GMP Material Specialist I
GMP Material Specialist I
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Job Description
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 III will work collaboratively with others performing various Good Manufacturing Practices (GMP) Warehouse processes. The ideal candidate possesses strong multi-tasking skills strong verbal and written communication skills and experience working in a fast-paced dynamic environment with limited supervision. Provides exceptional customer service to our customers internal and external.
This role will be based out of our Everett B18 facility and will initially follow a night shift schedule Monday through Friday from 9:00 PM to 5:30 AM (5x8). Please note that this schedule is subject to change as we plan to transition to a 4x10 rotation in the near future
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.
SKILLS
Ability to communicate clearly and interact constructively with peers.
QUALIFICATIONS
Required:
0-1 years of experience in materials management or inventory control positions in a cGMP environment.
0-1 years of experience handling and transacting lot-controlled inventory (preferably in a GMP environment).
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 truck 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.
Preferred:
APICS NAPM or CLM certification or equivalent training is highly desirable
Physical Requirements (US Only):
Ability to lift up to 40 pounds with or without assistance of tandem lift or other materials handling equipment.
Compensation
$17.50-$24.06/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 2500 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.Want 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.
Required Experience:
Director
Employment Type
Full-Time
