Chemical Engineer Salary in Iowa, USA

Competitive SalaryRelo: YesOur client company is seeking an experienced Environmental Engineer to bring environmental excellence to their workplace. A very challenging position but with a great corporate support structure for the candidate selected to learn and grow.You must be willing to:Direct the Environmental Compliance efforts for a highly technical liquid manufacturing operationUnite the team to attain outstanding results in the area of Environmental ComplianceCreate proactive Environmental Compliance through teaching/training/monitoring resultsRequirements (IF YOU DON’T HAVE THESE, DON’T APPLY):BS Chemical or Environmental Engineering (Advanced Degree preferred)MUST HAVE: Experience with Water/WasteWater1-2 years of prior Environmental Leadership experienceStrong knowledge of Environmental compliance/exceptional training skillsAbility to influence a manufacturing cultureSuperb attention to detail/compliance requirementsOur client requests resumes be submitted in Word Doc format, '97-2003, with contact information outside of a headerFull Time, Permanent PositionMust be authorized to work in the United States without company sponsorship needed now or futureEdwards Place of Employment is a BBB accredited business

Background:Nucor Steel Marion, Inc. is a division of Nucor Corporation, the largest recycler and the largest manufacturer of steel and steel products in North America. Marion's division manufactures a full line of specialty steel products needed for vital highway, construction, and agricultural industries. Nucor has been ranked No. 1 on Fortune Magazine's list of the World's Most Admired Companies in our industry, is included on Forbes list of America'sBest Large Employers, and recently has been added to Barron's list of 100 Most Sustainable Companies. The key to Nucor's success is that we care about the safety and well-being of our teammates and customers, the health and protection of our environment, and the relationships we establish in the communities where we live and work. At the heart of every Nucor division are the dedicated people who make up our team. We offer you a challenging and rewarding work environment where you can contribute to the success of over 31,000 Nucor teammates and be part of a history of long-term sustainability and stability.What We Offer:• Potential annual income of $93K-$108K, plus annual bonus, based on previous experience.• Unlimited growth potential - A chance to grow your career with a Fortune 500 industry leader known as North America's most diversified and sustainable steel and steel products company.• Full benefits package, including, Medical/Dental/Vision insurance, Long-Term Disability, Life Insurance, 3 weeks paid vacation within the first year, 10 paid holidays, Paid Parental Leave, Profit Sharing, 401K with company match, Nucor Stock Purchase Program, Tuition reimbursement program for teammate/spouse and a scholarship program for children of teammates.Basic Job Functions:The role of the Process Engineer will be to work with the Team on Safety, Quality, Production and Cost improvements throughout the melt shop. The Process Engineer will work collaboratively with the team to refine our process and reach team goals. The successful candidate should be willing to comply with a rotating work schedule working 12-hour shifts including nights, weekends, etc. as needed.Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times.Minimum Qualifications:• Must have a 4-year degree in Engineering or related fieldPreferred Qualifications:• 3-5 Years Steel/Manufacturing Experience in an industrial setting.• Prior Leadership experience.Nucor is an Equal Opportunity/Affirmative Action Employer - M/F/Disabled/Vets - and a drug - free workplace

EngineeringProcess EngineerProcess Engineer for Muscatine, IA to use chemical process engineering knowledge to support agricultural chemical manufacturing plant operations. Requires Bachelor's in Chemical Engineering, Biotechnology Engineering, or a closely related field & 4 years experience performing process design for chemical manufacturing facility(ies); monitoring key performance metrics; designing, planning & managing plant projects with significant business impact; leading critical troubleshooting efforts of unit operations, including chemical reactors and/or filtration; analyzing & making recommendations regarding improvements to chemical process operations to improve performance; ensuring production processes comply with environmental regulations; participating in safety & ISO9001 quality audits; providing initial cost estimation for new and/or modified processes; analyzing process hazards to minimize risks; performing checkout & startup assistance for capital projects in chemical production facility(ies); providing technical leadership to process optimization teams; using process control automation tools, including DeltaV; participating in process safety management procedures & analysis. Telecommuting permitted from home office location within reasonable commuting distance of Muscatine, IA up to 1 day per week.recblid qsukkxumt3w2jyyd899dctdalinrbu

