Trima Ltd. Israel Work Values

Daily Duties at Trima Ltd. Israel:

• Maintain Internal Audits (IA), special projects, and Annual reports • Administrator of Qsoft program • Maintain documents in compliance with cGMPs • Working closely with Quality Assurance other departments to resolve documentation issues and ensure compliance. • Identify and present ongoing initiatives for continuous improvements to the organization’s quality and compliance process. • Inspect and promote GMP and SOPs compliance in an FDA and EMEA regulated pharmaceutical manufacturing environment, ensuring product integrity, safety and compliance with standards. • Ensure strict adherence to and implementation of Company Safety and Work rules • Assess project issues and develop solutions to meet scientific, productivity, quality goals and objectives • Participate in required meetings, activities, and related projects and relevant interdepartmental activities • Provide training and guidance to staff regarding compliance and interpretation of regulations • investigate quality issues and implementing corrective actions; • Identify departmental strengths and weaknesses

What they like about Trima Ltd. Israel:

Working in an organization that is technologically advanced, creative, and innovative is critical in your assessment of hiring companies. Less important to you are stability of the organization, the length of time an organization has been in business, and the business' plans for the future. You prefer a fast-moving company that will take risks to achieve its goals and objectives. The length of time the company has been in business is irrelevant. Maintaining status quo is unnecessary. You thrive on change, uncertainty and the upside of potential business risks, especially those associated with innovation. Stability for the long haul is not nearly as important as is working in an atmosphere that is charged with a sense of urgency and constant change.

Tags

QA, CRA, CTA, Research, biothech, regulation affeirs, Pharmaceutical, Generic, sience, biology, biochemistry, mulecular, Internal Audits, Cell culture, microbiology, SOP, GMP, GCP, life sience, MS Office, cells culture, gene therapy, molecular biology, vascular cells, biotechnology, Endiogenesis, VSMC, signal transductins, GCPRs, TRKs, proteins, Enzymes, hormons, protein-expressiona-and-purification, DNA, RNA, elctrophoresis, cGMP Regulatory Compliance Support specialist, Vectors, transffection

Skills

1.Supervisor of all in vivo laboratory personnel and activities. Sole Study Director for all Good Laboratory Practice (GLP) studies, 2.Directed the group responsible for developing biological, chemical and sterilization qualification strategies. Indirectly supervised 10 - 15 peers and subordinates, 3.Determined all biological and chemical qualification testing of new and modified products or materials in compliance with industry guidelines., 4.Active participant with the development of domestic and international biocompatibility testing guidelines, 5.Keep abreast of international regulations and provide direction related to updated or new regulations or policies. E.g. GMP guidelines introduced to other departments , 6.Analyze and advise on quality approaches and techniques addressing product development, continuous improvement projects, and urgent issue task forces to ensure proper resolution and compliance, 7.Introduce of Risk assessment motives to QA web-reports led to early discovery of crucial problems (some systematic) which could cause disqualification of production batches. e.g. increase company efficiency, 8.Maintain library of regulatory guidelines, 9.Extensive meetings and trainings led Firm employees awareness to the importance of compliance to QA guides and by that lower the amount of invalid batches., 10.Positive atmosphere and encouragement of brain storming help in bringing out improvement ideas and to lift working motivation, 11.Managed a computer network system serving seven departments. (E.g. Manage registration tracking system including tracking submissions and updating registration database with Q-soft program – which I was Self study) . , 12.Molecular cloning technique: PCR, RT-PCR, Restriction digest, ligation, DNA/RNA gel electrophoresis, bacterial transformation, plasmid isolation and purification, plasmid transfection and generation of over expressed cell lines. Gene manipulation and d, 13.Protein analysis: protein expression in cell culture, SDS-PAGE electrophoresis, western blot analysis, isolation and purifications of proteins, co-immuno-precipitation technique, immuno-fluorescence technique and immuno-staining, 14.Culture experience: sterile work with various human and mouse cell cultures, bacterial cultures, cell transfection, treatment of cells with growth factors/inhibitors/drug, cell counts, 15.Bioinformatics: searching in GenBank, experience in genome/protein/cDNA databases analysis, BLAST and sequence alignment, genome comparison of various species, 16.Microbiology: diagnostic bacteriology, cultivation and isolation of bacteria, specialized culture media and culture conditions, testing antimicrobial susceptibility, 17.Microsoft office programs (e.g: Word. Excl, Power point, Access), Photoshop, Adobe Acrobat, Q-soft, Interwise

These are some of the questions we asked our climbers about their experiences with Trima Ltd. Israel: