Supervisor jobs in Avon, IN

Bilingual Production Supervisor *Must Be Bilingual in English and Spanish 6501 Julian Ave, Indianapolis, IN 46219 Monday - Thursday (Friday OT as needed) Day Shift: 5:00am - 3:30pm We are looking for an experienced Bilingual Production Supervisor to oversee our Personal Care products operation. You'll guarantee that manufacturing remains a smooth and efficient process by monitoring employees and organizing workflows. In our fast paced environment, the supervisor is an integral part of the manufacturing process. They must be competent and comprehend complex operations. You should also be able to optimize day-to-day activities while minimizing the costs. The goal is to ensure that production processes deliver products of maximum quality in a profitable manner. Key Responsibility: Promote safety-first culture that fosters an injury free workplace. Monitor and leads the production Work directly with Production manager to manage daily production numbers Follow and enforces established safety rules and regulations Follow all SOP's and Work Instructions and communicates improvements and changes as required Respond to emergencies and notify management immediately Monitors that goods are produced efficiently and to the correct quality standard Train/assist production employees on all SOP's (filling, packing, change over, sanitation etc.) Promote, motivate, and provides mentoring and guidance to employees Continuously looking for efficiencies and safety improvement(s) Follows and enforces GMP guidelines Works directly with maintenance to ensure productivity and minimal downtime. Excellent communication skills (leads 1st shift tier meeting, communicates daily production targets) Must have SAP production knowledge Must be Bilingual (English/Spanish) Education and Experience: Bilingual in English/Spanish required Bachelor's Degree Preferred 2+ years of supervisory experience in a manufacturing environment SAP experience required

We manufacture and market Splenda, the #1 brand in the low calorie sweetener category and the most recognized in the world. Heartland Food Products Group is a global leader in the consumer packaged goods (CPG) industry, producing low-calorie sweeteners, coffee, coffee creamers and liquid water enhancers. We make coffee, tea and water taste better and help people live happier, healthier and longer lives by making it easy to reduce sugar. We offer an excellent compensation and benefits package. Come grow with us! This role is not a remote opportunity, it is on-site at our Manufacturing Plant in Indianapolis, Indiana. 3rd shift available. Scope: The Production Supervisor directly supervises and coordinates the activities of production and operating workers, such as packers, machine operators, and blenders. The Supervisor will be responsible for establishing and achieving production goals, fostering relationships, promoting Health and Safety and the development of a well-trained and motivated staff. Essential Duties and Key Responsibilities: Enforces safety and sanitation regulations per food safety and quality guidelines. Responsible for initiating appropriate actions that address Food Safety concerns, including escalation to Quality and Management. Utilizes all food safety and food security guidelines, including Safe Quality Foods (SQF) good manufacturing practices and Hazard Analysis Critical Control Points. Directs and coordinates the activities of the employees engaged in the production or processing of goods, such as packers, machine operators, and blenders. Develops and motivates team to solve own day-to-day operational issues and achieve plant goals through ongoing communication and facilitation of team meetings. Coordinates daily inventories and supplies and other operational activities within or between departments. Plans and establishes work schedules, assignments, and production sequences to meet production goals. Inspects materials, products, or equipment to detect defects or malfunctions. Observes work and monitor gauges, dials, or other indicators to ensure that operators conform to production or processing standards. Conducts employee training in equipment operations and work and safety procedures or assigns employee training to experienced workers. Maintains records of employees' attendance and hours worked. Counsels employees about work-related issues and assists employees to correct job-skill deficiencies. Recommends or initiates personnel actions, such as hires, promotions, transfers, discharges, or disciplinary measures of direct reports. Interprets specifications, blueprints, job orders, and company policies and procedures for workers. Initiates and drives process improvements. Reads and analyzes charts, work orders, production schedules, and other records and reports to determine production requirements and evaluates current production estimates and outputs. Document all records outlined by company policies, such as production records, HACCP, good manufacturing policies, standard operating procedures, and food safety and quality plans. Oversees and completes production documentation, support documentation, and process control documentation throughout the facility. All other duties as assigned. Qualifications Bachelor of Science in Engineering required. Minimum of 2 years' experience in manufacturing and supervision. Superior analytical and critical thinking skills Proficient computer skills, including Microsoft Excel and Word Demonstrates essential problem-solving methods and initiative. Ability to perform under pressure and to solve problems independently Ability to communicate well with all employees and customers Physical Demands: Must be able to physically perform the functions of climbing, balancing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting, grasping, feeling, talking, hearing, and repetitive motions Must be able to work seated using a computer and phone for long periods of time. Must be able to work extended hours, such as daily overtime and an occasional weekend Must possess visual acuity to document company records Continuous walking throughout plant and distribution center. Lifting up to 50 pounds

Salary: $70k-$80k We are seeking a results-driven Transportation Supervisor to oversee shipping operations across a two-building facility. This role ensures customer orders are shipped accurately and efficiently while maintaining high productivity standards. Key Responsibilities Team Leadership: Hire, train, and develop team members, conduct performance reviews, and manage conflict resolution. Operational Oversight: Supervise daily shipping functions, monitor conveyor workflows, and troubleshoot inefficiencies. Budget & Metrics: Track labor hours and work completion levels to meet or exceed established budgets. Compliance: Maintain expert knowledge of shipping vendors and ensure all tasks comply with company safety and business standards. Qualifications Experience: Minimum of 4 years in a supervisory or lead role within a shipping or transportation environment. Skills: Strong leadership, analytical, and communication skills. Proficiency with basic PC applications is required. HAZMAT experience required. International Shipping experience required. Apply today to join a team dedicated to operational excellence!

Shift hours - 2:30 PM - 11:00 PM, with occasional adjustments based on the needs of 2nd and 3rd shifts. Location 6125 Guion Road, Indianapolis Indiana 46254 X ylem's Production Supervisor, you'll take charge of a high-performing ion-exchange resin team , driving reliable, high-quality production every day. You'll own daily operations, sharpen performance through audits and coaching, and move quickly to resolve issues and boost efficiency. Partnering with leadership, you'll spearhead process improvements, eliminate nonconformance, and enforce uncompromising safety and regulatory standards. 24 direct reports, including 7 CDL Class A Drivers ensuring compliance with DOT regulations, safe driving practices, and efficient route execution to meet delivery and service goals. Responsibilities: (Onsite Position) Standard work hours: 2:30 PM - 11:00 PM, with occasional adjustments based on the needs of 2nd and 3rd shifts. Expected to maintain a minimum 44-hour work week Primary oversight of 2nd shift operations, with additional responsibility for 3rd shift performance and coordination Maintain DOT compliance for all drivers, including required documentation, inspections, and certifications Manage a fleet of 7 vehicles, ensuring preventive maintenance, safe operation, and regulatory compliance Inventory Management Monitor and track inventory levels Order supplies and materials as needed Implement systems to optimize inventory management Conduct regular inventory audits to ensure accuracy and identify discrepancies Coordinate with purchasing department to ensure timely delivery of materials Safety And Compliance Enforce safety protocols and procedures Conduct regular safety training for production team members Ensure compliance with all relevant regulations and guidelines Conduct safety inspections and address any safety concerns or hazards Maintain accurate and up-to-date safety records. Qualifications A bachelor's degree in Business Administration, Supply Chain Management, or a related field with at least 2 years experience or equivalent work experience that provides exposure to fundamental theories, principles, and concepts. Strong analytical skills and proficiency in data analysis tools (e.g., Excel, SQL). In-depth understanding of inventory management principles and practices. Experience with inventory management software and systems. Ability to develop and implement inventory optimization strategies. Strong problem-solving skills and attention to detail. Xylem does not provide visa sponsorship for this position The estimated salary range for this position is $75,000 to $90,000. Starting pay is dependent on multiple factors, such as skills, experience and work location, and is not typically at the top of the range. At Xylem we offer a competitive compensation package with a generous benefit package, including Medical, Dental, Vision plans, 401(k) with company contribution, paid time off, paid parental leave and tuition reimbursement.

The Transportation Supervisor is responsible for overseeing yard operations, managing up to seven direct reports, and ensuring the efficient movement of inbound and outbound freight. This role requires a strong focus on performance metrics, data-driven decision-making, and continuous improvement initiatives. The ideal candidate will drive execution in a fast-paced environment while maintaining safety, compliance, and operational efficiency. Key Responsibilities Operational Leadership & Yard Management ● Oversee multiple yard operations, ensuring efficient trailer flow, dock assignments, and asset utilization. ● Ensure compliance with all safety protocols, DOT regulations, and company policies. ● Collaborate with internal teams, including Sortation, Outbound, and Carrier Management, to optimize transportation processes. ● Manage driver check-ins, trailer audits, and yard security to maintain operational integrity. People Management & Team Development ● Lead and develop a team of up to seven direct reports, providing coaching and performance feedback. ● Ensure adequate staffing and shift coverage to meet operational demands. ● Foster a culture of accountability, teamwork, and continuous improvement. ● Conduct regular performance reviews and support career development initiatives. KPI Ownership & Performance Management ● Monitor and drive performance against key transportation metrics, including:On-Time Performance (OTP) Trailer Dwell Time Dock-to-Stock Time Yard Utilization Efficiency Safety Compliance and Incident Rate Labor Productivity & Cost per Unit ● Lead daily and weekly business reviews (WBRs), providing root cause analysis (RCA) and corrective action plans (CAPs). ● Utilize data to drive process improvements and operational excellence. Continuous Improvement & Problem-Solving ● Identify and implement process improvements to optimize transportation efficiency and reduce costs. ● Utilize Lean, Six Sigma, or other process improvement methodologies to enhance operations. ● Develop action plans to address recurring operational challenges based on WBR insights. Qualifications & Requirements ● 3+ years of experience in transportation, logistics, or yard operations leadership. ● Strong analytical skills with experience in KPI management, root cause analysis (RCA), and corrective action planning (CAP). ● Proven ability to manage multiple yard operations and direct reports in a high-volume environment. ● Proficiency in transportation management systems (TMS), yard management systems (YMS), and data analytics tools. ● Strong problem-solving skills with a bias for action. ● Excellent communication and stakeholder management abilities. ● Bachelor's degree in Logistics, Supply Chain, Business, or related field preferred. Work Environment & Schedule ● Fast-paced, high-volume logistics environment. ● May require weekend or night shifts based on business needs.

The Judge Group is currently in search of a Production Manager for a large food manufacturing facility located in Indianapolis, IN area! Responsibilities: Confers with management personnel to establish production and quality control standards, develop budget and cost controls, and obtains data regarding types, quantities, specifications, and delivery dates of products ordered Leads Supervisors and Team Members in a high-speed food manufacturing and packaging environment Utilizes assigned resources to maximize manufacturing output, minimize waste/downtime, improve capacity and efficiencies and maintain product quality and integrity Consults with engineering personnel relative to modification of machines and equipment in order to improve production and quality of products Confers with Purchasing and Receiving to ensure raw material testing and usage are done. Raw material ordering for as many as sixty different raw materials is done in a way that minimizes extra truck loads at month end. Assists with Quality Control programs to safeguard product quality Conducts internal audits to ensure compliance with FDA USDA AIB and OSHA methods policies and procedures Completes raw material month end inventory explaining any variance to budget Plans and directs production activities and establishes production priorities for products in keeping with effective operations and cost factors Coordinates production activities with procurement, maintenance, and quality control activities to obtain optimum production and utilization of human resources, machines, and equipment Reviews and analyzes production, quality control, maintenance, and operational reports to determine causes of nonconformity with product formulations, and operating or production problems Requirements: Dairy or ESL Beverage (Extended Shelf-Life) experience required High speed food or beverage manufacturing experience required HPWS (High Performance Work Systems), HPWO (High Performance Work Organization), or HPWT (High Performance Work Team) experience preferred 5+ years of production management experience

