2,201 Pharmaceutical Analyst jobs in the United Kingdom

PE Global is recruiting Pharmaceutical Business Analyst for our pharma client based in Moorgate, London. The rate for this role is £33.04 PAYE or £44.43 Umbrella p/hour.

There are two contract durations on offer, a 6-month and an 11-month.

This will be a hybrid role - 2 days a week in the office. Pharma Industry or Biotech experience preferred.

Responsibilities:

1. Drive Performance Insights

• Analyse brand and market performance to identify risks and opportunities.
• Turn data into clear, actionable insights that support business planning.
• Track customer engagement and improve omni-channel effectiveness.

2. Shape Go-to-Market and Portfolio Strategy

• Help prioritise products and initiatives based on data and market trends.
• Guide commercial teams on where to focus resources for maximum impact.
• Lead the design and execution of the Sales Force Incentive Programme.

3. Lead Forecasting and Planning

• Build accurate forecasts using market data and historical trends.
• Ensure business assumptions are evidence-based and aligned with strategy.
• Support planning cycles with reliable, insight-driven inputs.

4. Prioritise Business Questions and Insights

• Identify key strategic questions that data can help answer.
• Highlight gaps in data or insights and help shape research priorities.
• Focus efforts on insights that drive measurable business outcomes.

5. Influence Strategy and Decision-Making

• Embed insights into business reviews and strategic planning.
• Deliver clear, compelling reports and presentations for senior leaders.
• Act as a strategic advisor across commercial and cross-functional teams.

6. Build Insight Capability Across the Business

• Coach teams on how to use data effectively.
• Promote data literacy and strategic thinking across departments.
• Foster a culture where insights drive decisions and innovation.

Requirements:

Essential

• Proven experience in the pharmaceutical, biotech, or healthcare industry preffered .
• Strong analytical and problem-solving skills with ability to translate data into strategy.
• Excellent stakeholder management and communication skills, including experience working with senior leaders.
• Experience in commercial strategy, business analytics, or performance management .
• Familiarity with UK healthcare system and NHS structure .
• Project management capabilities, including prioritisation and coordination across functions.
• Comfortable navigating ambiguity in fast-paced environments.
• Advanced proficiency in Microsoft Office (Excel, PowerPoint, etc.) .
• Degree in STEM (Science, Technology, Engineering, Maths) or Business-related field required.

Preferred

• Familiarity with CRM and marketing platforms (e.g., Veeva CRM, Veeva PromoMats, Salesforce Marketing Cloud ).
• Experience with data visualisation tools such as Power BI or Spotfire .
• Working knowledge of digital tracking and analytics platforms (e.g., Google Analytics, Hotjar ).
• Exposure to market research techniques and frameworks.
• Experience working in Agile teams or Agile environments.
• Understanding of back-end data infrastructure and digital metrics.
• Advanced degrees (MSc, MBA) are a plus but not essential.

Please note PE Global cannot assist with visa sponsorship. Candidates need their own visa valid for the entire duration of the contract.

PE Global is recruiting Pharmaceutical Business Analyst for our pharma client based in Moorgate, London. The rate for this role is £33.04 PAYE or £44.43 Umbrella p/hour.

There are two contract durations on offer, a 6-month and an 11-month.

This will be a hybrid role - 2 days a week in the office. Pharma Industry or Biotech experience preferred.

Responsibilities:

1. Drive Performance Insights

• Analyse brand and market performance to identify risks and opportunities.
• Turn data into clear, actionable insights that support business planning.
• Track customer engagement and improve omni-channel effectiveness.

2. Shape Go-to-Market and Portfolio Strategy

• Help prioritise products and initiatives based on data and market trends.
• Guide commercial teams on where to focus resources for maximum impact.
• Lead the design and execution of the Sales Force Incentive Programme.

3. Lead Forecasting and Planning

• Build accurate forecasts using market data and historical trends.
• Ensure business assumptions are evidence-based and aligned with strategy.
• Support planning cycles with reliable, insight-driven inputs.

4. Prioritise Business Questions and Insights

• Identify key strategic questions that data can help answer.
• Highlight gaps in data or insights and help shape research priorities.
• Focus efforts on insights that drive measurable business outcomes.

