Jobs and Careers

Project Manager-QA

Los Angeles, United Statesfull_timeVerifiedPosted 1 Apr 2026

💰 $115,000/yr($105,000/yr – $115,000/yr)

About the role

Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.

POSITION SUMMARY

Working knowledge of QS, cGMP, and Process Flows.  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.  

ESSENTIAL DUTIES AND RESPONSIBILITES including the following. Other duties may be assigned

Drives departmental projects to completion through providing leadership and management to all personnel and functions involved.

Management of projects to meet appointed timelines and achievement of required completion dates, including large scale Quality initiatives in new technologies to improve efficiency. This involves migrations, transitions and implementations in varying electronic formats.

Assists and supports department in routine functions to include but not limited to deviation investigations, CAPA processing, and customer complaint investigations as needed.

Perform review and approval tasks for the department as needed.

Identification of project scopes, required resources, resource assignment and management.

Responsible for monitoring and updating project status and communicating this information to management.

Responsible for identification and resolution of roadblocks and streamlining where possible.

Responsible for communication and coordination with other departments to streamline the transition of projects to routine operation.

Provide leadership for ongoing projects.

Participates in departmental meetings and cross functional team meetings as required.  Assembles cross-functional teams and/or facilitates team meetings as necessary.

Assume the decision-making responsibility for day-to-day operations considering staff input and collaborating with other GB functions.

Provide scientific and/or technical advice and counsel regarding projects as needed.

Communicates company and departmental goals to the department’s exempt and non-exempt employees.

Manages large complex projects to bring in on budget, on schedule and technically correct by revising, analyzing and reporting the results against business parameters.

Communicates with cross functional departments and support groups to improve departmental performance and efficiency.

Maintain a quality presence to ensure compliance with all regulatory requirements.

Maintain current knowledge of regulatory and industry standards.

Strict adherence to procedures and practices according to FDA regulations.

Strong emphasis on documentation according to FDA regulations.

REQUIRED EXPERIENCE/SKILLS & EDUCATIONAL QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

Bachelor of Science degree in Engineering, Biology, Chemistry, Biochemistry, Information Systems or closely related scientific/technical discipline is required.

Minimum of 5 years direct Quality experience in a pharmaceutical, GMP, or FDA regulated environment is required. In addition, experience in quality assurance, quality control, quality operations, or engineering function is preferred.