8 Manufacturing Companies jobs in Fraser
Sr Quality Control Engineer
48308 Rochester, Michigan
Endo International
Posted 4 days ago
Job Viewed
Job Description
**Why Us?**
We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life.
**Job Description Summary**
The Quality Engineer is a role within the Quality Control organization which oversees Computer System Validation (CSV) activities for all Quality Control software and equipment/instrumentation. The individual in this position will create, execute, review, and approve validation documentation, participate in cross-functional planning, and execution meetings as well as provide support for issue resolution.
Additionally, this role would be the Subject Matter Expert for Data Integrity for the Quality Control department. The role is responsible for identifying compliance and data integrity issues related to QC equipment and implement effective resolutions. The role provides assistance to Regulatory Agency inspections and audits in addition to providing guidance and recommendations for identified data situations.
**Job Description**
Scope of Authority
The incumbent in this position is specifically to focus Quality Control Laboratories and provides software/equipment/process solutions to the laboratory. The role will be responsible for creation, execution, and approval of validation for all QC software and equipment. Additionally, acts as a Subject Matter Expert for electronic Data Integrity topics.
Key Accountabilities
Accountability
Project Planning
Develop, manage, and oversee validation plans.
Define project timelines and provide updates to stakeholders.
Create and manage Capital Appropriation Requests.
Highlight, communicate and elevate issues as needed.
Equipment/ Software Onboarding
Oversee site validation activities (e.g., equipment, processes, computer system validation) to ensure compliance with cGMP.
Lifecycle management of Quality Control software and equipment.
Data Integrity
Identify compliance and data integrity issues related to QC equipment and implement effective resolutions.
Participate on management teams preparing for audits and inspections.
Safety
Follows EH&S procedures to ensure a safe work environment
Continuous
Other
Customer interface and meeting customer expectations
Qualifications
Education & Experience
+ Bachelor's degree in life science, physical science, or technology field with 6+ years' laboratory experience in QC functions in a GMP laboratory
+ Data Integrity assessment experience
+ Direct experience authoring/editing/executing validation documents for laboratory equipment and/or laboratory systems (LIMS, ELN, CDS)
+ Excellent knowledge of FDA regulations, ISPE guidelines and ISO standards
Knowledge
_Proficiency in a body of information required for the job_
_e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc._
+ Review and evaluate internal validation documentation (i.e., user requirement specifications, functional specifications, protocols, reports, etc.)
+ Perform review of vendor protocols and creation of in-house supporting documentation to deliver a complete package of qualification documentation
+ Develop and implement solutions to validation related discrepancies and deviations
+ Ensure compliance to data integrity requirements in a GMP environment
+ Computer System Validation (CSV) experience within the life sciences industry.
+ Experience working in a GMP Quality Control Laboratory.
Skills
&
Abilities
+ Work in compliance with Quality Management System requirements
+ Intermediate to advanced computer skills
+ Strong attention to detail. Highly productive, able to manage time and prioritize tasks to meet timelines
+ Experience with Customer interface and meeting customer expectations.
+ Regularly contributes and represents department/group on multi-disciplinary teams. Builds extensive relationships across the organization and has an in-depth understanding of all key department and how they interface with responsibilities.
+ Coordinate with end users and process owners to lead development of validation strategy for projects, systems, and processes.
+ Implement procedures, training and oversight to ensure the integrity of data generated to support testing processes.
+ Manage contractors supporting validation projects
+ Works independently on assessment using knowledge and work experience. Gathers input from colleagues and management to address issues.
Physical Requirements
+ Ability to lift 15 lbs.
+ Ability to walk across plant/laboratory
+ Travel up to 20% of the time may be required
**_Disclaimer:_** _The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required._
**EEO Statement:**
We firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
We want the best and brightest people to help us achieve our mission to develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering healthcare and are dedicated to supporting each other as we work to bring the best treatments forward. Our shared values of Integrity & Quality, Innovation, Drive, Collaboration and Empathy guide our team and enable us to deliver upon our vision of helping everyone we serve live their best life.
**Job Description Summary**
The Quality Engineer is a role within the Quality Control organization which oversees Computer System Validation (CSV) activities for all Quality Control software and equipment/instrumentation. The individual in this position will create, execute, review, and approve validation documentation, participate in cross-functional planning, and execution meetings as well as provide support for issue resolution.
