Total 84 transportation manufacturing production job vacancies in Health / Beauty / Fitness category in Singapore

To develop, maintain and ensure compliance with the Quality Management System (QMS) in collaboration with the AccountablePharmacist. To write, develop, maintain and assure implementation of policies and standard operating procedures (SOPs) and maintain thecontrolled documentation system in cooperation with the Accountable Pharmacist. To ensure that all activities, documentation, and procedures within the unit meet current legislation such as GMP, GCP, Health andSafety and COSHH. To assist in all aspects of internal and external audit of the aseptic service, including audits ofcurrent practice, and development of service improvement strategies. To be responsible for the local delivery of the pharmacy education and training strategy for production staff.

You will be able to find a full Job Description and Person Specification attached within the supporting documents or please click Apply now to view in Trac.

HOW MIGHT YOU DEFY IMAGINATION?

Amgen is one of the world’s leading independent biotechnology companies. For over 4 decades, Amgen has pioneered biotechnology breakthroughs, to bring state-of-the-art medicines from laboratory to the patient. Amgen has not only discovered and developed innovative human therapeutics, but has invested in cutting edge manufacturing capability and support services to deliver these exciting therapies to medical teams around the world. Japan and Asia Pacific (JAPAC) is the fastest growing region in Amgen. Now we are hiring an Snr/Occupational Health Nurse in Amgen Singapore Manufacturing.

Live

What you will do

Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics has changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people’s lives.

As the Snr/Occupational Health Nurse you will be responsible to lead the Occupational Health (OH) Program for Amgen Singapore, which includes key aspects of both care management of employees and strategic OH planning.

As an integral part of EHSS team and being part of Amgen OH network, this role reports to EHSS Director and dotted line to Global OH Lead/designate. As Amgen Singapore adopts a Total Workplace Safety and Health approach, this role is essential in building a holistic and integrated approach to manage the interactions between work, safety and health to promote the well-being of both employees and Amgen Singapore.

Other scopes include injury/illness care, medical surveillance exams & testing, wellness screening, fitness center oversight, compliance tracking & record keeping, travel health consultation, emergency response and disaster preparedness.

Responsibilities:

• Manage OH programs for Amgen to optimize health care and return to work, assess health risks and ensure health-based programs are developed, documented, and implemented in accordance with both Singapore regulatory and Amgen’s requirements.
• Lead the operational activities for OH facilities – first aid room, nursing room and provide resources and physical health clearance to fitness facilities’ accesses.
• Render emergency medical care for employees, for example first aid treatment. Lead the First Aid Program for the site and ensure the readiness of first aiders in emergency response situations.
• Follow up with designated workplace doctor (DWD) on occupational related incidents and update the Amgen Incident Database. Instrumental in ensuring that work related incidents are properly managed, timely communicated and followed-up.
• Set up, manage and/or monitor medical/health contracts and service level agreements with external DWD, to ensure it is in line with company procurement standards, and continuously improve case management protocols.
• Manage site OH medical records in accordance to local regulatory requirements and Amgen record retention policy, including first aid records, equipment maintenance/ calibration records etc.
• Monitor and manage employees on routine medical surveillance program. Lead the site in pre-employment and regular medical assessment activities.
• Render OH SME support and advice in site’s Wellness program for Amgen Singapore in accordance to Amgen Corporate and Singapore HPB program. Partner with site Wellbeing Lead for a holistic Total Workplace Safety and Health solution in Amgen Singapore. Some examples include leading the general/targeted/interventional health screening or management, as well as healthy food programs.
• Oversee the site’s Return-to-Work program, as well as work accommodation plans.
• Partner closely with key stakeholders such as Human Resources department in the management of related OH programs for employees.
• Support employees with traveling health requirements (e.g. travel kits, vaccinations etc.) as part of Travel Health Program management.

All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional tasks and responsibilities.

Win

What we expect of you

Required Qualifications

• Bachelor’s degree in nursing or relevant qualification with practicing certificate and 4 years of directly related experience OR
• Diploma in nursing or relevant qualification with practicing certificate and 8 years of directly related experience
• Nursing Administration/ Management/ Advance Leadership Diploma is highly desirable

Preferred Qualifications

• Relevant industrial experience specifically in manufacturing industry, with minimum 3-5 years’ experience in Occupational Health.
• Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff

Thrive

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

• Vast opportunities to learn and move up and across our global organization
• Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
• Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Your selection for this role will be subject to fulfilling the medical requirements of this job scope. If so, you will be informed of the medical check(s) that you may need to undergo. All medical related expenses incurred from this medical check shall be borne by the company.

