Trabajos laboratory en St AlbansCrear alertas

Technical Sales Engineer (Capital Equipment) North London & Home Counties £60,000 - £70,000 + Car Allowance + Bonus + Comprehensive Benefits Are you a technically minded Sales Engineer ready to make a real commercial impact? Join a market-leading organisation at the forefront of scientific instrumentation and capital equipment, trusted by customers across global manufacturing, R&D, and advanced-materials sectors. In this role, you'll take full responsibility for a thriving UK territory, building long-term customer partnerships, delivering tailored technical demonstrations, and providing innovative solutions to complex engineering challenges. You'll receive continuous product and sales training, backed by an expert applications and service team, giving you the support and structure needed to excel. With clear routes for career progression, this is an ideal opportunity for an ambitious technical-sales professional eager to move into senior commercial or technical-leadership positions. Join a globally respected company renowned for engineering excellence, customer focus, and continuous innovation offering stability, flexibility, and a collaborative culture where your contribution truly counts. This position would suit a Technical Sales Engineer with capital equipment experience looking for a new challenge within a lucrative patch. The Role • Deliver engaging technical demonstrations and bespoke solutions across a wide product range., • Manage the full sales process, from lead generation to deal closure., • Strong technical understanding with the ability to learn and communicate complex systems., • Proven B2B technical-sales experience, ideally within capital equipment, laboratory, or scientific instrumentation sectors. To apply or learn more about this opportunity, click "Apply Now" or contact Patrick Simper at Rise Technical Recruitment. Rise Technical Recruitment Ltd acts an employment agency for permanent roles and an employment business for temporary roles. The salary advertised is the bracket available for this position. The actual salary paid will be dependent on your level of experience, qualifications and skill set and will be decided by our client, the employer. Rise are not responsible or liable for any hiring decisions made by the end client. We are an equal opportunities company and welcome applications from all suitable candidates.

PermanentBased in Hemel Hempstead (occasional travel to clients)Full Time - 35 hour week£65,000 pa - £70,000 paSubject Matter Expert - Product Cybersecurity Working for a global company that are experts within their field ensuring standards within compliance testing activities. An equal opportunity employer, that are committed to diversity. As an SME Product cybersecurity expert, you will be responsible for serving as the main technical authority and providing thought leadership for cybersecurity compliance testing activities for connected consumer, industrial and medical products. This role combines product cybersecurity expertise, hands-on testing skills, and practical knowledge of different product cybersecurity standards and related regulations as well as the ability to understand new testing standards and methodologies for connected product cybersecurity compliance at global a scale. This role is crucial in helping our clients to bring secure connected products to market and comply with evolving cybersecurity regulations. The individual will leverage technical expertise to perform in-depth security evaluations, offer strategic testing and evaluation guidance, and contribute to our reputation as a trusted authority in IoT product cybersecurity. • To provide expert advice to internal teams and leadership, • To contribute to the company strategic positioning in the Product IOT cybersecurity area, • To interpret product IOT cybersecurity standards and related regulations understanding testing protocols and evaluation methodologies as well as required testing tools, • To manage the testing of client samples to ensure compliance to the relevant schemes under type test and audit tests, • To support project clients in conducting tests and in observing the results, • Working with certification teams to resolve issues found during testing, • To develop tests and automation to further expand our testing capabilities for new product cybersecurity regulations To serve as product cybersecurity technical compliance authority for our client you will lead the product cybersecurity, • Assist to maintain and improve test techniques for the IoT laboratory, • To lead the standards, review process required by the company strategy, • To research and identify new potential test equipment for the IoT laboratory, • Establish KPI's and report on compliance/accreditation/operational related issues, • Ensure that compliance processes are established, implemented and maintained and ensuring that they continue to meet accreditation requirements and remains effective, efficient and fit for purpose, • To provide technical assistance with customers, during any potential testing and certification journey, • To manage client's samples and testing to ensure that agreed timelines are met for the testing of samples, • To assist in the maintenance and continuous improvement on automated reporting tools, • Prepare Test Reports for clients and delivered on time as agreed in Operational Plan, • Maintaining CREST CPSA Level or equivalent qualification, • Support in the development of new testing services related to Product cybersecurity, • Demonstrate achievement of annual PDR objectives and delivery of our clients core values and behaviours, • Customer Focus - both internal and external, • Participation in the continual improvement of initiatives Person Specification:, • At least 5 years experience hardware cybersecurity testing (IoT devices), • Sound knowledge in the different IOT product cybersecurity regulations around the world, • Have practical knowledge and experience deliveringesting and assessment services against relevant standards and/or other relevant documents and procedures for IoT. It includes relevant experience with ETSI EN 303 645, ETSI TS 103 701, RED EN 18031, IEC 62443, UL2900 and OWASP standard, • Strong foundation in programming languages and networking is essential, • Understanding of microcontrollers (e.g., STM32, ESP32) and real-time operating systems (RTOS), • Proficiency with UART, JTAG, SPI, I2C for debugging and testing purposes, • Knowledge of different wireless protocols as Zigbee, Bluetooth, Wi-Fi, Cellular, LoRaWAN, • Bluetooth, Wi-Fi, Cellular, LoRaWAN, etc., and their attack surfaces, • Practical knowledge of Linux OS and others, • Good communication skills and the ability to write clear and concise reports, • Work well as part of a team, • Building relationship with external and internal client, • Ability to solve problems proactively Education - Bachelor's degree in any of the below fields:- Cybersecurity - Computer Engineering - Electrical/Electronic Engineering - Telecommunications - Information Technology Please let us know if we need to make reasonable adjustments to our process, please let us know about how we can best support you and make the adjustments that may be needed. Altitude-Recruitment Limited acting as an Employment Agency and Employment Business.

A leading pharmaceutical manufacturer is seeking a Quality Systems & QC Laboratory Electronic Systems Administrator to support and maintain electronic quality and laboratory systems in line with GMP, GAMP, and data integrity requirements. This role will play a key part in ensuring systems such as electronic QMS and QC laboratory applications remain compliant, validated, and fit for purpose. Responsibilities • Administer and support electronic QMS (e.g., TrackWise) and QC laboratory systems, • Support qualification and validation of equipment, processes, and electronic systems, • Maintain user access, data integrity controls, and system availability, • Coordinate system updates, upgrades, and vendor support activities, • Generate, review, and approve validation documentation and SOPs, • Troubleshoot system issues and provide user support and training Requirements • Experience supporting electronic QMS and/or QC laboratory systems in a GMP environment, • Working knowledge of CSV, GAMP, and data integrity principles, • Understanding of qualification and validation for equipment and electronic systems, • Strong analytical, documentation, and communication skills, • Comfortable working cross-functionally with IT, Quality, and external vendors About Planet Pharma: Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age. Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information: E:

With clear routes for career progression, this is an ideal opportunity for an ambitious technical‑sales professional eager to move into senior commercial or technical‑leadership positions. Proven B2B technical‑sales experience, ideally within capital equipment, laboratory, or scientific instru

Field Service Engineer, Medical Sterilisation Systems Autoclaves / Washer Disinfectors Overall Earnings £55,000+ Basic Salary £40,000 to £47,000 Bonus Overtime Circa £5,000 Hybrid Company Car Excellent Benefits Full and Comprehensive Product Training An opportunity for a field service engineer with experience of sterilisation systems, autoclaves or washer disinfectors to join a market leader with excellent training and career opportunities The Role - Field Service Engineer, Medical Sterilisation Systems Following expansion, they seek to recruit a customer focused Field Service Engineer, responsible for the service, installation, repair and general maintenance of their range of highly advanced sterilisation and endoscope washer disinfectors. Your Background - Field Service Engineer, Medical Sterilisation Systems To be considered for this exciting role you must be able to demonstrate: A strong background working in a field service or technical support role Previous experience working on endoscope washers, medical / laboratory autoclaves, sterilisation systems or washer disinfectors A HTM, STM or WTM qualification Impeccable customer service skills An interest in IT The ability to remain confident in customer facing environments The Company - Field Service Engineer, Medical Sterilisation Systems Well established supplier of specialist medical and laboratory equipment This instantly recognisable market leader is renowned for their forward-thinking products, support services and complete solutions that include sterilisation systems, washer disinfectors and autoclaves used within the healthcare, life sciences, pharmaceutical and industrial market sectors A market leader in a number of equipment technologies and enjoy 'best in class' status with a number of their innovative systems This vacancy is being advertised by TRS Consulting. The services advertised by TRS Consulting are those of an employment agency and / or an employment business. TPBN1_UKTJ

Talentmark are recruiting for a Quality Validation Associate, to join a well-established and successful global pharmaceutical company, based in Hatfield, Hertfordshire, on a permanent basis. Role: This role is responsible for ensuring that electronic systems within the Quality Control Laboratory and the Quality Systems operate in accordance with the requirements of the departmental Standard Operating Procedures. Key duties will include: Ensure the Electronic Quality Management System (QMS) and Quality Control Laboratory systems and software used to support the manufacture, packaging, testing, storage and distribution of marketed drug products comply with current GMP and company expectations. Provide input to the review and writing of any associated quality policies, systems and procedures as required and prepare and update SOPs and training materials for system administration activities, Qualification and Validation activities. Support the maintenance and administration of the Electronic QMS and Provide ongoing operation, maintenance and implementation of improvements to electronic systems. Support the effective management of the administration of QC laboratory system applications providing independence of access for administrator activities. Ensure Qualification and Validation of equipment, processes, systems is/are performed in line with procedures, GMP and GAMP guidelines for process, equipment and electronic systems, as and when required. Ensure the maintenance of procedures supporting Qualification and Validation and generate, review and approve Qualification and Validation documentation. Ensure user access to systems is maintained in line with procedures and support is provided to facilitate the set up and change management of system data and ensure continuous system availability and functionality. Support the Management of the relationships with external system providers for technical and helpdesk support and coordinate and lead system updates and upgrades with the system providers. Support the provision of training on the requirements for CSV and IT qualification and validation and support quality systems training of staff. Support the change control process to ensure the requirements of qualification and validation are included. Ensure procedures are in place for backup, archiving and retrieval of data on electronic systems. Support the Implementation of system upgrades and new software applications.Your Background: Educated to degree level or above in a scientific or related field with significant experience in a pharmaceutical industry role focused on Electronic Quality Systems. Proficient knowledge of electronic systems, CSV and GAMP requirements and the ability to understand and analyse user requirements to facilitate changes and system improvements. Good understanding of the requirements of data integrity and application to system management. Good understanding of Quality Control Systems and analytical software and electronic Quality Systems. Good understanding of GMP Guidelines and Regulations. Knowledge of the qualification and validation requirements for equipment and electronic systems. Excellent verbal and written communication skills.Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence

QC Analyst (Grade II) St Albans £32,000 Monday to Friday, 8am–4pm We are currently recruiting for an experienced QC Analyst (Grade II) to join a well-established UK pharmaceutical manufacturer based in St Albans, Hertfordshire. This is an excellent opportunity to join a growing organisation operating from a modern, state-of-the-art manufacturing facility with significant production capacity. The Role Reporting to the QC Supervisor and QC Lead Analyst, you will be responsible for completing training and carrying out routine analytical laboratory work in compliance with all regulatory and internal standards. You will be expected to work professionally and independently on assigned tests, product samples, or technical areas, maintaining full compliance with: Good Manufacturing Practice (GMP) Data Integrity standards Good Documentation Practice (GDP) Environmental, Health & Safety (EHS) requirements Internal SOPs At Grade II level, you will be recognised as having sufficient technical expertise to perform QC analysis independently across areas such as: Technical Services Incoming Materials Finished Product / IPC About the Company Our client is a highly respected UK-based pharmaceutical manufacturer with over 35 years of industry experience. They specialise in the manufacture and packaging of non-sterile solid dosage forms, including tablets and capsules, supplying a wide range of over-the-counter analgesic products to major retailers. Following a recent £14 million investment in a new headquarters and manufacturing facility, the company now produces over 2 billion tablets annually and continues to expand. Requirements Previous QC laboratory experience within a GMP-regulated pharmaceutical environment Strong understanding of GMP, GDP, and Data Integrity Ability to work independently and manage assigned workload Excellent attention to detail and documentation skills Package Salary: £32,000 40 hours per week Monday to Friday, 8am–4pm 28 days holiday (inclusive) Pension