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Join a High-Performing Team at Our Cutting-Edge Deeside Facility and Earn More While Staying Local! Boccard is driving growth in the new era of nuclear energy as a leading specialist in engineering, manufacturing, construction, and maintenance. With a strong order book, long-term projects, and no plant shutdowns, we’re investing in advanced technologies and infrastructure to shape the future of clean energy. We are looking for experienced NDT Quality Control Welding Inspectors to work at our fully digital manufacturing plant in Deeside. The successful applicant(s) will join an experienced team of quality engineers and QC inspectors, working closely with technical and production departments in the manufacture of nuclear fabrications. We offer a competitive hourly rate of £26.15, and with overtime (higher rate) opportunities, your earnings can increase significantly. For example, working just two hours of overtime from Monday to Thursday could boost your weekly pay by around 30%—and that’s without factoring in additional weekend overtime options. This means you can enjoy a competitive salary while staying local, close to home, without the need to travel abroad or relocate. Key Responsibilities: • Conduct inspections and non-destructive testing (NDT) to ensure compliance with specifications and safety standards., • Maintain accurate inspection records and report quality issues and corrective actions., • Ensure compliance with nuclear industry regulations and internal QA/QC procedures., • Collaborate with engineering and production teams to resolve quality concerns., • CSWIP 3.1 certification with experience as a welding inspector., • Certification in PCN Level 2 MPI and PCN Level 2 DPI., • Advanced knowledge of modern welding procedures., • Excellent communication skills and attention to detail., • Employer pension contribution scheme., • 25 days annual leave, plus bank holidays., • Ongoing investment in your training and development., • Employee Assistance Programme., • Overtime available. If you think this is the right role for you, apply now and join us in shaping the future of clean energy!

RRxCo is partnered with an exciting and fast-growing Biotech to hire a QA specialist to help bolster their resource. The UK-based business established in 2010 focusing on antibody, protein and peptide drug conjugate medicines and technology. The bioconjugation team was formed in 2011 and moved into a state-of-the-art facility in 2018. The facility has been built for containment; with the safety of their people and the environment in mind, and bespoke laboratories have been designed specifically to accommodate highly potent bioconjugations. Antibody Drug Conjugates combine the cell and tissue specificity of monoclonal antibodies with the cell-killing potential of highly potent small molecules and represent one of the fastest-growing sectors in the oncology field. Summary The Quality Assurance Specialist is responsible for maintaining the quality management systems, ensuring there is adequate QA support for production activities (including batch review), Project support, oversight of material management and approval of materials/ service providers, approval of validation documentation, audit support activities and other QA activities onsite. Deliverables • Responsible for document review (batch documents, logbooks, Protocols, SOPs, forms etc.), • Use Quality systems to ensure compliance (Documentation, Deviation CAPA, Change control etc), • Contributes to supplier quality assurance programme and new supplier qualification., • Supporting and leading quality related investigations, writing investigation reports and initiating/following up on corrective and preventative actions., • Use, support and maintain training systems, training programmes and training documentation., • Proactive administration of the Quality Management systems, metrics/KP! management and trending for Quality., • Works closely with all functions and departments to ensure efficient document review according to cGMP and other regulatory requirements are compliant., • Supports and lead in self-inspections, customer, and regulatory audits., • Is an integral part of the Quality Team, Coach, support and follow values., • Ability to work under pressure and leading Quality based projects., • Support and lead other activities like Data Integrity activities, Quality Risk Management, approving pre and post execution validation documents, Supporting batch release of clinical and commercial bulk drug substance/ API against product specification files., • MHRA and other regulatory guidelines knowledge, • Completion of additional duties reasonable to ensure the efficient running of the QA department. Profile of the individual • Minimum HND Biological subject and have a proven track record in QA in the pharmaceutical industry (or a related industry), • Minimum 5 years' experience in a QA role within either Pharmaceuticals or Biopharmaceutical environment. QA experience of dealing with QC and/or Manufacturing would be advantageous., • Experience using Microsoft Office of programs especially good knowledge in Word, Excel, PowerPoint, and formatting skills., • Knowledge and practical experience of GMP & GLP Systems., • Knowledge and practical experience of Quality systems, Data Integrity, Supplier Management and Quality Risk Management., • Numerical & investigative skills, Coach and support other functions in managing quality issues. Ability to work accurately, with attention to detail in documentation reviews., • Ability to prioritise and deal effectively with a varied workload., • Good communication skills with the ability to form strong working relationships with stakeholders at all levels across the organisation., • Approachable and friendly, with the confidence to constructively challenge results and performance when required. Desirable: • Trained external auditor for external suppliers. Trained trainer, mentor, and coach in Quality., • End to end QA knowledge on pharmaceutical manufacturing knowledge. Excellent technical reports writing skills, advanced Microsoft package skills. Leadership and soft skills proficiency., • Investigational Medicines product knowledge of Manufacturing and QA support.

