Find pharmaceutical quality control Jobs in dublin, d

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Senior Specialist MS&T

PSC Biotech -
Dublin, County Dublin

Apply Now

Job details

Permanent
1 day ago

Qualifications

Biology
Buffer (application)
Chemical Engineering
Lean
Data analysis skills
Master's degree
Six Sigma
Bachelor's degree
Continuous improvement
Technical writing
Chemistry
Manufacturing
Leadership

Full job description

Job Information

Date Opened

06/05/2026

Job Type

Contract

Industry

Pharma/Biotech/Clinical Research

Work Experience

5+ years

City

Dublin

State/Province

Dublin

Country

Ireland

Job Description

About PSC Biotech

Who are we?

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

‘Take your Career to a new Level’

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

Employee Value Proposition

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

Job Description

The Senior Specialist MS&T (DS Process Science) delivers a range of technical support to the Drug Substance Business: supporting technical investigations within the Integrated Process

Team, supporting significant projects in the MS&T laboratory, while creating an inclusive culture that energizes a Safety First, Quality Always, with a continuous improvement mindset.

Requirements

Primary Responsibilities

Leading, designing, supporting and executing experimental design, data analysis andinterpretation to resolve complex deviations.
Leading process improvement and troubleshooting with end-to-end product focus.
Assist in, and facilitate investigations, ensuring effective Root Cause Analysis and CAPAs.
Executing experimental design, data analysis and interpretation
Supporting the process sciences team during small scale model run execution, including buffer preparation, equipment set up, run execution, sampling and data
analysis.
Author and review standard operating procedures (SOPs), protocols and reports as required.
Support continuous improvement through Lean Six Sigma methodologies.
Supporting alignment and knowledge exchange with development organizations, other commercial nodes and external manufacturing partners.

Qualification and Experience

General Competencies

Demonstrated leadership and change management skills with a continuous improvement focus
Proven track record of delivering high performance through development and coaching of a team.
Evidence of continuous professional development.
Strong collaboration to promote knowledge sharing and implementation of best practices across the site.
Desire to continuously learn, improve and develop.

Technical

Demonstrated leadership and proven track record of delivering projects of technical complexity
Knowledge of and experience in applying Six Sigma and Lean methodologies.
Desirable evidence of continuous professional development.
Experience in drug substance process development, process characterisation studies, downstream technology, and/or process modeling.
Experience in designing and executing experimental programs in the laboratory. Working knowledge of statistical methods for DOE design and data analysis (e.g., JMP or Design
Expert software)
Technical experience in the drug substance manufacture of biological molecules at thelab, pilot and/or commercial-scale.
Experience with technology transfer, regulatory filing, and commercial drug substance manufacturing of biologics is a plus.
Technical writing skills.

Minimum Education/Experience

A Masters degree in Biological Sciences/Chemistry /Chemical Engineering/Biological Engineering with 2+ years experience or a Bachelor’s degree in Biological
Sciences/Chemistry /Chemical Engineering/Biological Engineering with 4+ years experience
Experience leading technical related projects.

Required Skills:

Data Analysis, Estimation and Planning, Immunochemistry, Immunology, Manufacturing Quality Control, Microbiology, Process Design, Process Improvements, Project Planning, Regulatory Compliance, Root Cause Analysis (RCA), Six Sigma, Standard Operating Procedure (SOP),Technical Support, Technical Writing, Technology Transfer

Apply Now

Refine Your Search

pharmaceutical quality control jobs in dublin, d

Senior Specialist MS&T

Lab IT Engineer

Senior Estimator

Eirdata Regional Manager ( Dublin / Leinster )

Senior Mechanical Engineer

Automation Engineer (Rockwell)

Senior CSA Design Engineer

Tax Risk & Controversy - Manager

Senior Estimator

Electrical Engineer

Senior Mechanical Design Engineer

Electrical Project Engineer

Senior Pharmacist - UPMC Sports Surgery Clinic, Dublin

Construction Project Director - UK, Ireland & Europe

Senior Electrical Engineer

Electrical Design Engineer

ISC E2E Value Stream Project Engineer

Senior Electrical Design Engineer

Electrical Project Manager - Dublin

Senior Electrical Engineer

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