
Unknown Employer · Watford
[https://www.bbacerts.co.uk/files/2024/03/site-image.jpg] Location: BBA Test, BRE Innovation Park, Bucknall Lane, Watford, WD25 9BA [https://res.cloudinary.co...
[https://www.bbacerts.co.uk/files/2024/03/site-image.jpg]
Location: BBA Test, BRE Innovation Park, Bucknall Lane, Watford, WD25 9BA
Expected Start Date: ASAP
Working for BBA
The British Board of Agrément (BBA) drives industry safety by providing services that help clients create accountability and
mitigate risk. Since 1966, the BBA has built its position as an independent certification body in the Construction and Civil
Engineering industries.
We have a rich heritage of expertise and skill, as well as rigorous and robust processes and procedures which equip us with an
acute focus on construction innovation of the future. Through extensive product and system research, testing and certification,
auditing, and inspection, the BBA helps to instil confidence throughout the construction and manufacturing supply chain in both
the UK and Global marketplaces.
🔗 [https://www.balfourbeatty.com/who-we-are/]About BBA [https://www.bbacerts.co.uk/]
The Package
YOUR MISSION The QC Analytical Scientist is responsible for the testing of gene therapy products and associated materials used for manufacturing to EU and FDA GMP requirements. JOB DESCRIPTION MAJOR ACTIVITIES * The testing of gene therapy products in accordance with product specifications to ensure all testing is completed within the required timelines in alignment with the production schedule. * Support testing requirements for the management of the facility including support of the environmental monitoring schedule. * Operation and maintenance of laboratory equipment ensuring all equipment is calibrated and suitable for use in alignment with the test schedule. * Record of out of specifications, non-conformances, investigations, analysis and implementation of corrective action(s) as applicable. * Assistance with the development and updating of SOPs and laboratory documentation. * Part of the Quality Control team, maintain the flow of information, ensuring appropriate communications are passed and information folders are maintained with most recent version/communication. * Ensure all training is undertaken in a timely manner as required to perform required activities. Support any training activities of other employees where required. * Maintain QC facilities to meet GMP requirements, conduct necessary checks to support any health authority, customer/stakeholder site visits. * Support with maintaining the Quality Management System and controlling of documents and assuring the data integrity of all data produced. * Support any external or internal audits where required. * Support with all reasonable managerial requests and ad-hoc tasks. * Work in a team manner with Production personnel. Additional Activities * Assist in the introduction of new analytical methodology for testing gene therapy products. KEY PERFORMANCE INDICATORS * All testing performed meets QC KPI requirements. * Internal quality control audits. * Plan, manage and record training effectively. KEY JOB COMPETENCIES * QC testing of products to GMP requirements. * Maintenance of Laboratories to GMP standards. * Analytical - Synthesizes complex or diverse information; collects and researches data and uses intuition and experience to compliment data. * Problem Solving - Identifies and resolves problems in a timely manner; gathers and analyses information skilfully; develops alternative solutions and works well in group problem solving situations. * Leadership - exhibits confidence in self and others; inspires and motivates others to perform well; effectively influences actions and opinions of others and accepts feedback from others. * Cost Consciousness - works within approved budget; develops and implements cost saving measures. * Motivation - achieves challenging goals; demonstrates persistence and overcomes obstacles; measures self against standard of excellence. * Planning/Organizing - prioritizes and plans work activities; uses time efficiently. * Professionalism - approaches others in a tactful manner; reacts well under pressure; treats others with respect and consideration regardless of their status or position; accepts responsibility for own actions; follows through on commitments. * Quality Management - looks for ways to improve and promote quality; demonstrates accuracy and thoroughness. * Oral Communication - speaks clearly and persuasively in positive or negative situations; listens and gets clarification; responds well to questions; demonstrates good presentation skills; participates effectively in meetings. * Written Communication - writes clearly and informatively; edits work for spelling and grammar; varies writing style to meet needs; presents numerical data effectively; able to read and interpret written information. * Responsible for ensuring that own work complies with GMP, Data Integrity and Good Documentation Practice (GDP) and is undertaken in accordance with applicable procedures. * Responsible for ensuring that own training is undertaken in a timely and GMP compliant manner before the task is undertaken. * Responsible for ensuring that any GMP documentation assigned to me e.g. (but not limited to) Issues, CAPAs, Change Controls, BMRs & audit/inspection actions is closed timely and in a RFT state. JOB RESPONSIBILITIES * Compliance with GMP. JOB BACKGROUND * Degree in Human Health or Sciences or equivalent relevant work experience in the pharmaceutical or other similar regulated industry (i.e. biologics,). * Demonstrate knowledge/experience of a GMP environment and quality control within a pharmaceutical or other regulated industry. * Proficiency in a body of information required for the job e.g. knowledge of EU and FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc. * Proficiency in IT, Microsoft Office software (Word, Excel and PowerPoint) preferred.
