Chemical Engineer Salary in St. Louis, MO

The Project Engineer is responsible for developing and implementing engineering solutions to problems and opportunities at MilliporeSigma's St. Louis, Missouri facility. The Project Engineer's responsibilities include: Provide project management and engineering for small, medium, and large capital projects, from project initiation through start-up, turnover, and project closure Develop project requirements, deliverables, schedules, and budget Manage capital project scope, budget, and schedule through project life cycle Procure necessary contractors, materials, and equipment to support projectsWork with General Contractors, skilled construction workers, internal skilled resources, and Engineers Coordinate schedules with stakeholders and manufacturing, manage the day-to-day project activity, and manage the knowledge transfer from end of project to manufacturing startup Responsible for the turnover package to site support teams including AutoCAD drawings, PM plans, spare parts, asset records, and knowledge transfer Attend seminars, conferences, and training to maintain and expand technical expertiseSupport departmental process improvement efforts based on annual objectivesResponsible for installation and maintainability of GMP utilities, facilities, and equipment (including automation equipment) such as but not limited to HVAC, compressed gases, process water, clean steam, chilled water, cleanrooms, isolators, HEPA filtration, etcSupport capital planning and reportingSupport the Management of Change process and utilizes good documentation practicesEnsure team utilizes safe work practicesIssue work permits regularlyPerform job hazard analysis, equipment assessments, failure fault trees, and risk assessments to drive continuously safe culturePurchase materials as neededEnsure/support GMP compliance (e.g. work order processing, good documentation practices, change management process, deviation review, CAPA assignments, etc.)Perform effective problem solving and root cause analysis to resolve issues, develop options, and prevent reoccurrenceCollaborate with Maintenance and Head of Engineering and Maintenance to deliver a 5yr strategic roadmap for capital expenditure projects, covering people, processes, systems, and infrastructure Manage multiple projects concurrentlyWork closely with the site EHS, Quality and Mechanical Integrity to develop engineering solutionsManage field construction work in support of projects Who You Are:Minimum Qualifications: Bachelor's Degree in Chemical Engineering, Mechanical Engineering, or other engineering discipline3+ years engineering experience within a pharmaceutical or chemical production environment1+ year managing capital engineering projects Preferred Qualifications: Experience of awareness of pharmaceutical standards, rules, and guidance documents (e.g., FDA, EU, IOS, ISPE, etc.) Experience in creating or managing the creation of engineering/construction bid packages Experience in managing construction work in support of projects GMP manufacturing, engineering, or compliance experience Environmental Engineering experience Excellent oral and written communication skillsRead and interpret internal and external regulatory agencies' policies, codes, standards, and regulations

Job DescriptionAs part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world's toughest challenges, like protecting the environment, making sure our food is safe or helping find treatments for cancer. Location/Division Specific InformationLocation: US - St. Louis, Missouri, site basedDivision: PSG - BiologicsIn the Biologics business unit of Thermo Fisher Scientific we deliver, from process development through commercial supply, we offer the expertise and resources necessary to help clients deliver innovative large molecule therapies. Placed in the forefront of our leading and groundbreaking businesses enabling clients to change lives with therapeutics for often unmet needs. How will you make an impact?The Manufacturing Sciences and Technology (MSAT) Director is responsible for leading all facets of Process Validation, Technology Transfer into manufacturing, GMP floor support and Continued Process Verification in accordance with current good manufacturing processes (cGMP). They will have a strong leadership and scientific mentorship to the MSAT team to ensure robust and reliable production processes are established through a meticulous technology transfer process to enable the site to meet and/or exceed client delivery commitments.This role will drive the planning, execution and customer interaction for the MSAT function during technology transfer from process development through to Commercial manufacturing. They will be accountable for all aspects of implementing, validating and monitoring robust and efficient manufacturing processes to produce human clinical trial and commercial products.What will you do? Leads the Manufacturing Science and Technology team and is responsible for process related