Equal Opportunity Statement

Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Job Description:

• Plan and co-ordinate weekly/monthly production and manpower schedules.
• Set and implement SOPs in line with cGMP to facilitate supervision for quality and process control.
• Implement and write reports for rework, scrap/loss disposal, process deviation, process validation, new process and change in process.
• Set and implement process flow structure and chart for compilation of process capacity and ability records.
• Prepare and implement work improvement program.

Job Requirement:

• Minimum Diploma in any course
• Good communication, analytical and leadership skill.
• Proficient in Microsoft Word and Excel.

TELE me at @jacechooo or WA me at https://wa.me/+6582976283 NOW!
Interested candidates please submit your resume to jacechoo@recruitexpress.com.sg

Jace Choo Oi Kei
Personnel EA License No.: R1875164
Recruit Express Pte Ltd (EA Licence No.: 99C4599)

Please refer to the JD/PD for full details on this post Please contact Sam Stone for further information or to arrange an informal visit samuel.stone@uhnm.nhs.uk 01782 674576

1. To prepare and prioritise cancer chemotherapy and medicines for injection including GMO class 1 and 2, using laminar airflow cabinets or isolator technology, providing all necessary in-process checks, within the clean room environment under the guidance of good manufacturing practice. 2. To prepare cancer chemotherapy for intrathecal use according to Department of Health guidelines, local trust policy and departmental procedures. 3. To work unsupervised if necessary in the preparation of cancer chemotherapy. 4. To follow carefully all standard operating procedures to ensure all products are made safely and efficiently in accordance with Good Manufacturing Practice legislation and guidelines. 5. To prepare all types of product documentation, with all types of calculations and the production of labels using the Prisym 2000 label software. 6. To assemble the raw materials and consumables required to prepare each individual product, ensuring total segregation of each preparation using a box or tray segregation system as defined in the standard operating procedure. 7. To assist with Clinical Trial stock control to include the production and checking of routine stock checks, ensuring stock rotation and expiry date checks are completed and investigating stock discrepancies. 8. To complete, maintain and file all relevant documents, records and reports. 9. To clean the pharmacy aseptic suite and support rooms following standard operating procedures and using specific methods of cleaning, ensuring appropriate quality control samples are taken and cleaning logs filled out. 10. To co-operate and participate in any training and development in production services, attending such study days and courses as necessary for service development. 11. To complete any environmental monitoring or operator validation tests requested by the quality assurance manager as appropriate to Clinical Trials. To provide effective communication with the R&D department, the research team, multidisciplinary team and various UK organisations and pharmaceutical companies. 13. To undertake general dispensary duties, in accordance with standard operating procedures and the legal framework for the supply of medicines: Labelling - generate accurate medication labels Dispensing - accurately dispense inpatient, outpatient and discharge prescriptions, including clinical trials, cytotoxic drugs and controlled drugs. Issue drugs - to healthcare professionals referring for advice when necessary. In collaboration with the pharmacy clinical trials team to ensure accurate record keeping of drug accountability of all clinical trials (both written and computer records). Reporting any exceptions of deficiencies to the pharmacy clinical trials support manager. To contribute to the efficient stock control of all clinical trial products by undertaking regular stock checks to ensure sufficient (IMP/trial-specific) in date stock for current and new patients. To record clinical trial drugs returned by the patients on appropriate drug accountability records and dispose of them according to the trial. To assist in the close-down and archiving of completed clinical trials. Organise trial monitor visits ensuring that both the pharmacy site files are drug returns are prepared in advance. To respond quickly and appropriately to all enquiries and queries, directing to most appropriate team member. To use the pharmacy computer and related technologies according to the needs of the department. To participate in the ordering and receipt of clinical trials products following trial protocols, study specific instructions and the departmental SOPs. To ensure that all trials are run in accordance with GCP, Good Manufacturing Practice and Good Dispensing Practice guidelines/department procedures and reporting any deviations to the pharmacy clinical trials support manager. To monitor appropriate storage of all clinical trial products ensuring storage condition records and accurate expiry records for all clinical trial products are kept up to date and archived for future reference according to GCP, GMP Guidelines. To ensure that pharmacy trial store and equipment is kept in a clean and usable workable condition. To attend GCP training/sessions as appropriate and to work to GCP at all times. To participate in the appraisal process and to undertake appropriate mandatory training. To assist with training of the Pharmacy Assistant and other pharmacy staff as required in dispensing clinical trials. To participate in audit projects to review clinical trial processes. To contribute and assist with advice to pharmacy staff about clinical trials. To participate in the departmental training programme including NVQ Level II. To be able to adhere to Standard Operational Procedures and policies without supervision To participate and maintain a record of continuing personal and professional development.

