Robert Van Paulino Email & Phone Number
Who is Robert Van Paulino? Overview
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Robert Van Paulino is listed as Bioprocessing Scientist at MeiraGTx, a with 395 employees, based in London, England, United Kingdom. AeroLeads shows a matched LinkedIn profile for Robert Van Paulino.
Robert Van Paulino previously worked as Industry Analyst EHSQ at Verdantix and Nuclear Medicine Radiopharmacy Technician (Band 7) at Maxxima Group. Robert Van Paulino holds Biosafety Practicioner, Biotechnology, Pass from The University Of Edinburgh.
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About Robert Van Paulino
Dedicated Bioprocessing Scientist with 1 year and 10 months of experience at MeiraGTx, specializing in GMP-compliant activities for sterile gene therapy products. Proven expertise in aseptic manufacturing techniques, ensuring the highest quality standards in clean room environments. Committed to GMP, Data Integrity, and GDP, contributing to contamination-free GMP batch manufacture. Strong leadership, effective problem-solving, and meticulous attention to detail. Focus on Health & Safety, Biosafety and 6S Operational Excellence (Opex – Culture).
Listed skills include Microsoft Excel, Microsoft Word, Customer Service, Microsoft Office, and 1 others.
Robert Van Paulino's current company
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Robert Van Paulino work experience
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Industry Analyst Ehsq
Bioprocessing Scientist
• Improved and executed GMP-compliant production processes for sterile gene therapy products, ensuring rigorous adherence to SOPs and GMP practices.• Demonstrated proficiency in aseptic manufacturing techniques, guaranteeing the production of intermediate sterile products at the highest standards.• Monitored and maintained clean room environments for compliant operations, ensuring a contamination-free GMP batch manufacture.• Implemented and managed projects for manufacturing waste… Show more • Improved and executed GMP-compliant production processes for sterile gene therapy products, ensuring rigorous adherence to SOPs and GMP practices.• Demonstrated proficiency in aseptic manufacturing techniques, guaranteeing the production of intermediate sterile products at the highest standards.• Monitored and maintained clean room environments for compliant operations, ensuring a contamination-free GMP batch manufacture.• Implemented and managed projects for manufacturing waste management, fostering sustainable and responsible practices and implementation of 6S methodology in the manufacturing facility, promoting continuous improvement, efficiency, and operational excellence.• Served as a Health and Safety Representative for manufacturing, contributing to a safe and secure working environment.• Completed the Biosafety Practitioner Level 1 course from the University of Edinburgh, enhancing knowledge in biosafety practices.• Utilized First Aid qualifications and rapid response skills to address health and safety concerns promptly.• Authored investigation reports, conducted risk assessments, and presented solutions in CAPA panels. Show less
Nuclear Medicine Radiopharmacy Technician (Band 7)
• Efficiently created and processed precise data sets from patient blood samples for GFR testing, ensuring accurate and reliable results.• Demonstrated independent and meticulous work in an in-vitro laboratory, handling aseptic production of diagnostic and therapeutic radioactive medicinal products within strict SOP parameters.• Executed precise preparation of Tc-99m standards, showcasing pipetting skills for consistent volumes of blood and radioactive samples.• Conducted a range of… Show more • Efficiently created and processed precise data sets from patient blood samples for GFR testing, ensuring accurate and reliable results.• Demonstrated independent and meticulous work in an in-vitro laboratory, handling aseptic production of diagnostic and therapeutic radioactive medicinal products within strict SOP parameters.• Executed precise preparation of Tc-99m standards, showcasing pipetting skills for consistent volumes of blood and radioactive samples.• Conducted a range of in vitro laboratory tests using unsealed sources of radioactivity, accurately calculating, and recording results on the Hospital Information System.• Ensured compliant stock levels and proper disposal of radioactive waste in accordance with SOPs.• Acted as a Radiopharmacy Operator under the Ionising Radiations (Medical Exposure) Regulations 2000, handling dispatch of radioactive materials and performing quality control tests on radiopharmaceuticals.• Active participant in Radiopharmacy staff meetings, contributing insights from monthly self-inspections (audits) to enhance operational excellence. Show less
Production Technician Supervisor
