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Catalent Pharma Solutions

<div>Project Manager
Position Summary:<ul><li>
Work Schedule: M-F 1st shift
</li><li>100% on-site</li></ul>
Catalent&rsquo;s Kansas City facility is home to our Oral &amp; Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Catalent Pharma Solutions in Kansas City, MO is hiring a Project Manager. Overall responsibility for the leadership and management of projects as assigned. Depending upon experience and knowledge manage projects that maybe simple and residing in one business line or site, or complex and reside within multiple business lines or may cross multiple Catalent sites. May take on Global PM, Multi site or Lead PM for clients
The Role:<ul><li>
Leads and builds multi-disciplinary project teams comprising of representatives from relevant 
functions and in some cases, cross-functional, multi-site activities for complex projects</li><li>
Manages the execution of the customer&rsquo;s requirements in accordance with an agreed-upon program of activities to achieve established goals and deliverables</li><li>
Compiles and maintains up-to-date project plans, identifies and captures new scope via proposals or change orders</li><li>
Ensures that key milestones in agreement with internal/external customers are achieved and good 
communication is maintained</li><li>
Tracks progress of all activities against plan and notifies the relevant personnel of changes, potential delays and/or issues</li><li>
Engrained in kick-off and methodical approach to managing the project throughout the duration of 
the project scope</li><li>
Understands escalation pathway and when necessary, has the ability to mitigate</li><li>
Demonstrates ability to facilitate risk assessment</li></ul>
The Candidate:<ul><li>
Bachelor's degree in a scientific discipline or equivalent combination of 
education and experience (Associate&rsquo;s degree and 2+ years of experience OR high school diploma 
and 4+ years of experience.</li><li>
Approximately 2 years of experience in project management, the pharmaceutical 
industry or appropriate business-related area preferred</li></ul>
Why you should join Catalent:<ul><li>
Defined career path and annual performance review and feedback process</li><li>
Diverse, inclusive culture</li><li>
Positive working environment focusing on continually improving processes to remain innovative</li><li>
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives</li><li>
152 hours of PTO + 8 paid holidays</li><li>
Several Employee Resource Groups focusing on D&amp;I</li><li>
Dynamic, fast-paced work environment</li><li>
Community engagement and green initiatives</li><li>
Generous 401K match</li><li>
Medical, dental and vision benefits effective day one of employment</li><li>
Tuition Reimbursement - Let us help you finish your degree or start a new degree!</li><li>
WellHub- program to promote overall physical wellness</li><li>
Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Project Manager, Biologics Analytical Services

<div>Supply Chain Planner
Position Summary:<ul><li>
Work Schedule: M-F 8am-5pm</li><li>
100% on-site</li></ul>
Catalent&rsquo;s Kansas City facility is home to our Oral &amp; Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Catalent Pharma Solutions in Kansas City, MO is hiring a Supply Chain Planner. The Supply Chain Planner oversee&rsquo;s all tasks associated with the development and maintenance of both the Master 
Production Schedule and the short-term daily production schedule using a variety of tools. Align with Project managers, Formulators, Product Leads and Operations to ensure forecasted work is scheduled and executed. Participate as a member of the Supply Chain Team.
The Role:<ul><li>
Partner with Project Managers, Formulators, Product Leads and Operations to 
Understand Client Forecasts/Needs and translate requirements into master schedule.</li><li>
Creation and modification of the long-range Master Schedule in GMP and shift specific 
short-term Production schedules.</li><li>
Maintain alignment with Planners to ensure shared resources are available as needed.</li><li>
Schedule Support Group activities that impact production and assist in facilitation of daily 
operations review meeting.</li><li>
Works with the BU Directors and Supply Chain Manager to review and revise rough cut 
capacity requirements and participate in S&amp;OP monthly process to help facilitate the monthly Operations review.</li><li>
Participate in all pre-launch activities as they relate to scheduling requirements.</li><li>
Work with Client Service Associates, Buyers and Projects Managers to schedule capacity, equipment and line personnel.</li><li>
Identifies and communicates conflicts to the BU and Supply Chain Management to obtain resolutions.</li><li>
Create and Modify ERP System elements to enable execution of operations- including Work Orders and Master Data/Transaction Data</li><li>
All other duties as assigned.</li></ul> 
The Candidate:<ul><li>
Business or scientific related degree, preferred</li><li>
 3-5 years of operational or scheduling experience, required.</li><li>
MRP experience required, JD Edwards preferred</li><li>
Previous experience in a discrete manufacturing, job shop environment preferred.</li><li>
Previous experience in a pharmaceutical environment, preferred.</li><li>
GMP Manufacturing experience, preferred.</li><li>
Solid dose clinical and development manufacturing experience, preferred.</li><li>
Finite Planning techniques/systems experience, preferred.</li></ul>
Why you should join Catalent:<ul><li>
Defined career path and annual performance review and feedback process</li><li>
Diverse, inclusive culture</li><li>
Positive working environment focusing on continually improving processes to remain innovative</li><li>
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives</li><li>
152 hours of PTO + 8 paid holidays</li><li>
Generous 401K match</li><li>
Medical, dental and vision benefits effective day one of employment</li><li>
Tuition Reimbursement - Let us help you finish your degree or start a new degree!</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Supply Chain Planner

<div>Senior Manager, Supply Chain
Position Summary:<ul><li>
Work Schedule: M-F 8am-5pm</li><li>
100% on-site</li></ul>
Catalent&rsquo;s Kansas City facility is home to our Oral &amp; Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Catalent Pharma Solutions in Kansas City, MO is hiring Senior Manager, Supply Chain. Catalent is a leading provider of advanced technologies and outsourced services for the pharmaceutical, biotechnology, and consumer health industry. The Kansas City Clinical Development &amp; Supply Planning and Production Control Manager meets cGMP (current Good Manufacturing Practices) expectations. This position is responsible for the business unit&rsquo;s demand planning, capacity planning, material planning, and production planning and scheduling with the objective to deliver clinical trial supplies and commercial marketed materials in a timely and efficient manner. This role will have critical input to the site&rsquo;s business and growth objectives and will be a key member of the Supply Chain leadership team.
The Role:<ul><li>
Lead the planning team including recruitment, development, coaching, mentoring, and retention for professional, highly effective team members.</li><li>
Accountable for maintaining effective planning and scheduling processes to ensure that site operations are forecasted and positioned for successful execution.</li><li>
Develop systems that make gaps between plan and actual visible to the organization.</li><li>
Develop capacity planning tools and monitor capacity (ongoing, short-, mid-, and long term) to ensure the optimal level of capacity is available to meet forecasted demand.</li><li>
Manage the period for Sales &amp; Operations Planning cycle to develop achievable short, mid and long-term operating plans. Included is the production scheduling of operations to meet financial &amp; performance goals.</li><li>
Manage the development of schedules for machine, man and material (raw materials, components, and outside services) based upon capacity and resources, execute the plan and make visual the results of execution.</li><li>
Participate in daily production meetings.</li><li>
Manage inventory levels to meet the objectives of the business plan, support the requirements of the manufacturing operation, and meet the needs of the customer.</li><li>
Provide training, mentoring and development of direct and indirectly reporting employees</li><li>
All other duties as assigned.</li></ul> 
The Candidate:<ul><li>
Bachelor&rsquo;s degree in operations management, production planning and control, supply chain management, industrial engineering, or related discipline is preferred.</li><li>
CPIM and/or APICS/ASCM certification preferred.</li><li>
Minimum of five years progressive production planning, control management, or equivalent customer service experience with manufactured or packaged products is required; including demand, production, inventory, and capacity planning.</li><li>
Experience hosting and leading client and internal inspections, including direct experience hosting and leading in the preparation, management, and follow-up relating to FDA inspections.</li><li>
5-8 years of progressively increasing leadership experience in a production or customer service environment is required.</li><li>
Advanced computer skills &ndash; including, but not limited to, Microsoft Office suite including Microsoft Access, and Inventory/ERP systems is required.</li></ul>
Why you should join Catalent:<ul><li>
Defined career path and annual performance review and feedback process</li><li>
Diverse, inclusive culture</li><li>
Positive working environment focusing on continually improving processes to remain innovative</li><li>
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives</li><li>
152 hours of PTO + 8 paid holidays</li><li>
Generous 401K match</li><li>
Medical, dental and vision benefits effective day one of employment</li><li>
Tuition Reimbursement - Let us help you finish your degree or start a new degree!</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Senior Manager, Supply Chain

Oakwood Systems Group

<div><div>Position Overview</div><div>
We are seeking a Technical IT Project Manager to lead the successful delivery of Data &amp; AI and Application Development initiatives for our professional services clients. This role blends hands‑on project leadership, technical fluency, and consultative client engagement.</div><div>
The ideal candidate is comfortable managing complex, multi‑disciplinary projects in a consulting environment, serving as a trusted advisor to clients while ensuring projects are delivered on time, on scope, and on budget.</div><div>
Key Responsibilities</div><div>
Project &amp; Delivery Leadership</div><ul><li>
Lead end‑to‑end delivery of Data &amp; AI projects (data platforms, analytics, reporting, AI/ML initiatives) and custom application development engagements.</li><li>
Manage all phases of the project lifecycle, including initiation, planning, execution, monitoring, and close‑out.</li><li>
Own project scope, schedules, budgets, risks, issues, dependencies, and change control.</li><li>
Coordinate cross‑functional teams including architects, developers, data engineers, and client stakeholders.</li></ul><div>
Client &amp; Consulting Engagement</div><ul><li>
Act as a trusted advisor to clients, translating business objectives into actionable technical delivery plans.</li><li>
Facilitate discovery sessions, requirements workshops, and solution planning discussions.</li><li>
Manage client expectations, communicate status, and proactively address risks and roadblocks.</li><li>
Support pre‑sales and solution scoping efforts, including estimates, timelines, and delivery approach.</li></ul><div>
Technical &amp; Methodology Alignment</div><ul><li>
Partner closely with technical leads on Azure‑based Data &amp; AI solutions, analytics platforms, and modern application architectures.</li><li>
Ensure adherence to Oakwood delivery methodologies (PMI‑based / agile‑hybrid approaches).</li><li>
Guide teams through Agile, Scrum, or hybrid delivery models as appropriate.</li><li>
Ensure quality, documentation, and governance standards are met.</li></ul><div>
Stakeholder &amp; Team Management</div><ul><li>
Serve as the primary liaison between clients, project teams, and Oakwood leadership.</li><li>
Build high‑performing, collaborative project teams.</li><li>
Provide clear direction, remove blockers, and promote accountability.</li></ul><div>
Required Qualifications</div><ul><li>
5+ years of experience as an IT Project Manager in a consulting or professional services environment.</li><li>
Proven experience managing Data &amp; Analytics / Data &amp; AI projects.</li><li>
Experience leading application development projects (custom software, web, or cloud‑native apps).</li><li>
Strong understanding of modern Microsoft‑centric environments (Azure, data platforms, app dev stacks).</li><li>
Demonstrated ability to manage complex projects with multiple workstreams and stakeholders.</li><li>
Excellent client‑facing, communication, and facilitation skills.</li></ul><div>
Preferred Qualifications</div><ul><li>
Experience with Azure Data Services (e.g., Azure Data Factory, Synapse, Databricks, Power BI).</li><li>
Familiarity with AI/ML initiatives, analytics platforms, or data modernization programs.</li><li>
Agile / Scrum experience (CSM, SAFe, or similar).</li><li>
PMP or equivalent project management certification.</li><li>
Experience supporting pre‑sales, estimates, or delivery planning in a consulting model.</li></ul><div>
Why Oakwood</div><ul><li>
Work on high‑impact, modern technology projects with leading clients.</li><li>
Collaborate with experienced consultants in Data, AI, Cloud, and App Development.</li><li>
Consulting‑first culture that values relationships, quality delivery, and professional growth.</li><li>
Opportunity to influence delivery strategy and client outcomes.</li></ul></div>

