Are you passionate about contributing to medical advancements and helping diagnose and treat diseases? As a Medical Technologist, you'll play a crucial role in the healthcare field, conducting tests on biological samples and providing essential data to medical professionals. With a sharp eye for detail and a dedication to accuracy, you'll ensure the quality and reliability of diagnostic results, making a significant impact on patient care and well-being.
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Quality Engineer
Location: ROBINSON 77
Expertise: Institutional Healthcare
Experience: 2 years
Our client is a well established medical devices company with a strong product portfolio. Work with cross-functional teams to ensure implementation and/or maintenance of QMS that are appropriate for Medical Devices / Life Sciences Manufacturing / Medical Devices Distribution and Services, complies with Commercial/Distribution Quality System such as GDPMD and may also include, but not limited to FDA 21 CFR Part 820, ISO 9001, ISO13485 and other applicable regulatory and statutory requirements. Support external audit by certification body and/or regulatory inspections by regulatory agencies e.g. US FDA. Coordinate, plan and perform internal audits of processes, facilities and documentation to assure compliance with internal procedures, FDA 21 CFR Part 820, ISO 9001, ISO 13485 and GDPMD regulations and requirements. Establish, maintain and update relevant QMS documentation. Support in the preparation of generation of metrics and reports to support Quality Management Review. Maintain calibration records for all manufacturing tools and equipments Interface with production, process, and test engineering to ensure that products are consistently produced and controlled as per ISO / Part 820 requirements Provide QA support in the design, development, sustaining and production of life science / medical device products, facilitating the application of change controls, inspection and testing, risk management activities and quality plan for new product introductions / existing products are in order to sustain product competitiveness while maintaining compliance to domestic and international regulations and standards. Conduct customer feedback/complaints and trend review, and drive appropriate continual improvement implementationWhat you should do nowApply to this job ad or send your CV across to me at e.ng@brunel.net for a confidential discussion.(Brunel International South East Asia Pte Ltd, Registration Number: 199603098R | Company License Number : 16S8067 | Eve Ng EAP Registration Number R2198025.)
Operations Administrator
Location: ROBINSON 77
Expertise: Back Office & Administrations
Experience: 1 years
The RoleWe are looking for an Operations professional to support the mobilization and onboarding of Consultants across regions. In this role, you will be responsible for onboarding the consultants. You will also provide global mobility support, assisting Consultants with work passes, relocation, and travel arrangements. Additionally, you’ll handle administrative tasks, manage team inboxes, and coordinate pre-employment requirements to ensure smooth operations. If you enjoy working cross-functionally and delivering exceptional service, this role is for you.Job Responsibilities1.General Understanding and processing of work pass applications including renewals and dependent passes. Ensure that Consultant has provided all required completed forms necessary for payrolling, tax-filing and enrolment of insurance. Checking and arranging of required due diligence including but not limited to background checks, Drug & Alcohol testing, OGUK medical, offshore related training etc. Update and maintain Consultant’s details are updated in our systems. Keeping track of Employment and visa expiry dates. Building good rapport with Consultants by providing care and quality services.2.Global Mobility Global Mobility services include but are not limited to assisting Consultants with working rights requirements, relocating to work location by sourcing for flights, accommodation, local transport, movers, schooling needs etc. On-boarding of new Consultant to their role by providing them with all required documentation (Client-specific policies, payroll calendar, timesheets, information on medical insurance etc). Liaising with Consultant on their mobilization/demobilization flights and hotels required for their business or rotation trip. Obtaining business visas as and when required.3.Support & Coordination Manage team mailboxes, respond to client’s queries within the SLA and ensure emails are routed to the appropriate teams for action. Perform daily administrative duties to ensure smooth running of Operations team. Registering eligible Consultants to medical insurance through the online portal and deactivation upon cessation of employment. Coordinating of pre-employment medical before Consultant’s commencement of work. Issuance of Certificate of Employment and other necessary letters & correspondence at Consultant’s request. Procurement of safety tools and PPE as per project requirements. Preparation of Purchase Order upon receiving of invoices from vendor for approval before sending it to Finance for processing of payment. Ad hoc Administrative duties assigned by the Operations Manager.Qualification and Experience Fresh graduates are welcome to apply as relevant training will be provided. Fresh and dynamic team player with good cooperation and communication skills. Proactive and meticulous. Positive attitude and willingness to learn.What We Can Offer You: Excellent corporate culture Friendly and supportive team Working with multinational and multicultural team Fun working environment Career development and opportunity Open and transparent communicationIn Brunel, we have built a truly sustainable and durable business model: connecting specialists to exciting career opportunities, supporting the development of these careers, and offering fair and equal employment.
Regulatory Affairs Manager (Pharma)
Location: ROBINSON 77
Expertise: Institutional Healthcare
Experience: 3 years
Our client is a global pharmaceutical company with a wide product portfolio Develop and implement regulatory strategies for new and existing products in the assigned regions. Provide guidance to the company regarding regulatory requirements and ensure compliance with all relevant regulations. Submission and coordination with H.S.A. and with Regional RA APAC & RA HO Collaborate with PIC for RA/QA of Business Partner/ Distributor in Hong Kong, Taiwan, and Brunei. Coordinate and liaise with necessary requirements for BE Study, CDP, BE site inspection, BE specific study. To facilitate critical submissions to H.S.A. as per commercial priority. Prepare a regulatory plan for submissions and renewals and ensure implementation as per agreed timelines. Provides up to date Registration status and estimated timeline for submission/ MA Approval. Proactively provides input on the current and upcoming New Regulation/Guideline and assess possible impact to registered/ upcoming registration product. Preparation of documentation for GMP accreditation and keep monitoring and record activities related to GMP. Provides support for all Pharmacovigilance / Quality Complaint Report. Recognize issues, roadblocks, and project risks, and proactively address these or raise to the attention of management with proposed solutions. Provide Technical support for Tender participation, Hospital listing and Medical enquiries.What you should do nowApply to this job ad or send your CV across to me at e.ng@brunel.net for a confidential discussion.(Brunel International South East Asia Pte Ltd, Registration Number: 199603098R | Company License Number : 16S8067 | Eve Ng EAP Registration Number R2198025.)
Medical technologist job role
As a Medical Technologist, you will be responsible for performing various laboratory tests on biological samples, analysing the results, and generating reports for medical professionals. You'll work in hospital or independent medical laboratories, helping diagnose and monitor diseases, contributing to medical research, and ensuring the smooth operation of the laboratory.
Medical technologist responsibilities
As a Medical Technologist in the healthcare field, you’ll be conducting vital laboratory tests on various biological samples and providing essential data for medical professionals. Your precise and accurate work will contribute to diagnosing and monitoring diseases, ultimately impacting patient care and well-being. Here are the key responsibilities of a medical technologist:
- Use established lab protocols to perform laboratory tests and accurately log the results.
- Perform comprehensive examinations of cells and microorganisms for disease detection.
- Inform clients of recollection protocols if a specimen is rejected.
- Identify, diagnose, and resolve issues that may arise with the laboratory equipment.
- Verify all test results and ensure correct matching with the respective specimens.
- Properly label and organise tests for easy retrieval and tracking.
- Study and analyse biological samples such as blood, urine, tissue, and spinal fluid to identify abnormalities and support medical diagnoses.
- Report findings to physicians and other medical professionals for further evaluation and treatment planning.
- Maintain a well-organised and adequately stocked laboratory environment.
Adhere to biohazard guidelines and follow proper safety protocols.
Medical technologist qualifications
To work in the field, Medical Technologists must hold a minimum of a bachelor's degree in medical technology, Clinical Laboratory Science, or a related field. A minimum of four years of experience as a medical technologist is often required.
Proficiency in managing electronic health record systems such as AdvancedMD and eClinicalWorks could also be required in some roles. Medical Technologists need to demonstrate in-depth knowledge of medical laboratory equipment, techniques, tests, and procedures, as well as advanced skills in preparing and analysing biological samples. Expertise in inventorying supplies and maintaining laboratory equipment is crucial.
Medical technologist skills
To be successful in this role, you’ll need specific skills to ensure accurate and reliable laboratory testing. Here are the key skills of a medical technologist:
- Proficiency in research and data analysis.
- Capability to multitask effectively and prioritise tasks in a fast-paced environment.
- Familiarity with biohazard guidelines and a commitment to following safety measures.
- Ability to stand for extended periods during laboratory procedures.
- Excellent attention to detail and the ability to handle complex laboratory tasks.
- Strong problem-solving and critical-thinking skills.
- Excellent verbal and written communication skills.
- Strong ability to comprehend and execute instructions accurately.