Additionally, this role would be the Subject Matter Expert for Data Integrity for the Quality Control department. The role is responsible for identifying compliance and data integrity issues related to QC equipment and implement effective resolutions. The role provides assistance to Regulatory Agency inspections and audits in addition to providing guidance and recommendations for identified data situations.
**Job Description**
Scope of Authority
The incumbent in this position is specifically to focus Quality Control Laboratories and provides software/equipment/process solutions to the laboratory. The role will be responsible for creation, execution, and approval of validation for all QC software and equipment. Additionally, acts as a Subject Matter Expert for electronic Data Integrity topics.
Key Accountabilities
Accountability
Project Planning
Develop, manage, and oversee validation plans.
Define project timelines and provide updates to stakeholders.
Create and manage Capital Appropriation Requests.
Highlight, communicate and elevate issues as needed.
Equipment/ Software Onboarding
Oversee site validation activities (e.g., equipment, processes, computer system validation) to ensure compliance with cGMP.
Lifecycle management of Quality Control software and equipment.
Data Integrity
Identify compliance and data integrity issues related to QC equipment and implement effective resolutions.
Participate on management teams preparing for audits and inspections.
Safety
Follows EH&S procedures to ensure a safe work environment
Continuous
Other
Customer interface and meeting customer expectations
Qualifications
Education & Experience
+ Bachelor's degree in life science, physical science, or technology field with 6+ years' laboratory experience in QC functions in a GMP laboratory
+ Data Integrity assessment experience
+ Direct experience authoring/editing/executing validation documents for laboratory equipment and/or laboratory systems (LIMS, ELN, CDS)
+ Excellent knowledge of FDA regulations, ISPE guidelines and ISO standards
Knowledge
_Proficiency in a body of information required for the job_
_e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc._
+ Review and evaluate internal validation documentation (i.e., user requirement specifications, functional specifications, protocols, reports, etc.)
+ Perform review of vendor protocols and creation of in-house supporting documentation to deliver a complete package of qualification documentation
+ Develop and implement solutions to validation related discrepancies and deviations
+ Ensure compliance to data integrity requirements in a GMP environment
+ Computer System Validation (CSV) experience within the life sciences industry.
+ Experience working in a GMP Quality Control Laboratory.
Skills
&
Abilities
+ Work in compliance with Quality Management System requirements
+ Intermediate to advanced computer skills
+ Strong attention to detail. Highly productive, able to manage time and prioritize tasks to meet timelines
+ Experience with Customer interface and meeting customer expectations.
+ Regularly contributes and represents department/group on multi-disciplinary teams. Builds extensive relationships across the organization and has an in-depth understanding of all key department and how they interface with responsibilities.
+ Coordinate with end users and process owners to lead development of validation strategy for projects, systems, and processes.
+ Implement procedures, training and oversight to ensure the integrity of data generated to support testing processes.
+ Manage contractors supporting validation projects
+ Works independently on assessment using knowledge and work experience. Gathers input from colleagues and management to address issues.
Physical Requirements
+ Ability to lift 15 lbs.
+ Ability to walk across plant/laboratory
+ Travel up to 20% of the time may be required
**_Disclaimer:_** _The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required._
**EEO Statement:**
We firmly believe in the principles of equal employment opportunity and strive to create an atmosphere where all employees, regardless of their race, color, creed, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability (including pregnancy), age, or military or veteran status, feel valued, respected, and empowered. Our commitment to EEO extends to every aspect of employment, including recruitment, hiring, training, promotions, compensation, benefits, transfers, terminations, and all other employment practices. We are dedicated to ensuring that all employment decisions are based on qualifications, skills, and merit.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
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0
Senior Quality Control Engineer
48201 Detroit, Michigan
$105000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a detail-oriented Senior Quality Control Engineer to join their automotive manufacturing team in Detroit, Michigan . This hybrid role requires a blend of on-site quality assurance activities and remote data analysis. You will be responsible for developing, implementing, and managing comprehensive quality control systems and procedures to ensure the highest standards of product quality and consistency. Your duties will include conducting rigorous testing, analyzing quality data, identifying areas for improvement, and collaborating with production and engineering teams to implement corrective actions. The ideal candidate will have extensive experience with quality management systems (QMS) such as ISO 9001 or IATF 16949, statistical process control (SPC), and various inspection techniques. You will lead quality audits, train inspection personnel, and contribute to the continuous improvement of manufacturing processes. Proficiency in quality analysis software and a strong understanding of automotive manufacturing standards are essential. This is an opportunity to play a pivotal role in maintaining and elevating the quality reputation of a leading automotive supplier. You will be integral to ensuring that every product meets or exceeds customer expectations and industry benchmarks.
