57 Pharmaceutical Manager jobs in the United Kingdom

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Role Details:

Project Manager – Pharmaceutical Project, Irvine Based

Altrad are currently expanding due to a number of project successes within our Major projects business across the Pharmaceutical & Life Sciences industries.

To support this growth we are looking to recruit a Project Manager with a proven track record in a Process industry and executing multi-disciplined projects from inception through completion, ideally based around process manufacturing, process equipment and containment though not necessarily in a Pharmaceutical environment.

The opportunity will be based at our client site facility on a full time basis in Irvine, Scotland to ensure delivery while working as part of an integrated project team.

Key Deliverables:

• Management and Coordination of Design delivery to ensure the engineering design solution for the work scope assigned is delivered to meet the project's requirements & schedule milestones.
• Project Manage work scope ensuring delivery to budget and schedule targets and complies technically with project requirements.
• Manage multi-discipline EPC or Client projects from inception through completion
• From Client Handover, define base line scope, programmes and allowances together with the strategy for delivery in accordance with client / Altrad procedures for management of projects including control of change
• Preparation of the Project Execution Plan for the execution of all project activities in accordance with the Company Business Operating Procedures and specific Client/contract requirements
• Manage project estimates, costs and cost reports and deliver monthly updates
• Deliver projects in alignment with pre-established policies and processes for clear communications to all parties involved in the project
• Manage the preparation and regular update of the Project Schedule against which all project deliverables are monitored and controlled.
• Preparation and delivery of client side procedural documents in support of project delivery

Key Responsibilities:

The appointed will manage projects from client handover, through to final completion and par of an integrated site team consisting core project disciplines including construction including feasibility, front end engineering, execution and handover in accordance with joint client / Altrad procedures for delivery of projects.

Key Accountabilities:

• Delivery of engineering to time and cost required.
• Effective execution of the assigned engineering Work Packages within the time, cost, and quality required.
• Ensure project changes impacting the assigned work scope are flagged, reported, authorised, and implemented effectively.
• Coordinate effective responses to site and vendor queries.
• Deliver complete customer satisfaction and deliver/close out on time, first time to specification and quality.
• Point of contact and liaison / communication between Company and Client.
• Project Budget management and authority for approval of project expenditure.
• Ensure compliance with the Company’s Quality Policy and Business Operating Procedures recognising specific Customer driven requirements as defined in the Project Execution Plan.
• Communicate to ensure complete awareness of all team/contractor members of interface roles and responsibilities to achieve global project objectives.
• Identify, review and manage project risk avoiding/minimising financial exposure.
• Manage Project Reporting throughout the life cycle of the project on an open, no surprises basis.
• Maintain a proficient, ethical and cooperative approach with Client, Contractors and Team Members.

Key Requirements:

• Strong knowledge of manufacturing in a process industry gained in an industrial environment and ideally including understanding of hazardous sites and COMAH.
• Experience of being site based and working in an integrated way with a client manufacturing team
• HNC/HND in an engineering discipline or Degree level qualification or equivalent in a technical or engineering discipline.
• Experience of leading a multi-discipline design engineering team within the process sector.
• Pharma sectors experience beneficial.
• Experience in full project life cycle including feasibility, FEED, Detailed design and Execute phases potentially via EPC/ EPCM.
• A track record in role of PM executing small to medium sized multi disciplined process and infrastructure projects.
• Site management exposure of multi-disciplined site construction, plant and services installation, testing and commissioning
• Experience of working within a project portfolio environment.

Why join us?

• Work on high-impact projects within a leading organisation at the forefront of the nuclear industry.
• Competitive salary and benefits package.
• Opportunities for career growth and professional development.
• Collaborative and dynamic work environment with a focus on innovation and excellence.

Altrad Babcock is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We make hiring decisions based on your experience, skills, and passion for making a difference. Everyone is welcome to apply.

