Experience

amaiaa beauty

• United States
• Personal Care Product Manufacturing
• 1 - 100 Employee

• Founder and Chief Beauty Officer

  • May 2017 - Present

  Having worked in the corporate worlds of Pharmaceuticals, Nutraceuticals, Generics and Cosmetics, for over 3 decades, I literally woke up one fine morning and decided to give up my current position to pursue the dream and inspiration bubbling inside me since I took an emotional journey in India, visiting the homeland of beautiful rare treasures, spices and ingredients. It is there my mother and her mother spoke to me, the result, 'amaiaa' was born. At amaiaa we believe that glamour should not come at the expense of nature. Amaiaa would like to announce the premiere of two facial elixirs, Atma and Saya, a daytime and nighttime formula created to encourage naturally glowing skin and promote education among young women in India. Developed through a hand-selected process, each facial elixir is comprised of an abundance of all-natural ingredients and essential oils, with highlighted notes of Indian Jasmine and Indian Sandalwood found throughout the mystical land of rich heritage and rare spices. At Amaiaa we believe that glamour should not come at the expense of nature, which is why our mission is to connect women to the rare treasures found in India because we know that a woman’s skin should reflect the radiance within. Amaiaa encourages women to “be their own favorite” by reminding them that beautiful skin is not achieved through the use of synthetic formulas but is a process that begins with nurturing the skin beneath the surface. India’s treasures include the brilliant and beautiful young women that contribute to its population. With every purchase of each elixir, Amaiaa will donate a portion of the proceeds to a young woman’s academic journey, empowering her to create a radiant future for herself. Please contact: +1 954 830 5848 www.amaiaa.com Please follow us on Facebook, Instagram, Titter and Pinterest, @amaiaabeauty Show less



Revlon

• Personal Care Product Manufacturing
• 700 & Above Employee

• Program Director

  • Apr 2016 - May 2017

  Leads, manages and grows the Revlon Consumer PMO. Supporting the creation and deployment of global innovation development processes and master plans across Color Cosmetics, Personal Care and Revlon sister brands including Almay, Color Beyond, and Gatineau and others. Responsible for a team of 15 program managers and planners. Leads, manages and grows the Revlon Consumer PMO. Supporting the creation and deployment of global innovation development processes and master plans across Color Cosmetics, Personal Care and Revlon sister brands including Almay, Color Beyond, and Gatineau and others. Responsible for a team of 15 program managers and planners.



G&W Laboratories

• United States
• Pharmaceutical Manufacturing
• 100 - 200 Employee

• Senior Program Manager, Technical Project Portfolio Management

  • May 2015 - Apr 2016

  Led a cross functional project teams and responsible for full life cycles from product development to filing submissions with FDA , to include ANDA, PAS, and CBE-30. Oversaw a multi-million dollar portfolio of up to 50 projects. Involved with new product development for semi solid formulation, gels, ointments, lotions, and suppositories. Planned, executed and led project teams to develop and deliver products. Achieved approval from FDA within 30 days through a timely and accurate PAS submission. Ensured a timely ANDA submission for a complex formulation. First to lead teams in the highly effective company “Project Team Model” working cross-functionally across G&W labs. Part of a focus team involved in building new process flows and maps taking the company into a future desired state. Effectively managed deficiency notifications received from FDA in a strict timelines to provide detailed responses Show less



ABJ Pharmaceutical Consulting

• Greater New York City Area

• Founder

  • 2014 - 2015

  An ultimate “end to end” data service that captures and streamlines all “big” data into real-time dashboards, graphics, and final data assumption reports, allowing efficient interpretation, review, and decisions by our clients which ultimately results in their product launches to the Global markets before potential competitors. Offering a comprehensive range of project management services with the ability to exceed stakeholders’ expectations through innovative project, program, or portfolio management services. Our scope of work ranges from Drug Discovery to Post Marketing Clinical Trials. Show less