You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac.

Please refer to the JD/PD for full details on this post Please contact Sam Stone for further information or to arrange an informal visit samuel.stone@uhnm.nhs.uk 01782 674576

The candidate will work under Good Manufacturing Practice (GMP) guidance and be actively involved in aseptic preparation of chemotherapy, parenteral nutrition and clinical trials. Working with isolators and laminar airflow cabinets, utilising specialist equipment such as EM2400 Compounder for the preparation of parenteral nutrition. To apply and ensure the principles of Good Clinical Practice (GCP) are adhered to in managing clinical trials, maintain records of dispensing, including clinical trial material. To participate in the internal ordering, stock control and distribution of aseptic and clinical trial products. To assist in the instruction and supervision of pharmacy assistants, pre-registration pharmacy technicians, pre-registration and diploma pharmacists and pharmacy students To participate in the induction and supervision of new pharmacy staff To participate in staff performance and appraisal schemes and contribute to the staff training sessions. To participate in staff rotas including if necessary early and late sessions, weekend and bank holidays. To participate in departmental audits and service improvement initiatives Prioritises own work load and that of other junior colleagues working within the same area Ensure routine tasks are carried out within work area Ability to work within tight time frames and under pressure within a busy environment. Responds and manages changes in workflow priorities as the day develops Skill to dispense complex medications and to undertake manipulations with accuracy and speed. Works within standard operating procedures. To actively participate in the continual improvement of the pharmacy service Implement policies and propose changes to practices, procedures for own area Implements SOPs within pharmacy technician teams Actively participates in and maintains near miss and incident recording You will be able to find a full Job description and Person Specification attached within the supporting documents or please click Apply now to view in Trac.

To ensure that all activities, documentation, and procedures within the unit meet current legislation such as GMP, GCP, Health and Safety and COSHH. To ensure and supervise the safe handling of cytotoxic, hazardous, and toxic materials. To be responsible for stock control for consumable items, drugs, and raw materials and the appropriate charging of all outgoing items. To assist the Chief Pharmacy Technician Production with the ordering of outsourced products including chemotherapy, TPN, and other Specials from commercial suppliers, and to ensure appropriate stock levels of these are maintained. To assist the Chief Pharmacy Technician Production, in collecting data for the Key Performance Indicators (KPIs) reports, and Quality Indicators (QIs). To assist in the internal and external audits of the aseptic service, and the subsequent approved action plans. To assist in the production aspects of clinical trials in liaison with the clinical trials team, and Good Clinical Practice (GCP). To prepare aseptic products within the isolator according to approved local SOPs, maintaining personal aseptic technique and validations. To promote and encourage reporting and learning from near-misses and errors within the service. To investigate errors in the unit, make recommendations and implement approved changes to practice in order to reduce the likelihood of reoccurrence. Please see the Job Description and the Persons Specification for further details about the job role.

Work following SOPs at all times Production Checking, ensuring all BMRs and related production documents are completed prior to Quality Release. Production checking ensuring all manufactured items have been visually inspected Identification, investigation and documentation of deviations Identification and reporting of errors To ensure reports from customers relating to product quality complaints or adverse drug reactions are documented and the essential minimum information is collected and forwarded to the Regulatory Affairs Department the same day they are received. To deal with any other duties which do not change the nature of this post. To act in a professional manner at all times in order to promote a positive image of the Company.

A Vacancy at Nottingham University Hospitals NHS Trust.


An exciting opportunity has presented for a senior pharmacist to join our cancer pharmacy team. We are looking to recruit to the post of Specialist Clinical Pharmacist – Pharmacy Production / Haematology. The post will be split 50:50 between working with direct clinical care in haematology and Pharmacy Production, offering the best of both worlds of cancer pharmacy.

