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Process Scientist - Job Opportunity at PE Global

Sligo, Ireland
Contract
Mid-level
Posted: June 5, 2025
On-site
EUR 65,000 - 85,000 annually based on Ireland's competitive biopharmaceutical market, with contract roles typically commanding 15-25% premium over permanent positions. The Sligo location may offer slightly lower compensation than Dublin but provides better work-life balance and lower living costs, making the total value proposition competitive for mid-level professionals.

Benefits

12-month contract duration providing focused project experience and flexibility for career transitions
Opportunity to work with leading biologics company offering exposure to cutting-edge pharmaceutical manufacturing processes
Direct collaboration with global science and quality teams enhancing international network and knowledge transfer
Training and supervisory responsibilities accelerating leadership development and team management skills

Key Responsibilities

Drive strategic development of manufacturing processes for new product introductions, directly impacting company's pipeline expansion and market competitiveness
Provide critical operational technical support for process issue resolution, ensuring manufacturing continuity and quality standards that protect patient safety
Execute comprehensive gap analysis and facility fit studies that determine feasibility and investment requirements for new product launches
Lead process safety and risk analysis initiatives that safeguard operations and ensure regulatory compliance across NPI activities
Monitor and analyze critical process data during manufacturing operations, enabling data-driven decisions that optimize production efficiency
Develop and maintain specifications for NPI materials and consumables, establishing quality standards that ensure product consistency
Lead complex risk assessments including PFMEA and EHS evaluations that protect both product quality and worker safety
Create comprehensive NPI documentation including transfer plans, protocols, and manufacturing batch records that enable successful product commercialization
Collaborate with global cross-functional teams on process development strategies that align with company's long-term product portfolio objectives
Lead product and process investigations that resolve manufacturing challenges and drive continuous improvement initiatives
Mentor and train operations personnel on NPI processes, building organizational capability and ensuring knowledge transfer for sustainable operations

Requirements

Education

Third level degree in a relevant engineering, science or technical discipline required. Masters Qualification in relevant technical discipline desirable.

Experience

3 years' experience in pharmaceutical process engineering, with relevant experience of batch processing, technical transfers, scale up, in a cGMP pharmaceutical or Biologics industry. Minimum of 1 years in a similar type of role. Minimum of 1 years within Pharmaceutical or Bio Industries.

Required Skills

Experience in new product introductions to Biologic facilities Strong technical and operational knowledge of unit operation within a fill finish facility Experience with batch processing Technical transfers Scale up experience cGMP pharmaceutical or Biologics industry knowledge Process safety and risk analysis Gap analysis and facility fit studies PFMEA and EHS risk assessments Process data monitoring and analysis
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Sauge AI Market Intelligence

Industry Trends

The biologics sector is experiencing unprecedented growth driven by personalized medicine and advanced therapeutics, with Ireland positioning itself as a global hub for biopharmaceutical manufacturing through significant government incentives and infrastructure investments. This trend creates sustained demand for process scientists specializing in NPI activities as companies race to bring innovative treatments to market. Regulatory environments are becoming increasingly stringent with enhanced focus on process validation and risk management, particularly in biologics manufacturing where product complexity demands sophisticated process control strategies. This regulatory evolution drives premium compensation for professionals with demonstrated expertise in cGMP environments and risk assessment methodologies. The shift toward continuous manufacturing and Industry 4.0 technologies in pharmaceutical production is creating opportunities for process scientists who can bridge traditional batch processing with emerging digital manufacturing paradigms, particularly in facility modernization and technology transfer projects.

Role Significance

Typically operates within a cross-functional team of 8-12 professionals including quality assurance specialists, regulatory affairs experts, and operations personnel, while interfacing with global teams of 20-30 members across multiple geographic regions.
This mid-level position carries significant technical responsibility with direct impact on product commercialization success, requiring independent decision-making on complex process development challenges while collaborating with senior global teams. The role bridges technical expertise with business objectives, positioning the incumbent as a key contributor to organizational growth.