Kurita America Inc is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, gender, gender identity, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with disability.Engineering Sales RepresentativeUS-IA-Des MoinesJob ID: 2024-2137Type: Full Time Exempt# of Openings: 1Category: SalesDes Moines, IAOverviewKurita America is part of the Kurita Group, one of the leading water solutions providers in the world. Established in 1949, the Kurita Group is comprised of an international network of approximately 8000 employees located in 18 countries.Located in Minneapolis, MN, Kurita America brings innovations to market through a holistic water management approach, incorporating state-of-the art equipment, chemistries, engineering, and services to conserve natural resources for a better, more sustainable world.Kurita’s corporate philosophy is to study the properties of water, master them and create an environment in which nature and humanity are in harmony Title: Sales & Service Water treatment Engineer - Selling Water Treatment Chemicals to clients all over the areaLocation: Des Monies, IA area Pay: $70-90K base salary based on experience PLUS commission We have an immediate need for a Water Treatment (this is TECHNICAL ENGINEERING) Account Manager located in or around the Des Monies, IA Area You will be primarily responsible for revenue and profit growth of our integrated programs, services and products in targeted accounts within your assigned region. You will be required to take a consultative sales approach with a strong emphasis on converting strategic competitive accounts. In addition, you will be required to build long-term relationships with an existing customer base by understanding their key business drivers, executing programs, and selling new technologies. ResponsibilitiesIncrease annual invoiced gross profit dollar amount $50,000 over previous year gross profit dollar totalsMeet objectives and goals as defined by the Regional Sales ManagerService accounts according to previous commitmentsMaintain key account base for regionQualificationsTechnical Bachelor's Degree or equivalent experience1+ years of successful technical sales or outside sales experiencePrefer water treatment or specialty chemical industry experiencePrefer working knowledge of boilers, cooling towers, and wastewater treatment systemsMust have a valid Driver's License and acceptable Motor Vehicle RecordNo immigration sponsorship offered for this roleThe qualified candidate will be subjected to post offer consumer background check and drug screen EEO/AA/F/M/Vet/DisabledPI240093161

The Director of Engineering and Facilities is a leadership position in UI Pharmaceuticals, a Contract Development and Manufacturing Organization (CDMO) located in the College of Pharmacy. This position is responsible for leading people and projects. The department employs process engineers and maintenance staff who are responsible for equipment and facility readiness in a GMP environment. The director is responsible for leading projects with significant departmental scope that have long term-financial, operational, and physical implications for the organization. As a people manager, this position hires, develops, evaluates, and implements personnel actions. Additionally, the director collaborates with Facilities Management, Manufacturing Operations, and Quality Control staff to support facility improvements, control systems and ongoing operations. Financial responsibilities include the development of a departmental budget, project cost projections and initiatives to reduce expenditures while maintaining systems and facility compliance.This is a highly regulated work environment and may require special gowning procedures and wearing of protective clothing over the head, face, hands, feet, and body and/or donning of other personal protective equipment to meet safety requirements. UI Pharmaceuticals is a Contract Development and Manufacturing Organization (CDMO) within the College of Pharmacy at the University of Iowa. Our mission is to improve quality of life by applying our pharmaceutical expertise to advance innovative products into clinical trials. Our vision is to be the premier partner for biotech, government and research institutions. We are located on the main campus in Iowa City, which offers a great place to live, top rated schools, a vibrant night life, and world class health care facilities. As a University of Iowa employee, you will have access to an excellent benefits package.We are expanding our capabilities while maintaining our culture focused on quality, customer service and community. Consider accelerating your leadership and technical skills by joining us on the next phase of our growth strategy.Key Areas of ResponsibilityCompliance Implement new policies and revise existing programs to ensure compliance with regulatory requirements and cGMP. Evaluate completed work to determine whether it meets specifications, standards, and regulations. Direct and implement modifications to bring project, facility, and processes into compliance. Oversee equipment listing and coordinate facility and control systems calibrations and associated PMs to keep facility GMP compliant. Manufacturing Lead start-up of sterile facility and process qualification of new manufacturing lines. Develop life cycle plans for all manufacturing equipment. Recommend design improvements to optimize manufacturing and safety procedures in accordance with divisional goals. Leadership Instill a safe and compliant work environment. Hire, develop and manage the performance of staff. Interpret and implement HR policies and procedures and assure staff are compliant with university policies and procedures. Training/Education Collaborate with Quality Assurance and Manufacturing Operations on the design, evaluation, and coordination of employee training on new equipment and processes. Be a Subject Matter Expert (SME) to other departments on the operation of equipment and facilities. Financial Develop departmental budget by recommending capital equipment, spare parts and service agreements for equipment and facilities. Provide oversight and control of departmental operating budget and project expenditures. Set financial priorities for projects and project budgets. Apply Process Improvement, Quality Engineering, and Management Engineering Concepts and Methodologies Maintain the engineering change control process and equipment assessments. Hands on process improvement and validation for pharmaceutical process equipment. Validate life cycle of equipment including authoring of validation master plans, URSs, FAT, SAT, IQ, OQ, PQ and engineering studies. For a complete job description, please contact Libby Kleppe at [email protected] Requirement M.S. in Engineering (preferably Chemical or Mechanical). Experience Required Minimum 5-7 years of related experience in a pharmaceutical, GMP environment, laboratory, or biological environment. This experience is evidenced by demonstration of knowledge and/or skills in areas such as: isolator operation, automated technologies, environmental controls, utilities (WFI and clean steam) aseptic processes. Experience or knowledge in quality control. Experience in qualifying facility, equipment, and control systems. Demonstrated ability to communicate effectively, orally and in technical writing, to a variety of constituents internal and external to the organization. Strong skills in developing SOPs, work instructions, validation documents, deviations, investigations, and batch records. Knowledge of pharmaceutical regulations, FDA, cGMP, EU, ISPE, etc. Intermediate skills creating and editing documents in MS Excel and Word or comparable programs. Professional experience working effectively with individuals from a variety of backgrounds and perspectives. Desirable Qualifications Pharmaceutical, Manufacturing, or Engineering project-related experiences including lyophilizer operation and/or maintenance. Experience with Process Mapping and/or project management. Understanding of Six Sigma and Lean manufacturing methodology. Experience operating under design control and GMP manufacturing. Experience with SCADA systems, Metasys systems, or JCI controls in heavy industries and pharmaceuticals. Microbiology and environmental monitoring experience. Application and Position Details In order to be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" to the submission: Resume Cover Letter Job openings are posted for a minimum of 14 calendar days. This job may be removed from posting and filled any time after the minimum posting period has ended. Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. 5 professional references will be requested at a later step in the recruitment process. For additional questions, please contact Libby Kleppe at [email protected]. Benefits Highlights Regular salaried position. Located in Iowa City, Iowa. Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans. For more information about Why Iowa? Click here. Additional Information Classification Title: Principal Engineer Appointment Type: Professional and Scientific Schedule: Full-time Work Modality Options: On Campus Compensation Pay Level: 6B Starting Salary Minimum: 115,000 Starting Salary Maximum: 135,000 Contact Information Organization: College of Pharmacy Contact Name: Libby Kleppe Contact Email: [email protected]

The Director of Engineering and Facilities is a leadership position in UI Pharmaceuticals, a Contract Development and Manufacturing Organization (CDMO) located in the College of Pharmacy. This position is responsible for leading people and projects. The department employs process engineers and maintenance staff who are responsible for equipment and facility readiness in a GMP environment. The director is responsible for leading projects with significant departmental scope that have long term-financial, operational, and physical implications for the organization. As a people manager, this position hires, develops, evaluates, and implements personnel actions. Additionally, the director collaborates with Facilities Management, Manufacturing Operations, and Quality Control staff to support facility improvements, control systems and ongoing operations. Financial responsibilities include the development of a departmental budget, project cost projections and initiatives to reduce expenditures while maintaining systems and facility compliance.This is a highly regulated work environment and may require special gowning procedures and wearing of protective clothing over the head, face, hands, feet, and body and/or donning of other personal protective equipment to meet safety requirements.UI Pharmaceuticals is a Contract Development and Manufacturing Organization (CDMO) within the College of Pharmacy at the University of Iowa. Our mission is to improve quality of life by applying our pharmaceutical expertise to advance innovative products into clinical trials. Our vision is to be the premier partner for biotech, government and research institutions.We are located on the main campus in Iowa City, which offers a great place to live, top rated schools, a vibrant night life, and world class health care facilities. As a University of Iowa employee, you will have access to an excellent benefits package.We are expanding our capabilities while maintaining our culture focused on quality, customer service and community. Consider accelerating your leadership and technical skills by joining us on the next phase of our growth strategy.Key Areas of ResponsibilityComplianceImplement new policies and revise existing programs to ensure compliance with regulatory requirements and cGMP.Evaluate completed work to determine whether it meets specifications, standards, and regulations. Direct and implement modifications to bring project, facility, and processes into compliance.Oversee equipment listing and coordinate facility and control systems calibrations and associated PMs to keep facility GMP compliant.ManufacturingLead start-up of sterile facility and process qualification of new manufacturing lines.Develop life cycle plans for all manufacturing equipment.Recommend design improvements to optimize manufacturing and safety procedures in accordance with divisional goals.LeadershipInstill a safe and compliant work environment.Hire, develop and manage the performance of staff.Interpret and implement HR policies and procedures and assure staff are compliant with university policies and procedures.Training/EducationCollaborate with Quality Assurance and Manufacturing Operations on the design, evaluation, and coordination of employee training on new equipment and processes.Be a Subject Matter Expert (SME) to other departments on the operation of equipment and facilities.Financial Develop departmental budget by recommending capital equipment, spare parts and service agreements for equipment and facilities.Provide oversight and control of departmental operating budget and project expenditures.Set financial priorities for projects and project budgets.Apply Process Improvement, Quality Engineering, and Management Engineering Concepts and MethodologiesMaintain the engineering change control process and equipment assessments.Hands on process improvement and validation for pharmaceutical process equipment.Validate life cycle of equipment including authoring of validation master plans, URSs, FAT, SAT, IQ, OQ, PQ and engineering studies.For a complete job description, please contact Libby Kleppe at [email protected] RequirementM.S. in Engineering (preferably Chemical or Mechanical).Experience RequiredMinimum 5-7 years of related experience in a pharmaceutical, GMP environment, laboratory, or biological environment. This experience is evidenced by demonstration of knowledge and/or skills in areas such as: isolator operation, automated technologies, environmental controls, utilities (WFI and clean steam) aseptic processes.Experience or knowledge in quality control.Experience in qualifying facility, equipment, and control systems.Demonstrated ability to communicate effectively, orally and in technical writing, to a variety of constituents internal and external to the organization.Strong skills in developing SOPs, work instructions, validation documents, deviations, investigations, and batch records.Knowledge of pharmaceutical regulations, FDA, cGMP, EU, ISPE, etc.Intermediate skills creating and editing documents in MS Excel and Word or comparable programs.Professional experience working effectively with individuals from a variety of backgrounds and perspectives.Desirable QualificationsPharmaceutical, Manufacturing, or Engineering project-related experiences including lyophilizer operation and/or maintenance.Experience with Process Mapping and/or project management.Understanding of Six Sigma and Lean manufacturing methodology.Experience operating under design control and GMP manufacturing.Experience with SCADA systems, Metasys systems, or JCI controls in heavy industries and pharmaceuticals.Microbiology and environmental monitoring experience.Benefits HighlightsRegular salaried position. Located in Iowa City, Iowa.Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans.For more information about Why Iowa? Click here.The University of Iowa is an equal opportunity/affirmative action employer. All qualified applicants are encouraged to apply and will receive consideration for employment free from discrimination on the basis of race, creed, color, religion, national origin, age, sex, pregnancy (including childbirth and related conditions), disability, genetic information, status as a U.S. veteran, service in the U.S. military, sexual orientation, gender identity, or associational preferences.recblid j72x4bv1aztprr9x4mnnhkocnbgr22

