Senior Manager, Quality Centers of Excellence (Princeton, Hybrid)
Quality engineer job in Jefferson City, MO
The Senior Manager, Centers of Excellence (CoEs) is responsible for establishing, leading, and optimizing one or more prioritized CoEs within the Global Quality Operations organization-such as Inspection Readiness, Audit Effectiveness, or other strategic focus areas. This role drives execution of CoE initiatives, develops tools and frameworks, and delivers performance metrics and dashboards to support continuous improvement and operational excellence. The ideal candidate will have strong global collaboration skills and experience working across cross-functional teams in a matrixed environment.
**Key Responsibilities**
**Centers of Excellence Leadership**
+ Lead the development and execution of one or more CoEs (e.g., Inspection Readiness, Audit Effectiveness) aligned with global quality priorities.
+ Establish CoE charters, operating models, and governance structures to ensure clarity and accountability.
+ Develop and maintain tools, templates, and guidance documents to support CoE objectives.
+ Collaborate with global and regional quality teams to ensure consistent implementation and adoption of CoE practices.
**Execution & Delivery**
+ Drive the day-to-day operations of assigned CoEs, ensuring timely delivery of initiatives and measurable outcomes.
+ Coordinate cross-functional working groups and facilitate workshops to gather input and share best practices.
+ Support the development and rollout of training and communication materials related to CoE initiatives.
**Metrics & Performance Tracking**
+ Define and track key performance indicators (KPIs) to measure CoE impact and effectiveness.
+ Develop dashboards and reporting tools to provide visibility to leadership and stakeholders.
+ Analyze data to identify trends, gaps, and opportunities for improvement.
**Global Collaboration & Stakeholder Engagement**
+ Partner with stakeholders across Regulatory Affairs, Clinical, Manufacturing, Compliance, and IT to align CoE efforts with broader quality strategies.
+ Serve as a point of contact for CoE-related inquiries and support global engagement and alignment.
+ Contribute to enterprise-wide business excellence initiatives as needed.
**Team & Project Support**
+ May supervise or mentor junior staff or contractors supporting CoE activities.
+ Provide project management support for CoE-related initiatives.
+ Promote a culture of collaboration, accountability, and continuous improvement.
**Qualifications**
Required
+ Bachelor's degree in life sciences, engineering, business, or related field.
+ 5-7 years of experience in pharmaceutical quality, operations, or business excellence roles.
+ Solid understanding of GxP principles and global regulatory expectations.
+ Experience supporting audit or inspection readiness programs.
+ Strong communication and collaboration skills across global teams.
+ Proficiency in MS Office and data visualization tools (e.g., Excel, Power BI, Tableau).
Preferred
+ Experience establishing or managing Centers of Excellence or similar operational frameworks.
+ Lean Six Sigma or similar continuous improvement certification.
+ Familiarity with quality management systems and digital tools.
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $131,153.00 - Maximum $196,075.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
BMS Quality Manager (BQM) - Data Center Design, Engineering and Construction
Quality engineer job in Jefferson City, MO
Meta is seeking an experienced Building Management System (BMS) Quality Manager to join our Data Center Engineering & Construction (DEC) Quality team. Our team's mission is to optimize the delivery of our Building Management Systems to ensure it is completed on time, is safe, robust, reliable, and conforms to our design and quality requirements. Role will be supporting internal cross-functional teams, lead installation and commissioning efforts, oversee quality, and quickly adapt in an evolving space.Our data centers are the foundation upon which our rapidly growing infrastructure efficiently operates, and our innovative services are delivered. Building and operating data centers the "right" way is synonymous with ensuring high uptime, capacity availability and capital conservation. The data center engineering team thinks from chip to chiller (or electrical substation), determining configurations and ensuring maximum efficiency of our compute infrastructure.
**Required Skills:**
BMS Quality Manager (BQM) - Data Center Design, Engineering and Construction Responsibilities:
1. Manage, onboard, and lead the General Contractor BMS Lead(s), the Control Systems Integrator (CSI) and Electrical and Installation (E&I) controls contractor s throughout all phases of the project, while developing efficiency improvements and incorporating lessons learned to ensure a safe, robust, reliable and functional controls system that adheres to Meta's design and quality requirements
2. Establish a clear vision and foster cross-functional collaboration, coordination, and support among on-site project teams, including the Meta BMS team, general contractors, Control System Integrators, and installation contractors
3. Drive consistency and standardization across all buildings and Control System Integrators and installation contractors
4. Review, understand and ensure project level adherence to the issued revision of the BMS PLC Playbook
5. Perform BMS inspections (wiring, installation, and commissioning) and validate the status/progress of the projects including supporting the project teams, both internal and external, starting from the early stages of Mechanical, Electrical and Plumbing (MEP) construction by working with project level Construction Managers (both internal and external) to check the health of the project (including schedule), working with the project teams and supporting Regional Quality Managers (RQMs). Align internally on program/project related communications to ensure a clear, consistent message to trade partners
6. Assess team performance, build relationships and to support the project benchmark and mock-up process of the BMS installations to assure consistency across the project while coordinating these efforts across multiple cross-functional partners, in a timely manner, to minimize re-work
7. Work with Construction Managers, Regional Quality Managers and General Contractors to ensure creation, accuracy and maintenance of logical schedule(s) for construction, commissioning, and packaged equipment BMS activities while leveraging this data to identify early finish dates for detailed design delivery
8. Coordinate and manage both packaged equipment factory installed controls audits and BMS commissioning audits to ensure specification/requirement adherence and track identified deficiencies through completion
9. Coordinate and lead large multi-stakeholder meetings on a regular basis and communicate discussions to all key stakeholders
10. Support custom tooling and their integration into the construction processes as well as supporting other cross-functional program/project initiatives that directly impact the delivery of the BMS while simultaneously working to identify and mitigate risk associated with these efforts
11. Travel domestically as needed (anticipated 40-50% travel)
**Minimum Qualifications:**
Minimum Qualifications:
12. Bachelor's degree (Engineering, Construction Management, or equivalent degree) or relevant work experience
13. 10+ years of experience with a combination of Instrumentation and Controls programming/installation, general contractor MEP coordination/project management, commissioning (both mechanical and electrical) of data centers, or other large scale mission critical buildings
14. Experience with Industrial Automation and Building Management Control Systems (i.e. PLC/DDC)
15. 3+ years of experience with programming/designing of HVAC control systems & Electrical Power Monitoring
**Preferred Qualifications:**
Preferred Qualifications:
16. Experience with PLC, SCADA and OPC UA systems
17. Experience with Schneider Electric Unity Pro, AVEVA, and Ignition platforms
18. Experience with Schneider Modicon and Rockwell Allen-Bradley PLC Platforms
19. Experience with Autodesk ACC Build and Procore Platforms
20. Certified in the following: cGMP, CAP (Certified Automation Professional), and/or PMP (Project Management Professional)
**Public Compensation:**
$144,000/year to $201,000/year + bonus + equity + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.
Quality Engineer (Onsite - Columbia, MO)
Quality engineer job in Columbia, MO
Thank you for your interest in joining Solventum. Solventum is a new healthcare company with a long legacy of solving big challenges that improve lives and help healthcare professionals perform at their best. At Solventum, people are at the heart of every innovation we pursue. Guided by empathy, insight, and clinical intelligence, we collaborate with the best minds in healthcare to address our customers' toughest challenges. While we continue updating the Solventum Careers Page and applicant materials, some documents may still reflect legacy branding. Please note that all listed roles are Solventum positions, and our Privacy Policy: *************************************************************************************** applies to any personal information you submit. As it was with 3M, at Solventum all qualified applicants will receive consideration for employment without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Job Description:
Quality Engineer (Solventum)
We are pleased to report that Solventum has successfully completed the sale of its Purification & Filtration (P&F) business to Thermo Fisher Scientific Inc. (Thermo Fischer). This is a significant milestone for the P&F business, allowing for the strategic investment and resources needed to sustain growth and deliver customer solutions. Please note that this position is scheduled to transfer to a local subsidiary of Thermo Fisher in your country. However, the position is in a country where the transfer of employees to Thermo Fisher is delayed until a later date. By joining Solventum during this transitional period, you will be able to work alongside an energized and mission-driven team who is experiencing this transition along with you. Until the transfer is complete, you will be employed by Solventum, and your employment is subject to all applicable terms and conditions as outlined in our employment agreement and company policies
The Impact You'll Make in this Role
As a Quality Engineer, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:
Providing product assurance engineering support for commercialized products including specification and design control, change management, risk management, investigations, and continuous improvement.
