4 jobs found

Junior Electrical Maintenance Engineer (Training on F-Gas) £38,000 - £40,000 + OTE £45,000 + 2k Call Out Bonus+ Training + Qualifications + Overtime Wrexham Are you a Junior Maintenance Engineer with an electrical qualification such as NVQ, BTEC or similar looking to work for a growing company that will provide ample training and qualifications in refrigeration to allow for further progression? Do you want to work for a company that invests in their staff through tailored development and offer plenty of overtime to help boost earnings? On offer is the opportunity to join a growing company who provide cold storage and logistic solutions to a number of clients in the Food and Pharmaceutical industries. They have been in operation for over 40 years going through a significant Expansion Program in the UK with huge investments in the next couple of years already planned. In this role you will carrying out PPM maintenance of Mechanical aspects of all cold storage machinery on site, working in an Electrically Biased team to ensure the continued operation of all the chillers. This role will also provide training on equipment and the opportunity to earn a qualification in Refrigeration. This role would suit a Junior Maintenance Engineer with Electrical bias who holds an electrical qualification such as an NVQ, BTEC or 17th/18th edition looking for career development and excellent overtime opportunities. The Role: Maintenance on cold storage equipment Following PPM schedule Training on equipment and refrigeration Monday - Friday (8am - 4:30pm) On call rota 1 in every 3 weeks Overtime 1.5x and 2x on Sunday The Person: Electrical Maintenance Engineer Manufacturing or Cold Storage background Electrical Qualification (NVQ, BTEC, 17th/18th Edition) Job Reference: BBBH22995a Maintenance Engineer, Maintenance, Electrical, HVAC, NVQ, 17th /18th Edition, BTEC, Technician, HVAC, PLC, Hydraulics, Fault Finding, Overtime, Days Based, Training, Refrigeration, Manufacturing, Warehouse, Cold Storage, PPM If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV. We are an equal opportunities employer and welcome applications from all suitable candidates. The salary advertised is a guideline for this position. The offered renumeration will be dependent on the extent of your experience, qualifications, and skill set. Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C's, Privacy Policy and Disclaimers which can be found at our website. JBRP1_UKTJ

General Information Title: Senior Scientist - Formulation Development Department: Formulation Development Site: Guildford, UK Reporting To: Associate director - Formulation Development Position Summary - To design and develop dosage forms as per the client's TTP within the set timeline and oversee laboratory operational activities of the UK Formulation Development team Essential Functions Lead and oversee experimental activities within assigned projects, ensuring alignment with study plans, SOPs, agreed timelines, and MedPharm's Quality Management System (QMS), while considering resource availability. These include but are not limited to the following: Provide expert guidance on the selection and preparation of solvent systems and execution of saturated solubility experiments. Lead the design and development of formulations for assigned projects, ensuring scientific rigor and alignment with project objectives. Manufacture and aliquoting of formulations for stability studies. Characterisation of formulations during the development phase and on developmental stability studies. Analyse and interpret study data to inform formulation strategy and decision making. Schedule and oversee laboratory work, ensuring efficient resource allocation. Lead and mentor team members through various stages of formulation development. Maintain effective communication with Study Director, Technical Oversights, and Project Managers. Contribute to Formulation Development updates in collaboration with internal stakeholders. Maintain operational expertise on equipment used in the laboratory and troubleshooting. Train other team members on equipment use. Maintain training records and review the training records of direct reports, where applicable. Ensure all activities comply with Health & Safety policies and COSHH regulations. Supervisory responsibilities Provide effective line management through regular one to ones, performance reviews, and oversight of staff training and development. Key Relationship Laboratory staff in Formulation development, Process Development and Analytical Heads of Departments Study Directors Laboratory Technicians Project managers Planning team 3rd Party suppliers and vendors Education and Experience Degree in Pharmaceutical Sciences, Chemistry, or related field (MSc/PhD preferred) Proven experience in formulation development Knowledge, Skills, and Abilities Knowledge of Formulation Science Knowledge of dosage forms including creams, ointments, gels, suspensions. Cosmetic development (Preferred but not essential) Experience in pre formulation and formulation development. Ability to work to tight deadlines. A methodical approach to work and highly organised. Ability to work independently and contribute to the team. Good communication skills (written and oral). IT literate. Ability to multi task, manage time efficiently and prioritise. Physical Demands and Work Environment While performing the duties of this job, there may be certain physical demands required for the position. Regular standing for extended periods while conducting laboratory experiments and processes. Frequent manual handling of laboratory glassware, raw materials, and small scale manufacturing components. Occasional lifting of items up to 10-15 kg, such as chemical containers or pieces of equipment. Repetitive movements associated with routine laboratory procedures. Other Duties You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked. Limitations and Disclaimer The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.

Pharmacy Manager GMP Pharmacy & Manufacturing Full Time The Medicines Evaluation Unit (MEU) Ltd is one of the UKs leading contract research organisations conducting clinical trials for the pharmaceutical industry.The organization holds MHRA Phase I Accreditation, together with an MHRA Manufacturing Licence MIA (IMP). Our state-of-the-art facility operates under strict Good Manufacturing Practices (GMP). The Role We are seeking a detail-oriented, proactive Pharmacy Manager to join our production team. As a Pharmacy Manager, you will assist the Head of Pharmacy to support operational functions of the MEU pharmacy department and GMP manufacturing facility. You will play a key role in supporting the preparation, packaging, dispensing and quality control of pharmaceutical products. This management role combines accuracy with strict compliance to Good Manufacturing Practice (GMP) guidelines. What we are looking For Essential Registered Pharmacist (GPhC) or equivalent relevant scientific qualification (e.g. Registered Pharmacy Technician). Significant experience in GMP sterile and Non-Sterile manufacturing, IMP handling, or clinical trial pharmacy operations. Strong working knowledge of EU GMP, GCP, UK Clinical Trials Regulations, and MHRA inspection requirements. Proven leadership and team management skills within a regulated environment. Excellent documentation, organisational, and communication skills. Demonstrated ability to manage workload and make decisions under inspection-ready conditions. Desirable Experience within an MHRA Phase I unit, CRO, or early-phase manufacturing environment. Experience with aseptic or sterile manufacturing. Knowledge of QMS tools, CAPA management, and risk-based approaches. Experience supporting facility design, qualification, or expansion projects. Personal Attributes Proactive, accountable, and quality-driven with strong attention to detail. Confident and calm under pressure with sound professional judgement. Collaborative and adaptable, capable of leading multidisciplinary teams. Committed to maintaining the highest standards of GMP and GCP compliance MEU will offer you. Competitive Salary & Benefits Package A supportive, safety-focused working environment 29 days annual leave plus bank holidays Company pension scheme Discretionary bonus and healthcare plan after a qualifying period Free secure on-site parking JBRP1_UKTJ