Onesource Enterprise Site Leader Milano

Onesource Enterprise Site Leader
Milano
Lombardia, Milano

Responsibilities**:

Location Milan, MilanoIT

Job ID JR-032824

Summary:

- Active and positive member of the account leadership team, leading the Scientific Services on site group and maintains open lines of communication with client representatives, end users, alliance partners, and operations managers.

- Manages scope including Service Level Agreements (SLA's) and developing, tracking and optimizing Key Performance Indicators (KPI's).

- Identify and communicate opportunities for cost savings and increased scope.

- Ensures day-to-day and long-range activities for defined Services scope are planned and that appropriate resources are available.

- Ensure that all programs and procedures for Scientific Services are properly implemented.

- Responsible for Scientific Services personnel including hiring, promotions, recognition, discipline, and performance management.

- Establishes/coordinates goal setting, performance reviews and incentive/salary administrative processes for direct reports and possibly those reporting to direct reports, utilizing appropriate tools.

- Ensures training records are maintained and up to date via direct reports.

- Communicates operating philosophy, objectives and expectations to Scientific Services personnel in a continuing effort to build the site team.

- Ensures all in scope services follows appropriate client procedures and Government regulatory codes.

- Supports PerkinElmer and Client audits.

- Communicates formally and informally with customer's staff.

- Responsible for identifying, sharing best practice, training and resources between sites

- Complies with all company policies and procedures and adheres to company standards.

- Performs other duties as required.

Competencies:

Qualification in business, Engineering or Chemistry, including related field of study and experience managing multi-million dollar budget in Laboratory and / or manufacturing Pharmaceutical environments.

A minimum of 10 years of experience and accomplishment while operating in regulated environments.

Must have demonstrable knowledge of FDA guideline interpretations, GMP, GLP and audit experience.

Provide demonstrated knowledge of Pharmaceutical, Biotech, and Medical Device industry products and services.

Broad knowledge of business processes to drive out costs in research and manufacturing of FDA regulated efforts.

A proven knowledge of, and experience of working with, the Life Science industry supplier base including analytical instrument OEM's, service providers and consumables vendors.

Provide demonstrated leadership, team building, strong organizational skills, project planning and management with a participatory management style.

Excellent presentation and communication skills and MS Office literacy required.