Technical IT Project Manager

Burns & McDonnell

<div>Description
The Senior Site Quality Specialist is responsible for the implemented quality program on projects to confirm projects are fabricated/installed, examined, tested, and documented in accordance with the project specifications, governing codes of construction, and contract documents.
<ul><li>Provide guidance to quality personnel relative to the scope, complexity and logistics of work.</li>
<li>Support specification reviews to develop the Construction Quality Plan for the project.</li>
<li>Effectively communicate with project personnel to ensure specifications and code inspections are understood and met.</li>
<li>Participate in preparatory meetings to communicate contractual requirements to the subcontractors to ensure quality objectives are achieved.</li>
<li>Proactively evaluate the implementation of the quality program (e.g. document management, material management, special processes, etc.) and when required, bring the attention of noncompliant processes to the project team.</li>
<li>Inspect fabricated/installed products and services to confirm they are in compliance with project specifications and drawings and results documented, as required.</li>
<li>Proactively evaluate installation activities and participate in project schedule look-ahead meetings to identify and discuss any upcoming complexities with the project team.</li>
<li>Evaluate quality verification documents to confirm all attributes are addressed as they are issued and confirm compliance with the specifications and drawings.</li>
<li>Generate accurate inspection reports daily. Update inspection databases to accurately track inspection status, results, and metrics.</li>
<li>Participate in the walk-down and turnover process and when required, perform and document acceptance inspections.</li>
<li>Lead quality meetings with client and subcontractors, if required.</li>
<li>Recommend enhancements and changes to the Quality Management System.</li>
<li>Confirm conditions adverse to quality (nonconformances) are identified, segregated, documented, dispositioned, and tracked through acceptance to closure.</li>
<li>Lead the development of Inspection and Test Plans (ITPs) with collaboration from the project team and confirm their implementation.</li>
<li>Review and confirm compliance of applicable materials, procedures, subcontractor quality submittals, and ITPs.</li>
<li>Assign Welding Procedure Specification to the weldments, if applicable.</li>
<li>Test and qualify welders in accordance with company welder testing procedures and code requirements, if applicable.</li>
<li>Monitor the implementation of the site welding program.</li>
<li>Manage and track welder to weld traceability.</li>
<li>Proactively communicate quality opportunities or concerns to the project team.</li>
<li>Understand and interpret discipline-specific codes, specifications, and client requirements.</li>
<li>Manage tracking project quality metrics.</li>
<li>Manage the project turnover deliverables are populated and correspond to project activities.</li>
<li>Lead Quality orientation on a project site, as needed.</li>
<li>Comply with all Safety &amp; Health requirements and participate in the Task Safety Observations (TSO's) to ensure adherence to safety standards.</li>
<li>Responsible for coaching, training and mentoring field quality personnel.</li>
<li>Performs other duties as assigned.</li>
<li>Complies with all policies and standards.</li>
</ul>Qualifications
<ul><li>High School Diploma/GED and 11 years relevant experience in managing the implementation of a quality program required.</li>
<li>Or Associate's Degree in Engineering, Construction Management, Welding Technology, Nondestructive Examination or related field and 9 years relevant experience in managing the implementation of a quality program required.</li>
<li>Or Bachelor's Degree in Engineering, Construction Management, Welding Technology, Nondestructive Examination or related field and 7 years relevant experience in managing the implementation of a quality program required.</li>
<li>Strong analytical and problem solving skills.</li>
<li>Advanced technical writing experience required.</li>
<li>Strong computer and communication skills.</li>
<li>Must be detailed oriented.</li>
<li>Certified Welding Inspector-AWS Required.</li>
</ul>This job posting will remain open a minimum of 72 hours and on an ongoing basis until filled.
EEO/Disabled/Veterans
Job Quality
Primary Location US-MO-Kansas City
Schedule: Full-time
Travel: Yes, 100 % of the Time
Req ID: 261589
Job Hire Type Experienced #LI-HMH #CDB N/A</div>

Senior Site Quality Specialist - Construction (Field)

