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- ...issues with drug product processing technologies and equipment. Identify and implement operational improvements for current and new sterile operations. Support commercial drug product manufacturing operations and contract manufacturing quality with technical evaluation...SuggestedContract work
- ...site and global procedures. Responsibilities Development and execution of CQV testing documentation for Clean Utilities for the Sterile Drug product facility. Responsible for meeting key project deliverables for safety, CQV schedule and quality of project-related...SuggestedContract workFor contractors
MALDI-TOF for Precise and Fast Microorganism Identification in Compliance with Updated EudraLex[...]
...identifying organisms with high accuracy — particularly crucial in light of the significant updates to EudraLex Annex 1 (Manufacture of Sterile Products) in August 2023. Implementation of Contamination Control Strategy (CCS): Operating in the pharmaceutical, cleanroom,...Suggested- ...client is one of the largest production units in the world! Our client produces, packs, and distributes in a high-tech environment, sterile injectable medicines. More than 1 million injectable medicines are produced, packaged, and distributed every day to 170 countries worldwide...SuggestedContract workWorldwide
- ...Senior Project / Contracts Manager to manage: # Phase 1: €15M hospital fit out to include Theatres; Treatment Rooms; Recovery Rooms; Sterile Rooms; Conference Rooms; Staff Rooms; Administration Rooms; etc – extensive M&E. # Phase 2: €20M infrastructure & associated civils...SuggestedFor contractors
- ...the absence of specified objectionable organisms. Good manufacturing practices require that objectionable organisms be absent from non-sterile nutritional and dietary products. Objectionable organisms are defined as microorganisms that may cause potential health hazards to...Suggested
- ...experts through comprehensive training. Become a trusted guide for customers - conducting piercings, educating on aftercare, maintaining a sterile environment, addressing questions and concerns throughout the process. Keep It Fresh: Maintain an Insta-worthy store with perfect...SuggestedPermanent employmentPart timeShift work
- ...testing of water, in-process and drug product release samples • Bioburden testing of water & in-process drug product samples • Sterility testing • Water sampling • Lab Support duties such as Biological Indicator testing, Growth Promotion, Media Preparation, Identifications...Suggested
- ...Endotoxin testing of water, in-process and drug product release samples Bioburden testing of water & in-process drug product samples Sterility testing Water sampling Lab Support duties such as Biological Indicator testing, Growth Promotion, Media Preparation,...SuggestedHourly payContract workWork at officeWeekend work
- ...manufacturing facilities. • Expertise in material and process flow knowledge (theory of constraints, lead time, transit times, etc.) for sterile production and distribution. • Experience handling strategic sourcing, negotiation of complex business issues and risk assessments a...SuggestedContract workWorldwide
- ...analysis including bioburden testing, endotoxin testing, microbial identification, Biological Indicator testing, BacT/ALERT testing, sterility checks, and growth promotion of media as required. - Carry out environmental monitoring including viable and non-viable...SuggestedFull timePart timeFlexible hours
- ...GPT confirms the suitability of culture media for various applications, including environmental monitoring, sterility testing, and microbial limits tests. By regularly performing GPT, companies can: Verify Media Quality Ensure that each batch of culture media can support...Suggested
- ...microbial recovery in microbiological assays, as required by GMP guidelines. Quantitative testing to assess the bioburden of non-sterile drug products and raw materials. Sensitive detection of bacterial endotoxins using the Limulus Amebocyte Lysate (LAL) assay to ensure...Suggested
£60.7k - £86.7k per annum
...doing: * Validation Engineer responsible for ensuring that the Validation activities associated with a Syringe Filling Line for a Sterile fill finish facility are in compliance with GMP and Quality Requirements. * Generation, execution, review and approval of CQV test...SuggestedContract work- ...sales goals. Experience or knowledge of healthcare technology or healthcare software related to track and trace, decontamination, sterile services, endoscopy, or theatres is highly desirable. Skilled in territory mapping and strategic planning, with the ability to analyse...SuggestedHybrid work
- ...for multiple regulatory agencies Expert knowledge of large molecule manufacturing processes (for biologics and/or vaccines) and sterility assurance requirements Ability to accurately interpret and apply regulatory expectations for a robust and compliant QMS Experience...Full timeContract workFor contractorsLong term contractVisa sponsorshipWork at officeLocal areaRemote workRelocationHybrid workFlexible hoursShift work3 days weekMonday to Thursday
- ...specification findings as appropriate. Report, standards, policy writing skills required. Equipment and process validation. Sterile Fill-Finish processes and equipment. Proficiency in Microsoft Office and job-related computer applications Excellent communication...Contract work
£39k - £40.8k per annum
...testing of water, in-process and drug product release samples * Bioburden testing of water & in-process drug product samples * Sterility testing * Water sampling * Lab Support duties such as Biological Indicator testing, Growth Promotion, Media Preparation, Identifications...Contract workWeekend work- ...investment in recent times. Core Responsibilities: Development and execution of CQV testing documentation for Utilities for the Sterile Drug product facility. Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related...Contract workFor contractors
€30.4k per annum
...efficient production processes. Perform cleaning of isolators, integrity checking, and pressure gauge checking to maintain a sterile environment. Carry out transfer sanitization into cabinets, perform volume and in-process checking to ensure accurate...WorldwideShift workNight shiftWorking Monday to Friday- ...Engineering or Relevant Experience 8+ years of experience in biopharma operations, with significant exposure to aseptic manufacturing, sterile drug product filling, and startup or capital projects environments. Proven ability to lead cross-functional teams and projects in...Hourly payFull timeContract workWork at officeHybrid work3 days week
£47.7k - £65k per annum
...and nights away when needed. A degree level education is beneficial, but not essential, as is experience working in a cleanroom or sterile environment. It is, however, essential you have a logical and methodical approach to finding faults and be comfortable with PLC troubleshooting...Permanent employmentLocal areaRemote workWork from homeHome officeNight shift- ...the NPI or post-NPI phases. Provide process development expertise for commercial drug product processing in specific areas such as sterile processing, process characterization, tech transfer and validation. Support commercial drug product manufacturing operations with...Worldwide
- ...products for international markets. We are now seeking an experienced Regulatory Affairs Manager as we expand and broaden our range of non-sterile oral products. Reporting to: Engineering Manager / EHS Team Role Function: The health and safety officer will ensure that...For contractorsFor subcontractorImmediate start1 day week