149 Control Analyst jobs in the United Kingdom

Job title: TRADE CONTROL ANALYST
Location: London, UK
Job reference #: 31770
Contract type: Permanent
Language requirements: Fluent in English; knowledge of Italian would be an advantage.

At Eni , we are looking for a Trade Control Analyst to join Eni Trade & Biofuels (ETB) in London , UK. Working closely with the front office and other teams within the middle office, you will be responsible for performing daily transaction validation and control activities focused on energy commodities (crude, products, and biofuels). The ideal candidate will have experience working with a variety of commodities, although we are open to considering experienced individuals with a particular focus on a single commodity.

About Eni Trade & Biofuels

ETB is at the cutting edge of sustainability and innovation in the global energy market. As a dynamic force within the Eni group, which is a leader in the energy transition, at ETB we are rapidly establishing ourselves as a key player in the new energy landscape. When you join ETB, you become part of Eni - a leading global energy company with over 32,000 employees in 61 countries. Eni is at the forefront of the energy industry, specializing in exploration, production, transport, marketing and trading of oil, natural gas and biofuels. ETB is the crude oil, refined oil products and biofuels trading and shipping company of Eni. We are a diverse and dynamic team of around 300 professionals distributed in three offices (Rome, London and Singapore) with the addition in Houston of Eni Trading & Shipping Inc. (ETS Inc) which handles marketing of oils and petroleum products for the US market. Our team is also involved in marketing Eni's oil equity productions, sourcing hydrocarbons and bio feedstocks, and managing the output of our traditional and green refineries.

Main responsibilities :

• Perform daily validation activities to ensure all financial and physical crude and product transactions are captured accurately and in a timely manner and ultimately validated in accordance with the company's procedures.
• Conduct daily checks on relevant prices (spot/forward) to ensure all market data is captured accurately and promptly.
• Support the oil, financial, and physical end-of-day processes in the relevant ETRM system, ensuring the timely generation of position and P&L reports.
• Carry out checks on unauthorised trades and monitor mandates/limits (e.g. tenor, quantity, value).
• Perform daily market conformity controls to monitor financial and physical oil transactions.
• Complete all required activities related to month-end and quarter-end checks for financial and physical oil.
• Ensure compliance with all internal and external regulations and respond promptly to all audit requests.
• Provide support to the Middle Office function regarding new products and non-standard deal approvals and monitor procedural compliance with new financial regulations (e.g. MiFID II, position limits) through first-level control execution.
• Support automation initiatives by promoting greater use of systems within the Trade Control team, eliminating manual spreadsheets, and fully supporting the implementation of relevant controls directly into trade capture systems.
• Manage ad hoc requests as required.

Skills and experience required :

• University degree in a numerate discipline (e.g. Finance, Mathematics or a quantitative-related field).
• Prior experience in a risk or trade control-focused role within the commodities industry.
• Strong knowledge of oil products.
• Understanding of control processes applicable in a trading or regulated environment.
• Familiarity with exchanges (e.g. ICE, CME, NYMEX, DME), Platts' Market on Close (MOC), E-Window, and other trading platforms.
• Highly proficient in Excel and VBA; knowledge of Python and Power BI would be an advantage.
• Strong organisational, time-management and team-working skills, with excellent attention to detail.
• Effective communication skills, with the ability to build relationships across a wide range of internal and external stakeholders.
• Results-oriented and proactive approach to work.
• Fluent in English; knowledge of Italian would be an advantage.

Why ETB
•

• Impactful Work : Join a team that plays a crucial role in Eni's Net Zero 2050 strategy, benefiting from Eni's strong trading position and global integration.
• Collaborative Culture : Experience a truly multicultural, supportive, and dynamic work environment.
• Career Growth : Rapid learning opportunities with potential for movement across teams and international roles.
• Work-Life Balance : Enjoy a balanced lifestyle with a comprehensive benefits package that may include health, well-being, and flexible working options.

How to apply :

• Applications are only accepted through our online application system.
• Please upload your CV in English .

About Eni

Eni is a global energy company operating in 61 Countries, with over 30,000 employees. Originally an oil & gas company, it has evolved into an integrated energy company, playing a key role in ensuring energy security and leading the energy transition. Eni's goal is to achieve carbon neutrality by 2050 through the decarbonization of its processes and of the products it sells to its customers. In line with this goal, Eni invests in the research and development of technologies that can accelerate the transition to increasingly sustainable energy. Renewable energy sources, bio-refining, carbon capture and storage are only some examples of Eni's areas of activity and research. In addition, the company is exploring game-changing technologies such as fusion energy - a technology based on the physical processes that power stars and that could generate safe, virtually limitless energy with zero emissions.

Working at Eni

At Eni we believe in enterprising people, capable of making a difference and making their contribution with passion and innovation, to respond to the global challenges of the energy transition. For us, the skills and attitudes of each individual , continuous training , and diversity and inclusion are fundamental. We promote flexible ways of working with particular attention to well-being, welfare and work life-balance. Eni will evaluate applications considering plurality and diversity as sources of enrichment. If your application is assessed to be among those most in line with the required profile, you will be contacted to continue the selection process. Whatever your ambition, at Eni you can find the tools to make it happen.

Energy for action takers

Group Controls Analyst

£45,000 + 10% bonus

Full-time Liverpool

Join a business at a crucial time of expansion

I'm recruitng for a Group Controls Analyst to join a fast-growing, values-led business in the North West. This brand-new role sits at the centre of a thriving finance function giving you the chance to help shape internal controls and influence the business as it continues to scale.

Making the m.

• Conducting chemical, physical, and microbiological testing on pharmaceutical samples using various analytical techniques (e.g., HPLC, GC, UV-Vis, Karl Fischer).
• Preparing reagents, standards, and solutions for analytical testing.
• Accurately documenting all testing procedures, results, and observations in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Performing method validation and equipment calibration activities.
• Troubleshooting analytical methods and equipment failures.
• Interpreting test results and identifying any deviations from specifications.
• Writing and reviewing analytical test methods, validation reports, and quality control procedures.
• Collaborating with other departments, including Research and Development and Production, to resolve quality issues.
• Maintaining a clean and organized laboratory environment.

• Degree in Chemistry, Pharmacy, Biochemistry, or a related field.
• Previous experience in pharmaceutical QC or analytical laboratory work.
• Proficiency with analytical techniques such as HPLC, GC, spectroscopy.
• Knowledge of GMP, GLP, and regulatory guidelines.
• Strong analytical and documentation skills.
• Ability to work autonomously and meet deadlines in a remote environment.
• Excellent communication and report-writing skills.

• Perform analytical testing of raw materials, intermediates, and finished products.
• Operate and maintain laboratory equipment, including HPLC, GC, and spectrophotometers.
• Prepare samples, reagents, and standards for analysis.
• Document all test procedures, results, and observations accurately.
• Ensure compliance with GLP, GMP, and other relevant regulatory guidelines.
• Participate in method validation and transfer activities.
• Investigate and report on out-of-specification (OOS) results.
• Maintain a clean, organized, and safe laboratory environment.
• Collaborate with R&D, Production, and Regulatory Affairs teams.
• Contribute to the continuous improvement of QC processes and procedures.

• Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related life science discipline.
• Proven experience working in a pharmaceutical quality control laboratory.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR, etc.
• Familiarity with pharmacopoeial standards (BP, USP, EP).
• Knowledge of GLP and GMP principles.
• Strong understanding of experimental design and data analysis.
• Excellent problem-solving and critical thinking skills.
• Meticulous attention to detail and accuracy.
• Good written and verbal communication skills.
• Ability to work effectively in a team-oriented environment.

