical support and training to personnel as well as cross-functional teams. Physical Attributes: * Lift, push pull, or move up to 55 pounds while wearing personal protective equipment, including respirators, for an extended time. Also able to move 300+ pounds with mechanical or team member assistance. * Perform tasks while wearing personal protective equipment, such as respirators or chemical protective clothing, for long durations. * Walk, reach above shoulders, stoop, kneel, twist, crouch, and/or stand and perform repetitive movements for extended periods of time. * Ability to talk, hear, taste and smell. Specific vision requirements of this job include close vision, distance vision, color vision, peripheral vision, depth vision, and the ability to adjust focus. Who you are: Minimum Qualifications: * Bachelor's degree in Chemistry, Biochemistry, Chemical Engineering or other scientific discipline OR * Associate Degree in Chemistry, Biochemistry, Chemical Engineering or other scientific discipline with 5 + years large scale chemical manufacturing experience Preferred Qualifications: * 1+ year production experience. * Detail oriented with excellent organizational, written, and verbal communication skills. * Logical approach to problem solving. * Experience with customer interaction. * Knowledge of Process Improvement methodology (e.g., PDSA, Lean Manufacturing, and/or Six Sigma). Pay Range for this position: $24.00 - $41.00. The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

The Mississippi State Chemical Laboratory (MSCL) is searching for an advanced laboratory analytical level analyst that performs highly technical and advanced scientific and/or instrumental analysis procedures in a specialized area, utilizing both standard and non-routine methodologies and procedures. This analyst will conduct analyses that rely on advanced instrumentation and complex computer software and develop and implement complex analytical techniques. This position is distinguished from the Laboratory Analyst II by the independent and self-directed nature of the work and by its required advanced knowledge in areas of inorganic chemistry, organic chemistry, or microbiology. Salary Grade: 13 Please see Staff Compensation Structure or Skilled Crafts and Service Maintenance Compensation Schedule for salary ranges. For salary grade UC, these positions are "Unclassified" and salary ranges are determined by the hiring department. Department Profile: The Mississippi State Chemical Laboratory (MSCL) is a state-appropriated regulatory agency for the State of Mississippi as well as a fee-for-service laboratory located on the campus of Mississippi State University. MSCL is dedicated to ensuring the quality and safety of fertilizers, pesticides, animal feeds, petroleum products, and manufactured and retail food. It provides fast, defensible, and reliable analytical data to: 1. The State's regulatory agencies, including MDAC Bureau of Plant Industry. 2. The State's federations and councils, such as the MS Farm Bureau and Delta Council. 3. The State's industries, including Poultry, Catfish, and Manufacturing. 4. The State's citizens. The MSCL adheres to the highest professional standards and provides quality analytical services in a timely manner. Essential Duties and Responsibilities: 1. Performs advanced scientific and/or instrumental analyses exercising independent judgment in data interpretation and evaluation of compliance with regulatory requirements as promulgated by federal agencies, state agencies, and other regulatory bodies. Advanced-level analytical techniques could include: GC, GC/MS, LC, HPLC, ICP, ICP/MS, microscopic, microbiological and/or other analyses as appropriate. 2. Provides technical expertise for all aspects of environmental analyses in a specialized area; where applicable, researches special environmental/analytical problems and writes reports of findings; participates in interdepartmental meetings on a range of specialized technical and/or scientific subjects as needed. 3. Develops, implements, and maintains appropriate QA/QC controls and procedures. Integrates technical knowledge of regulatory requirements and applicable standards into all laboratory practices and procedures in a specialized area. Manages special projects and assignments related to assigned specialized area. 4. Participates in proficiency studies to demonstrate analytical competency, to examine and investigate problematic areas, and to research and develop improved preparatory and/or analytical techniques. 5. Gathers, evaluates, and interprets analytical and environmental data to determine regulatory compliance, ambient conditions, and process control trending. 6. Troubleshoots and maintains sophisticated analytical instrumentation, performing day-to-day routine care and more complex periodic maintenance, as well as reporting, investigating, correcting, and documenting serious instrumental malfunctions and problems. 7. May review analytical data produced by other analysts and specialists, following established standards and requirements; evaluates data for integrity and validity of the results. 8. Trains and/or leads analytical personnel engaged in preparatory and analytical work in designated specialization; serves as a reference and provides technical assistance to project managers and other personnel. 9. Contributes to development and implementation of short and long-range laboratory plans and objectives; participates in inter-departmental meetings on organizational, technical, and/or scientific subjects when assigned. 10. Researches and acquires new knowledge in the field by reading, attending seminars and workshops. 11. Performs related duties as assigned. Minimum Qualifications: A professional employee must possess a bachelor's degree in chemistry (biochemistry, analytical, inorganic, and organic), toxicology, microbiology, or related field OR completion of a bachelor's degree program at an accredited college or university with a minimum equivalent of 34 semester hours in toxicology, chemistry, microbiology, or related field and a minimum of 6 years of analytical testing experience. Special Requirements: Requires a degree in chemistry, environmental science, biology, microbiology, or a related field, and three to five years of progressively responsible instrumental and/or scientific chemical analysis experience, or equivalent Preferred Qualifications: 1. Master's degree in chemistry or in a related field, 2. Demonstrate competence in the principles, methods, and techniques of analytical chemistry. 