Sample Bilingual Consultant Resume
Contact information
Briany S. Mansouri
17 Street
Oklahoma City
Oklahoma
Career objective
Looking for a challenging position of the Sample Bilingual Consultant Resume the reputed University with a view to use my wide experience for the benefit of the organization.
Bilingual bio/chemical engineer with 4 years experience in cGMP pharmaceutical manufacturing industry. Developed sound analytical, quantitative and project management skills having worked in scale-up/scale-down, new process development, process optimisation and technology transfer. Experienced in Quality by Design and Design of Experiment. Self-motivated with a willingness to accept change and heightened levels of responsibility.
PROFESSIONAL EXPERIENCE
FLAMBEAU EUROPLAST LTD, Ramsgate – Business Project Manager Feb – Sept 2010
Secured a 2.5m asset purchase and its consolidation, working closely with the managing director of Flambeau EuroPlast Ltd. Instrumental in the due diligence process, liaised with all stakeholders and performed commercial and operational due diligence for acquisition target. Worked with front-line staff through to Board level to achieve synergies.
Selected highlights:
Negotiated contracts worth 25,000 for acquisition site closure.
Delivered commercial, operational and IP due diligence questions.
Created schedule overlay of capacity and production data from own and acquisition site, including different production efficiency levels and shift hour scenarios. This determined which machines to keep and which products to discontinue for the merger of the two sites at year-end.
PFIZER LTD, Bioprocess Development Group, Pfizer Global Manufacturing Jan 2006 – May 2009
Downstream Processing Scientist
Worked on process development, scale-up, improvement, transfer and validation for a wide variety of biologics for Pfizer manufacturing sites world-wide. Experienced in all aspects of membrane filtration, chromatography, Expanded Bed Adsorption (EBA), precipitation and aseptic technique. Handled planning and structuring of parallel studies such as CTLA4, Anidulafungin, IgF1-r and Diphtheria and ensured studies’ criteria are met. Communicated important stagegates as part of a global team to US senior management via teleconference or face-to-face. Developed in-depth understanding of protein products in terms of processing, interactions and their formulations, impurities, side-product formation and how to control these.
Selected highlights:
Secured proof of concept for continuous processing as an alternative to Protein A chromatography by improving monoclonal antibody’s yield and purity by 20% and further proofed process application to other monoclonals. This alternate purification process guaranteed cost savings of 40% and more and has a potential for industry-wide application. Supported patent application until project was transferred to Pfizer colleagues in the US.
Completed cost analysis on Diphtheria harvest filter unit cost and their cleanability for Pfizer Nebraska under Laboratory Class III conditions. Delivered a more cost effective alternative with a saving of more than $175,000 per process cycle pre- optimisation.
Supported the manufacture and aseptic filling of New Chemical Entities (NCE) to supply product for use in pivotal stability, robustness and commercial trials.
Familiar in all aspects of GMP documentation, including authoring, reviewing, auditing batch records, batch record deviations, technology transfer documentation, experimental reports and validation protocols for scale-up processes.
Trained and project managed a new team of 10 colleagues from Ireland taking over our department’s function in all technical aspects, practices and procedures, ensuring GMP training compliance. Accomplished a smooth hand-over of projects, procedures and techniques and ensuring team remained motivated to deliver important project to a very tight deadline.
Completed Failure Modes and Effects Analysis (FMEA) to identify critical process parameters to design laboratory pre-qualification studies and secondary, augmented design using Design of Experiment software (DoE). Used DoE software to analyse and write up conclusions for FDA report write-up/ Bioprocess License Application (BLA).
Designed and carried out fermentation challenge studies which required working to tight deadlines, attention to detail and timely sample analysis.
PFIZER LTD, Bioprocess Development Group, Pfizer Global Manufacturing Feb 2005 – Jan 2006
Contract Analyst
Responsible for structuring and running studies and their analysis, oversight of daily laboratory activities, training and stock control.
Selected highlights:
Created a simplified purification process to include water as a solvent which increased the concentration of the purified product and reduced process costs.
Provided process engineering support and assisted with trouble-shooting at Pfizer contract manufacturer in Germany during monoclonal antibody process scale-up.
Harmonised key global process by travelling to Germany to provide bilingual support at less than 24 hrs notice for 100+ process deviations for a FDA Bioprocess Licence Application submission.
Planned and carried out EBA experiments as alternative to Protein A chromatography for second generation mAb process for harvest, concentration and purification step using AKTA explorer.
Responsible for auditing experimental write-ups. Acted as main contact for queries regarding records management.
OTHER EXPERIENCE
Business consultant, Kenya July – Aug 2009
Identified new economic opportunities for a community group in western Kenya. Selected and scheduled the group’s activities and visits to local projects, and organised and gave business training sessions.
Selected highlights:
Negotiated and secured an agreement for the community group to arrange sale of produce to a more reliable buyer.
Devised a focused and commercial structure addressing low profits for a community group of 25+ members.
Published articles on this voluntary consulting work with the Association of MBAs, The Independent and the University of.
POSITIONS OF RESPONSIBILITIES
Board of Directors, Animate Arts Company Ltd Since July 2010
Executive MBA Representative, Business School Sept 2008 – Aug 2010
Active member, Pfizer Adventure Racing Group Jan 2006 – May 2009
EDUCATION
Business School, Masters in Business Administration (expected 2:1) Sept 2008 – Jan 2011
University College London, MSc Biochemical Engineering (2:1) Sept 2003 – Sept 2004
University of Newcastle upon Tyne, BEng (Hons) Chemical and Process Engineering (2:2) Sept 1998 – June 2003
Industry placement at The Dow Chemical Company, Liquid Separations, Germany Sept 2001 – Aug 2002
References
Briany S. Mansouri
Manager
Wap Company.
Briany_Mansouri@gmail.com
