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Technician San Francisco

Location:
San Francisco, CA, 94015
Posted:
July 25, 2013

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Resume:

Mary Rose Magie P. Yap

Address: *** ******** *** **** **

Daly City, Ca. 94015

Phone: 650-***-****

E-mail: ********@*****.***

Objective: To acquire unique skills and experience for professional growth.

Skills and Abilities

Equipment operating skills- all related Genentech commercial and clinical filling equipments (TL and

IMA filler, Bosch vial washer and tunnel, Branson Ultrasonic system, Steris parts washer,

etc.) General lab equipments (centrifuge, pipette, spectrophotometer, scales, etc.)

Laboratory skills- General laboratory skills, knowledge of aseptic techniques.

Computer/software skills- Microsoft office, DMS, Trackwise, UNIX, Novamanage and Livelink.

Personal skills- Hardworking, able to work in groups or independently, very organized, a quick learner

and a motivated worker.

Education

2008 San Francisco State University SF, Ca. - Certificate on Clinical Trial Management

2000 San Francisco State University SF, Ca. - Bachelor of Science w/ concentration in Cell and

Molecular Biology

Professional Experience

June 2007- May 2008 Genentech, Inc. South San Francisco, Ca.

Documents and Data Analyst, SSF Manufacturing Shared Services

• Supported commercial cell culture purification and filling groups. Main duties involved

gathering, drafting and reporting, analyzing, presenting and updating data for both groups (i.e.

campaign monthly metrics, weekly metrics and discrepancies, ticket turn around tracking,

miscellaneous spreadsheets and scorecards).

• Supported Class A initiatives - documents, software and processes (develop SIPOC,

process maps and business documents for executing processes in cell culture purification group,

SAP, 5S, etc.).

• Supported side projects - inventory investigations to resolve system anomalies and

document audits for cell culture purification group.

• Assisted with driving and improving metrics and processes for commercial purification

and filling groups (i.e. improving ticket turn around, reducing discrepancies for commercial and

non-commercial filling).

December 2003- June 2007 Genentech, Inc. South San Francisco, Ca.

CPMF Technician for Clinical Filling Ops. (Start-up Technician)

• Project driven group derived from clinical manufacturing for the purpose of validating a new

clinical filling facility (CPMF). Main duties were to support all activities and facility needs

(facilities issue, stocking up supplies, assist vendors and contractors, R&D requests, facility

maintenance and improvement, submit work requests, designed parts for equipments, special

ordered materials and parts, Execute cGMP product fills and validation fills (QTPs), validate

equipments and facility, provide operations support on all activities, etc.)

• Acted subject matter experts for equipments in the facility (Westcapper, Steris parts washer, SIP

of portable tank skid, SIP of transfer line skid, Glycol cooling system for port. Tanks, CIP skid,

IMA filler, Finn-aqua autoclave). Responsible for creating SOPs, operation contact and assists in

validation of equipments, provide training, develop equipment improvements and

troubleshooting.

• Support filling operations and validation activities in the clinical and commercial manufacturing

facilities (i.e. Area 2 lyophilizer Project developed procedures, planned and gathered materials

and executed cycle development fills, media fills and qualification lots for Cathflo Activase).

Developed Tickets, related forms and SOPs, filling procedures, interventions and trouble shoot

systems based on cGMP.

January 2003-December 2003 University of California San Francisco SF, Ca.

Pulmonary Research Staff Research Associate I

• Processed and stored all Pulmonary Research clinical samples (Induced Sputum, Blood,

Nasal lavage and scrapings). Separated supernatant from cell pellets and prepared slides. Stored

and recovered samples. Determined sample total and differential cell counts. Analyzed cell

protein content using ELISA and Unicap. Purchased laboratory materials. Entered Data. In

charge of overall laboratory up-keep.

Aug. 2000-Jan. 2003 DPI-ChemRx Advanced Technologies SSF, Ca.

Manufacturing Associate I

• Synthesized drug-like compounds for drug companies following protocols. Wrote

production protocols for synthesizing each chemical library according to development synthesis

protocols. Purchased and inventoried materials for libraries to be synthesized. Coordinated

materials, protocols, scheduled chemical library start dates and end dates for QC analysis. Kept

track of chemical synthesis progress daily. Generated weekly and monthly reports to

management on progress of libraries in synthesis (no. of compounds in synthesis, to start

production and end production, no. of compounds purified and shipped).

Languages: English and Tagalog.

References: Available upon request.



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