Position Summary The Computer System Validation (CSV) Specialist is responsible for the governance, validation, and lifecycle management of all GxP-relevant computerised systems at site. This role ensures ongoing compliance with EU GMP Annex 11, MHRA Data Integrity
Company Description About AbbVie AbbVies mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on
Fusion Pharmaceuticals, part of the AstraZeneca Group, is redefining precision oncology with next‑generation radioconjugates that deliver powerful alpha‑emitting payloads directly to tumors. Our pipeline spans multiple first‑in‑class programs—backed by a GMP‑compliant, state‑of‑the‑art radiopharmaceutical facility in Hamilton,
Nexcella, Inc. Montreal / Hybrid Associate Director of Regulatory Affairs Our 3 Core Values Intelligence Integrity Initiative What You’ll Do The Director of Regulatory Affairs will support the regulatory strategy and execution for clinical trials conducted
Company Overview MHRA Hospitality is a Canadian multi-brand hospitality company focused on building and growing exceptional restaurant concepts across the country. Headquartered in Barrie, Ontario, MHRA provides the operational, franchise, marketing, real estate, training, HR, and business infrastructure
Job Summary Provide strong leadership and oversight to ensure responsibilities in regards to QA, QC and Compliance activities. The position is accountable for assuring the supply of quality products to Sun Pharma customers and markets, and
Nexcella, Inc. is seeking an Associate Director of Regulatory Affairs to guide regulatory strategy and execution for clinical trials under FDA/EMA/Health Canada/MHRA regimes. The role focuses on preparing, submitting, and maintaining regulatory documents to ensure compliance with
Associate Director of Regulatory Affairs Our 3 Core Values Integrity Initiative What You’ll Do The Director of Regulatory Affairs will support the regulatory strategy and execution for clinical trials conducted under FDA/EMA/Other Regulatory agencies regulations. This
Overview Replimune’s mission is to revolutionize cancer treatment with therapies designed to activate a powerful and durable full‑body anti‑tumor response, boldly transforming cancer care because patient’s lives depend on it. At Replimune, we live by our
Lead Pharmacists for Manufacturing and Accountable Pharmacist See attached job description with person specification for the full details. Please do take time to read the requirements of the role. The main responsibilities of this role are
How Youll Make An Impact Provide technical consulting services that leverage Ecolab’s expertise in chromatography resin performance, downstream purification, and regulatory change management to help commercial teams understand customer needs and increase account revenue. Act as
Principal Executive Search Consultant - Medical & Clinical Clinical Project Manager – Phase I PK/PD & Bioequivalence Studies (Generics) Location: Spain Employment Type: Full-time, Permanent About Us Im working with a forward thinking pharmaceuticals who are
Job Description Summary Managing, ensuring and improving capabilities to comply with external standards and regulations. Interprets internal and external business challenges and recommends best practices to improve products, processes or services. Stays informed of industry trends