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ll integrate innovation with strategy, leaving your mark across a tapestry of brands.. Ensure that project scopes fulfil relevant regulatory requirements including compliance with RB/MJN quality requirements, Food and Drug Administration (FDA) regulations, state and federal environmental health and safety (EHS) requirements, and Reckitt engineering guidelines.. Capable of managing multiple capital projects simultaneously with a variety of technical scopes e.g. (powder blending and transport, HVAC, liquid processing, packaging, robotics).. Reckitt offers eligible employees competitive benefits including medical, prescription, dental, vision, life and disability insurance; paid time off for vacation, sick, and Company recognized holidays; a 401(K) plan; generous paid parental leave; adoption and fertility support; tuition reimbursement; product discounts; and much more!. Job Segment: Environmental Health & Safety, Nutrition, Counseling, Healthcare
Managing New Product Introductions and addressing impacts on order management, software licensing and the installed base. Implementing the S&OP process in SAP IBP. We are specifically looking for a candidate with experience in supply chain operations and outsourced high-tech manufacturing.. - SAP IBP – Good to have. In addition, this role is eligible for the following benefits subject to company policies: medical, dental, vision, pharmacy, life, accidental death & dismemberment, and disability insurance; employee assistance program; 401(k) retirement plan; 10 days of paid time off per year (some positions are eligible for need-based leave with no designated number of leave days per year); and 10 paid holidays per year.
You’ll play a key role in scheduling, process improvement, cross-functional coordination, and employee development, all while championing Lean Manufacturing and a safety-first culture.. Conduct quality audits and oversee maintenance of QA/QC documentation. 5+ years of supervisory experience in manufacturing, fabrication, or modular assembly. Proficiency in Lean Manufacturing and/or Six Sigma practices. Knowledge of OSHA safety requirements and ISO-based quality systems
Lead Continuous Improvement – Utilize Lean principles, SPC, and DOE methodologies to analyze data, drive corrective actions, and optimize manufacturing processes.. Drive Supplier Quality Management – Work with vendors to establish and maintain quality expectations, ensuring reliable and consistent product performance.. Develop Quality Training Programs – Train internal teams on quality control processes, SPC, and corrective action strategies , fostering a culture of continuous improvement.. Experience – 3-5+ years of experience in quality control, process auditing, lean manufacturing, or engineering within a manufacturing environment.. Certifications (Preferred) – Six Sigma Green or Black Belt certification.
The Director, Western SCM Unit will lead a cross-functional team driving excellence in Import/Export Compliance, Logistics, and Supply Chain support while interfacing closely with other EDCS Units, PQ, and PST leaders to ensure stable supply for the Americas Region.. As the manufacturing network and global supply chain become more complex with the launch of biologic products and hhceco initiatives, the Director will oversee Global Logistics and Import/Export compliance for commercial, clinical, and research materials.. This includes the Eisai Customs and Border Protection (CBP) Compliance program and managing all freight identified by EISAI’s Importer of Record (IOR) number.. The Director will develop colleagues with expertise in relationship/project management, contract review and negotiation, demand planning, and logistics to manage effectively in a global networked business environment.. Negotiate critical Supply Agreements and Amendments to maintain alignment with PQA. Represent Supply in negotiations of supply agreements with key partners such as Biogen in association with the Alzheimer’s Collaboration Agreement.
Perform duties in computerized order entry, distribution of all supplies, linen, equipment, shipping and receiving of hospital merchandise.. No experience required yet preferred 1 year of work experience, including experience in one of the following areas: distribution, warehousing, shipping, receiving, logistics, material handling, customer service, inventory control, or other comparable service line.. Use appropriate Supply Chain technologies (Pyxis and SAP) to document movement of supplies. Perform cycle count on a regular basis to ensure accuracy of stock levels in all areas. Transport shipments from loading dock to stockroom and deliver packages to appropriate purchasers.
