Operations Lead
This job does not exist anymore.
Try running a new searchor browse our vacancies.
Or fill in the form below to receive job alerts.
| Job Type | Contractor |
| Location | Dublin |
| Area | Dublin |
| Sector | Operations & Manufacturing |
| Start Date | |
| Advertiser | Darcy Ainscough-Denton |
| Telephone | +353 1 574 6266 |
| Job Ref | 1002850 |
| Job Views | 142 |
- Description
- Team Horizon is seeking an Operations Lead (initial 12-month contract) for our client who are a leading biopharmaceutical company based in Dublin. In this role you will serve as primary production process owner responsible for New Product Introduction and Life Cycle Management Projects and process improvements projects. You will be operations point of contact for coordination of the manufacturing effort and will be responsible for driving process efficiencies as part of the project for operations. You will apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to ensure streamlined manufacturing operations are enabled in both vial and syringe facilities.
Why you should apply:
This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.
There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.
Our client is developing the capability to produce all its medicines in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Function as the site interface between the Product Delivery Teams (PDT’s), and the client’s Manufacturing operations.
Develop, review and approve generic batch records and parameter value lists across Formulation, Filling and Inspection.
Develop, review and update Production, Engineering, Operating Procedures & training materials.
Assist in providing training on scientific or technical aspects of the process/project.
Evaluate, plan, and implement solutions for process improvement opportunities.
Support scheduling and execution of Characterisation, Engineering and PPQ runs including ensuring all necessary pre-requisites are included on the schedule and assess process performance by observation of floor operations and review of performance data.
Provide troubleshooting support throughout the project and on the floor during execution of activities.
Hold people to account for delivery and behaviours within Product team.
Perform Job Hazard Assessments and Change Control Assessments to determine impact to Manufacturing.
Partner with Learning & Performance to define training strategy’s for NPI’s and complex projects.
Liaise with Quality Assurance to ensure that GMP standards are maintained in line with current SOP’s, batch documentation and licences.
Develop, review and update Protocols for manufacturing activities.
Documentation and approval of protocol deviations for manufacturing activities.
Liaise with Process Development regarding process changes in an effective and timely manner.
Own and lead change controls as required by the NPI Project Team.
Review and approve bills of materials.
Develop, review and update Product Quality Risk Assessments.
Any other duties as assigned.
What you need to apply:
Project Management and organizational skills, including ability to follow assignments through to completion.
Problem solving skills: Gathers data from key stakeholders, analyses and interprets information to develop solutions to technical problems of moderate complexity.
Negotiation and Influence skills.
Take initiative to identify and drive improvements.
Excellent verbal and written communication skills: Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls) and good Presentation skills.
Escalate issues professionally and in a timely manner.
Decision Making skills and confidence to challenge others on decisions that impact the manufacturing area.
Teamwork and Coaching others.
Ensures compliance within regulatory environment.
Demonstrated ability to work independently and deliver right first-time results under minimal direction.
Bachelor’s degree in a science discipline.
2+ years of biopharmaceutical manufacturing experience in Fill Finish or related manufacturing or GMP experience in the pharmaceutical or medical device industry.
Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.
