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 DRs CAPAs CCs 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 InvolvementEh&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 teams 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.Key Skills
Abinitio,Apache Tomcat,Ethernet,Hotel Management,Financial Planning & Analysis,AV
Employment Type : Full-Time
Experience : years
Vacancy : 1