23 Manufacturing jobs in Winterville

**Overview**
**Quality Control|** Hiring Immediately **|Kinston,NC**
**3rd shift**
**12:00 midnight-8:00am**
**Pay:$18.39- $27.04 based on experience**
Benefits Overview:
+ Medical, Dental, Vision
+ Prescription drug coverage
+ 401K with a company match
+ New Hire Wellness Bonus (see plan details)
+ Healthcare and Dependent day care flexible spending accounts
+ Corporate discounts
Our Social Responsibility platform features a robust, employee-led Give Back program, which includes a matching gifts plan, community grants initiative, and our annual Company-wide Month of Action campaign. With each of these initiatives, our employees are empowered and equipped to give back to their communities and support the non-profits important to them and their families. Through our Give Back program, we own our commitment to Social Responsibility and live our purpose of Packaging a Better Future.
**Responsibilities**
**Responsibilities:**
+ Measures product quality through the use of statistical methods, control charting, and process improvement techniques
+ Updates and maintains Quality Department computer databases and quality system files
+ Conducts various quality tests to ensure customer specifications are met
+ Accurately completes all required quality inspections, and quality systems documentations
+ Maintains work area in organized, safe and clean manner
+ Follow all Standard Operating Procedures, Safety Standards and Safe Work Practices
+ Assist and train production floor associates on quality topics to ensure customer specifications are met
+ Complete required calibration of quality test equipment and ensure proper use.
+ Tracks and coordinates non-conforming material
+ Maintains inventory of department quality supplies
+ Communicate pertinent information at shift change
**Qualifications**
**Qualifications:**
+ Must be able to effectively communicate (verbal/written) with various levels within the facility
+ Basic computer systems knowledge (Windows, Word, Excel). SAP, PowerPoint a plus
+ Experience with AIB or BRC quality systems a plus
+ Experience in a GFCI certification environment a plus
+ Other job duties as assigned by Team Leader
**Pactiv Evergreen** is now a part of Novolex. Novolex is a leading manufacturer of food, beverage, and specialty packaging that supports multiple industries, including foodservice, restaurant delivery and carryout, food processing, grocery and retail, and industrial sectors. Our innovative product portfolio is designed to meet the diverse needs of businesses worldwide and the millions of customers they serve. Through continuous investment in research and development, we are committed to engineering more sustainable choices for the future. Our extensive manufacturing network spans North America and Europe, including two world-class plastic film recycling centers. Discover more about Novolex, our 20,000+ family members and our commitment to innovation and sustainability at .
**Job Locations** _US-NC-Kinston_
**ID** _2025-27822_
**Category** _Operations_
**Position Type** _Full Time_
**Pay Type** _Hourly_

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Join Us and Make a Difference!**
At Thermo Fisher Scientific, your work will make a global impact. From protecting the environment to ensuring food safety and supporting life-saving cancer research, we address the world's toughest challenges.
**About The Role:**
We are looking for a dedicated Manufacturing Scientist to support the development and advancement of manufacturing processes for oral solid dosage (OSD) products in both traditional batch and continuous manufacturing environments. You will contribute to scaling up new processes, performing product validations and post-approval qualifications, and supporting routine manufacturing operations to ensure timely product release. You will collaborate closely with analytical, quality, and project management teams to drive successful process development and commercial execution.
**Key Responsibilities:**
+ Collaborate with cross-functional teams-including validation, operations, quality, analytical development, and process development-to support technical project activities.
+ Contribute scientific input to product and process development efforts within commercial manufacturing areas.
+ Assist in applying risk-based approaches to process scale-up and commercialization, supporting the development of mitigation strategies.
+ Draft and review batch records, protocols, and reports to support development, validation, and commercial production activities.
+ Support routine manufacturing operations by troubleshooting issues and ensuring timely product release, while building technical expertise as a product steward.
**Education**
Bachelor's degree in chemical engineering, chemistry, pharmacy, or a related field with 1+ years of experience, Master's degree or Ph.D. with no experience required.
**Experience**
+ Minimum of 1 year of experience in a pharmaceutical manufacturing or process development environment, including exposure to scale-up, technology transfer, or commercial support for immediate and controlled-release dosage forms; familiarity with continuous manufacturing is a plus.
+ Foundational understanding of GMP, regulatory expectations, and process validation principles.
