ALMA L. LASTRELLA
2263 Sun Valley Road ? Chula Vista, CA 91915
Cell  [Send email to request phone number] 39-1706 ? Home  [Send email to request phone number] 82-7472 
E-mail ?



Enclosed is a copy of my resume for your review. I am currently seeking for a
Clinical Laboratory Scientist/Lab Manager position in your company.

Please note, as you read my resume, that I offer excellent experiences and
skills. My work performance is thorough, resourceful, and detailed. I believe I
would be of immediate value to your company, and I welcome the challenge and
responsibility of proving my worth to an organization that appreciates quality
performance.

If, upon review of my qualifications, you feel that you have present or
prospective need for an individual with my skills, then I would like to arrange a
meeting to discuss the possibilities.
You may contact me at the above address and telephone number at your earliest
convenience.

Thank you for your consideration and reply. I look forward to hearing from you
in the near future.

Sincerely,



Alma L. Lastrella

Enclosure: Resume

















ALMA L. LASTRELLA

2263 Sun Valley Road  [Send email to request phone number] 39-1706
Chula Vista, CA 91915 

SUMMARY OF QUALIFICATIONS

A motivated, detail oriented and results driven Manager and Clinical Laboratory
Scientist with over 18 years of experience in the biotech, pharmaceutical and
healthcare industries. Excellent leadership, communication and teambuilding
skills with the ability to prioritize, set goals, and met objectives while
creating an atmosphere for achievement. Principal strengths include problem
analysis and resolution, process design and development, team motivation and
training.



PROFESSIONAL EXPERIENCE

Prometheus Laboratories 3/2007- Present
Sr. Laboratory Manager

? Manage and coordinate the daily activities of clinical laboratory operations
including quality control, troubleshooting, equipment maintenance and performance
of all assays.
? Managed the performance of assays in fields of Molecular Genetics (PCR),
Chemistry (HPLC, ELISA) and Immunology.
? Provides direct and constant supervision, training, annual competency
assessment and scheduling of Clinical Laboratory Scientists, Laboratory
Technicians and Equipment Technician.
? Responsible for interviewing, hiring and training employees; planning,
assigning and directing work; appraising performance; rewarding and disciplining
employees; addressing complaints and resolving problems.
? Responsible for testing and reporting of laboratory test results for all
disciplines approved by CAP, NY and CLIA.
? Responsible for technical studies designed to improve or validate clinical
laboratory testing methods.
? Initiates and coordinates process design and improvement activities such as:
quality, safety, document management and proficiency testing. 
? Participates in cost analysis and the departmental budgeting process.
? Assists with the implementation of test methods from R&D or external sources.
? Review and analyze equipment quotes and contracts and interacts with vendors
on special projects
? Departmental representative for cross -functional projects and leads
department meetings and project teams.
? Responsible for reviewing QC records and resolving problems.
? Responsible for instrument performance including: troubleshooting, repairs,
preventative maintenance and calibrations on all laboratory equipment
performance, maintenance and calibration.

Quest Diagnostics, Inc. San Diego, CA 2005- 2007
Laboratory Supervisor

? Managed the daily activities of the department including hiring, training,
competency, performance evaluation, counseling and scheduling of staff.
? Reviewed and monitored quality assurance indicators and daily quality control
procedures. 
? Performed validation of new equipment, controls and reagents and evaluation of
new or revised procedures.
? Responsible for enrollment, testing, evaluating, reporting, and follow-up on
CAP proficiency testing. 
? Performed investigation and troubleshooting of any testing or equipment
problems. 
? Participated as team member of the lab consolidation project and coordinated
the set-up and validation of instruments for the new STAT lab.
? Responsible for reviewing QC records and resolves problems as required
? Responsible for instrument performance and preventive maintenance.
? Performed laboratory testing and reporting patient results.