3. Field and laboratory work experience beyond the minimum required. Substitution allowed: A master's degree in chemistry, microbiology, or related field and a minimum of 3 years of relevant experience and demonstrated competence may be substituted to begin at the Laboratory Analyst III position. A professional employee with a doctoral degree in chemistry, microbiology, or related field with 1 year of relevant experience and demonstrated competence can begin work at the Laboratory Analyst III level. Knowledge, Skills, and Abilities: Knowledge of: • Principles of scientific analysis and established laboratory methodology. • Inorganic chemistry, organic chemistry, environmental sciences, biology, mathematics, microbiology and/or other related scientific fields. • Laboratory and chemical principles, terminology, material, equipment, procedures, and techniques. • Quality control and quality assurance techniques. • Regulatory requirements related to laboratory analysis. • Principles of laboratory ethics as applied to the production of valid analytical data. Ability to: • Independently learn and develop new complex laboratory procedures. • Perform complex laboratory analyses and produce high quality data. • Work safely with hazardous substances. • Perform QA/QC activities objectively and without outside influence. • Establish and maintain effective working relationships with coworkers and managers, including representative outside groups and agencies. • Research environmental and analytical problems. Skilled in: • Using complex analytical techniques including GC, GC/MS, LC, HPLC, ICP, ICP/MS, Microscopic, Microbiological and/or other analyses as appropriate. • Advanced data processing and reporting using spreadsheets, databases, and specialized software. • Interpreting analytical data and evaluating results. • Troubleshooting analytical problems. • Utilizing laboratory equipment and computers to conduct sample and data analyses. • Oral and written communication and communicating technical concepts. • Diagnosing and correcting problems with laboratory equipment and/or procedures. • Providing direction to staff engaged in specialization, including assigning, and reviewing work. • Demonstrating techniques and providing training to others. Knowledge of: • Principles of scientific analysis and established laboratory methodology. • Inorganic chemistry, organic chemistry, environmental sciences, biology, mathematics, microbiology and/or other related scientific fields. • Laboratory and chemical principles, terminology, material, equipment, procedures, and techniques. • Quality control and quality assurance techniques. • Regulatory requirements related to laboratory analysis. • Principles of laboratory ethics as applied to the production of valid analytical data. Ability to: • Independently learn and develop new complex laboratory procedures. • Perform complex laboratory analyses and produce high quality data. • Work safely with hazardous substances. • Perform QA/QC activities objectively and without outside influence. • Establish and maintain effective working relationships with coworkers and managers, including representative outside groups and agencies. • Research environmental and analytical problems. Skilled in: • Using complex analytical techniques including GC, GC/MS, LC, HPLC, ICP, ICP/MS, Microscopic, Microbiological and/or other analyses as appropriate. • Advanced data processing and reporting using spreadsheets, databases, and specialized software. • Interpreting analytical data and evaluating results. • Troubleshooting analytical problems. • Utilizing laboratory equipment and computers to conduct sample and data analyses. • Oral and written communication and communicating technical concepts. • Diagnosing and correcting problems with laboratory equipment and/or procedures. • Providing direction to staff engaged in specialization, including assigning, and reviewing work. • Demonstrating techniques and providing training to others. Working Conditions and Physical Effort • Fine Motor Skills: Laboratory analysts need good fine motor skills to handle delicate equipment, pipettes, and small samples with precision. This includes tasks such as pipetting, micro-dispensing, and manipulating small objects. • Visual Acuity: Good vision is essential for observing samples, reading measurements, and other tasks. Corrective eyewear may be necessary. • Color Vision: Some laboratory work may involve the ability to distinguish colors, especially in fields like histology or chemistry where color changes indicate reactions or results. • Manual Dexterity: Laboratory analysts must have the ability to perform tasks that require steady hands and coordination, including operating laboratory instruments, adjusting settings, and conducting intricate procedures. • Standing or Sitting: Depending on the laboratory and the specific job tasks, laboratory analysts may need to stand for extended periods while working at laboratory benches or sit at computer workstations for data analysis and reporting. • Lifting and Carrying: There may be a need to lift and carry laboratory supplies, equipment, or samples, which can vary in weight. The specific weight requirements will depend on the laboratory setting. • Bending and Stooping: Laboratory analysts may need to access samples, equipment, or lower shelves, which may require bending or stooping. • Wearing Personal Protective Equipment (PPE): PPE is mandatory. This can include wearing gloves, lab coats, safety goggles, and, in some cases, respirators. Comfortably wearing and using PPE is essential. • Repetitive Movements: Laboratory work often involves repetitive movements, such as pipetting, which can put strain on wrists and hands. Proper ergonomics and the use of ergonomic equipment can help reduce the risk of repetitive strain injuries. • Adequate Mobility: Laboratory analysts should have the ability to move around the laboratory space, reach equipment, and navigate safely in a potentially crowded environment. At this time, MSU is unable to offer H-1B visa sponsorship for this role. This applies until further notice. Instructions for Applying: Link to apply: *********************************** All applicants must apply online and attach a cover letter, current resume or curriculum vitae, and the complete contact information for at least three professional references. Restricted Clause: Position is contingent upon continued availability of funding. Equal Employment Opportunity Statement: Mississippi State University is an equal opportunity institution. Discrimination is prohibited in university employment, programs or activities based on race, color, ethnicity, sex, pregnancy, religion, national origin, disability, age, sexual orientation, genetic information, status as a U.S. veteran, or any other status to the extent protected by applicable law. Questions about equal opportunity programs or compliance should be directed to the Office of Civil Rights Compliance, 231 Famous Maroon Band Street, P.O. 6044, Mississippi State, MS 39762, **************. What do I do if I need an accommodation? In compliance with the ADA Amendments Act (ADA), if you have a disability and would like to request an accommodation in order to apply for a position with Mississippi State University, please contact the Department of Human Resources Management at tel: ************** or *******************. If you have any questions regarding this policy, contact the Department of Human Resources Management at ************** or *******************. Upon request, sections of this job listing are available in large print, and readers are available to assist the visually impaired.