+ Ability to contribute to cross-functional projects in a fast-paced, results-driven setting, with emerging skills in navigating compliance-related activities.
+ Solid understanding of Python or MATLAB for data analysis, along with basic proficiency in statistical tools relevant to process development.
+ Strong communication, problem-solving, and teamwork skills, with the potential to contribute to internal and client-facing technical discussions.
**Why Thermo Fisher Scientific?**
+ Career Development: Opportunities for learning, growth, and leadership.
+ Benefits: Competitive pay, healthcare, retirement plans, and more.
+ Inclusive Culture: We value different perspectives and cultivate an encouraging environment.
+ Purposeful Work: Join a team that's making a tangible difference in the world.
Do you thrive in dynamic environments and love solving sophisticated challenges? If so, we want to hear from you.
**Reasonable Accommodations**
We are committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the application process, please contact our HR team.
Thermo Fisher Scientific is an Equal Opportunity Employer. We value diversity and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Join Us and Make a Difference!**
At Thermo Fisher Scientific, your work will make a global impact. From protecting the environment to ensuring food safety and supporting life-saving cancer research, we address the world's toughest challenges.
**About The Role:**
We are seeking a dedicated Manufacturing Scientist to support the development of oral solid dosage (OSD) manufacturing processes in both batch and continuous manufacturing environments. Responsibilities include scaling up new processes, performing product validations and post-approval qualifications, and supporting routine operations to ensure timely product release. You may serve as the primary technical representative on client projects and will collaborate closely with analytical, quality, and project management teams to drive successful process development and commercialization. Experience with data science or statistical tools (e.g., Python, MATLAB) to support process optimization is desirable.
**Key Responsibilities:**
+ Collaborate with cross-functional teams to complete technical activities and provide scientific support for product and process development in commercial manufacturing.
+ Lead technical planning and serve as the primary scientific representative in client interactions, providing rationale for decisions and ensuring alignment across multiple projects.
+ Apply a risk-based approach to process scale-up and commercialization, developing and implementing mitigation strategies.
+ Prepare batch records, protocols, and reports to support development, validation, and routine commercial production.
+ Support routine manufacturing and act as technical steward for assigned products.
**Education**
Bachelor's degree in chemical engineering, chemistry, pharmacy, or a related field with 2+ years of experience, Master's degree or Ph.D. with no experience required.
**Experience**
+ Proven experience in a pharmaceutical manufacturing environment, with hands-on experience in product or process development, including scale-up and technology transfer for immediate and controlled-release dosage forms; knowledge of continuous manufacturing is preferred.
+ Strong understanding of GMP, regulatory compliance, and process validation requirements.
+ Demonstrated capability in coordinating complex projects and handling compliance-related obstacles in a fast-paced environment.
+ Proficient in Python or MATLAB for data analysis, with solid knowledge of statistical tools and their application to process development.
+ Excellent problem-solving, communication, and collaboration skills, with the ability to lead technical discussions across cross-functional teams and with external clients.
**Why Thermo Fisher Scientific?**
+ Career Development: Opportunities for learning, growth, and leadership.
+ Benefits: Competitive pay, healthcare, retirement plans, and more.
+ Inclusive Culture: We value different perspectives and cultivate an encouraging environment.
+ Purposeful Work: Join a team that's making a tangible difference in the world.
Do you thrive in dynamic environments and love solving sophisticated challenges? If so, we want to hear from you.
**Reasonable Accommodations**
We are committed to providing reasonable accommodations to individuals with disabilities. If you require assistance during the application process, please contact our HR team.
Thermo Fisher Scientific is an Equal Opportunity Employer. We value diversity and do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Sr Manufacturing Engineer
Requisition ID:
68930
Date:
Jul 8, 2025
Location:
Kinston, North Carolina, US
Department:
Engineering
Description:
At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
**Job Summary**
This role will work closely with production, maintenance, engineering, IT, and vendors to design, construct, install, validate, and maintain equipment, software, and data acquisition systems throughout their lifecycles.
**Essential Duties and Responsibilities**
+ Update programs to support current productions systems as well as work with teams to develop and create complete solutions to implement new systems.
+ Use engineering principles to design configurations and develop parameters for programmable/configurable devices to implement enhancements to the operation of equipment.
+ Create or modify pneumatic, hydraulic, mechanical, and/or electrical systems to support new or current manufacturing systems as well as create or update all supporting drawings and documentation.