Responsibilities:
Responsibilities:
- Develop and implement robust quality control plans and procedures.
- Conduct product testing, inspection, and validation processes.
- Analyze quality data to identify trends, root causes, and areas for improvement.
- Implement corrective and preventive actions (CAPA) to address quality issues.
- Lead internal quality audits and support external audits.
- Ensure compliance with QMS standards (e.g., IATF 16949).
- Train and mentor quality inspection personnel.
- Collaborate with production and engineering teams on quality initiatives.
- Manage non-conformance reporting and resolution.
- Contribute to continuous improvement efforts through quality tools and methodologies.
- Bachelor's degree in Engineering or a related technical field.
- 5+ years of experience in quality control/assurance, preferably in automotive manufacturing.
- Strong knowledge of QMS (ISO 9001, IATF 16949).
- Proficiency in SPC, FMEA, and root cause analysis tools.
- Experience with measurement and testing equipment.
- Excellent analytical, problem-solving, and documentation skills.
- Good communication and teamwork abilities for hybrid work.
- Experience with quality inspection and validation techniques.
- Relevant certifications (e.g., ASQ Certified Quality Engineer) are a plus.
Apply Now
1
Automotive Quality Control Engineer
48201 Detroit, Michigan
$90000 Annually
WhatJobs
Posted 8 days ago
Job Viewed
Job Description
A leading automotive manufacturer is seeking a highly meticulous and skilled Automotive Quality Control Engineer to join their team in Detroit, Michigan, US . This vital role will be responsible for ensuring that all automotive products meet stringent quality standards and customer expectations throughout the production lifecycle. You will implement and manage comprehensive quality control processes, conduct inspections, and analyze production data to identify and resolve quality issues. The ideal candidate will possess a Bachelor's degree in Mechanical Engineering, Automotive Engineering, or a related field, with significant experience in automotive quality assurance and control. Proficiency with quality management systems, such as ISO 9001 and IATF 16949, is essential. Responsibilities include developing and implementing quality inspection plans, analyzing defect data, and leading root cause analysis investigations. You will work closely with production teams, design engineers, and suppliers to address quality concerns and implement corrective and preventive actions. Strong problem-solving skills, attention to detail, and a deep understanding of statistical process control (SPC) are required. You will also be involved in supplier quality management, ensuring that incoming components meet specified standards. The ability to conduct audits and drive continuous improvement initiatives in quality performance is crucial. We are looking for a proactive and technically adept individual who is passionate about automotive quality and committed to upholding the highest manufacturing standards. This position offers a competitive salary, excellent benefits, and opportunities for professional growth within the automotive industry.
Apply Now
2
Creative Implementation Quality Control Lead
48222 Detroit, Michigan
Rocket Companies Inc.
Posted today
Job Viewed
Job Description
Rocket is a Detroit-based company made up of businesses that provide simple, fast and trusted digital solutions for complex transactions. The name comes from our flagship business, now known as Rocket Mortgage, which was founded in 1985. Today, we're a publicly traded company involved in many different industries, including mortgages, fintech, real estate and more. We're insistently different in how we look at the world and are committed to an inclusive workplace where every voice is heard. Apply today to join a team that offers career growth, amazing benefits and the chance to work with leading industry professionals.
You will play a key leadership role in championing the quality and accuracy of all creative assets across our channels. As the Creative Implementation QC Leader, your mission is to ensure every piece of work that reaches the market is flawless, consistent, and aligned with our brand. You'll support and mentor a team devoted to raising the bar for creative excellence. Your expertise will make a tangible impact on our brand's reputation and creative achievements.