About this role We are seeking an Account Manager with a strong foundation in B2B sales, ideally within technology or cybersecurity. This role combines new business development (hunting) with account growth (farming), offering the opportunity to build long-term client relationships while developing expertise in the IAM and PAM space. You will work closely with pre-sales, delivery consultants, marketing, and leadership to manage opportunities, support the full sales cycle, and contribute to CyberIAM’s continued growth. This is an excellent opportunity for someone with 1–4 years of sales experience who is ready to step into a specialist cybersecurity environment and grow into enterprise-level account management. Key Responsibilities As an Account Manager at CyberIAM, you will: • Identify and generate new business opportunities within enterprise and mid-market organisations., • Build and maintain a strong sales pipeline through proactive prospecting and relationship development., • Manage opportunities through the sales cycle with support from senior team members where required., • Develop strong, long-term relationships with clients and stakeholders., • Identify upsell and cross-sell opportunities within existing accounts., • Collaborate with pre-sales and delivery teams to align client needs with CyberIAM’s service offerings., • Contribute to account planning to drive revenue growth and client retention., • Maintain accurate pipeline forecasting and CRM records (HubSpot)., • Stay informed on IAM, PAM, and cybersecurity market trends., • Represent CyberIAM professionally in client meetings, virtual engagements, and industry events. What we’re looking for We want to hear from you if you have: • 2–4 years’ experience in B2B sales, account management, or business development., • Experience selling technology, SaaS, IT services, or cybersecurity solutions (strongly preferred)., • A track record of meeting or exceeding sales targets., • Confidence engaging with senior stakeholders and technical decision-makers., • Strong communication and relationship-building skills., • A consultative, solution-oriented sales approach., • Experience using CRM systems (HubSpot preferred) and LinkedIn Sales Navigator., • A proactive, self-motivated, and results-driven mindset., • Strong organisational skills and attention to detail., • Experience or exposure to IAM, PAM, or cybersecurity vendors such as CyberArk, SailPoint, Saviynt, Okta, Ping, or BeyondTrust is advantageous but not essential. What you bring to the table • Consistent pipeline generation and new opportunity creation., • Strong collaboration with technical and delivery teams., • Revenue growth across new and existing accounts., • Increasing confidence in managing more complex enterprise sales cycles over time., • Development into a trusted identity security advisor within your client base. What CyberIAM Offers • Career Growth: Structured training & certifications., • Time Off: 33 days holiday (incl. public holidays)., • Health & Wellbeing: AXA Healthcare & discounted gym membership., • Financial Perks: Up to 6% pension contribution (10% total)., • Work-Life Balance: Flexible working & a social fund., • Competitive Salary + Commission.

Job Title: Telesales Representative / Telesales Specialist Location: Cheshire (Hybrid – 3 days onsite) Industry: Validation Equipment Manufacturing (B2B) About the Company We are a leading manufacturer of validation equipment, supplying high-quality, compliant solutions to businesses across regulated industries. Known for our technical expertise, reliability, and customer service, we support organisations in meeting stringent quality and validation requirements. The Role We are seeking a driven and confident Telesales Representative to support our growing commercial team. This role focuses on outbound and inbound phone-based sales, engaging with business customers to promote and sell our validation equipment and related solutions. You’ll play a key role in generating new business opportunities, qualifying leads, and supporting the sales pipeline, working closely with field sales and technical teams. Key Responsibilities • Proactively contact prospective and existing business customers via phone and email, • Promote and sell validation equipment and associated solutions to B2B customers, • Qualify inbound leads and generate outbound opportunities, • Understand customer needs and match them with appropriate products, • Manage and update CRM records accurately, • Achieve individual sales targets and KPIs, • Support quotations, follow-ups, and order progression, • Collaborate with internal teams to ensure a smooth customer experience Skills & Experience • Previous experience in telesales, inside sales, or phone-based B2B sales, • Confident communicator with a professional phone manner, • Comfortable handling outbound calling and sales conversations, • Target-driven with a resilient, proactive mindset, • Strong organisational and follow-up skills, • Experience using CRM systems (desirable), • Background selling technical, industrial, or capital equipment is a plus, but not essential What We Offer • Competitive base salary with commission/bonus structure, • Hybrid working (3 days onsite in Cheshire), • Full product training and ongoing support, • Opportunity to sell high-quality, in-demand technical products, • Supportive team environment with opportunities for growth

