About Dawar Consulting
Sourced by ZipRecruiter
Industry
It services
Company size
11 - 50 Employees
Headquarters location
Newark, CA, US
Year founded
2009
$39 - $42/hr
Full-time
Medical, Dental, Vision, Retirement
Posted 5 days ago
Job description
Our client, a world leader in biotechnology and life sciences, is looking for a “Validation Engineer" based out in Tucson, AZ.
Job Duration: Long Term Contract (Possibility Of Extension & FT Conversion)
Rate: $39-$42/hr on W2
Company Benefits: Medical, Dental, Vision, Paid Sick leave, 401K
Job Summary:
We are seeking a proactive Validation Engineer with 1–3 years of experience in a regulated manufacturing environment such as medical devices, pharmaceuticals, or biotechnology. This on-site role focuses on process validation activities to ensure compliance with FDA, ISO, cGMP, and internal quality standards while supporting continuous improvement and operational excellence.
Key Responsibilities:
- Develop, write, review, and execute process validation and process verification protocols and reports
- Conduct risk assessments and support validation strategies for new and existing manufacturing processes
- Analyze and interpret validation data to ensure compliance with regulatory and internal quality requirements
- Collaborate with Manufacturing, Quality, and Design Transfer teams to resolve validation issues and implement corrective actions
- Support process optimization and continuous improvement initiatives to improve quality and efficiency
- Ensure compliance with FDA, ISO, cGMP, and internal regulatory standards
- Maintain validation documentation, traceability records, and audit-ready files
- Provide training and guidance on validation processes, procedures, and compliance requirements
Required Qualifications:
- Bachelor’s degree in Engineering, Life Sciences, or related field
- 1–3 years of experience in validation within a regulated manufacturing environment
- Knowledge of process validation principles, verification techniques, and industry standards
- Familiarity with FDA regulations, ISO standards, and cGMP requirements
- Strong technical writing, analytical, and problem-solving skills
- Excellent communication and cross-functional collaboration abilities
Preferred Experience:
- Medical device, biotech, or pharmaceutical industry experience
- Experience supporting audits, CAPA activities, and process improvement initiatives
- Familiarity with risk assessments and validation documentation practices
Key Skills:
Process Validation | Process Verification | FDA Compliance | cGMP | ISO Standards | Validation Protocols | Risk Assessments | CAPA | Technical Writing | Root Cause Analysis | Quality Systems | Continuous Improvement | Manufacturing Validation | Regulatory Compliance
If interested, please send us your updated resume at hr@dawarconsulting.com/kavitha@dawarconsulting.com .
dawarconsulting.com
Frequently asked questions
Q: What skills or qualities help someone succeed as a Validation Engineer?
A: To succeed as a Validation Engineer, key technical skills include proficiency in regulatory frameworks such as FDA and ISO 13485, as well as expertise in validation methodologies like risk-based validation and design control. Additionally, strong analytical and problem-solving skills, along with proficiency in programming languages like Python or SQL, are essential for developing and executing validation protocols. Soft skills such as effective communication, attention to detail, and a methodical approach to problem-solving also contribute to success in this role, enabling Validation Engineers to collaborate with cross-functional teams and ensure compliance with regulatory requirements.
Q: What is the career path for a Validation Engineer?
A: A Validation Engineer's career path typically begins with entry-level roles such as Validation Engineer or Junior Validation Specialist, where they gain hands-on experience in designing, implementing, and executing validation protocols for medical devices, pharmaceuticals, or other regulated products. As they progress to mid-level roles like Senior Validation Engineer or Validation Lead, they develop expertise in regulatory compliance, risk management, and team leadership, and may also take on responsibilities such as training and mentoring junior engineers. Senior Validation Engineers or Validation Managers often oversee large-scale validation projects, develop and implement validation strategies, and may also pursue certifications like CQE (Certified Quality Engineer) or CVA (Certified Validation Engineer) to further advance their careers.
