- Bachelor's degree in science, Chemistry, Biochemistry, Biology, or related science field.
- Minimum of one (1) year of experience in Laboratory GMP regulated environment.
- Two (2) plus years in a pharmaceutical manufacturing and cGMP environment
- GLIMS experience
- Technical communication (written & presentation) skills.
- Understanding of the fundamental business drivers for the company and apply this knowledge in their own work.
- Ability to interpret Company Quality Policies and Guidelines for daily application.
- Understanding and active application of regulatory/compliance requirements, including GMP and related regulations, and ability to interpret those regulations for implementation in the workplace.
- A knowledge of theories, processes, and procedures in the Quality Laboratory.
- Strong technical writing capabilities.
- Perform stability sample pulls using GLIMS and delivery to the laboratory, adhering to GMP processes and procedures.
- Perform receipt of stability samples from production units.
- Perform shipment of stability samples to external testing laboratories.
- Perform build and setup of stability studies in GLIMS.
- Able to clearly represent individual status/accomplishments.
- Actively promotes an inclusive culture.
- Properly documents, investigates, and identifies proactive measures to ensure right first-time achievements.
- Understand and apply Data Integrity concepts.
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Material Coordinator - Wilson, United States - IMS People
Description
Job Description
Job DescriptionLaboratory Sample / Material Coordinator - II
Duration: 6 Month Contract
Location: This is a 100% onsite role. Candidate should be flexible to come in earlier if needed Merck Road, Wilson, NC 27893
Hours: M-F 8:00am - 4:30pm
Qualifications:
Education Minimum Requirement:
Required Experience and Skills:
A successful candidate will exhibit:
Responsibilities: