Warning
This job advert has expired and applications have closed.
Visual Inspection and Logistics Coordinator
| Posting date: | 17 June 2024 |
|---|---|
| Salary: | £22,500 to £23,500 per year |
| Hours: | Full time |
| Closing date: | 05 July 2024 |
| Location: | G20 0XA |
| Remote working: | On-site only |
| Company: | Curia (Scotland) Limited |
| Job type: | Permanent |
| Job reference: | SWBK1706 |
Summary
We have an opportunity to join our Visual Inspection and Logistics team based at our Glasgow, G20 site in the role of Visual Inspection and Logistics Coordinator. This role is part of the overall production team, where you will be working within a friendly and supportive environment to undertake training and development. The Logistics team works together to achieve good manufacturing practices (GMP) and delivery of customer expectations on time and in full (OTIF). Working in Logistics, you are responsible for ensure all valuable product manufactured is fit for purpose, this is important work as our product could be saving someone’s life; we take pride in our work and are committed, to the creativity and credibility of our production team.
You will play a key part in the control, storage and labelling of the finished drug product and be responsible for the visual inspection of all vialled products for pharmaceutical use and ensuring that defective products are recognised, removed and reported in accordance with Good Manufacturing Practices (GMP).
This position requires a very good level of eyesight. You are permitted to wear prescription spectacles but a recent prescription test must be taken. Curia will arrange for a paid eye test for you and provide a contribution towards safety spectacles if required. Previous experience within a GMP environment is desirable. A friendly, can do attitude to learning is needed to be a successful member of the team and progress your career.
Responsibilities include:
• Curia will provide full training to progress you to approved Visual inspection of vialled products for pharmaceutical use; work is carried out under Good Manufacturing Practices (GMP).
• You will progress training, by carrying out standard operating procedures, learning during the flow of work, shadowing and testing products.
• The role involves carrying out manual visual inspection of filled vials, both freeze dried and liquid filled, using approved procedures for drug products. This is a repetitive task and breaks are assigned around every 55 minutes where other logistics tasks are assigned during this time. A level of fitness is required as there is a requirement to stand and focus as well as lift and pack finished goods for shipping.
• All work is traceable and process documentation is required at each step – you are required to follow strict good manufacturing practices to remove defective products based on agreed reject categories.
• You will complete and report on each inspection in batch manufacturing records in accordance with GMP.
• You will carry out sampling and labelling of raw materials and finished product
• Dispatching of material to clinical sites test houses and packaging facilities.
Product storage tasks
• Control of finished product storage and maintaining of storage areas.
• Document storage locations per batch in inventory
• Ensure storage areas are monitored and perform checks as directed by supervisor
Product labelling and dispatch
• Communication with clients regarding labelling, dispatch, stock control etc.
• Generation of product labels as per client instructions
• Labelling of product vials per agreed batch manufacturing instructions
• Arranging dispatch of materials to Client/Clinic sites as appropriate
• Book transportation to coincide with the size of dispatch to meet the clients delivery deadlines
• Review of dispatch temperature traces
• Preparation of material for dispatch world wide
• Completing dispatch paperwork to the highest standard to aid customs clearance
• Liaising with externa courier plus internal and external customers
Skills and Qualifications
• A good level of written and spoken English as well as knowledge of excel is an advantage.
You will play a key part in the control, storage and labelling of the finished drug product and be responsible for the visual inspection of all vialled products for pharmaceutical use and ensuring that defective products are recognised, removed and reported in accordance with Good Manufacturing Practices (GMP).
This position requires a very good level of eyesight. You are permitted to wear prescription spectacles but a recent prescription test must be taken. Curia will arrange for a paid eye test for you and provide a contribution towards safety spectacles if required. Previous experience within a GMP environment is desirable. A friendly, can do attitude to learning is needed to be a successful member of the team and progress your career.
Responsibilities include:
• Curia will provide full training to progress you to approved Visual inspection of vialled products for pharmaceutical use; work is carried out under Good Manufacturing Practices (GMP).
• You will progress training, by carrying out standard operating procedures, learning during the flow of work, shadowing and testing products.
• The role involves carrying out manual visual inspection of filled vials, both freeze dried and liquid filled, using approved procedures for drug products. This is a repetitive task and breaks are assigned around every 55 minutes where other logistics tasks are assigned during this time. A level of fitness is required as there is a requirement to stand and focus as well as lift and pack finished goods for shipping.
• All work is traceable and process documentation is required at each step – you are required to follow strict good manufacturing practices to remove defective products based on agreed reject categories.
• You will complete and report on each inspection in batch manufacturing records in accordance with GMP.
• You will carry out sampling and labelling of raw materials and finished product
• Dispatching of material to clinical sites test houses and packaging facilities.
Product storage tasks
• Control of finished product storage and maintaining of storage areas.
• Document storage locations per batch in inventory
• Ensure storage areas are monitored and perform checks as directed by supervisor
Product labelling and dispatch
• Communication with clients regarding labelling, dispatch, stock control etc.
• Generation of product labels as per client instructions
• Labelling of product vials per agreed batch manufacturing instructions
• Arranging dispatch of materials to Client/Clinic sites as appropriate
• Book transportation to coincide with the size of dispatch to meet the clients delivery deadlines
• Review of dispatch temperature traces
• Preparation of material for dispatch world wide
• Completing dispatch paperwork to the highest standard to aid customs clearance
• Liaising with externa courier plus internal and external customers
Skills and Qualifications
• A good level of written and spoken English as well as knowledge of excel is an advantage.