The post holder will work closely with the Pharmacy Production Unit, the Senior Clinical Pharmacists covering Haematology, Haematopoietic Stem Cell Transplantation (HSCT) and Advanced Therapy Medicinal Product
(ATMP) and the wider multi-disciplinary team.

Part of the Pharmacy Aseptic Services Unit supporting the aseptic preparation and release of high risk injectable or infusional products, as well as maintaining a high quality, safe and efficient level of service delivery.

You will undertake technical and clinical verification of all SACT prescriptions according to approved chemotherapy regimens and local and national standards after a period of competency-based training and assessment.



You will be working as part of a wide Cancer Pharmacy team to jointly provide an expert pharmacy service to Pharmacy Production Unit and the clinical directorate for the haematology. You will help to deliver and Systemic Anticancer Chemotherapy (SACT) prescription verification and clinical monitoring.

As a pharmacy expert in Production / Technical Services you will supervise and support pharmacy staff in the cytolab providing pharmaceutical care to patients under the oncology/haematology team and provide training for pharmacy staff on medicine related issues within the Pharmacy Cytolab. You will provide professional and clinical supervision for haematology pharmacy areas.

You will provide leadership and support for medicines optimisation ensuring that haematology patients receive the most appropriate treatment that is both safe and cost-effective .

With over 19,000 staff, we are one of the biggest employers in the city with a central role in supporting the health and wellbeing of our local population. We play a leading role in research, education and innovation.

Come and join our wonderful team at NUH. We are big believers in diversity and welcome new ideas to help develop our team in order to deliver world class healthcare to the vast patient populations we serve. With endless personal development opportunities available, at NUH we will endeavour to turn your job into a career!

We particularly welcome applications from people who identify as Black, Asian and Minority Ethnic, or Disabled, as we are striving to be better represented at NUH.

Please see attached full job description. The list below is not exhaustive of the JD,

Production / Technical Services

1. To assist in the overall management of all activities in the Pharmacy Production Unit at the City Hospital Campus of NUH to ensure services are maintained; informing the Assistant Head of Pharmacy - Production Services of workload changes likely to impact on safe working practices.
2. To maintain an awareness and knowledge of new medicines, chemotherapy regimens and service developments to inform workload and workforce planning. This includes being an active member of the appropriate NUH groups at the City Hospital Campus and also via liaison with lead cancer pharmacists and clinicians.
3. To support the Assistant Head of Pharmacy - Production Services and to provide professional advice and support to the various sections in the Pharmacy Production Department.
4. To provide professional support to the Production Management team, responsible for all aspects of the services within this aseptic preparation unit including the approval of all systems of work and documentation used in the unit.
5. To support and supervise a team of Pharmacists, Pre-registration Pharmacists, scientific, technical and other support staff in undertaking their day-to-day operational activities.
6. To maintain awareness and knowledge of industry development and best practice, ensuring that a comprehensive and up-date selection of reference texts and journals is maintained.
7. To maintain and further develop, where appropriate, links with relevant professional bodies and organisations e.g., General Pharmaceutical Council, MHRA, Department of Health, BOPA, Local cancer network.
8. To take the lead role and responsibility for the development, research and operational management of chemotherapy services and future commercial and in-house developments of service to patients to ensure the safe and timely provision of cytotoxic chemotherapy in line with GMP, Quality Assurance of Aseptic Services and Health and Safety.
9. To liaise with Quality Control over all aspects of quality assurance to ensure that production activities comply with nationally applicable good manufacturing practice standards and local policies and procedures. To carry out internal audit and report on findings at the appropriate forum. To engage in all aspects of the Quality Management System within the Pharmacy Production Department including the CAPA system and error monitoring systems.
10. To conduct and/or contribute to relevant clinical and other audits to facilitate clinical governance requirements. To reflect on and interpret the results of audits, address remedial points and implement change as required.
11. To assist in identifying staffing and recruitment issues and implementing change in the staff structure to accommodate change in service needs and / or to resolve issues. To evaluate the effect changes in workload, staffing and service development (capacity planning) have on service delivery and to ensure that appropriate actions are applied to ensure that the services operate at low risk to patients at all times. To participate in the recruitment of senior pharmacists and technicians.
12. To critically appraise published work in responding to questions raised by other health-care professionals including other pharmacists, and offer advice on conflicting or absent information.
13. Following all clinical protocols, to accurately interpret prescriptions for cytotoxic chemotherapy, intervening when necessary by raising concerns and queries with the appropriate chemotherapy trained pharmacist, nurse or doctor.
14. To check and release to the designated clinical areas, intrathecal chemotherapy in accordance with Trust and Department of Health policies and procedures.
15. To lead the maintenance and up-dating of the drug monograph files and expiry tables, including details of drug administration, manufacturing, instructions, labelling requirements and product expiry and storage (essential to the safe delivery of the service).
16. To take a lead role in the production and management of the documentation system required in the Cytolab Production Unit, ensuring the maintenance of all necessary record entries and audit processes.

