Analytical R&D Scientist
Company: Yoh, A Day & Zimmermann Company
Location: Belews Creek
Posted on: April 9, 2021
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Job Description:
Analytical Research and Development (AR&D) Scientist needed
for a --contract opportunity --for Yoh Scientific--------s client
located in the --High Point, NC --area. This position is with a
major pharmaceutical company. -- --If you meet the requirements,
please apply to this job and also feel free to follow up via email
to Rachita.Saxena@yoh.com. (Job#310960)
Pay Rate: $35.00
Hours: 8am-5pm
1 year W2 Contract
SUMMARY
As an Analytical Research and Development (AR&D) Scientist you
are expected to independently manage project activities and perform
all related administrative. -- Job functions include providing
analytical support to internal, and occasionally external,
pharmaceutical product development projects. -- Duties include, but
are not limited to, cleaning verification, method development,
validation, qualification and transfer, stability, raw material,
finished product testing and partnering with the Formulation
R&D team. -- The perfect candidate will possess the following
attributes.
------- -- -- -- -- Technical
-- -- -- -- -- -- -- -- -- An expert at developing and validating
test methods for pharmaceutical raw materials and finished products
for strength, impurities, identity and dissolution by HPLC, GC,
dissolution, spectroscopy, and traditional quantitative
analysis.
-- -- -- -- -- -- -- -- -- An expert at testing pharmaceutical raw
materials and finished products by internally developed and
compendial test methods.
-- -- -- -- -- -- -- -- -- An expert at troubleshooting analytical
and instrument problems and at performing OOS investigations.
-- -- -- -- -- -- -- -- -- An expert at GMPs as they pertain to the
R&D analytical group and pharmaceutical product
development.
-- -- -- -- -- -- -- -- -- A strong working knowledge of
descriptive organic chemistry.
-- -- -- -- -- -- -- -- -- A working knowledge of pharmaceutical
formulations development.
------- -- -- -- -- Leadership
-- -- -- -- -- -- -- -- -- Will be an experienced technical and
personal leader who leads by example.
-- -- -- -- -- -- -- -- -- Will be expected to mentor, lead and
develop lower level scientists.
-- -- -- -- -- -- -- -- -- Will effectively maintain open
communication within the R&D team, as well as external,
customers.
------- -- -- -- -- Administrative
-- -- -- -- -- -- -- -- -- Will have a strong command of the
English language with strong oral and written communication
skills.
-- -- -- -- -- -- -- -- -- Will have a solid working knowledge of,
and experience with, common office software and chromatographic
data acquisition systems.
-- -- -- -- -- -- -- -- -- Will have experience in providing
support for generating CMC sections of INDs, ANDAs and NDAs
(including 505b2).
-- -- -- -- -- -- -- -- -- Will be able to effectively work in
multidisciplinary teams within the department and company.
--
--
--
ESSENTIAL DUTIES AND RESPONSIBILITIES
------- -- -- -- -- Ensure that the work performed by direct
reports meet pharmaceutical industry and internal company standards
for quality and timeliness. -- Primary duties will include the
following.
-- -- -- -- -- -- -- -- -- Develop and validate methods to test
pharmaceutical raw materials and finished products for strength,
identity, impurities and dissolution performance by commonly used
techniques.
-- -- -- -- -- -- -- -- -- Test and release raw materials and
finished products in support of internal product development.
-- -- -- -- -- -- -- -- -- Test stability samples in support of
internal product development.
-- -- -- -- -- -- -- -- -- Administrate the departmental cleaning
verification program to support the Pilot Plant and the packaging
lines.
------- -- -- -- -- Plan, review and manage the activities
performed by direct reports. -- Such work must meet all appropriate
scientific, regulatory and safety standards, including GMPs, ICH,
OSHA and internal SOPs.
------- -- -- -- -- Accurately, clearly and completely communicate
the results of work, orally and/or in writing, to line management,
clients and/or others with a need to know.
------- -- -- -- -- Work with other internal colleagues and other
departments within the company as needed to facilitate the
successful development and launch of new products and technologies
and assist in trouble-shooting problems with currently marketed
products.
------- -- -- -- -- Represent the Analytical Development group by
participating in departmental and company project team
meetings.
------- -- -- -- -- Assist in preparing regulatory documents and
other communications with outside agencies, clients, and/or
colleagues from other corporate sites.
------- -- -- -- -- Write SOPs and other instructional documents
for the Analytical Development group.
--
QUALIFICATIONS (Minimum Education and Experience)
------- -- -- -- -- Bachelors, Masters or Ph.D. in Chemistry (a
focus on Analytical is preferred) with at least 2-6 years of
directly related experience, including at least 0-2 years of
directly related supervisory experience. -- Other educational
qualifications may be considered if accompanied by additional
related experience.
------- -- -- -- -- Must be fluent in spoken and written
English.
------- -- -- -- -- Must have a working knowledge of common office
and technical software.
------- -- -- -- -- Must be legally eligible to work in the United
States and must be able to pass a legally administered drug
screening.
SUMMARY
As an Analytical Research and Development (AR&D) Scientist you
are expected to independently manage project activities and perform
all related administrative. -- Job functions include providing
analytical support to internal, and occasionally external,
pharmaceutical product development projects. -- Duties include, but
are not limited to, cleaning verification, method development,
validation, qualification and transfer, stability, raw material,
finished product testing and partnering with the Formulation
R&D team. -- The perfect candidate will possess the following
attributes.
