7 Manufacturing jobs in Sugar Land

Our Supervisor, Manufacturing Operations (Warehouse) plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, you are responsible for supervising warehouse technicians in the warehouse. Warehouse personnel are responsible for receiving and picking materials used in compounding. The Supervisor will ensure personnel are using current Good Manufacturing Practices. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.This is a full-time role for our Mid shift, working Monday through Friday from 8:00 AM - 5:00 PM. This is a set, consistent schedule based on site in our Sugar Land, TX location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.What the Supervisor, Manufacturing Operations (Warehouse) Does Each Day:Supervises warehouse personnel on multiple shift operationOversees discrepancy and non-conformance investigations and documenting investigations on process/product deviations or non-conforming materialsMaintains records of movement of materials at the point of receipt in the warehouse to the point of useReviews documentation to ensure recording of processes, logs, batch records, and accounting of materials complies with policies, procedures, and Good Documentation Practices (GDP)Monitors the daily use of products throughout the process to ensure people and processes are in a continuous state of compliance with DEA regulations, company policies and procedures and safety requirementsUses ERP System, Infor, to input data, reference orders for pickingResponsible for training adherence for warehouse personnelDevelops and provides oversight to identification and implementation of appropriate corrective actions and preventive actionsDocuments in a timely manner all tasks requiring written records as specified in Standard Operating ProceduresManages material handling and movement with a sense of urgency as neededEnsures picking of batches meets production schedule and customer demandOur Most Successful Supervisor, Manufacturing Operations:Meets productivity standards; Completes work in timely manner; Strives to increase productivityFollows policies and procedures; completes administrative tasks correctly and on timePrioritizes and plans work activities; Sets goals and objectivesApproaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitmentsMinimum Requirements for this Role:High school Diploma or GED from recognized institution or organization required1 year of supervisory or management experience requiredSuccessful completion of certified in-house qualification programsAble and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodationMust be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visasAny of the Following Will Give You an Edge: Bachelor's Degree in Life Science or other related fieldExperience working with controlled substancesWorking knowledge of DEA regulatory requirements as well as all applicable SOPsWorking knowledge of safety standards, and their application, to continuously improve the safety culture and metricsBenefits of Working at Quva:Set, full-time, consistent work scheduleComprehensive health and wellness benefits including medical, dental and vision401k retirement program with company match22 paid days off plus 8 paid holidays per yearNational, industry-leading high growth company with future career advancement opportunitiesAbout Quva:Quva provides industry-leading health-system pharmacy services and solutions, including 503B sterile injectable outsourcing services and AI-based data software solutions that help power the business of pharmacy. Quva Pharma's multiple production facilities and industry-first dedicated remote distribution capabilities provide ready-to-administer sterile injectable medicines critical to patient care. Quva BrightStream partners with health systems to aggregate, normalize, and analyze large amounts of complex data across their sites of care, and through proprietary machine learning, transforms data into actionable insights supporting revenue optimization, script capture, inventory management, drug shortage control, and more. Quva's overall progressive and integrated platform helps health-systems transform pharmacy management to achieve greater value and deliver highest-quality patient care.Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

The Manufacturing and Field Engineering Manager will manage the build and commission of the ACOMP product. Previous experience working on field installations, startups, and commissioning of instrumentation, analyzers, or other complex equipment in industrial environments. They will work closely with the CTO and VP of Technology to manage the company's build and commissioning to meet accelerating demand for the company's products. This individual is highly motivated, organized, proactive, and has demonstrated the skills to successfully manage a team. Experience working in high-pressure situations and the ability to quickly solve unexpected issues are very important. Background in instrumentation, mechanical engineering, chemical engineering, chemistry, automation, and/or control systems engineering.

Key Responsibilities

Maintain constant communication with management, staff, and vendors to ensure proper operations of the organization

Manage field engineering and manufacturing team to manufacture and deploy quality products at customer sites

Works closely with the product engineering team to plan the execution of builds, installations, and startups with customers

Actively pursue strategic and operational objectives

Manage the manufacture: supply chain, final assembly, and interface with QA Manager for quality testing, including internal QC/QA, factory acceptance tests (FAT) and site acceptance tests (SAT) as and when appropriate

Manage manufacturing processes, assess personnel and define required personnel and contract needs for execution

Manage field engineering team's execution of builds, installations, and startups with customers. Ensures field engineers work with the product engineering team to provide feedback on system performance in the field, encounter issues, participate in design reviews, support R&D and testing.

