POSITIONS:
(Click on title to view job description)
CURRENT OPENINGS:
More positions coming soon
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| VTI is growing, and we require
experienced validation professionals for our various Offices.
We are one of America's leading Validation companies. Join
us and work in a friendly environment. We offer some of
the best salary and benefit packages in the industry.
If you are interested in a career opportunity with VTI
please submit a resume. |
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Our Employment Opportunity:
Validation Technologies strives to employ skilled professionals
who will significantly contribute to the success of our company.
Validation Technologies Benefits:
- Health insurance
- Dental Insurance
- Bonus Program
- Life Insurance
- Short Term Disability
- Long Term Disability
- 401K Plan
E-Mail to validation@validation.org
or fax at (858) 638-5532
VALIDATION SPECIALIST /
ENGINEER:
(Northern California - Bay Area)
Description:
Validation Technologies, Inc. is currently seeking Validation
Specialists / Engineers to work a variety of Bay Area projects.
This person will participate in validation and GMP compliance
activities for our clients within FDA regulated industries
including pharmaceutical, biotechnology, medical device, and
medical diagnostic.
Validation Specialists / Engineers will be responsible for
the development, execution, and final reporting for equipment
and utility IQ, OQ, PQ protocols. Other responsibilities include
maintaining direct communication with Project Managers and
clients to ensure that validation plans are properly implemented
in compliance with corporate and federal policies and procedures.
Requirements:
- Bachelor's or Master's degree in Engineering, Chemistry,
Life Science or related subject with 3+ years of experience
in either of the following industries biopharm, medical
device and pharmaceutical
- A thorough understanding of the GMP regulatory environment,
validation, and associated subjects
- An ability to work independently and follow instructions
- Excellent verbal and written communication skills
- Understand of critical Utility Qualification
- Proficiency in Windows and Microsoft Office applications
- Knowledge of Kaye(c) Validator / thermal validations a
plus
- Knowledge of cleaning and process validation a plus
E-Mail to validation@validation.org
or fax at (858) 638-5532
Sr. Validation Specialist
/ Engineer - U.S.
Description:
Develop & execute computer validation plans for pharmaceutical,
medical device and biotechnology industries regulated by FDA,
w/emphasis on system definition, requirements, specification
& traceability matrix for validation protocol design &
execution. Engage in regulatory compliance activities, include
inventory assessment, compliance audits, designing appropriate
remediation plans. br> Bachelor’s degree, or foreign
equivalent, in Biotechnology, Chemical Engineering, or Computer
Science plus 2 yrs of work exp in job offered. Interview/Work
Site: San Diego, CA, with extensive travel throughout North
America. Proof of authorization to work in the US required
if hired. Send this ad and your resume to Validation Technologies
Inc. 6540 Lusk Blvd., Suite C270, San Diego, CA 92121.
Requirements:
- Bachelor's degree in Engineering, Chemistry, Life Science
or related subject with 2+ years of experience in either
of the following industries biopharm, medical device and
pharmaceutical
- A thorough understanding of the GMP regulatory environment,
validation, and associated subjects
- An ability to work independently and follow instructions
- Excellent verbal and written communication skills
- Understand of critical Utility Qualification
- Proficiency in Windows and Microsoft Office applications
E-Mail to validation@validation.org
or fax at (858) 638-5532
VALIDATION SPECIALIST
/ ENGINEER:
(Canada - Toronto Area)
Description:
Validation Technologies, Inc. is currently seeking Validation
Specialists / Engineers to work a variety of Toronto Area
projects. This person will participate in validation and GMP
compliance activities for our clients within FDA regulated
industries including pharmaceutical, biotechnology, medical
device, and medical diagnostic.
Validation Specialists / Engineers will be responsible for
the development, execution, and final reporting for equipment
and utility IQ, OQ, PQ protocols. Other responsibilities include
maintaining direct communication with Project Managers and
clients to ensure that validation plans are properly implemented
in compliance with corporate and federal policies and procedures.
