Warehouse Delivery Driver, GMP/Pharmaceuticals

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe, creating a healthier and happier tomorrow.

Our mission is to work side by side with our customers in order to improve patients' lives by bringing new biopharmaceuticals to market.

JOB SUMMARY

The GMP Material Specialist II works collaboratively with others, performing various Good Manufacturing Practices (GMP) Warehouse processes.

The role requires strong multi-tasking skills, strong verbal and written communication skills, and experience working in a fast-paced, dynamic environment with limited supervision.

GMP Material Specialist provides exceptional customer service for our customers, internal and external.

While all GMP Material Specialists will be trained and asked to perform functions supporting GMP Warehouse processes, this position will primarily be driving the AGC Biologics truck between our campuses in Everett and Bothell.

ESSENTIAL JOB DUTIES / RESPONSIBILITIES

• Performs timely and accurate transactions in ERP and related inventory / data management systems.
• Supports monitoring, ordering, and handling of supplies and materials used in facilities and day to day operations.
• Dispenses materials to support manufacturing. Includes handling hazardous materials, detailed measurement / portioning, performing aseptic technique in a clean room setting
• Helps organize warehouse, ensure material identification, locations, movement, and quantities are timely, accurate, and correct.
• Understands and adheres to SOPs and cGMP compliance accurately reflecting material status, labeling, movement, UOM, and picking of raw materials and the handling, storage, and shipment of finished goods - under multiple storage conditions.
• Communicates at all levels to ensure proper materials management and inventory control objectives and strategies are achieved and supported as requested.
• Ensures warehouse safety standards are upheld, and notifies management staff of any issues, observations, or concerns regarding violations, or potential enhancements to department safety
• Maintains department standards

QUALIFICATIONS

Required :

• Commercial Drivers License, Class A preferred or obtained soon after hire date
• HAZMAT endorsement desired, must be obtained within 30 days
• 2+ years of driving experience with a clean driving record no DUIs + no more than 1 point on driving record + zero at-fault accidents in the past 5 years
• 2-3 years of experience in materials management or inventory control positions in cGMP environment.
• 2-3 years of experience handling and transacting lot-controlled inventory (preferably in a GMP environment).
• Forklift certification or obtained within 30 days after start date.
• Ability to work hours necessary to support production and / or maintenance activities.
• Ability to communicate verbally in addition to basic writing skills.
• Extended use and experience with ERP, MRP and inventory management systems
• Ability to complete HAZMAT training, a requirement of performing portions of the work
• Ability to operate hand truck, lift trucks and other equipment.
• IATA and / or hazardous good handling certifications completed or ability to immediately begin training and qualification and shipping training
• Basic Computer literacy and ability to perform accurate transactions.
• Basic mathematical skills.
• DOT Medical Card

Preferred :

APICS, NAPM, or CLM certification or equivalent training is highly desirable

Compensation

$21.19 - $29.14 / hour

Our culture at AGC Biologics is defined by the six core values : Knowledge, Trust, Quality, Ingenuity, Accountability and Teamwork.

Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents.

Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners, every step of the way.

We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells.

Our global network spans the U.S., Europe, and Asia, with cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado;

Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide.

Our commitment to continuous innovation fosters the technical creativity to solve our clients' most complex challenges, including specialization in fast-track projects and rare diseases.

AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. W ant to keep posted about our growth and learn more about our company?

Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly, collaborative culture that values personal initiative and professional achievement.

AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances.