Research Associate

Join our company that is thriving to improve human health. We're dedicated to creating an innovative and excellent culture that motivates our staff to realize their full potential. We're looking for passionate people who want to make a valuable contribution and who share our vision. Our global company provides a positive and dynamic work environment with opportunities for professional growth. You will have the chance to work in an international environment with supportive colleagues who will help you thrive.

JOB PURPOSE

Under direct supervision, uses fundamental concepts, practices, and procedures, together with particular platforms, to perform routine clinical sample processing.

These tasks may require the application of established techniques, procedures, and criteria. This includes the generation of revenue by conducting fee-for-service analyses of biological samples (e.g., blood, saliva, stool, urine, bacteria, etc) for external clients using various equipment (e.g., flow cytometers, centrifuges, incubators, analytical and statistical software, office equipment, etc.).

MAIN AREAS OF RESPONSIBILITY

• Develops and validates bioanalytical tests under the guidance of Scientists.
• Performs clinical sample analysis and clinical sample reporting.
• Ensures clear audit trails by performing quality control of all information and data generated.
• Assists with documents for projects (e.g., Lab Manuals, Validation Phase Plans, Method Development Plans, Sample Analysis Plans, Sample Analysis Reports etc.).
• Assists with multiple projects in a fast-paced laboratory environment.
• Management, monitoring and ordering of consumable stock thereby ensuring that sufficient reagents are available to perform assays.
• Stock takes (this includes stock management on a Laboratory information management system (LIMS)).
• Strong adherence to regulatory compliance and safety requirements involving good clinical laboratory practices (GCLP), standard operating procedures (SOP´s), Health & Safety policies, and other related documents.
• Assumes the responsibility of Study lead on projects as well as chief analyst on assay methods.
• Odoo timesheet and planning accurately and efficiently.

Ad-hoc

• Writes and/or reviews/validates SOP´s, standard working procedures (SWP´s), documents, forms, and spreadsheets.
• Documents and updates the installation, operation, and performance qualifications (IQ/OQ/PQ) of equipment e.g., new equipment, preventative maintenance (PM), services etc.
• Ensures that equipment being used for assays are fit for purpose and are not used outside of service dates (equipment custodian).
• Performs set-ups, start-ups, and verification of various analysers (e.g., electrochemiluminescence analysers, microplate readers, flow cytometers etc.) and laboratory equipment (e.g., centrifuges, pipettes, timers, and thermometers etc.).
• Performs daily good housekeeping (GHK) duties.
• Completes and maintains relevant documentation related to clinical trials such as overview documents, sample logistics tracking forms, worksheets, and method sheets etc.
• Ensures correct, timeous, and documented receipt of all sample as well as reagent deliveries including proper storage thereof (this includes locating and drawing of samples and reagents when needed).
• Assist with the training of other staff members in company procedures and validated methods

QUALIFICATION AND EXPERIENCE

• Bachelor's degree is usually required within a relevant to the field (e.g., Biology, Biochemistry and Cell Biology) with 1-2 years’ experience or at least 3 years of company experience in a relevant field of work is required.
• On-going general International Organization for Standardization (ISO), Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) awareness training needs to be provided to all staff. The job holder needs to ensure that he/she is up to date with the available training.
• Previous work experience in a relevant field with expertise in pipette handling, following standard protocols and using basic equipment (e.g., centrifuges, biosafety cabinets, plate washers and incubators)
• Previous work experience or a master’s degree (MSc) in a scientific field.
• Working within a good practice (GxP) and/or Good Clinical Laboratory Practice (GCLP) accredited environment.
The ideal candidate should have prior experience working with analysers e.g., electrochemiluminescence analysers, microplate readers, Flow cytometers etc.

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SKILLS AND COMPETENCIES

• On-going professional development is strongly encouraged; this may take the form of training, workshops, seminars etc.
• Good knowledge of written and spoken English
• Proficient in Excel and Microsoft

BENEFITS AT OUR COMPANY

• Competitive market salaries in each country
• Discretionary bonus based on performance each year (subject to company performance and budget)
• Annual Inflationary increases to salary (subject to budget and inflation)
• Training and Development opportunities, ensuring each employee has a personal development plan and identifying relevant courses to improve (including LinkedIn Learning)
• Identifying a Career path for promotion potential and working with Managers to determine milestones to be achieved.
• Locally applied benefits per country, including annual leave and competitive pension contributions.
• Flexible working options
• Statutory/Public Holidays – flexible to be taken when chosen or on the actual public holiday.
• Regular employee engagement and wellness surveys
• Regular communication and engagement through BambooHR announcements and Town Hall meetings
• Strong applicant tracking system for recruitment and ensuring the onboarding process is an enjoyable experience for all new employees.
• End of year celebratory functions.
• Social events & end of year function
• Family friendly leave for sick, paternity, maternity and parental
• Medical aid contribution
• Dental and vision plan
• 401K retirement plan contribution

ONLY CANDIDATES IN THE USA, UNLESS YOU HAVE A WORK VISA TO WORK IN THE USA.

PLEASE ENSURE THAT YOUR CV/RESUME IS SUMBITTED IN ENGLISH.