Technical Project Manager

Grifols

Technical Project Manager managing FDA submissions and quality projects in pharmaceutical industry. Leading cross-functional teams for project execution and compliance in a global healthcare company.

Posted 5/20/2026full-timeLos Angeles • California • 🇺🇸 United StatesMid-LevelSenior💰 $105,000 - $125,000 per yearWebsite

About the role

Key responsibilities & impact

Responsible for managing various facets of quality projects related to submissions to the FDA, review and approval of documents and the management of systems.
Develop production objectives, manage, and maintain project plans
Interface with various groups to ensure that objectives and timelines are met specifically for preparing complex technical submissions related to major facility projects
Review and approve protocols and final reports
Ensure implementation and maintain compliance of Methods Validation
Write and revise documents and procedures
Plan, direct and manage internal and contract manufacturing projects from concept to production using recognized project management tools including initiation, control and closure.
Formulate project objectives, approaches, schedules, risk assessments, budgetary constraints and manpower requirements in accordance with customer needs.
Lead cross-functional project team on project execution to meet objectives, on-time delivery and budget constraints
Establish and maintain timely and clear communication with project team, customers and suppliers.
Ensure appropriate processes are followed for effective and timely engagement of related parties in completion of designated project activities.
Provide regular status update to senior management.

Requirements

What you’ll need

Bachelor’s degree in the sciences or related field.
Supplemental training / education in business administration desirable.
Project management certification a plus
Minimum 5 years’ experience in pharmaceutical, medical device, plastic/parts design industry including 3 years in increasingly complex project management duties in a GMP product development / process improvement environment.
Working knowledge of QS, cGMP, Process Flows, Design Software, Schematics.
Must have sound knowledge of MS Office, MS Project, relational database.
Strong interpersonal skills and ability to communicate with all levels of the organization.
Ability to organize, prioritize and manage multiple responsibilities with low level of supervision.
Detail oriented with strong emphasis on accuracy and thoroughness.
Project management training (PMI preferred).
Knowledge of 2D/3D barcoding and electronic data transfer systems highly desirable.
Willing to travel domestically and internationally up to 20%.

Benefits

Comp & perks

Medical
Dental
Vision
life insurance
PTO
paid holidays
up to 5% 401(K) match
tuition reimbursement

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

project managementmethods validationdocument reviewprotocol approvalrisk assessmentbudget managementprocess improvementGMP2D/3D barcodingelectronic data transfer systems

Soft Skills

interpersonal skillscommunicationorganizationprioritizationdetail orientedaccuracythoroughnessleadershipteam collaborationtime management

Certifications

project management certificationPMI training