Lab Analyst II
Adecco Healthcare & Life Sciences is hiring a contract Lab Analyst II for our Pharmaceutical partner in Swiftwater, PA
The anticipated hourly wage for this position is between $38 and $41. Hourly wage may depend upon experience, education, geographic location, and other factors.
Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs.Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria
Summary:
This position is within the Analytical Support Section of the Quality Control Department, comprising a team of eleven professionals dedicated to achieving departmental objectives. The primary responsibilities include:
- QC Test Material Management
- International Shipments
- New Product Support
- Compendial Compliance
- Method Transfers
- Method Validation
- Support for Assay Lifecycle Program
The role focuses on managing the reference standard and critical reagent program, encompassing inventory oversight and international shipping in compliance with Regulatory Affairs. Additionally, it involves supporting the assay lifecycle program, which includes method validation and method transfers.
A key aspect of this position is participation in method transfers. The analytical methods involved span the company's entire product portfolio, including wet chemistry methods, compendial methods, GC, LC/MS, UV, CE, AA, ICP, various other instrumental methods, and cell-based assays.This offers exposure to a diverse array of testing techniques.
Key Responsibilities:
- Method Development/Optimization, Transfer, and Validation
- Support for Assay Lifecycle Program Management: Overseeing more than 200 methods across multiple disciplines.
- Inventory Management: Overseeing all QC materials in collaboration with multiple departments.
- Management of International Shipments: Ensuring compliance with Regulatory Affairs and all relevant laws.
Key Activities:
- Participate in project teams focused on method transfer and validation of QC Analytical Methods.
- Engage in project teams managing reference standards and critical reagents used in QC Testing.
- Author and review documents supporting departmental functions.
- Perform laboratory tasks in strict adherence to local documents and Federal Regulations.
- Manage multiple projects and work independently on assigned tasks, both individually and within teams.
- Maintain and optimize reference standard and reagent storage.
Basic Qualifications:
- BS Degree in Chemistry, Biology, Microbiology, or a related science field.
- A minimum of 2 years of experience in a cGMP environment.
- Proficiency in Microsoft Excel.
This role offers a comprehensive opportunity to engage with a wide range of analytical techniques and contribute to the advancement of quality control processes within the organization.
Pay Details: $38.00 to $41.00 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs.In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
- The California Fair Chance Act
- Los Angeles City Fair Chance Ordinance
- Los Angeles County Fair Chance Ordinance for Employers
- San Francisco Fair Chance Ordinance