The MSI Express Leadership Rotational Program is a two-year developmental program designed to provide hands-on experience in 3-4 different departments within MSI Express.. This program is designed to provide a well-rounded understanding of food manufacturing, supply chain logistics, financial planning, customer engagement, and human capital management.. Supply Chain – Understand logistics, inventory management, scheduling, and demand planning to optimize product flow and minimize disruptions.. Quality Assurance – Learn about compliance with food safety standards and regulatory guidelines, gaining expertise in FDA, NSF, and SQF requirements and standards.. ✅ No prior work experience required, but internship or co-op experience is a plus
Accentuate Staffing is assisting a growing printing company in the Fuquay area who is hiring a Supply Chain Associate to perform all supply chain functions for their production facility.. This is a direct hire opportunity offering excellent benefits working in the office 8am-5pm Monday-Friday.. Associate will streamline transportation and inventory management, analyzing shipping and delivery data. Associate will resolve Purchase Order discrepancy with customers, expedite orders. Candidates must be computer savvy with ERP systems, Oracle, SAP, AS400, or similar supply chain software
A world leader in the field of in vitro diagnostics for more than 60 years, bioMerieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety.. High School Diploma/GED with 4+ years of experience in electro-mechanical maintenance, troubleshooting and repairing of electro-mechanical systems.. Associate's Degree and 2+ years of experience in electro-mechanical maintenance, troubleshooting and repairing of electro-mechanical systems.. Strong attention to detail and GMP experience (including knowledge of change control, validation, and commissioning processes) desired.. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at , by email at , or by dialing 711 for access to Telecommunications Relay Services (TRS).
POSITION SUMMARY: The Senior Manager, Contract Manufacturing is responsible for the oversight of external manufacturing/packaging activities and day-to-day business management of assigned Contract Manufacturing Organization (CMO) relationships with accountability for ensuring supply of product to patients on-time and for driving continuous improvement in risk, performance, quality and total cost.. Lead coordination of resources across R&D, Quality, Regulatory, Finance, Supply Planning, Logistics and Technical Operations for the successful implementation and ongoing management of pharmaceutical finished product manufactured and packaged with CMOs. Implement, monitor, and deliver against key performance metrics in support of improving team, CMO and company performance.. Develop appropriate CMO relationships, including strategic alliances between key CMOs and internal stakeholders.. Conduct joint operations and business review meetings with each CMO at defined frequencies to monitor and improve performance.. Minimum of ten (10) years of combined experience within the pharmaceutical industry in the areas of manufacturing, direct material sourcing, quality, logistics, alliance or external manufacturing management or similar technical functions.
We trace our roots all the way back to the Irish Glass Bottle Company, founded in 1932.. Today we have a presence across Europe, Africa, and North America.. Did you know we produce metal and glass packaging which are permanent materials, meaning they can be infinitely recycled without any loss of quality?. We push the boundaries of what’s possible, pioneering new production methods, new design techniques and new ways to recycle and save energy.. Our aim is to reduce any negative environmental impact while remaining economically sustainable and socially responsible.
We focus on product innovation and development, supply chain, procurement and sourcing, manufacturing operations, service operations and capital asset programmes to drive both growth and profitability.. You’ll work with our clients to develop a supply chain strategy, optimise their supply chain footprint and logistics, manage transportation and distribution, and develop an integrated business planning solutions.. Demonstrates extensive abilities and/or a proven record of success in the following areas: - Leveraging extensive knowledge across end-to-end supply chain transformation, network strategy, supply chain analytics, process improvement and automation, supply chain technologies (strategy, master date mgmt., tech platform integration, etc.). Travel Requirements Up to 80% Job Posting End Date Learn more about how we work: PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy:.. For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws.
Labcorp is seeking to add a Supply Chain Associate – Onsite Inventory Control for our Greenfield, Indiana location.. The Supply Chain Associate will perform a variety of activities relating to inventory control, Greenfield site logistics, material or specimen shipping (domestic & international) and centralized receiving as assigned by Supervisor to meet company standards of quality, customer service, safety and productivity.. What to Expect Shift: Monday through Friday Hours: 7:00 am to 3:30 pm Location: Greenfield, IN Maintains responsibility for warehouse pick rates, pick errors and accuracy Maintains all product returns, cancelled orders and ensures items are returned to stock in a timely manner Ensures complete physical cycle count of assigned areas quarterly Accountable for accurate inventory data, proper transactional timing (i.e., receipts and usage data is processed each day.). May involve some overtime and weekend hours as needed Associate will be exposed to hazardous materials such as dry ice and controlled radiation testing materials Education and Qualification(s), required High school graduate or equivalent required Valid driver’s license 1-3 years’ directly applicable experience Associate should have excellent written and verbal communication skills, attention to detail, and organizational skills.. Preferred Experience in: Shipping, receiving, inventory management or delivery Experience with electric pallet jacks and forklifts Work experience using Bar Code/ Inventory Control Tracking equipment.