PRIMARY FUNCTION: Primarily responsible for verification of production processes, packaging, food safety and monitoring of operational sanitation. Responsible for proper documentation, inventory control, and release of hold product. Assist production Team Members, Team Leaders, and Supervisors in assuring that safe and quality products are produced according to specification. Performs all work in compliance with company policies, NCC Animal Welfare Guidelines and local, state and federal policies, laws and regulation RESPONSIBILITIES AND TASKS: Under minimal supervision, communicate with Production & QA Team Members, Team Leaders, and Supervisors to assure proper handling of all products and timely correction of deficiencies Monitor lines and paperwork throughout the day to assure specification compliance for each product Verify and help enforce GMP's Verify labels, lot codes, bags, boxes, and pallets are correctly adhered, printed, sealed, and stacked Verify receiving of incoming raw materials and ingredients, informs Shipping/Receiving Team Leader and QA Team Leader or QA Coach if any product does not meet specifications Assist Production with day to day quality problems to reach workable solutions Assure microbiological swabs and samplings are performed at correct times and correct positions Assist in making sure all quality and food safety policies and procedures are being followed Work in compliance with all company policies, NCC Animal Welfare Guidelines and local, state and federal policies, laws and regulations All other duties as assigned EDUCATION AND CERTIFICATIONS: High School Diploma or equivalent EXPERIENCE AND SKILLS: Minimum 1 year experience in quality assurance or 6 months Wayne Farms employee Intermediate math (add, subtract, multiply and divide) and computer skills Detail oriented Must have the ability to effectively communicate in English, both verbal and written, with internal and external customers in a timely and professional manner; ability to communicate in multiple languages preferred Sound work ethic, honesty and moral character SAFETY REQUIREMENTS: Follow departmental and company safety policies and programs Must wear Personal Protective Equipment (PPE) at all times in areas where required. PHYSICAL REQUIREMENTS: Stand up to 8 hours. Lift up to 60 lbs. Exposure to wet and dusty environment. Frequently reaching, bending, stooping, kneeling and crawling. Work around raw, live animal odors Ability to work nights, weekends, holidays and extended shift hours We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

An experienced Quality Control Laboratory Chemist is needed to support testing activities in a regulated laboratory environment. The role involves conducting chemical analyses on raw materials, in-process samples, finished goods, and stability samples to ensure product quality and compliance with industry standards. Key Responsibilities Conduct chemical testing on raw materials, in-process products, finished products, and stability samples. Operate, maintain, and calibrate analytical instrumentation (e.g., HPLC, GC, UV/VIS, FTIR). Prepare reagents and samples in alignment with established procedures. Accurately document and report results according to regulatory and quality system requirements. Support method development, validation, and transfer activities. Troubleshoot and investigate testing or equipment-related issues. Collaborate with cross-functional teams and provide mentorship to junior staff when needed. Required Qualifications 3 to 5 years of hands-on chemistry experience in a regulated QC or manufacturing laboratory. Proficiency with chromatography techniques, particularly HPLC and GC. Familiarity with additional analytical tools (e.g., UV/VIS, FTIR, AA, IC, ICP-MS, dissolution testing). Experience with laboratory software (e.g., Empower, Microsoft Office). Solid understanding of cGMP principles and quality systems (e.g., change control, deviations, CAPAs). Strong attention to detail, communication skills, and ability to manage multiple tasks in a fast-paced setting. Additional Information Degree preferred, but equivalent industry experience will be considered in place of formal education. Must be able to lift 50 lbs regularly and work on their feet for extended periods.

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us. Click on the link below to learn what our employees have to say about Evonik: ************************************************** This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. Responsibilites: * Has a sound understanding of the skills required to perform the following routine activities: * Environmental Monitoring - Monitoring of Classified Areas using a) active/passive air sampling methods and RODAC/swab surface sampling methods for the detection of bacteria and fungi; and b) CliMet air sampling methods for the detection of Total Particulates; trending of this data to detect anomalies, and characterize the transient and resident microflora. * Utilities -Testing of a) city water for total microbial count and the absence of enteric organisms; b) pre-treat water, clean steam and Water for Injection for total microbial count and presence of endotoxins; and c) nitrogen and process air for total microbial count and total particulates. * Utilizes classical microbiological methods for the identification of microorganisms. * Perform validation activities such as biological indictor recovery, bioburden rinse/swab, endotoxin rinse and endotoxin challenge vial testing. * Data analysis and entry into software systems such as Microbiology Information Management Systems (MIMS). * GMP Documentation - Document test results and conclusions in a GMP manner. Ensure test forms are complete before submission for approval. * Performs responsibilities in compliance with Evonik quality systems. * Adheres to all company safety, health and environmental policies, procedures and directives. * Conducts all laboratory activities in a safe manner by use of MSDS to establish chemical hazards, observes the appropriate laboratory procedures and reports all incidents that could threaten the safety of laboratory personnel Requirements: * Bachelor's degree in microbiology, biological sciences, or related field of study * Minimum 1 yr. experience in a clinical, academic, or industrial/pharmaceutical microbiology laboratories. * Experience in microbiological assays and testing. * Desired experience in environmental monitoring and trending. * Desired experience in the testing of utilities. * Excellent written and verbal communication skills. * Excellent organizational and leadership skills. * Proficiency in Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMP). * Excellent computer skills including experience with spreadsheets and databases. * Ability to use a respirator. * Ability to work with microorganisms and hot liquids. The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at *************************** Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Kelvin Seals [C] Company is Evonik Corporation