About the role
* Lead, support, and develop the quality control team, empowering a culture of accountability and high performance
* Oversee and execute the quality assurance process for all creative deliverables prior to publication or trafficking
* Guarantee that every asset meets brand, technical, and legal requirements for any channel or format
* Collaborate closely with creative, production, and external partners to tackle feedback and resolve discrepancies quickly
* Design, refine, and uphold quality control checklists, standard operating procedures, and best practices
* Track and report errors, root causes, and corrective measures to foster continuous improvement
* Assert the final approval on all assets by ensuring pixel-perfect accuracy, consistency, and compliance
* Provide training and set best practices for the team as quality procedures or industry standards evolve
About you
Minimum Qualifications
* 3 years of experience in creative quality control, production management, design, or a related creative field
* Strong understanding of creative production workflows across digital, video, and print channels
* Proven ability to identify errors and inconsistencies in high-volume creative output
* Exceptional organizational skills and keen attention to detail
* Demonstrated collaboration skills with cross-functional creative, production, and trafficking teams
* Proficient with creative software and tools
* Effective written and verbal communication skills
Preferred Qualifications
* Bachelor's degree in marketing, design, communications, or a related field
* Prior experience leading or mentoring others
* Background in managing or implementing quality control processes for omnichannel campaigns
* Knowledge of advertising compliance regulations and creative standards
* Ability to operate effectively in fast-paced, high-stakes environments and meet tight deadlines
* Experience training teams on quality standards and procedures
* Familiarity with quality assurance platforms or automated QC tools
* Foundational knowledge in AI-powered marketing and communications
What you'll get
Our team members fuel our strategy, innovation and growth, so we ensure the health and well-being of not just you, but your family, too! We go above and beyond to give you the support you need on an individual level and offer all sorts of ways to help you live your best life. We are proud to offer eligible team members perks and health benefits that will help you have peace of mind. Simply put: We've got your back. Check out our full list of Benefits and Perks.
About us
Rocket is a Detroit-based company made up of businesses that provide simple, fast and trusted digital solutions for complex transactions. The name comes from our flagship business, now known as Rocket Mortgage, which was founded in 1985. Today, we're a publicly traded company involved in many different industries, including mortgages, fintech, real estate and more. We're insistently different in how we look at the world and are committed to an inclusive workplace where every voice is heard. Apply today to join a team that offers career growth, amazing benefits and the chance to work with leading industry professionals.
This job description is an outline of the primary responsibilities of this position and may be modified at the discretion of the company at any time. Decisions related to employment are not based on race, color, religion, national origin, sex, physical or mental disability, sexual orientation, gender identity or expression, age, military or veteran status or any other characteristic protected by state or federal law. The company provides reasonable accommodations to qualified individuals with disabilities in accordance with applicable state and federal laws. Applicants requiring reasonable accommodations in completing the application and/or participating in the application process should contact a member of the Human Resources team, at
You will play a key leadership role in championing the quality and accuracy of all creative assets across our channels. As the Creative Implementation QC Leader, your mission is to ensure every piece of work that reaches the market is flawless, consistent, and aligned with our brand. You'll support and mentor a team devoted to raising the bar for creative excellence. Your expertise will make a tangible impact on our brand's reputation and creative achievements.
About the role
* Lead, support, and develop the quality control team, empowering a culture of accountability and high performance
* Oversee and execute the quality assurance process for all creative deliverables prior to publication or trafficking
* Guarantee that every asset meets brand, technical, and legal requirements for any channel or format
* Collaborate closely with creative, production, and external partners to tackle feedback and resolve discrepancies quickly
* Design, refine, and uphold quality control checklists, standard operating procedures, and best practices
* Track and report errors, root causes, and corrective measures to foster continuous improvement
* Assert the final approval on all assets by ensuring pixel-perfect accuracy, consistency, and compliance
* Provide training and set best practices for the team as quality procedures or industry standards evolve
About you
Minimum Qualifications
* 3 years of experience in creative quality control, production management, design, or a related creative field
* Strong understanding of creative production workflows across digital, video, and print channels
* Proven ability to identify errors and inconsistencies in high-volume creative output
* Exceptional organizational skills and keen attention to detail
* Demonstrated collaboration skills with cross-functional creative, production, and trafficking teams
* Proficient with creative software and tools
* Effective written and verbal communication skills
Preferred Qualifications
* Bachelor's degree in marketing, design, communications, or a related field
* Prior experience leading or mentoring others
* Background in managing or implementing quality control processes for omnichannel campaigns
* Knowledge of advertising compliance regulations and creative standards
* Ability to operate effectively in fast-paced, high-stakes environments and meet tight deadlines
* Experience training teams on quality standards and procedures
* Familiarity with quality assurance platforms or automated QC tools
* Foundational knowledge in AI-powered marketing and communications
What you'll get
Our team members fuel our strategy, innovation and growth, so we ensure the health and well-being of not just you, but your family, too! We go above and beyond to give you the support you need on an individual level and offer all sorts of ways to help you live your best life. We are proud to offer eligible team members perks and health benefits that will help you have peace of mind. Simply put: We've got your back. Check out our full list of Benefits and Perks.
