53 Pharmaceuticals jobs in Harlow

• Develop, optimize, and scale-up manufacturing processes for pharmaceutical products.
• Conduct process development studies, including formulation, reaction kinetics, and purification methods.
• Write and execute process validation protocols (IQ, OQ, PQ) and reports.
• Troubleshoot and resolve process deviations and implement corrective and preventive actions (CAPAs).
• Ensure all manufacturing processes comply with GMP, regulatory guidelines (e.g., FDA, EMA), and company standards.
• Collaborate with R&D to transfer new products from laboratory scale to commercial manufacturing.
• Design and implement process improvements to enhance yield, reduce costs, and improve efficiency.
• Prepare technical documentation, including batch records, SOPs, and technical transfer packages.
• Provide technical support and training to manufacturing personnel.
• Participate in process hazard analyses and risk assessments.
• Stay updated on industry best practices and emerging technologies in pharmaceutical manufacturing.

• Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Engineering, or a related field.
• Minimum of 6 years of experience in process development and manufacturing within the pharmaceutical or biopharmaceutical industry.
• Strong understanding of GMP regulations and pharmaceutical process validation.
• Proven experience with process scale-up and technology transfer.
• Knowledge of various pharmaceutical manufacturing technologies (e.g., solid dosage, sterile manufacturing, biologics).
• Excellent analytical, problem-solving, and troubleshooting skills.
• Strong technical writing and communication skills.
• Ability to work effectively in a cross-functional team environment.
• Experience with process simulation software is a plus.
• Detail-oriented with a strong commitment to quality and safety.

Smart4 Sciences - QC Goods In Inspector - Pharmaceuticals

We are supporting a leading pharmaceutical manufacturer in their search for a Goods In Inspector to join their Quality team. This is a fantastic opportunity for someone with a keen eye for detail and a background in QC, laboratory work, or pharmaceutical operations to play a key role in ensuring compliance, safety, and quality of incoming materials.

Key Responsibilities

• Inspect and sample incoming packaging components and raw materials against specifications and procedures.

• Raise non-conformance reports for any materials outside of specification.

• Clean and maintain warehouse staging areas, airlocks, and sampling booths in line with SOPs.

• Maintain accurate and compliant records in line with cGMP requirements.

• Support effective liaison with warehouse, packaging, and manufacturing teams to ensure timely sampling.

• Manage laboratory waste disposal in accordance with procedures.

• Follow personal hygiene and safety standards, ensuring a safe working environment.

About You
We're looking for someone with:

• Previous experience working in a laboratory or QC environment.

• Understanding of GMP and working to Standard Operating Procedures.

• Strong IT skills, including Microsoft Word and Excel.

• Excellent attention to detail and record-keeping skills.

• Fluency in written and spoken English, with the right to work in the UK.

This is a great chance to develop your career in pharmaceutical quality within a supportive and regulated environment. Our client offers training, career progression, and a collaborative team culture.

If you're detail-oriented and eager to build a career in pharmaceutical quality, we'd love to hear from you. Please apply today or contact Gareth Gooley at Smart4 Sciences on for a confidential discussion.

Smart4 Sciences - QC Goods In Inspector - Pharmaceuticals

We are supporting a leading pharmaceutical manufacturer in their search for a Goods In Inspector to join their Quality team. This is a fantastic opportunity for someone with a keen eye for detail and a background in QC, laboratory work, or pharmaceutical operations to play a key role in ensuring compliance, safety, and quality of incoming materials.

Key Responsibilities

• Inspect and sample incoming packaging components and raw materials against specifications and procedures.

• Raise non-conformance reports for any materials outside of specification.

• Clean and maintain warehouse staging areas, airlocks, and sampling booths in line with SOPs.

• Maintain accurate and compliant records in line with cGMP requirements.

• Support effective liaison with warehouse, packaging, and manufacturing teams to ensure timely sampling.

• Manage laboratory waste disposal in accordance with procedures.

