Assurance Manager Salary in St. Louis, MO

Job DescriptionWhen you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you'll be supported in achieving your career goals.Location/Division Specific InformationWork Location: St. Louis, MO (on-site)Group: Pharma Services GroupDivision: Drug Substance DivisionHow will you make an impact?We are searching for a Manager, Manufacturing Sciences with education and experience in biopharmaceutical processing or a related field. This member of our team provides technological input in the development, validation, and transfer of manufacturing processes. The Manager, Manufacturing Sciences routinely supports the Process Engineering team as technical owners of customer programs in a manufacturing environment and will be highly involved and act as a subject matter expert in defining and shaping Thermo Fisher Scientific's own technology programs.This role will collaborate with internally with supervisors/managers and technicians in the Operations department, Quality Assurance, fellow Engineers, and scientists in Process Development and with the client as a Process Engineer program lead or as a Process Engineering subject matter expert. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success. What will you do?Draft, review and approve Standard Operation Procedures, and Job Aids and consult internally to ensure scientifically sound and robust procedures. Collaborate with the process development to develop standardized methodologies and learn/explore/initiate new methodologies for conducting unit operations at the manufacturing scale including cell culture, harvest, and purification. Contribute to Internal and Customer meetings based upon sound evidence without supervision. Initiate and lead internal projects and lead client projects and manage timelines with minimal support from supervision. Actively identify error proofing opportunities and initiate and drive engineering initiatives to improve practices and procedures without supervision. Provide scientific expertise for GMP deviations by assessing, reviewing and approving the impact of major deviations on both the product quality and the validation of the process or consults the process engineering team and internal teams on product impact. Initiate and lead changes to equipment and process design, proactively and without supervision. Consult on non-standard/challenging process design and/or validation strategies. Draft, review and approve Manufacturing Batch Records, Performance Qualifications, Process Validation protocols, process flow diagrams, automation methods, and Bill of Materials, ensuring the process is technically accurate and designed for Manufacturing. Draft, review, and approve Process control documents, campaign summary report and process validation reports. Acts as subject matter expert to troubleshoot design flaws, ensure process design is scientifically sound and robust and within the validated process and regulatory guidelines. Reviews, analyzes and trends process data without supervision Provide technical feedback on documents created by other departments, such as Tech Transfer Protocols and SOPs. Troubleshoot technical challenges on the manufacturing floor as needed for a 24/7 manufacturing facility. Support our MSAT team with additional tasks to improve the site, ensure patient safety, and deliver for our customers. Provides development and training for Process Engineers/Scientists. How will you get here?EducationBachelor's degree required in a scientific field, preferably in engineering or the biochemistry field, with 8+ years of experienceMaster's degree with 6+ years of experience or PhD with 3+ years of experience will be consideredExperienceExperience within a GMP Environment / Biologics / Pharma Industry highly preferredExperience in a leadership role is requiredKnowledge, Skills and AbilitiesFollow Environmental, Health and Safety policies and procedures and ensure a safe and healthy workplace environment. Ability to self-motivate, prioritize work and time. Demonstrates a foundation in general scientific practices, principles, and concepts. Writes and communicates effectively. Ability to work both independently and as part of a team. Knowledge of current Good Manufacturing Practices and US/EU regulations. Advanced knowledge of statistical methods used for Pharmaceutical Process Analysis is a plus. Proficient in Microsoft Word and Excel. Ability to stand for prolonged periods of time and gown into manufacturing areas. 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 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.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.Accessibility/Disability AccessJob Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

