55 Pharmaceuticals jobs in Harlow
Financial Accountant (Pharmaceuticals)
Posted today
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Financial Accountant for a pharmaceutical business based in London seeking qualified ACA/ACCA/CIMA accountants
Your new company
I am supporting a Global Specialist Pharmaceutical company looking for a Financial Accountant to join their growing team. This is a great opportunity to join the company at an exciting time of growth, and work alongside impressive finance leaders that will help with your development. The client is open to candidates with industry experience or from practice with relevant client exposure.
Your new role
Reporting to the Financial Controller, your responsibilities will include:
- Contribute to the preparation of annual statutory financial statements for the group and its subsidiaries in accordance with UK IFRS, ensuring full compliance with all relevant reporting standards.
- Collaborate with external auditors throughout the audit process, responding to enquiries and facilitating the timely resolution of any issues raised.
- Drive improvements in financial reporting processes and internal controls, supporting the manager’s commitment to accuracy, efficiency, and regulatory compliance.
- Provide support in tax-related activities, including VAT submissions, corporate tax calculations, and annual tax disclosures
- Assisting with cash flow management
- Perform monthly balance sheet reconciliations
- Assisting with ad hoc projects
What you'll need to succeed
The client is seeking a Fully Qualified Accountant (ACA, ACCA, CIMA) coming from either practice or industry. Relevant sector or client exposure is ideal, as well as strong stock and distribution knowledge. You’ll have strong collaboration skills and thrive in a fast-paced environment.
What you'll get in return
A competitive salary of £60,000–£65,000, plus a 10% performance bonus and a comprehensive benefits package. You’ll be supported in expanding this role further, working alongside accomplished finance leaders who are committed to your professional development.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call Catherine now.If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career. #
Senior Regulatory Affairs Specialist - Pharmaceuticals
Posted 2 days ago
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The ideal candidate will have extensive experience in regulatory affairs within the pharmaceutical or biotechnology sector, demonstrating a proven ability to manage multiple projects and meet strict deadlines. You will be involved in strategic regulatory planning, providing expert advice to R&D, clinical, and commercial teams on regulatory requirements and submission pathways. This position requires exceptional analytical and communication skills, with the ability to interpret complex scientific and regulatory information and translate it into clear, concise documentation. Collaboration with cross-functional teams and external partners will be a key aspect of the role. This position offers a hybrid working model, allowing for a balance of remote work and in-office collaboration at our **London, England, UK** headquarters. You will be instrumental in bringing innovative medicines to patients by ensuring successful regulatory submissions and maintaining compliance throughout the product lifecycle. This is a challenging and rewarding opportunity for a dedicated regulatory professional to make a significant impact.
Key Responsibilities:
- Prepare, review, and submit regulatory submissions (e.g., NDAs, MAAs, variations) to global health authorities.
- Develop and implement regulatory strategies for product development and lifecycle management.
- Ensure compliance with all applicable pharmaceutical regulations and guidelines.
- Liaise with regulatory agencies, manage correspondence, and respond to queries.
- Provide regulatory input and guidance to R&D, clinical, manufacturing, and commercial teams.
- Maintain regulatory submission files and databases.
- Conduct regulatory intelligence activities to stay informed of evolving requirements.
- Participate in regulatory inspections and audits.
- Review promotional materials for regulatory compliance.
- Contribute to the development of SOPs and departmental processes.
Qualifications:
- Degree in Pharmacy, Life Sciences, Chemistry, or a related field.
- Minimum of 6 years of experience in pharmaceutical regulatory affairs.
- In-depth knowledge of global regulatory guidelines (MHRA, EMA, FDA, ICH).
- Proven experience in preparing and submitting regulatory dossiers.
- Excellent written and verbal communication skills, with strong attention to detail.
- Strong analytical and problem-solving abilities.
- Ability to manage multiple projects and work effectively in a team environment.
- Experience with regulatory information management systems is a plus.
Lead Chemical Process Engineer - Pharmaceuticals
Posted 19 days ago
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Job Description
Responsibilities:
- Lead the design, development, and optimization of chemical processes for pharmaceutical manufacturing, from lab scale to commercial production.