Production Manager - 1st Shift A well-established manufacturing organization is seeking an experienced Production Manager to oversee daily operations at its Indianapolis facility. This role is responsible for driving safe, efficient, and high-quality production while leading and developing production teams in a fast-paced environment. The Production Manager will partner closely with cross-functional teams to meet customer demand, improve processes, and support continuous improvement initiatives. Key Responsibilities Lead and manage day-to-day production operations to ensure safety, quality, delivery, and productivity targets are met Supervise, coach, and develop production supervisors and hourly team members Plan and coordinate production schedules to align with customer requirements and business objectives Track and analyze key performance indicators including safety, quality, scrap, downtime, and throughput Drive continuous improvement initiatives focused on efficiency, cost reduction, and waste elimination Ensure compliance with all safety standards, company policies, and regulatory requirements Partner with Engineering, Quality, Maintenance, and Supply Chain teams to resolve production issues Support hiring, onboarding, training, and performance management efforts within production Participate in process improvement, equipment upgrades, and capital planning initiatives Qualifications Proven experience as a Production Manager or senior Production Supervisor in a manufacturing environment Background in automotive, plastics, injection molding, or component manufacturing strongly preferred Demonstrated ability to lead, motivate, and develop teams on the production floor Experience with production planning, scheduling, and performance metrics Working knowledge of lean manufacturing and continuous improvement methodologies Strong problem-solving, communication, and organizational skills Why Consider This Opportunity Stable manufacturing environment with long-term growth potential Opportunity to lead plant-level operations and influence performance Hands-on leadership role with visibility across operations Team-oriented culture focused on quality, safety, and continuous improvement

FULLBEAUTY Brands™ is the premier fashion and lifestyle destination for the plus size customer. We are an online and catalog marketplace offering a curated collection of the finest family of plus size brands and thousands of products. POSITION SUMMARY: As a Warehouse Supervisor, you will provide leadership and general supervision to your employees in a dynamic, high volume, multi-shift fulfillment center. Supervisors will have an active role in all aspects of an employee's time with FBB, including but not limited to onboarding, training, development, discipline, and performance review. Supervisors will also grow their careers by learning the fundamentals of supervision and leadership with ongoing professional development. Supervisors will be expected to effectively manage their time to plan and organize duties and tasks ensuring successful completion. Supervisors will support the Operations Manager and ensure timely, accurate product receipt, order fulfillment, and optimization of resources and processes. Supervisors are expected to manage and lead people to ensure compliance with company policies/procedures, continual process improvement and drive employee initiatives to create and promote an environment where employees are engaged, empowered, and committed to success. PRIMARY RESPONSIBILITIES: Manage department quality to ensure all orders are shipped 100% accurately; customer service and quality are the first focus of a supervisor. Meet and exceed expected Key Performance Indicators that include customer service metrics, safety, department efficiency and work in process carryover. Responsible for identifying and correcting safety hazards in areas of responsibility; creating a safe work environment and a safety mindset among team members; addressing all safety issues and concerns throughout the operation. Retain staff through engaging with employees and ensuring they feel valued. Train, develop and mentor hourly staff to drive career growth for team members. Promote a fun culture and an open environment that promotes teamwork throughout the facility. Maintain effective communication with all levels of the organization, throughout numerous departments (HR, Building Services, IT, Engineering, Logistics, etc.) Understand business priorities while anticipating and addressing potential challenges. Meet assigned deadlines for projects. Drive innovation, proactively look for and identify operational constraints while working to eliminate them. Develop a work environment that welcomes change, accepts challenging the norm and drives innovation. MINIMUM QUALIFICATIONS: Previous supervisory or leadership experience Prior warehouse or distribution experience Proficiency with Microsoft Office programs (primarily Word and Excel) Knowledge of labor relations and experience working in a union environment Knowledge/experience in transportation environment (i.e., shipping, receiving and inventory management, distribution, or dispatch) Knowledge/experience working with warehouse management system(s) Bilingual language skills (Spanish or Burmese a bonus) WHY JOIN FULLBEAUTY? Competitive Health Benefits (Medical, Dental & Vision) Employer HSA Contribution 401K Match Employee Assistance Program Wellness Initiatives 30% Associate Merchandise Discount Across our Family of Brands Employee Discount on Travel, Cell Phone Plans and More Generous Paid Time Off Program Promote From Within Culture Commitment to Being an Equal Opportunity Employer Life Insurance Benefits Internal charity that supports FULLBEAUTY Brands' associates and their immediate family members during times of extreme hardship FULLBEAUTY Brands™ is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, sexual orientation, gender identity, disability or protected veteran status.