Job Details Sylacauga - Sylacauga, AL Full Time 4 Year Degree Day ManufacturingDescription The Quality Control Chemist will play a crucial role in ensuring the excellence and consistency of our chemical products through rigorous testing and analysis. Position is full-time at the Sylacauga, AL plant laboratory reporting to the Director of Quality and Process Chemistry. (approximately 40 hours): Monday through Friday with flexibility to work additional hours and different schedules during peak customer demand times. Essential Duties & Responsibilities Conduct Quality Control Testing: Execute a variety of chemical and physical analyses on raw materials, intermediates, and finished products to guarantee compliance with established quality standards. Utilize analytical instrumentation, including but not limited to ICP-OES (Inductively Coupled Plasma Optical Emission Spectroscopy), HPLC (High Performance Liquid Chromatography), Gas Chromatography, Karl Fisher, Viscometer, Specific Gravity, and pH to perform quantitative and qualitative analyses. Perform method validation and verification for new testing methods in the laboratory. Data Analysis and Troubleshooting: Perform data analysis, identify trends, and troubleshoot issues, taking corrective actions as necessary. Compliance and Approval Checks: Ensure products meet specifications and conduct final product approval checks. Confirm label claims adhere to quality control specifications. Documentation, Record-Keeping, and Quality Assessment: Maintain meticulous and precise records of all testing procedures, results, and any deviations from anticipated outcomes. Generate Certificates of Analysis (CoA) for each product batch, providing comprehensive documentation of quality specifications. Assess daily quality parameters and quality systems, covering cross-checks, raw materials, calibration, maintenance, procedures, training, auditing, and oversight of analytical testing. Document standard operating procedures and identify trends in testing results using data analysis from daily result entries. Training and Support: Train new quality chemists, and provide technical support to stakeholders, investigating quality problems and implementing actions to follow up. Troubleshoot and Investigate: Identify and investigate any discrepancies from quality standards, collaborating with production and relevant departments to promptly resolve issues. Handle basic issues and problems under direct supervision, escalating more complex issues to appropriate staff. Continuous Improvement: Participate in continuous improvement initiatives by suggesting and implementing enhancements to existing testing methods and processes. Compliance and Safety: Guarantee that all quality control activities adhere to industry regulations and safety standards. Contribute to maintaining a safe, clean, and orderly laboratory environment. Other duties - Perform additional duties as assigned. Qualifications Qualifications Proficient understanding of analytical techniques and instruments. Exceptional attention to detail and accuracy in documentation. Ability to work independently and collaboratively in a team setting. Strong communication skills with the ability to convey complex information clearly. Education/Experience Bachelor or Master's degree in Chemistry or related field. 2+ years' work experience in plant nutrition formulation/development desired. Physical Requirements 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 individual with disabilities to perform the essential functions. While performing the duties of this job the employee is regularly required to talk or hear. The employee is frequently required to sit and use hands to touch, handle, or feel. Prolonged periods sitting at a desk and working on a computer. The employee is occasionally required to stand, walk, reach with hands, and arms, climb or balance and stoop, kneel, or crouch. The employee is occasionally required to lift up to fifty pounds. The vision requirements include close vision and ability to adjust focus. Employees must be able to stand for extended periods of time. Working 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. The employee will primarily be in a laboratory setting onsite, with occasional plant walk throughs to assist in quality related matters. The noise level in the work environment is typically minimal, with normal chemical manufacturing duties occurring daily. The statements herein are intended to describe the general nature and levels of work performed by employees, but are not a complete list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of the employer.

Job Title: Quality Control Chemist About the Company: IPS Corporation is a global, market-leading provider of solvent cements, adhesives, and specialized plumbing products. Founded in 1954 in Los Angeles, CA, IPS began by producing clear cements for laminating acrylic sheets for aircraft canopies. Today, IPS, with its three operating companies, has eight manufacturing plants and nine distribution centers supporting sales to a diverse set of end markets in 85 countries. About Weld-On: Weld-On Adhesives, the largest subsidiary of IPS Corporation, is the pioneer and leading manufacturer of Weld-On solvent cements, primers, and cleaners for PVC, CPVC, ABS and other plastic piping systems. Weld-On products are globally recognized as the premium products for joining plastic pipes and fittings and are used by professional installers around the world in a variety of applications such as, but not limited to, construction (residential & commercial), industrial (chemical process, water treatment, mining, etc.), irrigation (landscaping & agricultural) and others. About the Job: We are seeking a Quality Control (QC) Chemist to join our team at the Weld-On Adhesives manufacturing facility in Hartsville, TN. Reporting directly to the Quality Manager, this role plays a critical part in ensuring that all products meet the highest quality standards through rigorous analytical testing and inspection. The QC Chemist will also collaborate with cross-functional teams to support new product introductions, validation processes, and compliance with certification requirements Responsibilities: * Perform quality assurance testing using Gas chromatography, Infrared spectroscopy, viscometers, moisture analyzers, and other analytical techniques to verify product conformance with specifications. * Maintain and calibrate laboratory equipment to ensure accuracy, reliability, and compliance with standards. * Develop, write, and implement Standard Operating Procedures (SOPs) for laboratory processes and equipment usage. * Accurately record and document QC test results, deviations, and corrective actions in compliance with internal protocols and customer requirements. * Conduct lab experiments to support new formula introduction, validation, and troubleshooting of quality issues. * Assist with product certification and compliance activities, including audits, testing, and sample submissions. Education/ Experience Qualifications: * Bachelor's degree in Chemistry, Polymer Science, Materials Science, or a related field. * Minimum of 3 years of relevant experience in the chemical industry, preferably in adhesives, sealants, or coatings. * Strong technical expertise in chemical formulation, quality control, and analytical testing. * Familiarity with regulatory requirements and standards related to hazardous chemicals. * Proficiency in data analysis, with the ability to identify trends and draw valid conclusions; experience with statistical tools is a plus. * Excellent written and verbal communication skills, with the ability to collaborate effectively across all organizational levels and with external partners. * Comfortable working in a global, multi-disciplinary team environment. * Willingness to travel up to 25%. This description reflects management's assignment of essential functions; it does not proscribe or restrict the tasks that may be assigned. Weld On is an equal opportunity employer and makes employment decisions without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other status protected by law.

