Process Co-ordinator
Process Co-ordinator
Posted on :
01-08-2025
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1 Vacancy
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Job Description
Work Schedule
12 hr shift/nightsEnvironmental 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 materialsJob 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 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 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.
Employment Type
Full-Time
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