+ Analyze data to identify opportunities to create new systems which support the advancement of manufacturing operations.
+ Manage projects by creating teams and utilizing techniques and processes throughout the entire project lifecycle: Initiating, Planning, Executing, Monitoring/Controlling, and Closing.
+ Write or approve all necessary documentation to design, purchase, install and maintain new equipment and systems. For example, user specifications, request for quotes, design requirements, functional requirements, functional procedures, acceptance and validation protocols.
+ Train team members on functional procedures and troubleshooting techniques to support and maintain equipment and systems.
+ Lead activities with maintenance, engineering, and vendors to create, install, and validate new equipment and systems.
+ Assist corporate and other facilities as needed to troubleshoot complex problems or support standardized equipment and systems.
+ Any other duties as required.
**Education**
+ Bachelor's Degree related field required
**Work Experience**
+ Minimum 5 years related work experience required and
+ previous experience in a manufacturing working environment and/or industrial setting required and
+ experience with Project Management processes and techniques preferred
**Preferred Knowledge, Skills and Abilities**
+ Proficient in AutoCAD and Microsoft Office based programs including Project and Visio.
+ Knowledge of terminal services for remote support of equipment and systems.
+ Have a functional understanding of cGMPs
+ Able to comply with the company's safety policy at all times
+ Able to comply with the company's quality policy at all times
**Travel Requirements**
10%: Up to 26 business days per year
**Physical Requirements**
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
**Additional Requirements**
+ Self-motivated and solution-oriented personality.
+ Excellent written and verbal skills.
+ Good communication, project management, and interpersonal skills.
+ Good organizational skills.
+ Effective problem-solving skills.
+ Must wear safety toe shoes, safety goggles, and hearing protection, as required, in production areas.
+ Must follow and comply with Plant's Dress and Hygiene Code (SOI).
+ Must follow and comply with all Company and Plant policies, procedure (SOIs), rules and State and Federal laws
#LI-TH1
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

**Manufacturing Production Operator**
**Position Summary**
Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.
The Manufacturing Production Operator is responsible for cleaning equipment as well as dispensing, sifting, and blending of good manufacturing practice (GMP) commercial batches in an oral solid dosage (OSD) environment. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
Shift: Monday - Thursday 4 pm - 2:30 am ?
This position is 100% on-site at the Greenville site.
**The Role**
+ With close oversight, operate equipment needed to dispense and sift scale-up, bio-batches, full commercial scale batches, and CTM batches.
+ Ensure all batch records and logbook entries are accurately documented and compliant with SOPs and FDA cGMP guidelines.
+ Assist with setup, manufacturing, and changeovers with adherence to SOPs and safety requirements.
+ All other duties as assigned.
**The Candidate**
+ High school diploma or equivalentwith at least 1 year of manufacturing or related experience or completion of Grads2Work Program or BioWorks certificate program required.
+ Required to obtain internal forklift operation certification.
+ Position requires the ability to lift 50 lbs unassisted, and push and pull in excess of 100 lbs.
+ Majority of work day is performed while standing and walking.
+ Requires the use of hands for simple grasping and fine manipulations.
+ Ability to occasionally bend, stoop, twist, and have full range of motion in upper and lower extremities.
+ Exposure to hazardous chemicals, other active chemical ingredients, dust, fumes, gases, skin and respiratory irritants, moving machinery parts, and damp, humid and wet environments.
+ Must be able to use a variety of tools, equipment, and machinery.
+ This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent.
**Why You Should Join Catalent**
+ Competitive medical benefits and 401K
+ 152 hours of PTO + 8 Paid Holidays
+ Dynamic, fast-paced work environment
+ Opportunity to work on Continuous Improvement Processes
**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 . 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 & 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- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

**Pharmaceutical Manufacturing Specialist**
**Position Summary**
Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Catalent's Greenville, N.C. facility specializes in end-to-end turn-key solutions for oral solid dosage forms, including integrated formulation development, analytical services, commercial manufacturing, and packaging. This state-of-the-art facility has had over $100M of investments in recent years and features fit-for-scale capacity with potent handling capabilities, ideal for orphan or targeted drug development.
