GMP Material Specialist III
GMP Material Specialist III
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Our purpose is to bring hope to life by enabling lifechanging 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 multitasking skills strong verbal and written communication skills and experience working in a fastpaced dynamic environment with limited supervision. Provides exceptional customer service to our customers internal and external.
ESSENTIAL JOB DUTIES/RESPONSIBILITIES
Assist supervisor with training personnel and creation of job aids for warehouse and materials management functions ERP functions.
Perform timely and accurate transactions in ERP and related inventory/data management systems. Ability to perform all functions as primary receiver or shipper.
Support monitoring ordering and handling of supplies and materials used in facilities and manufacturing operations.
Dispenses materials to support manufacturing. Includes handling hazardous materials detailed measurement/portioning performing aseptic technique in a clean room setting.
Help organize and clean warehouse ensures material identification status location movement and quantities are accurate timely and correct.
Identify opportunities for process improvement related to warehouse operations processes and procedures to produce reduction of labor or improvement in quality or accuracy.
Conduct cycle counts inventory/discrepancy research and coordinates year end physical count.
Understand and adhere to SOPs and cGMP compliance regarding materials control in multiple storage locations and conditions. Understands rules and regulations on hazmat shipping domestically and internationally as well as procedures and shipping requirements for safe transit of high value materials via parcel or freight.
Focus on receiving packing and shipping of biologics and hazardous goods.
Participate in the creation and maintenance of job aids training materials and qualification processes deviation/CAPA/CRs. Ability to initiate Deviation/CAPA and Change Request as needed.
Ensures warehouse safety standards are upheld and notifies management staff of any issues observations or concerns regarding violations or potential enhancements to department safety. Ability to generate Job Safety Analysis suggestions.
SKILLS
Ability to communicate clearly and interact constructively with peers and other departments.
QUALIFICATIONS
Required:
A minimum of 58 years of experience in materials management or inventory control positions in cGMP environment and at least 8 years experience handling and transacting lotcontrolled inventory (preferably in a GMP environment).
Extended use and experience with ERP MRP and inventory management systems
Ability to handle key inventory item processing; API Cell Banks Vial Pulls.
Ability to regularly generate process and initiate improvement suggestions to support key initiatives proposed by management.
Ability to complete HAZMAT training a requirement for 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.
Good attention to detail with strong organizational skills.
Preferred:
DOT H endorsement a plus.
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.
SCHEDULE & LOCTAION
Monday Friday
This role reports out of our warehouse in Everett Washington
COMPENSATION
$25.65 $35.27
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 sidebyside with our clients and partners every step of the way. We provide worldclass development and manufacture of mammalian and microbialbased 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 cGMPcompliant 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 fasttrack 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
