Senior Validation Engineer

INCOG BioPharma Services; Fishers (IN); On-site; USD 80,000 - 130,000; Full time

Job summary

INCOG BioPharma Services is looking for a skilled Senior Validation Engineer to join their Validation Department in Fishers, IN. The role involves executing validation activities in a sterile injectables environment, supporting capital projects, and ensuring compliance with industry standards. Applicants should have a strong background in validation, excellent communication skills, and a degree in a STEM field. This position presents an opportunity to contribute to meaningful projects and work in a collaborative environment focused on technical excellence.

Qualifications

• 5-8 years of experience in Validation or related discipline.
• 4+ years GMP experience required.
• Physically capable of working onsite.

Responsibilities

• Perform Qualification activities on utilities, equipment and laboratory systems.
• Review facility changes and provide input on re-validation and re-qualification of equipment.
• Develop and modify SOPs, WIs, and guidelines for equipment validation.

Skills

Validation expertise

Communication

Analytical skills

Education

Bachelor’s degree or higher in STEM discipline

Job description

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Join to apply for the Senior Validation Engineer role at INCOG BioPharma Services

INCOG BioPharma is seeking a highly motivated Senior Validation Engineer with validation expertise to join our team. The Senior Validation Engineer is a key individual contributor role within the INCOG BioPharma Validation Department. The Senior Validation Engineer is responsible for understanding and implementing validation requirements for a sterile injectables manufacturing facility. The ideal candidate has subject matter expertise and practical experience in qualification and validation.

The Senior Validation Engineer will partner with internal customers to meet the needs of client projects, facility upgrades, capital expansion projects, and laboratory systems. They will possess a demonstrated ability to influence positive outcome without direct reporting authority.Additionally, they must thoroughly understand and be able to adapt to the changing needs of a manufacturing environment.

Essential Job Functions:

• Perform Qualification activities on utilities, equipment and laboratory systems. This includes, but is not limited to, clean utilities, autoclave, washer, filler, laboratory instruments, controlled temperature units, etc.
• Interact with clients to provide validation support including but not limited to, customer product launches, new equipment qualifications.
• Support and provide validation oversight for capital expansion projects/build outs
• Take ownership in the development and modification of Standard Operating Procedures (SOPs), Work Instructions (WIs) and guidelines for equipment validation policies, standards, procedures, and templates
• Review facility changes and provide input on re-validation and re-qualification of equipment
• Assess risks involved in processing steps related to equipment, developing and/or reviewing validation requirements and design deliverables
• Engage in a cross functional team and work closely with other supporting groups including Engineering and Operations to support and monitor validation and process improvement efforts
• Conduct validation qualifications in accordance with all applicable protocols and identify associated protocol excursions.
• Identify industry trends in validation and expectations of regulatory agencies and propose program modifications as appropriate to align with current requirements.
• Special Job Requirements:
• Bachelor’s degree or higher in STEM discipline
• 5-8 years of experience in Validation or related discipline
• 4+ years GMP experience required or other regulated industry
• Physically capable of working onsite
  
  

Additional Preferences:

• Master's degree or higher preferred
• Computer System Validation experiencepreferred
• Cleaning Validation experience preferred
• VHP & Steam Sterilization experience preferred
  
  

Additional info about INCOG BioPharma Services:

At INCOG BioPharma we have built a world-class CDMO for parenteral injectable drugs. Our culture and priorities are different by design: focused on building long-term value for our customers, we are committed to a service-culture mindset, technical excellence, and a collaborative and team-centered approach to doing business.

If you crave the challenge of creating systems from scratch and believe you have insights for a better way of doing business, which benefits customers by ensuring quality outcomes and accelerating their route to market, we want to hear from you. Unless otherwise specified, all positions are based out of our Fishers, IN offices. Please note, we are a smoke-free campus.

INCOG BioPharma is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. All employment decisions at INCOG BioPharma are based on business needs, job requirements and individual qualifications, without regard to race, color, religion or belief, sex (including pregnancy), age, physical disability, sexual orientation, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics.

By submitting your resume and details, you are declaring that the information is correct and accurate.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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