- Conduct process simulations, feasibility studies, and techno-economic assessments.
- Develop detailed process flow diagrams (PFDs) and piping & instrumentation diagrams (P&IDs).
- Oversee pilot plant operations and scale-up activities, ensuring successful technology transfer.
- Implement process improvements to enhance yield, reduce costs, and improve safety and environmental performance.
- Ensure all process designs and operations comply with relevant regulatory requirements (e.g., FDA, EMA) and GMP guidelines.
- Collaborate with multidisciplinary teams, including R&D, manufacturing, quality assurance, and engineering.
- Provide technical guidance and mentorship to junior process engineers.
- Troubleshoot and resolve complex process-related issues in manufacturing.
- Author and review critical process documentation, including batch records and validation protocols.
- Master's or PhD in Chemical Engineering or a related discipline.
- A minimum of 7 years of progressive experience in chemical process engineering, with a significant focus on the pharmaceutical or biotechnology industry.
- In-depth knowledge of pharmaceutical manufacturing processes, equipment, and GMP requirements.
- Proven experience in process design, scale-up, and technology transfer.
- Proficiency in process simulation software (e.g., Aspen Plus, HYSYS) and P&ID development tools.
- Strong understanding of chemical reaction engineering, thermodynamics, and mass transfer.
- Excellent analytical, problem-solving, and project management skills.
- Exceptional communication, leadership, and interpersonal abilities.
Senior Pharmaceutical Research Scientist
Posted today
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Key Responsibilities:
- Lead the design and execution of complex biological experiments to investigate disease mechanisms and identify potential drug candidates.
- Develop and optimize in vitro and ex vivo assays for target engagement, efficacy, and mechanism of action studies.
- Analyze and interpret large datasets using statistical and bioinformatics tools, presenting findings clearly and concisely to diverse audiences.
- Collaborate closely with cross-functional teams, including medicinal chemists, pharmacologists, and toxicologists, to advance projects towards clinical development.
- Stay abreast of the latest scientific literature and emerging technologies in relevant therapeutic areas.
- Mentor and guide junior scientists, fostering a collaborative and high-performance research environment.
- Contribute to the development of research strategies and proposals.
- Ensure all laboratory activities are conducted in compliance with company policies and regulatory guidelines.
- Maintain meticulous records of experiments and data.
Qualifications:
- Ph.D. in Molecular Biology, Biochemistry, Pharmacology, or a related life science discipline.
- A minimum of 5 years of post-doctoral or industry experience in pharmaceutical research, with a strong track record of publications and successful project contributions.
- Extensive experience in assay development, execution, and data analysis, with proficiency in relevant software.
- Deep understanding of mammalian cell culture techniques, molecular biology techniques (e.g., PCR, Western blotting, ELISA), and genetic manipulation (e.g., CRISPR).
- Familiarity with computational biology tools and approaches is highly desirable.
- Exceptional problem-solving skills and the ability to work independently and as part of a remote team.
- Excellent written and verbal communication skills, with the ability to present complex scientific information effectively.
- Proven ability to manage multiple projects simultaneously and meet deadlines.
This role is based in London, England, UK , but is entirely remote, requiring reliable internet connectivity and a dedicated home workspace. Join us in shaping the future of medicine through cutting-edge research, all while enjoying the flexibility of a remote-first culture.
Senior Pharmaceutical Research Scientist
Posted 1 day ago
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Key Responsibilities:
- Design and execute complex experiments to identify and validate drug targets and develop novel drug candidates.
- Conduct in-vitro and in-vivo studies to assess the efficacy, safety, and pharmacokinetics of potential therapeutics.
- Analyze and interpret experimental data, drawing robust conclusions and making strategic recommendations.
- Prepare detailed research reports, scientific publications, and presentations for internal and external audiences.
- Collaborate effectively with cross-functional teams, including medicinal chemists, biologists, and pharmacologists, both remotely and in person.
- Contribute to the development and optimization of research methodologies and protocols.
