Scientist I

ACM Global Laboratories; York and North Yorkshire; On-site; GBP 27,000 - 37,000; Full time

Job summary

ACM Global Laboratories in the United Kingdom seeks a Scientist I to join the Laboratory team to analyze clinical samples on automated and manual platforms, operating under Good Clinical Practice standards. The role involves supervised work and adherence to SOPs.

Responsibilities include setting up and maintaining equipment, performing sample analyses, supporting instrument validations, and contributing to quality documentation, CAPA, deviation reports, and change controls.

Qualifications

• BSc or higher in a relevant scientific subject.
• Experience with SOPs and quality systems is preferred.

Responsibilities

• Set up and maintain laboratory equipment per SOPs.
• Perform sample analysis on automated and manual platforms.
• Assist in instrument and method validations as required.
• Contribute to revision of department SOPs with ACM functions.
• Document and complete quality records (Quality Issue, CAPA, deviation, change control).
• Maintain general housekeeping and support procurement, stock checks, and clean environment.
• Participate in internal and external quality assessments.

Skills

Laboratory operations

Sample analysis

Quality documentation

GCP compliance

Education

BSc or higher in a relevant scientific subject

Tools

SOP adherence

Job description

Schedule: Tuesday - Friday 9:00 AM - 5:00 PM, Saturday 8:00 AM - 4:00 PM

SUMMARY

The Scientist I is expected to form part of Laboratory team performing analysis of clinical samples on both automated and manual platforms, working to Good Clinical Practice (GCP) standards. The Scientist I performs activities under supervision.

RESPONSIBILITIES

• Setup and maintenance of laboratory equipment in line with standard operating procedures (SOPs)
• Performing sample analysis
• Assist in instrument and method validations where required
• Contribute to revision of department specific SOPs in conjunction with other ACM functions
• Document and complete any quality documentation (Quality Issue, CAPA, deviation, change control) as appropriate within the required timeframes
• Participate fully in the general housekeeping of the laboratory, including procurement, stock check and maintaining a clean and tidy working environment
• Assist in other operational areas where required (e.g. Sample Management, Logistics)
• Participate in internal and external quality assessment as required
• Participation in all activities that seek to ensure compliance with GCP guidelines and accreditation schemes (e.g. CAP)
• Comply with policies for the safe, secure and confidential processing and storage of patient / client data and other laboratory information
• Any other duties as defined and requested by Operational Management
• The post-holder is responsible for ensuring that all the above processes are performed in accordance with: Definitive study protocols, the current ICH Guideline for GCP, UK Clinical Trial Statutory Instruments, current Health and Safety Legislation and ACM HR policies, other legislation that is relevant to the responsibilities of the post, and ACM SOPs

MINIMUM QUALIFICATIONS

• BSc or higher in a relevant scientific subject

PREFERRED QUALIFICATIONS

• N/A

PHYSICAL REQUIREMENTS:

M - Medium Work - Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects; Requires frequent walking, standing or squatting.

Rochester Regional Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, sex (including pregnancy, childbirth, and related medical conditions), sexual orientation, gender identity or expression, national origin, age, disability, predisposing genetic characteristics, marital or familial status, military or veteran status, citizenship or immigration status, or any other characteristic protected by federal, state, or local law.