Reviewing and approving IQ/OQ/PQ documents and validation documents to qualify and validate new equipment and processes.
Participating in and leading customer audits, ISO 9001 audits, ISO 13485 audits, internal audits, and other activities to identify improvement opportunities.
Providing quality assurance and control for products used in FDA regulated industries, including control of incoming materials, review of in-process tests and release tests and device history records.
Working with manufacturing engineers and other personnel to solve product quality issues.
Leading investigations, corrective action responses, trending and monitoring for nonconforming materials, complaints, and supplier issues.
Interacting with Division quality personnel and outside suppliers to ensure product quality and performance.
Driving quality improvement using engineering best practice, statistical techniques, and Lean Six Sigma methodologies.
Your Skills and Expertise
To set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications:
Bachelor's Degree or higher (completed and verified) from an accredited institution
Additional qualifications that could help you succeed even further in this role include:
Bachelor's degree or higher in Manufacturing/Industrial Engineering, Chemical Engineering, Mechanical Engineering, Statistics/Mathematics from an accredited institution
Three (3) years of engineering experience in a private, public, government or military environment
Experience with quality systems such as Quality Manuals, ISO-13485, 21 CFR Part 210, 211 and 820, metrology, calibration, auditing and supplier management
Working knowledge of root cause analysis tools and techniques
American Society for Quality, Certified Quality Engineer (CQE) certification or willingness to obtain
Proficiency in the use of statistical and quality engineering tools such as exploratory data analysis, basic statistics, Gage R&R, Analysis of Variance, Failure Modes and Effects Analysis, Statistical Process Control and Capability, acceptance sampling, correlation and regression, and experimental design
Excellent verbal and written communication skills
Proficient in MS Office (Word, Excel, PowerPoint, Access) and writing/using data queries, extracts and analysis
Skills including organization, resilience, collaboration, and curiosity.
Work location:
Onsite: Columbia, MO
Travel: May include up to 5% domestic travel
Relocation Assistance: is not authorized
Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status).
Supporting Your Well-being
Solventum offers many programs to help you live your best life - both physically and financially. To ensure competitive pay and benefits, Solventum regularly benchmarks with other companies that are comparable in size and scope.
Applicable to US Applicants Only:The expected compensation range for this position is $95,825 - $117,120, which includes base pay plus variable incentive pay, if eligible. This range represents a good faith estimate for this position. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate's relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental & Vision, Health Savings Accounts, Health Care & Dependent Care Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences and Retirement Benefits, etc.). Additional information is available at: *************************************************************************************** of this position include that corporate policies, procedures and security standards are complied with while performing assigned duties.
Solventum is committed to maintaining the highest standards of integrity and professionalism in our recruitment process. Applicants must remain alert to fraudulent job postings and recruitment schemes that falsely claim to represent Solventum and seek to exploit job seekers.
Please note that all email communications from Solventum regarding job opportunities with the company will be from an email with a domain *****************. Be wary of unsolicited emails or messages regarding Solventum job opportunities from emails with other email domains.
Solventum is an equal opportunity employer. Solventum will not discriminate against any applicant for employment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status.
Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly.
Solventum Global Terms of Use and Privacy Statement
Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at Solventum are conditioned on your acceptance and compliance with these terms.
Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application you will be asked to confirm your agreement with the
terms.
Auto-ApplyQuality Engineer Co-Op
Quality engineer job in Columbia, MO
Watlow is a global technology and manufacturing leader who provides world class engineering expertise through innovative thermal products and systems, enabling our customers to thrive. We are making a positive impact every day as our solutions enrich the lives of people everywhere. We have been providing breakthrough thermal solutions for nearly a century. Our corporate values guide us uncompromisingly to always do the right thing, continually learn and improve, respect everyone, and lead with service and humility.
The Co-op positions at Watlow offer a 6-8-month immersive experience for students seeking more than a typical internship. This program allows participants to step away from their academic studies and engage in real-world engineering challenges directly tied to the company's strategic objectives.
Located at one of Watlow's manufacturing center of excellence (MCOE's), co-op participants will work on impactful projects in design, testing, automation, and manufacturing development. They will have the opportunity to apply classroom knowledge to real-world manufacturing projects while collaborating closely with mentors and experienced engineers.
Co-ops development skills may include learning how to:
Collaborate with technicians working on first articles to support system acclimation and onboarding.
Lead investigations and analysis of non-conforming defects, with emphasis on top recurring issues.
Conduct Root Cause Analysis (RCA), investigations, and develop Corrective and Preventive Actions (CAPAs).
Participate in 8D corrective action processes for both customer-driven and internal projects.
Drive process control improvements using Statistical Process Control (SPC) tools and equipment.
Identify and monitor process parameters for early detection of nonconformance.
Apply statistical methods to solve complex process control issues.
Engage in emergent learning opportunities to expand technical knowledge and cross-functional collaboration.
Qualifications:
Currently enrolled in an accredited university pursuing a bachelor's or master's degree in mechanical, industrial, electrical engineering, computer science, or a similar field.
Available to take a semester off from school to work at a Watlow facility.
Ability to start in between January 2026 OR June of 2026.
Additional Co-op Perks:
Housing stipend or corporate housing available.
Comprehensive onboarding and immersion plan.
Mentorship program and networking opportunities.
Opportunity to participate in and support local STEM and charitable initiatives.
The Watlow co-op program offers students a chance to be part of a team working on projects that matter. It provides valuable experience beyond the classroom, allowing participants to build their engineering careers in a meaningful way.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
Industrial Engineer - Startup Manufacturing
Quality engineer job in Columbia, MO
Job DescriptionDescription:
ThermAvant Technologies, LLC designs and manufactures high-performance custom thermal management solutions, including advanced heat sinks and heat spreaders utilizing Oscillating Heat Pipe (OHP) technology. Our solutions serve terrestrial and aerospace applications. ThermAvant operates an AS9100D/ISO9001-certified facility in Columbia, Missouri.
Position Overview:
We are seeking a proactive Industrial Engineer to join our dynamic startup manufacturing team. The ideal candidate will be instrumental in developing and optimizing manufacturing processes, integrating new technologies, and scaling production efficiently. This role requires close collaboration with manufacturing engineers and cross-functional teams to drive continuous improvement and meet rapidly evolving production demands.
Key Responsibilities:
Design, develop, and implement efficient manufacturing processes for new and existing products.
Collaborate with manufacturing engineers to integrate new machinery and technologies into production lines.
Assist in development of production schedule processes to ensure timely delivery and optimal resource utilization.
Implement level loading strategies to balance workloads and maximize throughput.
Conduct time studies and workflow analyses to identify bottlenecks and areas for improvement.
Lead initiatives to scale production volumes rapidly while maintaining quality and efficiency.
Develop and maintain standard operating procedures (SOPs) and work instructions.
Utilize lean manufacturing principles and continuous improvement methodologies to enhance processes.
Monitor key performance indicators (KPIs) and implement corrective actions as needed.
Ensure compliance with safety, quality, and regulatory standards.
Requirements:
Required Qualifications:
Bachelor's degree in industrial engineering, Manufacturing Engineering, or a related field.
Minimum of 3 years of experience in an industrial engineering role within a manufacturing environment, preferably in a startup setting.
Proficiency in developing and optimizing manufacturing processes and workflows.
Experience with production scheduling, capacity planning, and level loading techniques.
Strong analytical and problem-solving skills.
Excellent communication and interpersonal skills.
Ability to work collaboratively in a fast-paced, team-oriented environment.
Familiarity with lean manufacturing principles and continuous improvement methodologies.
Preferred Qualifications:
Experience with integrating new machinery and technologies into manufacturing processes.
Knowledge of advanced manufacturing technologies, such as automation and additive manufacturing.
Proficiency in using manufacturing software tools for scheduling and process optimization.
#IndustrialEngineer #EngineeringCareers #ManufacturingJobs #ProcessImprovement #LeanManufacturing
#SixSigma #SupplyChainJobs #OperationsEngineering #EfficiencyExpert #ContinuousImprovement
Bilingual Customer Quality Specialist
Quality engineer job in Jefferson City, MO
The Quality Assurance (QA) Specialist is responsible for analyzing the efficiency and effectiveness of individual case analysts. The QA Specialist reviews cases, interactions and evaluates them for compliance with standardized process requirements in both English and Spanish languages.
**Key Responsibilities:**
The QA Specialist reviews cases, emails, and recorded telephonic interactions and evaluates them for compliance with standardized process requirements. Requirements may include soft skills in phone calls, clear communication in emails, and an adherence to directive in case work. Based on the review, the Quality Analyst provides a concise written analysis of the work reviewed along with feedback and coaching recommendations to improve the performance of the program.
**Required minimum qualifications:**
+ Bachelor's Degree or equivalent OR 4 years of relevant experience in lieu of degree.
+ Experience following defined processes.
+ Must be a US Citizen or Authorized to work in the US (if not a citizen) and a resident of the US for at least 3 years within the last 5 years.
+ Must have fluent written and verbal English and must be fluent verbal Spanish.
+ Candidates that do not meet the required qualifications will not be considered
**Preferred qualifications:**
+ Experience with CMS's 1095-A
+ Advanced proficiency with MS Office including SharePoint, Teams, Excel, Word, and PowerPoint
+ Strong verbal and written communication skills
+ Familiarity with process improvement systems such as Lean Six Sigma, Agile, and others.
+ Previous Federal Government experience.
**Compensation Ranges**
Compensation ranges for ASM Research positions vary depending on multiple factors; including but not limited to, location, skill set, level of education, certifications, client requirements, contract-specific affordability, government clearance and investigation level, and years of experience. The compensation displayed for this role is a general guideline based on these factors and is unique to each role. Monetary compensation is one component of ASM's overall compensation and benefits package for employees.
**EEO Requirements**
It is the policy of ASM that an individual's race, color, religion, sex, disability, age, sexual orientation or national origin are not and will not be considered in any personnel or management decisions. We affirm our commitment to these fundamental policies.
All recruiting, hiring, training, and promoting for all job classifications is done without regard to race, color, religion, sex, disability, or age. All decisions on employment are made to abide by the principle of equal employment.
Physical Requirements
The physical requirements described in "Knowledge, Skills and Abilities" above are representative of those which must be met by an employee to successfully perform the primary functions of this job. (For example, "light office duties' or "lifting up to 50 pounds" or "some travel" required.) Reasonable accommodations may be made to enable individuals with qualifying disabilities, who are otherwise qualified, to perform the primary functions.
**Disclaimer**
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job.
17.75
EEO Requirements
It is the policy of ASM that an individual's race, color, religion, sex, disability, age, gender identity, veteran status, sexual orientation or national origin are not and will not be considered in any personnel or management decisions. We affirm our commitment to these fundamental policies.
All recruiting, hiring, training, and promoting for all job classifications is done without regard to race, color, religion, sex, veteran status, disability, gender identity, or age. All decisions on employment are made to abide by the principle of equal employment.
Construction Quality Technician - Columbia, MO
Quality engineer job in Columbia, MO
Job Description
Job purpose
The Quality Technician performs and documents routine field and laboratory testing/inspections as required by the Project Quality Management Plan and/or as directed by a Quality Manager.
Duties and responsibilities
Testing Concrete for Air Content, Slump, and Temperature.
Making concrete cylinders/beams in the field for early or 28-day acceptance.
Nuclear Gauge Density Testing on Soil and Aggregate bases.
Using core drill to cut concrete cores on various pavements.
Measuring, trimming, and capping concrete cores.
Perform Concrete Plant Inspections
Sample aggregates and soils at jobsites, concrete plants, and quarries.
Break cylinders and cores for strength determination.
Maintain and calibrate company owned testing equipment.
Filling out, documenting, and submitting all reports that correlates with the above duties and responsibilities as required by the Owner.
Be reliable, possess a good attitude and strong work ethic.
Be a team player.
Perform other duties as assigned.
Qualifications
Below qualifications are not required for hire but must be acquired within one year of hire date.
MoDOT certifications for Concrete Field, Concrete Strength, Soil Denstity and/or Field Density and Aggregate Tech.
Nuclear Density Gauge Safety and Hazmat/Transportation Training Certification.
Railroad Safety Training.
30-hour OSHA training.
Ability to deal effectively and tactfully with a wide variety of individuals in person, via telephone and in writing. Excellent customer relations skills.
Ability to work independently and resolve practical problems, keeping all appropriate parties aware of issues or risks.
Have a strong work ethic.
Excellent verbal and written communication skills.
Understand basic behavior-based safety programs and enforce company's safety policies.
Must have and maintain a valid driver's license.
Must be able to pull trailers and maintain a DOT medical examination card.
Working conditions
Outside environment, exposure to all weather conditions and temperature extremes. Site specific exposure to hazardous materials requiring proper use of Personal Protective Equipment. Noise levels are site specific and may be subject to PPE.
Physical requirements
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 frequently required to stand; walk; use hands to handle/feel objects, tools, or controls; and reach with hands and arms.
You are occasionally required to climb or balance and stoop or kneel.
You must regularly lift and/or move up to 50 pounds. Specific vision abilities required by this job include distance vision, peripheral vision, depth perception, and the ability to adjust focus.
The position requires that you will walk the construction site, climb ladders, climb stairs, and walk on uneven ground.
Position will require employee to spend a large portion of their time on the project sites.
Millstone Weber is an Equal Opportunity Employer and has long led the industry in training and hiring a diverse and inclusive workforce. To accomplish our goals of quality, innovation and continuous improvement, we are committed to partnering with employees and subcontractors who share our company values and seek to continually exceed the expectations of project owners. We strive to maintain a work environment that provides all employees with an opportunity to be successful without regard to race, creed, color, religion, sex, sexual orientation, gender identity, national origin, disabled Veterans and Vietnam Era Veterans, age, or physical/mental condition. As part of that policy, we adopt and support the Equal Opportunity Laws that are designed to promote the full realization of equal employment opportunity through a positive continuing program.
Quality Area Lead - Jefferson City, MO
Quality engineer job in Jefferson City, MO
Job Title: Quality Area Lead - 3rd Shift Hours: M-F 12:00AM to 08:30AM; Training will be held on day shift Pay: $34.91/hour + Shift Differential ($6.28/hr) while working nights TYPE: HOURLY Minimum Education and Experience: + College Bachelor's degree preferred
+ Minimum 3 years related work experience, preferably in a quality environment
General Scope of Position: The Quality Lead role will have ownership of the performance of quality throughout the LIV area. They are required to lead autonomously, motivate and develop their team. This role is the business facing lead for the area, ensuring partnership across End to End Supply Chain operations.
Job Skills/Tasks:
Essential Functions:
+ Accountable for performance of the following:
+ Safety
+ 100% completion of risk assessments, SQC audits, SBO's for direct reports.
+ World class execution of 5S and GMP within their area.
+ Team's execution to the f-tag program.
+ Quality
+ Lead Quality Technicians
+ Report and review E-Incidents to suppliers
+ Participate in Internal Auidt program
+ Investigate MQI's with a cross functional team to prevent reoccurrence
+ Communicate holds to planning
+ Manage the rework area and instructions
+ Utilizes SAP QM and Unilever specifications including PLM and JDA TNT system and support verification of use for quality purposes.
+ Ensure all Area equipment validations are completed using IQ, OQ, PQ.
+ Calibrations of all department equipment
+ Owner of SOP and work instruction for Area to ensure updated regularly.
+ Supports effort to complete and maintain internal and external audits and certifications.
+ Responsible of traceability compliance and auditing to ensure compliance e.g includes annual mock recall exercises.
+ Ensures proper onboarding of new hires in department.
+ Oversee Cleaning and Disinfection execution on shift.
+ Supports and participates in Quality Pillar activities for UMS program.
+ Drives quality focused improvement activities, reducing quality losses.
+ Utilizes advanced knowledge of category and technology details and requirements to support site innovation and changes.