activities enabling Drug Substance manufacturing of Biologic's.Is responsible for facility fit assessment, tech transfer activities, coordination of process start-up activities including Engineering Runs, GMP/clinical, PPQ and routine commercial runs, and resulting risk mitigation activities.Is responsible for Process Validation and Continued Process Verification activities.Supports manufacturing activities with active process monitoring and data trending, process deviation resolution, process improvements and scientific expertise in the Drug Substance fieldProvides strong technical leadership to process engineers, scientists and associates for clinical and commercial production.Coordinates scientifically and/or technically based process improvements of clinical and commercial manufacturing processes. Offers molecule steward and drive process lifecycle management initiative in accordance to customer's molecular strategy as needed.Actively liaises with external customers and internal partners to facilitate execution of customer projects.Operate as key point of contact for Joint Steering Committees engaging with senior level executives both internally and externally.Represent the St. Louis site as a domain expert during external and internal regulatory compliance inspections.Support the authoring, reviewing and approving of regulatory applications for customers as well as support responses to regulatory agencies.Build and responsibly manage operational budgets for the MSAT organization of the site.Responsible for recruitment and development of MSAT staff, ensuring effective utilization of resources through strong leadership, performance management and robust employee development plans.Drive continuous improvements and establish best-in-class MSAT capabilities by improving the enabling processes and systems.Works multi-functional with process development, manufacturing, quality assurance, quality control, supply chain, and facilities departments to effectively transfer, maintain and commercialize processes in the facility.Ensure that changes to existing processes or the introduction of new processes are carried out and documented according to approved change control procedures and in compliance with cGMP requirements.Requirements:PhD in Biotechnology, Chemical or Pharmaceutical Engineering, or related field, with minimum of 8 years of relevant experience; orM.S./M.A. in Biotechnology, Chemical or Pharmaceutical Engineering, or related field, with minimum of 12 years of relevant experience; orB.S./B.A. in Biotechnology, Chemical or Pharmaceutical Engineering, or related field, with minimum of 14 years of relevant experience.Knowledge, Skills, Abilities7+ years in a leadership role of sciences / technology groups in a fast-paced production environment.Broad experience in all process areas (Upstream cell culture, downstream processing, buffer and media preparation) and ancillary processes (CIP, SIP).Proficiency in working with multicultural and cross-disciplinary project teamsGood GMP knowledgeCustomer-centric mentalityExperience in leading teamsExcellent organization, planning, problem solving and critical thinking skillsExcellent writing, communication and presentation skillsEnergy and drive (committed, drive for results)Willingness to travel up to 10%Benefits:We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company pension, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation.Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one distributed team of 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.EEO/Reasonable Accommodation:Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and chip in to our singular mission-enabling our customers to make the world healthier, cleaner and safer.Apply today! http://jobs.thermofisher.comThermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status

Document Control SpecialistSt. Louis, MO, USA Req #578Thursday, April 4, 2024Company: Pioneer Industrial CorporationAbout Us Pioneer Industrial Corporation is a prominent corporation known for its expertise in sourcing, manufacturing, and servicing industrial equipment across various industries including refining, oil and gas, power, chemical, petrochemical, pulp & paper, food & beverage, and pharmaceutical sectors. Their wide range of industrial equipment encompasses Pressure Relief Valves (PRVs), Control Valves, Line Valves, Electric Actuators, Instrumentation, Pumps, Blowers, Mechanical Seals, and Fluid Sealing applications. With a commitment to quality and customer satisfaction, Pioneer Industrial offers comprehensive solutions to meet the diverse needs of their clients in the industrial sector. Join Pioneer Industrial Corporation and be part of a dynamic team driving innovation and excellence in the industrial equipment industry.SummaryWe are seeking a meticulous and organized Document Control Specialist to join our team. The ideal candidate will be responsible for managing the pre-order and post-order documentation process for