Downstream Technical Services Specialist

Overview

Job Title : Downstream Technical Services Specialist

Introduction to role : Are you ready to make a difference in the world of biopharmaceuticals?

As a Downstream Technical Services Specialist, you'll play a pivotal role in supporting the cGMP manufacture of biological bulk drug substances at Alexion's facility in Blanchardstown, Dublin.

Your expertise will be crucial in technology transfer, process validation, and routine commercial manufacturing for Downstream processes.

Collaborate with various departments to ensure successful facility startup and process qualification, while driving timely completion of milestones related to new product introduction and process validation.

Are you up for the challenge?

Responsibilities

Provide process expertise in Downstream purification processes including buffer preparation, purification, viral reduction steps, and DS formulation.

Author and review technical documentation, gap assessments, protocols, reports, and validation documentation.

Lead or support the continuous process verification program at ADMF.

Support the introduction and changes of raw materials and consumables.

Collaborate with Quality, Supply Chain, and Manufacturing Operations to ensure material availability and release.

Identify and implement process improvements for yield and cycle time reduction.

Generate documentation protocols and lead plant supporting studies at commercial scale.

Provide on-the-floor support for troubleshooting processing issues and lead investigations into process deviations.

Lead key process changes using change control systems.

Ensure compliance with Quality and Safety standards, liaise with global groups, and provide technical support during audits.

Author and review CTD sections for regulatory submissions.

Serve as a subject-matter expert during regulatory agency inspections.

Essential Skills / Experience

Minimum 3+ years' experience in Technical Services / Process Development / Manufacturing Support in a biological bulk drug substance manufacturing organization

Technical and operational knowledge of multiple unit operations in cell culture processing

Comprehensive understanding of cGMP requirements for biopharmaceutical manufacturing

Good interpersonal skills coupled with demonstrated ability to effectively work in a matrix organization, and in local group settings

Ability to present and defend technical and scientific approaches in both written and verbal form

Ability to drive for results independently and adapt to rapidly changing priorities

Experience of Technology Transfer activities is advantageous

Knowledge or experience of start-up or systems would be ideal

Detail orientated

Technical writing competency

Desirable Skills / Experience

B.Sc.

in Biochemistry, Biology, Chemistry or equivalent, or B.Eng.

Process or Chemical Engineering

M.Sc.

or other postgraduate qualification in Biochemistry, Biology, Chemistry or equivalent, or B.Eng.

Process or Chemical Engineering.

Experience of authoring CMC sections of regulatory submissions

When we put unexpected teams in the same room, we unleash bold thinking with the power to inspire life-changing medicines.

In-person working gives us the platform we need to connect, work at pace and challenge perceptions.

That\'s why we work, on average, a minimum of three days per week from the office.

But that doesn\'t mean we\'re not flexible.

We balance the expectation of being in the office while respecting individual flexibility.

Join us in our unique and ambitious world.

At AstraZeneca, you\'ll find an environment where innovation thrives and your contributions are valued.

Our commitment to serving patients drives everything we do, fostering a culture of inclusiveness and integrity.

With a rapidly expanding portfolio, you\'ll have the opportunity to grow alongside exceptional leaders and peers who are dedicated to making a difference.

Embrace the entrepreneurial spirit and autonomy of a leading biotech while enjoying tailored development programs that align your growth with our mission.

Ready to join us on this exciting journey?

Apply now and be part of a team that\'s redefining the future of healthcare!

Date Posted

18-Sep-2025

Closing Date

01-Oct-2025

Our mission is to build an inclusive and equitable environment.

We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process.

We welcome and consider applications from all qualified candidates, regardless of characteristics.

We offer reasonable adjustments / accommodations to help all candidates to perform at their best.

If you have a need for any adjustments / accommodations, please complete the section in the application form.

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