Hamlyn Williams

About the Company

Placing Talent that Makes A Difference.

Talent attraction and retention are critical to our client’s success; Hamlyn Williams’ mission is to support and enable this through the delivery of high-quality staffing solutions.

Founded in 2011, we are a global organisation with local offices across North America and Europe, and over 160 colleagues. We cover the Financial Services, Cyber Security, Professional Services, Technology, Life Sciences and Manufacturing industries.

Our people are ambitious, we persevere for our customers success, and work with pride. We are investing in our people strategy and have recently relaunched the Hamlyn Williams way (HW way) and Career Pathway, your route to success. There has never been a better time to join Hamlyn Williams.

Visit www.hamlynwilliams.com for more information.

Listed Jobs

Company Name

Hamlyn Williams

Job Title

Commissioning Engineer

Job Description

We are looking for an experienced Commissioning Engineer to join an exciting automation and manufacturing project. This role offers a unique opportunity to work on critical systems in high-performance environments, with a focus on hands-on engineering tasks and technical problem-solving.

Role Overview:
60% hands-on engineering: Perform commissioning, validation, troubleshooting, and control panel reviews.
40% project coordination: Engage in meetings, scheduling, and reviewing technical documentation.

Key Requirements:
5+ years of commissioning experience in automation or manufacturing systems.
Expertise in BMS and Allen Bradley systems.
Strong knowledge of HVAC systems and related commissioning processes.
Proficient in:
Wiring diagrams, loop/point tests, and troubleshooting.
Instrumentation, sequence tests, and system validation.
Reviewing P&IDs, documentation, control panels, and FATs.
Prior experience in datacentre environments is highly desirable.

This is an excellent opportunity for a skilled engineer to work on cutting-edge automation systems within a supportive and collaborative team. For more details or to apply, reach out:
i.chowdhury@hamlynwilliams.com - +44 7389042558
Schedule a call: https://calendly.com/i-chowdhury-hamlynwilliams/30min

London, United Kingdom

Hybrid

07-01-2025

Company Name

Hamlyn Williams

Job Title

Cyber Security Specialist

Job Description

Our client is a leading electrical organization based in France. They are on the look-out for an experienced SIEM & Cloud Security Specialist to join their team

This is a remote contract role
5 days a week - 6 months as a start

Role:
You will lead efforts to manage, optimize, and migrate the existing SIEM infrastructure to Microsoft Sentinel. This includes enhancing threat detection, supporting SOC teams, and implementing advanced cloud security strategies.

Responsibilities:
Optimize Rapid7 InsightIDR
Analyze the current SIEM environment.
Improve detection rules, workflows, and integrate critical systems.
Provide technical support and propose immediate optimizations.
Plan & Execute Migration to Microsoft Sentinel
Design a migration strategy and manage data dependencies.
Configure Sentinel, including alert rules, dashboards, and workflows.
Scale Sentinel with advanced features and ensure comprehensive monitoring.
Establish Advanced Cloud Security
Implement Azure security policies and automate governance processes.
Support SOC teams in threat management and vulnerability remediation.
Documentation & Training
Develop detailed configuration and migration documentation.
Train internal teams on Sentinel use and optimization.

Requirements
Must have EU citizenship
Technical Expertise:
Proven experience with Rapid7 InsightIDR and Microsoft Sentinel.
Strong knowledge of Microsoft Azure security services.
Proficiency in SIEM migration, data analysis, and incident response.
Certifications (Preferred):
AZ-500 (Microsoft Azure Security)
SC-200 (Microsoft Security Operations)
Skills:
Project management and collaboration in complex environments.
Excellent communication, including technical and non-technical audiences.
Proactive, self-motivated, and detail-oriented.
Languages:
Fluent in English (mandatory); French (optional)

Benefits
Pay: 750e - 800e per day
Remote Working

If you or someone you know is interested in this position please apply through the link or email me at s.mooney@hamlynwilliams.com

France

Hybrid

21-01-2025

Company Name

Hamlyn Williams

Job Title

Validation Engineer

Job Description

We are seeking a skilled Validation Engineer with expertise in single-use technology (SUT) to support validation activities related to bioreactors, mixing systems, and other disposable process equipment used in biopharmaceutical manufacturing. The successful candidate will be responsible for the development and execution of validation protocols (IQ/OQ/PQ), ensuring compliance with GMP, FDA, EMA, and industry standards. This role is critical in ensuring the reliability, efficiency, and regulatory compliance of bioprocessing equipment.

Key responsibilities:
Develop, execute, and document validation protocols (IQ, OQ, PQ) for single-use bioreactors, mixing systems, and other process equipment.
Ensure compliance with GMP, FDA, EMA, ISO, and industry standards related to single-use technology.
Perform risk assessments and gap analyses for single-use components to ensure process integrity.
Collaborate with cross-functional teams, including Manufacturing, Quality Assurance, Process Development, and Regulatory Affairs, to support validation efforts.
Investigate and resolve validation deviations, anomalies, and non-conformances.
Author and review Standard Operating Procedures (SOPs), User Requirement Specifications (URS), and Validation Master Plans (VMPs).
Lead and participate in FAT, SAT, and commissioning of single-use systems.
Conduct performance qualification studies, including sterility, extractables & leachables testing, and integrity testing.
Stay updated with industry trends, technological advancements, and regulatory changes affecting single-use technologies.
Provide training and technical support on validation processes to internal stakeholders.

Qualifications:
Bachelor’s or Master’s degree in Engineering, Biotechnology, Biochemistry, or a related field.
5+ years of validation experience in the biopharmaceutical or medical device industry.
Hands-on experience with single-use bioreactors, mixing systems, and filtration assemblies.
Strong knowledge of GMP, FDA 21 CFR Part 11, ISO 13485, USP, and ICH guidelines.
Experience with risk-based validation approaches and industry best practices.
Familiarity with data integrity principles, electronic validation systems, and automation is a plus.

Please get in touch if you are interested in applying!

England, United Kingdom

Hybrid

30-01-2025