Biibhr

Senior Engineer I, Manufacturing Sciences

Ireland · Work style not stated · Full time

Apply on the employer’s site ↗See how well you match this job

You apply directly with the employer. ROLIVA does not submit applications from this page and is not the employer.

About the role

Description from the employer’s posting. Check the employer’s page for the current version.

  • EmployerBiibhr
  • LocationIreland
  • Work styleWork style not stated
  • Employment typeFull time
  • Employer posted

About This Role:
As a Senior Engineer I, you will play a pivotal role in providing hands-on process and manufacturing sciences expertise to support technology transfers and ongoing clinical and commercial manufacturing programs. This position is integral to enabling critical manufacturing sciences activities, including new technology transfers, process performance qualifications (PPQs), and complex manufacturing investigations. Your consistent on-site presence will be essential for effective support of manufacturing operations, allowing for direct collaboration with manufacturing, engineering, quality, and partner functions. By observing process execution in real time, you will facilitate immediate technical intervention and accurate problem definition. Your leadership will be crucial in driving strategic initiatives and business process optimization, ensuring practical, executable, and sustainable solutions within the manufacturing environment. Focused on parenteral drug product manufacturing, this role is crucial for the successful execution of manufacturing strategies and strengthening cross-functional alignment.

Show full description

This role requires working on site for 5 days per week in Athlone.

What You’ll Do:

Provide hands-on, on-site technical leadership during manufacturing operations, making timely decisions during live processing for issue resolution.

Lead rapid process and product impact assessments and corrective and preventive actions (CAPAs) requiring immediate access to the manufacturing floor.

Engage daily with Manufacturing, Quality, and Process Engineering to ensure accurate development and execution of SOPs and batch records.

Perform real-time manufacturing campaign data review and trending using tools such as Tableau, Power BI, Statistica, and SIMCA.

Support technology transfers from development and external partners to manufacturing facilities, assessing process and facility fit.

Partner closely on-site with various teams to ensure rapid alignment and execution during active transfers.

Work alongside manufacturing and engineering teams to develop tests ensuring process execution as intended.

Identify optimization initiatives to improve productivity and process robustness through on-site observation.

Coordinate technical reports and data supporting deviations, CAPAs, and technology transfer optimization.

Serve as an on-site subject-matter expert in biopharmaceutical manufacturing and/or process development.

Support regulatory filings, requests for technical queries (RTQs), inspections, and audits as needed.

Who You Are:
You possess a keen ability to independently analyze complex technical issues and are adept at evaluating manufacturing data to identify improvement opportunities. Your skills in designing, executing, and communicating studies are exceptional, and you thrive in in-person engagements with cross-functional teams. Your strong presence on the manufacturing floor ensures accurate translation of process knowledge into execution, and your leadership style strengthens accountability and alignment across functions. You are committed to staying on the cutting edge of biopharmaceutical manufacturing, bringing your expertise and passion for process optimization to every project.

Required Skills:

Bachelor's Degree in a relevant field.

Strong technical expertise in manufacturing sciences/technical development for biologics or other parenteral drug products.

Proficiency in data analysis tools such as Tableau, Power BI, Statistica, and SIMCA.

Excellent communication and collaboration skills to engage with cross-functional teams.

Preferred Skills:

Experience supporting regulatory activities, including filings, inspections, audits, and interactions with global health authorities.

Proven track record in strategic initiatives and business process optimization within a manufacturing environment.

Demonstrated ability to lead technology transfers and manage complex manufacturing investigations.

Job Level: Professional

Why Biogen?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Staying safe while you apply

  • Never pay to apply, interview or accept an offer. ROLIVA never asks you for payment to apply to a job.
  • Apply only through the official “Apply on the employer’s site” button, on the employer’s own site, and check that a recruiter’s email uses that employer’s own domain rather than a free email address.
  • Be cautious of an offer made with no real interview, or pressure to decide quickly or share financial details early.

Does something look wrong with this listing? Use “Report broken link” in the role details, or read ROLIVA’s full job-safety guidance ↗.

Preparing for this role with ROLIVA

  • Check the fit.

    Compare the requirements with the experience you have confirmed, including gaps.

  • Prepare honestly.

    Build interview stories and application drafts from your own evidence.

  • Keep track.

    Save the role and record your own application status and follow-ups.

Create a free workspace or log in.

Software engineer jobs in Ireland

ROLIVA currently lists 152 open roles like this in Ireland.

Employers hiring for this

  • Elastic16 open roles
  • Toast13 open roles
  • Analog Devices11 open roles
  • Medtronic9 open roles
  • MongoDB7 open roles

Top skills asked for

Listings whose description mentions each term. A mention is not a requirement.

At a glance

  • Employment typeFull time
  • SenioritySenior
  • Employer posted
  • Added to ROLIVA
  • Last checked

Skills in this posting

Skills ROLIVA found in the employer’s own description above. A mention is not a requirement.

Tableau Power BI

Explore similar roles

Similar jobs