Vylla Home's national footprint and full-service model provide a truly progressive approach to the real estate process, creating extraordinary experiences for both our customers and sales agents. As part of the Carrington and Vylla family of companies, we provide nearly every aspect of homeownership under one roof - from real estate with Vylla Home to title, settlement and escrow services with Vylla Title and Escrow, mortgage lending with Carrington Mortgage Services, LLC and more! We offer our agents: True partnership in your real estate business to support your career goals and development. Competitive commission splits - keep your commission and set your own value! Unlimited opportunity to earn what you are worth. No upfront or monthly fees. We don't make money until you do. Reasonable flat rate transaction fees. No hidden costs, and you don't pay until you close! Qualified leads, assets and referrals - many unique options to increase your business. We are also a leading REO brokerage and provide multiple REO lead resources. Free CRM tool (including a custom mobile app for when you're on the go!), marketing tools, transaction management system, e-signatures and more. Customized training, live demos and a library of industry-relevant resources available 24/7. We also offer the Ninja Selling sales platform and training for agents to increase productivity - all at no cost to you! Customizable marketing resources including agent websites, printed and digital materials, social media assets, tools, support and training. Face-to-face broker support and coaching - true mentorship! Dedicated resources from Vylla and Carrington's family of companies (including lending, title and settlement services along with superior customer service from our homeownership concierge team) Back office support including dedicated transaction coordinators and an agent services resource team “Best of both worlds” environment with local offices and support as well as the backing of a large, established and nationwide institution Incentive program to earn cash if you help grow our team and refer new agents onboard Resources for your clients including a mobile app for home search, moving discounts from local vendors and more. Flexible schedules and control over your personal and professional growth as an agent A fun, positive culture where our community, or Vyllage as we call it, supports one another and gives back Apply today! What will make you successful at Vylla? An active Real Estate license Drive and ambition to succeed as part of an innovative, fast-growing team Complete focus on the customer experience Strong communications skills and ability to build a network of engaged customers and prospects Ability to multi-task and take initiative, strong work ethic Vylla is an equal opportunity employer. It is the policy of the company that applicants be considered for positions for which they qualify without regard to race, color, religion, gender, national origin, ancestry, age, marital status, sexual orientation, veteran's status, physical or mental disability or any other legally protected category. Vylla will make reasonable accommodations for known physical or mental limitations of a qualified applicant or employee with a disability unless the accommodation will impose an undue hardship on the company. EEO/AAP Employer

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world. Responsibilities: The Warehouse Lead Operator assists the Warehouse Supervisor in supporting site operations by directing and performing material handling tasks according to current standard operating procedures and work instructions. The role requires interpersonal communication skills, initiative, and attention to detail for safe and efficient operations. Basic Requirements: * High school diploma or equivalent * Three years of experience in pharmaceutical/GMP environments * Proficiency in reading, writing, and communicating in English * Current certification for operating powered industrial equipment (e.g., forklifts, reach trucks, swing-reach trucks) Additional Skill Preferences: * Experience with RF scanners and computer systems such as SAP, MES, & WMS * Experience handling hazardous materials * Ability to work with and learn new digital systems * Demonstrated ability to lead and train others in departmental tasks Key Responsibilities: * Ensure adherence to Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) in a regulated environment * Enforce standards for housekeeping, safety, and environmental compliance throughout warehouse areas according to procedures * Provide coaching and guidance to employees in assigned areas * Assign daily and weekly work schedules to warehouse operators * Serve as acting leader in the absence of the Warehouse Supervisor as needed * Conduct routine inspections for health and safety compliance * Assist the Warehouse Supervisor in reviewing, updating, and creating procedures * Participate in deviation investigations relating to area responsibilities * Safely operate warehouse docks and ramps for loading/unloading containers and trailers * Operate powered industrial equipment safely and efficiently to maintain material flow * Collaborate with supervision, counterparts, and safety representatives to implement improvements from safety incident investigations or projects * Receive and inspect inbound raw materials, packaging, and miscellaneous items into inventory using WMS systems * Maintain accurate inventory records in SAP/WMS * Label materials according to health, safety, quality, transport regulations, and customer requirements * Participate in warehouse audits related to quality, safety, and inspection readiness * Pick and prepare materials to meet manufacturing and shipping schedules * Comply with transportation regulations and shipping requirements * Support other warehouse functions as assigned, including cycle counting and material handling duties at manufacturing nodes * Align individual and team activities to defined metrics and goals Additional Requirements / Information: * The Warehouse Lead Operator role is night shift-based: 5:45 pm - 6:00 am on a rotational schedule of three nights on, two nights off, two nights on, and three nights off * May include occasional non-scheduled call-in times for plant emergencies * Ability to bend, reach, and lift items up to 50 pounds * Ability to work periodically in refrigerated storage areas Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (******************************************************** for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status. Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), en Able (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $25.60 - $37.55 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly

Pay Range: $65,000 - 75,000, depending on experience Rate Frequency: Salaried Schedule: Monday through Thursday, from 4:00 PM to 2:30 AM. Click here to experience a Day in the Life of our Teammates! Uncap Your Potential at America's Largest Coca-Cola Bottler - Pour Your Passion into Purpose! We're more than beverages-we're building meaningful careers and vibrant communities. Join our team where your talent meets purpose, and every teammate directly shapes our success. * Career Growth: Clear pathways to advance and develop your career * Competitive Benefits: 401(k) match + health coverage + employee stock purchase plan * Purpose-Driven: Create meaningful impact in the communities you serve * Professional Development: Dedicated training + personalized mentorship Join us - your refreshing new chapter starts here! Job Overview The Supervisor MFG Warehouse is responsible for supervising all areas of Warehouse Operations in a MFG Center or Hub including, but not limited to, clerks, pallet builders, checkers, loaders, forklift drivers, etc. by providing leadership to the team, training and evaluating Warehouse Personnel and Processes, and maintaining the ability to provide expertise and hands-on assistance in any area of Warehouse Operations when required. The Warehouse Supervisor is responsible for performance management and will lead the interviewing of potential candidates, provide direction of work to the assigned team, and provide guidance and support to any specific area of responsibility and/or Team as designated by the Warehouse MFG Manager. The Supervisor MFG Warehouse reports to the Manager MFG Warehouse and handles issues occurring within the Warehouse regarding processes or personnel while promoting all policies, safety procedures, goals, expectations, and CCCI's Purpose and Values. Duties & Responsibilities * Supervises and directs the daily activities of warehouse teammates to ensure the safe and successful completion of all related daily warehouse activities and operations. * Verifies and ensures all applicable Warehouse processes are followed, including, but not limited to, the processes for handling damaged product check-in, etc. * Trains and supervises a staff of warehouse personnel and evaluates processes striving for continuous improvements. * Communicates with other departments and internal/external stakeholders as it relates to identified process improvements, quality, Out-of-Stocks (OOS ), Carrier issues, Loading issues, etc. * Manages and models the safety culture and strives for 100% compliance concerning safety policies and procedures. * Supervises, leads, and motivates a team to deliver results by communicating company goals, safety practices, and deadlines; engaging and developing teammates through effective performance management, coaching, and training; issuing corrective action, implementing continuous improvement methods while maintaining customer focus, and embodying company purpose and values to inspire servant leadership. * Leads in interviewing potential candidates. Knowledge, Skills, & Abilities * Ability to lead, coach, teach, and train in a manner that aligns with Company Purpose. * Extensive knowledge of all Warehouse Processes and Warehouse Systems. * Ability to prioritize, multi-task, and think proactively. * Strong communication skills - written and oral. * Computer skills: Microsoft Office Applications (Word, Excel, Outlook) and Internet Explorer. * Ability to work in a fast-paced atmosphere while walking and repetitively lifting 30 lbs. * Ability to lift up to 75 lbs. * Ability to collaborate within a team environment. * Ability to coordinate and organize efficient and dependable warehouse processes. * Ability to adapt to needs of role in different work areas throughout the workday and meet minimum expectations of those different work areas. * Ability to read and interpret instructions from computer screen. * Attention to detail and ability to differentiate our packages. * Ability to work/lead in a noisy and non-climate controlled (Hot in summer/Cold in winter) environment. * Intentional self-starter who takes initiative and proactively seeks out value-add opportunities. Minimum Qualifications * High school diploma or GED * Knowledge acquired through 1 to 3 years work experience * Minimum of 1 - 2 years experience supervising or leading people in a warehouse environment. Preferred Qualifications * PIT (Powered Industrial Truck) Certification * Certification to be secured after 90-day probationary period Work Environment Noisy and non-temperature-controlled environment including high and low-temperature environments Equal Opportunity Employer - All qualified applicants will be considered for employment without regard to disability, protected veteran status, or any other characteristic protected by applicable law. Nearest Major Market: Indianapolis

