Senior Packaging & Labelling Engineer: Validation Lead

Corin Group; Cirencester; On-site; GBP 58,000 - 63,000; Full time

Benefits offered by this job

Pension

Private medical insurance

Life assurance

Eye tests

Referral bonus

Job summary

Corin Group in Cirencester is seeking a Senior Packaging & Labelling Engineer to join the Validation & Sterility Assurance team onsite. You will lead packaging and labeling validation across a global portfolio, support regulatory compliance, and mentor a small team in a highly regulated medical device environment.

The role involves development and delivery of training, collaboration with Regulatory Affairs, R&D, Quality, Operations, and external partners, and ensuring deadlines are met.

Qualifications

• Strong analytical, investigative, and problem-solving skills.
• Excellent attention to detail.
• Ability to manage multiple priorities and complex technical projects.
• Strong written and verbal communication skills with the ability to influence stakeholders at all levels.
• Previous experience mentoring, coaching, or supervising others.
• Experience leading validation projects within a medical device manufacturing environment.

Responsibilities

• Monitor and validate packaging and labelling for medical devices.
• Lead validation projects and cross-functional collaborations.
• Review and approve labels, packaging BOMs, and technical documentation.
• Deliver training to operational teams and participate in recruitment when needed.
• Handle regulatory compliance activities and responses to authorities.
• Act as auditee during internal, customer, and regulatory audits.
• Mentor and develop junior team members.

Skills

Analytical skills

Problem-solving

Attention to detail

Communication

Mentoring

Validation leadership

Education

Degree in science/engineering

Job description

Corin Group in Cirencester is seeking a Senior Packaging & Labelling Engineer to join the Validation & Sterility Assurance team onsite. You will lead packaging and labeling validation across a global portfolio, support regulatory compliance, and mentor a small team in a highly regulated medical device environment.

The role involves development and delivery of training, collaboration with Regulatory Affairs, R&D, Quality, Operations, and external partners, and ensuring deadlines are met.