Invenergy drives innovation in energy. Powered by decades of entrepreneurial experience and unparalleled execution, we solve the energy challenges facing our customers and communities. We provide power generation and storage solutions at scale around the world to create a cleaner energy future. We develop. We build. We own. We operate. We are Invenergy.Job DescriptionAbout the SiteBlue Bird Solar is a 139MW-AC solar powered generation facility located in Warrenton MO, utilizing TMEIC inverters, NEXTracker trackers, with an attached substation.Position OverviewAs an Operations & Maintenance Manager you will be responsible for managing the Blue Bird Solar Farm.ResponsibilitiesManage all aspects of the day to day operation of the facility in a safe and environmentally sound manner.Prepare and implement plant operating and maintenance procedures ensuring compliance with all Federal, State and Local requirements.Recruit, select, train and manage plant operating, maintenance and administrative staff.Prepare annual operating budgets and periodic status reports.Interface and coordinate with local customers and suppliers.Procure parts, materials, services and support resolution of technical issues.Ensure compliance with all project safety, environmental and contractual responsibilities.Provide a high level of professionalism and technical expertise.Perform routine Quality Assurance checks of solar technician work.Assist solar technicians from time to time in various solar maintenance and troubleshooting activities.Required SkillsHigh School diploma or equivalentA minimum of six (6) months of supervisory experience.Computer proficiency with Microsoft Office software.Excellent verbal and written communications skills.Must be able to work outdoors in inclement weather, climb portable ladders without assistanceThis position may require the ability to remotely manage new projects within a region, so candidate must be willing to travel up to 50% as business needs warrant.Willing to work nights during scheduled and unscheduled maintenance activitiesAbility to move and manipulate up to 45 kg (100 pounds).Valid driver's license and acceptable driving record.Eligible to work in the United States without the need for employer visa sponsorship now or in the futurePreferred Education and/or Work ExperienceTechnical degreeExperience in power generation facilitiesA minimum of 10 years of experience in a manufacturing or skilled trade environment.Experience with PV maintenance, including DC systems, AC medium voltage systems, and network communications and monitoringExperience with the operation of various SCADA systemsSkilled in the use of testing equipment and tools such as Thermographic Electrical Inspection, I-V Curve Tracing, Meggers, and Ground Fault DetectionStrong Analytical and Diagnostic capabilities to troubleshoot and correct problems foundKnowledge of National Electrical Code (NEC), NFPA, and other standard practicesAbility to read and understand electrical single-line and three-line diagrams / schematicsIndividuals receiving conditional offers of employment will be subject to drug testing and must receive a negative result to begin working for the company.BenefitsEligible for medical, dental, vision, 401(k), profit sharing, bonus, paid time off, etc.Invenergy LLC is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to, among other things, race, color, religion, sex, sexual orientation, gender identity, national origin, age, status as a protected veteran, or disability.

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

Establish and maintain working professional relationships with the project design team, company field and office personnel, subcontractors, and vendorsLead the preparation of construction documentsAdminister contracts with owner, subcontractors, and vendorsManage value engineering effortsPrepare and process all paperwork and documents to owner, project design team and subcontractors in a timely and complete mannerEnsure compliance with construction permitsPrepare and maintain project schedule and budgets, communicating changes to project personnel as neededReview, approve, and process draw requests and payments to suppliers and subcontractorsWork with owner in transitioning the project from construction to residential operations.Address all project completion and warranty issues and prepare final close-out documentationManage budget and financial reportingInterpret and analyze reports to ensure adherence to project budget.Manage the Quality Assurance/Quality Control (QA/QC) program.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.3+ years of Construction Project Management experienceStrong background in Commercial ConstructionStrong oral and written communication skillsProficient in Microsoft Office Suite and ProCoreThe ability to work in a fast paced work environmentAbility to work independently and as part of a teamThe desire to grow their career professionallyThe desire to drive the growth of a highly reputable General ContractorThe desire to mentor some of the younger Project ManagersStrong track record with client relationshipsDetail orientedGood time management skillsGround up experience is preferredProven ability to deliver commercial construction projects on time and on budgetMust be able to work in a multiple-project environmentCapable of problem solving and experience with complex detailed projects

