Quality Control Analyst, Biochemistry & GMP Lab
Overview
You will own document authoring and revision for GMP raw materials testing in a biochemistry lab at LanceSoft. You will execute experiments and procedures with limited supervision, ensuring compliance with regulatory standards. This role sits on the QC Raw Materials team, supporting daily operations for manufacturing release. You will drive instrument and method projects from initiation to documentation, collaborating with biochem staff and lab managers. The work directly impacts product quality and regulatory readiness, offering hands-on experience with Matlab and chemometric software.
What You'll Do6
- 1Execute experiments and procedures as detailed by the lab manager and staff, completing 75% of assigned tasks in GMP environments.
- 2Write and revise protocols, test methods, and SOPs to maintain compliance with quality control practices.
- 3Drive instrument and method projects from planning to execution, attending project meetings and coordinating with team members.
- 4Revise existing documents to support daily operations of the QC Raw Materials department.
- 5Perform laboratory activities including sample testing and data collection for raw material release.
- 6Collaborate with the biochem team to ensure timely completion of 079 activities and uphold quality standards.
Requirements6
- 1Bachelor's degree in chemistry, biology, or biochemistry.
- 2Laboratory experience preferred, with hands-on work in GMP or regulated environments.
- 3Experience with Matlab or other chemometric software.
- 4Ability to author and revise technical documents including protocols and SOPs.
- 5Strong attention to detail with a focus on regulatory compliance.
- 6Effective communication and teamwork skills for cross-functional collaboration.
Salary Insight
$73 - $77k per year
Location
Required Skills
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