Manufacturing Process Specialist

Morgan McKinley; Dún Laoghaire-Rathdown; Sur place; EUR 90 000 - 130 000; Plein temps

Résumé du poste

Morgan McKinley seeks a Senior Specialist Manufacturing with deep aseptic drug product knowledge to own and optimize critical manufacturing processes. You will lead process documentation, drive CAPAs, and steer continuous improvements across the aseptic operations, collaborating with Quality, Validation, Engineering, and Manufacturing teams.

The role emphasizes safe, compliant operations, pro-active problem solving, and delivering reliable performance in a high-paced environment.

Qualifications

• Bachelor’s degree in Science, Engineering or related discipline.
• 5+ years in aseptic Drug Product manufacturing or related cGxP environment.
• Experience with regulatory compliance and cGMP.
• Strong written and verbal communication for cGxP documentation.

Responsabilités

• Act as SME and single point of contact on site and network projects.
• Lead process ownership and drive safety, quality, and compliance.
• Direct initiatives to improve reliability and efficiency of manufacturing processes.
• Lead or support investigations and CAPA implementation to prevent recurrence.
• Identify and lead continuous improvement projects within assigned area.

Connaissances

Aseptic manufacturing knowledge

cGxP/good documentation

CAPA and investigations

SOP authoring and revision

Cross-functional collaboration

Formation

BSc in Science/Engineering

Description du poste

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.

As a Specialist Manufacturing, 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 the manufacturing operations. You are someone who contributes to the development of new principles and concepts, who wants to be challenged and can lead change from a manufacturing operations perspective.

Supporting key areas of the business, the Process Owner Lead will direct initiatives that improve the reliability and efficiency of manufacturing processes in addition to day-to-day support related to unplanned event troubleshooting, investigations, CAPA identification and implementation.

Primary responsibilities:

• Perform as a knowledgeable subject matter expert (SME), and single point of contact on site and network projects and programs, to advance manufacturing and aseptic operations through ownership of the assigned processes and taking a proactive approach to safety, quality, and compliance by actively seeking opportunities to remove error traps.
• Accountable for process documentation (e.g., SOPs, Training, Electronic Batch Records, Risk Assessments) in assigned area of responsibility. Gatekeeper (develop, review and update) of process documentation to maintain structure and control over generation and revision ensuring the documents clearly and correctly direct the process.
• Leading and/or providing input to strategic initiatives that will improve and develop processes for the future.
• 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.
• Use subject matter expertise to identify and lead continuous improvement projects in assigned area of responsibility. Ensure project timelines are met, challenges identified, mitigations are in place and communication plans delivered to all stakeholders.
• 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 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 timeline.
• Remain current on state-of-the-art for systems and processes and advise on the appropriate adoption and use of new techniques and technology.
• Ability to lead change from an aseptic operations perspective is a plus.

What you need to apply:

• Bachelor’s degree in Science, Engineering or related discipline with 5 + years’ experience in aseptic Drug Product Manufacturing or related cGxP manufacturing experience.
• 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 upscale 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.