Job DescriptionDescription: Volumod of is a new start up modular manufacturing group of partners located in Indianapolis, Indiana. Volume is looking to change the lives of thousands of individuals and families in the State of Indiana by providing rapid response, high quality single and multi-family housing solutions to communities in need of affordable housing. Our investors are also proven community developers who share a mission to create affordable modular homes for Indiana by leveraging renewable resources, designing smart homes, and caring for people. Our Vision is to see the people of Indiana renewed by great jobs and homes that improves lives. Volume is a fully integrated business model designed to manufacture modular solutions for our investors who provide the opportunity to control each project and all manufactured product from land to lockup. The factory is forecasted to manufacture up to 214 modules / 32,000 square feet of product per month by the end of 2021, and for an additional ramp up in capacity of 25% by the end of 2022. We plan to build more than 2075 modules / 1,000,000 square feet over the first four years. Volumod is currently seeking a Production Supervisor. The Production Supervisor is responsible for leading plant employees in a manufacturing and assembly environment for off-site construction of modular homes. This position plans, executes, and assigns work, implements policies and procedures, and recommends improvements in production methods, equipment, operating procedures and working conditions. This position drives continuous improvement through the plant operation and leads the workforce as necessary to maintain a high level of morale. Functional Duties: Lead and train employees to support different departments. Interviewing, hiring, training, and development of production workers. Delegate and prioritize alignment of resources to production areas as needed. Exhibit exceptional leadership and communication skills. Driving employee engagement. Support quality assurance and continuous improvement processes. Balance safety, quality, cost, & productivity to achieve positive results. Read and interpret architectural, structural, mechanical blueprints. Properly operate power tools, and associated equipment. Lead and support various construction/production processes as needed including the installation of framing, flooring, ceilings, roofing, windows, doors, etc. Lead weekly safety meetings with production team members and promote a safe working environment. Lead crew meetings to communication key production topics and engage with the workforce. Demonstrate commitment to an injury-free environment and ensure employee adherence to safety program standards. Leverage Lean manufacturing principles to drive production team and resource utilization efficiency. WE ARE NOT ACCEPTING CANDIDATES FROM STAFFING FIRMS Requirements: Required Education and Experience requirements: High School Diploma, GED, or Four years of experience leading highly effective production teams. Good people skills, good attitude, and the ability to operate as part of a team. Effectively communicate and understand both verbal and written instructions. An accountable attitude with a commitment to accuracy Experience applying Lean manufacturing principles to drive continuous improvement. Detail oriented and comfortable with manufacturing process Preferred Experience requirements: Offsite / Modular Construction Experience Minimum of 8 years' experience in residential, modular and / or multi-family construction preferred but not required. Physical Requirements: Prolonged periods of standing, walking, stooping, bending. May have periods of sitting at a desk and working on a computer. Must be able to lift up to 50 pounds at times. Benefits: Our people are the organization' greatest asset. We are proud to offer a full range of employee benefits. This full-time position offers a competitive base salary with bonus potential, paid time-off and paid holidays. Medical/Dental/Vision Insurance, and a 401k Plan with a 100% employer match Year-Round Production Indoor Climate Controlled EnvironmentBenefit Conditions: Waiting period may apply Only full-time employees eligible Typical end time: 4PM Typical start time: 7AM Work Remotely No Benefits: 401(k) 401(k) matching Dental insurance Employee assistance program Health insurance Health savings account Life insurance Paid time off Retirement plan Tuition reimbursement Vision insurance