RRxCo is partnered with an exciting and fast-growing Biotech to hire a QA specialist to help bolster their resource. The UK-based business established in 2010 focusing on antibody, protein and peptide drug conjugate medicines and technology. The bioconjugation team was formed in 2011 and moved into a state-of-the-art facility in 2018. The facility has been built for containment; with the safety of their people and the environment in mind, and bespoke laboratories have been designed specifically to accommodate highly potent bioconjugations. Antibody Drug Conjugates combine the cell and tissue specificity of monoclonal antibodies with the cell-killing potential of highly potent small molecules and represent one of the fastest-growing sectors in the oncology field. Summary The Quality Assurance Specialist is responsible for maintaining the quality management systems, ensuring there is adequate QA support for production activities (including batch review), Project support, oversight of material management and approval of materials/ service providers, approval of validation documentation, audit support activities and other QA activities onsite. Deliverables • Responsible for document review (batch documents, logbooks, Protocols, SOPs, forms etc.), • Use Quality systems to ensure compliance (Documentation, Deviation CAPA, Change control etc), • Contributes to supplier quality assurance programme and new supplier qualification., • Supporting and leading quality related investigations, writing investigation reports and initiating/following up on corrective and preventative actions., • Use, support and maintain training systems, training programmes and training documentation., • Proactive administration of the Quality Management systems, metrics/KP! management and trending for Quality., • Works closely with all functions and departments to ensure efficient document review according to cGMP and other regulatory requirements are compliant., • Supports and lead in self-inspections, customer, and regulatory audits., • Is an integral part of the Quality Team, Coach, support and follow values., • Ability to work under pressure and leading Quality based projects., • Support and lead other activities like Data Integrity activities, Quality Risk Management, approving pre and post execution validation documents, Supporting batch release of clinical and commercial bulk drug substance/ API against product specification files., • MHRA and other regulatory guidelines knowledge, • Completion of additional duties reasonable to ensure the efficient running of the QA department. Profile of the individual • Minimum HND Biological subject and have a proven track record in QA in the pharmaceutical industry (or a related industry), • Minimum 5 years' experience in a QA role within either Pharmaceuticals or Biopharmaceutical environment. QA experience of dealing with QC and/or Manufacturing would be advantageous., • Experience using Microsoft Office of programs especially good knowledge in Word, Excel, PowerPoint, and formatting skills., • Knowledge and practical experience of GMP & GLP Systems., • Knowledge and practical experience of Quality systems, Data Integrity, Supplier Management and Quality Risk Management., • Numerical & investigative skills, Coach and support other functions in managing quality issues. Ability to work accurately, with attention to detail in documentation reviews., • Ability to prioritise and deal effectively with a varied workload., • Good communication skills with the ability to form strong working relationships with stakeholders at all levels across the organisation., • Approachable and friendly, with the confidence to constructively challenge results and performance when required. Desirable: • Trained external auditor for external suppliers. Trained trainer, mentor, and coach in Quality., • End to end QA knowledge on pharmaceutical manufacturing knowledge. Excellent technical reports writing skills, advanced Microsoft package skills. Leadership and soft skills proficiency., • Investigational Medicines product knowledge of Manufacturing and QA support.

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You'll act as the go-to technical specialis.

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You'll act as the go-to technical specialis.

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Job description:Asset Technical SpecialistHello! Thanks for stopping by.

Temporary: 5-6 months | Fully Remote (UK-based).We're resourcing for a data migration project and are looking for a Product Data Analyst to work alongside an IT Project manager on a 3DX implementation.This role is focused on building and validating a structured classification standard for engineerin

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Technical Support Lawyer (New Homes), 5+ Years PQE, Remote / Hybrid, £Competitive – An exciting new role for a Technical Support Lawyer to join a friendly and supportive team. As a Technical Support Lawyer, you will play an integral role in supporting a busy residential conveyancing team by provi

The role involves managing on-site content updates, coordinating third-party platform usage, and assisting technical SEO initiatives.

Reporting to the Customer Support Manager, you will be the "Integration Whisperer" for our most complex technical challenges. Bridge the communication gap by explaining complex 401 Unauthorized errors or technical hurdles to CFOs and Procurement Leads in layman's terms.

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A leading distributor of off‑grid energy is seeking an EC&I Technician to design, develop, install, and commission control systems across the UK.The role involves fault-finding and ensuring compliance with industry standards.This position offers hybrid working and a supportive environment.The idea

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Technical environment: This is a technical role within the Tech team, involving direct interaction with customer technical teams.

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Technical Claims Specialist page is loaded## Technical Claims Specialistlocations: London, United Kingdomtime type: Full timeposted on: Posted Todayjob requisition id: R264With a company culture rooted in collaboration, expertise and innovation, we aim to promote progress and inspire our c

They are seeking a Technical Officer to join their dynamic team, reporting directly to the Operations & Technical Director. In addition, the Technical Officer will provide support with operational and logistics‑related quality improvements.

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