About us
Rocket is a Detroit-based company made up of businesses that provide simple, fast and trusted digital solutions for complex transactions. The name comes from our flagship business, now known as Rocket Mortgage, which was founded in 1985. Today, we're a publicly traded company involved in many different industries, including mortgages, fintech, real estate and more. We're insistently different in how we look at the world and are committed to an inclusive workplace where every voice is heard. Apply today to join a team that offers career growth, amazing benefits and the chance to work with leading industry professionals.
This job description is an outline of the primary responsibilities of this position and may be modified at the discretion of the company at any time. Decisions related to employment are not based on race, color, religion, national origin, sex, physical or mental disability, sexual orientation, gender identity or expression, age, military or veteran status or any other characteristic protected by state or federal law. The company provides reasonable accommodations to qualified individuals with disabilities in accordance with applicable state and federal laws. Applicants requiring reasonable accommodations in completing the application and/or participating in the application process should contact a member of the Human Resources team, at
View Now
3
Senior Pharmaceutical Quality Control Analyst
48201 Detroit, Michigan
$88000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory facility in Detroit, Michigan . This critical role focuses on ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis. Responsibilities include performing analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques such as HPLC, GC, UV-Vis, and FTIR. You will be responsible for reviewing and interpreting test data, preparing analytical reports, and ensuring all laboratory activities comply with Good Manufacturing Practices (GMP) and regulatory guidelines.
The ideal candidate will have extensive experience in pharmaceutical quality control and a strong understanding of analytical chemistry principles. You will be involved in method validation, equipment calibration and maintenance, and troubleshooting laboratory issues. Collaboration with R&D, manufacturing, and regulatory affairs departments is essential. This position requires meticulous attention to detail, excellent documentation skills, and a commitment to maintaining the highest standards of quality. Experience with LIMS (Laboratory Information Management System) is desirable. This is an excellent opportunity to contribute to the development and production of life-saving medications in a dynamic and growth-oriented environment. Our client offers comprehensive benefits and professional development opportunities.
Key Qualifications:
The ideal candidate will have extensive experience in pharmaceutical quality control and a strong understanding of analytical chemistry principles. You will be involved in method validation, equipment calibration and maintenance, and troubleshooting laboratory issues. Collaboration with R&D, manufacturing, and regulatory affairs departments is essential. This position requires meticulous attention to detail, excellent documentation skills, and a commitment to maintaining the highest standards of quality. Experience with LIMS (Laboratory Information Management System) is desirable. This is an excellent opportunity to contribute to the development and production of life-saving medications in a dynamic and growth-oriented environment. Our client offers comprehensive benefits and professional development opportunities.
Key Qualifications:
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific field.
- Minimum of 5 years of experience in pharmaceutical quality control or analytical laboratory setting.
- Proficiency in analytical instrumentation (HPLC, GC, etc.) and associated software.
- Thorough understanding of GMP, FDA regulations, and quality assurance principles.
- Excellent analytical, documentation, and problem-solving skills.
- Ability to work independently and as part of a team.
Apply Now
4
Senior Pharmaceutical Quality Control Analyst
48201 Detroit, Michigan
$85000 Annually
WhatJobs
Posted 14 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their state-of-the-art facility in Detroit, Michigan, US . This critical role ensures the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a deep understanding of analytical chemistry, pharmaceutical regulations (e.g., GMP, FDA), and advanced laboratory techniques. You will be responsible for performing complex analytical tests on raw materials, in-process samples, and finished products, interpreting results, and documenting findings meticulously. This position involves method development and validation, instrument calibration and maintenance, and contributing to the continuous improvement of quality control processes. You will also collaborate with research and development teams, production, and regulatory affairs to ensure compliance and product integrity.
Key responsibilities include:
Key responsibilities include:
- Performing quantitative and qualitative analysis of pharmaceutical samples using various analytical techniques (e.g., HPLC, GC, UV-Vis, AAS, KF titration).
- Developing, validating, and troubleshooting analytical methods according to regulatory guidelines.
- Calibrating, maintaining, and performing performance qualification (PQ) on laboratory instruments.
- Interpreting analytical data, preparing detailed reports, and ensuring accuracy of results.
- Reviewing and approving laboratory testing records and deviations.
- Participating in internal and external audits and inspections.
- Providing technical guidance and training to junior analysts.
- Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPA).
- Maintaining laboratory inventory and ensuring compliance with safety protocols.
- Contributing to the improvement of quality systems and processes.
Apply Now
5
Traveling Quality Control Manager - MSG - Data Centers
48222 Detroit, Michigan
Turner Construction Company
Posted 2 days ago
Job Viewed
Job Description
Division: Critical Facilities-Data Centers
Project Location(s): Milwaukee, WI 53201 USA
Minimum Years Experience: Travel Involved: Job Type: RegularJob Classification: ExperiencedEducation:Job Family:ConstructionCompensation:Salaried Exempt
* This position is for a full time traveling assignment supporting an Advanced Technology project, which includes our Data Center, Pharmaceutical, Industrial/Manufacturing, and EV/Battery/Renewables market segment groups (MSG). *
Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents. Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff.
Reports to: Project Manager or Project Executive
Essential Duties & Responsibilities*:
* Manage the development and implementation of the project-specific QA/QC Plan in coordination with the project team, the owner/architect team and the contract documents.
* Assure that sufficient, qualified specialized staff is assigned to provide the required knowledge and experience to execute the plan.
* Maintain a collaborative working relationship with owners, architects, consultants, subcontractors and vendors to ensure that the project-specific QA/QC Plan delivers a fully compliant project.
* Lead, supervise and develop all Turner QA/QC staff, including providing input on or completing performance appraisals.
* Ensure strict adherence to ethics and compliance requirements at all times.
* Develop a comprehensive working knowledge and understanding of the contract documents (including Turner's contract, plans, specifications and applicable codes).
* Develop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements.
* Implement project-specific QA/QC Plan in coordination with the project safety plan.
* Understand the project execution plan and coordinate QA/QC procedures at appropriate stages of the work, in line with the project schedule.
* Continually improve strategies and tools to efficiently and effectively document, track and record compliance with the contract documents.
* Execute the project-specific QA/QC Plan in a manner that engages all project staff, subcontractors, vendors and consultants.
* Execute the project-specific QA/QC Plan in a manner that engage all project staff, subcontractors, vendors and consultants.
* Conduct testing and inspections and arrange for third-party testing and inspections. Analyze and report the results.
* Expand the development of the plan as the project progresses as appropriate to expand the project by continually improving procedures.
* Direct removal and replacement of, and document all non-compliant materials and/or workmanship. Document compliance after corrective work is completed prior to starting any subsequent work.
* Research and apply additional QA/QC and Lean procedures to enhance the quality of project delivery.
* Oversight of project close-out and quality reports.
#LI-SO2
Qualifications: Bachelor's Degree with a minimum of five years' experience or equivalent combination of education, training and/or experience and construction experience that bridges both field and engineering responsibilities. Knowledge of the construction process, means and methods, and materials, their characteristics, installation procedures and tolerances. Strong computer skills and a familiarity with Microsoft Office Suite. Knowledge of Turner's project management software and leadership skills. Very strong verbal and written communication skills are required. Proven leadership qualities and skills with the desire to teach and mentor staff. May require QA/QC certification depending on specific project.
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and taste or smell. The employee is frequently required to stand and walk. The employee is occasionally required to climb or balance and stoop, kneel, or crouch. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Work Environment: While performing the duties of this job, the employee regularly works on-site at the construction work site where the employee is exposed to moving mechanical parts; high precarious places; fumes or airborne particles; outside weather conditions and risk of electrical shock. The noise in these work environments is usually moderate to very loud.