- Mentor and guide junior research scientists and laboratory technicians.
- Stay current with the latest advancements in pharmaceutical sciences, therapeutic areas, and relevant technologies.
- Ensure strict adherence to Good Laboratory Practice (GLP) and regulatory guidelines.
- Manage research projects, including planning, resource allocation, and timeline management.
- Participate in scientific meetings and conferences to present findings and foster collaborations.
- Spend necessary time in the London-based laboratory as required by the hybrid schedule.
- PhD in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry experience in pharmaceutical research and drug discovery.
- Demonstrated expertise in relevant areas such as target validation, assay development, or in-vivo models.
- Strong analytical and problem-solving skills, with a track record of scientific innovation.
- Excellent written and verbal communication skills, with the ability to communicate complex scientific information clearly.
- Experience working in a hybrid research environment, including the ability to work effectively in a laboratory setting in London, England, UK .
- Proficiency in data analysis software and scientific literature databases.
- Ability to work independently and as part of a collaborative team.
- Strong understanding of regulatory requirements in the pharmaceutical industry.
Senior Pharmaceutical Research Scientist
Posted 1 day ago
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Lead Pharmaceutical Research Scientist
Posted 5 days ago
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Job Description
Responsibilities:
- Lead and manage research projects focused on identifying and validating new drug targets and developing novel therapeutic molecules.
- Design, execute, and interpret complex experiments in areas such as molecular biology, pharmacology, and medicinal chemistry.
- Supervise and mentor a team of research scientists and technicians, fostering a collaborative and high-performing research environment.
- Develop and implement robust research protocols and methodologies to ensure scientific rigor and reproducibility.
- Analyze experimental data, interpret results, and contribute to the preparation of scientific publications, patents, and regulatory submissions.
- Collaborate closely with internal departments, including clinical development, manufacturing, and regulatory affairs, as well as external academic and industry partners.
- Stay updated with the latest scientific literature, emerging technologies, and industry trends relevant to drug discovery.
- Ensure compliance with all relevant safety, ethical, and regulatory guidelines within the laboratory setting.
- Contribute to strategic planning for the research and development pipeline, identifying future opportunities and challenges.
Qualifications:
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, Medicinal Chemistry, or a closely related field.
- Minimum of 7 years of post-doctoral research experience in the pharmaceutical or biotechnology industry.
- Demonstrated experience in leading and managing research teams and projects.
- Proven track record of success in drug discovery, with publications in peer-reviewed journals and/or patent filings.
- Expertise in one or more key therapeutic areas (e.g., oncology, immunology, neurology).
- Strong understanding of drug development processes, from target identification to preclinical studies.
- Excellent analytical, critical thinking, and problem-solving skills.
- Superb written and verbal communication skills, with the ability to present complex scientific information clearly.
- Experience with laboratory automation and high-throughput screening techniques is advantageous.
- Ability to thrive in a fast-paced, collaborative, and deadline-driven environment.
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Senior Pharmaceutical Research Scientist
Posted 5 days ago
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Responsibilities:
- Lead and execute cutting-edge research projects focused on identifying and validating novel drug targets and therapeutic modalities.
- Design, optimize, and perform complex in vitro and ex vivo assays to assess compound efficacy, safety, and mechanism of action.
- Analyze and interpret experimental data, troubleshoot issues, and develop innovative solutions to research challenges.
- Prepare detailed research reports, technical documentation, and scientific presentations for internal teams and external stakeholders.
- Contribute to the writing of regulatory submissions and scientific publications.
- Mentor and guide junior scientists, fostering a collaborative and high-performance research environment.
- Collaborate with cross-functional teams, including medicinal chemistry, pharmacology, toxicology, and clinical development, to advance projects through the development pipeline.
- Stay current with the latest scientific literature, emerging technologies, and industry trends in relevant therapeutic areas.
- Manage research budgets and resources effectively, ensuring project timelines are met.
- Contribute to the intellectual property strategy by identifying patentable inventions.
- Ph.D. in Pharmacology, Biochemistry, Molecular Biology, or a related life science discipline.
