Quality Control Lab Analyst

LanceSoft Europe; Montrose; On-site; GBP 30,000 - 50,000; Full time

Job summary

An established industry player is seeking a Quality Lab Analyst to support laboratory activities at the Montrose site. This role involves ensuring effective routine analysis, coordinating with various departments, and adhering to compliance standards. The ideal candidate will have a strong background in quality control and analytical techniques, contributing to continuous improvement initiatives and supporting staff training. If you're passionate about operational excellence and quality assurance in the pharmaceutical sector, this opportunity is perfect for you.

Qualifications

• Experience in a Quality Control lab with analytical techniques is essential.
• Ability to perform routine analysis and troubleshoot production issues.

Responsibilities

• Ensure effective and prompt routine analysis in the quality lab.
• Coordinate with departments for smooth product flow and efficiency.

Skills

Chromatography

Analytical Techniques

Quality Control

Good Laboratory Practice (cGLP)

Data Management (M-ERP)

Job description

This range is provided by LanceSoft Europe. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from LanceSoft Europe

Director Delivery Services at LanceSoft, Inc.

Role: Quality Lab Analyst

Location: Angus, Scotland DD10 8EA

Duration: 12 months

There may be scope for shifts later, so please check if they are open to shift work. For now, shifts are during the day, 09:00 AM to 05:30 PM.

Previous employment in a Quality Control lab or equivalent with competency in analytical techniques such as chromatography and classical tests is required.

Description:

The quality team supports the Montrose site by managing operational quality laboratory activities in a safe, compliant, and efficient manner.

The purpose of the Quality Analyst role is to:

1. Ensure routine analysis is completed effectively and promptly.
2. Coordinate with other parts of the quality directorate for smooth product flow.
3. Support interfaces with other departments at Montrose for efficiency.
4. Escalate significant quality or compliance issues appropriately and promote continuous improvement.
5. Perform routine analysis on IPC, raw materials, manufactured, and stability samples using classical and chromatographic techniques, utilizing IT systems like M-ERP for data management.
6. Provide analytical support for non-routine samples and troubleshoot production issues.
7. Operate with integrity, a positive attitude, and a collaborative spirit.
8. Participate in activities like procedure reviews, validations, risk assessments, and process improvements.
9. Adhere to current Good Laboratory Practice (cGLP) standards.
10. Engage in audits such as GMP, 5S, and self-inspections.
11. Support continuous improvement initiatives using GPS tools and value-for-money principles.
12. Contribute to staff training and development, including learning new techniques.
13. Work safely and compliantly, supporting laboratory safety and operational procedures.
14. Meet site strategic requirements, including ZIPs, ZAPs, and quality metrics.
15. Manage deviations, change controls, and improvement actions professionally and timely.
16. Support additional analyses at the Montrose site as directed by the Laboratory Leader.

Seniority level

• Associate

Employment type

• Contract

Job function

• Science, Research, and Manufacturing

Industries

• Pharmaceutical Manufacturing and Biotechnology Research

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