Associate Director, Project Management

Join Grifols To Improve Healthcare

Would you like to join an international team working to improve the future of healthcare? Grifols is a global healthcare company that has been working to improve the health and well-being of people around the world since 1909. 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.

Job Summary

This position is responsible for overall project management at the Grifols Biologicals LLC (GB) manufacturing site.

Essential Job Duties

Develop and manage project schedules to track key milestones and project completion.

Track a project through all phase gates of project initiation, planning, implementation, and closure.

Manage resource allocation and project prioritization of key projects.

Generate Risk Mitigation Plans and Risk Register for medium to large projects to ensure successful project completion.

Generate Project Plans for large projects to summarize project scope, qualification strategy, submission strategy and timeline.

Lead and manage medium to large plant projects that impact capacity expansion, reliability, process improvement, and quality / compliance.

Generate Risk Assessments for implementation of projects prior to closure of change control.

Coordinate on-time project implementation with supporting groups such as Manufacturing, Quality Assurance, Facilities, Maintenance, Validation, Quality Control, Quality Operations, and Materials Management.

Ensure on-time Product Release by tracking the completion and closure of impacted change requests and associated qualifications (following plant shutdowns).

Lead and manage scheduling of shutdown and startup activities to ensure on-time start of production.

Support monthly project update reports of key plant projects and present to GB management.

Be curious to ask probing questions to ensure teams understanding of project objectives and requirements, facilitate discussions to clarify roles & responsibilities, and alignment on timelines.

Expertly utilize soft skills like leadership, communication, critical thinking and emotional intelligence to ensure team engagement and collaboration.

Successfully identify and remove roadblocks that prevent meeting the project schedule. Identify when escalation is required to higher level management to mitigate critical project delays.

Lead and support Continuous Improvement Projects and Initiatives (i.e. Kaizens, Value Stream Mapping, DMAIC etc.).

Conduct Lessons Learned for plant shutdowns and key projects as needed.

Requirements

Bachelor of Science degree in Engineering, Biology, Chemistry, Biochemistry or closely related scientific / technical discipline is required. PMP Training and Certification desired.

Typically requires a minimum of 10 years of related experience. Project or technical leadership experience required. Direct and Cross-functional Supervisory or management experience preferred.

Requires understanding of principles and qualification requirements for a range of systems and equipment, including ultrafiltration, CIP, chromatography, reactor tanks, centrifuges, filter presses, etc.

Knowledge of cGMPs, FDA regulations, and industry guidelines.

Strong technical writing skills.

Ability to inspire high performance in others and align team.

Ability to lead, motivate, guide, train, coach and develop personnel.

Demonstrated project management skills.

Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions.

Must be proactive, results oriented, and have strong attention to detail.

Self-starter with strong work ethic and the ability to exercise good judgment.

Ability to effectively prioritize multiple tasks to meet deadlines.

Strong interpersonal skills with the ability to interact with personnel at all levels in a team.

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

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

Provide leadership for ongoing Validation projects.

Participates in departmental meetings and cross functional team meetings as required.

Assembles cross-functional teams and / or facilitates team meetings as necessary.

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

Strict adherence to procedures and practices according to FDA regulations.

Strong emphasis on documentation according to FDA regulations.

Adhere to departmental corporate safety policies.

Must be flexible with working hours in order to accommodate the 24 hour, 7 day plant operation.

Occupational Demands

Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Frequent hand movement of both hands with the ability to make fast, simple movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations with occasional travel within the United States. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions and plans work schedules to meet goals. Frequently interacts with others, relates sensitive information to diverse groups. Must work with diverse groups to obtain consensus on issues. Ability to apply abstract principles to solve complex conceptual issues.

The estimated pay scale for the Associate Director, Project Manager role based in Los Angeles, CA, is $150,000 to $190,000 / per year. Additionally, the position is eligible to participate in up to 15% of the company bonus pool. We offer a wide variety of benefits including, but not limited to : Medical, Dental, Vision, PTO, up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression.