Aida R. Ramirez

**** ***** ******

Downey, California, 90240

562-***-****(H) 562-***-****(C)

Objective: A position in Quality or Operations that utilizes my skills and

enhances my career goals and opportunities in management.

Qualifications:

. Extensive process, engineering and management experience in the medical

device industry.

. Proven ability to successfully manage projects and people.

. Demonstrated communication, listening and motivational skills with

supervision experience with direct reports along with management positions.

. An analytical and resourceful self-starter.

Strengths:

Analytical Communication Motivator Discipline

Work Ethics Process Development FDA Standards Planning

Skills: MS Word, Excel, Windows

Education:

. B.S. Chemical Engineering, Universidad Autonoma de Santo Domingo,

Dominican Republic.

. Master in Production Management, Universidad Tecnologica de Santo

Domingo, Dominican Republic.

. Master in Quality Assurance, Universidad Autonoma de Santo Domingo,

Dominican Republic.

May 2013 - Present Life Cycle Herbal Products Los Angeles, CA

Quality Control Coordinator: Responsible for managing all quality control

activities, including in process inspection, and final product release.

Responsible of document control, writing and revising standard operation

procedures (SOP's), updating all documents including Master Manufacturing

Records (MMR's), and training production workers on cGMP. Also managing the

Corrective Action Request (CAR's) for customer complaints, Out of

Specification (OOS), Label Control, and deviations on in process product.

Material Review Board member responsible for keeping track of on hold

stock. Conduct final review, audit, and sign off for all Batch Production

Records (BPR's) prior to the release of finished products.

January 1993 - April 1997 Alpha Therapeutic Los Angeles, CA

Manufacturing Quality Control Supervisor: Responsible for managing all

quality control activities, including raw material inspection, in process

inspection, and final product release; also supervised four (4) Quality

Control Inspectors in three different shifts.

Jan 1991 - May 1992 Abbott Laboratories Dominican Republic

Process Engineer: Responsible for coordinating and executing protocols for

all new products and new production lines. In charge of the validation of

all new equipment for the processing of all medical devices assembled at

this plant. Also trained to be the head of the calibration department for

this facility.

June 1986 - Jan 1991 Cartonera Hernandez Dominican Republic

Quality Control Manager: Responsible for managing all activities in the

Quality Control Department, including inspection of raw materials, in

process and final inspection of all products; in addition, was responsible

for the supervision of six (6) quality control inspectors in three

different shifts; was also responsible for system tracking all customer

complaints.

References: Are available upon request.

Contact this candidate