Hello Associates,

I have a very immediate need for Quality Control Chemist II for my client
in Buena, NJ (100% interview with in 24/hr)
Kindly go through the below position and do let me know your interest.
Kindly share suitable profiles at  fah...@mirthconsulting.net

*Job Title*:* Quality Control Chemist II*

*Duration: 6 Months Contract to Hire”*


*Location: Buena, NJ Maxx* *Rate : $40 /Hr on C2C*
*H4 EAD, EAD GC, Green Card , US Citizen only required…..*



*Job Summary:*



A Quality Control Chemist II is responsible for providing accurate and
timely testing of in-process, finished product, stability, and raw material
samples, to support the production schedule. This person will also ensure
the safety and reliability of products produced in compliance with quality
and regulatory requirements.



*Reporting Relationships: None*



*Essential Responsibilities:*



Perform QC testing of in-process, finished product, stability and raw
material samples using techniques such as HPLC, GC, viscosity, wet
chemistry techniques, specific gravity, and TOC as directed by the
supervisor

Maintain up-to-date documentation. Enter all raw data directly into the
notebook and promptly calculate all test results.

Peer review notebooks and test results generated by other QC team members.

Critically evaluate and interpret experimental data. Immediately inform
supervisor of issues and assist in the resolution of complex problems.

Maintain laboratory equipment and instrumentation in good working order,
following appropriate procedures for usage, clean-up and maintenance.

Maintain and follow all laboratory systems, GMPS, safety, and housekeeping
requirements.

Prepare and review SOPs, as required.

Perform Quality Inspection functions, assist with water sampling and
monitoring.

Support sampling and testing for cleaning validation, process validation,
and method validation as required.

Keep supervisor informed of all key quality findings and issues.

Assume other activities and responsibilities from time to time as directed.



*Qualifications:*



Education: Bachelor's degree in Chemistry, Engineering or other Physical
Sciences

Minimum 2-5 years of experience in medical device and/or pharmaceutical QA
or QC role

Working knowledge in the quality systems for the medical device and/or
pharmaceutical industry

Working knowledge in FDA 21 CFR Parts 11, 210, 211, and 820 and ICH quality
system requirements

Ability to work collaboratively in a professional and effective manner
across all company departments

Experience in using computer programs (MS Word, Excel, and Access)

Strong verbal and written communication skills



*PHYSICAL DEMANDS:*



While performing the duties of this job, the employee is regularly required
to stand. The employee is frequently required to walk; sit; use hands;
talk; and hear. The employee is occasionally required to reach with hands
and arms; climb or balance; stoop; kneel; crouch. The employee must
occasionally lift and or move up to 25 pounds. Specific vision abilities
required by this job include close vision, distance vision, and color
vision.

The physical demands described here are representative of those that must
be met by an employee to successfully perform the essential functions of
this job. Reasonable accommodations may be made to enable individuals with
disabilities to perform the essential functions.

This job description is not all-inclusive. It acts as a guideline and is
subject to change over time. Additional duties may be assigned based on
business needs

--------------------------------------------------------------------------------

Thanks & Regards.

Syed Faheem | Technical Recruiter

[image: http://www.mirthconsulting.net/assets/images/mirth2.png]

6353 N  Claremont Ave Chicago, IL. 60659

Direct: 312-872-9208, 312-428-5615.

fah...@mirthconsulting.net|
<fah...@mirthconsulting.net%7C%20%20www.mirthconsulting.net%7C>

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