Work Schedule

12 hr shift/nights

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials

Job Description

Job Description

Join our extraordinary team as a SWC6 Process Co-ordinator at Thermo Fisher Scientific Inc. and be at the forefront of manufacturing excellence! This role offers you the chance to work in a high-reaching environment where your skills will be applied to their fullest potential.

Position Location: UK - Swindon – Kingfisher Drive

Responsibilities:

Successfully acquire and maintain a GMP license, ensuring compliance at all times.Coordinate team adherence to site metrics, including DR’s, CAPA’s, CC’s, IDHammer tickets.Step in for the Manager – Commercial Operations as needed, taking responsibility for all associated activities.Ensure team members are multi-skilled to perform tasks perfectly, safely, and in strict compliance with procedures.Keep team training up to date, ensuring the right curricula are assigned.Deliver the weekly production schedule by ensuring timely availability of skills, materials, components, equipment, and documentation.Lead investigations and author minor deviations with detailed knowledge of products and processes.Ensure real-time completion of batch documentation, with daily routine checks and compliant BMR entries.Set and communicate performance measures and targets, leading tier 1 huddle meetings.Actively participate in Practical Process Improvement (PPI) and Operational Excellence initiatives.Support the introduction of new products, equipment, and processes.Lead consumable orders and usage for financial control.Serve as team EDMS author and approver, ensuring accurate and timely management of documentation.Maintain facility cleanliness in line with 5s principles.Identify and implement Lean process improvements, reducing waste and non-value adding activities.

Gmp:

Coach and mentor staff to ensure products are manufactured and documentation completed in accordance with GMP, SOPs, and other regulatory requirements.Conduct timely deviation and complaint investigations to identify root causes and close corrective/preventative actions.Complete surveillance audits and support Self-Inspection audits.Maintain a high level of cleanliness and orderliness at all times.Work towards achieving a Silver License badge for aseptic filling if applicable.

People Management:

Develop an encouraging and successful work environment, providing mentorship to your team.Handle team People tasks: recruit diverse talent, train, set goals, provide feedback, and conduct appraisals.

Role model the 4i values:

Integrity – Intensity – Innovation – Involvement

Eh&s:

Understand and adhere to emergency procedures and safe systems of work.Ensure compliance with environment, health and safety, and security policies and procedures.Report and investigate all accidents, near misses, and rule breaches promptly.

Minimum Requirements/Qualifications:

Validated experience leading, supervising, and motivating a team.Proactive approach with the ability to lead your team’s workload, priorities, and development.Technical writing skills for reports, investigations, and SOPs.Experience in pharmaceutical or regulated production operations, such as the food industry.Leadership experience and supervisory management qualifications, preferably to NVQ level 3 or equivalent.Lean manufacturing and/or Lean Six-Sigma training and experience desirable.