Timo Grimmon Email & Phone Number

Billericay, Gb

Oxford, Oxfordshire, United Kingdom

London, England, United Kingdom

- Contribute to the day to day maintenance of the quality management system and compliance at the MeiraGTx UK site- Take ownership of roles in various improvement projects - Asses the compliance and suggested CAPA actions for Quality Events at the MeiraGTx UK site- Work intra-departmentally with excellent written and verbal communications- Author and review Quality documentation- Ensure inspection readiness for various departments- Performed Runner and Document Retriever duties during client/partner audit- Keeping up to date and training out upskilling session for root cause analysis to London site- Taken ownership of customer complaint management and medical device SME trainee- Perform complex root cause investigations- Review, revise and approve complex root cause investigations from all departments, giving advise on the investigations and the implementation of robust and effective CAPAs.

London, England, United Kingdom

- Responsible for the organization of training and development of a team of ten bioprocessing scientists- Used 1-2-1’s, Team meetings, Team building activities and developmental planning to help operator progression, resulting in multiple operators at MeiraGTx and Oxford Biomedica promoted.- Promoted safety, continuous improvement, quality event closure and GxP compliance within the team- Took ownership of purification and finial filling processes, working to maintain GMP compliance and process readiness at all times through the use of frequent area-of-ownership inspections- Completed in-depth investigation, root cause analysis, CAPA actions and Change Controls for complex quality events in collaboration with QA and coached team members on owned investigations.- Participated and contributed to high level, inter-departmental meetings to ensure smooth operations- Work closely with QA to resolve day to day processing issues in compliance with procedure.- Routinely first contact for emerging manufacturing issues and engage in rapid response assessments and containment with relevant parties and QA.- Engage with reviewing, editing, authoring and approving SOP’s and Batch documentation.- Responsible for final manufacturing review and sign off on Batch documentation to high standard.- Responsible for planning and executing weekly and monthly quality audits of areas of ownership- Train out and encourage a Data Integrity (Adherence to ALCOA+) and GDocP culture.- Pro-actively spot and engage in resolving data integrity and procedural compliance gaps.

London, England, United Kingdom

In this role I lead a team of three bioprocessing scientist in the day to day manufacturing activities for clinical stage therapeutics. It involves collaborating with Tech Transfer streamline our GMP production capabilities, proactively work to improve safety and compliance and champion the personal and technical development for the members of my team.

Oxford

- Prioritised departmental KPI’s, quality document deadlines and upheld safety precautions of the team.- Responsible for writing and reviewing quality documents inc. Deviations, Change Control and CAPA’s- Create training and trained team members on executing SOP’s and championed data integrity and RFT.- Developed time management and interdepartmental communication abilities due to high pressureenvironment of Covid-19 Vaccine manufacturing under scrutiny of Astra Zeneca and regulatory bodies.- Ownership of GMP8 manufacturing suite, keeping it inspection ready and compliant at all times- Qualified Aseptic Technique trainer and Gowning Qualification Trainer- Train forty new operators in novel process featuring PALL Allegro Systems in coordination with MSAT

Oxford, United Kingdom

- Capable operator with GxP compliant experience in and outside of the cleanroom.- Engaged in the day to day manufacturing activities from preparing and preforming processes to sanitising the cleanrooms.- Experienced in maintenance and harvest of adherent HEK cell culture form small scale flasks to 10 layer cell factories.- Experienced in maintenance and harvest of suspension HEK cell culture from small scale shaker flasks to 200L bioreactors. -Contributed to the validation of the new TFDF process step introduced into the suspension production platform.- Experienced in downstream purification of product using the AKTA chromatography platform and cartridge filtration. - Experienced in Vaporised Hydrogen Peroxide (VHP) treatment of the cleanrooms to ensure sanitisation together with a 3rd party contractor- Experience using LIMS system

Manchester

Became familiar with the maintenance of CHO cell culture and a range of analytical techniques including GCMS (Gas Chromatography- Mass Spectrometry), Single metabolite assays, protein identification, Western's, SDS-page, PCR, CHO cell transient transfection and fluorescent microscopy.

Nanjing, Jiangsu, China

Took initiative after the release of official air pollution numbers in Nanjing, China, in ordering pollution filter masks from Singapore and distributing the masks (Totobobo Masks) to members of the international and local community. For this venture I managed the financial, logistical and marketing aspects of the effort and personally delivered the masks to costumers while communicating with Totobobo masks for continued supplies.

Nanjing, Jiangsu, China

Translated documents from Dutch/German to English for other BASF sites for the local site. This helped develop my time management skills as translations were given set due dates.Greatly improved my communicative skills as the job involved communicating technical information across three languages.

Master Of Science (M.Sc.), Biotechnology, First Class

Activities and Societies: University of Manchester Water poloMy masters project allowed me to work with Dr. Alan Dickson and Dr. Edward.

International Baccalaureate, 34 Ib Points

Activities and Societies: - Swim Squad (Captain) - Football team - Volleyball team - Orchestra - Water Polo Club (Founder and Captain)•.