Ran Rippa
Clinical and Production Laboratory Manager at Medical Electronic Systems- Claim this Profile
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English Full professional proficiency
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Hebrew Native or bilingual proficiency
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Spanish Limited working proficiency
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Bio
Boris Pertsikov, Ph.D.
I was Ran Rippa's colleague for two and a half years at Trima's analytical R&D. I have worked with him and identified him as team head of analytical R&D. Ran managed the development of analytical methods for generic pharmaceutical products, for example: tablets, capsules, liquid formulations (lotions and syrups) and semi-solid formulations (creams, ointments and gels). Ran Rippa has experience in development and validation of analytical HPLC and dissolution methods. He demonstrated a creativity, solving complicated separations of excipients, impurities and the active ingredients using liquid chromatography. Ran gained plenty of knowledge and experience in the stability testing of finished products. He showed professional knowledge in GMP, issuing analytical methods, SOP's, development and validation protocols and reports. Ran successfully managed analytical R&D projects and was responsible for the analytical data submitted to the regulators. He was defending on the product until it was approved. Ran's relationships with the colleagues and mangers were professional and with a great will to do any task required. Respectfully, Dr. Boris Pertsikov Head of Analytical R&D Team
Boris Pertsikov, Ph.D.
I was Ran Rippa's colleague for two and a half years at Trima's analytical R&D. I have worked with him and identified him as team head of analytical R&D. Ran managed the development of analytical methods for generic pharmaceutical products, for example: tablets, capsules, liquid formulations (lotions and syrups) and semi-solid formulations (creams, ointments and gels). Ran Rippa has experience in development and validation of analytical HPLC and dissolution methods. He demonstrated a creativity, solving complicated separations of excipients, impurities and the active ingredients using liquid chromatography. Ran gained plenty of knowledge and experience in the stability testing of finished products. He showed professional knowledge in GMP, issuing analytical methods, SOP's, development and validation protocols and reports. Ran successfully managed analytical R&D projects and was responsible for the analytical data submitted to the regulators. He was defending on the product until it was approved. Ran's relationships with the colleagues and mangers were professional and with a great will to do any task required. Respectfully, Dr. Boris Pertsikov Head of Analytical R&D Team
Boris Pertsikov, Ph.D.
I was Ran Rippa's colleague for two and a half years at Trima's analytical R&D. I have worked with him and identified him as team head of analytical R&D. Ran managed the development of analytical methods for generic pharmaceutical products, for example: tablets, capsules, liquid formulations (lotions and syrups) and semi-solid formulations (creams, ointments and gels). Ran Rippa has experience in development and validation of analytical HPLC and dissolution methods. He demonstrated a creativity, solving complicated separations of excipients, impurities and the active ingredients using liquid chromatography. Ran gained plenty of knowledge and experience in the stability testing of finished products. He showed professional knowledge in GMP, issuing analytical methods, SOP's, development and validation protocols and reports. Ran successfully managed analytical R&D projects and was responsible for the analytical data submitted to the regulators. He was defending on the product until it was approved. Ran's relationships with the colleagues and mangers were professional and with a great will to do any task required. Respectfully, Dr. Boris Pertsikov Head of Analytical R&D Team
Boris Pertsikov, Ph.D.
I was Ran Rippa's colleague for two and a half years at Trima's analytical R&D. I have worked with him and identified him as team head of analytical R&D. Ran managed the development of analytical methods for generic pharmaceutical products, for example: tablets, capsules, liquid formulations (lotions and syrups) and semi-solid formulations (creams, ointments and gels). Ran Rippa has experience in development and validation of analytical HPLC and dissolution methods. He demonstrated a creativity, solving complicated separations of excipients, impurities and the active ingredients using liquid chromatography. Ran gained plenty of knowledge and experience in the stability testing of finished products. He showed professional knowledge in GMP, issuing analytical methods, SOP's, development and validation protocols and reports. Ran successfully managed analytical R&D projects and was responsible for the analytical data submitted to the regulators. He was defending on the product until it was approved. Ran's relationships with the colleagues and mangers were professional and with a great will to do any task required. Respectfully, Dr. Boris Pertsikov Head of Analytical R&D Team
Experience
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Medical Electronic Systems
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United States
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Medical Equipment Manufacturing
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1 - 100 Employee
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Clinical and Production Laboratory Manager
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Jul 2023 - Present
Manage the laboratory personnel to ensure that they are trained to perform all aspects of the laboratory procedures and protocols. Maintain the laboratory and laboratory equipment including calibration of equipment, repair, and upkeep so that it is functioning per the company standards. Perform clinical trials. Meet regulatory ISO 13485 standards and prepare the laboratory for regulatory inspections. Develop review and provide input into all laboratory and clinical trial protocols, and procedures. Coordinate with the R&D Lab Manager and the Clinical Director for product continuity from R&D to Production. Hire laboratory personnel based on budgeted positions or growth in coordination with the CEO. Provides input for the annual budget for personnel. Show less
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MediCane Health Incorporated.