Environmental Industrial Processes - Sustainable Minerals and Metals Do you want to make a difference for the mineral industry and the environment? IFE has an open position within mineral processing and extractive metallurgy in the Environmental Industrial Processes Department. The position is part of the Sustainable Minerals and Metals group (SUMM), which works within IFE’s strategic area of critical raw materials. The group works with both primary and secondary processing of critical minerals and has a strong international position in this field. We are looking for a strong candidate who can help increase the group’s capacity and expertise. The ideal candidate has education and work experience in mineral processing or extractive metallurgy, based on either primary or secondary raw materials. A relevant PhD is an advantage, as is relevant industrial experience. We are seeking someone who can work independently, contribute actively to the research group, communicate well in English, and bring a positive and collaborative attitude. Since much of the work is carried out in collaboration with industry and other research groups, good communication skills are important, and some travel should be expected. The main tasks will include scientific work, planning and following up laboratory activities, developing new research projects, building customer relations, project management, and scientific publishing. We offer a scientist position with access to excellent infrastructure, competitive salary and working conditions, flexible tasks and working hours, and opportunities to contribute to the development of a sustainable mineral industry in Norway and Europe. The work will be carried out in an active and growing research team at IFE, together with inspiring, social, and ambitious colleagues. The group has a strong international position within hydrometallurgy, processing of radioactive materials, and upscaling. The work is performed in collaboration with leading Norwegian and European companies and research institutions. Job description In this position, you will work on various projects and your tasks will include: • Iniate and write research project proposals ranging from direct funded projexcts to large EU-projects • Project management with close industry collaboration • Close cooperation with other department at IFE, research partners and industry • Safety work/HSE related to infrastructure, instruments and daily work • Communication and dissemination activities: Customer meetings, Consortia generation with industry and funding bodies, presentation of results in relevant arenas (e.g. conferences, seminars), publication of scientific papers, etc. • Identification of intellectual property assets (patenting, etc.) when relevant • Install and build experimental set-ups • Design, conduct and manage experimental work related to extractive metallurgy • Thermodynamic modelling • Process simulation Qualification requirements • Engineering degree or MSc in process engineering, metallurgy, chemistry or similar. A PhD degree in relevant area is preferable • Experience in the minerals and metals area from R&D and/or industry. Of special interest are knowledge and experience within hydrometallurgy, pyrometallurgy and/or mineral processing • Experience in planning and managing experimental facilities (reactors, mixer-settler units, autoclaves and other equipment, test rigs and instrumentation), from laboratory to prototype scale • Hands‑on experience with chemical and materials characterization using ICP, XRF, XRD, and SEM‑EDS, including method development, data interpretation, and quality assessment • Experience with processing of both secondary raw materials (e.g. industrial residues, recycled materials) and primary mineral resources • Competence in industrial process design, simulation and thermodynamic modeling tools is an advantage (e.g. ASPEN, HYSYS, OLI, HSC) • Good written and oral communication skills in English is requiered. Good Norwegian knowledge is an advantage • Good overview and knowledge of Norwegian mineral and process metallurgy, with particular insight into hydrometallurgy‑related industry is an advantage • Ability to link fundamental chemistry with industrial process development Personal qualities • Ability to take initiatives and highly result and solution-oriented • Ability to work independently as well as within the research team • Quality-oriented, responsible, dedicated and structured • Motivated to learn new industrial processes and the scientific and technical challenges around them • Good oral and written communication skills • Flexible, versatile and open to work on a varied range of experimental facilities We offer • Exciting and challenging work in an interdisciplinary, international and growing environment within an broad network of academic and industrial partners. • Participation in scientific projects of high international level in the field of environmental process technology and material science. • Stimulating and positive work environment. • Good pension benefits. • Competitive salary terms and working conditions. • A workplace that will promote the employees’ health, environment and safety. IFE is subject to the Security Act, which includes requirements for the organisation’s management of critical national information, as well as other relevant legislation concerning the management of sensitive information. On this basis, it is a prerequisite for employment that the applicant is suitable from