- Minimum of 5 years of post-doctoral or industry research experience in drug discovery and development.
- Extensive hands-on experience with a range of molecular and cellular biology techniques (e.g., Western blotting, ELISA, flow cytometry, cell-based assays).
- Proven track record of successfully contributing to drug discovery programs, evidenced by publications and/or patents.
- Strong understanding of disease pathophysiology and relevant assay development.
- Excellent analytical, critical thinking, and problem-solving skills.
- Superb data analysis and interpretation capabilities, with proficiency in relevant software.
- Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and concisely.
- Demonstrated ability to work effectively in a team-oriented environment, as well as independently.
- Experience with small molecule or biologic drug discovery is highly desirable.
- Familiarity with CRO management is a plus.
Principal Pharmaceutical Research Scientist
Posted 6 days ago
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Job Description
Responsibilities:
- Lead and manage research projects from early-stage discovery through to preclinical development, ensuring scientific rigor and timely execution.
- Design and implement in vitro and in vivo experimental models to assess drug efficacy, safety, and pharmacokinetics.
- Develop and validate novel assays for high-throughput screening and target validation.
- Analyze and interpret complex biological data, drawing meaningful conclusions and formulating next steps.
- Supervise and mentor junior scientists and research associates, fostering a collaborative and high-performing team environment.
- Stay at the forefront of scientific literature, identifying new research avenues and technologies relevant to therapeutic areas of interest.
- Prepare comprehensive research reports, regulatory documents, and patent applications.
- Present research findings at internal scientific meetings and external conferences.
- Collaborate effectively with cross-functional teams, including chemistry, toxicology, and clinical development.
- Contribute to the strategic planning and prioritization of the drug discovery portfolio.
Qualifications:
- PhD in Pharmacology, Molecular Biology, Biochemistry, or a related life sciences discipline.
- A minimum of 8 years of post-doctoral research experience in the pharmaceutical industry or a closely related field.
- Demonstrated expertise in drug discovery, with a strong publication record and/or patent contributions.
- Extensive experience with various biological assays, cell-based models, and potentially animal models.
- Proficiency in data analysis software and statistical methods.
- Proven ability to lead projects, mentor staff, and work effectively in a multidisciplinary team.
- Excellent written and verbal communication skills, with the ability to articulate complex scientific concepts.
- Strong strategic thinking and problem-solving capabilities.
- Familiarity with regulatory requirements and drug development processes is highly desirable.
- A passion for scientific innovation and a commitment to advancing patient care.
Senior Pharmaceutical Research Scientist
Posted 6 days ago
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Job Description
Key responsibilities include:
- Leading independent research projects in drug discovery and development, from target validation to lead optimization.
- Designing and conducting in vitro and in vivo experiments to evaluate drug candidates.
- Developing and validating bioassays and screening methodologies.
- Interpreting complex experimental data and providing insightful analysis.
- Contributing to the generation of intellectual property through patent applications.
- Collaborating effectively with multidisciplinary teams, including chemists, biologists, and toxicologists, in a virtual environment.
- Preparing detailed research reports, scientific presentations, and manuscripts for publication.
- Staying abreast of the latest scientific advancements and emerging technologies in pharmaceutical R&D.
- Mentoring junior scientists and contributing to a culture of scientific excellence.
- Ensuring adherence to all regulatory guidelines and ethical standards in research.
The ideal candidate will hold a Ph.D. in Pharmacology, Medicinal Chemistry, Biochemistry, or a closely related field, with a minimum of 6 years of post-doctoral or industry research experience in drug discovery. Demonstrated expertise in a specific therapeutic area (e.g., oncology, neuroscience, infectious diseases) and hands-on experience with relevant assays and technologies are essential. Strong analytical, problem-solving, and critical thinking skills are paramount. Excellent written and verbal communication skills are required for effective virtual collaboration and dissemination of scientific findings. The ability to work autonomously, manage multiple research projects, and contribute significantly in a remote setting is critical. If you are a dedicated scientist driven by the potential to develop life-changing medicines, we invite you to apply.