Global Quality Junior CSV Engineer

To contribute to project workstreams across core functions such as sales, commercial operations, procurement, and planning on a global scale. This position offers a CSV engineer the opportunity to play a pivotal role within a major business transformation programme, engaging with projects that impact the organisation worldwide.

MAIN DUTIES & RESPONSIBILITIES

• Assist in the development, implementation, and maintenance of Computer System Validation (CSV) documentation in compliance with regulatory requirements and Good Practice (GxP) standards.
• Support the validation of computerized systems across the company.
• Participate in risk assessments and impact analyses for new and existing computer systems.
• Collaborate with cross-functional teams such as Operational Quality, IT, Operations, Project Management and Test teams to ensure systems meet user requirements and regulatory guidelines.
• Assist with deviation investigations, change controls, and corrective and preventive action (CAPA) processes related to CSV activities.
• Remain up-to-date with the latest regulations, guidance documents, and industry best practices related to CSV and governing regulations.
• Support audits and inspections by providing relevant CSV documentation and expertise.
• Support the delivery of CSV projects with basic project management skills.
• Support the delivery of a global CSV plan in collaboration with Business, Technology and Quality teams.
• Contribute to the continuous improvement of CSV processes.
• Promote a culture of quality excellence that encourages ethical conduct and commitment to compliance.
• This role will involve some international interaction and some international travel.

QUALIFICATION, EXPERIENCE & SKILLS REQUIRED

• Suitable for Graduate with Bachelor’s degree in Engineering, Life Sciences, Computer Science, or a related discipline.
• Familiarity with GxP regulations (GMP, GDP, GCP, etc.) and their impact on computerised systems.
• Excellent written and verbal communication skills, with the ability to produce clear and concise technical documentation.
• Strong analytical and problem-solving abilities.
• Ability to work both independently and collaboratively within a team environment.
• Attention to detail and a commitment to maintaining high-quality standards.

QUALIFICATION, EXPERIENCE & SKILLS DESIRABLE

• Previous experience (e.g., internship, placement, or project) in a pharmaceutical or regulated environment.
• Knowledge of software development lifecycles, IT infrastructure, or data integrity principles.
• Understanding of risk management and change control processes.
• Familiarity with audit processes and regulatory inspections.
• Proficiency with electronic systems such as document management systems, SDLC management systems, testing systems.
• Strong organisational skills with the ability to manage multiple tasks and priorities.

Culture at Uniphar

• We have a People First approach, we do the right thing and take a stand for our people.
• We foster a strong Entrepreneurial Spirit where Adaptability, Commitment & Resilience is embodied in our way of working.
• We have a Common Purpose that connects our diversified businesses and people.
• Finally, Trust is at the heart of how we operate.

As we are a global team, there is flexibility to be based in one of Uniphar’s offices or work from home. There may be a need for face to face meetings in other locations, as needed. There may also some flexibility required in order to interact with colleagues or clients in their time zones (i.e. it’s not a ‘9 to 5’ type of job). In return, you will be joining an environment that understands how inter-twined work and life have become - and both the benefits and challenges that brings - and therefore offers a flexible, progressive way of supporting it through our Hybrid Working philosophy.