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Genovice Jobs (NOW HIRING)

Genovice

Validation Engineer (Contract)

Indianapolis, IN · Hybrid

$80K - $150K/hr

Overview Our client, an innovative and fast-growing pharmaceutical manufacturing company, is seeking an experienced Equipment Validation Engineer to support validation efforts across its cGMP ...

Genovice

Engineering Project Manager

Indianapolis, IN

$110K - $160K/hr

Engineering Project Manager - CAPEX Location: Indianapolis, IN Duration: 6-month contract Department: Engineering Industry: Pharmaceutical Manufacturing Position Summary Our client is seeking an ...

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Genovice information

What is the difference between Genovice vs Genovice?

AspectGenoviceGenovice
CertificationsTypically requires basic programming or software development certificationsSame certifications often applicable, depending on specific role
Work EnvironmentPrimarily in software development teams, tech companies, or IT departmentsSimilar work environment, focused on coding, testing, and software deployment
Industry UsageCommonly used in tech, software, and IT industriesSame industry usage, often overlapping in job functions
Job Search & ComparisonOften compared with software developer or programmer rolesSimilar roles with slight variations in responsibilities

Genovice and Genovice are closely related roles within the software development field, sharing similar certifications, work environments, and industry usage. They are often compared because of overlapping responsibilities and skills, making them interchangeable in many contexts. Understanding the specific job description can help clarify the differences, but generally, they serve similar functions in tech teams.

What are Genovices?

Genovices are entry-level professionals or trainees who are new to a specific field or industry. They typically undergo training or apprenticeship to gain practical experience and foundational knowledge in their chosen area. Genovices work under the supervision of more experienced staff and gradually take on more responsibilities as they grow in their roles. The term is often used to describe individuals at the beginning of their career journey, learning the essential skills required to advance.

What are the key skills and qualifications needed to thrive as a Genovice, and why are they important?

I'm sorry, but 'Genovice' is not a recognized real-world professional occupation, so I cannot provide a valid response.
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Genovice jobs near you

Validation Engineer (Contract)

Genovice

Indianapolis, IN • Hybrid

$80K - $150K/hr

Full-time

Re-posted 6 days ago

Job description

Overview

Our client, an innovative and fast-growing pharmaceutical manufacturing company, is seeking an experienced Equipment Validation Engineer to support validation efforts across its cGMP manufacturing and laboratory operations. This role offers the opportunity to contribute to high-impact projects in a cutting-edge, regulated environment focused on therapeutic production.

This is a contract role with strong potential for extension. Local candidates are preferred, but hybrid arrangements may be considered for candidates willing to travel on-site to Indianapolis 2–3 days per week.

Key Responsibilities

  • Author, review, and execute IQ/OQ/PQ protocols for a range of GMP manufacturing and laboratory equipment.

  • Support commissioning, qualification, and validation of new and existing equipment including:

    • Cleanroom and HVAC systems

    • Bioprocessing and fill/finish equipment

    • Laboratory instruments

    • Radiation shielding and containment systems

  • Collaborate cross-functionally with Engineering, Quality, Manufacturing, and Regulatory teams to ensure validation activities align with project timelines and compliance standards.

  • Assist with deviation investigations, change controls, and CAPA implementation related to equipment validation.

  • Ensure all validation activities comply with FDA, USP, ICH, and cGMP regulatory requirements.

  • Maintain thorough and audit-ready documentation throughout the validation lifecycle.

Qualifications

  • Bachelor’s degree in Engineering, Life Sciences, or a related technical field.

  • Minimum 3–5 years of hands-on validation experience in the pharmaceutical, biotech, or pharmaceutical industry.

  • Strong working knowledge of equipment qualification (IQ/OQ/PQ) and relevant regulatory guidance.

  • Familiarity with GAMP 5, FDA 21 CFR Part 11, and risk-based validation approaches.

  • Excellent written and verbal communication skills.

  • Ability to work independently, manage priorities, and contribute in a fast-paced environment.

  • Experience in pharma, sterile manufacturing, or working with radioactive materials is a plus but not required.

Details

  • Start Date: ASAP or within 2–3 weeks

  • Duration: 6–12 months, likely to extend

  • Location: Hybrid – Onsite 2–3 days/week in Indianapolis, IN (travel support may be available for non-locals)

  • Compensation: Competitive hourly rate (based on experience)