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Technical and Engineering

We are hiring for various Technical and Engineering roles.

Working within a multi-disciplinary team, the successful candidates will be placed in roles based on their academic background and/or their technical experience in a pharmaceutical or equivalent highly regulated industry.

• The purpose of the roles are, for example, to provide technical support, through identification and qualification of new products and process introduction (NPI) and implementation of process improvement opportunities within our existing commercial operations.
• The roles are best suited to individuals with a Scientific or Engineering degree, or those with relevant technical experience within a manufacturing, packaging, or engineering environment.

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Formulation Development

We are hiring for various roles in Formulation and Process Development including:

• Scientist / Engineer Levels I, II and III
• Senior Scientist / Engineer Levels I and II
• Technical Leader Levels I and II

Successful candidates will be placed at the appropriate level based on their academic background and experience in pharmaceuticals or related industries.

Requirements:

• A third level education in Chemical/ Process Engineering, Pharmacy, Chemistry, or a similar scientific or engineering discipline.
• Applicants will be supported through a bespoke training and development program.

Role Overview:

The purpose of this role is to lead the development of all aspects of the formulation and processes used in the manufacture of new and existing drug products, specifically focusing on oral solid and non-sterile dosage forms from phase 1 to phase 3 clinical trials. As a scientist, the candidate will be very hands-on with development in collaboration with our clients, acting as a key stakeholder for scientific contributions to the team, development planning, and GMP strategies. Additionally, the role involves the commercialization of products and supporting projects until successful validation. Overall, the Formulation Team coordinates the manufacture by liaising with various stakeholders to ensure production is completed to the required quality and on time. Documentation is also a key part of this role, where scientists are required to accurately capture data, interpret it scientifically, and compile technical reports to the highest standards.

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Project Management

Project Management is central to all operations at Almac Pharma Services. The Project Manager serves as the primary contact for clients and will lead a multidisciplinary team from various Almac departments to meet client requirements. Supported by a Project Coordinator, the Project Manager will be assigned to multiple projects overseeing multiple Client accounts.

Almac Pharma Services has three distinct project management groups, each specialising in different business areas:

1. Pharmaceutical Development: This group focuses on the early stages of drug development, including formulation, clinical trial material manufacturing, and analytical services. They ensure that new pharmaceutical products are developed efficiently and meet regulatory standards.
2. Packaging Process Validation: This team specialises in validating packaging processes to ensure that products are safely and securely packaged. They work on designing, testing, and validating packaging solutions that comply with industry standards and client specifications.
3. Ongoing Commercial Supply: This group manages the supply chain for commercial products and the relationship between Client and Almac. They oversee the production, packaging, and distribution of pharmaceutical products to ensure a continuous and reliable supply to the market.

Each group plays a crucial role in supporting client requirements and ensuring the successful delivery of pharmaceutical services.

This diverse field offers individuals the chance to enhance their skills and knowledge in a dynamic, fast-paced environment.

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Analytical Lab Based Opportunities

Our expert lab teams are responsible for undertaking analysis in support of drug product manufacture, from early phase development to commercial release. Within our specialised testing laboratories, we possess experience in a wide range of analytical techniques and utilise the most advanced equipment and software packages available to ensure that all testing is performed to the highest standards. Our labs operate on a full flex schedule.

To facilitate the growth and continuous improvement of our laboratory services, we are recruiting for a range of current and future roles in the following areas:

Lab Based roles

• Lab Technician
• Lab Analyst/Senior Analyst
• Raw Materials Analyst
• Cleaning Verification Analyst

Lab Supervisor/Management Roles

• Technical Leader
• Team Leader

Lab Support Roles

• Lab Instrument Technician
• Lab Data Systems Specialist

Lab Technician, Lab Instrument Technician, and Lab Data Systems Specialist roles are suitable for candidates with a Science based A-Level (or equivalent qualification) and no third level qualification.

All other roles are suitable for graduates with a Pharmaceutical Science/Chemistry/Microbiology, or similar Life Sciences degree, and for experienced professionals who have worked in a laboratory environment.

Successful candidates will be assigned to the appropriate level based on their academic background and experience in pharmaceuticals or related industries. Applicants with no previous experience are welcome and will be supported through a bespoke training and development program.

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Quality

The Quality Assurance (QA) department plays a crucial role in ensuring that medicines produced are safe and effective, and that APS adheres to all regulations and guidelines set by health authorities, such as the MHRA. QA supports the entire production process, from compilation of batch records and procedures that govern the operations, to assessing the impact when things don’t go as planned.

Our teams include:

• Quality Operations: Responsible for ensuring the manufacturing, Packaging and distribution of our Pharmaceutical Products comply with regulatory standards and our internal Quality Processes through understanding of the principles of GMP & GDP.  
• Quality Compliance: Responsible for ensuring the Pharmaceutical Quality System, including procedures and processes, adhere to regulatory requirements.  
• Product Quality: Responsible for ensuring each batch of product manufactured meets the required quality standards before it is certified for use.  
• Technical Quality: Responsible for ensuring that our systems and processes meet the required quality standards. It is a GMP requirement that manufacturers control the critical aspects of their operations through qualification and validation over the life cycle of the product and process. This ensures systems and processes are fit for purpose and ultimately ensures the safety of our patients.  

Who the role is suited to: Our roles are best suited for people with a Chemical/Process Engineering, Pharmacy or Chemistry degree, in lieu of this, applicants with experience in a Scientific or Engineering industry will be welcome.

Levels of experience: Graduates with no previous industry experience are welcome and will be supported through a bespoke training and development program.

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GMP Operations

Role overview

As an Operator within our Production team based in Loughborough, you will be responsible for ensuring the smooth and efficient running of process development activities within the department.

You will be involved in a wide range of manufacturing activities for oral solid dose pharmaceuticals, either as part of a team or unsupervised. You will:

• Prepare processing areas and assemble equipment, with appropriate training.
• Complete cleaning of processing areas and equipment, including appropriate storage of equipment and consumables during and after processing campaigns
• Ensure all processing and non-processing areas are maintained to a high level of cleanliness.
• Ensure batch documentation is completed accurately.
• Work according to GMP and EHS requirements.

The standard shift pattern for the role is Monday to Friday, 8:30 – 16:30. Successful candidates may be expected to work changing shift patterns to enable us to meet clients project demands.

Successful candidates will be graded based on their level of experience and provided with structured training and development opportunities to enable them to progress within the team

Requirements

• GCSEs (or equivalent) at Grade C or above in English Language, Math and Science.
• Proven experience of working well within teams

The following would also be beneficial but is not essential:

• Experience in a manufacturing environment within the pharmaceutical industry.
• Experience in set up, operation and clean down of process equipment.
• Involved in blending, compression/encapsulation and coating processes.

Additional Information

Please note, we are recruiting for current and future vacancies, with CVs assessed as part of an ongoing process.

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