Job Title: Quality Control Laboratory Chemist Department: Quality Control Reports To: Quality Control Manager Employment Type: Full-Time | On-Site Compensation: Median $23-$25/hour (commensurate with experience) About the Role Our client is seeking an experienced Quality Control Laboratory Chemist to join their Quality Control team. In this role, you will play a critical part in ensuring the quality and compliance of human and veterinary drug products by conducting a wide range of chemical analyses in a GMP-regulated laboratory environment. This position requires a strong background in chromatography and a proven track record of working within cGMP standards. Key Responsibilities Perform chemical analyses on raw materials, in-process products, finished products, and stability samples. Operate, maintain, and calibrate analytical instruments (HPLC, GC, etc.). Prepare reagents and samples in compliance with SOPs and regulatory requirements. Accurately document and report test results according to GMP guidelines. Contribute to method development, validation, and transfer activities. Troubleshoot and investigate testing or equipment-related issues. Collaborate with QC team members and cross-functional departments. Mentor and support junior chemists when needed. Qualifications & Requirements 3-5 years of direct hands-on experience in a GMP-regulated QC or manufacturing laboratory. Strong background in chromatography (HPLC, GC, UV/VIS, FTIR). Experience with analytical tools such as AA, IC, ICP-MS, and dissolution testing. Proficiency with Empower, Microsoft Office, and laboratory data systems. Solid understanding of cGMP, quality systems, and regulatory compliance (change control, deviations, CAPAs). Excellent attention to detail, communication, and organizational skills. Ability to multitask and prioritize in a fast-paced environment. Note: Applicants with only academic or research lab experience will not be considered. A degree is not required. Relevant industry skills and experience are what matter most. Physical Requirements Must be able to lift 50 lbs. or more daily. Ability to stand, walk, or sit for 8+ hours per day.

