SYNGENE
Career Opportunities: study Personnel (Microbiologist) Life sciences discipline
(B.Sc./ M.Sc./ B.V.Sc./ M.V. Sc / M. Pharm)
JOB
PURPOSE (Briefly describe the objectives of the job):
As a
Study Personnel - Genetic Toxicology:
Responsible
for assisting in Genetic toxicology (Bacterial reverse mutation test, In vitro
Chromosomal aberration and micronucleus test; In vivo Chromosomal aberration
and micronucleus test) studies are carried out to the required scientific and
regulatory standard and review and approve the study data.
You
will be familiar with conducting all work in compliance with applicable
regulatory requirements governing the work in which they are involved, such as
GLP.
KEY
RESPONSIBILITIES:
Assist
in conduct of study in compliance with the Principles of Good Laboratory
Practice.
Comply
with the instructions given in the study plan and appropriate Standard
Operating Procedures applicable to their involvement in the study. Any
deviation from these instructions should be documented and communicated
directly to the Study Director, and/or if appropriate, the Principal
Investigator(s).
Record
raw data promptly and accurately and in compliance with Principles of Good
Laboratory Practice, and ensure the quality of their data.
Exercise
health precautions to minimize risk to them and to ensure the integrity of the
study. Communicate to the appropriate person any relevant known health or
medical condition in order that they can be excluded from operations that may
affect the study.
Sampling
(Quarantine, Sentinel, feed, Air
sampling, Monthly monitoring rooms and water) and analysed on timely basis.
EDUCATIONAL
QUALIFICATION:
To
be successful in this position, you will need to hold a degree or above in a
life sciences discipline (B.Sc./ M.Sc./ B.V.Sc./ M.V. Sc / M. Pharm).
WORK EXPERIENCE:
0 to
2 years of experience as study personnel.
TECHNICAL
/FUNCTIONAL SKILL:
You
should have good understanding and hands on Experience of Genetic
toxicology. Preferably have knowledge of
related disciplines, slide reading, cell culture handling and microbial counting.
Ideally,
you should be working in, or have Experience within contract research,
pharmaceutical companies or have an academic background related to a toxicology
discipline.
BEHAVIORAL/MANAGERIAL
SKILLS:
You
need to demonstrate:
A
proactive attitude towards internal and external customer satisfaction and the
highest standards of scientific quality and regulatory compliance.
Good
written and spoken communication skill.
Have
a meticulous attitude towards consistency of 100% quality in study plan,
reports and related material.
Be
aware of study status at all times and anticipate problems that may affect
timing, quality or integrity and take appropriate action to resolve such
problems.
OTHER
JOB REQUIREMENTS:
Basic
familiarity with Microsoft Office Suite.
Computer
skills, commensurate with Essential Functions and including ability to learn a
validated system.
Ability
to work extended hours beyond normal work schedule to include, but not limited
to, evenings, weekends, extended shifts and/or extra shifts, sometimes on short
notice.
Ability
to work under specific time constraints.
TO APPLY CLICK HERE
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