Engineering, Procurement, and Construction (EPC) projects. This role requires attention to detail, excellent organizational skills, and the ability to collaborate effectively with cross-functional teams to ensure accurate and timely documentation management throughout the project lifecycle.Responsibilities Pre-Order Documentation Management Coordinate with project managers, engineers, and procurement teams to collect, review, and organize pre-order documentation such as technical specifications, drawings, vendor quotes, and contractual agreements. Ensure all pre-order documents comply with company standards, client requirements, and regulatory guidelines. Maintain an organized and easily accessible document repository for pre-order documentation, utilizing document control software or other relevant systems. Post-Order Documentation Management: Manage the receipt, review, and processing of documentation related to orders placed with vendors and subcontractors. Verify the accuracy and completeness of post-order documents, including purchase orders, material certifications, and supplier documentation. Work closely with the procurement team to track the status of orders and ensure timely delivery of required documentation. Document Control Procedure Develop and maintain document control procedures and workflows specific to EPC projects, ensuring adherence to industry best practices and project requirements. Implement efficient filing systems and naming conventions to facilitate easy retrieval and tracking of documents. Train project team members on document control processes and procedures as needed. Quality Assurance Conduct regular audits of document control processes to identify areas for improvement and ensure compliance with quality standards. Collaborate with internal and external stakeholders to address any discrepancies or issues related to documentation. Communication and Collaboration Serve as a primary point of contact for document-related inquiries from project teams, clients, vendors, and regulatory authorities. Foster strong communication and collaboration across departments to facilitate the exchange of information and documentation throughout the project lifecycle. Requirements Bachelor's degree in Engineering, Business Administration, or related field. Proven experience (1-3 years) working in document control, preferably within the EPC industry or similar project-based environments. Proficiency in document management software and tools Strong understanding of document control best practices, standards, and regulatory requirements. Excellent attention to detail and organizational skills. Effective communication and interpersonal abilities. Ability to work independently and collaboratively in a fast-paced environment. Familiarity with engineering drawings, technical specifications, and contractual documents. Certification in document control (e.g., Certified Document Controller) is a plus. #pioneerindustrial#FCG-L#LI- IP1 No Agencies, PleaseOther details Pay Type Salary

JOB DESCRIPTION Wood Applied Intelligence CEC Controls ( A Wood company) is currently recruiting for Senior Control Engineers to join our team in St. Louis, MO.This position will report to the appropriate manager in this location. We are looking for Senior Control Engineers that must be able to lead and perform the design of control systems, from start to finish, as well as the engineering and field start up for the "System Integration in the Electrical Controls" Industry for manufacturing. Experience in industries related to Automotive automation and controls preferred. Demonstrated troubleshooting skills are absolutely necessary. This is an ideal opportunity for an individual with solid experience to manage and lead a growing engineering team. Responsibilities: Performing Design of Automation control systems, requirements which will include: Review specifications and standard practices. Establishing non-standard designs as required. Follow internal and customer standards as required Create system map layouts, sequence of operations, drawing packages, PLC logic, and HMI screens. Specify Panel and field material by creating Electrical Bill of Material's (EBM's) Batch experience preferred Field duties and responsibilities include: Assisting in installation oversight Start-up and Debug at customers facilities Launch and Standby support Lead Responsibilities: Provide oversight and quality control for local engineering team Mentor junior to mid-level engineers in skill-set and career growth #LI-RemoteRESPONSIBILITIES Qualifications: Education: Associates Degree in Electrical Engineering, Bachelor Science Electrical Engineering, Chemical Engineering or Bachelor Science Electrical Engineering & Technology, or equivalent relevant work experience with a technical degree 12+ years of industry experience working for a systems integrator; must include control panel and circuit design (in it's totality) non-standard designs, system map layouts, sequence of operations, reviewing cycle