• Supervised staff inside and outside clean room areas, ensuring a steady workflow and promoting a strong work ethic.• Delegated tasks to complete daily orders, maintain equipment, and manage stock levels within designated areas.• Proficient in understanding complex machinery, including Isolators, Autoclaves, and capsule machines.• Assisted in validating new equipment, cleaning agents, and developing new complex processes.• Ensured staff awareness and competence in performing… Show more • Supervised staff inside and outside clean room areas, ensuring a steady workflow and promoting a strong work ethic.• Delegated tasks to complete daily orders, maintain equipment, and manage stock levels within designated areas.• Proficient in understanding complex machinery, including Isolators, Autoclaves, and capsule machines.• Assisted in validating new equipment, cleaning agents, and developing new complex processes.• Ensured staff awareness and competence in performing standard operating procedures (SOPs) and GMP adherence.• Trained new employees and pre-reg pharmacists in GMP and SOP standards.• Collaborated with Quality Control in the development and research of clinical trials, procuring suitable equipment, implementing technical procedures, and recording data.• Updated SOPs in conjunction with the Senior Pharmacist and Chief Technician.• Proposed and commented on changes to departmental policies and procedures, assisting in their implementation.• Liaised with ward staff and pharmacists daily to determine CIVAS and cytotoxic requirements, preparing doses as necessary.• Ensured differential pressures and environmental conditions met correct limits, maintaining equipment at GMP standards.• Formulated and printed worksheets and labels for products using the pharmacy computer system, ensuring stability before compounding.• Manufactured CIVAS, cytotoxic, clinical trials, sterile, and non-sterile products in accordance with SOPs and GMP principles.• Assisted in computing Cytotoxic, Non-sterile, and CIVAS manufactured products on the JAC system for stock control, cost calculation, and assignment to the appropriate consultant.• Dispensed products according to orders from external customers or home care.• Addressed possible near misses, deviations, and raised CAPAs, change controls, and UE’s. Assisted in investigations related to risk management and Root Cause Analysis (RCAs). Show less
Sterile Operations
• Demonstrated full understanding of specific environments, process flows, and equipment operations.• Proficient in troubleshooting mechanical issues related to specific equipment.• Expertise in utilities, including HVAC operations, pressure cascade control, WFI, and steam generation.• Responsible for the preparation, assembly, sterilization, and aseptic filling of products.• Ensured processing records compliance with approved procedures and production programs.• Coordinated… Show more • Demonstrated full understanding of specific environments, process flows, and equipment operations.• Proficient in troubleshooting mechanical issues related to specific equipment.• Expertise in utilities, including HVAC operations, pressure cascade control, WFI, and steam generation.• Responsible for the preparation, assembly, sterilization, and aseptic filling of products.• Ensured processing records compliance with approved procedures and production programs.• Coordinated section activities, liaised with other sections, and organized daily work operations.• Upheld high standards of cGMP and Health & Safety in all activities.• Reviewed SOPs, BPRs, and related documentation, generating reports for microbiology and leadership.• Assisted team leaders and management in specific investigations.• Maintained equipment compliance through regular maintenance, calibration, and validation.• Facilitated cross-shift handovers through clear verbal communication.• Proficient in gas and liquid filtration principles, troubleshooting filter testing problems.• Conducted sterile transfers and operated clean in place systems for department-specific equipment.• Expertise in troubleshooting and operating various equipment, including sterilization and freeze-drying.• Assisted in management of Heat Treatment, including training new staff and operating AHT ovens for sterilization.• Analysed and interpreted statistical data from Yokogawa charts, understood incubation processes, and organized product storage in incubation and cold rooms. Show less
Pharmaceutical Production Technician