Maintenance Supervisor - Automation & Technical Systems Burlington, NC | $80,000 - $95,000 + Annual Bonus and relocationLead a team of 16 maintenance technicians across multiple shifts in this newly created role at a growing manufacturer.. Drive equipment reliability and minimize downtime in a 24/7 production environment.. Join a growing organization where you can shape a new role and drive technical excellence.. Equal Opportunity Employer M/F/D/V
With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year.. Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/ systems needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, water for injection, etc.. Ability to analyze problems, develop and propose engineering solutions in a scientific manner using data-driven techniques and analyses (e.g., Data Analytics, Root Cause Analysis (RCA), Statistical Process Control (SPC), Six Sigma, Predictive Maintenance, etc.. and familiarity with GMP quality systems/processes such as change control, non-conformances, corrective and preventative actions, and qualifications/validation. Understanding of capital projects in a GMP Biopharmaceutical Production facility including procurement, construction, startup, and validation
Our newer Active Pharmaceutical Ingredients (API) facility in Clayton, NC sits on 825,000 square-feet of state-of-the-art equipment, and houses the Fermentation, Recovery and Purification in the production of ingredients for Novo Nordisk's innovative oral products.. Gain extensive knowledge of the full external production life cycle such as aseptic manufacturing (vials, PFS, cartridges), inspection and/or assembly & packaging operations including critical equipment & processes. May consider an Associate's Degree in Pharmacy, Engineering, Automation, or relevant field of study from an accredited university with a minimum of ten (10) years of experience in pharmaceutical manufacturing, including assembly, packing, and/or device assembly required, preferably in a pharmaceutical environment. Minimum of eight (8) years of experience in pharmaceutical manufacturing, including aseptic production, assembly, packing, and/or device assembly required, preferably in a pharmaceutical environment. Thorough validation knowledge and experience required (product/tech transfer preferred)
The Supply Chain 3PL Manager is responsible for oversight of operations at Civica's third-party logistics (3PL) partner in Durham, NC and any 3PL partners added to the network in the future. Oversee on-site daily operations of Civica product and materials at partner 3PL facilities and coordinate product shipments to and from the Petersburg site to meet the production and distribution schedules. Perform cycle counts according to procedures to ensure accuracy within Civica and the 3PL's warehouse management systems. Bachelor's degree in related area and 5+ years in Supply Chain and/or Warehouse Management, with increasing responsibility in a cGMP environment. Project Management, Operational Excellence, and/or Lean/Six Sigma experience preferred.
Strong attention to detail which translates in SOP authoring, developing training tools, and improving user interface in MES or HMIs. Participates and/or lead cross functional teams in the development and implementation of strategies associated with the area for the following initiatives: Continuous Improvement, Root Cause Analysis (RCA), Failure Modes Effect Analysis (FMEA), Operational Standards for Supply Chain Excellence (OSSCE).. Work with EWM, IDS and Master Data Team to support launch and ticket builds and process order releases.. Experienced as a technician/operator in a pharmaceutical manufacturing environment.. 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), enAble (for people with disabilities).
Your expertise in procuring parts, managing inventory, and asset linkages, coupled with CMMS planning and inventory management, will underpin the efficiency and effectiveness of our Maintenance, Manufacturing, Metrology, and Engineering teams.. Provide CMMS planning and perform PM revisions to maintain a high standard of preventive maintenance practices.. Manage CMMS inventory system operations, including purchasing, receiving, and issuing inventory based on work order and PM demand.. You possess a strong working knowledge and competency in Computerized Maintenance Management Systems (CMMS), making you a valuable asset to any team.. Strong working knowledge and competency in Computerized Maintenance Management Systems (CMMS).
Johnson & Johnson is currently seeking a Senior Maintenance Supervisor to join our MAKE Asset Management Organization located in US Large Molecule Drug Substance Site located in Wilson, North Carolina.. The new facility will expand production of innovative biologic medicines in areas including oncology, immunology, and neuroscience.. Supervises a team of multi-craft maintenance technicians and is accountable for conducting effective performance management.. Experience in green or brown field GMP MFG facility start-up including process systems, automation, utilities, facilities, and operations.. Employees may be eligible to participate in the Company's consolidated retirement plan (pension) and savings plan (401(k