17. To ensure that computer software used in chemotherapy manufacture is regularly reviewed and updated as appropriate and to take the lead on e-prescribing at Cytolab
18. To assist in the maintenance of the Validation Master Plan across the Pharmacy Production Department to ensure its continuing development and validity.
19. To contribute to the submission of business cases to secure funding for new pharmacy staff, equipment, premises or services for the advancement of pharmacy services in the Pharmacy Production Department.
20. To assist in the formal management of contracts with external customers.
21. To take a lead role in risk management, Health and Safety assessment and evaluation, including COSHH, for the Cytolab Production Department
22. To support the Assistant Head of Pharmacy – Production Services in the development and delivery of timely performance reports. To help develop performance indicators that clearly demonstrate the contribution that staff in the Cytolab Production Department make to patient care and to the business of the Pharmacy Production Department, maintain a capacity plan and acting on it as appropriate
23. To support the Head of Pharmacy in specific pharmacy management issues and projects and to contribute to the overall organisation, administration and management of the NUH Pharmacy department e.g. rota management, workload analysis and staff deployment.

Clinical Haematology coverage

1. The post-holder will be be providing clinical pharmacy service for Haematology patients, for both inpatients and outpatients, including reviewing our transplant patients and complex haematology patients working alongside other pharmacists working in the haematology team.

2. To act as a clinical role model for junior pharmacists within the team and demonstrate the ability to provide service that ensures the safe, clinically effective and cost-efficient use of medicines and the ability to check clinically screened dispensed prescriptions.

3. To contribute to the development and implementation of strategies to improve safe medicines use across the Trust.

4. To ensure compliance with commissioned frameworks, FOC and EAMS agreements, and FOI requests for patients in the haematology directorate alongside other pharmacists working in the haematology team.

5. To act as an Independent Non-medical Prescriber, in accordance with the Health &Social Care Act 2001, specialising in haematology clinical area if and when capacity allows.

6. Day to day clinical management of the patients within haematology speciality on allocated days, ensuring necessary/appropriate medications are available for assessment and treatment needs of the speciality.

7. Provide support to the overall Cancer Pharmacist teams for patients within the speciality, including screening of prescriptions where needed

Education and Training

To take a lead role in the development, introduction, implementation, training and evaluation of new technologies in relation to chemotherapy provision. In conjunction with production and quality control staff and the pharmacy department’s training team, to ensure that all staff (including Resident Pharmacists and Pre registration pharmacists) who undertake production activities within the Cytolab Production Department possess the necessary skills to do so safely. This involves ensuring their training, assessment and validation of competence is effectively carried out. In conjunction with the lead production training technician to regularly review and update training packages to reflect current best practice and latest evidence.

Other Duties

1. To participate in rostered flexible shift working including evening, weekend and bank holiday arrangements in line with service commitments. To participate in the early and late duty, weekend and Bank Holiday working in accordance with departmental rotas, in order to fulfil contractual obligations.
2. Undertake any other duties that may reasonably be required as agreed by senior staff.
3. Prioritise workload to ensure customer and patient needs and expectations are met.
4. Ensure office areas are kept clean and tidy.
5. Participate as an appraisee in the departmental individual professional development review and KSF competency processes, supporting and working towards identified objectives and training requirements in order to maintain and continuously develop performance

6. Undertake annual mandatory training e.g. manual handling, fire, security, basic life support etc.

GENERAL DUTIES
In addition to the key job responsibilities detailed in this job description all employees at Nottingham University Hospitals NHS Trust are expected to comply with the general duties as outlines in the trust policies and procedures to include safe guarding,, information governance, Health and safety, governance, and Health and Well being.

