QC Chemist / QC Analyst / Laboratory Technician
at ARO Scientific Ltd
Widnes, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 28 Apr, 2025 | GBP 28000 Annual | 29 Jan, 2025 | 2 year(s) or above | Completion,Paperwork,Powerpoint,Outlook,Communication Skills,Microsoft Office,Excel | No | No |
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Description:
QC CHEMIST / QC ANALYST / LABORATORY TECHNICIAN
We are seeking a highly motivated individual to join our energetic and focused team within the laboratory department. The QC Chemist will work in conjunction with the Technical Manager to ensure that the laboratory is operated, maintained, and developed to particularly high standards. The QC Chemist will be responsible for maintenance and improvement of key processes, as well as working with staff at all levels to achieve a consistently high standard of analysis within the laboratory and production department. Due to the high level of accuracy that is required in the role, we are looking for someone that has great mathematical and literacy skills with exceptional attention to detail.
ESSENTIAL SKILLS/TECHNIQUES
· Ability to work independently and as part of a team
· Hands-on attitude and willingness to learn new skills
· High level of attention to detail and accuracy, both practically and on completion of paperwork
· Familiarity of working in an ISO 17025 accredited laboratory
· Be able to work to tight timelines and manage time effectively
· Contact with external bodies will require applicants to have excellent communication skills and a proven track record of establishing and maintaining relationships at all levels
· Proactive approach and attitude to given tasks
· Proficient with Microsoft Office (Excel, PowerPoint, Outlook)
PREFERRED SKILLS
· Experience/knowledge in physical / chemical processing procedures
QUALIFICATIONS AND EDUCATION REQUIREMENTS
Minimum: - BSc (Hons) degree in a scientific subject plus 2 years’ experience in an ISO 17025 laboratory setting OR at 5 years’ experience in an ISO 17025 laboratory setting.
Desirable: - MSc in Chemistry subject plus 2 years’ experience in an ISO 17025 laboratory setting.
Responsibilities:
· Perform batch disposition and stability activities.
· Manufacturing of raw materials / chemicals to final product specifications.
· Analytical testing of raw materials, intermediate and final products in accordance with Quality Management System (QMS) requirements.
· Perform stability and homogeneity study programme activities, storage of in process, and final products samples and retention sample management.
· To produce test results in accordance with the documented procedures, standards, and specifications.
· To ensure testing/sampling activities are maintained in compliance with ISO 17025, QMS and Company requirements.
· Assisting in equipment periodic reviews, monitoring, and maintaining calibration status of equipment within the Quality Control department.
· Preparation and update of SOPs, instructions and protocols and other Quality Control documentation
· Actively contribute to department and site audit readiness requirements including any continuous improvement initiatives.
· Assist in investigation of quality incidents and other problem-solving forums and complete QMS documentation in a timely manner.
· To ensure that the laboratory working areas are safe, clean, and tidy environments in which to work.
· Ensuring the confidentiality of all customer information obtained or created during the performance of laboratory activities, except as required by law.
· Operating, maintaining and calibrating laboratory equipment. Responsibility for specific departmental items of equipment (maintenance, calibration, cleaning).
· Maintaining and updating all technical data with respect to SDS & CoA’s.
· To carry out allocated work in accordance with documented in-house procedures, in an expeditious manner.
· Stock control of critical raw materials and assist with company stock takes.
· Supporting the development of efficient work procedures.
· Participating in the development of the company’s in-house capabilities.
· To work in a safe manner that is in accordance with the Company Health & Safety Policy, and to ensure good health and safety practices are always followed.
· To integrate into the team and maintain a strong harmony and morale throughout the laboratory department.
REQUIREMENT SUMMARY
Min:2.0Max:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
BSc
Proficient
1
Widnes, United Kingdom