Total 3 manufacturing production job vacancies in tr1 2ax

Hours of Work:

40 Hours per week working on a rotational shift.
Monday to Friday 06.45am to 3.15pm and 3.00pm to 11.30pm

The role:

Working in a team, you will be required to set up the machinery before each production run. This will involve getting materials ready to be processed, ensuring they are correctly placed, and all other operating procedures are followed.
This will involve manual handling and measuring and handling chemicals.

Machine operating and minding, stopping the machines to problem solve and fix any issues during production.
Cleaning down the machinery after each production run.

Acorn by Synergie acts as an employment agency for permanent recruitment.

Proud member of the Disability Confident employer scheme

Use the Pharmacy Wellsky stock control computer system. To assist with stock control including the investigation of any discrepancies. As determined by the Lead Technicians supervise occasional visitors to the department, ensuring security, safety, and confidentiality is always maintained during the visit. To co-ordinate and prioritise workflow relating to cancer chemotherapy, parenteral nutrition, CIVAS, other non-cytotoxic products, non-sterile manufacturing, and radiolabelled kits under direction of senior technicians. This will include worksheet generation, calculations, raw material assembly and labelling. To prepare cancer chemotherapy for intrathecal use according to Department of Health guidelines, Local Trust policy and departmental procedures. To complete the initial check of cytotoxic, non-cytotoxic, CIVAS and parenteral nutrition batches prior to compounding. This will be achieved by completing and achieving the Pharmacy Workforce Development South Pre and In-Process Checking accreditation. To supervise senior assistant technical officers, assistant technical officers, and students within the pharmacy technical services unit. To Train and carry out competency assessments for senior assistant technical officers, assistant technical officers, rotational technicians under the guidance and direction of senior technicians. To carefully follow all standard operating procedures and work instructions to ensure that all products are made safely and efficiently in accordance with Good Manufacturing Guidelines. To assist with the preparation of draft documents pertaining to new products and procedures under guidance and supervision of senior technicians. To participate in production of clinical trials products completing all necessary documentation as required by the study protocols.

Use the Pharmacy Wellsky stock control computer system. To assist with stock control including the investigation of any discrepancies. As determined by the Lead Technicians supervise occasional visitors to the department, ensuring security, safety, and confidentiality is always maintained during the visit. To co-ordinate and prioritise workflow relating to cancer chemotherapy, parenteral nutrition, CIVAS, other non-cytotoxic products, non-sterile manufacturing, and radiolabelled kits under direction of senior technicians. This will include worksheet generation, calculations, raw material assembly and labelling. To prepare cancer chemotherapy for intrathecal use according to Department of Health guidelines, Local Trust policy and departmental procedures. To complete the initial check of cytotoxic, non-cytotoxic, CIVAS and parenteral nutrition batches prior to compounding. This will be achieved by completing and achieving the Pharmacy Workforce Development South Pre and In-Process Checking accreditation. To supervise senior assistant technical officers, assistant technical officers, and students within the pharmacy technical services unit. To Train and carry out competency assessments for senior assistant technical officers, assistant technical officers, rotational technicians under the guidance and direction of senior technicians. To carefully follow all standard operating procedures and work instructions to ensure that all products are made safely and efficiently in accordance with Good Manufacturing Guidelines. To assist with the preparation of draft documents pertaining to new products and procedures under guidance and supervision of senior technicians. To participate in production of clinical trials products completing all necessary documentation as required by the study protocols.