We are looking for a detail-oriented Validation Engineer to join our client based in Philadelphia on a 12 months contract. You will be responsible for ensuring that manufacturing processes, equipment, and systems meet the required standards and regulations.
Key Responsibilities:
- Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and systems.
- Conduct risk assessments and develop mitigation strategies.
- Ensure compliance with regulatory requirements (FDA, EMA, etc.).
- Conducting regular inspections, performing calibrations, identifying areas for improvement, and alerting management of potential issues.
- Collaborate with cross-functional teams to support validation activities.
- Maintain accurate and detailed documentation of validation activities.
- Investigate and resolve validation-related issues.
- Participate in continuous improvement initiatives.
Required Qualifications:
- Bachelor’s degree in Engineering, Life Sciences, or a related field.
- Minimum of 5 years of experience in validation within the pharmaceutical industry.
- Strong knowledge of regulatory requirements and guidelines.
- Strong attention to detail and organizational skills.
Contract:
- 40 hours per week
- Start Date: ASAP
- Contract Length: 12 months
- Philadelphia, PA
- W2 only
