What are the responsibilities and job description for the Laboratory Analyst II position at Aequor Technologies LLC?
This position will be in the Analytical Support Section of the Quality Control Department which consists of eleven team members working together to support the department goals. The main activities of the role are as follows :
QC Test Material Management
International Shipments
new product support
compendial compliance
method transfers
method validation
support Assay Lifecyle Program
The main responsibilities will be to support the reference standard and critical reagent program, which includes inventory management, international shipping in compliance with Regulatory Affairs. Also support the assay lifecycle program which includes method validation and method transfers.
A key component to this role will be involvement in method transfer.
The analytical methods included for this position will be the entire company portfolio of products which includes wet chemistry methods, compendial methods, GC, LC / MS, UV, CE, AA, ICP, various other instrument methods, and cell-based assays. There is opportunity for exposure to a variety of test method techniques. The analytical and biological methods included for this position will be the entire company portfolio of products which includes wet chemistry methods, compendial methods, GC, LC / MS, UV, CE, AA, ICP, various other instrument methods, and cell-based assays.
KEY RESPONSIBILITIES :
General Method development / optimization, method transfer and method validation
Support Assay Lifecycle Program Management of more than 200 methods from multiple disciplines
Inventory management of all QC materials working across multiple departments
Manage International Shipments for QC in compliance with Regulatory Affairs and all relevant Government and Shipping company laws.
KEY ACTIVITIES :
Participate in project teams involved in the method transfer / validation of QC Analytical Methods
Participate in project teams involved in the management of reference standards and critical reagents used in QC Testing
Author and Review documents in support of the department functions
Perform laboratory tasks in strict compliance with local documents and Federal Regulations
Ability to manage multiple projects and work independently on assigned tasks as an individual contributor and in teams
Maintain and optimize reference standard and reagent storage
BASIC QUALIFICATIONS :
BS Degree in Chemistry, Biology or Microbiology (Preferred) or Science with 2 years experience in a cGMP environment. Experience with Microsoft Excel is required.
