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Project Manager, Automation, Biopharma

Company: GForce Life Sciences
Location: Oceanside
Posted on: January 16, 2022

Job Description:

Consultant, Project Manager, Automation, Biopharmaceutical

Summary
Our client, a research-based biopharmaceutical company focused on the discovery, development, and commercialization of innovative medicine is seeking a Senior Project Manager to support their biologics site in an operational readiness program to prepare for drug manufacturing/phase III product development.

Duties / Expectations of Role
Facilitate small to large complex projects with teams composed of cross-functional and geographically dispersed members
Support execution of automation projects using DeltaV
Provide leadership and direction to assigned project teams through application of expertise in project management tools and processes.
Institute comprehensive work breakdown structures for all team deliverables; track and follow up on implementation of team decisions.
Ensure high levels of communication with project teams, support resources and management.
Identify resource and schedule constraints, key risks and issues to be resolved, and proactively drive the development of contingency and/or risk mitigation plans.
Support the coordination and cascading of plant operations key performance indicators; maintain and report applicable department metrics.
Develop, implement, manage an effective standardized approach to program/project management with regards to compliance with company standards, schedule milestones, resources, and costs (including capital and operational).

Mandatory Requirements
5+ years in biopharmaceuticals or highly regulated industry
Experience with Processes and/or typical MES applications in biopharmaceuticals.
3-5 years minimum of Project Management experience, leading automation projects.
Process control system experience with knowledge of various hardware products, technologies and services deployed for process control systems such as DeltaV, plus interfaces with other systems.
Ability to navigate GMP manufacturing areas; knowledge in all GMP to comply with CFRs and ICH Q7
Experience in varied and progressively challenging operations roles with the biopharmaceutical/pharmaceutical industry and possess a strong knowledge of GMP manufacturing, quality and/or regulatory processes and challenges.

Term & Start
12+ month contract
Must be onsite in San Diego County 3 days per week

Keywords: GForce Life Sciences, Oceanside , Project Manager, Automation, Biopharma, Executive , Oceanside, California

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