• Spearheaded the manufacturing of specialized veterinary products, including compounding suspensions, solutions, and external pastes such as Levothyroxine, Dantrolene syringes, and Trilostane solution.• Assisted in upholding the integrity of the production environment, ensuring strict compliance with SOP, MHRA, and GMP standards.• Conducted regular calibration of scales, balances, and other equipment as per SOP requirements.• Executed thorough cleaning routines on a daily, weekly… Show more • Spearheaded the manufacturing of specialized veterinary products, including compounding suspensions, solutions, and external pastes such as Levothyroxine, Dantrolene syringes, and Trilostane solution.• Assisted in upholding the integrity of the production environment, ensuring strict compliance with SOP, MHRA, and GMP standards.• Conducted regular calibration of scales, balances, and other equipment as per SOP requirements.• Executed thorough cleaning routines on a daily, weekly, monthly, and quarterly basis in both sterile and non-sterile environments.• Led the manufacturing of sterile products within isolators, including Deslorelin, Tacrolimus, and Omeprazole, and oversaw bulk production of various items, including filling, pastes, and syringes.• Played a pivotal role in product development, conducting trials and calculating concentrations for process validation, particularly for products like Trilostane suspensions.• Assisted in upholding the integrity of the production environment, ensuring strict compliance with SOP, MHRA, and GMP standards.• Implemented company policies for personal protection, diligently managing stock of Personal Protective Equipment (PPE).• Upheld a safe and clean work environment by strictly adhering to current good manufacturing practices (cGMP), standard operating procedures, and legal regulations; actively monitored the environment.• Played a pivotal role in product development, conducting trials and calculating concentrations for process validation, particularly for products like Trilostane suspensions.• Ensured in-process checks at each step of the manufacturing process for all products, guaranteeing strict adherence to Good Manufacturing Practices (GMP) by all operatives.• Managed laboratory operations by maintaining a steady workflow through effective organization, collaboration with other departments, and proactive planning; motivated staff by fostering communication and creating a friendly work environment. Show less
Colleagues at MeiraGTx
Other employees you can reach at meiragtx.com. View company contacts for 395 employees →
Michael Passineau
Colleague at MeiragtxWexford, Pennsylvania, United States
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Amanda Cullen
Colleague at MeiragtxLondon, England, United Kingdom
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Muzzammil Patel
Colleague at MeiragtxLondon, England, United Kingdom
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Ela Balda
Colleague at MeiragtxEnnis, County Clare, Ireland
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Cameron Hughes
Colleague at MeiragtxDunstable, England, United Kingdom
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SG
Sarah Goeminne
Colleague at MeiragtxGhent Metropolitan Area, Belgium
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Paul Batcheler
Colleague at MeiragtxAddlestone, England, United Kingdom
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CB
Chandler Bing
Colleague at MeiragtxParis, Île-De-France, France
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Timo Grimmon
Colleague at MeiragtxWestcliff-On-Sea, England, United Kingdom
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Darren Walsh
Colleague at MeiragtxLimerick, County Limerick, Ireland
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Robert Van Paulino education
Biosafety Practicioner, Biotechnology, Pass
Cs50 Computer Science, Computer Science
Python, Computer Programming
Bsc(Hons) Biological Sciences, Biology/Biological Sciences, General, Upper Second-Class Honours (2:1)
Education record
Education record
Frequently asked questions about Robert Van Paulino
Quick answers generated from the profile data available on this page.
What company does Robert Van Paulino work for?
Robert Van Paulino works for MeiraGTx.
What is Robert Van Paulino's role at MeiraGTx?
Robert Van Paulino is listed as Bioprocessing Scientist at MeiraGTx.
Where is Robert Van Paulino based?
Robert Van Paulino is based in London, England, United Kingdom while working with MeiraGTx.
What companies has Robert Van Paulino worked for?
Robert Van Paulino has worked for Meiragtx, Verdantix, Maxxima Group, Royal Free London Nhs Foundation Trust, and Bpl Plasma.
Who are Robert Van Paulino's colleagues at MeiraGTx?
Robert Van Paulino's colleagues at MeiraGTx include Michael Passineau, Amanda Cullen, Muzzammil Patel, Ela Balda, and Cameron Hughes.
How can I contact Robert Van Paulino?
You can use AeroLeads to view verified contact signals for Robert Van Paulino at MeiraGTx, including work email, phone, and LinkedIn data when available.
What schools did Robert Van Paulino attend?
Robert Van Paulino holds Biosafety Practicioner, Biotechnology, Pass from The University Of Edinburgh.
What skills is Robert Van Paulino known for?
Robert Van Paulino is listed with skills including Microsoft Excel, Microsoft Word, Customer Service, Microsoft Office, and Management.
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