GMP Engineer

Indianapolis, Indiana

Katalyst Healthcares & Life Sciences
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Responsibilities:

Plan and execute commissioning activities for new equipment or systems.

Develop protocols and test plans for IQ, OQ, and PQ.

Ensure correct installation and performance of equipment/systems.

Maintain detailed records of commissioning and qualification activities.

Generate comprehensive qualification reports in compliance with regulatory requirements.

Stay updated on industry regulations (FDA, GMP, GAMP) and ensure compliance.

Implement and maintain validation procedures per regulatory guidelines.

Work closely with cross-functional teams, engineers, and regulatory affairs personnel.

Collaborate with vendors to ensure equipment meets specifications.

Identify and address issues during the commissioning and qualification process.

Develop and implement corrective and preventive actions (CAPAs).

Perform risk assessments to identify potential issues affecting equipment/system performance.

Mitigate risks through appropriate actions and documentation.

Requirements:

Bachelor's degree in engineering, Science, Business, Management, or related field.

Minimum five (5) years of experience in a commercial/industrial construction environment.

At least five years of related experience (preferred).

Excellent verbal and written communication skills.

Proficiency in Microsoft Office (Excel, Visio, Outlook, Word, etc.).

Strong understanding of industry regulatory requirements (FDA, GMP, GAMP).

Experience with commissioning and qualification processes.

Proficiency in generating and maintaining documentation.

Strong problem-solving and troubleshooting skills.

Effective communication and interpersonal skills.

Attention to detail and commitment to quality.

Ability to work in a team and independently.

Date Posted: 13 May 2024
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