IMEG

<div>IMEG is hiring a Senior Electrical Engineer in Kansas City, MO, to lead the delivery of large and highly complex building projects as a project manager or lead engineer. You&rsquo;ll work closely with a team of engineers and consultants to provide project direction, engineering solutions, and advice to clients to ensure positive outcomes. You will also support budget accountability, mentor and train team members, and collaborate with cross-functional partners to meet project goals and client expectations.
Principal Responsibilities
<ul><li>Lead design efforts for the analysis of electrical systems, utilizing engineering software and tools to create detailed designs, specifications, and calculations according to code requirements and IMEG standards
</li><li>Perform site assessments and develop detailed analysis and technical reports
</li><li>Partner with clients to understand needs, gather project requirements, and communicate technical information effectively
</li><li>Build and maintain client relationships through professional communication
</li><li>Provide in-process design reviews of electrical system design, calculations, specifications, and project correspondence
</li><li>Implement IMEG quality control processes to ensure engineering designs and solutions meet IMEG quality standards, industry standards and client requirements
</li><li>Provide technical assistance in resolution of field issues with minimal support from senior staff
</li><li>Train, mentor, and motivate staff
</li><li>Prioritize safety in all aspects of engineering work; identify and mitigate potential safety risks associated with electrical systems
</li><li>Collaborate with multidisciplinary teams, including other engineers, architects, and project managers, to deliver integrated solutions that meet project goals
</li><li>Stay up to date with industry trends, emerging technologies, and best practices in electrical engineering; contribute to research, development, and innovation efforts within IMEG
</li><li>Participate in project interviews and project presentations
</li></ul>Required Qualifications and Skills
<ul><li>Bachelor of Science (BS) Degree in Electrical Engineering, or equivalent, required
</li><li>Professional Engineer (PE) License preferred
</li><li>10 years of experience minimum required, 12 preferred, in the building design consulting industry
</li><li>Adept in the technical aspects of one&rsquo;s discipline; advanced proficiency in technical and analytical skills including proficiency of principles of circuit theory, electromagnetism, power systems, and electronics as they relate to electrical systems
</li><li>Knowledge of Illumination Engineering Society (IES) Standards and reference material resources such as NFPA Link, TechStreet, MadCAD, and Facility Guideline Institution (FGI)
</li><li>Advanced proficiency of Master Specification editing and software such as eSPECS; Proficient with Adobe or Bluebeam Revu
</li><li>Ability to mentor, train, motivate, and lead others
</li><li>Ability to perform final quality control check in their area of expertise
</li><li>Ability to sell work and develop client relationships
</li><li>Strong training and mentoring skills
</li><li>Excellent communication and interpersonal skills; Ability to clearly communicate in both oral and written communication to individuals or groups
</li><li>Ability to work collaboratively in a team environment
</li><li>Attention to detail and problem-solving skills
</li><li>Proficient with MS Office Suite including but not limited to Word, Excel, and Outlook
</li><li>Ability to travel up to 20% with occasional overnight stays
</li></ul>This position is not eligible for sponsorship.
Why Join Us IMEG puts people first&mdash;with a strong focus on career growth, work-life balance, and meaningful impact. As a 100% employee-owned firm, we offer the resources of a national design leader with the close-knit culture of a local office. You&rsquo;ll collaborate across disciplines, contribute to innovative, sustainable projects, and shape the communities we serve. Join a team where your ideas are valued, your development is supported, and your work truly matters.
 