5. Influence Strategy and Decision-Making

• Embed insights into business reviews and strategic planning.
• Deliver clear, compelling reports and presentations for senior leaders.
• Act as a strategic advisor across commercial and cross-functional teams.

6. Build Insight Capability Across the Business

• Coach teams on how to use data effectively.
• Promote data literacy and strategic thinking across departments.
• Foster a culture where insights drive decisions and innovation.

Requirements:

Essential

• Proven experience in the pharmaceutical, biotech, or healthcare industry preffered .
• Strong analytical and problem-solving skills with ability to translate data into strategy.
• Excellent stakeholder management and communication skills, including experience working with senior leaders.
• Experience in commercial strategy, business analytics, or performance management .
• Familiarity with UK healthcare system and NHS structure .
• Project management capabilities, including prioritisation and coordination across functions.
• Comfortable navigating ambiguity in fast-paced environments.
• Advanced proficiency in Microsoft Office (Excel, PowerPoint, etc.) .
• Degree in STEM (Science, Technology, Engineering, Maths) or Business-related field required.

Preferred

• Familiarity with CRM and marketing platforms (e.g., Veeva CRM, Veeva PromoMats, Salesforce Marketing Cloud ).
• Experience with data visualisation tools such as Power BI or Spotfire .
• Working knowledge of digital tracking and analytics platforms (e.g., Google Analytics, Hotjar ).
• Exposure to market research techniques and frameworks.
• Experience working in Agile teams or Agile environments.
• Understanding of back-end data infrastructure and digital metrics.
• Advanced degrees (MSc, MBA) are a plus but not essential.

Please note PE Global cannot assist with visa sponsorship. Candidates need their own visa valid for the entire duration of the contract.

• Perform a variety of chemical and physical tests on pharmaceutical products using sophisticated analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
• Analyze raw materials, intermediates, and finished goods to confirm identity, purity, and potency.
• Prepare reagents and solutions required for testing procedures.
• Accurately document all test results, observations, and deviations in laboratory notebooks and electronic systems.
• Calibrate and maintain laboratory equipment, ensuring it is in optimal working condition.
• Follow Standard Operating Procedures (SOPs) meticulously and ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
• Investigate out-of-specification (OOS) results and deviations, contributing to root cause analysis.
• Participate in method validation and transfer activities.
• Contribute to internal audits and regulatory inspections.
• Maintain a clean and organized laboratory workspace.

• Bachelor's degree in Chemistry, Pharmaceutical Science, Biochemistry, or a related scientific discipline.
• Minimum of 2 years of experience in pharmaceutical quality control or a related analytical laboratory role.
• Hands-on experience with analytical instrumentation such as HPLC, GC, spectroscopy techniques.
• Proficiency in GMP and other relevant regulatory guidelines.
• Strong understanding of pharmaceutical testing methodologies.
• Excellent attention to detail and accuracy in data recording and reporting.
• Ability to interpret analytical data and identify potential issues.
• Good problem-solving skills and the ability to work independently.
• Effective written and verbal communication skills.
• Familiarity with laboratory information management systems (LIMS) is a plus.

• Perform chemical and physical analysis on raw materials, intermediates, and finished pharmaceutical products.
• Utilize various analytical techniques including HPLC, GC, FTIR, UV-Vis, and wet chemistry.
• Ensure all testing is conducted in compliance with GMP, GLP, and relevant pharmacopoeial standards.
• Accurately document all experimental data, observations, and results in laboratory notebooks and LIMS.
• Calibrate, maintain, and troubleshoot laboratory equipment.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Prepare and standardize reagents and solutions.
• Contribute to method validation and transfer activities.
• Maintain a clean and organized laboratory environment.
• Participate in internal and external audits.

• Bachelor's degree in Chemistry, Pharmaceutical Science, or a related field.
• Proven experience in a pharmaceutical Quality Control laboratory setting.
• Hands-on experience with HPLC, GC, and other relevant analytical instrumentation.
• Knowledge of GMP and GLP regulations.
• Familiarity with pharmacopoeial methods (BP, USP, EP).
• Strong understanding of analytical chemistry principles.
• Excellent documentation skills and attention to detail.
• Ability to work independently and as part of a team.
• Good problem-solving skills.

