Find Qc analyst Jobs in Greystones County Wicklow

Biochemical QC Analyst
Neogen —Bray, County Wicklow
- Full-time
- Analysis skills
- No degree
- Quality control
QC Analyst
SGS —Wicklow, County Wicklow
- €43,000–€48,000 a year
- Full-time
- Analysis skills
- No degree
- Organisational skills
Quick apply
QC Laboratory Technician
PSC Biotech —Dublin, County Dublin
- Presentation skills
- No degree
- Organisational skills
5d

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QC Laboratory Technician
PSC Biotech —Dublin, County Dublin
Ensure compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current good manufacturing Practices (cGMP) in the…
5d
QC Analyst
Servier —Arklow, County Wicklow
Ensure thorough understanding and adherence to all relevant and current SOPs and Work Instructions. A Bachelor’s degree in Chemistry, Biology, Biochemistry,…

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Biochemical QC Analyst

Neogen -
Bray, County Wicklow

Apply Now

Job details

Full-time

Qualifications

Biochemistry
Analysis skills
Quality control
Chemistry
Quality systems
Manufacturing
Communication skills

Full job description

It's fun to work in a company where people truly believe in what they are doing!

Are you an experienced quality control professional with a strong understanding of biochemical analysis, validation processes and regulated manufacturing environments? We are seeking a Biochemical QC Analyst to support validation activities, analyse quality data and help ensure products are manufactured in line with applicable regulatory requirements, internal standards and current industry practices.

Key Responsibilities

Prepare installation, testing and validation procedures, protocols and related documentation in accordance with regulatory and internal quality requirements.
Compile, review and analyse validation and quality control data, identifying trends, discrepancies and areas for improvement.
Prepare clear validation reports and make evidence-based recommendations for process improvements or corrective actions.
Investigate and troubleshoot validation or quality-related issues, supporting root cause analysis and practical resolution.
Maintain accurate validation documentation, records and files in line with good documentation practice and data integrity expectations.
Collaborate with cross-functional teams to support compliant manufacturing and continuous improvement initiatives.

Job Requirements

Relevant third-level qualification in Biochemistry, Chemistry, Biotechnology, Pharmaceutical Science or a related scientific discipline.
Previous experience in a QC, validation or quality role within a regulated manufacturing, pharmaceutical, biotechnology or life sciences environment.
Working knowledge of validation principles, quality systems, GMP and applicable regulatory expectations.
Strong analytical skills with the ability to interpret data, prepare reports and recommend appropriate actions.
Excellent attention to detail and a commitment to accurate documentation and compliance.
Effective communication and problem-solving skills, with the ability to work both independently and as part of a team.

What We Offer

A standard benefits package.
The opportunity to contribute to quality and compliance in a regulated scientific environment.
A professional, collaborative workplace where continuous improvement and high standards are valued.
Supportive team engagement and opportunities to develop your technical and quality expertise.

If you are ready to take the next step in your quality control career and apply your scientific expertise in a regulated manufacturing setting, we'd love to hear from you. Join our team and help support the delivery of high-quality products through robust validation and quality practices.

Come Be Part Of A Mission that Matters!

From inside the farm gate to our dinner plates, Neogen protects the world’s food supply. Through a variety of animal healthcare products, to food safety solutions for dangerous bacteria, allergens, toxins, drug residues and much more, Neogen is there — and you can be too.

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