Biopharmaceutical Process Technologist Amgen Ireland

Position Overview: Process Technologist in Manufacturing

We are seeking diligent and technically skilled Process Technologists to join our global Manufacturing & Operations teams. In this vital hands-on role, you will be responsible for executing and supporting the core production processes that create our life-changing biologic medicines. You will operate at the intersection of science, technology, and strict regulatory compliance, ensuring that every batch meets the highest standards of quality, safety, and efficacy. This position is the operational engine of our therapeutic production, ideal for individuals who thrive in structured, precise environments and are motivated by contributing to a mission that impacts patient lives worldwide.

This is a shift-based, on-site role within one of Amgen’s state-of-the-art manufacturing facilities. You will become an integral part of a highly trained team responsible for the reliable production of complex biologic drug substances or drug products.

Key Responsibilities & Operational Impact

Your daily work will directly contribute to the reliable supply of critical medicines. Your primary duties will include:

• GMP Manufacturing Operations: Execute routine and complex production operations according to established Standard Operating Procedures (SOPs) and Batch Records in a cGMP (current Good Manufacturing Practice) environment. This includes activities within upstream cell culture, downstream purification, formulation, fill/finish, or packaging operations.

• Aseptic Technique & Process Monitoring: Perform operations within cleanroom environments, utilizing strict aseptic technique. Monitor and control critical process parameters (CPPs) using sophisticated process automation systems (e.g., DCS, SCADA) and manual checks.

• Equipment Operation & Troubleshooting: Safely operate, set up, and perform basic troubleshooting on major bioprocessing equipment such as bioreactors, chromatography skids, filtration systems, vial washers, filling lines, and lyophilizers.

• Documentation & Compliance: Maintain impeccable real-time documentation. Complete batch records, logbooks, and work orders with a high degree of accuracy and attention to detail. Actively participate in investigations for process deviations or non-conformances.

• Safety & Quality Advocacy: Adhere to all safety protocols, including those for hazardous materials and high-pressure systems. Uphold a culture of quality by following procedures, identifying potential risks, and advocating for best practices in every task.

• Continuous Improvement: Participate in root cause analysis and contribute ideas for process optimization, lean manufacturing initiatives, and safety improvements. Support technology transfer and validation activities for new processes.

Candidate Profile: Qualifications and Attributes

We are looking for operational professionals with a strong technical foundation and a commitment to quality. The successful candidate will demonstrate:

Essential Technical Competencies & Experience:

• An Associate’s degree, Bachelor’s degree, or equivalent qualification in Biotechnology, Chemical Engineering, Biochemistry, Microbiology, Pharmaceutical Sciences, or a related STEM field.

• 1-3 years of relevant experience in a cGMP manufacturing environment within the biotechnology, pharmaceutical, or related regulated industry (e.g., medical devices, diagnostics). Recent graduates with strong co-op or internship experience in a GMP setting will be considered.

• Practical, hands-on experience with bioreactor operations, purification systems, or automated filling/packaging equipment is highly desirable.

• Fundamental understanding of aseptic processing, cleanroom behaviors, and microbial control.

• Strong mechanical aptitude and the ability to follow complex technical instructions with precision.

• Proficiency with basic computer systems for documentation and process control.

Core Professional Attributes:

• An unwavering commitment to safety, quality, and compliance in every action.

• Excellent attention to detail and procedural discipline.

• Effective teamwork and communication skills, with the ability to work collaboratively in a dynamic, shift-based environment.

• A proactive, problem-solving mindset and the ability to remain calm under pressure.

• Flexibility to work various shifts (including nights, weekends, and holidays) as required by a 24/7 manufacturing operation.

• Fluency in the local language of the applied-for site and professional proficiency in English.

Global Employment Offering: Compensation & Benefits

Amgen is committed to investing in our workforce with a comprehensive, competitive total rewards package tailored to major employment regions.

• Competitive Compensation Package: We offer a strong base salary, shift differential pay for non-standard hours, and annual performance-based bonus potential. Compensation is benchmarked competitively within each local market (Ireland, Germany, Canada, Singapore, USA).

• Global Career Pathways: This role offers a defined career ladder within Global Operations. Opportunities for advancement into specialist, supervisory, or technical support roles are clear and supported by our commitment to internal talent development.

• Industry-Leading Benefits Program:

  • Health & Wellbeing: Comprehensive medical, dental, and vision plans for employees and eligible dependents.

  • Financial Security: Competitive retirement/pension plans (e.g., 401(k) with company match in USA, PRSA in Ireland, RRSP in Canada), life insurance, and income protection plans.

  • Paid Time Off & Flexibility: Generous holiday/vacation entitlements, personal days, and sick leave aligned with local norms. We support work-life balance through structured shift patterns.

  • Career Investment: Robust onboarding and continuous training on GMP, safety, and advanced technical skills. Tuition reimbursement programs to support further education.

• Purpose-Driven Culture: Work in a mission-oriented environment where you can see the direct link between your daily tasks and patient outcomes. Experience our inclusive culture through team events and site-wide meetings.

Application Process: Steps to Join Amgen

Amgen is an Equal Opportunity Employer and values diversity in its workforce. We encourage applications from all qualified candidates regardless of nationality, background, or identity.

Our hiring process is designed to be thorough and to ensure a mutual fit:

1. Online Application: Submit your CV/resume and complete your profile via our official careers portal (link below). Tailor your application to highlight relevant technical coursework, laboratory skills, and any GMP or bioprocessing experience.

2. Recruiter Screening: A preliminary conversation with a Talent Acquisition professional to discuss your background, career interests, and the specifics of the role and location.

3. On-Site/Virtual Interview Panel: Engage with the Hiring Manager and potential peers in a panel interview. This will include behavioral and situational questions and a detailed discussion of your technical knowledge and hands-on experience.

4. Site Tour & Practical Discussion: For on-site roles, a facility tour or virtual walk-through may be arranged, followed by further discussions with senior operations staff.

5. Offer & Onboarding: Successful candidates will receive a formal offer letter. Our global onboarding program is designed to integrate you seamlessly into Amgen and your local team.

Begin a Career with Purpose at Amgen

If you are a technically minded professional seeking a stable, rewarding career where precision meets purpose, we invite you to apply. This is more than a manufacturing job; it is an opportunity to be part of a team that delivers hope to patients around the world.

To Apply for Opportunities in Ireland, Germany, Canada, Singapore, or the USA:

APPLY ONLINE HERE: Amgen Global Careers Portal

• Primary Hiring Locations Include:

  • Ireland: Dun Laoghaire (County Dublin)

  • Germany: Munich, Augsburg

  • Canada: Burnaby (British Columbia), Mississauga (Ontario)

  • Singapore: Tuas

  • USA: West Greenwich (Rhode Island), Thousand Oaks (California), Juncos (Puerto Rico), Holly Springs (North Carolina), and other major sites.

• Amgen thanks all applicants for their interest. Only those selected for an interview will be contacted. All applications are treated with the highest level of confidentiality.

• Candidates of all nationalities with the legal right to work in the specified countries are welcome to apply.