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Israel
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Analytical Laboratory Manager
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Feb 2022 - Feb 2023
Led and managed Analytical R&D and QC activities in the analytical laboratory for an international pharmaceutical company focused on developing and marketing cannabis-based medications. Conducted quality control tests for clinical trials, stability studies, and internal analytical studies and issued certificates of analysis. Developed and validated analytical methods for raw materials in-process monitoring and drug products. led laboratory investigations following irregularities (OOS, OOT, abnormal results) producing appropriate CAPA. Oversaw stability testing studies conducted in out-source laboratories. Show less
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Entera Bio Ltd.
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Biotechnology
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1 - 100 Employee
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Analytical Laboratory Manager
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Nov 2014 - Feb 2022
Led and managed Analytical R&D and QC activities in the analytical laboratory for a biotech company specializing in oral delivery of large molecules (hormones, proteins, etc.). Conducted quality control tests for clinical trials and stability studies. Developed and validated analytical methods for raw materials, in-process materials, and drug products. Led the analytical issues for the company's preclinical and clinical trials. Managed tech transfer of analytical methods to CMOs and service laboratories in Israel and abroad (England, USA, China). Established a quality assurance management system. Managed the procurement process of equipment and reagents. Recruit and trained researchers. Supervised the stability tests carried out in the company's laboratories and external laboratories. Show less
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Ministry of Education
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Education Administration Programs
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700 & Above Employee
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Natural Sciences Teacher
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Aug 2012 - Oct 2015
● Taught Natural Sciences – Chemistry, Biology, and Physics ● Taught Natural Sciences – Chemistry, Biology, and Physics
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SOREQ Nuclear Research Center, Isorad Ltd. Pharmaceutical Division
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Yavne, Center District, Israel
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Analytical R&D and Quality Assurance Consultant
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2011 - 2012
Provided external professional consulting on analytical development and quality assurance issues for the ‘Isorad’, a company that develops and manufactures radiopharmaceuticals for the diagnostic and therapeutic Medicare market. Provided external professional consulting on analytical development and quality assurance issues for the ‘Isorad’, a company that develops and manufactures radiopharmaceuticals for the diagnostic and therapeutic Medicare market.
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Trima Pharmaceutical Products
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Israel
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Team Head - Analytical R&D
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2004 - 2011
Planned and managed the development of analytical methods for drug products in various applications, including tablets, capsules, syrups, creams, ointments, foams, and gels, for a company that develops, manufactures, and markets generic pharmaceutical products. Planned and directed the validation of analytical methods for many varied drug products. Led the stability studies of new drug products ensuring that products met their shelf-life specifications, reporting in a timely manner to the management. Wrote many analytical methods for a wide variety of raw materials and finished products. Issued validation and development protocols and reports. Directed and issued drug substances and drug product release and shelf-life specifications. Issued the company standard operating procedures (SOPs). Issued the analytical R&D documents for registration files and responded to regulatory authorities regarding analytical questions that arose from registration files. Show less
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Peptor
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Biotechnology Research
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QC and Analytical R&D Manager
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2003 - 2004
Managed an analytical lab team for a biotech company developing peptide-based pharmaceuticals. Oversaw quality control tests, stability studies, analytical and bio-analytical development, purification, and identification of peptides. Managed the outsourcing of analytical projects, including development and validation, in Israel and worldwide. Supported the audits of Aventis on the subcontractor's site. Represented the company's analytical issues in audio conferences with Aventis, Managed an analytical lab team for a biotech company developing peptide-based pharmaceuticals. Oversaw quality control tests, stability studies, analytical and bio-analytical development, purification, and identification of peptides. Managed the outsourcing of analytical projects, including development and validation, in Israel and worldwide. Supported the audits of Aventis on the subcontractor's site. Represented the company's analytical issues in audio conferences with Aventis,
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Chemagis
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Analytical R&D Research Analyst and Manager Assistant
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1994 - 2003
Developed and validated analytical methods for the QC laboratory of a company that develops, manufactures, and markets active pharmaceutical ingredients (APIs). Solved analytical issues for the regulatory affairs department, R&D teams, and production department. Issued company standard operating procedures (SOPs). Wrote and issued the company's specifications and methods worksheets while managing change controls and maintaining efficient document flow to the Manufacturing, QC, and QA departments. The company's safety guide instructs the teams on safety, to enable work in a safe work environment for all employees. Responsible for the company’s bank of standards, ensuring that all standards are tested on time for Retest/Expiry Date and supplies efficiently to the clients. Show less
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Education
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The Hebrew University
M.Sc., Biochemistry -
The Hebrew University
B.Sc., Chemistry