QC Scientist - Weekend Shift Department: Quality Control - Analytical Team Schedule: Friday to Monday | 4x10 Hour Shifts | Flexible Start Times (7 AM-5 PM or 8 AM-6 PM) Job Title: QC Scientist Job Description Join our team as a QC Scientist where you will leverage numerous analytical tools for large molecule analysis including HPLC, UPLC, CGE, iCE, and Cell Based Analyses. This role supports GMP manufacturing for commercial product and stability testing. Prior experience in a cGMP environment is required. Pay:$28-$38 Responsibilities + Perform HPLC, UPLC, CGE, iCE, Cell Based Analyses, and Compendial Testing on In-Process, DS release, and stability samples, ensuring timely project delivery. + Review laboratory data packets and author laboratory investigations as assigned. + Conduct GMP testing using HPLC and UPLC test methods such as Reverse Phase, SEC, and CEX. + Compile data for documentation of test procedures and prepare reports. + Collaborate with team members and departments like quality assurance and data reviewers. + Contribute to the development of new concepts, techniques, and standards. + Recognize and report invalid, lab incident, out-of-specification, or out-of-trend results; recommend solutions. + Perform all duties in compliance with SOPs, GMP, and safety guidelines. + Participate in laboratory activities, perform safety inspections, and order supplies. Essential Skills + 0-5 years of proven experience in a GMP regulated environment, preferably pharmaceuticals. + Experience with analytical techniques and required instrumentation such as HPLC, UPLC, CGE, iCE, UV, pH, Osmolality, and cell-based bioassays. + Knowledge of GMP regulations in a cGMP manufacturing environment. + Working knowledge of scientific principles for a wide range of analytical techniques. + Proficiency with EMPOWER, MS Office, and laboratory computer programs. Additional Skills & Qualifications + Bachelor's degree in chemical pharmaceutical, biology, chemistry, biotechnology, or related field. + Prior use of EMPOWER is preferred. + Good organization and planning skills. + Attention to detail and a positive, collaborative demeanor. Work Environment You will be part of a newly formed team of 6 Scientists and 1 Supervisor supporting the weekend shift within a QC Analytical team of over 80 members. The role involves 3-6 months of training and testing on each test before progressing. Work in a pharmaceutical lab setting doing bench work. Shifts are 4-10 hour days from Friday to Monday, with flexible hours between 7am-5pm or 8am-6pm. Job Type & Location This is a Contract to Hire position based out of Berkeley, Missouri.Job Type & Location This is a Contract to Hire position based out of Berkeley, MO. Pay and Benefits The pay range for this position is $28.00 - $38.00/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 Berkeley,MO. Application Deadline This position is anticipated to close on Dec 19, 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 actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Are you ready to embark on a career where innovation meets excellence? At Jost Chemical Company, we're on a mission to push the boundaries of chemical manufacturing, delivering high-quality products that make a positive impact on global industries. If you're passionate about chemistry, dedicated to precision, and eager to contribute to a company that values both innovation and integrity, explore our exciting job opportunities. Join us in shaping the future of chemical manufacturing at Jost Chemical Company, where your career is more than just a job - it's a journey of growth and achievement. Then, this position is right for you! Founded in 1985, Jost Chemical is a global leader in the manufacture of high purity mineral salts for the nutritional, pharmaceutical and specialty markets. Expansion, growth of capabilities, and investment in people, lab and production equipment have been a part of Jost's company culture for 35 years. To learn more about Jost Chemical please visit ******************** Our offer: * Shift Differential * Medical/Dental/Vision Plan Insurance, Short and Long-Term Disability and Life Insurance first of the month following 60 days. * 401k plan which includes safe-harbor contribution and discretionary match. * Paid Time Off (PTO) Employees eligible first day of employment. * 9 Company Paid Holidays (72 hours) each year. * Uniforms Provided * Foot Protection- annual allowance for all laboratory, maintenance and production employees. * 24-hour access to our free, on-site fitness center. * We provide Individual development, on-the-job training, and development programs designed to enhance your professional growth and development while ensuring you feel valued, inspired and appreciated at work. Jost Chemical is an equal opportunity employer and affirmatively seeks diversity in its workforce. We consider applicants, and make all employment decisions, without regard to race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, or any other legally protected status. We are committed to recruiting and retaining the best talent in the chemical manufacturing industry. Background * Works under general direction of the Quality Control Manager in a c-GMP regulated manufacturing environment operating under Q7A standards. * Employees in positions at this level of the series exercise a considerable degree of independence in conducting a wide range of experiments requiring expertise in the application and adaptation of numerous research techniques and produce desired results. Tasks * Perform analytical testing using wet chemistry techniques and instrumentation on c-GMP regulated products following compendial methods (USP/NF, EP, FCC, JP etc). * Perform microbiological testing on c-GMP regulated products using compendial methods. * Perform routine and non-routine testing using basic and advanced laboratory instrumentation and adhere to a strict calibration / preventative maintenance program. * Interpret analytical data and assist chemical operators and chemical engineers with applying this data to the manufacturing process. * Write research methods, results, and conclusions for publication; may present at professional conferences. * Review scientific literature, abstracts, and applicable method papers; identify appropriate application for current or anticipated research projects. * Maintain data integrity in both written and digital form. * Prepare laboratory test solutions and perform standardizations of volumetric solutions. * May be required to inventory and order laboratory supplies, instruments, and reagents. * Maintain a clean and organized work area. * Maintain and enhance site safety. * Instruct other personnel in specific areas of quality control laboratory testing. * Data mining and trending; Process Validation support; Root Cause Analyses; Problem Solving Tools use; Statistical Data trending; Support for Non-conformance Investigations; Production support activities. Specifications * A.S or B.S. Chemistry or related technical field that included instrumentation, or industry experience. * 0-2 years professional level chemist experience. Knowledge of: * Theories, principles, and methods of instrumental and wet chemistry * Method development and method validation * Mathematics and statistics * Basic analytical laboratory equipment * MS Office software package Skill in: * Working effectively and efficiently on multiple projects at once * Working effectively in a team environment * Responding to rapidly changing demands Ability to: * Lead and/or train others in assigned activities * Follow compendia and other test methods * Develop creative solutions to more varied research procedural problems * Design and manage projects * Identify, gather, process, and record data accurately * Maintain quality, safety, and/or infection control standards * Operate and maintain laboratory equipment * Communicate effectively, orally and in writing (including documenting research methods, results, and conclusions) * Exercise independent judgment

Microbiology Lab Tech needs 1 year microbiology testing experience, Microbiology Lab Tech requires: Bachelors degree in science field or relevant work experience Skilled in use of PC software and Microsoft Office (Excel, Word, PowerPoint) Experience with SAP, relevant ISO standards, and/or auditing preferred Ability to work on multiple projects and priorities Minimum 1 year experience with microbiological testing required Experience with hygienic sampling & hygienic plating required Microbiology Lab Tech duties: Finished product and raw material testing Gram-staining Stocking of inventory, media, and reagents, managing laboratory waste Environmental monitoring including testing process water, air sampling, and swabbing of equipment (limited) Plate reading and communication of results

A Microbiology Laboratory Technician I (LabTech I) reports to the Laboratory Manager. The LabTech I performs research and analysis activities, processes chemistry and microbiology samples, and provides maintenance tasks necessary to support the Phigenics Analytical Services Laboratory (PASL). This position has no supervisory responsibilities. Job Duties Understand PASL services, operations, and testing methods for waterborne pathogens Basic understanding of field testing equipment and supplies Receive and log in chemistry or microbiology samples Prepare materials and reagents for processing chemistry or microbiology samples; record observations and measurements, and report results Under direct supervision, provides analysis of the samples according to the standard operating procedures (SOPs). Records sample location data and results in the database Communicates accurate and timely results to clients and the sales team Assists in the maintenance of quality system records to comply with accrediting agencies Assists with ordering, receipt, inspection, and stocking of supplies Performs lab maintenance, including, but not limited to: Clean lab equipment and wash glassware, vials, and filters Clean and store materials used for testing Discard old chemistry or microbiology samples Prepares reports as necessary Education and Experience A bachelor's degree in Chemistry, Biology, or a related field is required 0-2 years of experience as a lab technician or related field Works under direct supervision from the Lab Manager Accuracy and attention to detail are strong requirements Excellent verbal and written communication skills are strongly required Skills with standard concepts, practices, and procedures within a particular field Performs tasks successfully using instructions, pre-established guidelines, and standard procedures to perform work Experience with MS Office, spreadsheets, word processing, and other computer programs Minimal travel required Physical Demands and Work Environment Regularly required to sit, use hands and fingers; handle, feel, talk, and hear. Frequently required to reach with hands and arms. Occasionally required to stand; walk; climb or balance; stoop, kneel, crouch, or crawl, and taste or smell. Regularly lift and /or move up to 10 pounds, frequently lift and/or move up to 25 pounds, and occasionally lift and/or move up to 50 pounds. Phigenics LLC is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, creed, color, religion, alienage or national origin, ancestry, citizenship status, age, disability or handicap, sex, marital status, veteran status, sexual orientation, arrest record, or any other characteristic protected by applicable federal, state or local laws. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

