Pharma Operations Lead
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| Job Type | Permanent |
| Area | Sligo, Ireland |
| Sector | ManagementOperations & Manufacturing |
| Start Date | |
| Advertiser | Hilda Lynn |
| Telephone | +353 98 33013 |
| Job Ref | #1002602 |
| Job Views | 201 |
- Description
- 2602 - Pharma Operations Lead
Team Horizon is seeking a Pharma Operations Leader to be part of our clients’ leadership team in our in Sligo. The purpose of this role is to lead a dynamic pharmaceutical manufacturing team to produce life enhancing medicines. The successful person will lead and facilitate the safe operations of the manufacturing team in a dedicated hormone pharmaceutical processing facility in line with all safety, regulatory and organisational requirements.
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, helping to ensure continuity of supply of our medicines as they expand internationally.
What you will be doing:
Supervision and execution of pharmaceutical processing activities in the facility and support locations, to meet clearly stated operating objectives. Daily reporting on the status of all operations and support activities.
Team leadership, motivation, and direction to maximise the effectiveness of their manufacturing team.
The Pharma Operations Leader must clearly communicate task details and goals to their team members, to allow the pharmaceutical technicians to work effectively.
Resource planning to ensure the required personnel are available to run manufacturing operations safely and efficiently.
Planning and co-ordinate of training requirements within the team and training of new team members.
Measurement, reporting and ownership of key departmental performance metrics, such as yield, rate, usage, attendance, overtime, etc.
Responsible for verification and update of manufacturing control system transactions accurately and in a timely fashion.
Responsible for manufacturing compliance with all safety, environmental and quality related SOP’s.
Work closely with the other shift leaders to ensure interdepartmental activities are planned and executed safely.
Develop direct reports by securing appropriate training, assigning progressively challenging tasks and managing mid-year and annual reviews.
Assist and co operate with HR in the management of employee relations issues.
Interacts with internal and external customers, by meeting regularly, responding to requests and explaining procedures.
Lead the identification, implementation, and execution of key department and Site Strategies.
Schedules human and material resources within a department or section in conjunction with near-term plans to ensure their availability; carries out operations within an established budget.
Adheres to and supports all EHS & E standards, procedures, and policies.
What you need to apply:
A diploma in a relevant science/engineering discipline and/or suitable experience 3 years’ experience of batch processing operations in an FDA/HPRA regulated industry with detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry.
3 years’ experience of operating in a highly automated environment.
3 years suitable direct supervisory experience or training.
Previous experience of supervising a team environment with active participation in proactive improvement programs.