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ProPharma

Freelance/Contract Automation Engineer Consultant

Hybrid

Glasgow, United kingdom

Senior

Freelance

26-09-2025

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Skills

Monitoring Research Data collection Databases Organization Front-end Development

Job Specifications

Company profile

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world's largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Job description

We are currently supporting a life-sciences client based in Scotland as they require interim support within their Automation group. At present we have a 9 month contract which can offers hours anywhere from 20-37.5 a week (flexible) and requires 1 week in 4 onsite in the Glasgow area (hybrid). This project is to commence immediately; it offers an excellent hourly rate and we are ideally searching for independent Consultants to support us with this project.

Responsibilities included:

Configure, install and manage Ignition gateways, including module installation, OPC connections, and database connections.
Connect Ignition to various data sources, including equipment PLCs, Cognex vision systems, databases, file repositories, and more.
Design and develop HMI and SCADA screens, dashboards, and reports within the Ignition platform - focussing on the Perspective module.
Implement data collection and logging from manufacturing equipment to facilitate real-time monitoring and historical analysis.
Collaborate with cross-functional teams, including business, production, IT, and engineering, to understand requirements and deliver effective solutions. Work with IT/Automation teams to ensure a suitable back-end database structure.
Troubleshoot and resolve issues related to the Ignition system, data connectivity, and application performance.
Develop and maintain technical documentation for the Ignition system, including design specifications, user manuals, and standard operating procedures.

Skills required

Must be educated to a BSc or higher within engineering or Computer Science discipline (or another technical field)
Thorough experience working in inductive automation ignition platforms or similar including HMI/SCADA
Excellent knowledge of Front-end development principles
User Interface & User experience design understanding would be highly desirable
Experience with industrial protocols and an understanding of relational databases
Excellent stakeholder skills
Can perform the project to the desired requirements set out in the job description

Additional Information

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

About the Company

At ProPharma, we help pharmaceutical, biotechnology, and medical device companies bring life-changing therapies to market. From early development through clinical, regulatory approval, and commercialization, we provide expert guidance to navigate complex challenges and accelerate success. Our mission is simple: improving patient health and safety by delivering the highest-quality regulatory, compliance, clinical research, pharmacovigilance, and medical information services throughout the entire product lifecycle. With over... Know more