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Top Tech Jobs & Startup Jobs
Biotech • Pharmaceutical
The Quality Control System Administrator ensures the successful rollout and support of third-party business applications such as LIMS. Responsibilities include maintaining and managing installations, troubleshooting user issues, managing user accounts, and collaborating with development teams to deliver software releases.
Top Skills:
Lims
Biotech • Pharmaceutical
The Quality Control Sr. Analyst I is responsible for driving laboratory activities in GMP testing, conducting training for new hires, and interacting with QC personnel. This role includes authoring SOPs, reviewing documentation, improving QC systems, and handling laboratory investigations related to test failures.
Top Skills:
BiochemistryMolecular Biology
Biotech • Pharmaceutical
The Quality Control Analyst I performs routine lab activities supporting GMP testing for QC. Responsibilities include performing drug product analysis, maintaining compliance with documentation, and communicating lab issues. The analyst also participates in improving QC systems and laboratory maintenance tasks.
Top Skills:
Qpcr
Biotech • Pharmaceutical
The Quality Control Analyst I is responsible for performing laboratory activities supporting GMP testing. Duties include endotoxin testing, gram staining, bioburden testing, and maintaining compliance with documentation practices. The analyst communicates lab issues, participates in investigations, and contributes to improving QC procedures and systems within a GMP environment.
Top Skills:
BiochemistryMolecular Biology
Biotech • Pharmaceutical
The Manager of Quality Assurance oversees activities related to the manufacturing of cell and gene therapy products, ensuring compliance with quality systems, cGMP guidelines, and regulatory requirements. Responsibilities include batch record review, employee training, maintaining document control, and participating in inspections and continuous improvement activities.
Biotech • Pharmaceutical
The Specialist I in Quality Assurance will handle routine activities in manufacturing, focusing on the creation and review of GxP controlled documents, managing the document lifecycle, and ensuring compliance with quality standards. This includes editing, formatting, and archiving documents and supporting inspections as needed.
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