for adhering to all health and safety guidance, provided by the Company. EXPERIENCE WE ARE LOOKING FOR:- Experience from a directly relevant biotechnology or pharmaceutical industry Experience of working in a busy laboratory environment D or MD/Ph.D in relevant scientific discipline, Master’s degree or native equivalent with more »
regulatory requirements and market dynamics is not necessary but a strong advantage •Proven experience within a CDMO or a similar commercial role within biotechnology, pharmaceutical and life-science consulting industry is advantageous •Excellent written and verbal communication skills, with the ability to present findings and recommendations in a clear and more »
RPi)To support the Head of Quality in ensuring the provisions of the licences are observed. Company Overview: Our client is a rapidly growing pharmaceutical wholesaling company involved in the procurement and supply of unlicensed medicines into the NHS and Private Hospital sector in the UK. They aim to deliver more »
relevant Microsoft platforms, tools, technologies, patterns, and techniques related to MSFT suites, Azure tools, integration, and data is required.Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred.Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. FHIR more »
or an MBA. 5+ Years' experience in Strategy, Management Consulting or Industry; with a dedicated focus and background on Healthcare and Life Sciences; (i.e., Pharma, Biopharma, Biotech and Medical Device). Proficiency with Microsoft Office, including Word, Excel, and PowerPoint; (experience in computer programming software (e.g., VBA) or other role more »
with various relevant Microsoft platforms, tools, technologies, patterns, and techniques related to Azure tools, integration, and data is required.Experience with industry/domains like pharmaceutical, finance, HR, sales, marketing, and manufacturing is highly preferred.Experience with healthcare industry regulations, data security and compliance standards (e.g. GDPR), and EDI standards (e.g. FHIR more »
wider business. Flexibility to work across multiple sites in London Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies. Proclinical Staffing is an equal opportunity employer. more »
programme | Recognition awards | Free Parking Bespak Holmes Chapel is an Investors in People silver award winner who employs over 300 people and are a pharmaceutical Contract Development and Manufacturing Organization (CDMO) that offers development and manufacturing solutions for a variety of medical products. Our products include medical devices such as more »
Title:Global Strategic Sourcing Director (GSSD) External Resources & Mobility ServicesCompany:Ipsen Pharma (SAS)Job Description:The Global Strategic Sourcing Director is responsible for developing, implementing, and leading the Global Sourcing strategy for the External Resources & Mobility Services, with an indicative portfolio spend of c. 150M & anticipated significant future growth.You will more »
Type: PermanentWork Hours: Full TimeContact: Jas GujralEmail: cv@nexusjobs.comTelephone: 020 7488 6900Job DescriptionSenior Information Security AnalystOur Client is a leading global company specialising in pharma products.They are looking to recruit a Senior Information Security Analyst with at least 5 to 7 years expertise in Technology Security.The Senior Information Security Analyst more »
Stevenage, Hertfordshire, United Kingdom Hybrid / WFH Options
GlaxoSmithKline
development processes, and ensure efficient deployment and monitoringPreferred Qualifications/Experience:If you have the following characteristics, it would be a plus:Understanding of pharmaceutical industry data and domain knowledge within CMC.Knowledge of GxP compliance requirements and experience implementing them in data engineering projectsPlease take a copy of the Job more »
development processes, and ensure efficient deployment and monitoringPreferred Qualifications/Experience:If you have the following characteristics, it would be a plus:Understanding of pharmaceutical industry data and domain knowledge within CMC.Knowledge of GxP compliance requirements and experience implementing them in data engineering projectsPlease take a copy of the Job more »
Brentford, Middlesex, United Kingdom Hybrid / WFH Options
GlaxoSmithKline
development processes, and ensure efficient deployment and monitoringPreferred Qualifications/Experience:If you have the following characteristics, it would be a plus:Understanding of pharmaceutical industry data and domain knowledge within CMC.Knowledge of GxP compliance requirements and experience implementing them in data engineering projectsPlease take a copy of the Job more »
working with minimum supervision under pressure to tight deadlines with customer focus. Requirements : Bachelors degree in applicable field (e.g Science, Engineering) or equivalent (e.g Pharma, Biopharm, Life Science, Biotech) Good Experience in Quality Assurance; Problem Solving, Analytical and Continual Improvements. Certified Lead Auditor in ISO 9001:2015 or more »
ensuring equipment performance? We are seeking a highly motivated Equipment Validation Specialist to play a vital role in maintaining the integrity and efficiency of pharma manufacturing processes. In this role, you will be responsible for: Defining and executing equipment validation activities , ensuring all equipment meets the required standards. Coordinating and more »
have any questions, please contact Ingrid Aymes at i.aymes@proclinical.com Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies. Proclinical Staffing is an equal opportunity employer. more »
level in science or equivalent experience. Minimum 5- 7 years of experience in the Regulatory Affairs regulatory experience with new product introduction within the pharmaceutical industry covering both UK National and European regulations Strong communication and project management skills Proficiency in the use of MS Office suite (Excel, PowerPoint) Ability more »
support for the company’s initiatives. Requirements: Bachelor's degree in a relevant field (think: Business, Life Sciences, Engineering). Strong experience in the pharmaceutical realm, where you've honed your project management skills. A deep-seated understanding of GMP and GDP guidelines. A proven track record of launching products more »
world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.For more information, please visit viforpharma.comWe want CSL to reflect the world around usAs a global organization with employees in 35+ more »
Cardiff, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include more »
Cardiff, South Glamorgan, Wales, United Kingdom Hybrid / WFH Options
Gyrus Medical Ltd An ATL Technology Company
/Engineering/Quality orientated qualification Minimum of 3 years experience working in a QA/QS environment, preferably within the medical device or pharmaceutical industry. Knowledge of ISO13485:2003 and Medical Device Directive MDD 93/42/EEC Knowledge of FDA QSR Part 820 Computer literate to include more »
software, data analytics tools, process mapping software). Ability to leverage technology solutions to streamline processes, enhance efficiency, and drive innovation. Experience in PV pharma or Life Sciences industry-specific processes and best practices. Awareness of Operating of operating frameworks such as, CCMP, Lean Six Sigma, ITIL V4, GDPR, ISO27000 more »
Weybridge, England, United Kingdom Hybrid / WFH Options
Clinigen
Clinigen is a rapidly growing global specialty pharmaceutical and services company with a unique combination of businesses. Our divisions operate in a complex global regulatory environment and ensure that vital medicines are delivered securely on time and wherever they are needed in the world. We are currently 1,100 people more »
maintaining the GMP facilities and equipment in accordance with maintenance and validation programmes. The successful applicant will operate within and contribute to a GMP Pharmaceutical Quality System including change control, preventive actions, deviation management and document control. Excellent interpersonal and communication skills are essential, as is the ability to work more »
/create new SOPs Where change controls require participation in the packaging part, raise packaging specifications and check Master Batch Packaging records from Central Pharma Support Team with the process of movement of goods for products and materials through SAP system, including, purchasing, receiving, moving from site to site etc. more »
