Senior Validation Engineer

LAPORTE L.C.C.; King of Prussia (Montgomery County); Hybrid; USD 90,000 - 130,000; Full time

Job summary

A leading consulting engineering firm is looking for a Senior Validation Engineer to manage validation projects in the pharmaceutical sector. The role involves developing validation strategies, overseeing documentation, and conducting risk assessments, requiring significant industry experience and a degree in engineering. Join a supportive team focused on professional growth and flexibility in a hybrid work environment.

Benefits

Competitive salary

Comprehensive benefits

PTO

Qualifications

• 10 years direct work experience in GMP/pharmaceutical environment.
• Experience in writing and executing equipment qualification documents (IQ/OQ/PQ).
• Familiarity with Current Good Manufacturing Practices.

Responsibilities

• Develop validation plans outlining strategy, scope, and timelines.
• Oversee validation protocols and documentation management.
• Conduct risk assessments and develop mitigation strategies.

Skills

Attention to Detail

Communication Skills

Flexibility

Education

S. degree in engineering field

Tools

Computerized Systems Validation

ISPE GAMP5

Job description

Validation Engineer (Senior, 10 year's of experience)

Full-time, hybrid, some travel required. Must be within reasonable distance to King of Prussia, PA.

We’re seeking a full-time process & validation engineer to join our expanding team and contribute to the validation and management of projects in the pharmaceutical, biopharmaceutical, and medical device manufacturing areas. LAPORTE is a consulting engineering firm which has been in business for 25 years. Today, the company has 25 offices across North America and Europe, and over 480 employees with a passion for engineering.

Join us for a competitive salary, compensatory PTO, comprehensive benefits, and a supportive work environment that emphasizes professional growth. We believe in a flexible working environment that values work-life balance while encouraging efficiency and creativity on a daily basis.

The Process and Validation Engineer will

• Carry out all aspects of a validation project for our Biopharmaceutical clients including: authoring and/or executing Validation Master Plan (VMP), User Requirements Specifications (URS), Risk Assessments (RA), Design Qualification (DQ), Factory Acceptance Test (FAT), Site Acceptance Test (SAT), Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Process Validation (PV) protocols/reports in accordance with corporate and departmental procedures.

Responsibilities to include:

• Validation Planning: Develop validation master plans outlining the validation strategy, scope, and timelines for the project.
• Documentation Management: Oversee the creation, review, and approval of validation protocols, reports, and other documentation required for validation activities.
• Risk Assessment: Conduct risk assessments to identify potential validation issues and develop mitigation strategies to address them.
• Protocol Execution: Oversee the execution of validation protocols, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for equipment and systems within the QC building.
• Commissioning Support: Collaborate with the commissioning team to ensure a seamless transition from construction to operation, verifying that systems and equipment are installed correctly and function as intended.
• Standard Operating Procedure: Provide technical input with respect to Standard Operating Procedures (SOP) development. Revise or develop SOPs in compliance with industry standards and cGMP.
• Participate on cross-functional teams to assist with Out of Specification (OOS), Deviation investigation, CAPA and Change Controls write-up.
• Perform Periodic Review for various validated systems including computerized systems, laboratory equipment, manufacturing equipment, infrastructure systems. Analyze information, draw the right conclusions based upon technical knowledge of the systems, and work effectively with different groups across site to determine status, gaps and corrective actions.
• Maintain up-to-date knowledge of validation requirements, practices, and procedures and coach other members of the team participating in validation activities.

Qualifications:

• S. degree in engineering field or relevant equivalent
• Prior experience writing and executing equipment qualification documents (IQ/OQ/PQ) required.
• Minimum 10 years of direct work experience in a GMP/pharmaceutical environment within the US, writing and executing commissioning and validation.
• Excellent knowledge of the Current Good Manufacturing Practices.
• Ability to work in a team environment with excellent communication skills.
• Ability to demonstrate a sense of urgency, flexibility and accountability.
• Flexibility to travel to the client site on a frequent basis.
• Meticulous attention to detail.
• Experience in working in cleanrooms and familiar with gowning requirements.
• Prior experience performing GxP risk assessments such as Functional Risk Assessments (FRA) or Failure Mode and Effect Analysis (FMEA)
• Experience in Aseptic Processing
• Familiarity with current industry standards for facilities, utilities, and equipment qualification.
• Familiarity withComputerized Systems Validation and ISPE GAMP5 and 21 CFR Part 11.
• Ability to exercise independent judgment in methods, techniques and evaluation criteria for obtaining results.

Send us your application today. We look forward to meeting you!

The LAPORTE team

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