QC Analyst

QC Analyst - 23 Month Contract (Temporary)QC Analyst - 23 Month Contract (Temporary)

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Who We Are

BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.

Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.

Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best – people with the right technical expertise and a relentless drive to solve real problems – and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.

About Technical Operations

BioMarin's Technical Operations group is responsible for creating our drugs for use in clinical trials and for scaling production of those drugs for the commercial market. These engineers, technicians, scientists and support staff build and maintain BioMarin's cutting-edge manufacturing processes and sites, provide quality assurance and quality control to ensure we meet regulatory standards, and procure the needed goods and services to support manufacturing and coordinating the worldwide movement of our drugs to patients.

QC Analyst – In-Process

23 Month Contract (Shift)

Shift Role - Onsite Only - Shanbally, Cork

Closing date Wednesday 11th June 2025

Exciting opening in a newly 5S certified Analytical lab within QC In-Process team at BioMarin. This is a very diverse role which encompasses all the in-process testing (both analytical and microbial) for the Drug substance and Drug product facilities on site. In addition, the in-process team support testing for all incoming raw materials and testing of the incoming packaging materials for the pack lines.

Due to the fast-paced nature of the in-process group the team is a shift based team, operating a 4 cycle shift pattern (see below).

QC In-Process are a high-performing, team-based group, where colleagues are flexible, multi-skilled and empowered to make decisions. QC In-Process operates to an extremely high standard of quality and compliance.

A high level of initiative, energy and motivation are key role requirements, as well as organizational skills.

Reporting to the QC Team Lead/Manager, the primary role of the QC Analyst is to provide support to internal customers by providing quality testing and delivering results in accordance with GMP standards.

Other responsibilities include:

• Perform primary review of QC raw data and trend results
• Prepare protocols, summaries, and reports—often for direct submission to pharmaceutical regulatory agencies
• Draft/Update QC SOPs
• Act as technical resource (SME) and train other analysts in areas of expertise
• Evaluate results against defined acceptance criteria
• Conduct and document laboratory investigations to completion
• Maintain the laboratory in an inspection-ready state
• Interact directly with regulatory agency inspectors during audits
• Interface with other BioMarin departments (Manufacturing, Quality Assurance, Facilities, etc.) and contractors as necessary
• Other Duties as assigned.
  
  

Desirable Skills:

• Excellent communication skills both written and verbal
• Customer focus; takes personal responsibility for speed; quality and accuracy of delivery
• Self-motivated and ability to work under pressure
• Team Leadership – active participation team development and continuous improvement including standard work and 5S
• Successful track record in achieving goals as part of a team within a growing, dynamic environment
• Demonstrated adaptability and flexibility to support a growing organization
  
  

Education:

• BSc in a scientific/engineering discipline with 5+ years (MSc with 3+ years) of relevant (cGMP) laboratory experience.
  
  

Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.

Equal Opportunity Employer/Veterans/Disabled

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.Seniority level

• Seniority levelMid-Senior level

Employment type

• Employment typeContract

Job function

• Job functionQuality Assurance
• IndustriesBiotechnology Research and Pharmaceutical Manufacturing

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