Disclosure and Barring Service Check
This post is subject to the Rehabilitation of Offenders Act (Exceptions Order) 1975 and as such it will be necessary for a submission for Disclosure to be made to the Disclosure and Barring Service (formerly known as CRB) to check for any previous criminal convictions.

UK Registration
Applicants must have current UK professional registration. For further information please see NHS Careers website (opens in a new window).


This advert closes on Monday 9 Sep 2024

Please see Job description for full details Service Delivery To coordinate with the Senior Operational Lead regarding preparation of Clinical Trial medicines to ensure a safe and efficient service. To ensure that all IMP activities undertaken within the Production Unit comply with GMP/GDP/GCP, Health and Safety and COSHH legislation and that all work documentation and procedure manuals meet these regulations. To support senior staff in the day-to-day management of clinical trials staff and workload in the allocated preparation area. To ensure that all staff working on Clinical Trials in Production are trained and competency assessed in the tasks they undertake. Clinical trials To lead on the set-up and implementation of Clinical Trials requiring preparation or manufacture to ensure GMP, GCP, full protocol, CTA, and IMPD compliance. To generate quality technical agreements, commercial and supply agreements in response to acceptance of a clinical trial, liaising regularly with the trial sponsor. To generate or contribute to the continued maintenance of trial specific IMPDs in liaison with the local site QA, QP, QC department and trial sponsor. To lead on generation of batch specific documentation such as training logs, batch manufacturing records and any other required trial specific documentation. To supervise the clinical trials co-ordinator and clinical trials workload on a day to day basis and report regularly on the status of clinical trials to the production manager highlighting any resource requirements. To oversee the manufacture of clinical trials and training on trial specific protocols and manufacturing methods to ensure other staff are aware of the trial-specific requirements of the batch/product. To supervise trainee pharmacists, STP students and trainee Production technicians when rotating through Production Clinical Trials. To ensure effective communication is maintained with clinical trial sponsors and/or contract partners for any aspect of the Production Clinical Trial service delivery. To be responsible for ensuring all Clinical Trial Site Master Files are updated and maintained contemporaneously in accordance with data integrity principles to be audit ready at all times. Governance and Quality To ensure that the Clinical Trial Pharmaceutical Quality Management system is maintained and developed in accordance with the MS(Specials) and MIA(IMP) license requirements and in response to changes in regulations and legislation. To undertake a regular review of all quality exceptions according to department procedures. To author and review deviation reports and change controls along with other PQS documents and assist in risk-based decision making on product quality and final product disposition from a production perspective in liaison with QA and the QP. To support and document change through the Quality Management System to both reduce risk and drive innovation in clinical trial activities and the overall clinical trials service. To ensure all changes to the Quality Management System are effectively communicated via the change control process to all grades of staff. By example and effective communication to create an environment of quality improvement. To review and develop Standard Operating Procedures to ensure compliance with current and future clinical trial, manufacturing and regulatory requirements. To participate in sponsor or other customer related audits for clinical trials including agenda writing, ensuring appropriate staff are aware and present at the audit. To review with the QA team and QP any clinical trial related audit reports, draw up an action plan for compliance achievement and communicate appropriately with the auditor to ensure timely close out of items raised. To contribute to regulatory inspections involving the MIA(IMP) licence. To ensure that all staff are aware of the relevant Standard Operating Procedures, that these are well maintained and kept up to date with technological and regulatory updates to drive optimal performance of the clinical trials service. Training and Education To induct all new staff to the department into the clinical trials service and introduce the clinical trials team members and their roles. To prepare activity competency records relevant to clinical trials related activities and assess staff competence in completing such activities To regularly update the wider production and quality teams in new clinical trials / batches / products being introduced to the department through presentations and team meetings. To assist with the induction, training and assessment of staff working in the unit.