time, studies and dimension switch layouts, design packages, design logic, enter logic, and the design of Smart Displays Knowledge of System Architecture, including non-standard material, control panel power requirements and/or distribution Capable of reviewing the specifications and standard practices (internal hardwired and logic standards, general specifications and scope of work) Technical knowledge and skills required : RSLogix 5, 5000 RS Networx for DeviceNet, ControlNet, EtherNet IP DriveExecutive, DriveExplorer PanelBuilder PDS, 1400e; 32, RSView Studio Technical knowledge/skills considered an asset: Ford NextGen standards; GM G12 standards, Microsoft Office Suite, Siemens Capable of assisting with installation, and debugging with no additional support Ability to work independently and in a team atmosphere Authorization to work lawfully in the US without sponsorship from Wood is required Physical Requirements: Able to climb a 2-story ladder Be able to cover, on foot, a reasonable distance on a job site

The Quality Engineer is responsible for developing, reviewing, and managing the execution of validation activities, and ensuring that the qualifications are consistent with the user's/manufacturer's requirements and quality standards. Interact cross-functionally with Manufacturing, Project Management, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and MaintenanceCreate and execute protocols for equipment, methods, analytical instrumentation, and cleaning, process controls, and facility including but not limited to FAT/SAT/IOQ and PQ documentsUtilize GDP in a GMP atmosphere while generating protocols and reviewing documents. Review and generate closing reports for executed protocolsCreate validation schedules, coordinate execution efforts with contractors, production operators, production engineers, customers, and quality assurance staff membersWork through a Management of Change system to determine the impact of proposed changes to the qualification status of equipment, software, or facilitiesDevelop/Establish an overall plan for qualifying new equipment or new/upgraded facility and establishing the proper controls for the introduction of equipment/facility and/or changes under proper quality standards (e.g. FDA, EU, ISO, ISPE, etc.)Identify and establish revalidation requirementsWrite and execute qualification packages, technical reports, and validation master plansDevelop cleaning validation protocols for equipment and facilitiesDevelop clean/dirty hold times This is a Hybrid role requiring 3 days per week onsite. Minimum Qualifications:Bachelor's Degree in Biomedical Engineering, Chemical Engineering, Chemistry, or Biochemistry Preferred Qualifications:2+ years of experience in quality or a quality support role2+ years of experience with equipment or validation, in a cGMP manufacturing setting or related industrial laboratory environmentAbility to utilize GDP during document creation and reviewWorking knowledge of current regulatory guidelines and standardsAbility to apply and incorporate regulatory standards, rules, and guidance. (e.g. FDA, EU, ISO, ISPE, etc.) Experience in a fast-paced environment with the ability to adjust to changing prioritiesDetailed-oriented work standardsSound understanding of Quality Risk Management conceptsRSREMD

At MilliporeSigma an exciting opportunity now exists to be a member of a critical Life Science manufacturing facility in St. Louis, MO. In this role, you will assist in the research and troubleshooting of defective products in order to identify potential root cause failure. Responsibilities:Identify key process parameters, define their impact on product quality, and subsequently develop and modify formulations, methods and controls to meet quality specificationsUtilize your processing insights to recommend and implement improvements, modifications, or additions to document workSupport the maintenance of production records and documentsAs you grow in your position, manufacturing supervisory duties may be includedAs the facility is highly team-oriented, the opportunity exists to attend cross-functional meetings with R&D, Engineering, and Operations teamsYou will work with outside contractors and other vendors to manage changes to site automation systemsIn this role you will maintain and adhere to project timelines/schedule and costWho You Are:Minimum Qualifications:Bachelor's Degree in Chemical Engineering, Chemistry, Biochemistry, Mechanical Engineering or other Science or Engineering discipline3+ years of experience in engineering Preferred Qualifications:Master's Degree in Chemical Engineering, Chemistry, Biochemistry, Mechanical Engineering or other Science or Engineering discipline 3+ years of experience in process engineeringBlack Belt certificationProven ability to maintain and adhere to project timelines, schedule and cost Ability to communicate and lead cross-functional meetings with R&D, Engineering, and Operations teamsAbility to fill in for supervisor and support QC and QARSREMD