FELIPE Cabello
Pursuing Master’s degree in Environmental Health & BSc in Marine Biology both from UNIVERSITY OF PUERTO RICO. Worked as Sr. Process Facilitator at JOHNSON & JOHNSON CO. & Production Supervisor at MCNEIL (J&J)Las Piedras, Puerto Rico.
| Headline: | Entrepreneur |
| Skills: | Business, Languages, Leadership, Management |
| Groups: | [INACTIVE] EnterPRize 2010 |
| Interested in: | Brainstorming, Finding business partners, Finding cofounders, Finding team mates, Meeting new people, Professional opportunities, Promoting my startups, Recruiting for my startup |
| Schools: | University of Puerto Rico System |
WORK EXPERIENCE
| Employer: | MCNEIL (J&J)Las Piedras, Puerto Rico. |
| Position: | Production Supervisor |
| Description: | Provide technical support to enhance regulatory investigations and non- conformance issues.
Investigate, identify root causes, establish effective CAPA’s, and complete non- conformance reports within acceptable time frame. Directly responsible for monitoring and auditing process areas such as dispensing, formulation, granulation and blending. Monitor and coordinate manufacturing operations and all supporting activities such as validation, process compliance improvements, quality initiatives, and project management. |
| Employer: | JOHNSON & JOHNSON CO |
| Position: | Sr. Process Facilitator |
| Time period: | January 2005 - December 2009 |
| Description: | As a team player, maintained a high level of compromise in the completion of business plans normally above 3% improvement, helping in exceeding site profit plan expectations.
Reviewed, implemented and trained personnel in an extensive Good Manufacturing Practices GMP’s initiatives to become ready for a new manufacturing facility and FDA inspections. Co-lead the introduction of a generic product, on time and with high quality, which represented several MM in profits. Assisted in the development and implementation of business strategies to achieve targeted goals of 99% in customer satisfaction, inventory levels and spare parts inventory. |
| Employer: | Metrocover |
| Position: | General Manager-Self employment |
| Time period: | January 2003 - December 2005 |
| Description: | Developed and established a small distribution operation of my own invention (patented) product, Metrocover.
Developed, coordinated and complete the patenting of a new product until it final approval (Design Patent # 6,583,359B1. Developed strategies for manufacturing, packaging, distribution and marketing of product. Finalized negotiation with two leading chain of hardware stores to sale my product. Successfully market and reaches break even point 4 months after product lunch. |
| Employer: | WYETH AYERST LEDERLE, INC |
| Position: | Process Flow Assurer |
| Time period: | January 2001 - December 2003 |
| Description: | Support the Sterile Formulation and filling activities by planning, organizing, and monitoring the established QA programs to assure compliance with cGMP’s and regulatory agencies.
Established programs to improve batch record reviews, manufacturing instructions, in-process verifications, and final dispositions processes. |
| Employer: | ASTRA-ZENECA PHARMACEUTICALS |
| Position: | Production Supervisor |
| Time period: | January 1996 - December 2001 |
| Description: | Reported to Production Manager with responsibilities for the production functions of finished product operation of solid dosage, including packaging and distribution of all the drug presentations (High Unit Dose, Bulks, bottles and blisters).
Ensured an effective and efficient production process with an excellent quality. Maximized the productivity level with effective in-process verification techniques, proper material utilization, and continuous improvement programs. |
| Employer: | AMGEN MANUFACTURING INC |
| Position: | Manufacturing Section Head |
| Time period: | January 1992 - December 1996 |
| Description: | Reported to Manufacturing Director, responsible for the filling and packaging operations.
Directed start-up operations to establish the different stages of the manufacturing processes including components preparation, aseptic filling, labeling, and packaging. Selected, evaluated, and purchased the equipment to be used for the sterile manufacturing of Vials and Syringes products. Responsible for regulatory audits, performance qualifications, validation, calibration, and transfer of new technology; as well as Process Mechanics Support, and Printing room activities. Performed equipment evaluations and executed IQ’s, OQ’s, PQ’s and PV’s for equipments and processes. |
| Employer: | MOVA PHARMACEUTICAL INC |
| Position: | QA Auditor/Product Disposition Supervisor |
| Time period: | January 1990 - December 1992 |
| Description: | I supported the plant compliance activities by monitoring, auditing and collecting data to measure processes execution. Exposed to internal and external auditors as a team member to determine objective quality improvements opportunities.
Reported to Quality Operations Head. As Team member I maintained the highest quality level in compliance to GMP’s by auditing manufacturing subcontractors. |
| Employer: | MOVA PHARMACEUTICAL INC. |
| Position: | Product Disposition Supervisor |
| Time period: | January 1988 - December 1990 |
| Description: | Performed batch record reviews and released incoming manufacturing materials, packaging components, and process documentation records.
Conducted quality audits in manufacturing and packaging areas for acceptable product characteristics and conformance with plant formulas and procedures. |
EDUCATION
| University: | University of Puerto Rico System |
| Degree: | Environmental Health, MSc |
| University: | University of Puerto Rico System |
| Degree: | Marine Biology, BSc |
INFORMATION
| Memberships: | PDA (Parental Drug Association)
IOPP (Institute of Packaging Professionals) USPTO (United State Patent & Trademark Office) Registered Inventor |
FELIPE's Startups (1)
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Metrocover
Metrover is a electric meter console cover to protect and improve the appearance of the ordinary the electric meter panel in every houses.