Thermo Fisher Scientific

• United States
• Biotechnology Research
• 700 & Above Employee

• Program Director

  • 2013 - 2013

  - Successfully implemented a major strategic alliance and served as single point of contact for Strategic Partner - Oversaw alignment of internal processes and procedures across all sites to establish a solid infrastructure for efficient and seamless post-project transfer to Strategic Partner - Effectively communicated implementation and operational activities to all stakeholders and relevant third parties - Managed project timelines and milestones to ensure on-time initiation of trials Show less



Thermo Fisher Scientific

• United States
• Biotechnology Research
• 700 & Above Employee

• Senior Global Project Manager

  • 2010 - 2012

  - Managed extensive projects, including oversight of overall project coordination and communication - Improved cross-functional business process activities and implemented the improvements while leading cross-functional teams locally and globally - Developed and presented successful proposals to optimize supply while managing patient dosing regimens - Assessed clinical protocols and other client-supplied study specifications to make recommendations resulting in more optimized and effective study performance Show less



Mundipharma

• Pharmaceutical Manufacturing
• 700 & Above Employee

• Projects Manager

  • 1999 - 2010

  - Oversaw company operations, served as a Subject Matter Expert, and led numerous project teams to support global company initiatives - Efficiently managed projects resulting in consistent on-time completion and optimized allocation of resources throughout sites across the EU - Enhanced professional development opportunities for internal teams to assist with team member growth - Managed a team of Project Coordinators overseeing clinical studies (Phases I–IV), new drug safety evaluations, and stability studies for international research and development projects - Managed section budget and advised Mundipharma and associated companies regarding resource management, outsourcing, and budgeting - Oversaw comprehensive records for all operations undertaken by the section, ensuring accurate generation and maintenance of records - Ensured all work was conducted in compliance with relevant codes of practice dictated by prevailing authorities (SOP, cGxP, UK, EU, FDA, etc.) for all clinical manufacturing, packaging, storing, and distribution - Provided expert scientific, technical, and regulatory advice relating to trial, packaging, and label design, resulting in the most appropriate presentation of dosage forms, packaging, and labeling for each project - Coordinated the provision of clinical supplies, including planning and distribution, for all clinical studies - Assisted multidisciplinary Chemistry-Manufacturing-Controls (CMC) and medical project sub-teams Show less



Ethical Pharmaceuticals

• Cambridge, United Kingdom

• Senior Quality Assurance Executive

  • 1997 - 1999

  - Performed cGxP audits, prepared reports of findings, and monitored the effectiveness of corrective actions - Audited and reviewed clinical trial medication supplies batch documentation and clinical trial project reports for cGxP compliance - Investigated and prepared reports related to adverse quality events - Performed cGxP audits, prepared reports of findings, and monitored the effectiveness of corrective actions - Audited and reviewed clinical trial medication supplies batch documentation and clinical trial project reports for cGxP compliance - Investigated and prepared reports related to adverse quality events



Therapeutic Antibodies - TAB London Limited

• St Bartholomews Medical College, London UK

• Senior Microbiologist, Quality Control Supervisor

  • 1994 - 1997

  - Ensured accurate and consistent performance of all required Laboratory Quality Control procedures according to applicable specifications and strict adherence to cGLP and cGMP guidelines - Ensured accurate and consistent performance of all required Laboratory Quality Control procedures according to applicable specifications and strict adherence to cGLP and cGMP guidelines



Martindale Pharmaceuticals Limited

• Harold Hill, Essex United Kingdom

• Microbiologist

  • 1994 - 1994

  - Responsible for microbiological monitoring of all raw materials, in-process bulk products, and finished products according to applicable procedures and specifications with strict adherence to cGLP, cGMP, and Health and Safety regulations - Responsible for microbiological monitoring of all raw materials, in-process bulk products, and finished products according to applicable procedures and specifications with strict adherence to cGLP, cGMP, and Health and Safety regulations