The Senior Quality Assurance Specialist is a systems and product support role that will initiate and manage the implementation and maintenance of quality systems supporting operations, quality, and product compliance. This may include support and management of the Deviation and CAPA Program, Complaint and Customer Notification Program, Internal audit Program, Change Control Management, Document and Record Control, Training Program and product support functions supported by the Quality Systems. The Senior Quality Assurance Specialist is a highly motivated and meticulous individual with excellent problem-solving and communication skills. The Senior Quality Assurance Specialist responsibilities focus on enhancing manufacturing site by providing expertise in advanced problem solving and implementation of corrective and preventative actions. The Senior Quality Assurance Specialist works closely with internal team members, stakeholders, collaborators, and participating facilities to ensure that root cause analysis is conducted in a timely manner to achieve goals. Additional responsibilities include:Provides Root Cause Analysis (RCA) support using performance improvement tools (e.g.,5 Why, Is/Is not, fishbone) and methodology, in addition to project management support for systemwide root cause analysis.Utilizes project management tools and methodologies to track and communicate the status of RCA and provides regular updates to the RCA Teams, ensuring the team is informed of status updates of the root cause analysis.Develops appropriate communication plans and strategies to ensure information is openly communicated.Demonstrates leadership in developing and implementing quality system initiatives in areas of Operations and Product Support.Recognize those areas of quality systems that exhibit an opportunity for improvement (ex. Documentation management, Training, Nonconformance management etc.) based upon business, customer, and regulatory requirements and develop, implement, and maintain these Quality Systems to ensure a level at or above industry standards.Support the Development of project plans for specific quality system initiatives and process improvements.Maintains current understanding of quality systems for business units and applies and interprets regulations in making business decisions and risk assessments. Establishes and maintains collaborative relationships within the system in order to obtain information and content from leaders and front-line staff to foster successful root cause analysis completion.Act as initial contact with Product Engineering, R&D, Production, and other support groups requesting additional information for regulated products, product status, or quality support. Lead change team assessment of end-to-end impact for product, process, systems, assay/method, and equipment change controls.Develops and manages best practices and tools for improvement, plan execution, and project management.Support product initiatives or custom business opportunities.Lead Administrative user for TrackWise Quality Management System Software.Ensure personnel are treated with respect and dignity with an emphasis on providing a strong avenue for communication and company values.Act as Lead Auditor of Internal Auditing TeamsConduct Training (individual, group, departmental & the entire Quality System)Participation in customer audits, regulatory audits, registration audits as a Subject Matter Expert of applicable Quality Management SystemsWho you are:Minimum Qualifications:Bachelor's degree in Life Sciences discipline, (Chemistry, Pharmacy, Chemical or Process Engineering) along with 4+ years of experience in Quality System (i.e., ISO environment) with experience in a specific QA job functionorBachelor's degree in any discipline along with 10+ years of Quality System (i.e., ISO environment) with experience in a specific QA job functionor Master's degree or PhD Degree in Chemistry, Biochemistry, Biology, Pharmacy or Engineering along with 3+ years of Quality System (i.e., ISO environment) with experience in a specific QA job functionLocation: onsite 3506 South Broadway, St Louis, MO - 3 days per week in office Preferred Qualifications:Knowledge of ISO 9001 and ISO 13485.Knowledge of ISO 9001 and ISO 13485 and regulatory compliance issues (i.e., FDA, USDA, ICH, IVDR, EDQM) related to biologic derived materials, and prior experience working in a controlled/regulated environment.Current fine chemical industry knowledge &/or experience.Excellent computer skills, including proficiency in MS Word, MS Excel, MS Access, MS Project, MS PowerPoint, and ability to learn and operate using other specific application software (SAP, Trackwise, etc.) Excellent communication (verbal & written) and customer services skills Excellent writing skills and experience writing technical documentation & reports Ability to simultaneously manage multiple tasks/priorities Excellent problem-solving skills/abilities Good time management and negotiating skills Capacity for independent work Data analysis, presentation, and experimental design knowledge Project management experience RSREMD

Establish and maintain working professional relationships with the project design team, company field and office personnel, subcontractors, and vendorsLead the preparation of construction documentsAdminister contracts with owner, subcontractors, and vendorsManage value engineering effortsPrepare and process all paperwork and documents to owner, project design team and subcontractors in a timely and complete mannerEnsure compliance with construction permitsPrepare and maintain project schedule and budgets, communicating changes to project personnel as neededReview, approve, and process draw requests and payments to suppliers and subcontractorsWork with owner in transitioning the project from construction to residential operations.Address all project completion and warranty issues and prepare final close-out documentationManage budget and financial reportingInterpret and analyze reports to ensure adherence to project budget.Manage the Quality Assurance/Quality Control (QA/QC) program.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.3+ years of Construction Project Management experienceStrong background in Commercial ConstructionStrong oral and written communication skillsProficient in Microsoft Office Suite and ProCoreThe ability to work in a fast paced work environmentAbility to work independently and as part of a teamThe desire to grow their career professionallyThe desire to drive the growth of a highly reputable General ContractorThe desire to mentor some of the younger Project ManagersStrong track record with client relationshipsDetail orientedGood time management skillsGround up experience is preferredProven ability to deliver commercial construction projects on time and on budgetMust be able to work in a multiple-project environmentCapable of problem solving and experience with complex detailed projects

