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SalaryHOW WE CARE FOR YOU:
At ACM Global Laboratories we are dedicated to getting health care right. Our robust benefits and total rewards foster employee wellbeing, professional development and personal growth. We care for your career while improving patients’ lives.
- Comprehensive Benefits Package
- Career Advancement Opportunities
- Comprehensive Career Pathways
- Auto enrollment Pension
SUMMARY
The Scientist IV is expected to form part of the Laboratory team performing analysis of clinical samples on both automated and manual platforms, working to Good Clinical Practice (GCP) standards.
ACM Global Laboratories is a growing international organisation that provides continued opportunities for internal advancement. At ACM you will be part of a team that is focused on improving people’s lives where you are supported by leadership and colleagues. We are backed by a large healthcare network in the complex and rewarding field of advanced laboratory science. Your voice is heard, and with that, you have an ability to make an impact on the organisation and influence your professional growth.
STATUS: Full Time
LOCATION: 23 Hospital Fields rd York, England [Onsite]
DEPARTMENT: Laboratory
SCHEDULE: Tuesday to Saturday; Days
ATTRIBUTES:
- BSc in Biomedical Sciences or equivalent.
- A minimum of 6 yrs experience within clinical biochemistry required
- Individuals must demonstrate the ability and possess the experience to be a subject matter expert for assays / platforms within the laboratory
KEY RESPONSIBILITIES
- Analysis. Performing analysis on clinical trials samples to the required standards within the determined timeframes. Designated as a subject matter expert for assays / platforms within the laboratory. Ability to troubleshoot assays / platforms within the laboratory
- Work withinternal and external parties to ensure continued compliance of assays /platforms within ACM. Supervision and training of laboratory personnel
- Quality. Write, review and revise laboratory and ACM wide SOPs in conjunction with other ACM functions. Document and complete any quality documentation (Quality Issue, CAPA, deviation, change control) as appropriate within the required. Lead the internal and external quality and regulatory audits as required. Work with operational management to maintain and improve quality standards and performance within the laboratory. Work in conjunction with Senior Scientific staff to evaluate Quality Control (QC) performance (internal and external QC).
- Maintenance. Setup and maintenance of laboratory equipment in line with standard operating procedures (SOPs). Ensuring all relevant maintenance is performed and documented as per SOPs. Lead the laboratory phase of validation activities (equipment and assay) alongside Research and Development ensuring deliverables meet required timeframes and requirements. Participate fully in the general housekeeping of the laboratory, including stock management and maintaining a clean, tidy and compliant working environment.
Job Type: Full-time
Benefits:
- Company pension
- Cycle to work scheme
- Free parking
- Health & wellbeing programme
- Life insurance
- On-site parking
- Referral programme
- Relocation assistance
Schedule:
- 8 hour shift
- Day shift
Ability to commute/relocate:
- YO10 4DZ: reliably commute or plan to relocate before starting work (preferred)
Application question(s):
- Will you now or in the future require sponsorship?
Work Location: In person
