Validation Engineer Entry Level

VALIDATION ASSOCIATES LLC - 4.0

Columbus, GA Job Details Full-time $30 - $33 an hour 1 day ago Benefits Opportunities for advancement Qualifications Pharmaceutical regulatory compliance Good documentation practices (GDP)

FDA 21 CFR

Part 11 GMP Production validation processes Pharmaceutical company experience Quality assurance experience within pharmaceutical industry Biomedical regulatory compliance Full Job Description 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.