Duties And Responsibilities To aseptically prepare high quality Cytotoxic/MABS/EAMS etc. in accordance with departmental procedures, Good Manufacturing Practice and COSHH regulations ensuring that all work complies with all regulatory frameworks and standards. Ensure that cleaning in all areas of the production unit is completed according to GMP and departmental policies and procedures. To ensure ingredients and disposables are assembled, disinfected and transferred through the Aseptic Services Unit appropriately. To accurately prepare worksheets and labels for aseptic products using the units computer system using JAC and iQEMO program if required. To assist with the preparation of a variety and routine complex documentation within the aseptic unit. To assist with the recording and analysis (where appropriate) of data, both manually and on the computer. Actively participates in the departments training, accreditation, validations and re-validation program. To be responsible for the maintenance of stock in the Aseptic Unit including evaluating stock levels within the Aseptic Unit assisting the ordering Technician to ensure adequate stock is maintained at all times. Ensure all Environmental monitoring plates are received and stored in the correct manner to ensure they are protected from contamination. Prepare environmental samples and checking detailed documentation for dispatch to QCNW To be responsible for routinely receiving, analyzing and documenting complex Environmental Reports from QCNW and referring any variances to senior staff in a timely manner, to determine best course of action eg resolving issues. Undertake any mandatory training, updates and courses in line with local and Trust policies. To complete all Aseptic Services Unit competency-based training packages. To participate in and co-operate with, individual personal assessment, continuing professional development and continuing education programmes to develop personal competencies and knowledge base. When appropriate to demonstrate activities to, work experience students, pre-registration pharmacists, pharmacy technicians, student pharmacy technicians and staff undergoing induction. Where appropriate, propose improvements to procedures e.g SOPs in own work area Communication and Leadership Communicate with other team members regarding activities within the Aseptic Services Unit may involve sensitivity and/or complex information. Carry out and plan on-going general administration tasks according to the Aseptic Unit on-going requirements and refer queries to the appropriate person. To ensure effective communication channels are maintained by all staff and any disagreements are dealt with promptly and in line with the Trusts respect policy. Participate in staff discussions during internal meetings and as part of a group when required. Finance: To effectively manage a designated stockholding to ensure that stock wastage is minimised. To assist the Senior/Specialist Technicians in managing the Aseptic Services stock takes. To comply with legal and Trust requirements relating to the purchase, supply, use safe custody and destruction of medicines within Pharmacy and other areas of the Trust. 12 Freedom to act Effort and Environment Factors: Demonstrable skills for manipulation of pharmaceutical products. The post holder must have the ability to lift and handle pharmaceutical items. The post holder must have the ability to work in a cleanroom environment. Regular use of a PC for data inputting and training. Policy: To be responsible for the adherence and upholding of all Trust and departmental policies and procedures. To comply with the updated national guidance and local Trust policy for the Safe Administration of Intrathecal Chemotherapy. Other Duties: The provision of a high-quality service delivered in a professional and courteous manner is a requirement of all staff employed by the Pharmaceutical Service. I It will be a requirement of the post holder to participate in the Aseptic On-Call preparation service for chemotherapy outside normal working hours on a rotational basis. To participate in a Saturday / Sunday and Bank Holiday rota, when the service requires which may be on a regular/rotad basis. Undertakes any other duties of a similar nature requested by the Production Manager/Deputy, or the Director of Pharmacy Responsibility for Patient Care Maintains compliance with Rules and Guidance to Good Manufacturing Practice and any other local, regional and national guidance documents Assists with the maintaining Quality Assurance Standards in accordance with National, Regional and local requirements Participates in ensuring that the aseptic service complies with clinical governance strategies, including risk management assessments of working practices, reporting of clinical incidents, pharmacy error reporting schemes, intervention monitoring and risk reduction strategies Regularly analyse documented GMP Observations, referring issues to Lead Technician and Production manager/Deputy where non-compliance or deviation identified.

JOB RESPONSBILITIES:

• Provide support for operational and technical activities

• Machine & Equipment maintenance / calibration

• Establish SOP and machine manual to provide comprehensive servicing and maintenance programmes

• Identify areas of process improvement and automation to implement work improvement programmes to achieve desired machine efficiency and reject rate

• Plan, evaluate and improve technical/engineering projects for cost and productivity

• Implementation of industrial safety practice to ensure compliance

• Any other ad-hoc tasks as assigned

JOB REQUIREMENTS:

• Min Degree in Electrical / Mechanical Engineering or related discipline
• Training provided - No exp needed

Medical Device MNC

Up to $3.6K

Interested candidates, please forward your resume to kevynhuang@recruitexpress.com.sg

Consultant: Huang Jingsheng Kevyn (R1333338)

Recruit Express Pte Ltd (99C4599)