24 Permanent GMP Jobs with Hybrid or WFH Options

this role you must have the right to work in this location. Key Responsibilities: For this role, you will assist with compliance on all GMP/GDP and GCP regulations guaranteeing adherence to GxP and data integrity legislation. Serve as the System Owner/Administrator role for GxP IT systems more »

for purpose QMS. Conduct GCP process, vendor, and investigator site audits. Support GxP Quality needs in Development & Precision functions, e.g. GVP, GLP, GDP/GMP & CSV. Requirements: Strong GCP Quality experience in biotech/pharma which spans clinical trial phases I to III. Expert in GCP global regulations and guidance more »

the management and improvement of quality systems processes to ensure both EU and US regulatory compliance to relevant company standards and Good Manufacturing Practice (GMP). The successful applicant will: Implement and monitor established policies and procedures to ensure compliance with necessary regulatory bodies in the areas of: Corrective and … Work in accordance with Company Quality Standards, procedures and processes and comply with the requirements of Good Documentation Practice (GDP) and Good Manufacturing Practice (GMP). Deputise for Senior Quality Systems Engineer when required, to ensure progression of departmental commitments. We are looking for someone who has: Minimum A level … Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include MS Word, Excel and MRP Knowledge of GMP and audits Ability to work with minimal supervision and use initiative. Good interpersonal skills and the ability to communicate well in English both written and more »

GCLP, CLIA, CAP, ISO15189 laboratory requirements Experience in CLSI, NYDOH and other industry standards for assay validation; Understanding of IVD regulations including QSR regulations, GMP manufacturing, ISO13485, and FDA and EU medical device regulations. Preferred Qualifications & Skills: Please note the following skills are not necessary, just preferred, if you do more »

purpose QMS - Execution of GCP process, vendor, and investigator site audits - Support GxP Quality needs in Development & Precision functions, e.g. GVP, GLP, GDP/GMP & CSV - Escalation of compliance risks/issues to line management QUALIFICATIONS: As Associate Director, Clinical QA you will require: - A relevant life science degree - Extensive more »

promoted internally. We need someone who has experience working in a Pharma/life science environment who has good knowledge of working in a GMP/GxP environment. This is a strategic role and requires someone who has previous regional experience with some auditing experience. The role is based from more »

experience leading IT at a senior management level Track record of delivering results quickly Experience in delivering IT services to customers Work in a GMP or highly regulated environment Preferred Experience: Experience of agile product development Experience of Lean Six Sigma Infrastructure delivery (networking, hardware) to customers Experience with data more »

pharmaceutical industry and familiarity with clinical trials. Advanced Excel skills (conditional formatting, hyper-linking, etc.). Ability to interpret and apply Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP) guidelines. Experience with collaboration tools (SharePoint, Dropbox, etc.). more »

HTML/CSS) Experience using a Tag Management System (ideally Google Tag Manager) Experience with Web Analytics and AdTech deployment (ideally Google Analytics and GMP/Facebook) Experience with multiple Web Analytics tools Experience with multiple Tag Management Systems Experience using JavaScript to deploy A/B and MVT tests more »

as part of the remuneration. Experience: Experienced project engineer or project manager in a pharmaceutical setting A strong understanding and hands on experience of GMP Engineering or validation experience is essential Exposure to the full validation lifecycle and the ability to walk through the full CQV phase Hands on experience more »

a company car or generous car allowance. So, if you're an experienced project engineer/project manager with a deep understanding of pharmaceutical GMP, hands-on experience in engineering or validation, and a knack for knocking projects out of the park, we want to hear from you! Don't more »

Quality Systems (FDA/ISO) within a regulated environment, and ERP/ASCP (SAP preferred) High understanding of Supply Chain Finance. Good Manufacturing Processes (GMP) Experience successfully collaborating with internal and external stakeholders on complex projects. Further information provided upon application. ECS Recruitment Group Ltd is acting as an Employment more »

Google Tag Manager, Google Analytics 4 and other site analytics software, as well as working with Advertising Platform analytics, such as Google Marketing Platform (GMP), Facebook and Google Ads etc. and troubleshooting when required. You will become a specialist with Looker studio and assist on the development and maintenance of more »

similar role. Paid, owned, website, & commerce data experience. Strong knowledge of key digital platforms, CRM, data and web analytics providers, including Adobe Marketing Cloud, GMP, GCP, Meta and other partners. Strong knowledge of data management, analytics with experience of deploying data & analytics projects across large accounts. Have managed multi- million more »

undertake project work from across XPS ensuring that day to day Administration work and resource is unaffected. Our APT team undertakes projects such as: GMP rectification/equalisation Buy-in/Buy-out Data Cleansing Ad hoc projects for example scheme closures, benefit rectifications, liability reduction exercises McCloud implementation: Public more »

values, promoting an ethical, positive company culture To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in more »

values, promoting an ethical, positive company culture To maintain consistent and documented compliance with all relevant Safety, Health and Environmental (SHE), Good Manufacturing Practice (GMP), Data Integrity (DI), quality and best practice requirements Preparation and approval of validation documentation or management of the process (fulfilling the Quality Assurance role) in more »

CAPAs, deviations, change controls and supplier qualification. 2. Make sure that the CMO batch documentation are compliant to GXP standards, including the review of GMP documentation. 3. You will work closely with the Quality Specialist, and assist in regulatory inspections and customer audits. 4. You will generate, retrieve, manage, and … the following on your profile and past history: 1. Relevant degree in a relevant life sciences discipline 2. Proven industry experience working in a GMP environment (preferred), or , GLP, GDP, GCP 3. A working knowledge and practical experience with document/Quality Management Systems, and Electronic Document Management Systems Key … Words: QA | Quality Assurance | QMS | Quality Management Systems | Clinical | GMP | GxP | Biotechnology | QDM | Quality Document Management Systems | Electronic Document Management Systems | Drug Discovery | CAPA | Deviations more »

RESPONSIBILITIES Develop and oversee a robust quality management system in line with pharmaceutical industry regulations, including Good Distribution Practices (GDP) and Good Manufacturing Practices (GMP). Establish quality policies, procedures, and guidelines to ensure the consistent and compliant handling, storage, and distribution of pharmaceutical products. Implement quality assurance programs, including … 8+ years) in quality management and loss prevention, preferably in the pharmaceutical or logistics industry. Strong understanding of pharmaceutical regulations and quality standards (GDP, GMP). Proven track record of successfully implementing quality management systems and loss prevention strategies. Excellent leadership, communication, and interpersonal skills. Analytical mindset with the ability more »

s products. Provide US and European regulatory intelligence, train Subject Matter Experts and provide internal consultancy for quality compliance implementation and FDA/EU GMP/GDP remediation projects in the Dechra Internal Manufacturing network. Frequent global travel is required with this role, and you will need to travel to … manufacturing network (as required) across the product's registered lifecycle in compliance with all applicable ISO, ICH, FDA, EU, and national regulatory requirements for GMP/GDP. Lead GMP/GDP audits for Dechra DPMS based on specific expertise, criticality, and complexity. Periodically assess the liability, regulatory and/or … networks are all being adequately monitored. Recruit, lead, train and develop, as required, the team of quality and compliance experts (specialised in auditing different GMP/GDP areas) across the business, to keep the business abreast of ongoing developments through benchmarking activities, whilst proactively identifying and addressing any gaps relating more »

be responsible for supporting the Quality Management System (QMS) and verifying the adherence of manufactured products for human use, in line with current Good Manufacturing Practice (cGMP). As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous … To be successful in this role, were looking for you to have: A-level qualifications (or equivalent Worked within an established Quality System (e.g. GMP, ISO) Writing and producing scientific reports The following criteria would also be beneficial to your application, but is not essential: Bachelors degree (or equivalent) in more »

and vision systems integrated within packaging equipment including interfaces with enterprise systems. • Responsible for providing cGMP compliant control systems as per GAMP5 and EU GMP Annex 11. General Responsibilities (Safety, Quality, Customer, Cost and Innovation) • To ensure that operations conducted are performed in accordance with the requirements of corporate standards … within the production facility. • Management of the design, development, maintenance and troubleshooting of automated systems, ensuring they are compliant as per GAMP5 and EU GMP Annex 11. • Successful delivery of automation projects to meet strategic business objectives. • Execute or facilitate automation design solutions in accordance with stakeholder requirements and business … at gate reviews. • Responsible that Good Engineering Practices (GEP) are employed in the design, installation and commissioning of assets. • Responsible that Good Manufacturing Practices (GMP) are employed, including activities determined from user requirement specifications (URS) through to qualification. • Coordination of specialist contractors undertaking work packages, ensuring safe systems of work more »

support the delivery of QA activities for their assigned portfolio of projects and provide advice to support the development, implementation and continuous improvement of GMP quality systems across the development functions and support implementation of agreed global standards. Essential Criteria · Appropriate scientific degree with experience (3-5 years) of working … within a pharmaceutical GMP environment, preferably within a pharmaceutical development organisation · A broad understanding of Quality Systems and GMP is essential · An understanding of the pharmaceutical/drug development process We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of more »

Teams London £45,000 - £80,000 per annum Opportunity for a strong pensions actuary to specialise further with a market leader in Risk Settlement, GMP Equalisation and Member Options- working from day one in one of these specialist teams. Comopany client is representing a leading consultancy with an opportunity for … a strong pensions actuary to specialise further in their market leading Risk Settlement, GMP Equalisation or Member Options teams. Youll be working from day one in one of the listed specialist teams and will have the opportunity to become an expert in a thriving area of the industry and develop more »