Key Projects

Leading technical transfer projects for new biological products from development to commercial manufacturing scale Implementing process validation protocols for regulatory submissions and market authorization Conducting facility modernization assessments and equipment qualification programs Developing risk mitigation strategies for complex manufacturing processes involving sensitive biological materials

Success Factors

Demonstrated ability to navigate complex regulatory requirements while maintaining operational efficiency, as biologics manufacturing faces the most stringent compliance standards in the pharmaceutical industry Strong analytical and problem-solving capabilities essential for troubleshooting sophisticated biological processes where minor variations can significantly impact product quality and patient safety Excellent communication and collaboration skills crucial for working effectively with diverse global teams and translating technical concepts for various stakeholder audiences Adaptability and continuous learning mindset necessary to keep pace with rapidly evolving biotechnology and manufacturing technologies Project management proficiency required to coordinate multiple NPI activities simultaneously while meeting critical timeline and quality milestones

Market Demand

High demand driven by Ireland's position as Europe's second-largest biopharmaceutical manufacturing hub, with over 50 global pharmaceutical companies operating facilities and continuous expansion of production capacity requiring specialized NPI expertise.

Important Skills

Critical Skills

cGMP compliance expertise is absolutely essential as biologics manufacturing operates under the most stringent regulatory oversight, with any compliance failures potentially resulting in significant financial and reputational consequences for the organization Process risk assessment capabilities are critical given the complexity and sensitivity of biological products, where process variations can have severe implications for product efficacy and patient safety Technical transfer experience is vital for NPI success, as the ability to successfully scale processes from development to commercial manufacturing directly impacts product launch timelines and market success

Beneficial Skills

Digital manufacturing and data analytics skills are increasingly valuable as the industry adopts Industry 4.0 technologies and advanced process control systems Project management certification would enhance effectiveness in coordinating complex NPI activities across multiple functional areas and geographic regions Regulatory affairs knowledge provides additional career flexibility and deeper understanding of the commercial implications of process development decisions

Unique Aspects

The role offers direct exposure to cutting-edge biologics manufacturing in Ireland's rapidly expanding biopharmaceutical sector, providing experience with the most sophisticated pharmaceutical production technologies
Significant emphasis on global collaboration distinguishes this position, offering networking opportunities and cross-cultural project experience valuable for international career development
The combination of technical leadership responsibilities with hands-on operational support creates comprehensive skill development across the full spectrum of process science activities
Focus on NPI activities provides exposure to the complete product lifecycle from development through commercialization, offering broader business perspective than routine manufacturing support roles

Career Growth

Progression to senior technical roles typically occurs within 2-3 years with demonstrated success in NPI projects, while transition to management positions may require 3-5 years depending on leadership development and business needs.

Potential Next Roles

Senior Process Scientist or Principal Scientist roles focusing on strategic process development and cross-site technology transfer leadership Process Development Manager positions overseeing entire NPI portfolios and managing technical teams Regulatory Affairs Specialist roles leveraging deep process knowledge for submissions and agency interactions Manufacturing Excellence or Continuous Improvement leadership positions driving operational optimization

Company Overview

PE Global

PE Global operates as a prominent staffing and recruitment specialist serving Ireland's thriving life sciences sector, with particular strength in pharmaceutical and biotechnology placements. The company maintains extensive relationships with multinational pharmaceutical companies and emerging biotech firms, providing access to premium contract and permanent opportunities across Ireland's established biopharmaceutical corridor.

Recognized as a leading recruitment partner in Ireland's life sciences sector, PE Global benefits from the country's strategic position as a European pharmaceutical manufacturing hub and maintains strong relationships with both established pharmaceutical giants and innovative biotech companies establishing Irish operations.
This Sligo-based opportunity reflects Ireland's distributed biopharmaceutical manufacturing landscape, where major companies have established significant operations outside Dublin to leverage regional talent pools, competitive operating costs, and government incentives supporting rural industrial development.
Contract roles through PE Global typically offer exposure to established pharmaceutical companies with mature operational cultures emphasizing compliance excellence, continuous improvement, and global collaboration, providing valuable experience for career advancement in the international biopharmaceutical industry.
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