+ Supports the quality Digital agenda.
+ Ensure all supply's are ordered in a timely manner.
+ All other duties as assigned.
+ Productivity
+ Glidepath with area plan as well as overall factory plan.
+ Build strategic plan to execution targets for their department and program.
+ Utilization of shift handover checklist to ensure seamless communication across shifts.
+ Participation in daily Planning meeting to ensure alignment to area strategy.
+ Cost/Labor
+ Manage area labor to budget.
+ Complete department payroll
+ Data Integrity
+ Understand all quality data entry, and reporting.
+ Ability to coach others on proper usage.
Competencies:
Skills Required:
+ Ability to develop leaders.
+ Strong sense of self-accountability and thrives in an autonomous environment.
+ Flexible work schedule to ensure support across their teams of varying shifts.
+ Verified and demonstrated technical skills in manufacturing operations.
+ Proficient in Microsoft Office.
+ Planning
+ Understand and utilize data to drive decisions and align resources.
+ Lead discussions and decision making.
+ Manage multiple workstreams simultaneously.
+ Leadership
+ Ability to gain buy-in and motivate their area team as well as cross-functional team members.
+ Execute performance escalation standards.
+ Teamwork
+ One Team mindset.
+ Bias for Action.
+ Drives for solutions.
Personal Protective Equipment:
+ Refer to department specific PPE assessment
Promotional Progression: (List and Describe)
+ This is a developmental role that could lead to increasing leadership within Unilever. In this role you will be challenged to develop your area leadership team and ensure performance across all shifts. This position will require thorough knowledge of the operations environment and experience developing teams.
Why work for Unilever (******************************************************** | Culture for Growth (****************************************************** | Every Voice Matters (******************************************************************************************************************************************* | Global Reach (********************************* | Strategy | Unilever (*********************************************** | Unilever Global Website (************************** |
Employment is subject to verification of pre-screening tests, which may include drug screening, physical and background check.
*Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents
#TER123
------------------------------------
At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee.Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities.For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal (**************************************************************************************************
Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check.
If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment.
#LI-DNP
Job Category: Supply Chain
Job Type: Full time
Industry:
Quality Engineer
Quality engineer job in Moberly, MO
Job Description
Work Eligibility: Must be a U.S. Citizen or a permanent lawful resident of the U.S.
Plans and directs activities concerned with the development, application, and maintenance of quality standards for processes, materials, and products. Assists quality personnel with daily quality requirements for production and provide support to other departments as required on quality issues.
Preferred Educational Experience:
Bachelors degree in Engineering field or equivalent work experience.
Preferred Work Experience:
Minimum of six (6) years experience in quality and manufacturing. Auditing experience preferred.
Essential Functions:
Ability to perform all safety critical functions. The product must be built to the designated specs approved and can not be deviated or substituted. The control, performance and tolerance are essential for the part to function so that it does not jeopardize public safety or it's compliance with government regulations.
Must be able to recognize and call the critical characteristic symbols as listed on the blueprints.
Develop and implement methods and standards of inspection, testing, and evaluation to meet customer requirements during the APQP process.
Establish and maintain programs to evaluate the precision and accuracy of production, measuring, and test equipment (gage calibration) utilizing measurement system analysis process.
Assist Purchasing with a qualified vendor base and work with them to ensure proper control/change process is followed.
Devise sampling procedures and related forms / instructions for recording, evaluating, and reporting quality and reliability data.
Performs Gauge R &Rs
Perform SPC Analysis
Assist the production teams on issues related to corrective and preventive actions.
Participate on new product development teams to insure a smooth transition of new products to the manufacturing floor and completion of all quality documentation.
Develop and implement methods and procedures for disposition of discrepant material.
Provides assistance with customer quotations by evaluating quality specifications.
Support Sales through customer visits on product quality issues required.
Assist Purchasing in the development of a qualified vendor base and work with them to resolve quality issues.
Go on technical reviews with customers.
Interpret customer specific specifications-ID Critical characteristics, working knowledge of APQP.
Understand PPAP requirements to customers and knowledge of SPC.
Understand PFMEA control plans and process flow.
MRB Delegation and Authority/Disposition
Demonstrated working knowledge of AIAG Core Tools
Follow all 6S & Safety Guidelines
Safety
Sort
Straighten
Scrub
Standardize
Sustain
Non Essential Functions:
Organize and implement quality audits, including resolution of non-conformance's.
Supervise quality personnel as required by Quality Manager.
Performs other duties as assigned.
Understand zero PPM and zero defects.
Project Timing Charts
Qualifications and Desired Skills
Organizational management skills
Communications skills
Work well with others
Office equipment
Computer skills
Problem solving
Analytical skills
Time management
Physical Requirements:
Data entry
80% of the time sitting
Some bending/stooping
Lifting less than 35lbs
Climate controlled environment
Color perception and vision requirements
AAP/EEO Statement:
It is the policy of Orscheln Products to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law.
Powered by ExactHire:184765
Chemical Engineer I
Quality engineer job in Columbia, MO
As a **Chemical Engineer I** here at Solstice, you will impact the company's growth and competitiveness by contributing to technical excellence, innovation, and safety in chemical engineering projects. **You will report directly to our Plant Manager, and you will work out of our Columbia, MO location. Relocation is not offered.**
**KEY RESPONSIBILITIES**
+ Manage capital projects to support site Annual Operating and Strategic Operation Plans
+ Analyze, optimize, and troubleshoot existing processes to ensure safe and efficient 24/7 operation
+ Collaborate with technical and R&D resources to understand our products & process to help support customer needs and their process
**Responsibilities**
Key Responsibilities
+ Collaborate with senior engineers and cross-functional teams to support the development and implementation of chemical processes and solutions
+ Conduct research and analysis to identify areas for process improvement and optimization
+ Assist in the design and testing of chemical processes and equipment
+ Ensure compliance with safety regulations and industry standards
+ Provide technical support and troubleshooting for process-related issues
**Qualifications**
**YOU MUST HAVE**
+ Bachelor's degree at a minimum from an accredited institution in a technical discipline such as science, technology, engineering, mathematics
+ Strong problem-solving and analytical skills
+ Familiarity with safety regulations and industry standards
+ Strong ability to multitask and work with a team
**WE VALUE**
+ Minimum of 1 year of experience in chemical engineering or related field
+ Advanced degree in Chemical Engineering or related field
+ Experience with batch processes
+ Experience with managing capital projects
+ Ability to work collaboratively in a team environment
+ Passion for safety, sustainability, and compliance
+ Strong technical expertise in chemical engineering principles
**US PERSON REQUIREMENT**
Due to compliance with U. S export control laws and regulations, candidate must be a U.S. citizen, permanent resident, or have asylum or refugee status in U.S.
**COMPENSATION**
The annual base salary range for this position is 71k-95k. Please note that this salary information serves as a general guideline. Solstice considers various factors when extending an offer, including but not limited to the scope and responsibilities of the position, the candidate's work experience, education and training, key skills, as well as market and business considerations.
**BENEFITS OF WORKING FOR SOLSTICE ADVANCED MATERIALS**
In addition to a competitive salary, leading-edge work, and developing solutions side-by-side with dedicated experts in their fields, Solstice Advanced Materials employees are eligible for a comprehensive benefits package. This package includes employer-subsidized Medical, Dental, Vision, and Life Insurance; Short-Term and Long-Term Disability; 401(k) match, Flexible Spending Accounts, Health Savings Accounts, EAP, and Educational Assistance; Parental Leave, Paid Time Off (for vacation, personal business, sick time, and parental leave), and 12 Paid Holidays.
The application period for the job is estimated to be 40 days from the job posting date; however, this may be shortened or extended depending on business needs and the availability of qualified candidates. Posting updated 12/09/2025.
_Solstice Advanced Materials is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status._
**About Us**
**Job Identification** 106019
**Job Category** Engineering
**Locations** 6400 N Brown Station Rd, Columbia, MO, 65202, US
**Hire Eligibility** Internal and External
**Relocation Package** US & CAN Domestic Tier 1
**US Person** Due to U.S. export control laws, candidates must be U.S. citizen, U.S. permanent resident, or have protected status under asylum or refugee.
