Future Tech Jobs
Future Tech Jobs
The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.
This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.
This role involves managing the post-launch lifecycle of the CFC CRM platform across global markets, ensuring its stability, compliance, and continuous optimization. The Senior Director will work closely with various teams to prioritize market needs, manage configurations, and ensure successful adoption and value realization from CRM investments.
The Quality Oversight and Compliance Director at Pfizer is responsible for developing and maintaining quality plans, ensuring inspection and audit readiness, and providing quality oversight of process deviations and investigations. This role involves interpreting and applying global regulations, driving compliance, and collaborating with stakeholders to identify and mitigate risks, ensuring the quality and integrity of Pfizer's medicines and vaccines.
The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...
This role involves working in a lab-based GCP environment, supporting translational pathology and biomarker programs. Responsibilities include maintaining quality standards, managing clinical and research specimens, performing laboratory assays, and collaborating with cross-functional teams to ensure laboratory activities align with project needs.
This role involves providing high-quality medical information to healthcare professionals, developing digital content for HCP and patient websites, and generating insights to support brand strategies. You will work closely with cross-functional teams to ensure clear and compliant scientific communication, focusing on Respiratory, Immunology, and Vaccines.
This role involves leading the development of global regulatory strategies for drug development programs, managing regulatory activities, and collaborating with cross-functional teams. The position requires extensive experience in regulatory affairs, with a focus on global health authorities and regulatory submissions.
This role involves leading the clinical operations strategy and execution across Recursion’s full clinical portfolio, from early-stage studies to pivotal trials and submission support. The VP will build scalable operating models, manage global trials, and ensure operational excellence in a data-driven, patient-centered, and technology-enabled environment.
The Product Development Scientist will work on the development and improvement of diagnostic products, from feasibility to launch, ensuring compliance with quality standards. Responsibilities include participating in product development phases, troubleshooting issues, and collaborating on technical analysis and material testing.
This role involves leading a small QA team, ensuring compliance with regulatory standards, and overseeing quality systems and validation activities. Responsibilities include report writing, internal and external audits, and driving continuous improvement initiatives.
This role involves managing regulatory maintenance for a high-complexity pharmaceutical portfolio, ensuring compliance and timely submissions to global health authorities. The candidate will lead strategic regulatory input across cross-functional teams, respond to complex queries, and support continuous improvement initiatives. It's a key position influencing patient access to medicines through robust lifecycle management.
This role involves driving regulatory strategy and execution for neuroscience products across global markets, with a focus on preparing high-quality submissions and managing interactions with health authorities. The manager will coordinate clinical trial applications, support approvals, and ensure compliance throughout the product lifecycle. Collaboration with cross-functional teams is essential to translate scientific data into regulatory outcomes.
The Scientist role involves reviewing clinical data, writing technical reports, and ensuring regulatory compliance for medical devices. You will work closely with a scientific and clinical team to produce high-quality documentation for product approvals, focusing on safety, efficacy, and meeting strict regulatory standards.
