Medical devices / Manchester / ISO13485 / £30,000 - £35,000 / Quality Manager My client is seeking a Quality Manager to join their fast-growing company in Manchester. This company specialise in medical devices in a very exciting field, where they need someone to come on board and join the team to help the company and quality team grow. Position: Quality Manager Salary: £30,000 - £35,000 - 6-month salary review, 10% bonus. Location: Manchester if you are interested in this position then please do get in touch as I would be keen to discuss the role in more detail, if you could send me your most updated CV through to I can then review your experience and get in touch. Medical devices / Manchester / ISO13485 / £30,000 - £35,000 / Quality Manager

Salary: £30,000 - £42,000 DOE + OTE: £8,000 + Pension + Healthcare + Company Car + Phone + Laptop Location: Cambridge, Oxford & London Requirements of the Bioprocess Sales Specialist: PhD or MSc in Bioprocess or related subject such as Vaccine Production, Fermentation, Cell Culture, Molecular Biology etc. Knowledge in Bioprocess at all scales (Lab scale, Pilot scale, Production scale) Demonstrable understanding of the Biotech industry, production facilities and a bioprocess production or process development platform Ability to effectively sell to a diverse customer base including teams of scientists, engineers, and other highly technical team members Ability to drive the Bioprocess strategies execution at Strategic Accounts at short, mid and long term Thorough understanding of the Bioprocess workflow and how to position differentiated products Full, clean and valid Driver's License Responsibilities of the Bioprocess Sales Specialist: Drive incremental sales growth in the Bioprocess Portfolio in the Golden Triangle region of the UK (Oxford, Cambridge and London) This individual will also be responsible for protecting and defending the existing Bioprocess business in the territory defined above as well as executing the Bioprocess strategy at Strategic Accounts level Achieve and exceed sales targets by developing a strong incremental portfolio Execute on business development with a good understanding of all regulations to develop a partnership approach based on Quality compliance, profitability and differentiation Ability to Collaborate with Strategic Account Managers, Business teams and Product Line Managers Company My client is a leading international pharmaceutical and laboratory equipment supplier Their innovative products and services are helping businesses across the globe to implement complex and quality-critical biomanufacturing and laboratory processes The Bioprocess division is a leading international provider of integrated solutions for the biopharmaceutical industry An extensive portfolio of products, technologies and services, we cover wide areas of the biopharmaceutical process chain, ranging from fermentation, cell cultivation, filtration and purification to media storage and transportation This division is a leader in process filtration, fermentation and fluid management Single-use products provided by my client have become established in nearly all process steps and play an important role in the manufacture of biopharmaceuticals You must have full right to work in the UK to be considered for this role. Langton Howarth also operates a recommend a friend referral scheme. So, if you know someone who could be good for this job, email your nominated candidate's name and contact details in confidence via email too, and we'll ensure you receive £100 of vouchers from a high street retailer of your choice!

We are currently recruiting for a Senior Laboratory Scientist (SLS) to join our Formulations Analysis Section in Harrogate. It is an exciting opportunity that will offer you the chance to become part of an exceptionally talented staff community that helps to bring the miracle of medicine to the market sooner. A Senior Laboratory Scientist (SLS) is expected to assist in the supervision and training of junior staff, and to take on additional supervisory roles when necessary, as well as being involved in method development. Additionally a SLS will be responsible for the organisation and efficient running of a number of Toxicology / Molecular Toxicology, Pharmacology or Short-Term Toxicology studies. SLS will have the responsibility of managing up to five operational staff. Responsibilities and duties Full participation in Company Quality Programme Maintenance of duties learned as a Laboratory Scientist 3 Should have the attitude and capability to perform any supervisory role that is required and act as a deputy to the area supervisors in their absence. The capability of managing a number of staff in an area or shift. To assist in the planning and scheduling of studies. To run all aspects of a number of assigned studies from study set up, to the reporting stage with minimal supervision, communicating with all relevant Covance personnel during this period and meeting the Company assigned time-frames. To communicate with the Dispensary Scheduler and Financial Analyst, any study related matters that may effect Dispensary revenues or workload. To respond to client queries relating to assigned studies - and assisting in any related client visits. To ensure, wherever possible the studies are performed using the Dispensary computer system. To ensure full compliance with GLP / SOPs at all times. Ensure time-sheets are accurately completed to ensure accurate study financial records. To undergo training in relevant modules of departmental programmes and to attend any other training recommended by the Supervisor or Manager, to develop managerial skills. To resolve any problems which may prevent efficient operation of studies and to liaise with supervisors and the Manager where necessary. To abide by company / departmental safety regulations at all times. To supervise and train junior staff to ensure their work is of the correct standard. To ensure operational areas are maintained in a clean and tidy state. To ensure that good communication and working relationships are maintained within the department and with the department's customers. To be aware of resources of the department such as stores requisitions and outside purchasing. To respond constructively to QA comments and to convey these comments to the relevant personnel. To carry out method development work and the setting up of studies, liaising with Study Directors and clients when necessary. Education: A Science Degree (ideally chemistry based) Experience: Work experience with GC essential for this role - method development, trouble shooting, maintenance, SD experience. By joining us you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. To submit your application for this Senior Laboratory Scientist opportunity, please click 'Apply' to be redirected to our Covance careers page.

Principal Designer Manchester £35,000 to £40,000 Permanent My client are looking for a dynamic and highly motivated professional to fulfil the role of Principal Designer in their Manchester office. The successful candidate will possess a strong background within a similar role and must have relevant CDM experience..... click apply for full job details

Science Solutions are recruiting for a Regulatory Specialist for a leading chemicals / consumer goods manufacturer based in Manchester. Key responsibilities: Product & Chemical Safety Assessments Create formulation and finished goods safety data sheets in multiple languages. Conduct chemical formulation & finished goods safety assessments together with simulated exposure scenarios. Determine correct label elements to ensure regulatory compliance for the country of sale. Communicate relevant information to allow NPD teams to incorporate all necessary attributes into product design to ensure regulatory compliance in sales region. Regulatory Compliance Ensure product regulatory compliance in region and country of sale. Remain up to date with all relevant legislation in region and country affecting products including but not limited to: REACH, GHS, CLP, Transport, Biocidal Products, Aerosol and Detergents regulations. Work closely with distributors to ensure regulatory compliance in region and country. Communicate with suppliers to ensure relevant regulatory information is made available. General Responsibilities Gather, evaluate, organise and communicate regulatory information appropriately. Respond quickly and appropriately to internal and external customer requests for regulatory support. Interact and participate in all areas of the business to remain familiar with products and services. Manage change and lead regulatory based projects as appropriate. Conduct regular assessments of the industry environment and likely changes to establish potential business impact. Provide education throughout the business to communicate appropriate legislative developments and potential impact. Continuously review and seek to improve information creation and flow, systems & processes to ensure efficient servicing of internal and external customer requirements. Knowledge and experience: Possess degree level education in relevant scientific area, chemistry preferred. Minimum 5 years' experience working in a similar industry environment, preferably in fast moving consumer goods (FMCG) with regulatory compliance responsibilities for the EMEA region. In depth knowledge of REACH, CLP, Detergent and Aerosol regulations. Practical experience of developing multi-lingual safety data sheets and product labels, with knowledge of the Safeware Quasar (GHS Pro) environment essential. Dangerous Goods Safety Advisor qualification essential (education will be provided). Awareness of product waste packaging regulations. Experience of SAP enterprise software environment preferred. IT literate Microsoft Office.