------- -- -- -- -- Technical
-- -- -- -- -- -- -- -- -- An expert at developing and validating
test methods for pharmaceutical raw materials and finished products
for strength, impurities, identity and dissolution by HPLC, GC,
dissolution, spectroscopy, and traditional quantitative
analysis.
-- -- -- -- -- -- -- -- -- An expert at testing pharmaceutical raw
materials and finished products by internally developed and
compendial test methods.
-- -- -- -- -- -- -- -- -- An expert at troubleshooting analytical
and instrument problems and at performing OOS investigations.
-- -- -- -- -- -- -- -- -- An expert at GMPs as they pertain to the
R&D analytical group and pharmaceutical product
development.
-- -- -- -- -- -- -- -- -- A strong working knowledge of
descriptive organic chemistry.
-- -- -- -- -- -- -- -- -- A working knowledge of pharmaceutical
formulations development.
------- -- -- -- -- Leadership
-- -- -- -- -- -- -- -- -- Will be an experienced technical and
personal leader who leads by example.
-- -- -- -- -- -- -- -- -- Will be expected to mentor, lead and
develop lower level scientists.
-- -- -- -- -- -- -- -- -- Will effectively maintain open
communication within the R&D team, as well as external,
customers.
------- -- -- -- -- Administrative
-- -- -- -- -- -- -- -- -- Will have a strong command of the
English language with strong oral and written communication
skills.
-- -- -- -- -- -- -- -- -- Will have a solid working knowledge of,
and experience with, common office software and chromatographic
data acquisition systems.
-- -- -- -- -- -- -- -- -- Will have experience in providing
support for generating CMC sections of INDs, ANDAs and NDAs
(including 505b2).
-- -- -- -- -- -- -- -- -- Will be able to effectively work in
multidisciplinary teams within the department and company.
--
--
--
ESSENTIAL DUTIES AND RESPONSIBILITIES
------- -- -- -- -- Ensure that the work performed by direct
reports meet pharmaceutical industry and internal company standards
for quality and timeliness. -- Primary duties will include the
following.
-- -- -- -- -- -- -- -- -- Develop and validate methods to test
pharmaceutical raw materials and finished products for strength,
identity, impurities and dissolution performance by commonly used
techniques.
-- -- -- -- -- -- -- -- -- Test and release raw materials and
finished products in support of internal product development.
-- -- -- -- -- -- -- -- -- Test stability samples in support of
internal product development.
-- -- -- -- -- -- -- -- -- Administrate the departmental cleaning
verification program to support the Pilot Plant and the packaging
lines.
------- -- -- -- -- Plan, review and manage the activities
performed by direct reports. -- Such work must meet all appropriate
scientific, regulatory and safety standards, including GMPs, ICH,
OSHA and internal SOPs.
------- -- -- -- -- Accurately, clearly and completely communicate
the results of work, orally and/or in writing, to line management,
clients and/or others with a need to know.
------- -- -- -- -- Work with other internal colleagues and other
departments within the company as needed to facilitate the
successful development and launch of new products and technologies
and assist in trouble-shooting problems with currently marketed
products.
------- -- -- -- -- Represent the Analytical Development group by
participating in departmental and company project team
meetings.
------- -- -- -- -- Assist in preparing regulatory documents and
other communications with outside agencies, clients, and/or
colleagues from other corporate sites.
------- -- -- -- -- Write SOPs and other instructional documents
for the Analytical Development group.
--
QUALIFICATIONS (Minimum Education and Experience)
------- -- -- -- -- Bachelors, Masters or Ph.D. in Chemistry (a
focus on Analytical is preferred) with at least 2-6 years of
directly related experience, including at least 0-2 years of
directly related supervisory experience. -- Other educational
qualifications may be considered if accompanied by additional
related experience.
------- -- -- -- -- Must be fluent in spoken and written
English.
------- -- -- -- -- Must have a working knowledge of common office
and technical software.
------- -- -- -- -- Must be legally eligible to work in the United
States and must be able to pass a legally administered drug
screening.
--
Opportunity is Calling, Apply Now!
Recruiter: Rachita Saxena
Rachita.Saxena@yoh.com
What--------s In It For You?
We welcome you to be a part of one of the largest global staffing
companies to meet your career aspirations. Yoh--------s network of
client companies has been employing professionals like you for over
65 years in the U.S., UK and Canada. Join Yoh--------s extensive
talent community that will provide you with access to Yoh--------s
vast network of opportunities and gain access to this exclusive
opportunity available to you.
------- -- -- -- -- -- -- -- -- -- -- Medical, Dental & Vision
Benefits
------- -- -- -- -- -- -- -- -- -- -- 401K Retirement Saving
Plan
------- -- -- -- -- -- -- -- -- -- -- Life & Disability
Insurance
------- -- -- -- -- -- -- -- -- -- -- Direct Deposit & weekly
ePayroll
------- -- -- -- -- -- -- -- -- -- -- Employee Discount
Programs
------- -- -- -- -- -- -- -- -- -- -- Referral Bonus Programs
Yoh makes finding and applying for jobs simple. Partner with Yoh to
find the right opportunities across multiple industries in the US
and UK. Find out more here!
Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer.
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, disability, or status as a
protected veteran. Visit
https://www.yoh.com/applicants-with-disabilities to contact us if
you are an individual with a disability and require accommodation
in the application process.PandoLogic. Keywords: R&D Scientist,
Location: Belews Creek, NC - 27009
Keywords: Yoh, A Day & Zimmermann Company, Winston-Salem , Analytical R&D Scientist, Other , Belews Creek, North Carolina
Click
here to apply!
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