Aseptic Process Owner Lead - Dun Laoghaire, Dublin

Office/Project Location: Dun Laoghaire, Dublin

Employment Type: Contract

Work Location:  Site Based

Pay: €55 - €65 per hour

Experience: 10+ years

Visa: EU passport or Stamp 4 visa required

Aseptic Process Owner Lead - Dun Laoghaire, Dublin

Our client is a leading international Biotechnology company with a state of the art aseptic manufacturing facility in Dun Laoghaire, South Dublin. 

The plant is one of the most dynamic in Ireland and is currently undergoing rapid expansion and capital investment. 

This is an excellent opportunity to get experience into Ireland's leading aseptic manufacturing plant.

An exciting and rare opportunity has presented for an Aseptic Process Owner Lead. 

This is a senior role in the organisation and requires in-depth technical and operational knowledge of aseptic Drug Product manufacturing processes; Parts/Components Preparation, Formulation, Syringe Filling, Vial Filling, Lyophilisation and Capping.

The Site Aseptic Process Owner Lead will continue to build on the site and network aseptic processing knowledge and represent the Dublin site at a global level across the manufacturing network.

As the Site Aseptic Process Lead you will be an established professional who is a self-starter, capable of applying advanced process knowledge and creativity to complete complex assignments related to aseptic operations. 

You are someone who contributes to the development of new principles and concepts, who wants to be challenged and can lead change from an aseptic operations perspective.

Perform as a knowledgeable subject matter expert (SME), and single point of contact on site and network projects and programs, to advance aseptic operations

Leading and/or providing input to strategic initiatives that will improve and develop Manufacturing processes for the future including Contamination Control and Aseptic Process Simulations (APS)

Contribute in a team environment to operational issues pertaining to processes as they arise and provide expertise and support to help resolve escalated technical issues as required

Remain current on state-of-the-art for systems and processes and advise on the appropriate adoption and use of new techniques and technology.

Involved in the daily business management systems and reporting, have a clear understanding of what is happening in the assigned area of responsibility. Monitor any process trends (Personnel and Environmental Monitoring), including business performance metrics. 

Identify actions that will enable the process and the Manufacturing areas better achieve and surpass metrics in the future

Lead and/or Support investigations that impact on safety, quality and/or compliance of the processes, ensuring thorough investigations are conducted and actionable CAPAs, to prevent future reoccurrence, are implemented within agreed timelines

Requirements

Bachelor’s degree in Microbiology or related discipline with 10 + years’ experience in the pharmaceutical industry

Experience with regulatory compliance in cGMP manufacturing and in-depth knowledge of Eudralex Volume 4, Annex 1 Manufacture of Sterile Medicinal Products.

Proven ability to work in a high paced matrix organization and effectively influence change and escalate issues professionally and in a timely manner

Excellent Decision-Making skills and confidence to challenge others respectfully and professionally on decisions that impact the manufacturing area

Proactive and works well with others in a collaborative, fast-paced goal-driven environment

Interacts well with diverse groups (Manufacturing, Validation, Engineering, Quality etc) and maintains strong working relationships with internal and external collaborators

Demonstrated ability to coach, mentor and/or cross train colleagues within core technical areas

Excellent verbal and written communication skills: 

Strong Technical writing skills for cGxP documentation (e.g. investigations, procedures, change controls) and good Presentation skills.

Package

Contract role - Hourly rate €55 - €65 per hour

Minimum 12 month contract with the possibility of an extension. 

Onsite expectations: The team are required to do a minimal 3 days per week onsite.

However, the initial expectations are for you to be more present onsite to help integrating into the team, familiar with the site and projects, and benefit from face-to-face time and meetings. 

Depending on their capabilities and speed of development, the long-term goal is to offer 3 days onsite per week.

Contact

Karen McHugh is the consultant managing this position.

If you area Aseptic Process Owner Lead interested in roles based in Dublin , you can contact Karen by e-mail at karen@jobcontax.com Karen or phone 353 1 7979720 for a confidential chat.

JobContax do not send CVs to clients without candidate permission.

With over 50 years of technical recruitment experience, JobContax is the leading recruiter of Aseptic Process Owner Leads in Dublin and Ireland.

Due to the large volume of applications, JobContax may not be able to respond to every individual.

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