Description The Manufacturing Supervisor 2 is a senior supervisor position that is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor support and review of MBR's, providing coaching and feedback to operations team. Strategic operator development and career path mentorship. Involvement in manufacturing deviation investigations and CAPA implementation. Batch planning and scheduling and providing process continuous improvement initiatives. Influencing the accomplishments of companywide and team goals and objectives as well as inspiring team members while consistently modeling ALP values in all interactions. This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) The Manufacturing Supervisor will constantly evaluate the internal processes and procedures and work to create a productive space while maintaining the highest possible quality standards. Essential Job Functions:· Batch and resource detail schedule planning.· Provide floor support and real time batch record review.· Provide technical support, oversite and team leadership in manufacturing batch activities.· Coordinate the development of individual team members with routine one on ones, training oversite and training opportunities.· Develop and improve current processes to maintain and control the formulation and filling operations.· Attend cross functional leadership meetings, support client audits and tours.· Attend daily batch release and deviation triage meetings as representative for operations.· Assure compliance with cGMP requirements (current good manufacturing practices)· Perform GEMBA walks and checks for process improvements. Special Job Requirements:· 2-4 years demonstrated working knowledge of aseptic manufacturing operations.· 1-2 years in a people leadership role· Knowledge of process control, quality engineering, sampling requirements, statistical techniques, and process capability· Familiarity with relevant quality and regulatory requirements and trends and cGMP's· Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders.· Knowledge of Aseptic techniques and processing at INCOG Biopharma. Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

The Manufacturing Supervisor 2 is a senior supervisor position that is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor support and review of MBR's, providing coaching and feedback to operations team. Strategic operator development and career path mentorship. Involvement in manufacturing deviation investigations and CAPA implementation. Batch planning and scheduling and providing process continuous improvement initiatives. Influencing the accomplishments of companywide and team goals and objectives as well as inspiring team members while consistently modeling ALP values in all interactions. This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) The Manufacturing Supervisor will constantly evaluate the internal processes and procedures and work to create a productive space while maintaining the highest possible quality standards. Essential Job Functions: * Batch and resource detail schedule planning. * Provide floor support and real time batch record review. * Provide technical support, oversite and team leadership in manufacturing batch activities. * Coordinate the development of individual team members with routine one on ones, training oversite and training opportunities. * Develop and improve current processes to maintain and control the formulation and filling operations. * Attend cross functional leadership meetings, support client audits and tours. * Attend daily batch release and deviation triage meetings as representative for operations. * Assure compliance with cGMP requirements (current good manufacturing practices) * Perform GEMBA walks and checks for process improvements. Special Job Requirements: * Knowledge of process control, quality engineering, sampling requirements, statistical techniques, and process capability * Familiarity with relevant quality and regulatory requirements and trends and cGMP's * Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders. * Knowledge of Aseptic techniques and processing at INCOG Biopharma. * 2-4 years demonstrated working knowledge of aseptic manufacturing operations. * 1-2 years in a people leadership role Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

Anticipated salary range: $80,900 - $115,500 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: 12/28/2025*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. What Manufacturing Engineering contributes to Cardinal Health Manufacturing Engineering is responsible for developing manufacturing processes, production floor layouts and associated tools. Reviews new designs for manufacturability. Designs process improvements to reduce product cost, process cycle time and improved product quality. Shift/Schedule 40 hours weekly Weekend Shift Friday - Sunday 3x12s - 7 :00am - 7:30pm Monday 4 hours - 7:00am - 11:00am Must be flexible to work other hours and days as needed Responsibilities Supervises Manufacturing Engineering staff and oversees daily activities, and production schedules as it pertains to those delivery systems. Trains, coaches, mentors, develops, and provides direction to staff Conducts performance appraisals for direct reports. Responsible for Equipment and Facilities sustainment efforts and activities. Up to and including scheduling, performing, and documenting routing maintenance and break/fix operations. Works with EHS and RSO to adhere to Radiation Safety Program (Best Practices and Policies) Ensures attainment of budget objectives through effective financial management and optimal utilization of resources. Acts as liaison to ensure and take an active role in developing and maintaining positive working relationships with customers, suppliers, and corporate contacts through regular interactions. Ensures internal quality and regulatory standards are maintained at or above an acceptable level. Ensures positive working relationships with all CAH employees through regular interactions, team building, and active listening. Oversees and is accountable for safety for all employees and security of the facility. Ensures operational procedures are followed with and adhere to federal, state, local, and company regulations. Prepares regular reports and analysis for management, customer correspondence, succession plans, and employee documentation. Ensures high quality products and services are delivered to customers (both internally and externally); and works within their abilities to resolve complaints. Conducts staff meetings. Participates in organization-wide conferences and training activities. Operates under well-controlled and closely monitored conditions (GMP), which are highly regulated by State and Federal agencies and internal quality and regulatory professionals. Exposure to very low radiation levels from radiopharmaceuticals suitable for human use. Employees receive specific training in keeping with regulatory guidelines and are monitored for exposure. Qualifications Bachelor's degree or equivalent experience in related field preferred 4 years related pharmacy experience preferred Experience with cGMP preferred Experience with formulation and filling preferred Aptitude for supervisory skills Proven customer service skills Ability to negotiate, influence, and resolve customer/employee problems or conflicts to meet the needs of external and internal customers Ability to be innovative in troubleshooting complex problems Ability to promote teamwork within manufacturing location and region by treating staff members with respect. Ability to lift up to 80 lbs. Flexibility to work various shifts and rotate schedules Comfortable working in a nuclear environment What is expected of you and others at this level Manages department operations and supervises professional employees, frontline supervisors and/or business support staff Participates in the development of policies and procedures to achieve specific goals Ensures employees operate within guidelines Decisions have a short-term impact on work processes, outcomes, and customers Interacts with subordinates, peer customers and suppliers at various management levels may interact with senior management Interactions normally involves resolution of issues related to operations and/or projects Gains consensus from various parties involved 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

