This role is listed by an employer that holds a live Home Office sponsor licence on the Skilled Worker route.
Closest occupation match: SOC 2131, IT project managers. Home Office going rate for this occupation: £58,200 a year.
Individual eligibility depends on personal circumstances. These figures are public reference information, not advice or a verdict on this job.
ALTEN is a global engineering and technology consultancy operating across over 35 countries worldwide. We partner with industry leaders across sectors including Aeronautics, Aerospace, Defence, Naval, Automotive, Energy, Rail, IT and many more to deliver innovative engineering solutions that drive technological advancement & support sustainable transformation.
Our teams of passionate and agile engineers work on cutting-edge projects that shape the future of technology and sustainability. At ALTEN, we empower talented engineers to innovate, solve complex challenges, and deliver impactful solutions that build tomorrow’s world—today.
Join us and start building tomorrow’s world today!
As a Technical Project Manager, you will join our Hertfordshire team to support our activities within the pharmaceutical manufacturing sector.
You will be responsible for leading and managing technical projects across the Quality Control laboratory, ensuring laboratory systems, equipment, and processes remain compliant, efficient, and fit for purpose. Working closely with Quality, IT, Manufacturing, and external stakeholders, you will oversee electronic laboratory systems, equipment lifecycle management, method transfers, new product introduction activities, and laboratory compliance initiatives within a GMP-regulated environment.
Location: Hertforshire
On Site: Full - time on site
Clearance: Clearable
Experience Level: Senior (5+ years)
Key Responsibilities:
Lead and manage all technical projects within the Quality Control laboratory
Manage and develop a team of technical specialists supporting laboratory systems and equipment
Oversee the lifecycle management of QC electronic systems, including LIMS, CDS, and associated laboratory software
Ensure laboratory equipment and systems remain compliant with GMP, Data Integrity requirements, and company procedures
Develop and maintain a five-year equipment replacement and investment plan
Lead New Product Introduction (NPI) and Method Transfer activities within the QC function
Manage compliance-related initiatives including global changes, pharmacopeia updates, and regulatory requirements
Drive change management activities to ensure laboratory systems and equipment remain operational and compliant
Review and approve SOPs, quality documents, and technical procedures
Coordinate education and training programmes relating to specialist equipment and software
Work with cross-functional stakeholders to deliver technical improvements and laboratory optimisation projects
Monitor project progress, risks, budgets, and resource requirements
Support inspections, audits, and regulatory interactions as required
Required Skills:
Strong knowledge of pharmaceutical Quality Control laboratory operations
Experience managing QC equipment and electronic laboratory systems
Knowledge of LIMS, CDS, and laboratory software platforms
Understanding of equipment qualification, validation, and lifecycle management
Experience leading technical projects within a regulated environment
Strong understanding of GMP requirements and Data Integrity principles
Excellent communication, stakeholder management, and leadership skills
Ability to gather, analyse, and translate user requirements into practical solutions
Strong organisational and project management capabilities
Ability to interpret complex technical and scientific information and communicate findings effectively
Required Qualifications:
A Bachelor’s or Master’s degree in Engineering , or equivalent military experience .
Significant experience working within a pharmaceutical Quality Control laboratory environment
At least 2 years of experience managing QC equipment and electronic laboratory systems
Experience supporting technical change, validation, qualification, or laboratory compliance activities
Desirable Skills:
Experience as a LIMS or CDS administrator
Knowledge of laboratory instrument qualification and computer system validation (CSV)
Experience supporting method transfers and analytical technology implementation
Familiarity with pharmacopeia compliance activities and regulatory submissions
Experience managing multidisciplinary technical teams
Understanding of continuous improvement and laboratory digitalisation initiatives
Knowledge of laboratory automation technologies
Why join us?
We bring together entrepreneurial, tech-driven people to deliver innovative solutions for leading companies.
At ALTEN, you’ll work on exciting projects, supported by ongoing learning, mentoring, and clear career development tailored to your goals.
Join a passionate team and help build tomorrow, today.
In short you get:
A personalised career path and a rewarding management style
A huge diversity of engineering projects and industries
Private Medical Insurance
Cycle & Tech Scheme
Employee assistance programme
Life insurance & Pension Scheme
Social atmosphere, regular gatherings & team buildings
Flexible way of working (role dependent)
We are proud to support the Armed Forces Covenant & actively encourage applications from members of the Armed Forces community, including veterans, reservists, service leavers, and military spouses/partners. We recognise the value of military skills and experience and are committed to ensuring that no applicant is unfairly disadvantaged during our recruitment and selection processes.
ALTEN is committed to fostering a diverse and inclusive workplace and values the strength that comes from a global mix of backgrounds and perspectives. We welcome applications from all suitably qualified candidates, regardless of background or protected characteristics under the Equality Act 2010. If you require any reasonable adjustments during the recruitment process, please let us know.
This role may require you to have or be willing to go through Security Clearance. As part of the onboarding process candidates will be asked to complete a Baseline Personnel Security Standard; details of the evidence required to apply may be found on the government website Gov.UK. If you are unable to meet this and any associated criteria, then your employment may be delayed, or rejected . Details of this will be discussed with you at interview.
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All rolesLast verified against our ingestion on 8 October 2026; sponsor register dataset 2026-09-25.