* May perform other duties as assigned.
Turner is an Equal Opportunity Employer - race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by applicable law.
Project Location(s): Milwaukee, WI 53201 USA
Minimum Years Experience: Travel Involved: Job Type: RegularJob Classification: ExperiencedEducation:Job Family:ConstructionCompensation:Salaried Exempt
* This position is for a full time traveling assignment supporting an Advanced Technology project, which includes our Data Center, Pharmaceutical, Industrial/Manufacturing, and EV/Battery/Renewables market segment groups (MSG). *
Position Description: Responsible for planning, coordinating and developing the project-specific Quality Assurance/Quality Control (QA/QC) Plan that incorporates the policies and procedures necessary to deliver the project fully compliant with the contract documents. Manage, supervise, and administer the implementation of the project-specific QA/QC Plan and QA/QC staff.
Reports to: Project Manager or Project Executive
Essential Duties & Responsibilities*:
* Manage the development and implementation of the project-specific QA/QC Plan in coordination with the project team, the owner/architect team and the contract documents.
* Assure that sufficient, qualified specialized staff is assigned to provide the required knowledge and experience to execute the plan.
* Maintain a collaborative working relationship with owners, architects, consultants, subcontractors and vendors to ensure that the project-specific QA/QC Plan delivers a fully compliant project.
* Lead, supervise and develop all Turner QA/QC staff, including providing input on or completing performance appraisals.
* Ensure strict adherence to ethics and compliance requirements at all times.
* Develop a comprehensive working knowledge and understanding of the contract documents (including Turner's contract, plans, specifications and applicable codes).
* Develop engineering procedures, including document control, submissions management, creation and tracking of Requests For Information (RFIs), material samples, documentation and tracking of potential cost changes, documentation and tracking of approved change orders within budgetary requirements.
* Implement project-specific QA/QC Plan in coordination with the project safety plan.
* Understand the project execution plan and coordinate QA/QC procedures at appropriate stages of the work, in line with the project schedule.
* Continually improve strategies and tools to efficiently and effectively document, track and record compliance with the contract documents.
* Execute the project-specific QA/QC Plan in a manner that engages all project staff, subcontractors, vendors and consultants.
* Execute the project-specific QA/QC Plan in a manner that engage all project staff, subcontractors, vendors and consultants.
* Conduct testing and inspections and arrange for third-party testing and inspections. Analyze and report the results.
* Expand the development of the plan as the project progresses as appropriate to expand the project by continually improving procedures.
* Direct removal and replacement of, and document all non-compliant materials and/or workmanship. Document compliance after corrective work is completed prior to starting any subsequent work.
* Research and apply additional QA/QC and Lean procedures to enhance the quality of project delivery.
* Oversight of project close-out and quality reports.
#LI-SO2
Qualifications: Bachelor's Degree with a minimum of five years' experience or equivalent combination of education, training and/or experience and construction experience that bridges both field and engineering responsibilities. Knowledge of the construction process, means and methods, and materials, their characteristics, installation procedures and tolerances. Strong computer skills and a familiarity with Microsoft Office Suite. Knowledge of Turner's project management software and leadership skills. Very strong verbal and written communication skills are required. Proven leadership qualities and skills with the desire to teach and mentor staff. May require QA/QC certification depending on specific project.
Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and taste or smell. The employee is frequently required to stand and walk. The employee is occasionally required to climb or balance and stoop, kneel, or crouch. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Work Environment: While performing the duties of this job, the employee regularly works on-site at the construction work site where the employee is exposed to moving mechanical parts; high precarious places; fumes or airborne particles; outside weather conditions and risk of electrical shock. The noise in these work environments is usually moderate to very loud.
* May perform other duties as assigned.
Turner is an Equal Opportunity Employer - race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by applicable law.
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6
Assembly Line- 2nd & 3rd shifts
48091 Warren, Michigan
AtWork Group
Posted 12 days ago
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Job Description
A forklift drops of a crate of parts to your assembly line, all less than 15 pounds. You will take the parts out of the crate and hang them on racks. The racks will move through a machine that puts zinc plating on them and when they come out of the o Assembly line, Assembly, Manufacturing, Staffing
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