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization, partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington, Indiana, US and Halle/Westfalen, Germany, we offer a wide range of delivery systems including pre-filled syringes, liquid/lyophilized vials, diluents for reconstitution, powder-filled vials and sterile crystallization. Our product types include biologics and small molecules, cytotoxics, highly potent compounds, diluents for reconstitution and vaccines - which are all directly injected into patients worldwide. As such, there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards. While our primary focus is cGMP manufacturing, we offer many support services including formulation and development, lyophilization optimization, global regulatory support and secondary packaging. Our teams are driven to help clients scale, innovate and bring life-changing medicines to patients worldwide. Why join Team Simtra? Because we: Make it HAPPEN - We bring a growth mindset to every opportunity, developing new skillsets and exceeding our expectations and those of our customers. Make it TOGETHER - We work as one, respecting each voice and tapping into our unique strengths across teams-so we can solve problems in new ways. Make it RIGHT - We hold ourselves to a high standard of excellence, fulfilling our commitments to the customer, their patients, and our team members. Make it COUNT - We take pride in our day-to-day work, knowing the impact we make - taking on challenges big and small to improve patient health. The role: The Supervisor, Aseptic Operations is a member of the Operations Leadership Team and reports directly to the Manager, Aseptic Operations. They lead a team of Operations personnel engaged in manufacturing of sterile injectable drug products. The Supervisor, Aseptic Operations provides decision making and oversight to ensure compliance to all standard operating procedures and batch records. They must communicate effectively with Operations support departments (Quality, Technical Services, Engineering & Maintenance, etc.), multiple levels of management, and other customer support departments. The Supervisor, Aseptic Operations builds an environment where partnership, productivity, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product. 3rd Shift Schedule: 10pm - 8:30am (Monday - Thursday) Its responsibilities: Understand, follow, coach, and lead their teams to execute production activities in accordance with current Good Manufacturing Practices (cGMP). Provide guidance, support, direction and leadership through positive interactions with all personnel during daily operations. Interview, hire, mentor, and develop staff. Conduct annual performance reviews for all direct reports. Assists in setting performance objectives and development plans. Supervise the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities in order to meet customer requirements including deadlines and quality standards. High percentage of Gemba (shop floor) presence. Review, approve, and manage documentation for batch and system records. Assist in release of product for distribution. Assist in meeting product release time goals. Implement and support training programs designed to enable staff to consistently carry out all manufacturing processes with strict compliance to cGMPs and EHS regulations. Develop and implement performance measurement and internal auditing programs in order to routinely evaluate operational efficiency and quality. Implement changes as needed based on assessments. Lead technical reviews, investigations and process improvement projects. Provide manufacturing input into integration and validation of new equipment and processes. Resolve technical, material and cGMP problems that may impact project deadlines. Provide guidance and troubleshooting assistance as needed during a deviation in the process; applying Root Cause Analysis (RCA) tools when applicable. Obtain qualification to perform select critical operation processes. Represent the company during audits and inspections. Desirable qualifications: Bachelor's Degree in a science, engineering, or business discipline strongly preferred High School diploma or GED required Minimum 2 years of manufacturing or operations support experience required Minimum 1 year leadership experience required Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: Microsoft Dynamics, Veeva, PowerBI, Trackwise, etc.) Physical / safety requirements: Ability to stand or sit for extended periods of time Ability to lift up to 50 pounds Ability to push/pull heavy wheeled objects (i.e.: tanks, carts, pallet jacks, etc.) Must be able to perform overhead work (i.e.: sanitizing walls and ceilings) Physical coordination/flexibility to allow gowning for clean room environments Use applicable personal protective equipment, including safety shoes/toe caps, gloves, eye protection, heat resistant wear and hearing protection Dexterity and physical condition to perform some level of repetitive motion tasks Ability to wear respirator usage when product or task requires Eyesight to ensure effective inspection of equipment and/or filled units (corrective lenses acceptable) Use of hands and fingers to manipulate office equipment is required Must be able to gown qualify for Grade A/B areas (filling) In return, you'll be eligible for[1]: Day One Benefits Medical & Dental Coverage Flexible Spending Accounts Life and AD&D Insurance Supplemental Life Insurance Spouse Life Insurance Child Life Insurance Short and Long-Term Disability Insurance 401(k) Retirement Savings Plan with Company Match Time Off Program Paid Holidays Paid Time Off Paid Parental Leave and more Adoption Reimbursement Program Education Assistance Program Employee Assistance Program Community and Volunteer Service Program Employee Ownership Plan Additional Benefits Voluntary Insurance Benefits Vision Coverage Accident Critical Illness Hospital Indemnity Insurance Identity Theft Protection Legal and more Onsite Campus Amenities Workout Facility Cafeteria Credit Union [1] Current benefit offerings are in effect through 12/31/25 Disclaimer This job description is intended to provide the minimum knowledge, skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements. Equal Employment Opportunity Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Data Privacy To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: **********************************

Job Title: Training Supervisor Reports to: Training Manager Job Status: Exempt, FT SHEIN is a global online fashion and lifestyle retailer, offering SHEIN branded apparel and products from a global network of vendors, all at affordable prices. Headquartered in Singapore, with more than 16,000 employees operating from offices around the world, SHEIN is committed to making the beauty of fashion accessible to all, promoting its industry-leading, on-demand production methodology, for a smarter, future-ready industry. Position Summary As the Training Supervisor, you will lead the development, implementation, and oversight of tailored training programs for warehouse employees. This role requires creating comprehensive materials, conducting interactive sessions, evaluating performance, and ensuring strict policy adherence. Job Responsibilities Provide technical writing resources to ensure accurate work instructions are developed and maintained for all processes. Ensure associates are trained on individual job functions and training is documented. Ensure all regulatory and safety requirements are incorporated into company policies and associates are appropriately trained. Develop and conduct initial new associate and refresher programs to ensure all company and regulatory requirements are met. Develop, coordinate, and/or conduct job-specific and process training programs to ensure associates are trained on their job functions. Collaborate with department heads and HR to assess needs, measure effectiveness, and align training with goals. Maintain training records, track progress, and generate reports on outcomes and performance. Stay updated on industry trends, best practices, and technological advancements in training methods. Participate in meetings, committees, and projects focused on continuous improvement initiatives. Perform other duties as assigned. Job Requirements: 2 years of relevant work experience Experience with warehouse management or inventory systems Ability to adhere to the 7S program Strong understanding of warehouse operations, safety regulations, and compliance. Excellent communication, organizational, and leadership skills. Proficiency in MS Office and training software/tools. Benefits and Culture Healthcare (medical, dental, vision, prescription drugs) Health Savings Account with Employer Funding. Flexible Spending Accounts (Healthcare and Dependent care) Company-Paid Basic Life/AD&D insurance Company-Paid Short-Term and Long-Term Disability Voluntary Benefit Offerings (Voluntary Life/AD&D, Hospital Indemnity, Critical Illness, and Accident) Employee Assistance Program Business Travel Accident Insurance 401(k) Savings Plan with discretionary company match and access to a financial advisor Vacation, paid holidays, floating holidays, and sick days Employee discounts Free swag giveaways SHEIN is an equal opportunity employer committed to a diverse workplace environment.