If you wish to be considered please apply using the link and start your journey with Altrad…

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• Developing, implementing, and maintaining the Quality Management System (QMS) in accordance with regulatory requirements.
• Ensuring adherence to GMP, GLP, and other relevant industry standards across all operations.
• Leading and managing internal and external audits, inspections, and regulatory submissions.
• Overseeing the deviation and CAPA (Corrective and Preventive Actions) management process.
• Reviewing and approving batch records, validation protocols, and other critical quality documentation.
• Managing the change control process to ensure all changes are properly assessed, documented, and implemented.
• Developing and delivering quality training programs to staff.
• Monitoring and reporting on key quality metrics and performance indicators.
• Leading and mentoring the Quality Assurance team.
• Collaborating with cross-functional departments to resolve quality issues and drive continuous improvement.

• Supervising and guiding the Quality Control team, including training, performance management, and professional development.
• Developing, validating, and implementing analytical methods for raw materials, in-process samples, and finished products.
• Ensuring compliance with all relevant regulatory requirements (e.g., MHRA, FDA) and company SOPs.
• Managing the QC laboratory budget, equipment calibration, and maintenance.
• Reviewing and approving QC testing data, batch records, and deviation reports.
• Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPAs).
• Participating in internal and external audits and inspections.
• Collaborating with Production, QA, and R&D departments to resolve quality issues and support product lifecycle management.
• Staying current with pharmacopoeial requirements and regulatory updates.
• Driving continuous improvement initiatives within the QC department.
• Ensuring a safe working environment within the QC laboratory.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 7 years of progressive experience in pharmaceutical quality control, with at least 3 years in a supervisory or managerial role.
• In-depth knowledge of GMP, ICH guidelines, and relevant regulatory frameworks.
• Strong experience with various analytical techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Proven ability to lead and motivate a team.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong documentation and reporting skills.
• Experience with laboratory information management systems (LIMS) is a plus.
• Adaptability to work effectively in a hybrid environment, balancing on-site oversight with strategic planning.

Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly and is positioned well for an exciting future of continued expansion.

We are seeking a proactive, client-focused, and results-driven Client Engagement Manager to join our high-performing Global Business Development team. Reporting to the VP of Business Development, you will be responsible for generating sales leads for the Managed Access Division, supporting targeting and conference strategies, and collaborating with Marketing to strengthen the division’s online presence.

In this role, you will work closely with both the Marketing and Business Development teams to drive effective lead generation across all target assets and companies. You will also support visibility strategies through conference participation and digital engagement.

Key Responsibilities:

• Generate sales leads for the Business Development team against a pre-defined list of target assets and companies
• Support qualification of target assets against pre-agreed criteria
• Client outreach through social media, telephone, email and conference attendance
• Create compelling and client specific ‘hooks’ to generate interest in Clinigen offering and secure direct client contact opportunities for BD team
• Identify target people against key target assets to ensure outreach to correct decision makers
• Support horizon scanning for appropriate conferences and liaise with conference organisers to assess suitability, provide feedback and summaries to VP BDMA.
• Support BD prior to and during industry conferences to drive lead generation activities where appropriate
• Work with Marketing function to ensure full coverage of target assets and companies, maintaining high levels of awareness and supporting Thought Leadership positioning
• Create innovative ways to drive lead generation and get to target people quicker
• Work with VP BDM to maintain elements of the BD MA sharepoint site and develop SME status with regards to Salesforce use
• Work with Marketing function to ensure utilisation of content direct to target assets, people and companies
• Work with internal Clinigen stakeholders to ensure utilisation of existing Clinigen relationships where appropriate

Requirements

• Highly motivated and driven self-starter looking to progress into a commercial/sales/marketing environment
• Science/pharma background to enable identification of correct ‘hook’ to provoke lead and ensure credibility with prospect
• Ability/desire to travel internationally
• Excellent written and verbal communication skills
• Genuine passion for pharma industry and Clinigen offering with view to progress career quickly
• Good understanding of social media (LinkedIn primarily)
• Strong networking and interpersonal skills with ability to develop strong relationships with internal and external stakeholders
• Strong commercial intelligence and selling skills

Benefits

• 27 days holiday, plus bank holidays
• Discretionary Bonus
• Pension contributions & Life Assurance scheme
• Flexible Benefits Platform
• Annual salary review
• Independent financial advice service
• Enhanced Employee Assistance Programme
• Shopping discounts with retailers
• Long service awards
• Recognition scheme & employee of the year awards

Interested? We would love to hear from you, please apply today for consideration.