Are you a talented Validation Engineer seeking new opportunities in the US? Join Validation Associates LLC, a specialist pharmaceutical recruitment & staffing consultancy, focused on providing expert services in the life sciences industry.
Responsibilities:
- Perform equipment qualification, process validation, and cleaning validation activities.
- Develop and execute validation protocols, including IQ/OQ/PQ.
- Conduct risk assessments, root cause analysis, and failure mode effects analysis (FMEA).
- Collaborate with cross-functional teams to ensure compliance with regulatory standards.
- Maintain accurate documentation and reports related to validation activities.
- Stay updated on industry regulations and guidelines.
Requirements:
- Bachelors or Master's degree in Engineering, Life Sciences, or related field.
- Previous experience in validation activities within the pharmaceutical or medical device industry.
- Familiarity with regulatory guidelines, including FDA regulations and 21 CFR Part 11.
- Strong problem-solving and analytical skills.
- Knowledge of GMP, GDP, and quality systems.
- Proficiency in validation software and tools.
- Excellent communication and teamwork abilities.
Benefits:
- Competitive compensation package.
- Exciting opportunities in the life sciences industry.
- Continuous professional development and training programs.
- Collaborative and supportive work environment.
- Career growth and advancement opportunities.
