Laboratory Analyst II

Job Summary

Shift: M-F 8-4:30PM; Fully onsite position

Role

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.

location: Swiftwater, Pennsylvania

job type: Contract

salary: $40.00 - 42.30 per hour

work hours: 8 to 4

education: Bachelors

Responsibilities

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
  
  

Qualifications

Required Qualifications

• BS Degree in Chemistry, Biology or Microbiology or Science
• 2 years experience in a cGMP environment.
• Experience with Microsoft Excel is required.
• Experience with wet chemistry methods, compendial methods, GC, LC/MS, UV, CE, AA, ICP, various other instrument methods, and cell-based assays.
  
  

skills: Quality control, MS-EXCEL, Biology, Chemistry, Microbiology, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.

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