Document Quality Control Specialist - Bedford, United States - Adecco USA

Adecco USA Bedford, United States

3 weeks ago

Description

A Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science.

In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group.

This position will report to the Sr. Manager, QC and Sample Management.
Note that this is a 4-month temp/contract role starting in early June 2024 for a medical leave coverage. This is a fully remote position, but you MUST be located in the Northeast. The work hours are Monday-Friday 8:00am-5:00pm. The pay range is $ /hr. - depending on your level of experience.

Key Responsibilities:

Conduct Quality Control (QC) review of Bioanalytical data (LC-MS/MS, ELISA, qPCR, etc.) and study-related documentation generated in-house or at the CROs in support of regulated or non-regulated studies. Ensure that all information contained within the reports is accurate.
Upload, review, and edit all documents in SharePoint.
Participate in formatting reports generated in-house and providing report templates to CROs, as needed.
Perform QC review of packing slips, sample manifests, and critical reagent documentation.
Participate in authoring/editing new or approved Bioanalytical lab guidelines.
Perform routine QC review of Electronic Lab Notebooks (ELN) to ensure adherence to guidelines.
Perform audit of finalized reports and maintain errata list.
Check DMPK trackers for accuracy of entries and consistency of use.
Train on LIMS system to receive samples and access sample inventory

Required Skills & Experience:
Bachelor's Degree in a scientific or healthcare discipline.
Minimum of 4 years of relevant experience working in a pharmaceutical, CRO, biotech or similar organization preferred.
Knowledge of GxP regulations.
Excellent attention to detail and organizational skills.

Must have excellent oral and written communication skills and demonstrated ability to work effectively in a fast-paced environment where multiple concurrent projects must be completed in a specified timeframe.

Proficient in standard Microsoft Office tools:
Word, Excel, and PowerPoint.
Ability to take directions well and multi-task.
Demonstrated proficiency with LIMS/LabVantage and sample management is a plus.
Working knowledge of bioanalytical assays (LCMS/MS, immunoassays, etc.) is a plus.

Pay Details:
$50.00 to $75.00 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/DisabledTo read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to Company will consider qualified applicants with arrest and conviction records subject to federal contractor requirements and/or security clearance requirements.

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