Bioanalytical Sciences QC Analyst

TN Ireland; Dublin; On-site; EUR 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Bioanalytical Sciences QC Analyst to join their team in Dublin. This role offers an exciting opportunity to work in a leading aseptic manufacturing facility, contributing to quality control processes and ensuring compliance with industry standards. The successful candidate will engage in various QC activities, including sample management and analytical testing, while also driving continuous improvement initiatives. If you have a passion for biopharmaceuticals and a keen eye for detail, this position could be your next career step.

Qualifications

• 1-2 years of quality control experience in biopharmaceuticals or related fields.
• Experience with regulatory compliance in cGMP manufacturing and testing.

Responsibilities

• Responsible for QC activities including reagent management and GMP document review.
• Implement continuous improvement projects and support a lean culture.

Skills

Biopharmaceutical QC Experience

Regulatory Compliance

Technical Writing

Analytical Techniques

Project Management

Education

Bachelor's Degree in Life Sciences

Tools

GMP Documentation

Laboratory Equipment

Job description

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Bioanalytical Sciences QC Analyst, Dublin

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Client:

JobContax

Location:

Dublin, Ireland

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

1089c7692052

Job Views:

4

Posted:

06.05.2025

Expiry Date:

20.06.2025

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Job Description:

Employment Type: Contract

Work Location: Site based

Experience: 2 + years

Visa: EU passport or Stamp 4 visa required

Our client is a leading international Biotechnology company with a state of the art aseptic manufacturing facility in Dun Laoghaire, South Dublin.

The plant is one of the most dynamic in Ireland and is currently undergoing rapid expansion and capital investment.

This is an excellent opportunity to get experience into Ireland's leading aseptic manufacturing plant.

Under minimal supervision, responsible for one or more of the following activities in QC including: Reagent management, media preparation, GMP document review and management, sample and data management and some analytical testing.

Contributes to team by ensuring the quality of the tasks/services provided by self.

Contributes to the completion of milestones associated with specific projects or activities within team

The role undertakes implementing continuous improvement projects and supporting a lean culture and Right First Time (RFT). The role also represents the QC unit by liaising with internal and external customers.

With a high degree of technical flexibility, work across diverse areas within the lab

Plan and perform routine tasks with efficiency and accuracy.

Review, evaluate, back-up/archive, and approve analytical data.

Troubleshoot, solve problems and communicate with stakeholders.

Participate in audits, initiatives, and projects that may be departmental or organizational in scope.

Evaluate lab practices for compliance and operational excellence improvement on a continuous basis.

May participate in lab investigations.

May provide technical guidance.

May train others.

May contribute to regulatory filings.

May represent the department/organization on various teams

May interact with outside resources.

Requirements

1-2 years of biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical or medical device industry.

Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.

Understanding and application of principles, concepts, theories and standards of GMP QC analytical laboratories. Deepens technical knowledge through exposure and continuous learning

Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery

Some / limited experience in a wide variety of analytical techniques including but not limited to Cell-Based Potency Bioassays, Immunoassays, Cell Culture and Aseptic Technique

Take initiative to identify and drive improvements

Excellent verbal and written communication skills

Strong Technical writing skills for GMP documentation (e.g. investigations, procedures, change controls)

Escalate issues professionally and on a timely basis

Teamwork and Coaching others

Negotiation and Influence skills

Project Management and organizational skills, including ability to follow assignments through to completion

Demonstrated ability to work independently and deliver right first time results

Work is guided by objectives of the department or assignment

Follows procedures

Refers to technical standards, principles, theories and precedents as needed

May set project timeframes and priorities based on project objectives and ongoing assignments. Recognizes and escalates problems

Demonstrated leadership and communication skills

Auditing documentation and operation process

Demonstrated ability to interact with regulatory agencies

Package

Minimum 12 month contract with the possibility of an extension.

Onsite expectations: 5 days per week as this is a lab-based role.