SAP Software Engineer - Data Conversions, Data Quality, and Reporting
Quality engineer job in Jefferson City, MO
**_What Application Development & Maintenance contributes to Cardinal Health_** Information Technology oversees the effective development, delivery, and operation of computing and information services. This function anticipates, plans, and delivers Information Technology solutions and strategies that enable operations and drive business value.
Application Development & Maintenance performs configuration or coding to develop, enhance and sustain the organization's software systems in a cross-functional team environment through adherence to established design control processes and good engineering practices. This job family programs and configures end user applications, systems, databases and websites to achieve the organization's internal needs and externally-facing business needs. Application Development & Maintenance partners with business leaders, investigates user needs and conducts regular assessments, maintenance and enhancements of existing applications.
The SAP Software Engineer focused on Data Conversions, Data Quality, and Reporting is responsible for designing, developing, and maintaining data solutions that ensure data integrity and enable effective business intelligence. The role combines technical skills in data migration and ETL processes with an understanding of data governance and reporting tools.
**_What is expected of you and others at this level_**
+ Applies comprehensive knowledge and a thorough understanding of concepts, principles, and technical capabilities to perform varied tasks and projects
+ May contribute to the development of policies and procedures
+ Works on complex projects of large scope
+ Develops technical solutions to a wide range of difficult problems
+ Solutions are innovative and consistent with organization objectives
+ Completes work; independently receives general guidance on new projects
+ Work reviewed for purpose of meeting objectives
+ May act as a mentor to less experienced colleagues
**_Responsibilities_**
+ Design and execute data conversion strategies for SAP implementations and upgrades, including data extraction, transformation, and loading (ETL) from legacy systems into SAP.
+ Utilize SAP data migration tools such as SAP Data Services, LSMW, and Migration Cockpit to perform data loads and conversions.
+ Develop and maintain technical specifications, data mapping documents, and transformation rules.
+ Collaborate with business and technical teams to gather data requirements and ensure seamless data flow across systems.
+ Establish and maintain data quality frameworks to ensure the accuracy, consistency, and integrity of master and transactional data in SAP.
+ Perform data profiling, cleansing, and validation to identify and resolve data discrepancies before and after migration.
+ Define and monitor data quality metrics and key performance indicators (KPIs).
+ Work with business data stewards to correct data quality issues and promote data governance policies and standards.
+ Design, develop, and implement reporting solutions, dashboards, and analytical models using SAP technologies like SAP Analytics Cloud (SAC), SAP BW/4HANA, or SAP Fiori.
+ Translate business needs into technical specifications for reports and ad-hoc queries.
+ Optimize report performance and data extraction processes for efficiency.
+ Provide support and training to end-users on reporting tools to enable data-driven decision-making
**_Qualifications_**
+ Bachelor's Degree in related field preferred or equivalent work experience preferred
+ Proven experience in SAP Data Conversions, migrations and ETL processes.
+ Proficiency with SAP data tools such as SAP Data Services, SAP BW/HANA or SAP Analytics Cloud
+ Strong knowledge of SQL, data modelling and database concepts
+ Experience with SAP modules and data structures (e.g., Master Data, Financials, Supply Chain, OTC, PTP processes).
+ Excellent analytical, problem solving and communication skills
+ Ability to work both independently and collaboratively with cross-functional teams
**Anticipated salary range:** $94,900 - $135,600
**Bonus eligible:** No
**Benefits:** Cardinal Health offers a wide variety of benefits and programs to support health and well-being.
+ Medical, dental and vision coverage
+ Paid time off plan
+ Health savings account (HSA)
+ 401k savings plan
+ Access to wages before pay day with my FlexPay
+ Flexible spending accounts (FSAs)
+ Short- and long-term disability coverage
+ Work-Life resources
+ Paid parental leave
+ Healthy lifestyle programs
**Application window anticipated to close:** 01/20/2026 *if interested in opportunity, please submit application as soon as possible.
The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate's geographical location, relevant education, experience and skills and an evaluation of internal pay equity
_Candidates who are back-to-work, people with disabilities, without a college degree, and Veterans are encouraged to apply._
_Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal_ _Opportunity/Affirmative_ _Action employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law._
_To read and review this privacy notice click_ here (***************************************************************************************************************************
Network Reliability Engineer
Quality engineer job in Jefferson City, MO
GovCIO is currently hiring for Network Reliability Engineer to support our client's contract needs.The Network Reliability Engineer will support, maintain, optimize, monitor, and participate in troubleshooting efforts for a mature network environment for a large Government Agency.This position is located in the within the United States and is fully remote position.
**Responsibilities**
The ideal candidate will have extensive experience with SolarWinds Network Performance Monitor (NPM), Network Configuration Manager (NCM), NetFlow Traffic Analyzer (NTA), and SolarWinds Security Event Manager (SEM). Candidate will also have substantial experience with developing and maintaining interactive webpage dashboards related to SolarWinds suite. Highly desirable skills would include experience with CISCO switches and routers, CISCO specific monitoring systems, packet capture systems, packet broker switches, and automation provisioning. Additional skills that would provide value include experience with COTS DDI products, load balancers, NAC, AAA systems, SSL certificate management, and proxy systems.
+ Perform Incident Response support by monitoring ticket system and taking appropriate actions on network related Incidents.
+ Manage, maintain, and support existing SolarWinds instance which monitors and generates alerts for network equipment.
+ Manage, maintain, and support existing interactive webpage dashboards through programming and database calls to SolarWinds and various other systems utilizing SWQL Studio.
+ Participate in troubleshooting sessions involving connectivity issues for infrastructure and applications by using SolarWinds and/or analyzing packet capture data, syslogs and related log data.
+ Use network diagnostic tools to reduce outage times by quickly identifying network related anomalies and issues.
+ Generate root cause analysis for issues diagnosed on the network.
+ Use network diagnostic tools to proactively address network anomalies and issues as well as optimize network performance.
+ Develop and maintain technical documentation as it pertains to the systems being managed.
+ Ensure compliance with security standards, policies, and best practices for IT systems and data protection.
+ Train and mentor internal teams on efficiencies gained by utilizing SolarWinds to monitor and diagnose network anomalies and issues.
**Qualifications**
Bachelor's with 5 - 8 years (or commensurate experience)
Required Skills and Experience
+ 5+ years of experience in monitoring and managing network equipment.
+ Experience with Incident and Request ticketing systems.
+ Strong knowledge and experience with SolarWinds and related dashboard activities.
+ Strong knowledge of networking protocols (TCP/IP, HTTP/HTTPS, DNS, etc.).
+ Solid knowledge of SNMP as it relates to SolarWinds implementations.
+ Solid network and cybersecurity fundamentals knowledge.
+ Fundamental knowledge of MPLS and WAN routing principles.
+ Fundamental knowledge of IPv4 and IPv6 protocols.
+ Basic understanding of Red Hat Enterprise Linux (RHEL 8/9) to administer Apache2 web server.
+ Basic understanding of Application Programming Interface (API) utilization to extract performance and informational data from various vendors.
+ Basic understanding of Bash shell scripting, Python, PHP, Perl, Java Script, MySQL database.
+ Proficiency with Microsoft Office suite.
+ Familiarity with cloud service providers (AWS, Azure, Google Cloud).
+ Familiarity with Data Center network environments.
+ Strong ability to work as part of a team, but also possess the drive and ability to perform duties autonomously if the project demands it.
**Clearance Required:** Must be able to obtain and maintain a HUD Public Trust
**Company Overview**
GovCIO is a team of transformers--people who are passionate about transforming government IT. Every day, we make a positive impact by delivering innovative IT services and solutions that improve how government agencies operate and serve our citizens.
But we can't do it alone. We need great people to help us do great things - for our customers, our culture, and our ability to attract other great people. We are changing the face of government IT and building a workforce that fuels this mission. Are you ready to be a transformer?