The Pharmaceutical Manufacturing Specialist has a primary focus on new technology and business moving into Commercial Manufacturing Operations as well as serves as a liaison with other functional teams to lead/support commercial manufacturing operations and cross-functional execution. The Pharmaceutical Manufacturing Specialist provides on-the-floor oversight, direction, and support to manufacturing personnel to ensure timeliness and accuracy in the completion of assigned work. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.
**Shift:** Monday - Thursday 4 pm - 2:30 am ?
This position is 100% on-site at the Greenville site.
**The Role**
+ Frontline interface between the Commercial Manufacturing team, internal support teams as well as external clients to lead/support project work requiring cross-functional support. Assist in Commercial, Technical Transfer, Engineering and Development batches.
+ Maintain the inventory system for raw materials components; train and assist others in the use of the inventory system.
+ Assist in decisions on equipment selection, placement, and procedures to use equipment most effectively.
+ Ensure manufacturing area and equipment are maintained in accordance with company and regulatory requirements.
+ Recognize potential problems and provide input on corrective action(s), assist in completion of resolutions for issues in Commercial Manufacturing Operations.
+ Identify and recommend opportunities for improved efficiencies, client service and teamwork within Commercial Manufacturing Operations.
+ Troubleshoot equipment, process issues, and escalate problems that require quality assurance or Maintenance involvement; provide leadership and support for the timeliness and accuracy in the completion of Commercial Manufacturing operations.
+ Support and occasionally lead under supervision the scheduling and planning of client project work to ensure the highest levels of efficiency and quality standards are met.
+ Other duties as assigned.
**The Candidate**
+ High school diploma or equivalent with at least 5 years of experience in pharmaceutical Oral Solid Dosage (OSD) manufacturing required OR
+ Associate degree with at least 4 years of experience in pharmaceutical Oral Solid Dosage (OSD) manufacturing.
+ Demonstrated proficiency in Oral Solid Dosage (OSD) manufacturing operations related to Dispensing, Granulation, Compressing/Encapsulation and Coating. Must have previous experience with inventory management systems and be able to learn QAD (inventory Management System) to assist in the timely start and completion of batches and documentation.
+ This position requires that a respirator be worn for your safety, and as such, employment is contingent upon being able to complete a medical evaluation with satisfactory results. The medical evaluation is conducted via an external vendor assigned by Catalent.
+ Position requires the ability to lift 50 lbs. unassisted, and push and pull in excess of 100 lbs.
**Why You Should Join Catalent**
+ 152 hours of PTO + 8 paid holidays.
+ Medical, dental and vision benefits effective day one of employment.
+ Defined career path and annual performance review and feedback process.
**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 . 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 & 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- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

Adv Manufacturing Engineer
Location:
Kinston, NC, US, 28504
Company Description:
Crown Equipment Corporation is a leading innovator in world-class forklift and material handling equipment and technology. As one of the world's largest lift truck manufacturers, we are committed to providing the customer with the safest, most efficient and ergonomic lift truck possible to lower their total cost of ownership.
**Job Posting External**
**Company Description:**
Crown Equipment Corporation is a leading innovator in world-class forklift and material handling equipment and technology. As one of the world's largest lift truck manufacturers, we are committed to providing the customer with the safest, most efficient and ergonomic lift truck possible to lower their total cost of ownership.
**Responsibilities:**
+ Responsible for the advancement of manufacturing technology, product introduction, Plant or Corporate strategy, and project management of large manufacturing projects at a plant or corporate level.
+ Work closely with other manufacturing and non-manufacturing functions such as product engineering, quality engineering, purchasing, safety, environmental, industrial design, accounting, other plant functions, and manufacturing management to develop and implement solutions consistent with the goals of the Company.
**Minimum Qualifications:**
+ 8-15 years related experience
+ Bachelor Degree in Manufacturing, Mechanical, Industrial Engineering or related
+ Non-degree considered if 12+ years of related experience along with a high school diploma or GED
+ Frequent travel (6-20%).
+ Frequent overnight stays (6-20%)
**Preferred Qualifications:**
+ Manufacturing Engineering Degree.
+ CAD layout, simulation, process capability theory and statistical process control (SPC) and project management.
+ Excellent communication, interpersonal, and organizational skills.
If you possess these qualifications and wish to be considered for this position, please complete your candidate profile and submit an application.
