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Global Engineering C&Q Manager

AbbVie

Dublin, Ireland

Full time

Posted :2 years ago

Executive Assistant to Site Lead & Site Senior Leadership Team

AbbVie

Dublin, Ireland

Full time

Posted :2 years ago

QC Supervisor (Metrology)

AbbVie

Dublin, Ireland

Full time

Posted :2 years ago

QC Manager

AbbVie

Dublin, Ireland

Full time

Posted :2 years ago

QC Chemist /Lab Analyst (HPLC/GC)

AbbVie

Dublin, Ireland

Full time

Posted :2 years ago

QA (Quality) Operations Manager

AbbVie

Cork, Ireland

Full time

Posted :2 years ago

AbbVie

Global Engineering C&Q Manager

Posted :2 years ago

Job location

Dublin, Ireland

Job category

All

Job type

Full time

Job Descriptions

Job Description

Planning and coordination of C&Q activities in line with a risk-based approach (RBV).

Articulate and incorporate all C&Q deliverables into project scheduling tools and delivery outputs.

Help standardize the C&Q approach across the network.

Assessment of third-party C&Q support and / or the assessment of individual candidates for specific project roles.

Manage C&Q teams / team coordinators to deliver key GE lead projects across the network.

Track project progress in line with agreed schedules week on week.

Support issue resolution through close working ties with the cross functional teams.

Support protocol execution and reporting activities when required.

Provide guidance and advisement to C&Q personnel.

International Travel to support C&Q execution and management of FAT’s as well as on site execution activities.

Work closely with key GE members and central services personnel to upskill.

Requirements

Degree / Diploma in an Engineering or science-based discipline.

3-5 years’ experience in the pharmaceutical industry in a C&Q / Validation role.

Strong understanding of Pharmaceutical Regulatory Requirements.

Multi-disciplinary experience: Facilities, Utilities & Equipment, validation.

Previous experience in a project management role would be beneficial

Experience in Risk based Verification (RBV).

Experience with aseptic fill finish and OSD manufacturing practices.

High degree of knowledge of all relevant EU/FDA regulations.

Demonstrated ability to coordinate activities in an efficient and effective manner.

Experience with paperless validation solutions such as Kneat would be beneficial.

Ability to work closely with key project stakeholders to maintain project delivery schedules and limit any potential delays.

Qualifications

Bachelor Degree in Engineering (Level 7) , Third level qualification in a Science or Engineering

Skills

Project management
People Management
Management Skills
Project Planning
Leadership Skills

Experience

138