Biotechnology/ Pharmaceuticals Sample Resume

This sample resume is for professionals with extensive experience in biotechnology, pharmaceuticals and project coordination and regulatory compliance in toxicology, oncology, GMP and GLP settings.

SUMMARY
Seeking position where more than 10 years of
experience in biotechnology, pharmaceuticals and
project coordination will add value. Will relocate to
Anywhere within 30 days.
PROFILE
Extensive research experience includes pre-clinical
data reporting/processing, QA, project coordination
and regulatory compliance, in toxicology, oncology,
GMP and GLP settings.
Track record of consistent achievement for ABC Company’s
Proven management skills. Experienced supervising
laboratory operations, QA efforts and teams of up to
14 professionals on animal-based toxicology research
and other assignments.
ABC Company Vice President said: “His role within
ABC Company continued its evolution … He has
met each new role with enthusiasm and motivation. Tom
is always learning and is eager to apply his new
skills to new opportunities.”
KEYWORDS
biotechnology, bio-technology, bio-tech, biotech,
pharmaceuticals, project coordination, pre-clinical
research, data reporting, data processing, QA,
quality assurance, regulatory compliance, toxicology,
oncology, GMP, GLP, good manufacturing practices,
good laboratory practices
EDUCATION
Master of Science Degree: Management,University, Anywhere, USA
Graduate Courses in Advanced Biology, Polytechnical Institute, Anywhere, USA
Bachelor of Science Degree: Biology,University, Anywhere, USA
EXPERIENCE
Coordinator, Controlled Substances:ABC Company, Anywhere, USA (2003-present).
Support research by managing storage of controlled
drugs, as well as purchasing and inventory.
Chosen to fill demanding position handling four
separate functions: coordinating storage and
disposition of controlled substances; purchasing
laboratory and feed supplies; processing requisition
entries; and managing and monitoring two feed rooms.
Ensure 100% compliance with DEA guidelines. Procure
laboratory materials for two North American sites.
Perform inventories and data input for Toxicology
Department.
Complete high volumes of work. Increased efficiency
by organizing controlled substance room to
effectively monitor and combine all schedule I, II,
III, IV and V drugs.
Toxicology Administrator, ABC Company, Anywhere, USA (1993-2002).
Provided support for Mammalian Toxicology operating
areas, including customer satisfaction and follow-up,
quality and client issues. Worked with every major
Fortune 500 pharmaceutical firm.
Carried out wide range of activities, reporting to
Vice President of Mammalian Toxicology.
Played key role in bringing Covance to world-class
quality level. Analyzed client surveys to identify
problem areas. Refined ISO-9001 processes to
continually improve quality levels.
Created monthly quality reports covering research
operations globally.
Planned and led tours of research facility at a
campus for prospective and existing clients.
Maintained 100% retention of research clients with
effective contact and follow up on reporting, data
efficacy and satisfaction. Served as point person on
all quality/service issues.
Cited by Vice President for “working effectively
across all 4 sites and providing me with highly
reliable data covering a variety of client monitoring
and quality system activities.”
Research Assistant: ABC Company, Anywhere, USA (1991-1993).
Worked closely with veterinarians. Assisted on and
performed surgical procedures.
Performed health screens on studies for
pharmaceutical client firms; completed X-rays and
drug inventories. Initiated and updated standard
operating procedures.
Reported to Director of Laboratory Animal Medicine.
Supervisor, ABC Company, Anywhere, USA (1988-1991).
Supervised 14 employees performing toxicology
research.
Managed all pre-clinical research efforts, monitored
health of animals, updated all training files and
coordinated ad hoc projects.
Led efforts to significantly increase quality levels
by setting up automated processes and winning buy-in
from all personnel in department.
Research Assistant: University Hospital,
Anywhere, USA (1983-1987).
Performed tissue cultures for amniotic cell
assessment in Genetics Department.
Successfully developed and initiated double
screening/confirmation for growing, incubating and
preparation of slides with amniotic cells for
microscopic evaluation.
Performed all tissue culture for amniocentesis.
Developed film for chromosomal analysis, using dark
room techniques. Also gained extensive knowledge of
aseptic technique.
Quality Assurance Engineer: ABC Company, Anywhere, USA (1980-1982).
Designed and implemented quality program for Class
III critical medical device (Membrane Oxygenator) in
Extracorporeal Medical Specialties Department.
Analyzed pre-clinical and clinical data. Performed
continuous failure mode analysis charting and audited
program for compliance with contract manufacturing
regulatory guidelines.
ADDITIONAL INFORMATION
Prior experience in US Army; promoted to Captain and
received Bronze Star during combat.
Computer skills include Word, Excel and Vistant
logistics system.