If you have any questions regarding this Job Requisition, please contact Rose Mary Jones in the Human Resources Department at extension **15569.**
EOE Veterans/Disabilities
**Work Authorization:**
Crown will only employ those who are legally authorized to work in the United States. This is not a position for which sponsorship will be provided. Individuals with temporary visas or who need sponsorship for work authorization now or in the future, are not eligible for hire.
No agency calls please.
**Compensation and Benefits:**
Crown offers an excellent wage and benefits package for full-time employees including Health/Dental/Vision/Prescription Drug Plan, Flexible Benefits Plan, 401K Retirement Savings Plan, Life and Disability Benefits, Paid Parental Leave, Paid Holidays, Paid Vacation, Tuition Reimbursement, and much more.
EOE Veterans/Disabilities

**Overview**
The Warehouse Manager - Manufacturing is responsible for overseeing all aspects of warehouse operations, including forecasting, shipping, sourcing, scheduling, capacity planning, and personnel management. This role supports production and sales goals while ensuring effective coordination of logistics and distribution activities. The ideal candidate will lead the warehouse staff, drive operational efficiency, and enhance product flow and customer satisfaction.
**Responsibilities**
**Key Responsibilities:**
· Manage product forecasting, shipping, sourcing, and scheduling to support sales, marketing, and operational goals.
· Lead capacity planning for production lines, ensuring production loading, targets, and goals are met.
· Supervise, coach, and develop warehouse employees to ensure high performance, safety, and adherence to company policies.
· Coordinate and implement new product development logistics and system requirements.
· Establish and enforce warehouse policies and goals aligned with customer and business needs.
· Provide leadership in customer service and transportation logistics.
· Develop warehouse plans to improve inventory flow, product distribution, and storage efficiency.
· Collaborate on policy and procedural development to support quality and cost efficiency.
· Analyze inventory trends, perform network distribution studies, and optimize delivery and order fulfillment strategies.
· Maintain accurate records, generate reports, and ensure compliance with internal standards.
· Coordinate logistics activities with both internal teams and external customers.
**Qualifications**
**Qualifications:**
· Bachelor's degree in Logistics, Supply Chain Management, or a related field.
· Minimum 6 years of relevant business experience, preferably in supply chain or warehouse operations.
· Proven experience in managing and developing warehouse teams.
· Strong written and verbal communication skills.
· Excellent organizational skills with attention to detail and the ability to multi-task and prioritize effectively.
· High analytical ability and strategic mindset for logistics and inventory optimization.
**Pactiv Evergreen** is now a part of Novolex. Novolex is a leading manufacturer of food, beverage, and specialty packaging that supports multiple industries, including foodservice, restaurant delivery and carryout, food processing, grocery and retail, and industrial sectors. Our innovative product portfolio is designed to meet the diverse needs of businesses worldwide and the millions of customers they serve. Through continuous investment in research and development, we are committed to engineering more sustainable choices for the future. Our extensive manufacturing network spans North America and Europe, including two world-class plastic film recycling centers. Discover more about Novolex, our 20,000+ family members and our commitment to innovation and sustainability at .
Located 96 miles southeast of Raleigh Durham airport, Kinston is a city in Lenoir County, North Carolina, with a population of 21,677 as of the 2010 census. It has been the county seat of Lenoir County since its formation in 1791. Kinston is located in the coastal plains region of eastern North Carolina. In 2009, Kinston won the All-America City Award.
The plant was built in 1993 with an addition in 1995, manufactures paper cups and cartons, and has approximately 350 employees.
**Pactiv Evergreen** is committed to a diverse and inclusive workforce. Pactiv Evergreen is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, sex (including pregnancy), sexual orientation, religion, creed, age national origin, physical or mental disability, genetic information, gender identity and/or expression, marital status, veteran status or other characteristics or statuses protected by law. For individuals with disabilities who would like to request an accommodation, please call ( or email
All information will be kept confidential according to EEO guidelines and applicable laws.
Our Social Responsibility platform features a robust, employee-led Give Back program, which includes a matching gifts plan, community grants initiative, and our annual Company-wide Month of Action campaign. With each of these initiatives, our employees are empowered and equipped to give back to their communities and support the non-profits important to them and their families. Through our Give Back program, we own our commitment to Social Responsibility and live our purpose of Packaging a Better Future.
#LI-TM1
**Job Locations** _US-NC-Kinston_
**ID** _2025-27442_
**Category** _Operations_
**Position Type** _Full Time_
**Pay Type** _Salaried_