Some travel maybe required within Canada and U.S.
Requirements:
- Bachelor's or Master's degree in Engineering, Chemistry,
Life Science or related subject with 3+ years of experience
in either of the following industries biopharm, medical
device and pharmaceutical
- A thorough understanding of the GMP regulatory environment,
validation, and associated subjects
- An ability to work independently and follow instructions
- Excellent verbal and written communication skills
- Understand of critical Utility Qualification
- Proficiency in Windows and Microsoft Office applications
- Knowledge of Kaye(c) Validator / thermal validations a
plus
- Knowledge of cleaning and process validation a plus
E-Mail to validation@validation.org
or fax at (858) 638-5532
COMPUTER SYSTEM
VALIDATION SPECIALIST(Canada and U.S.)
Description:
Validation Tecnologies, Inc. is currently seeking Computer
System Validation Specialists in Canada and the U.S. to work
a variety of projects. This person will participate in computer
validation and 21 CFR Part 11 compliance activities for our
clients within FDA regulated industries including pharmaceutical,
biotechnology, medical device, and medical diagnostic.
Computer System Validation Specialists must have expertise
in computer validation, 21 CFR Part 11 assessments and remediation
planning and the software development lifecycle approach.
Responsibilities may include performing 21 CFR Part 11 assessment
and remediation planning, compliance audits, commissioning,
and development, execution, and final reporting on computerized
systems.
Preference will be given to individuals who have strength
in any combination of the following systems and areas: PLCs,
SCADA, Oracle, DCS, Millennium, SAP, Oracle, ERP/MRP, LIMS
systems, Laboratory Instrumentation, Document Management,
and other healthcare computer systems. Some travel maybe required
within Canada and U.S.
Requirements:
- Bachelor's or Master's degree in IT or Computer Science
related subject, or equivalent work experience
- Knowledge of FDA regulations and their impact on computerized
systems validations
- An ability to work independently and follow instructions
- Excellent verbal and written communication skills
- Expertise in 21 CFR Part 11 assessments and remediation
planning, and the software lifecycle approach
- Proficiency in Windows and Microsoft Office applications
- A thorough understanding of the GMP regulatory environment
and computer validation
- Expertise in 21 CFR Part 11 assessments and remediation
planning, and the software lifecycle approach
E-Mail to validation@validation.org
or fax at (858) 638-5532
PHARMACUETICAL VALIDATION
PROJECT MANAGER(Europe and U.S.)
Description:
Validation Tecnologies, Inc. is currently seeking Pharmaceutical
Validation Project Manager to manage multiple projects at
facilities through out the US and Europe. Minimum requirements:
B.S. degree in chemical engineering or biotechnology field,
ten years experiences in pharmaceutical/biotechnology/Chemicals
validation, including common validation, validation of computerized
systems, validation project management, and dealing with both
US and European pharmaceutical regulatory agencies.
Preference will be given to individuals who have strength
in any combination of the following systems and areas: PLCs,
SCADA, Oracle, DCS, Millennium, SAP, Oracle, ERP/MRP, LIMS
systems, Laboratory Instrumentation, Proces Validation Equipment
and Instrumentation Qualification, Document Management, and
other healthcare computer systems. Some travel maybe required
within Europe and U.S.
Requirements:
Requirements:
- Minimum requirements: B.S. degree in chemical engineering
or biotechnology field
- Knowledge of FDA regulations and their impact on computerized
systems validations
- An ability to work independently and follow instructions
- Excellent verbal and written communication skills
- Expertise in 21 CFR Part 11 assessments and remediation
planning, and the software lifecycle approach
- Proficiency in Windows and Microsoft Office applications
- A thorough understanding of the GMP regulatory environment
and computer validation
- Must understand U.S. and Europe Regulations
- Must have project management experience and be able to
manage staff.
E-Mail to validation@validation.org
or fax at (858) 638-5532
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