Company:
MEDVACON
Location: Kansas City
Closing Date: 23/10/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Company Description
MEDVACON Life Sciences works with leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.
Our focus is providing consulting and talent acquisition services for cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.
Job Description
Validation representative for laboratory validation activities, including Equipment Qualification and systems administration. In addition, provide technical guidance as a SME with respect to validation/process deviations and change controls as pertains to validation impact.
This is on W2 only
No expenses
ONSITE
SHIFT - M-F 8-4PM -DURATION
1 YEAR WITH OPTION TO EXTEND
Qualifications
Bachelors in related Field or 2-10 years of Scientific or Engineering experience
3+ years work exp in project/process engineering and validation of FDA-covered processes, as well as QA experience in a pharmaceutical environment.
Additional Information
Please attach a WORD resume to your submission
All of your information will be kept confidential according to EEO guidelines.
ON-SITE only
This is a contract role and does not offer benfits
40-hour week
1 YEAR WITH OPTION TO EXTEND -
MEDVACON Life Sciences works with leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.
Our focus is providing consulting and talent acquisition services for cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.
Job Description
Validation representative for laboratory validation activities, including Equipment Qualification and systems administration. In addition, provide technical guidance as a SME with respect to validation/process deviations and change controls as pertains to validation impact.
This is on W2 only
No expenses
ONSITE
SHIFT - M-F 8-4PM -DURATION
1 YEAR WITH OPTION TO EXTEND
Qualifications
Bachelors in related Field or 2-10 years of Scientific or Engineering experience
3+ years work exp in project/process engineering and validation of FDA-covered processes, as well as QA experience in a pharmaceutical environment.
Additional Information
Please attach a WORD resume to your submission
All of your information will be kept confidential according to EEO guidelines.
ON-SITE only
This is a contract role and does not offer benfits
40-hour week
1 YEAR WITH OPTION TO EXTEND -
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MEDVACON