a security perspective. Note that relevant applicants will be asked questions that are necessary to ascertain this. This includes questions about any ties to countries that the PST has classified as a ‘high-risk country’ in its open threat assessment. Background checks are performed as part of our recruitment process. We view diversity as a strength in our work. We therefore encourage all qualified candidates to apply regardless of age, gender, disability, sexual orientation, religion and ethnic background. We place great emphasis on your personal suitability for the position. KontaktinformasjonHilde Synnøve Tellesbø, Avdelingsleder, +47 99460629, Hilde.Tellesbo@ife.no Dyugu Yilmaz, Senior Scientist, +47 45843479, Duygu.Yilmaz@ife.no ArbeidsstedInstituttveien 2007 KJELLER Nøkkelinformasjon:Arbeidsgiver: Institutt for energiteknikk (IFE) Referansenr.: 5133011475 Stillingsprosent: 100% Permanent position Søknadsfrist: 14.08.2026
OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personalised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines. ** This position is a fixed-term contract, ending in December 2028 ** Our Medical Affairs Scientists are knowledgeable individuals who are passionate about ensuring that OGT’s products are safe, effective, and fit for purpose, thus allowing them to be available globally and state of the art. You will play an integral role in the delivery of internal and external analytical and clinical performance data for a range of OGT products. What you’ll be doing for us: To work as part of a team in executing tasks as directed, but not limited to, the following activities: * Contribute to the documentation and infrastructure of the department by overseeing the writing of internal and external protocols, study plans and reports * Participate in the design, implementation and delivery of any required studies * Identify and engage external laboratories, clinicians, and partners to obtain clinical performance data * Support and coordinate external studies, including collaboration, data sharing, and contracting activities * Collaborate with internal and external stakeholders to support project delivery * Manage and coordinate projects activities from initiation through to completion * Analyse and interpret data across diagnostic techniques and deliver scientific, clinical, and analytical reports in a timely manner * Ensure timely and accurate reporting of study results * Provide clinical/scientific input for product brochures, catalogues and other marketing materials when required * Contribute to the quality management system and infrastructure of the department by providing input into internal protocols and implementation of CAPAs, change controls and improvements * Support validation activities for team equipment and software, and support maintenance of risk management documentation in line with ISO 14971 * Provide training and support to medical affairs analysts and assistants as appropriate * Provision of analytical teaching within and outside of the medical affairs team as appropriate * Analysis of FFPE and haematological specimens using manual microscopes and automated software * Support karyotype analysis of G banding and reverse DAPI FISH images * To complete any other tasks as commensurate with the level and nature of the post as delegated by the line manager. What we are looking for in you Essential * A bachelor’s degree in molecular biology, biochemistry, genetics, biotechnology, or similar subject is required * Knowledge of FISH and/or cytogenetics techniques and their clinical applications * Understanding of clinical diagnostics, laboratory workflows, or molecular testing * Ability to engage confidently with external partners, including laboratories, clinicians, and collaborators * Proven ability to proactively drive activities forward * Experience drafting study protocols or similar technical/scientific documentation * Understanding of study design considerations, including objectives, endpoints and data requirements * Strong organisational and project coordination skills, managing activities from initiation through to completion * Ability to interpret clinical or diagnostic data, including comparison across different testing methodologies * Experience handling sensitive or clinical data, with an understanding of data quality and governance requirements * Excellent communication skills, both written and verbal. Desirable * Cytogenetics experience in an NHS laboratory or equivalent * Experience in data acquisition, clinical studies, or external collaborations * Experience setting up or supporting contracts, agreements, or study arrangements with external partners * Familiarity with disease areas, sample types, and appropriate testing approaches * Awareness of commercial or customer-facing environments, particularly in diagnostics or life sciences * Experience supporting clinical performance evaluations, validation, or regulatory activities * Experience in cytogenetics and or Karyotype analysis. In return you will receive: * Competitive salary * Pension Scheme (10% non-contributory) * Private Health Insurance * Private Dental Insurance * Group Income Protection * Group Life Assurance * 25 days holiday plus UK bank holidays * High Street Discount Scheme. Application is via CV and a one-page covering letter outlining your suitability for the role, salary expectations and notice period. Please note that we will need to establish your right to work during the recruitment process.