Job Information
Merck Associate Director, Regulated Bioanalytics, Integrated Program Logistics & Sample Management in Lower Gwynedd, Pennsylvania
Job Description
The Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) Regulated Bioanalytics Department is seeking an Associate Director to lead our Regulated Bioanalytics Sample Management group located at our company's state-of-the-art AdVAnce research facility in West Point, PA. At this new facility, we will combine the power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation of timely, high-quality regulated bioanalytical data. As the AdVAnce facility will not be fully constructed and ready for occupancy until 2026, initial roles will complete training and perform work primarily at our company's Springhouse Innovation Park facility in Lower Gwynedd Township, PA.
The individual will be responsible to lead all aspects of sample management operations, including deployment and troubleshooting of automated sample stores and liquid handlers, managing staff receiving and processing clinical study samples, and maintain highly compliant lab processes. The individual will also support efforts to implement and enhance Laboratory Information Management Systems (LIMS) or other applications used by the team. The candidate should be current on state-of-the art technologies and is expected to champion evaluation of new technologies and optimize processes. Representing the lab during quality and regulatory audits will be required.
Education Minimum Requirement:
- B.A./B.S. in Biology, Molecular Biology, Chemistry, Biochemistry, Engineering, Biotechnology, or related discipline with at least 7 years, M.S. with at least 5 years, or Ph.D. with 3 years experience in a related field
Responsibilities:
Manage the development, implementation, operation, and troubleshooting of automation solutions (i.e. sample stores, liquid handlers, etc.) within the sample management laboratory that addresses the receipt, aliquoting, and storage of regulated clinical samples and reagents
Lead staff through automated and manual sample receipt, processing, aliquoting, & distribution, ensuring efficiency and quality in sample management operations
Evaluate and validate new or updated applications (e.g. LIMS, automation systems, etc.) that enable improved sample management processes
Partner with IT on interfacing sample management automation data and systems into LIMS or other inventory management applications
Serve as an internal subject matter expert on new and existing automated liquid handler and automated samples store technology and capabilities
Train other sample management staff on sample management processes and the use of lab automation
Author SOPs or job aids associated with sample management systems and processes
Perform responsibilities in compliance with departmental SOPs and regulatory guidances (e.g., GxP)
Serve as lab lead during internal or external regulatory audits
Required Experience & Skills:
Experience leading sample management staff within a GxP regulated lab
Experience working with lab automation, such as liquid handlers, robotics, or automated sample stores
Experience implementing and validating new or updated lab applications such as a laboratory information management system (LIMS) or related system
Strong verbal and written communication skills and comfortable interacting with a variety of on-site and off-site collaborators
Ability to communicate effectively in presentations to stakeholders in partner organizations, to write technical reports, and to participate on cross-functional teams
Ability to build and maintain strong relationships with site leaders, corporate management, and other stakeholders to ensure effective communication of plans and issues
Strong attention to detail with the ability to multi-task and handle multiple responsibilities simultaneously
Ability to prioritize projects and resources to deliver required level of output and support
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Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
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Employee Status:
Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable
Shift:
Valid Driving License:
Hazardous Material(s):
Job Posting End Date:
12/22/2024
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Requisition ID: R326630