• Follow personal hygiene and safety standards, ensuring a safe working environment.

About You
We're looking for someone with:

• Previous experience working in a laboratory or QC environment.

• Understanding of GMP and working to Standard Operating Procedures.

• Strong IT skills, including Microsoft Word and Excel.

• Excellent attention to detail and record-keeping skills.

• Fluency in written and spoken English, with the right to work in the UK.

This is a great chance to develop your career in pharmaceutical quality within a supportive and regulated environment. Our client offers training, career progression, and a collaborative team culture.

If you're detail-oriented and eager to build a career in pharmaceutical quality, we'd love to hear from you. Please apply today or contact Gareth Gooley at Smart4 Sciences on for a confidential discussion.

• Design, execute, and interpret complex research experiments in drug discovery.
• Lead and mentor a team of research scientists and technicians.
• Develop and validate novel biochemical and cellular assays.
• Conduct high-throughput screening (HTS) campaigns.
• Investigate mechanisms of action for potential drug candidates.
• Analyze and present research findings to internal and external stakeholders.
• Manage project timelines, resources, and budgets effectively.
• Collaborate with cross-functional teams, including chemistry, DMPK, and toxicology.
• Stay abreast of the latest scientific literature and technological advancements.
• Contribute to the preparation of patent applications and scientific publications.
• Ensure compliance with GxP guidelines and laboratory safety standards.
• Identify and evaluate new therapeutic targets and drug development opportunities.

• Lead and mentor a team of research associates and scientists in a cutting-edge drug discovery laboratory.
• Design, develop, and implement experimental strategies to identify and validate novel therapeutic targets across various disease areas.
• Oversee the execution of complex research projects, ensuring timely and high-quality data generation.
• Analyze and interpret experimental data, drawing robust conclusions and making informed recommendations for project progression.
• Contribute to the strategic planning and prioritization of drug discovery projects within the R&D pipeline.
• Develop and maintain strong collaborative relationships with internal teams (e.g., DMPK, CMC, Clinical) and external partners (academic institutions, CROs).
• Prepare and present research findings at internal meetings, scientific conferences, and in peer-reviewed publications.
• Ensure compliance with all laboratory safety regulations, ethical guidelines, and company policies.
• Contribute to the development of intellectual property through invention disclosures and patent applications.
• Manage research budgets and resources effectively.
• Stay abreast of the latest scientific literature, technological advancements, and competitive landscape in pharmaceutical R&D.
• Assist in the recruitment and training of new research personnel.

• Ph.D. in Molecular Biology, Pharmacology, Biochemistry, or a related life science discipline.
• A minimum of 7 years of post-doctoral research experience in the pharmaceutical or biotechnology industry, with a significant focus on drug discovery.
• Proven experience in leading and managing scientific teams and projects.
• Demonstrated expertise in target identification and validation, assay development, and lead optimization.
• Strong understanding of key therapeutic areas (e.g., oncology, immunology, CNS).
• Hands-on experience with relevant laboratory techniques and instrumentation.
• Excellent analytical, problem-solving, and critical thinking skills.
• Exceptional written and verbal communication skills, including experience in presenting complex scientific data.
• A strong publication record and/or patent filings.
• Ability to work effectively in a collaborative, fast-paced, and dynamic research environment.
• Experience with hybrid work models and remote collaboration tools is desirable.

• Lead and direct pharmaceutical research projects in a specialized therapeutic area.
• Design and execute complex in vitro and in vivo experimental studies.
• Develop and validate novel assays and methodologies.
• Analyze and interpret scientific data to drive research decisions.
• Mentor and manage a team of research scientists and technicians.
• Contribute to the strategic planning of the research pipeline.
• Prepare research reports, publications, and patent applications.
• Collaborate effectively with cross-functional teams and external partners.
• Stay at the forefront of scientific advancements in pharmaceutical research.
• Ensure compliance with laboratory safety protocols and ethical guidelines.