In our Electrical team, you&rsquo;ll contribute to building and infrastructure projects through power distribution, lighting, and specialty electrical systems.
Electrical Team Highlights
<ul><li>Design power distribution, lighting, and specialty electrical systems for buildings and infrastructure
</li><li>Support solutions ranging from medium-voltage campus power systems to facility interior electrical layouts
</li><li>Contribute to systems including emergency power, uninterruptible power supply (UPS), and renewable energy integration
</li><li>Coordinate closely with multidisciplinary design teams to deliver integrated, code-compliant solutions focused on safety and reliability
</li></ul>Locations available: Kansas City, MO
Apply today to help deliver safe, reliable, code-compliant electrical solutions that make a meaningful impact for clients and communities.
IMEG , an employee-owned corporation, is committed to investing in employees&rsquo; futures through professional development programs and opportunities for career advancement. We offer a comprehensive benefits package including generous PTO, flexible schedule, and assistance with tuition reimbursement. Additionally, employees are eligible to enroll in health, dental, vision, and life insurance on their first day of employment.
Want to learn more about IMEG and our other amazing career opportunities? Please visit https://www.imegcorp.com/careers/ .
IMEG is committed to providing equal employment opportunities in all employment practices, without regard to race, color, religion, sex (including sexual orientation or gender identity), gender, national origin, disability, age, genetic information (including family medical history), parental status (including pregnancy, childbirth or related medical conditions including lactation), ethnic origin, hair type (including hairstyle or hair texture), citizenship status, marital status, military service, veteran&rsquo;s status, political affiliation, non-merit-based factors, or any other characteristic protected by law. In accordance with antidiscrimination law, it is the purpose of this policy to put into effect these principles and mandates. IMEG prohibits discrimination and harassment of any type. IMEG conforms to the spirit as well as to the letter of all applicable laws and regulations.
All applicants have the right to request access, correction, and deletion of their personal information from our system. In order to make a request, please email careers@imegcorp.com.</div>

Senior Electrical Engineer

<div>Lead Label Specialist
Work Summary<ul><li>
Work Schedule: Monday to Friday 2:30pm - 11:30pm with training on first shift</li><li>
100% based on-site in Kansas City</li></ul>
Catalent&rsquo;s Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions&mdash;from science and engineering to operations and logistics.
The Lead Label Specialist provides support to the Project Management Team, Operations Team and our customers by designing, printing and inspecting labels for use in clinical and commercial packaging and distribution. The Lead Label Specialist is tasked with overseeing all projects that run through Label Control while following the master schedule. Organization, leadership and strong attention to detail are a few of the required traits of this position.
The Role<ul><li>
Creation of GSA jobs, including the importing of verification data.</li><li>
This role may also include performing the role of LSO for the KCM site. These additional responsibilities include: set up and modification of users; creation/modification of sites within GSA; creation/modification of Clients within GSA; and training local users among other responsibilities outlined per SOP.</li><li>
Good Project manager, client and team rapport. Ability to communicate, educate and assist in all areas of label control.
</li><li>Attend Kick off meetings and assist in ensuring that each kickoff meeting has representation. Set a standard of what is expected and assist in holding team accountable. Knowledgeable about campaigns and the requirements.</li><li>
Organization and manage assigned projects with the ability to prioritize while assisting others in managing theirs. Utilize and be able to help others use WorkFront.</li><li>
Assist with enforcing the master schedule with a commitment to hitting OTD. Prioritize self with a big picture of the team. Promote teamwork where necessary to accomplish tasks.</li><li>
Provide regulatory audit and client audit support.</li><li>
Other duties assigned.</li></ul>
The Candidate<ul><li>
High-school diploma or GED required</li><li>
1+ years of clinical labelling experience or related pharmaceutical operations experience preferred</li><li>
Knowledge regarding design control, documentation, risk management and processes such as FMEA, Design Verification, and URS is a plus.</li><li>
Ability to communicate effectively with project managers, customers, and other personnel.</li><li>
Supervisory skills and experience strongly recommended</li><li>
High level of attention to detail.</li><li>
Excellent documentation skills.</li><li>
Strong problem solving and analytical skills.</li><li>
Excellent written, verbal and interpersonal communication skills, including the ability to present information.</li><li>
Demonstrate a willingness to share skills and information with others.</li><li>
Demonstrated ability to read, write, and speak clear English.</li></ul>
Why you should join Catalent<ul><li>
Career growth with a clear path and regular performance reviews</li><li>
Day-one benefits: medical, dental, vision</li><li>
401(k) match, tuition reimbursement, and wellness perks</li><li>
Paid time off: 152 hours + 8 holidays</li><li>
Inclusive culture with Employee Resource Groups and community initiatives</li><li>
Discounts from 900+ merchants via Perkspot</li><li>
A mission-driven workplace where your work helps save lives</li></ul>
Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process. 
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written &amp; signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond&mdash; it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE.</div>

Lead Label Specialist

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