• Perform a variety of analytical tests on raw materials, in-process samples, and finished products using techniques such as HPLC, GC, UV-Vis spectroscopy, and titration.
• Prepare reagents, solutions, and standards required for analytical testing.
• Operate and maintain laboratory equipment, ensuring proper calibration and functionality.
• Accurately document all testing procedures, results, and observations in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Analyze and interpret test data, identifying deviations and out-of-specification results.
• Investigate deviations and non-conformances, contributing to root cause analysis.
• Write and review analytical test methods and validation reports.
• Maintain a clean and organized laboratory environment, adhering to safety protocols.
• Participate in internal audits and inspections.
• Collaborate with R&D, production, and regulatory affairs departments to resolve quality-related issues.

• Bachelor's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline.
• Proven experience working in a pharmaceutical QC laboratory environment is essential.
• Hands-on experience with common analytical instruments like HPLC, GC, and UV-Vis spectrophotometers.
• Strong understanding of analytical chemistry principles and techniques.
• Familiarity with GMP, GLP, and relevant regulatory guidelines (e.g., ICH).
• Excellent attention to detail and accuracy in data recording and analysis.
• Strong written and verbal communication skills.
• Ability to work effectively both independently and as part of a team.
• Proficiency in using laboratory information management systems (LIMS) is an advantage.
• A proactive approach to problem-solving and continuous improvement.

• Perform a wide range of analytical tests on raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, spectroscopy, wet chemistry).
• Develop, validate, and transfer analytical methods according to relevant guidelines (e.g., ICH, USP, EP).
• Analyze and interpret test results, ensuring accuracy and completeness.
• Document all laboratory activities, including test procedures, results, and deviations, in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).
• Investigate out-of-specification (OOS) results and out-of-trend (OOT) data, identifying root causes and implementing corrective and preventive actions (CAPAs).
• Maintain laboratory equipment, ensuring it is calibrated, qualified, and in good working order.
• Contribute to the preparation of regulatory submission documents and respond to queries from health authorities.
• Train and mentor junior analysts, providing guidance on analytical techniques and laboratory procedures.
• Participate in internal and external audits, ensuring compliance with regulatory standards.
• Collaborate with other departments, including R&D, Manufacturing, and Regulatory Affairs, to resolve quality issues.
• Stay updated on current industry trends, scientific advancements, and regulatory changes affecting pharmaceutical quality control.
• Ensure the safe handling and disposal of chemicals and laboratory waste.

• A Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
• A minimum of 5 years of hands-on experience in a pharmaceutical Quality Control laboratory.
• Proficiency in analytical techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
• Strong understanding of GMP, GLP, and relevant regulatory guidelines (e.g., ICH, FDA, EMA).
• Experience with method development and validation is essential.
• Excellent analytical, problem-solving, and critical thinking skills.
• Strong documentation and report-writing abilities.
• Good communication and interpersonal skills, with the ability to work effectively in a team.
• Experience with laboratory information management systems (LIMS) is a plus.
• The ability to work independently and as part of a collaborative team in a laboratory setting.

• Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR, titration).
• Develop, validate, and implement new analytical methods according to regulatory guidelines (e.g., ICH, GMP).
• Troubleshoot and maintain analytical instrumentation, ensuring accuracy and reliability of results.
• Interpret test results, prepare comprehensive analytical reports, and document all activities in compliance with Good Manufacturing Practices (GMP).
• Investigate out-of-specification (OOS) results and deviations, recommending corrective and preventive actions (CAPAs).
• Collaborate with R&D, production, and regulatory affairs teams to support product development and lifecycle management.
• Mentor and train junior analysts, providing technical guidance and support.
• Participate in internal and external audits, ensuring compliance with quality standards.
• Contribute to the continuous improvement of quality control processes and laboratory operations.
• Manage and maintain laboratory consumables and reagents inventory.

• BSc or MSc in Chemistry, Pharmaceutical Sciences, or a related discipline.
• Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
• Proficiency in operating and maintaining analytical instruments such as HPLC, GC, and spectrophotometers.
• Strong knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceutical testing.
• Excellent analytical, problem-solving, and documentation skills.
• Ability to work independently and as part of a team in a fast-paced environment.
• Experience with method validation and transfer is essential.
• Good communication skills, both written and verbal.