Validation Engineer

Alliance Biotech Solutions (ABS) is a quality partner providing first in class solutions to the biotech and life sciences industries.

While our offers are limitless, we are focused on providing Engineering, Qualification, and Compliance solutions for our clients.

ABS employees are our product for the industry, and therefore our #1 priority because without them ABS cannot exist. They strengthen us in everything we do.

We recognize their value as contributors (individual and / or teams) for our partners. Encouraging growth and stretching their potential is paramount to success, and achievements for all.

Position Responsibilities

• Interfacing with your project manager (PM) and understanding your scope among projects supporting clients.
• Must be able to work independently or in a team environment, interacting with individuals at all levels in an organization, teams, and departments.
• Familiarity and sound understanding of common Qualification documentation and practices including, but not limited to Standard Operating Procedures (SOP’s), User Requirements Specifications (URS), Risk Assessments (RA), Validation Plans (VP), Requirements Trace matrix (RTM) Data Integrity Assessment (DIA)
• Plan, initiate and implement Change Control activities
• Writing and executing, Installation Operational Qualification (IOQ) and Performance Qualification (PQ) protocols and Summary Reports including thorough resolution of protocol deviations.
• Ability to work on multiple projects simultaneously
• Provides ongoing support for equipment throughout the system lifecycle including revalidation, troubleshooting, and deviation management

Experience

• 2-7 years’ experience performing commissioning, qualification and validation activities in an cGMP manufacturing and / or laboratory environments
• Familiarity with common validation equipment and systems; data loggers and paperless validation systems
• Maintaining an up-to-date knowledge of validation requirements, practices, and procedures including an understanding on GxP, GAMP5, cGMP, CFRs (Part 11, 210, and 211), FDA / EU regulatory requirements and associated guidance documents

Skills and Abilities

Good technical problem-solving and troubleshooting skills

High attention to detail

Great interpersonal and organizational skills.

Ability to multi-task and take initiative to accomplish assigned tasks accurately while taking established deadlines into account

Willing and able to thrive in unusually fast paced and changing environments

Ability to change priorities in response to company demands while continuing to deliver results

Benefits

Industry competitive wage as a full-time employee

Flexible Paid Time Off

Bonus plans

Medical, Dental and Vision Insurance with low employee cost

Employer paid long term and short-term disability

401k plan with employer contributions

Alliance Biotech Solutions is an Equal Employment Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, national origin, ancestry, citizenship status, military status, protected veteran status, religion, creed, physical or mental disability, medical condition, marital status, sex, sexual orientation, gender, gender identity or expression, age, genetic information, or any other basis protected by law, ordinance, or regulation.

Alliance Biotech Solutions does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Alliance Biotech Solutions, and Alliance Biotech Solutions will not be obligated to pay a placement fee.

All persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.