To control parts room inventory, identify, order, catalog, store, account for and issue machine parts, supplies and materials used by division. ESSENTIAL POSITION RESPONSIBILITIES Control parts room inventory, identify orders, catalog, store, account for issue parts and materials using software. Maintains organization and cleanliness of the parts room. Receives shipments of inventory and ensures orders are correct. Initiates and maintains all required records pertaining to maintenance parts and consults with engineers/vendors as needed. Participates as a member of the Team . Participates in ongoing development, communication and implementation of team concepts, programs and policies; coordinates work to ensure B.E.S.T. practices with all team members. Attends appropriate team meetings. As a member of the Team, fosters strong cohesiveness regarding all major issues; e.g., direction, annual plan, budget, policy changes, etc. Accepts responsibility to quickly identify any areas that lack cohesiveness, bringing them to the attention of the team leader and working with the team in a supportive manner to resolve issues and actively look for ways, and reinforces actions needed, to achieve synergy possible within the larger organization. Simmons Operating systems principles and objectives: Is familiar with Simmons' established operating systems (e.g. quality, security, office environment, company policies); understands the responsibility to maintain familiarity with the systems and this position's role in support of these systems - including a consideration of the impact of individual actions on the systems and the responsibility to communicate concerns and improvement ideas. Performs other duties as necessary in support of business objectives: This position description is intended to guide the activities of the Parts Room Attendant and is not intended to limit the thinking and creativity of the person to the work of this function nor is it intended that this describe all the work that may be required of the person in this position. Physical Activities: Ability to work in a wet, noisy, dusty, humid, hot or cold environment that has an unpleasant odor. Ability to walk and stand on feet for the entire shift. Ability to lift and carry up to 50 lbs. Frequent pulling, pushing and reaching. Requires frequent bending, stooping, kneeling, squatting. Requires working from step ladders. Ability to work with various chemicals and identify and use PPE in accordance with MSDS/SDS sheets. Personal Protective Equipment (PPE): safety footwear Travel: Technical Experience: Industry Experience: Preferred e xperience or knowledge in mechanical equipment, sources of supply, and parts catalog interpretation. Minimum Education : Ability to read, write and speak English. Must have basic math skills. Preferred Education : High School Diploma or G.E.D.