Interface with customers on a regular schedule to ensure systems are operating in the field, this includes customer value calls with support by business development, regular communications for service events and any customer issues

Manage field engineering team, including the execution of requirements for all service agreements (e.g. scheduled PM visits, emergency service calls, spare parts, etc.), manage contract renewals, and develop an overall system for managing all of these activities

As needed support of Business Development in late-stage customer engagements - support with FEED process for handoff to project engineering

Requirements

• 5+ years' work experience in an operations position, including management roles. Ideally in petrochemical or related industrial applications working in-field installation, startup, and commissioning of process instrumentation, analyzers or other equipment
• B.S. in mechanical engineering, electrical, chemical engineering, chemistry or very closely related technical discipline
• Management experience of production or field engineering team members
• Contract manufacturing/supply chain management experience
• Cost and schedule management
• Project planning and management experience
• Must be capable of executing on work product without significant delegation support
• High mechanical, hands-on aptitude for fluidic, instrumentation, and/or analyzer equipment with demonstrated success working with these
• Previous roles working in or serving process industries or similar industrial manufacturing environments
• Excellent written and verbal communication skills. Very good at interacting with a team and with external stakeholders and customers
• Demonstrated experience in the management of a team in a small and growing company

• Experience with equipment for polymer processes or on-site experience
• Knowledge or experience with polymer-related processes and equipment

• Salary commensurate with experience
• Health, dental, and vision benefits with 100% of premiums covered by us
• 401K w/ up to 6% match
• Paid Time Off (Vacation and Holidays)
• $75/mo Gym Stipend
• Learning and Development Stipend

• Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.
  

• Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.
  

Job Scope

The Supply Chain Planner and Buyer is responsible for all supply and demand planning tasks necessary to ensure an uninterrupted flow of Instrument, Reagent, and Bioassay products to customers. This role creates and implements production plans that are both material and resource feasible and serves as the primary point of contact regarding product availability. The Supply Chain Planner and Buyer manages the business relationship between Luminex and it's suppliers to purchase goods and services for the company at the lowest total cost. This role is also responsible for leading and supporting key supply chain projects and process improvement initiatives.

Key Duties and Responsibilities

• Utilizes demand forecasts and sales trends to create and maintain demand plans, capacity plans, and master production schedules.
• Interfaces with manufacturing, materials, logistics, technical support, purchasing and R&D to ensure availability of necessary raw materials.
• Ensures that raw material shortages are identified and resolved in a timely manner.
• Drives the resolution process of MRP exceptions and resolves MRP discrepancies.
• Provides Order Management and Sales with shipment commitments.
• Reviews open order reports and other indicators to ensure a timely delivery of finished goods to support customer demand.
• Identifies, negotiates, and resolves conflicts with respect to material and capacity availability and order promising.
• Notifies Order Management, Manufacturing, and other internal stakeholders whenever an existing shipment commitment is in jeopardy and recommends alternatives on how the requested demand could be satisfied.
• Assists Order Management, Sales, and Marketing in setting priorities when demand exceeds supply.
• Maintains inventory levels within established goals and guidelines and recommends adjustments in stocking levels.
• Monitors and implements actions to minimize raw material and finished goods scrap.
• Helps to maintain Bill of Material (BOM) structures as required.
• Participates as a reviewer/approver in the Engineering Change Order (ECO) process.
• Reviews cycle count and/or physical inventory records and resolves any discrepancies.
• Maintains scheduling parameters such as lead times, lot sizes, scales, safety stocks, and other item attributes for all planned items.
• Ensures that all processes are conducted according to approved procedures.
• Ensures completion of manual product system planning and associated documentation for production as required.
• Manages the tactical business relationship between the supplier and Luminex, and ensures the communications are clear and appropriate.
• Identifies, evaluates, and manages supply risk exposure and devises risk mitigation measures.
• Investigates and drives corrective actions to receiving and accounting problems related to purchase orders.
• Scope of work and actions are collaboratively managed with Supervisor.
• Ensures that all processes are conducted according to approved procedures.
• Works closely with manufacturing, quality, and engineering to resolve issues for current sourced solutions.

• Excellent written and oral communication skills.
• Ability to handle the pressure of meeting tight deadlines.
• Ability to work independently with minimal supervision.
• Highly organized with proven time management and prioritization skills.
• Ability to work in a fast-paced environment.

Education, Experience, and Qualifications

• Bachelor's Business, Supply Chain, Engineering, Science, or equivalent
• 1+ Years Experience in Supply Planning, Demand Planning, or Master Scheduling
• 1+ Years Experience in a Medical Device, Pharma, or other Healthcare field
• 1+ Years Experience using an ERP system in a manufacturing environment.
• 1+ Years Experience in using Microsoft Office, Excel, Word, and PowerPoint
• 1+ Years Experience with Oracle E-Business Suite (EBS)
• 1+ Years Experience in a GMP and/or FDA regulated environment.
• Certified in Production and Inventory Management (CPIM)-APICS
• CSSBB - Six Sigma Black Belt

What we offer

Receive a competitive salary of $85,000 - $92,000 annually and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world.

We currently are not sponsoring candidates for this role.