**What You Can Expect**
**Interview & Hiring Process**
If you are selected to move forward through the process, here's what you can expect:
+ During the Interview Process
+ Virtual video interview conducted via video with the hiring manager and/or team
+ Camera must be on
+ A valid photo ID must be presented during each interview
+ During the Hiring Process
+ Enhanced Biometrics ID verification screening
+ Background check, to include:
+ Criminal history (past 7 years)
+ Verification of your highest level of education
+ Verification of your employment history (past 7 years), based on information provided in your application
**Employee Perks**
At GovCIO, we consistently hear that meaningful work and a collaborative team environment are two of the top reasons our employees enjoy working here. In addition, our employees have access to a range of perks and benefits to support their personal and professional well-being, beyond the standard company offered health benefits, including:
+ Employee Assistance Program (EAP)
+ Corporate Discounts
+ Learning & Development platform, to include certification preparation content
+ Training, Education and Certification Assistance*
+ Referral Bonus Program
+ Internal Mobility Program
+ Pet Insurance
+ Flexible Work Environment
*Available to full-time employees
Our employees' unique talents and contributions are the driving force behind our success in supporting our customers, which ultimately fuels the success of our company. Join us and be a part of a culture that invests in its people and prioritizes continuous enhancement of the employee experience.
**We are an Equal Opportunity Employer.** All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender, gender identity or expression, sexual orientation, national origin, disability, or status as a protected veteran. EOE, including disability/vets.
**Posted Pay Range**
The posted pay range, if referenced, reflects the range expected for this position at the commencement of employment, however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, education, experience, and internal equity. The total compensation package for this position may also include other compensation elements, to be discussed during the hiring process. If hired, employee will be in an "at-will position" and the GovCIO reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, GovCIO or individual department/team performance, and market factors.
**Posted Salary Range**
USD $90,000.00 - USD $120,000.00 /Yr.
Submit a referral to this job (*********************************************************************************************************************************
**Location** _US-Remote_
**ID** _2025-7212_
**Category** _IT Infrastructure & Network Engineering & Operations_
**Position Type** _Full-Time_
Assistant Manufacturing Engineer
Quality engineer job in Tipton, MO
This position supports manufacturing engineering activities within the plant, focusing on process development, documentation, and communication between design and production. The role ensures compliance with ISO quality standards and contributes to continuous improvement initiatives in welding, fabrication, and overall manufacturability.
Job Purpose
Support manufacturing engineering activities to ensure efficient production processes, compliance with quality standards, and effective communication between design and production teams.
Key Responsibilities
Assist the Manufacturing Engineer and Plant Manager in daily operations and project tasks.
Review engineering drawings for manufacturability and provide feedback to design teams.
Distribute approved drawings to the Production Department.
Assist in defining welding and fabrication processes to meet quality and safety standards.
Create and maintain weld maps for production documentation.
Act as a liaison between the Production Department and Design Engineering to resolve technical issues and ensure smooth workflow.
Requirements
Responsibilities:
Ensure manufacturing processes comply with ISO 9001 quality requirements.
Maintain accurate documentation for weld maps and process instructions.
Support continuous improvement initiatives in manufacturing processes.
Communicate effectively between departments to resolve technical issues promptly.
Authorities:
Recommend changes to manufacturing processes for improved efficiency and quality.
Approve distribution of drawings to Production after review for manufacturability.
Escalate design or production issues to the Manufacturing Engineer or Plant Manager.
Qualifications
Education: Bachelor's degree in Engineering or equivalent work experience.
Technical Skills:
Knowledge of welding and fabrication processes.
Familiarity with Autodesk Inventor (preferred).
Other Requirements: Strong communication and organizational skills; ability to work collaboratively across departments.
Senior Manager, Global Quality Management - Clinical
Quality engineer job in Jefferson City, MO
The Senior Manager of Global Quality Management (GQM) supports the execution of clinical quality activities to ensure compliance with Good Clinical Practice (GCP), regulatory requirements, and internal standards across global clinical trials. This role provides hands-on quality oversight, supports audit and inspection readiness, and collaborates with internal teams and external partners to maintain high-quality standards throughout the clinical development lifecycle.
**Key Responsibilities**
**Clinical Study Support**
+ Serve as a GCP quality resource to clinical teams during study planning, conduct, and close-out.
+ Support the review of study documents (e.g., protocols, monitoring plans, vendor agreements) for quality and compliance.
+ Assist in identifying and resolving quality issues, protocol deviations, and potential noncompliance.
+ Collaborate with Clinical Operations, Regulatory Affairs, and Medical Affairs to embed quality practices throughout the study lifecycle.
**Inspection Readiness**
+ Support inspection readiness activities including mock audits, documentation reviews, and training coordination.
+ Maintain inspection readiness tools, trackers, and communication plans.
+ Participate in regulatory inspections and assist in preparing response documentation.
**Audit Program Execution**
+ Contribute to the development of the annual audit plan using risk-based approaches.
+ Coordinate and support investigator site, vendor, and internal process audits.
+ Track audit findings and ensure timely implementation of corrective and preventive actions (CAPAs).
+ Monitor audit trends and escalate recurring issues to senior leadership.
**Quality Systems & Compliance**
+ Support the implementation and continuous improvement of clinical quality systems, SOPs, and policies.
+ Assist with deviation management, root cause analysis, and CAPA tracking related to clinical activities.
+ Stay current with evolving global GCP regulations and industry best practices.
**Collaboration & Team Support**
+ Partner with internal stakeholders and CROs to ensure consistent quality oversight.
+ May mentor junior staff or contractors.
+ Contribute to cross-functional initiatives that promote a culture of quality and compliance.
**Qualifications**
Required
+ Bachelor's degree in life sciences or related field; advanced degree a plus.
+ 6-8 years of experience in clinical quality assurance or clinical research within the pharmaceutical or biotech industry.
+ Solid understanding of GCP, ICH guidelines, and global regulatory requirements.
+ Experience supporting inspection readiness and participating in audits or inspections.
+ Strong communication, organizational, and problem-solving skills.
+ Ability to travel domestically and internationally as needed.
+ Proficiency in MS Office (Word, Excel, PowerPoint).
**Preferred:**
+ Experience with TrackWise or similar quality management systems.
+ Prior collaboration with CROs and external vendors.
+ Exposure to FDA or other health authority inspections.
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $131,153.00 - Maximum $196,075.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Production Engineering
Quality engineer job in Jefferson City, MO
Production Engineers (PEs) at Meta are specialized software engineers who develop the underlying infrastructure for all of Meta's products and services, forming the backbone of every major engineering effort that keeps our platforms running smoothly and scaling efficiently.PEs work across Meta's product and infrastructure teams to ensure our services are reliable, performant, and capable of supporting billions of users. This means writing high‑quality code, solving complex problems in live production, and tackling challenges that impact over 2 billion people worldwide.Our PEs are embedded in teams across the spectrum - from products like Instagram, WhatsApp, Oculus, and Videos to critical backend services such as Storage, Cache, and Networking. The team brings together diverse levels of experience and backgrounds. Working alongside some of the best engineers in the industry, you'll contribute to code and systems that go into production and are used by millions every day. In Production Engineering at Meta, we navigate uncharted waters daily - solving problems at a scale few others face.
**Required Skills:**
Production Engineering Responsibilities:
1. Own back-end services which handle fleet management, front-end services such as WhatsApp / Instagram / Facebook / Meta Ads, infrastructure components that drive Meta's advances in AI, core services which are used by every team at Meta, the world's largest MySQL deployments, networking systems and everything in between
2. Write and review code, develop documentation and capacity plans, and debug the hardest problems, live, on some of the largest and most complex systems in the world
3. Together with your engineering team, you will share an on-call rotation and be an escalation contact for service incidents
4. Partner alongside the best engineers in the industry working on the coolest stuff around, the code and systems you work on will be in production and used by billions of people all around the world
**Minimum Qualifications:**
Minimum Qualifications:
5. 6+ years of experience in *nix (Linux or another UNIX-like OS) and Network fundamentals
6. 6+ years of coding experience in an industry-standard language (e.g. Java, Python, C++, PHP/Hack, Rust, Go)
7. Experience learning software, frameworks and APIs
8. Experience with Internet service architecture capacity planning and/or handling needs for urgent capacity augmentation
9. Knowledge of common web technologies and/or Internet service architectures (such as LAMP or MEAN stacks, CDN, Load Balancing techniques, etc.)
