Investigation Reviewer
Gurabo, PR, US, United States
Job Description
The
Investigation Reviewer
to support a pharmaceutical manufacturing operations.Review and approve manufacturing investigations for solid and parenteral processes, including deviations, batch failures, and out-of-specification results. Collaborate with cross-functional teams (Production, Quality Control, Engineering, Regulatory Affairs) to gather relevant data and support root cause analysis. Evaluate corrective and preventive actions (CAPAs) for effectiveness and alignment with quality standards. Maintain documentation integrity and ensure timely closure of investigations.
Requirements
Bachelor's degree in Chemistry, Biology, Engineering, or related field. Minimum 5 years of experience in pharmaceutical manufacturing, with direct involvement in solid and parenteral dosage forms. Strong understanding of GMP, FDA, and other regulatory guidelines. Experience with investigation systems. Excellent analytical, writing, and communication skills.
Job Types: Full-time, Contract
Work Location: In person
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Job Detail
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Job IdJD5525271
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationGurabo, PR, US, United States
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EducationNot mentioned