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.