10. Experience configuring and running infrastructure level applications, such as Kubernetes, Terraform, MySQL, etc
11. Bachelor's degree in Computer Science, Computer Engineering, relevant technical field, or equivalent practical experience
**Preferred Qualifications:**
Preferred Qualifications:
12. BS or MS in Computer Science
**Public Compensation:**
$147,000/year to $208,000/year + bonus + equity + benefits
**Industry:** Internet
**Equal Opportunity:**
Meta is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender, gender identity, gender expression, transgender status, sexual stereotypes, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also consider qualified applicants with criminal histories, consistent with applicable federal, state and local law. Meta participates in the E-Verify program in certain locations, as required by law. Please note that Meta may leverage artificial intelligence and machine learning technologies in connection with applications for employment.
Meta is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know at accommodations-ext@fb.com.
Industrial Engineer - Startup Manufacturing
Quality engineer job in Columbia, MO
Full-time Description
ThermAvant Technologies, LLC designs and manufactures high-performance custom thermal management solutions, including advanced heat sinks and heat spreaders utilizing Oscillating Heat Pipe (OHP) technology. Our solutions serve terrestrial and aerospace applications. ThermAvant operates an AS9100D/ISO9001-certified facility in Columbia, Missouri.
Position Overview:
We are seeking a proactive Industrial Engineer to join our dynamic startup manufacturing team. The ideal candidate will be instrumental in developing and optimizing manufacturing processes, integrating new technologies, and scaling production efficiently. This role requires close collaboration with manufacturing engineers and cross-functional teams to drive continuous improvement and meet rapidly evolving production demands.
Key Responsibilities:
Design, develop, and implement efficient manufacturing processes for new and existing products.
Collaborate with manufacturing engineers to integrate new machinery and technologies into production lines.
Assist in development of production schedule processes to ensure timely delivery and optimal resource utilization.
Implement level loading strategies to balance workloads and maximize throughput.
Conduct time studies and workflow analyses to identify bottlenecks and areas for improvement.
Lead initiatives to scale production volumes rapidly while maintaining quality and efficiency.
Develop and maintain standard operating procedures (SOPs) and work instructions.
Utilize lean manufacturing principles and continuous improvement methodologies to enhance processes.
Monitor key performance indicators (KPIs) and implement corrective actions as needed.
Ensure compliance with safety, quality, and regulatory standards.
Requirements
Required Qualifications:
Bachelor's degree in industrial engineering, Manufacturing Engineering, or a related field.
Minimum of 3 years of experience in an industrial engineering role within a manufacturing environment, preferably in a startup setting.
Proficiency in developing and optimizing manufacturing processes and workflows.
Experience with production scheduling, capacity planning, and level loading techniques.
Strong analytical and problem-solving skills.
Excellent communication and interpersonal skills.
Ability to work collaboratively in a fast-paced, team-oriented environment.
Familiarity with lean manufacturing principles and continuous improvement methodologies.
Preferred Qualifications:
Experience with integrating new machinery and technologies into manufacturing processes.
Knowledge of advanced manufacturing technologies, such as automation and additive manufacturing.
Proficiency in using manufacturing software tools for scheduling and process optimization.
#IndustrialEngineer #EngineeringCareers #ManufacturingJobs #ProcessImprovement #LeanManufacturing
#SixSigma #SupplyChainJobs #OperationsEngineering #EfficiencyExpert #ContinuousImprovement
Quality Area Lead - Jefferson City, MO
Quality engineer job in Jefferson City, MO
Job Title: Quality Area Lead - 3rd Shift
Hours: M-F 12:00AM to 08:30AM; Training will be held on day shift
Pay: $34.91/hour + Shift Differential ($6.28/hr) while working nights
TYPE: HOURLY
Minimum Education and Experience:
College Bachelor's degree preferred
Minimum 3 years related work experience, preferably in a quality environment
General Scope of Position: The Quality Lead role will have ownership of the performance of quality throughout the LIV area. They are required to lead autonomously, motivate and develop their team. This role is the business facing lead for the area, ensuring partnership across End to End Supply Chain operations.
Job Skills/Tasks:
Essential Functions:
Accountable for performance of the following:
Safety
100% completion of risk assessments, SQC audits, SBO's for direct reports.
World class execution of 5S and GMP within their area.
Team's execution to the f-tag program.
Quality
Lead Quality Technicians
Report and review E-Incidents to suppliers
Participate in Internal Auidt program
Investigate MQI's with a cross functional team to prevent reoccurrence
Communicate holds to planning
Manage the rework area and instructions
Utilizes SAP QM and Unilever specifications including PLM and JDA TNT system and support verification of use for quality purposes.
Ensure all Area equipment validations are completed using IQ, OQ, PQ.
Calibrations of all department equipment
Owner of SOP and work instruction for Area to ensure updated regularly.
Supports effort to complete and maintain internal and external audits and certifications.
Responsible of traceability compliance and auditing to ensure compliance e.g includes annual mock recall exercises.
Ensures proper onboarding of new hires in department.
Oversee Cleaning and Disinfection execution on shift.
Supports and participates in Quality Pillar activities for UMS program.
Drives quality focused improvement activities, reducing quality losses.
Utilizes advanced knowledge of category and technology details and requirements to support site innovation and changes.
Supports the quality Digital agenda.
Ensure all supply's are ordered in a timely manner.
All other duties as assigned.
Productivity
Glidepath with area plan as well as overall factory plan.
Build strategic plan to execution targets for their department and program.
Utilization of shift handover checklist to ensure seamless communication across shifts.
Participation in daily Planning meeting to ensure alignment to area strategy.
Cost/Labor
Manage area labor to budget.
Complete department payroll
Data Integrity
Understand all quality data entry, and reporting.
Ability to coach others on proper usage.
Competencies:
Skills Required:
Ability to develop leaders.
Strong sense of self-accountability and thrives in an autonomous environment.
Flexible work schedule to ensure support across their teams of varying shifts.
Verified and demonstrated technical skills in manufacturing operations.
Proficient in Microsoft Office.
Planning
Understand and utilize data to drive decisions and align resources.
Lead discussions and decision making.
Manage multiple workstreams simultaneously.
Leadership
Ability to gain buy-in and motivate their area team as well as cross-functional team members.
Execute performance escalation standards.
Teamwork
One Team mindset.
Bias for Action.
Drives for solutions.
Personal Protective Equipment:
Refer to department specific PPE assessment
Promotional Progression: (List and Describe)
This is a developmental role that could lead to increasing leadership within Unilever. In this role you will be challenged to develop your area leadership team and ensure performance across all shifts. This position will require thorough knowledge of the operations environment and experience developing teams.
Why work for Unilever | Culture for Growth | Every Voice Matters | Global Reach | Strategy | Unilever | Unilever Global Website |
Employment is subject to verification of pre-screening tests, which may include drug screening, physical and background check.
*Any coverages for health insurance and retirement benefits will be in accordance with the terms and conditions of the applicable plans and associated governing plan documents
#TER123
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At Unilever, inclusion is at the heart of everything we do. We welcome applicants from all walks of life and are committed to creating an environment where everyone can thrive/succeed. All applicants will receive fair and respectful consideration, and we actively support the growth and development of every employee.
Unilever is an Equal Opportunity Employer/Protected Veterans/Persons with Disabilities.
For more information on your federal rights, please see Know Your Rights: Workplace Discrimination is Illegal
Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check.
If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at NA.Accommodations@unilever.com. Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment.
#LI-DNP
Auto-ApplyQuality Engineer
Quality engineer job in Moberly, MO
Work Eligibility: Must be a U.S. Citizen or a permanent lawful resident of the U.S.
Plans and directs activities concerned with the development, application, and maintenance of quality standards for processes, materials, and products. Assists quality personnel with daily quality requirements for production and provide support to other departments as required on quality issues.
Preferred Educational Experience:
Bachelors degree in Engineering field or equivalent work experience.
Preferred Work Experience:
Minimum of six (6) years experience in quality and manufacturing. Auditing experience preferred.
Essential Functions:
Ability to perform all safety critical functions. The product must be built to the designated specs approved and can not be deviated or substituted. The control, performance and tolerance are essential for the part to function so that it does not jeopardize public safety or it's compliance with government regulations.
Must be able to recognize and call the critical characteristic symbols as listed on the blueprints.
Develop and implement methods and standards of inspection, testing, and evaluation to meet customer requirements during the APQP process.