Sharp Chula Vista Medical Center, Chula Vista, CA 2005- 2006
Clinical Laboratory Scientist III ?Generalist (Part-time)

? Performed pre-analytical and post analytical test processes in Chemistry,
Coagulation, Urinalysis, Hematology, Microbiology and evaluates results relative
to the diagnosis, assessment and treatment of disease.
? Reviewed Quality Control systems, data, and outcomes for analytical testing
and processes.
? Coordinated and completed processes in place to meet standards established to
maintain quality testing.
? Analyzed errors and follow-trough with investigation, corrective action,
documentation and notification to appropriate caregiver and lab leadership.
? Reviewed quality assurance indicators and monitors in place and works with the
laboratory team to meet the established thresholds. 


American Red Cross, San Diego CA 1998- 2005
Southern California National Testing Laboratory 
Manager, Operational Support 2003 ? 2005

? Provide leadership to laboratory personnel including Equipment Technicians,
Document Control Specialists and Development Implementation Specialist.
? Managed laboratory equipment processes and supply including inventory,
validation, preventive maintenance activities, data management systems and system
security.
? Coordinated the planning and performance evaluation, installation, validation
and implementation of new or revised tests, procedures, instrumentation and
software for the laboratory.
? Performed investigation, documentation and monitoring of laboratory equipment
problems and deviations. 
? Updated and maintained a database for validations, master equipment list,
equipment preventive maintenance, equipment maintenance schedules and system
security for entire site.
? Performed review, update, training and implementation of procedures in
compliance with FDA, CLIA, CAP, NY, AABB, and GMP/GLP regulations.
? Implemented an automated equipment management system in the lab using MAXIMO
for preventative maintenance schedule and QC activities.
? Participated in annual budget by preparing reports, and justifications for new
equipment, reagents, and additional personnel.
? Project Manager for the Master Validation Plan for new equipment, test methods
and procedures
? Member of the Quality Audit team and a certified Problem Management Level 3
team leader.

Night Production Manager 2000- 2003

? Managed the PM shift daily operations, testing activities and review of assay
results for automated and manual test processes. 
? Provided leadership and management oversight to all 3 supervisors and 20
laboratory staff including Laboratory Technicians and Clinical Laboratory
Scientists.
? Monitored and reviewed production and testing records in compliance with SOPs,
CFR, cGMP,GLP, ISO and other applicable federal, state and local regulations.
? Coordinated the hiring, development, evaluation, training, competency
assessment, counseling and supervision of assigned management and laboratory
staff.
? Conducted investigations on testing and equipment problems, errors and other
potential problems that affect test performance or results. 
? Performed internal/external audits and inspections, and developed and
implemented corrective actions (CAPA) for any non-conforming (NCMR) and variances
in testing process.
? Participated in safety committee activities and ensured compliance with safety
policies and procedures in the work area.
? Responsible for site safety, safety awards, and accident reports and
investigations.

Laboratory Supervisor 1998- 2000

? Provide supervision, guidance and leadership. including orientation, training,
competency, performance evaluation, and discipline to 15 Laboratory personnel
(Lab Technicians, Laboratory Assistants and Clinical Laboratory Scientist).
? Performed NAT and proficiency testing, review and reporting test results and
review of equipment maintenance, calibrations and quality control. 
? Monitored workflow and scheduling of staff in the laboratory.
? Participated in writing and performing departmental validations and SOPs.
? Monitored and maintained reagents and supply inventory.
? Investigated and corrected technical problems in test procedures, reagents and
equipment.
? Prepared SOP?s test plans and final reports for test methods and software
validations.




Alvarado Hospital Medical Center, San Diego, CA 1997 ? 2003
Clinical Laboratory Scientist II-/Generalist 
IVF Lab- Embryologist

IVF Laboratory of San Diego, San Diego CA 1994- 1997
(Acquired by Alvarado Hospital in 1997)
Clinical Laboratory Scientist II/Embryologist 

Quest Diagnostics Inc., San Diego CA 1993- 1999
Clinical Laboratory Scientist II ?Toxicology Department

Miles Pharmaceutical Inc. (Bayer Corporation), San Diego, CA 1991- 1993
Clinical Laboratory Scientist I 





EDUCATION 

Bachelor of Science in Medical Technology 

 LICENSE

California Clinical Laboratory Scientist License ? MTA 35456 


PROFESSIONAL MEMBERSHIPS

Clinical Laboratory Management Association 
California Association for Medical Laboratory Technology