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" 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.
Quals
Qualifications
Education Minimum Requirement:
" Bachelor s degree in Science, Chemistry, Biochemistry, Biology, or related science field.
Required Experience and Skills:
" 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.
A successful candidate will exhibit: -
" 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.
NOTE:
This is a 100% onsite role. Candidate should be flexible to come in earlier if needed.
Positions available: 2
Date Posted: 16 May 2024
Job Expired - Click here to search for similar jobs