The Lab Analyst role reports to the Plant Chemist/Lab Leader as part of the site quality assurance laboratory. The Lab Analyst is responsible for using analytical methods to provide prompt and accurate testing of industrial chemicals for conformance to quality specifications, for operational process control, to fulfill special customer requirements, or in support of troubleshooting or improvement projects. Responsibilities & Accountabilities * Follow all safety rules and actively promote safety through reporting safety observations, performing job safety analyses, completing safety inspections and walkthroughs, participating in safety meetings, etc. * Directly responsible for understanding, promoting and upholding the Eastman Basic Safety Expectations * Perform routine testing to determine and report final product quality status to manufacturing * Perform routine testing to support unit production as specified by the manufacturing units * Accurately input all data into LIMS system and record test results in a legible manner on designated forms * Check operation of testing equipment, troubleshoot equipment to identify and/or correct source of problem, and notify the chemist of any abnormalities or maintenance requirements * Conduct job tasks in a professional manner utilizing good housekeeping practices and laboratory technique

Responsible for performing inspection, testing, and verification of raw materials, in-process components, and finished stamped metal products to ensure compliance with company standards, customer specifications, and regulatory requirements. This role plays a critical part in maintaining product quality, preventing defects, and supporting continuous improvement initiatives. Split shift between 2nd and 3rd. Hours are 7pm - 3:30am. How You Will Help Perform inspections using appropriate measuring tools (e.g., calipers, micrometers, gauges, templates, visual standards). Conduct first piece, in-process, and final inspections per quality procedures and control plans. Read and interpret blueprints, technical drawings, and customer specifications. Document inspection results and maintain accurate records in quality systems, forms, or databases. Identify, report, and quarantine non-conforming material; assist with root-cause analysis and corrective actions. Verify compliance with customer and internal quality requirements. Communicate quality concerns to production, engineering, and leadership. Assist with calibration of inspection equipment and ensure proper use. Follow all safety requirements and promote a safe working environment. Support continuous improvement, lean manufacturing, 5S, and quality system initiatives. What You Will Bring Required: * High school diploma or GED. * Prior manufacturing experience (preferably in metal stamping or related field). * Ability to read and interpret blueprints and technical drawings. * Proficient with measurement tools and inspection techniques. * Strong written and verbal communication skills. * Basic computer skills (Excel, data entry, QMS software, etc.). Preferred: * 1-3 years of experience in quality inspection or quality assurance in metal fabrication, stamping, or machining. * Experience with CMM or optical measurement systems. * Certification such as ASQ Certified Quality Inspector (CQI) is a plus.

Work Your Magic with us! Start your next chapter and join EMD Serono. Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Your Role: The Quality Control Analyst for St. Louis Cell Marque is responsible for performing and analyzing assays to ensure the quality and consistency of our products. This role requires understanding and hands-on experience with various IHC, ELISA, bioburden, etc, techniques, and a commitment to maintaining rigorous quality standards. This position will work with oversight of the St. Louis Cell Marque QC Supervisor. Key Responsibilities: * Perform and analyze assays on tissue samples and other biological materials. * Prepare reagents, solutions and controls for assays. * Operate and maintain laboratory equipment. * Document and maintain accurate records in accordance with good documentation practices. * Identify trends and anticipate quality issues using data analytics. * Assist QA teams in ensuring overall product and process quality. * Adhere to all safety regulations and laboratory protocols. Who You Are: Minimum Qualifications: * Bachelor's Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc.) Preferred Qualifications: * Hands-on experience performing and analyzing IHC assays in a quality control or research setting. * Understanding of IHC principles, techniques, and applications. * Proficiency in using laboratory equipment and software * Knowledge of quality control principles and practices. * Excellent analytical, problem-solving, and troubleshooting skills. * Strong attention to detail and ability to maintain accurate records. * Excellent communication and interpersonal skills. * Ability to work independently and as part of a team. * Understanding or experience with ISO & FDA regulations. RSREMD * Pay Range for this position: $23.00-$36.00 per hour. * The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

What we offer Explore a world of opportunities with us. Look ahead with us and help shape innovative solutions to make our world more sustainable and life healthier, more vibrant and more comfortable. At Evonik, you have the chance to explore, thrive, and grow alongside 33,000 colleagues. Among attractive career paths and high-quality development programs, we not only offer performance-based remuneration and occupational health benefits but also hybrid and flexible working environments with #SmartWork. Bring your fresh perspective, develop your strengths, break out your mold, and find a career that fits your dreams with us. Click on the link below to learn what our employees have to say about Evonik: ************************************************** This position is responsible for conducting routine microbiological testing, documentation, and data analysis, of utilities, raw materials, facilities and equipment. Additionally, the microbiology technician will be responsible for upkeep of the laboratory, laboratory supplies, and other various routine laboratory tasks. Responsibilites: Has a sound understanding of the skills required to perform the following routine activities: Environmental Monitoring - Monitoring of Classified Areas using a) active/passive air sampling methods and RODAC/swab surface sampling methods for the detection of bacteria and fungi; and b) CliMet air sampling methods for the detection of Total Particulates; trending of this data to detect anomalies, and characterize the transient and resident microflora. Utilities -Testing of a) city water for total microbial count and the absence of enteric organisms; b) pre-treat water, clean steam and Water for Injection for total microbial count and presence of endotoxins; and c) nitrogen and process air for total microbial count and total particulates. Utilizes classical microbiological methods for the identification of microorganisms. Perform validation activities such as biological indictor recovery, bioburden rinse/swab, endotoxin rinse and endotoxin challenge vial testing. Data analysis and entry into software systems such as Microbiology Information Management Systems (MIMS). GMP Documentation - Document test results and conclusions in a GMP manner. Ensure test forms are complete before submission for approval. Performs responsibilities in compliance with Evonik quality systems. Adheres to all company safety, health and environmental policies, procedures and directives. Conducts all laboratory activities in a safe manner by use of MSDS to establish chemical hazards, observes the appropriate laboratory procedures and reports all incidents that could threaten the safety of laboratory personnel Requirements: Bachelor's degree in microbiology, biological sciences, or related field of study Minimum 1 yr. experience in a clinical, academic, or industrial/pharmaceutical microbiology laboratories. Experience in microbiological assays and testing. Desired experience in environmental monitoring and trending. Desired experience in the testing of utilities. Excellent written and verbal communication skills. Excellent organizational and leadership skills. Proficiency in Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GMP). Excellent computer skills including experience with spreadsheets and databases. Ability to use a respirator. Ability to work with microorganisms and hot liquids. The Evonik Group adopts an Equal Employment Opportunity (EEO) approach. Candidates are assessed based on their educational qualifications, experience, job competencies and potential and shall not be discriminated against on the basis of race, ethnicity, age, gender, religion, nationality, disability or sexual orientation or other classifications protected by local, state, or provincial regulations. Your Application To ensure that your application is proceeded as quickly as possible and to protect the environment, please apply online via our careers portal. Further information about Evonik as Employer can be found at *************************** Please address your application to the Talent Acquisition Manager, stating your earliest possible starting date and your salary expectations. Your Talent Acquisition Manager: Kelvin Seals [C] Company is Evonik Corporation

The Lab Analyst role reports to the Plant Chemist/Lab Leader as part of the site quality assurance laboratory. The Lab Analyst is responsible for using analytical methods to provide prompt and accurate testing of industrial chemicals for conformance to quality specifications, for operational process control, to fulfill special customer requirements, or in support of troubleshooting or improvement projects. Responsibilities & Accountabilities * Follow all safety rules and actively promote safety through reporting safety observations, performing job safety analyses, completing safety inspections and walkthroughs, participating in safety meetings, etc. * Directly responsible for understanding, promoting and upholding the Eastman Basic Safety Expectations * Perform routine testing to determine and report final product quality status to manufacturing * Perform routine testing to support unit production as specified by the manufacturing units * Accurately input all data into LIMS system and record test results in a legible manner on designated forms * Check operation of testing equipment, troubleshoot equipment to identify and/or correct source of problem, and notify the chemist of any abnormalities or maintenance requirements * Conduct job tasks in a professional manner utilizing good housekeeping practices and laboratory technique Experience & Education * Minimum of 1 years laboratory experience in a technical environment *Bachelor's/Associate's degree in a STEM field, such Chemistry or Chemical Technology preferred, but not required Job Skills * Strong attention to detail and safe work practices * Familiarity in GC, HPLC, and wet chemistry techniques * Ability to work in a team/collaborative environment * Strong communication and multitasking skills * Computer skills: Microsoft Office (Outlook, Word, Excel, PowerPoint), and LIMS preferred * Experience with cGMP and ISO 9001 requirements a plus Schedule * Position requires working a rotating 12- hour shift. Successful applicants must be flexible and willing / able to provide overtime coverage when needed (including evenings and holidays) and work a 12-hour rotating shift schedule (days and nights) if needed to support business requirements. Brown & Root Industrial Services is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, disability, sex, sexual orientation, gender identity or expression, age, national origin, veteran status, genetic information, union status and/or beliefs, or any other characteristic protected by federal, state, or local law. BENEFITS: Brown and Root offers a selection of competitive lifestyle benefits which include a 401K plan with company match, medical, dental, vision, life insurance, AD&D, flexible spending account, disability, paid time off, and flexible work schedule. We support career advancement through professional training and development. The Lab Analyst role reports to the Shift Team Leader/Lab Manager as part of the site quality assurance laboratory. The Lab Analyst is responsible for using analytical methods to provide prompt and accurate testing of industrial chemicals for conformance to quality specifications, for operational process control, to fulfill special customer requirements, or in support of troubleshooting or improvement projects. Responsibilities & Accountabilities * Follow all safety rules and actively promote safety through reporting safety observations, performing job safety analyses, completing safety inspections and walkthroughs, participating in safety meetings, etc. * Directly responsible for understanding, promoting and upholding Basic Safety Expectations both for themselves and the people around them * Perform routine testing to determine and report final product quality status to manufacturing * Perform routine testing to support unit production as specified by the manufacturing units * Accurately input all data into LIMS system and record test results in a legible manner on designated forms * Check operation of testing equipment, troubleshoot equipment to identify and/or correct source of problem, and notify the chemist of any abnormalities or maintenance requirements * Conduct job tasks in a professional manner utilizing good housekeeping practices and laboratory technique.