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RssMedical Device Sales Representative

Hi. I am a Chemical Engineer with 14 years of excellent experience in the manufacturing of pharmaceutical products. I have a BS in Chemical Engineering, a MS in Manufacturing Engineering, and a Certification in Biotechnology Practices. My background had given me the experience to be part of the most challenging projects in the pharmaceutical company I actually work for. But right now, I am looking for new endeavors and would like to make a career change. For all these years, I have been working mostly with equipment in a manufacturing environment. Right now, I feel this urgent need of working directly with the people that require a pharmaceutical product or medical device to improve the quality of their lives. I understood, I need to be in touch with the people, this has become my dream job. I would like a job as a medical device sales representative working directly with doctors and patients, even in surgery or medical procedures, and teaching people how to use the devices. Certainly, I do not have the experience as a medical sales representative but in my vast experience as a process engineer, I had attained the necessary skills to be a successful sales representative in the medical device world. Please take a look at my resume having in mind my strong desire for this career change, more than my experience in sales, and please consider me for any opening you may have in PR, Ft. Lauderdale or Miami areas. Feel free to contact me anytime at my personal phone number (787) 486-5430 or email maricel_flores@hotmail.com, so we can discuss more in detail my qualifications.

Process Engineer

Carolina, PR

About Me

Industry:

Engineering & Architecture

Occupation:

Process Engineer
 

Education level:

Master

Will Relocate:

Yes

Location:

Carolina, PR

Work Experiences

9/1997 - Present

(private)

Individual Contributor

  • Coordinate and conduct projects of the Process Engineering Group (PEG) qualification work. Review and approve validation documents, maintain and develop PEG projects' schedules, coordinate project activities between departments, and represents the PEG in regulatory and in-house inspections. Actively participate in safety, health and environmental studies and company teams as a representative of the PEG. Assists PEG Team Leader in development plans for the professional growth of the PEG group. Advice and guarantee that all activities comply with company and regulatory agencies quality standards in the projects/area of responsibility assigned. Actively participate to avoid/investigate deviation during the start-up and validation activities. Evaluate equipment/systems/process modifications to ensure compliance with the validated state in order to prevent quality issues that could affect the compliance of the process. Conduct facilities walk-thru and be in charge of the generation of quality, compliance and good engineering practices deficiencies lists to develop improvement strategies within systems, projects or areas assigned. Make contributions to the correction of cGMP issues. Support and participate during the audits and inspections of the area of responsibility. Guarantee that teamwork is effectively trained in the procedures, guidelines and regulations to avoid not compliance events. Ensure satisfactory Safety, health and Environmental (SHE) performance within the teamwork and actively participate in management SHE improvement actions.

Education

2007

Certification Degree

University of Puerto Rico

  • Biotechnology Practices

2004

Master Degree

Polytechnic University Of PR

  • Manufacturign Engineering

1995

Bachelor Degree

University of Puerto Rico

  • Chemical Engineering