Company:Bionique Testing Laboratories LLC
Job Description:Summary:The Manager for Systems and Equipment Validation is responsible for overseeing the qualification or validation lifecycle of computerized systems, equipment, utilities, and related processes to ensure compliance with regulatory requirements (e.g., FDA, EMA, ICH, GAMP, GMP, ISO). This role ensures that validation activities are properly planned, executed, and documented, and that quality standards are maintained throughout the system and equipment lifecycle.
Key Accountabilities and Responsibilities:Validation Oversight:
- Lead and manage qualification or validation strategies for computerized systems (CSV), laboratory information management systems, lab equipment, and utilities.
- Review and approve validation documentation including URS, risk assessments, IQ/OQ/PQ protocols, test scripts, and final reports.
- Ensure adherence to internal SOPs and global regulatory guidelines (e.g., 21 CFR Part 11, Annex 11, GAMP 5).
Quality Assurance (QA) Support:
- Coordinate with QA in cross-functional project teams (e.g., for new system implementations or equipment commissioning) and may represent Bionique's Quality Systems with internal or external stakeholders.
- Participate in change control, deviation investigations, and CAPAs related to validated systems and equipment.
- Provide QA oversight during system lifecycle events such as upgrades, decommissioning, and requalification.
Audit & Compliance:
- Support internal and external audits (regulatory agencies, clients) related to validation and system/equipment compliance.
- Maintain up-to-date knowledge of applicable regulations, standards, and industry best practices.
Team & Stakeholder Collaboration:
- Supervise and coach direct reports including establishing goals, performance management, career development planning, and providing support and guidance on an ongoing basis throughout the employment lifecycle to achieve goals
- Collaborate closely with all internal departments and external vendors to ensure timely and compliant validation activities.
- Train personnel on validation and compliance practices as needed.
Documentation & Metrics:
- Maintain validation master plans (VMP), equipment master lists, and associated quality documentation.
- Monitor and report key performance indicators (KPIs) for validation activities.
Additional duties as assigned
Qualifications:- Bachelor's degree in a scientific, engineering, or related technical discipline (e.g., life sciences, chemistry, engineering).
- 5+ years of relevant experience in quality assurance or validation within a GMP-regulated industry.
- Strong knowledge of validation principles (CSV, equipment, facilities, utilities) and applicable regulatory guidelines.
- Demonstrated experience in authoring and reviewing validation documentation.
- Excellent communication, analytical, and organizational skills.
- Familiarity with quality systems such as LabVantage, ZenQMS, BlueMountain, Veeva, or similar is a plus.
- Certification (e.g., ASQ, ISPE) or training in GAMP, risk-based validation, or data integrity is a strong advantage.
Physical Demands and Work Environment:- Prolonged periods of sitting on a chair, working at a desk, and working on a computer and/or telephone
- Pushing/Pulling/Lifting up to 25 pounds
- Standing/Walking/Mobility: must be able to stand to open files and operate office and laboratory equipment for prolonged periods; mobility to move between offices and colleagues required
- Must successfully pass a pre-employment physical and medical evaluation; specific immunizations may be required
- Must be able to wear required personal protective equipment (PPE)
Compensation:- The base compensation range for this role is between $95,000/yr - $110,000/yr.