• Perform analytical testing of raw materials, intermediates, and finished pharmaceutical products using methods such as HPLC, GC, UV-Vis Spectroscopy, and titrations.
• Prepare reagents, standards, and samples according to approved procedures.
• Operate and maintain laboratory equipment, ensuring calibration and performance are within specifications.
• Document all testing procedures, results, and observations accurately and comprehensively in laboratory notebooks and electronic systems.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective actions.
• Ensure all activities comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Participate in method validation and transfer activities.
• Review and approve test data and batch release documentation.
• Contribute to the continuous improvement of laboratory processes and quality systems.
• Maintain a safe working environment by adhering to all safety protocols and procedures.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues.
• Assist in the preparation for internal and external audits.

• Bachelor's or Master's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline.
• Proven experience in pharmaceutical quality control or a related laboratory setting.
• Hands-on experience with analytical instrumentation commonly used in pharmaceutical analysis (e.g., HPLC, GC, Karl Fischer titrator, FTIR).
• Strong understanding of GMP, GLP, and relevant regulatory requirements.
• Excellent data analysis and interpretation skills.
• Proficiency in scientific documentation and record-keeping.
• Strong problem-solving abilities and attention to detail.
• Ability to work independently and manage priorities effectively in a remote work environment.
• Effective communication and teamwork skills, even in a virtual setting.
• Knowledge of pharmacopoeial methods (e.g., USP, EP).
• Commitment to maintaining the highest standards of quality and scientific integrity.

• Performing analytical tests on pharmaceutical products using techniques such as HPLC, GC, UV-Vis, and titration.
• Testing raw materials, intermediates, and finished goods to ensure they meet specifications.
• Accurately documenting all testing procedures, results, and observations in compliance with GMP guidelines.
• Maintaining and calibrating laboratory equipment to ensure accuracy and reliability.
• Investigating out-of-specification (OOS) results and participating in deviation investigations.
• Assisting in the validation of analytical methods and equipment.
• Preparing and reviewing quality control documentation, including reports and certificates of analysis.
• Collaborating with R&D, production, and regulatory affairs departments.
• Staying updated on current Good Manufacturing Practices (cGMP) and relevant regulatory guidelines.

• Performing analytical tests on pharmaceutical samples.
• Operating and maintaining laboratory instrumentation.
• Analyzing test results and ensuring compliance with specifications.
• Documenting all laboratory activities according to GMP.
• Assisting with method development and validation.
• Participating in internal and external audits.
• Adhering to all safety protocols in the laboratory.
• Troubleshooting analytical issues.

• Performing analytical tests on pharmaceutical raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, and titration.
• Preparing reagents, solutions, and standards required for analytical testing.
• Operating, calibrating, and maintaining laboratory equipment and instrumentation.
• Documenting all testing procedures, results, and deviations in accordance with company SOPs and regulatory requirements.
• Reviewing and interpreting analytical data, identifying any out-of-specification (OOS) results and participating in investigations.
• Ensuring all laboratory activities comply with GLP, GMP, and other relevant regulatory standards.
• Preparing Certificates of Analysis (CoA) for tested materials.
• Maintaining a clean and organized laboratory environment.
• Participating in method validation and transfer activities as needed.
• Assisting with internal and external audits as required.

• Performing analytical testing on pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titration).
• Preparing reagents, solutions, and standards for analytical testing.
• Documenting all laboratory activities, test results, and deviations accurately and in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
• Interpreting test results and comparing them against specifications, reporting any out-of-specification (OOS) results to the QC Manager.
• Calibrating and maintaining laboratory equipment, ensuring it is in good working order.
• Participating in method validation and transfer activities.
• Assisting with the investigation of deviations, out-of-specification results, and customer complaints.
• Contributing to the continuous improvement of QC laboratory processes and procedures.
• Maintaining a safe and organised laboratory environment, adhering to all safety regulations.
• Ensuring compliance with regulatory requirements from bodies such as the MHRA and FDA.
• Participating in internal and external audits as required.