Find Document control Jobs in Cork County Cork

QC Analyst - 4 Cycle Shift (TEMPORARY)
BioMarin —Cork, County Cork
- Full-time
- Engineering
- Master's degree
- Bachelor's degree
Medical Scientist Haematology (Part Time Hours)
Mercy University Hospital —Cork, County Cork
- €45,279–€75,148 a year
- Part-time
- Acute care
- Rehabilitation centre
- Quality control
Quick apply
9h
External Manufacturing Supply Manager
GE HEALTHCARE —Cork, County Cork
- Engineering
- ERP systems
- Project management
Workplace Solutions - EMEA Senior Contract Specialist - Associate/VP, Cork — Share Plan Services
JPMorganChase —Cork, County Cork
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
1d
Project Manager: Civil Projects
Roadform —Cork, County Cork
- AutoCAD
- Microsoft Office
- Contracts
Site Engineer - Cork
McGinty & O'Shea —Cork, County Cork
- Civil Engineering
- Construction Management
- Communication skills
Quantity Surveyor
Lanstephen —Cork, County Cork
- Full-time
- Analysis skills
- Project management
- IT
- Annual leave
Quick apply
2d
International Tax Manager
Arlo Technologies, Inc. —Cork, County Cork
- Full-time
- No degree
- AI
- Communication skills
Senior Electrical Engineer
PM Group —Cork, County Cork
- Project management
- Electrical Engineering
- Communication skills
Senior Principal Digital IC Design Engineer
onsemi —Cork, County Cork
- Full-time
- Doctoral degree
- English
- Master's degree
- Work from home
Senior Civil Engineer
Easyfresh —Cork, County Cork
- €52,994.64–€82,958.83 a year
- Full-time
- AutoCAD
- Bachelor's degree
- Construction
Quick apply
3d
Security Architect
Forcepoint International Technology Limited —Cork, County Cork
- Full-time
- Azure
- Computer Science
- AWS
Quick apply
11h

More jobs to discover

Find similar jobs that you might be interested in.

Medical Scientist Haematology (Part Time Hours)
Mercy University Hospital —Cork, County Cork
MUH reserves the right to create a panel for this post from which permanent, fixed term and specified purpose vacancies of a full or part time duration may be…
€45,279–€75,148 a year
Quick apply
9h

I want to receive the latest job alerts for document control in cork county cork

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

document control jobs near cork county cork

Site Engineer jobs in Cork, County Cork

QC Technician jobs in Cork, County Cork

Quantity Surveyor jobs in Cork, County Cork

Security Architect jobs in Cork, County Cork

Tax Manager jobs in Cork, County Cork

Site Engineer jobs in County Cork

Site Engineer jobs in County Kerry

Site Engineer jobs in Louth, County Louth

Technician jobs in Dublin, County Dublin

Qc Technician jobs in Tipperary, County Tipperary

Language Specialist jobs in Dublin, County Dublin

Senior Network Engineer jobs in Dublin, County Dublin

Hospital Play Specialist jobs in Dublin, County Dublin

Senior Contract Specialist jobs in Dublin, County Dublin

Senior Business Analyst jobs in Dublin, County Dublin

Retail Store Manager jobs in Dublin, County Dublin

Quantity Surveyor jobs in Wexford, County Wexford

Chartered Valuation Surveyor jobs in Dublin, County Dublin

Quantity Surveyor jobs in County Kerry

Quantity Surveyor jobs in Galway, County Galway

QC Analyst - 4 Cycle Shift (TEMPORARY)

BioMarin -
Cork, County Cork

Apply Now

Job details

Full-time | Temporary

Qualifications

Engineering
Master's degree
Bachelor's degree
Organisational skills
Communication skills

Full job description

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 Control (Shift Role)

Location: BioMarin – QC In‑Process | 4‑Cycle Shift Pattern

An exciting opportunity has arisen for a QC Analyst to join BioMarin’s QC In‑Process Control team, based in a newly 5S‑certified analytical laboratory. This role offers excellent exposure across both Drug Substance and Drug Product manufacturing, in a fast‑paced, highly compliant GMP environment.

The QC In‑Process team delivers comprehensive in‑process analytical and microbiological testing, supporting manufacturing operations across the site. In addition, the team performs testing of incoming raw materials and packaging materials to support downstream pack line activities.

Due to the critical, around‑the‑clock nature of in‑process testing, this role is part of a 4‑cycle shift team, supporting continuous manufacturing operations.

QC In‑Process is a high‑performing, team‑based group, where colleagues are flexible, multi‑skilled, and empowered to make decisions. The team operates to an exceptionally high standard of quality, compliance, and safety, with a strong focus on continuous improvement, standard work, and 5S.

This role requires a high level of initiative, energy, and motivation, together with strong organisational skills and the ability to thrive in a dynamic manufacturing environment.

Role Responsibilities

Reporting to the QC Team Lead, the QC Analyst is responsible for supporting internal customers by delivering high‑quality, compliant test results in accordance with GMP standards.

Key responsibilities include, but are not limited to:

Perform primary review of QC raw data and trend results
Prepare protocols, summaries, and reports, including documents submitted directly to pharmaceutical regulatory agencies
Draft and update QC Standard Operating Procedures (SOPs)
Act as a technical subject matter expert (SME) and provide training and support to other analysts in areas of expertise
Evaluate analytical and microbiological results against defined acceptance criteria
Conduct and document laboratory investigations through to completion
Maintain the laboratory in a constant state of audit and inspection readiness
Interact directly with regulatory agency inspectors during audits and inspections
Interface with other BioMarin functions including Manufacturing, Quality Assurance, Facilities, and external contractors as required
Other duties as assigned

Desirable Skills and Attributes

Excellent written and verbal communication skills
Strong customer focus, with personal accountability for speed, quality, and accuracy of delivery
Self‑motivated, with the ability to work under pressure in a fast‑paced environment
Team‑oriented, with active participation in team development and continuous improvement, including standard work and 5S
Demonstrated success in achieving goals as part of a high‑performing team in a growing organisation
Proven adaptability and flexibility to support an evolving operational environment

Education and Experience

BSc in a scientific or engineering discipline with 5+ years of relevant cGMP laboratory experience
or
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.

Apply Now

Refine Your Search

document control jobs in cork county cork

QC Analyst - 4 Cycle Shift (TEMPORARY)

Medical Scientist Haematology (Part Time Hours)

External Manufacturing Supply Manager

Workplace Solutions - EMEA Senior Contract Specialist - Associate/VP, Cork — Share Plan Services

Project Manager: Civil Projects

Site Engineer - Cork

Quantity Surveyor

International Tax Manager

Senior Electrical Engineer

Senior Principal Digital IC Design Engineer

Senior Civil Engineer

Security Architect

More jobs to discover

I want to receive the latest job alerts for document control in cork county cork

Related Searches

Explore jobs in more locations

QC Analyst – In‑Process Control (Shift Role)

Role Responsibilities

Desirable Skills and Attributes

Education and Experience

Jobseeker tools

Employer Tools

Browse

Stay Connected