Technical Services Engineer – Product/Process
POSITION PURPOSE
As part of the Technical Services function the Technical Services Engineer – Product/Process will be responsible for supporting the development & optimization of aseptic pharmaceutical manufacturing processes, ensuring compliance with regulatory standards, and driving continuous improvement initiatives as well as Technical Transfer, Alternate Source Qualification and New Product Introductions. This role involves collaboration with cross‑functional teams, including Production, Quality, Regulatory and Engineering, to enhance efficiency, scale‑up processes, perform NPIs and troubleshoot manufacturing challenges.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Process Development & Optimization:
* Design, develop, and optimize pharmaceutical manufacturing processes, ensuring robust, scalable, and cost‑effective production.
* Conduct and document process risk assessments (e.g., FMEA) and implement risk‑mitigation strategies.
* Lead investigations into deviations, non‑conformances, and root cause analyses.
* Support scale‑up, tech transfer, ASQ and commercialization of new products in respect of study design, protocol generation and reporting of outcomes.
Validation & Compliance:
* Preparation and execution of Process Validation (PV) protocols (e.g., PPQ) and Continued Process Verification (CPV).
* Generation of change controls aligned with site procedures to support product/process changes.
* Ensure all process changes comply with cGMP, FDA, EMA, and other regulatory requirements.
* Support regulatory filings (e.g., CMC sections of regulatory filings) with process data and technical justifications.
Manufacturing Support & Troubleshooting:
* Provide on‑the‑floor technical support for routine manufacturing operations, deviations, and process issues.
* Collaborate with production and quality teams to ensure consistent process performance.
* Analyze process data trends to drive continuous improvement and reduce variability in critical quality attributes (CQAs).
NPI, Technical Transfer & Scale‑Up:
* Support technology transfers between development, pilot, and commercial‑scale manufacturing.
* Work closely with R&D, and Site Operations teams to ensure smooth process transitions.
* Define critical process parameters (CPPs) and critical quality attributes (CQAs) for robust transfer and/or scale‑up.
* Identify and implement process improvements using Lean, Six Sigma, and other problem‑solving methodologies.
* Evaluate and introduce new technologies to enhance efficiency, reduce waste, and improve yield.
* Support cost‑reduction initiatives while maintaining quality and compliance.
Perform other duties as assigned.
QUALIFICATIONS & SKILLS
The qualifications listed below are representative of the minimum knowledge, skill, and/or ability required.
* Education: Bachelor’s or Master’s degree in Chemical Engineering, Pharmaceutical Engineering, Biotechnology, or a related field.
* Experience: 3–7 years of experience in pharmaceutical manufacturing, process engineering, or technical services.
* At least two years experience in sterile injectables or biologics manufacturing.
* Technical Skills:
* Strong knowledge of aseptic processing, terminal sterilization, and lyophilization.
* Experience with process validation (PPQ), DOE, and statistical process control (SPC).
* Proficiency in cGMP, Annex 1, FDA, EMA, and ICH guidelines for sterile products.
* Proficient in the generation of cGMP documentation e.g. protocols, report, change control etc.
* Practical experience with filling machines, isolators, autoclaves, depyrogenation tunnels, and lyophilizers, modes of operation, critical process parameters etc.
* Good knowledge of aseptic behaviours, filter integrity testing, single use systems etc.
* Proficiency in data analysis tools (e.g., Minitab) and process modeling software.
* Soft Skills:
* Strong analytical and problem‑solving skills.
* Excellent communication and cross‑functional collaboration abilities.
* Ability to manage multiple projects in a fast‑paced environment.
Preferred Qualifications:
* Six Sigma or Lean Manufacturing certification.
* Experience with automation systems (e.g., SCADA, MES).
* Knowledge of process analytical technology (PAT).
Seniority level
Mid‑Senior level
Employment type
Contract
Job function
Industries: Engineering Services, Pharmaceutical Manufacturing, and Biotechnology Research
Location: Galway, County Galway, Ireland
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