The Quality Assurance Specialist provides compliance oversight across the MilliporeSigma Quality Management System (QMS) in collaboration with site personnel. As a QA Specialist you are responsible for the implementation and maintenance of Quality Systems and processes to ensure internal and external compliance and the promotion of quality practices that meet or exceed required guidelines and regulatory requirements. Responsibilities: include maintenance and continuous improvement of the overall Quality Program.Improve quality systems in ISO and non-GMP production environments.Drive quality improvement in multiple departments.Complete a high volume of work to meet department goals.Communicate the status of operations and bring critical deviations to the attention of your manager.Communicate with coworkers and interact with other departments on a regular basis.Complete and have accurate work consistently with quality guidelines.Assist in maintaining department KPIs through on time CAPAs, Deviations, Complaints and Change Controls.Assist in compliance with Life Science and site quality policies and procedures.Represent the site during customer and regulatory audits.Perform internal audits.Assist in the investigation of customer complaints. Contribute to Root Cause Investigations & Effectiveness Checks of Nonconforming IncidentsConduct Quality System Training Documentation control activities include management of the electronic documentation management system, and the ability to write, review or approve Operation Procedures, Specifications, Master Manufacturing & Packaging Procedures and other controlled documents.Physical Requirements: 70-100% Office Environment, 10-30% On-the-QA floor activities/observation.Give site tours of facilities including use of stairs.Who you are:Minimum Qualifications:Bachelor's degree in Life Sciences discipline, (Chemistry, Pharmacy, Chemical or Process Engineering) along with 3+ years of experience in Quality System (i.e., ISO environment) with experience in a specific QA job functionorBachelor's degree in any discipline along with 5+ years of Quality System (i.e., ISO environment) with experience in a specific QA job functionor Master's degree or PhD Degree in Chemistry, Biochemistry, Biology, Pharmacy or Engineering along with 2+ years of Quality System (i.e., ISO environment) with experience in a specific QA job functionLocation: onsite- St Louis, MO - 3 days per week in office Preferred Qualifications:Good computer skills, including proficiency in MS Word, MS Excel, MS Access, MS Project, MS PowerPoint, and ability to learn and operate using other specific application software (SAP, Trackwise, etc.) Excellent communication (verbal & written) and customer services skills Good writing skills and experience writing technical documentation & reports Ability to simultaneously manage multiple tasks/priorities Good problem-solving skills/abilities Good time management and negotiating skills Capacity for independent work Environmental conditions: Varies depending on specific job responsibilities.

**Beacon Hill Exclusive** Client in St. Louis is in search for a Quality Manager-Manufacturing. The id eal candidate will need a minimum of 5 years in Quality & Manufacturing as well as management of staff, must have ISO9000 experience and the ability to analyze data and have experience with Root Cause Corrective Action events. Responsibilities include hands on effectiveness of quality processes, create detailed work instructions, monitor and implement testing to ensure the processes are working and make adjustments as needed and manage, develop and train QC Inspectors and production line. Salary to $120K plus bonus. For immediate consideration please apply and send your resume to [email protected] or call 314-563-2588.Beacon Hill is an Equal Opportunity Employer that values the strength diversity brings to the workplace. Individuals with Disabilities and Protected Veterans are encouraged to apply.If you would like to complete our voluntary self-identification form, please click here or copy and paste the following link into an open window in your browser: https://jobs.beaconhillstaffing.com/eeoc/Completion of this form is voluntary and will not affect your opportunity for employment, or the terms or conditions of your employment. This form will be used for reporting purposes only and will be kept separate from all other records.Company Profile: Founded by industry leaders to set a new standard in search, career placement and flexible staffing, we deliver coordinated staffing solutions with unparalleled service, a commitment to project completion and success and a passion for innovation, creativity and continuous improvement.Our niche brands offer a complete suite of staffing services to emerging growth companies and the Fortune 500 across market sectors, career specialties/disciplines and industries. Over time, office locations, specialty practice areas and service offerings will be added to address ever changing constituent needs.Learn more about Beacon Hill Staffing Group and our specialty divisions, Beacon Hill Associates, Beacon Hill Financial, Beacon Hill HR, Beacon Hill Legal, Beacon Hill Life Sciences and Beacon Hill Technologies by visiting www.beaconhillstaffing.com . We look forward to working with you.Beacon Hill. Employing the Future (TM)

