Sr. Validation Specialist

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Job ID:

774

Location:

Greenville, SC 

Category:

Manufacturing, Pharmaceutical, Science

Salary:

47,000-55,000 per hour
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Job Views:

8592

Zip Code:

29605

Employment Type:

Full time

Posted:

03.16.2017
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Job Description:

CRS is seeking qualified candidates for a Sr. Validation Specialist position available in the Greenville area. This position is direct hire with a thriving manufacturing company.

Major Responsibilities Include:
-Develop process design reports, validation master plans, and process performance qualifications protocols.
-Execute protocols for process qualifications, installation and qualification of equipment, and processes in the facility.

Pay:
Salary ranges from $47,000-$55,000, depending on experience and qualifications.

Work Schedule:
Generally Monday-Thursday from 7am-3:30pm. Must be able to work other shifts as needed.

Next Steps:

Apply online now and visit CRS to speak to a recruiter Monday-Friday from 8am-11am/1pm-4pm at:

128 White Horse Court
Greenville, SC 29605

Call 864-277-1163 for more info.

Job Requirements:

Requirements:
-Engineering, chemistry, or other science related college degree.
-Validation experience including cleaning, process performance, etc.
-Technical writing ability.
-Experience in a pharmaceutical or other cGMP related setting is strongly preferred.
Company Info
Contingent Resource Solutions (CRS) 337 Spartangreen Blvd.
Duncan, United States

Phone: 8284896923
Web Site: www.crshireright.com

Company Profile




Company Info


Contingent Resource Solutions (CRS)
337 Spartangreen Blvd.
Duncan, United States
Phone: 8284896923
Web Site: www.crshireright.com

Sr. Validation Specialist

col-narrow-left   

Job ID:

774

Location:

Greenville, SC 

Category:

Manufacturing, Pharmaceutical, Science

Salary:

47,000-55,000 per hour
col-narrow-right   

Job Views:

8592

Zip Code:

29605

Employment Type:

Full time

Posted:

03.16.2017
col-wide   

Job Description:

CRS is seeking qualified candidates for a Sr. Validation Specialist position available in the Greenville area. This position is direct hire with a thriving manufacturing company.

Major Responsibilities Include:
-Develop process design reports, validation master plans, and process performance qualifications protocols.
-Execute protocols for process qualifications, installation and qualification of equipment, and processes in the facility.

Pay:
Salary ranges from $47,000-$55,000, depending on experience and qualifications.

Work Schedule:
Generally Monday-Thursday from 7am-3:30pm. Must be able to work other shifts as needed.

Next Steps:

Apply online now and visit CRS to speak to a recruiter Monday-Friday from 8am-11am/1pm-4pm at:

128 White Horse Court
Greenville, SC 29605

Call 864-277-1163 for more info.

Job Requirements:

Requirements:
-Engineering, chemistry, or other science related college degree.
-Validation experience including cleaning, process performance, etc.
-Technical writing ability.
-Experience in a pharmaceutical or other cGMP related setting is strongly preferred.