The Manufacturing Supervisor 2 is a senior supervisor position that is responsible for overseeing production operations, ensuring that all work completed is within appropriate timeframes, delivering daily expectations and assignments. Providing on floor support and review of MBR's, providing coaching and feedback to operations team. Strategic operator development and career path mentorship. Involvement in manufacturing deviation investigations and CAPA implementation. Batch planning and scheduling and providing process continuous improvement initiatives. Influencing the accomplishments of companywide and team goals and objectives as well as inspiring team members while consistently modeling ALP values in all interactions. This individual will ensure that all work is carried out in accordance with regulatory requirements, Good Manufacturing Practices (cGMP) and Standard Operating Procedures (SOPs) The Manufacturing Supervisor will constantly evaluate the internal processes and procedures and work to create a productive space while maintaining the highest possible quality standards. Essential Job Functions: · Batch and resource detail schedule planning. · Provide floor support and real time batch record review. · Provide technical support, oversite and team leadership in manufacturing batch activities. · Coordinate the development of individual team members with routine one on ones, training oversite and training opportunities. · Develop and improve current processes to maintain and control the formulation and filling operations. · Attend cross functional leadership meetings, support client audits and tours. · Attend daily batch release and deviation triage meetings as representative for operations. · Assure compliance with cGMP requirements (current good manufacturing practices) · Perform GEMBA walks and checks for process improvements. Special Job Requirements: · Knowledge of process control, quality engineering, sampling requirements, statistical techniques, and process capability · Familiarity with relevant quality and regulatory requirements and trends and cGMP's · Strong communication skills and the ability to build relationships with colleagues across all levels of the organization, including business managers, operations leaders, and technical leaders. · Knowledge of Aseptic techniques and processing at INCOG Biopharma. · 2-4 years demonstrated working knowledge of aseptic manufacturing operations. · 1-2 years in a people leadership role Additional info about INCOG BioPharma Services: At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business. If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus. INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics. By submitting your resume and details, you are declaring that the information is correct and accurate.

**Anticipated salary range:** $80,900 - $115,500 **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:** 12/28/2025*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. **_What Manufacturing Engineering contributes to Cardinal Health_** Manufacturing Engineering is responsible for developing manufacturing processes, production floor layouts and associated tools. Reviews new designs for manufacturability. Designs process improvements to reduce product cost, process cycle time and improved product quality. **_Shift/Schedule_** + 40 hours weekly + Weekend Shift + Friday - Sunday 3x12s - 7 :00am - 7:30pm + Monday 4 hours - 7:00am - 11:00am + Must be flexible to work other hours and days as needed **_Responsibilities_** + Supervises Manufacturing Engineering staff and oversees daily activities, and production schedules as it pertains to those delivery systems. + Trains, coaches, mentors, develops, and provides direction to staff + Conducts performance appraisals for direct reports. + Responsible for Equipment and Facilities sustainment efforts and activities. Up to and including scheduling, performing, and documenting routing maintenance and break/fix operations. + Works with EHS and RSO to adhere to Radiation Safety Program (Best Practices and Policies) + Ensures attainment of budget objectives through effective financial management and optimal utilization of resources. + Acts as liaison to ensure and take an active role in developing and maintaining positive working relationships with customers, suppliers, and corporate contacts through regular interactions. + Ensures internal quality and regulatory standards are maintained at or above an acceptable level. + Ensures positive working relationships with all CAH employees through regular interactions, team building, and active listening. + Oversees and is accountable for safety for all employees and security of the facility. + Ensures operational procedures are followed with and adhere to federal, state, local, and company regulations. + Prepares regular reports and analysis for management, customer correspondence, succession plans, and employee documentation. + Ensures high quality products and services are delivered to customers (both internally and externally); and works within their abilities to resolve complaints. + Conducts staff meetings. Participates in organization-wide conferences and training activities. + Operates under well-controlled and closely monitored conditions (GMP), which are highly regulated by State and Federal agencies and internal quality and regulatory professionals. + Exposure to very low radiation levels from radiopharmaceuticals suitable for human use. Employees receive specific training in keeping with regulatory guidelines and are monitored for exposure. **_Qualifications_** + Bachelor's degree or equivalent experience in related field preferred + 4 years related pharmacy experience preferred + Experience with cGMP preferred + Experience with formulation and filling preferred + Aptitude for supervisory skills + Proven customer service skills + Ability to negotiate, influence, and resolve customer/employee problems or conflicts to meet the needs of external and internal customers + Ability to be innovative in troubleshooting complex problems + Ability to promote teamwork within manufacturing location and region by treating staff members with respect. + Ability to lift up to 80 lbs. + Flexibility to work various shifts and rotate schedules + Comfortable working in a nuclear environment **_What is expected of you and others at this level_** + Manages department operations and supervises professional employees, frontline supervisors and/or business support staff + Participates in the development of policies and procedures to achieve specific goals + Ensures employees operate within guidelines + Decisions have a short-term impact on work processes, outcomes, and customers + Interacts with subordinates, peer customers and suppliers at various management levels may interact with senior management + Interactions normally involves resolution of issues related to operations and/or projects + Gains consensus from various parties involved _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 (***************************************************************************************************************************