MilliporeSigma in St. Louis, MO is seeking a Project Manager to lead projects and initiatives as well as continued administrative tasks primarily focused on bidding and order fulfillment for our Customs and Bulks business. Project stakeholders include leadership and individual contributors in R&D, Production, Quality Assurance, Quality Control, Marketing, Procurement and Material Management functions. Responsibilities: Build custom product and service proposals for external and internal customers with input from all functions required to fulfill orderBid and order fulfillment for bulk inquiries and custom projects and ensure proposals are compatible with the capability and capacity of the operations site fulfilling the orderFacilitate customer interactions with operations sites by hosting technical discussions and ensuring proper communication and intellectual property controlCoordinate with operations to determine costs and lead times for bulk and custom opportunities. Define and plan with limited starting information and assemble teams with specialized skillsets for specific projects Maintain regular progress and milestone communication to stakeholders and be responsible for documentation and systems setup for Custom and new product introductionWrite, review, and obtain approval for operations documents and set up of new products in SAP and document control systems such as eDOC or MangoAid in continuous process improvements aimed at decreasing lead times and increasing the competitive quality of our products and servicesMaintain proactive safety and quality standardsMaintain and manage project costs to budget Who You Are:Minimum Qualifications: Bachelor's degree in Chemistry, Biology, Chemical Engineering or other Science or Engineering field 3+ years of project management experience Preferred Qualifications:Master's degree in Chemistry, Biology, Chemical Engineering or related Science or Engineering discipline with 2+ years of industry experienceFamiliarity with project management software and toolsProject management certificationCustomer interface experienceTechnical knowledge of chemical or biologics processingKnowledge of manufacturing processes and challengesTechnical writing experienceHigh level organization and communication skills Demonstrated skill in Project Planning and executionTeam leadership experienceProficient in MS Office suiteExperience working within and/or lead multisite, cross functional project teamsExcellent communication skills, both verbal and writtenExperience pivoting priorities based on business needsProven proficiency in planning and scheduling, problem solving, project management, time management, prioritization & decision-making skills.Proficient with MS SharePoint, MS Project, Smartsheets, Wrike, MS Access, Statistical Analysis, Process Flow software and other project management toolsRSREMD

Establish and maintain working professional relationships with the project design team, company field and office personnel, subcontractors, and vendorsLead the preparation of construction documentsAdminister contracts with owner, subcontractors, and vendorsManage value engineering effortsPrepare and process all paperwork and documents to owner, project design team and subcontractors in a timely and complete mannerEnsure compliance with construction permitsPrepare and maintain project schedule and budgets, communicating changes to project personnel as neededReview, approve, and process draw requests and payments to suppliers and subcontractorsWork with owner in transitioning the project from construction to residential operations.Address all project completion and warranty issues and prepare final close-out documentationManage budget and financial reportingInterpret and analyze reports to ensure adherence to project budget.Manage the Quality Assurance/Quality Control (QA/QC) program.MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.3+ years of Construction Project Management experienceStrong background in Commercial ConstructionStrong oral and written communication skillsProficient in Microsoft Office Suite and ProCoreThe ability to work in a fast paced work environmentAbility to work independently and as part of a teamThe desire to grow their career professionallyThe desire to drive the growth of a highly reputable General ContractorThe desire to mentor some of the younger Project ManagersStrong track record with client relationshipsDetail orientedGood time management skillsGround up experience is preferredProven ability to deliver commercial construction projects on time and on budgetMust be able to work in a multiple-project environmentCapable of problem solving and experience with complex detailed projects