Establish and maintain programs to evaluate the precision and accuracy of production, measuring, and test equipment (gage calibration) utilizing measurement system analysis process.
Assist Purchasing with a qualified vendor base and work with them to ensure proper control/change process is followed.
Devise sampling procedures and related forms / instructions for recording, evaluating, and reporting quality and reliability data.
Performs Gauge R &Rs
Perform SPC Analysis
Assist the production teams on issues related to corrective and preventive actions.
Participate on new product development teams to insure a smooth transition of new products to the manufacturing floor and completion of all quality documentation.
Develop and implement methods and procedures for disposition of discrepant material.
Provides assistance with customer quotations by evaluating quality specifications.
Support Sales through customer visits on product quality issues required.
Assist Purchasing in the development of a qualified vendor base and work with them to resolve quality issues.
Go on technical reviews with customers.
Interpret customer specific specifications-ID Critical characteristics, working knowledge of APQP.
Understand PPAP requirements to customers and knowledge of SPC.
Understand PFMEA control plans and process flow.
MRB Delegation and Authority/Disposition
Demonstrated working knowledge of AIAG Core Tools
Follow all 6S & Safety Guidelines
Safety
Sort
Straighten
Scrub
Standardize
Sustain
Non Essential Functions:
Organize and implement quality audits, including resolution of non-conformance's.
Supervise quality personnel as required by Quality Manager.
Performs other duties as assigned.
Understand zero PPM and zero defects.
Project Timing Charts
Qualifications and Desired Skills
Organizational management skills
Communications skills
Work well with others
Office equipment
Computer skills
Problem solving
Analytical skills
Time management
Physical Requirements:
Data entry
80% of the time sitting
Some bending/stooping
Lifting less than 35lbs
Climate controlled environment
Color perception and vision requirements
AAP/EEO Statement:
It is the policy of Orscheln Products to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law.
Manufacturing Engineer Co-Op
Quality engineer job in Columbia, MO
Working at Watlow Watlow is a global technology and manufacturing leader who provides world class engineering expertise through innovative thermal products and systems, enabling our customers to thrive. We are making a positive impact every day as our solutions enrich the lives of people everywhere. We have been providing breakthrough thermal solutions for nearly a century. Our corporate values guide us uncompromisingly to always do the right thing, continually learn and improve, respect everyone, and lead with service and humility.
* The Co-op positions at Watlow offer a 6-8-month immersive experience for students seeking more than a typical internship. This program allows participants to step away from their academic studies and engage in real-world engineering challenges directly tied to the company's strategic objectives.
* Located at one of Watlow's manufacturing center of excellence (MCOE's), co-op participants will work on impactful projects in design, testing, automation, and manufacturing development. They will have the opportunity to apply classroom knowledge to real-world manufacturing projects while collaborating closely with mentors and experienced engineers.
Co-ops development skills may include learning how to:
* Design and build fixturing for product manufacturing.
* Conduct experiments to aid manufacturing cell design.
* Perform Gauge Repeatability and Reproducibility studies.
* Develop lean manufacturing standard work.
* Aid in the development of work instructions for manufacturing operators.
* Test and analyze new and existing products (heaters, sensors, controllers, or software).
* Build prototypes and participate in prototype and equipment design reviews.
* Handle fabrication, tooling, wiring, and building control panels.
* Complete reliability, experimental, and validation testing.
* Setup and program automated assembly and inspection equipment.
* Evaluate laboratory results.
Qualifications:
* Currently enrolled in an accredited university pursuing a bachelor's or master's degree in mechanical, industrial, electrical engineering, computer science, chemical engineering or a similar field.
* Available to take a semester off from school to work at a Watlow facility.
* Ability to start in January 2026 OR June of 2026.
Additional Co-op Perks:
* Housing stipend or corporate housing available.
* Comprehensive onboarding and immersion plan.
* Mentorship program and networking opportunities.
* Opportunity to participate in and support local STEM and charitable initiatives.
The Watlow co-op program offers students a chance to be part of a team working on projects that matter. It provides valuable experience beyond the classroom, allowing participants to build their engineering careers in a meaningful way.
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment visa at this time.
Manager, Global Product Quality - Controlled Substances
Quality engineer job in Jefferson City, MO
The Manager, Global Product Quality - Controlled Substances is responsible for ensuring that all activities related to controlled substances across the product lifecycle meet Good Manufacturing Practices (GMP) and comply with global regulatory requirements, including DEA regulations. This role partners closely with R&D, Supply Chain, Product Development, and Warehousing & Distribution teams to ensure robust quality oversight and regulatory compliance in the handling, storage, manufacturing, and distribution of controlled substances.
**Key Responsibilities**
+ Product Oversight:
Provide GMP oversight and guidance during the drug development process including review and approval of documentation and collaboration and oversight of suppliers/contract manufacturers. Act as a liaison with regulatory agencies and internal compliance teams regarding controlled substance matters.
+ Quality & Compliance:Serve as the quality and compliance lead for controlled substances, ensuring adherence to DEA regulations and other global controlled substance requirements (e.g., Health Canada, EMA, ANVISA). Develop, implement, and maintain global SOPs and standards for the compliant handling, storage, transportation, and distribution of controlled substances.
Ensure warehousing and distribution operations meet all applicable regulatory and internal quality requirements, including security, inventory reconciliation, and chain-of-custody controls.
+ Audit & Inspection Readiness:Support DEA inspections, audits, and regulatory submissions, ensuring readiness and robust documentation.
+ Process Optimization:Oversee and enhance quality systems related to product quality complaints, CAPA, deviations, and change control for controlled substances.
+ Data Analysis & Reporting:Monitor and analyze compliance metrics and trends to identify risks and drive continuous improvement initiatives.
+ Cross-functional Collaboration:Collaborate with R&D, Supply Chain, Product Development, and Manufacturing to ensure quality and compliance are integrated throughout the lifecycle of controlled substance products.
+ Training & Documentation:Provide training and guidance to global teams on controlled substance regulations, GMP expectations, and best practices.
**Qualifications**
Required
+ Bachelor's degree in Chemistry, Engineering, Life Sciences, or a related field.
+ Minimum 5 - 7 years of experience in a regulated industry (pharmaceutical or medical device), with 3-5 years in in pharmaceutical quality, with specific experience in controlled substances and commercial quality operations.
+ Demonstrated expertise in DEA regulations and compliance, including registration, quota management, recordkeeping, and reporting.
+ Strong understanding of GMP requirements and global regulatory expectations for controlled substances.
+ Experience managing quality systems (e.g., deviations, CAPA, change control, complaints) in a regulated environment.
+ Proven experience in warehousing and distribution controls, including security, inventory management, and transportation compliance for controlled substances.
+ Excellent communication, collaboration, and project management skills.
+ Ability to work effectively in a global, cross-functional, and matrixed environment
Preferred Experience
+ Experience with electronic Quality Management Systems (eQMS) such as Veeva, TrackWise, or similar.
+ Certification in DEA compliance, Quality Assurance, or Regulatory Affairs.
**Competencies**
**Accountability for Results -** Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
**Strategic Thinking & Problem Solving -** Make decisions considering the long-term impact to customers, patients, employees, and the business.
**Patient & Customer Centricity -** Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
**Impactful Communication -** Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
**Respectful Collaboration -** Seek and value others' perspectives and strive for diverse partnerships to enhance work toward common goals.
**Empowered Development -** Play an active role in professional development as a business imperative.
Minimum $104,640.00 - Maximum $156,400.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate's job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.
**Application Deadline** : This will be posted for a minimum of 5 business days.
**Company benefits:** Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.
Come discover more about Otsuka and our benefit offerings; ********************************************* .
**Disclaimer:**
This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.
Otsuka is an equal opportunity employer. All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.
If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability. You can request reasonable accommodations by contacting Accommodation Request (EEAccommodations@otsuka-us.com) .
**Statement Regarding Job Recruiting Fraud Scams**
At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives. They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.
Please understand, Otsuka will **never** ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.
Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.
To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website ******************************************************* .
Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka's call center at: ************. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: ******************* , or your local authorities.
Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. ("Otsuka") does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka's application portal without a valid written search agreement in place for the position will be considered Otsuka's sole property. No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.