Industrial Engineer Salary in Marietta, GA

Civil Project ManagerMarietta, Georgia Salary: $85,000 - $90,000 (DOE) + Bonus Structure (Guaranteed $25,000 1st year) + 401(k) + Insurances (Dental, Vision, Life) + Company Vehicle and Fuel Allowance + Company PhoneAre you a Project Manager from a civil background who is eager to join a company who will support your career aspirations?Are you a Project Manager eager to join a rapidly growing contractor offering full industry training in a specialist field?On offer is the chance to earn a great annual salary with a brilliant bonus scheme (with a guaranteed 1st year bonus of $25,000) and work on multiple projects across the residential, commercial and industrial sectors.Having established themselves as a leading contractor, with a growth rate of over 1 million within the last 2 years, they are undertaking their mission to expand through the addition of excellent team members to fulfil a large pipeline of projects. This is a great time to join the time with potential to further progress onto senior/leadership roles.In this role, you will be based in the Georgia office where you will have the exciting opportunity to work on a combination of projects within the Construction Industry including pressure grouting projects, structural support projects, earth retention, and slab jacking projects.This is an amazing opportunity that offers a great salary for your expertise. In addition, this company will support your career aspirations in the coming years through mentorship and vital experience, enhancing your experience within the industry.The role:Overseeing and managing pressure grouting from inception to completionOrganizing sub bids, in house take offs, design-build estimating, subcontractor bid qualification, proposal presentation to clientsManagement of all project documentationLeading regular project meetings with clients, architects and engineersAdhering to AIA and OSHA standardsPurchasing and managing materials and resourcesThe Person: Must come from a Civil background Minimum of 2-5 years' experience as a Project Manager within the Construction Industry, ideally with knowledge on Civil Construction/EngineeringUS Work AuthorizationA Valid Driving LicenseEnjoys working independently, and is flexible with an open schedule

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: Marietta, OH (on-site)Group: Laboratory Products GroupDivision: Laboratory Products DivisionThe Marietta Manufacturing site is a part of the Laboratory Products Division. Our laboratory equipment products are used primarily by pharmaceutical companies for drug discovery and development and by biotechnology companies and universities for life science research to advance the prevention and cure of diseases and enhance quality of life. Our offering consists of equipment, accessories, and services for sample preparation, storage and protection, and analysis.How will you make an impact?You will succeed in this role if you enjoy resolving problems and improving existing processes.What will you do?Establish and optimize manufacturing processes, methods and procedures to assure product conformance, quality and cost effectiveness.Resolve production issues and keep production running to support customer requirements until corrective actions can be implemented. Partner with Set-up, Maintenance, Quality, Operators, and other groups as needed to accomplish this.Uses fact-based analysis to identify gaps (NCRs, systemic problems, etc.) and develop corrective and preventive actions to address. Responsible for timely implementation of countermeasures.Identify and implement Continuous Improvement projects and/or general improvement projects, applying Lean methodologies and PPI tools.Coordinate and direct investigations in new processes, materials and technologies, providing training for the operation as needed.Coordinate and complete the validation process for new processes and equipment.Provide technical assistance and expertise to manufacturing in problematic situations, implementing corrective action and providing training as the need arises.Establish and maintain manufacturing specifications, i.e., BOM, routings, set up sheets and other related technical recommendations and documentation.Represent manufacturing engineering on New Product Development teams, ensuring new products that are brought to market are capable of being manufactured to accepted specifications.Prepares capital appropriation requests and owns administering the approved project capital.May coordinate and present manufacturing plans at design review meetings with R&D and Business leadership.How will you get here?EducationBachelor's degree in Engineering or related field is required (Mechanical or Industrial preferred)Experience2+ years of relevant experienceKnowledge, Skills and AbilitiesOutstanding attention to detail and interpersonal skillsSelf-starter, independent and detailedAbility to work in a fast paced environmentAbility to maintain a high degree of confidentialityEffective time management and prioritization skillsHighly effective verbal and written communication skillsAbility to respond quickly to sight and sound and the ability to read gauges, dial, meters, and instructionsThis position has not been approved for relocation assistance.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.

POSITION SUMMARY:In this exciting role as an Validation Senior Quality Engineer, you will design or plan protocols for equipment or processes to produce tissue-based products, biologic drug products and medical device products meeting internal and external purity, safety and quality requirements. This position will ensure compliance with all applicable, regulatory requirements, company policies, and standards. You will have the opportunity to drive a culture of continuous improvement by deploying sound engineering fundamentals to achieve quality objectives and ultimately yielding better patient outcomes.ESSENTIAL DUTIES AND RESPONSIBILITIES:Manage projects, efforts, and changes of moderate complexity and scope including but is not limited to, process performance qualifications, sterilization validations, stability studies, packaging simulated distribution studies, equipment validations, etc.Communicate quality standards and requirements within the organization.Project management with a focuses on planning and organizing a project and its resources from initiation through planning, execution, monitoring and control through closure.Collaborate with engineering and manufacturing functions to ensure quality standards are in place.Participate in continuous improvement activities that directly impact performance measures.Leads product quality investigations in support of CAPA, complaints and nonconforming material processes.Collect, analyze and interpret statistical data, performs analyses and provide reports as required.Takes an active role in leading, and reviewing design and manufacturing changes.Assists with internal and external audit activities.Leads Quality Assurance and product quality improvements in cross-functional initiatives.Supports day-to day manufacturing activities.Specialize in the areas of production control, incoming material, product evaluation and reliability, inventory control, and development as they apply to product or process quality.Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.Overlook and participate change approval process for risk assessment, verification, and validation.Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.PROBLEM SOLVING:Performs advanced areas of work for the professional fieldIdentifies key barriers/core problems and applies problem-solving skills in order to deal creatively with complex situations. Troubleshoots and resolves complex problems.Makes decisions under conditions of uncertainty, sometimes with incomplete information, that produce effective end resultsDECISION MAKING/SCOPE OF AUTHORITY:Independently performs assignments with instruction limited to results expected. Determines and develops approach to solutionsReceives technical guidance only on unusual or complex problems or issuesMay manage elements/portions of a budget/projectSPAN OF CONTROL/COMPLEXITY:Seasoned professional contributor with responsibility for an advanced area of work in the professional fieldMay be responsible for entire projects or functions having modest scope/impact or portions of projects having considerable scope/impact to department resultsEDUCATION/EXPERIENCE:BS degree in Science, biomedical, mechanical, industrial or similar engineering discipline3+ years of Quality Assurance /Engineering experience in an FDA-regulated industryPrefer cGMP pharmaceutical industry, biologics industry experience; medical device or tissue processing industries consideredPrefer Certified Quality Engineer (CQE) or other similar Quality/reliability certificationsPrefer Six Sigma certificationKnowledge of FDA, AATB, ISO, and other state/federal/international regulations and standardsExperience in utilization of statistical techniques such as the design of experiments, hypothesis testing, SPC, etc.SKILLS/COMPETENCIES:Excellent oral, written, and interpersonal communication skillsProficient in Microsoft Office (Excel, Word, etc.) Organized, flexible, and able to multi-task while maintaining a high level of efficiency and attention to detailMust show aptitude to develop appropriate skills needed for the job