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QPS Career
Opportunities USA
SENIOR/RESEARCH SCIENTIST - ADME
Responsibilities
include:
►Metabolite identification,
profiling and isolation from in vivo and in vitro samples to support
drug discovery, and delivery and development.
►Must have strong knowledge
in drug metabolism or organic chemistry and hands-on skills in
mass spectrometry and separation science.
►Experience with radiolabeled
compounds and radiochemical detection is a plus.
Candidate must possess:
PhD
in Analytical/Bioanalytical Chemistry, Organic Chemistry and Pharmaceutical
Chemistry with 0-2 years experience working in the area of drug
metabolism or MS with at least 5 years of relevant experience
are preferred.
ASSOCIATE
SCIENTISTS - BIOMARKER
Responsibilities
include:
►Participation in development
and validation of novel immunoassays, enzymes assays and cell-based
assays to support various drug discovery and development projects.
►Validation of commercially
available immunoassays and bioassays.
Application of various assay methods for routine sample analysis.
►Evaluate significance
of data and report findings
Maintain lab instrumentation and smooth operation of facilities
►Anticipate workload peaks
and manage flow to optimize productivity, while maintaining quality
of work.
Candidates must possess:
►Be able to follow procedures
and work towards the development of skills for trouble shooting
and study design.
►Have knowledge of GLP
►Hands on experience in
ELISA and cell culture and protein purification, conjugation
Minimum education: BS in Science and at least 1 year of hands-on
lab experience.
ASSOCIATE SCIENTISTS - BIOANALYTICAL
Responsibilities
include:
►Set-up, document and
monitor sample analysis procedures
►Assist in method development
and perform method validation
►Document results and
accurately record observations in accordance with GLP's and SOP's.
►Coordinate work flow
and satisfy needs of other ongoing studies.
►Demonstrate effective
teamwork
►Coordinate daily/weekly
workload to achieve changing priorities
►Run multiple interrelated
scientific studies simultaneously
►Organize and conduct
work assignments in a safe manner and according to SOP's and GLP
regulations
►Function independently
in set-up and conduct a variety of studies
Candidates must possess:
►BS in Biology, Pharmacy,
Chemistry, Biochemistry, Toxicology or related science with at
least 2 years of hands-on laboratory experience.
►Must be able to troubleshoot
and repair lab equipment and recognize technical problems. Must
have working knowledge of GLP's and other regulatory and safety
standards and demonstrate effective teamwork.
SCIENTIST
(ASSOCIATE OR STAFF)
Responsibilities
include:
►Support company efforts
in development of sustained delivery formulations for potential
drug candidates
►Assist in design, performance
and evaluation of experiments
►Evaluate formulation
performance in-vitro and in-vivo animal models
►Assist in addressing
formulation issues of potential drug candidates
►Conduct solid and solution
stability studies, as well as dissolution studies
►Prepare reports, summaries,
protocols, batch records and quantitative analyses
►Maintain high level of
professional expertise through familiarity with scientific literature
►Follow and prepare all
necessary SOP's.
Candidates must possess:
►Experience in analytical
development and validation such as HPLC, GPC and protein stability
testing.
►Experience with controlled
and sustained release formulations is strongly preferred.
►Understanding of the
importance of preformulation to formulation development is a plus.
►Must have excellent interpersonal,
multi-tasking, communication, presentation and analytical skills.
Must be able to troubleshoot procedures and contribute to troubleshooting
study design. Must exercise initiative, have the ability to examine
data and solve problems and make decisions with independence.
BS or MS
in Chemistry, Biochemistry, Pharmaceutics or related scientific
field with 2-4 years of relevant experience.
QPS' total
rewards system is designed to be competitive, motivational, fair,
and consistent with the objectives and values of the Company.
QPS' Compensation program ensures that pay is linked to performance
contribution and that employees are compensated in alignment with
the external marketplace. Performance is evaluated with salary
actions/merit increases performed on an annual basis. Bonuses
and awards are also a part of QPS' total rewards approach; and,
as such, are linked to individual, team, and company performance.
QPS Benefits
Include:
Located in
the Northeast U.S.'s major bio-tech corridor, QPS offers competitive
compensation and benefits programs to its full time employees,
including:
Paid Vacation /Sick/Personal Time
Paid Holidays, including a floating holiday
BlueCross-Blue Shield Medical
MetLife Dental (including orthodontia for up to 18 years of age)
MetLife Short Term and Long Term Disability
MetLife Group Life Insurance
MetLife Additional Individual & Family Life Insurance
QPS, LLC 401(k) Plan with Company Match
Delmarva Blood Bank Membership to Employees Working in DE Location
Credit Union Membership to Employees Working in DE Location
Federal and State Benefits such as COBRA, FMLA, Workers Compensation
Military Leave, Jury/Witness Duty Leave
Paid Bereavement Leave
Paid Wedding Leave
Opportunity to Bank Vacation
Employer-Sponsored Family Social Events
Qualified candidates may submit their resume to careers@questpharm.com
or via fax to (302) 369-5602. QPS is proud to be an equal opportunity
employer.
You
may also use our Contact Form.
EEO/AAP Notice: QPS is a federal contractor/subcontractor subject
to all provisions of Executive Order 11246, Section 503 of the
Rehabilitation Act, and the Vietnam Era and subsequent Veterans
Readjustment Acts.
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