Validation Engineer

Kindeva Drug Delivery; St. Louis (MO); On-site; USD 80,000 - 130,000; Full time

Job summary

Kindeva Drug Delivery seeks a Validation Engineer to enhance product safety and efficacy through rigorous validation of processing equipment. The ideal candidate will have a strong scientific background, practical experience in validation practices, and a commitment to maintaining high compliance standards in pharmaceutical manufacturing.

Qualifications

• 3+ years related validation experience and/or training.
• Must be able to read and analyze scientific documents.

Responsibilities

• Responsible for protocol execution of basic processing equipment.
• Assist with validation activities performed by outside validation companies.
• Help determine process capability of new equipment.

Skills

Knowledge of cGMP

Analytical skills

Attention to detail

Education

BS in Chemistry, Biochemistry, Microbiology, Engineering, Pharmacy or related science

Tools

Pharmaceutical processing equipment

Labeling/packaging equipment

Job description

Join to apply for the Validation Engineer role at Kindeva Drug Delivery

3 days ago Be among the first 25 applicants

Join to apply for the Validation Engineer role at Kindeva Drug Delivery

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

The Validation Engineer will assist in the development of inspection, assembly and packaging product manufacturing equipment qualification/validation, process validation protocols, and performs testing. The engineer generates validation protocols using templates and is responsible for protocol execution of various types of basic processing equipment under the direction of Validation Manager.

Role Responsibilities

• Responsible for protocol execution of basic processing equipment including (but not limited to) the following: Manufacturing Facilities, Inspection Equipment, Assembly Equipment, Packaging Equipment and Refrigerators (cold storge).
• Assist to determine process capability of new equipment through execution of approved protocols and assures defined parameters are incorporated into respective operating procedures and batch records.
• Assist with validation activities performed by outside validation companies; assures that department and company policies are adhered to.
• Assist with the Site Change Management Program to keep all finished products, equipment, processes and facilities in compliance with contemporary industry standards and regulatory filings
  
  

Basic Qualifications

• BS in Chemistry, Biochemistry, Microbiology, Engineering, Pharmacy or related science; or equivalent combination of education and experience.
• 3+ years related validation experience and/or training
  
  

Preferred Qualifications

• Knowledge of cGMP and internal SOPs and general knowledge of associated industry and regulatory guidance documents.
• Sound working knowledge of the operation of various pharmaceutical processing equipment, labeling/packaging equipment and integrated inspection equipment.
• Ability to read, analyze and interpret common scientific and technical journals; comprehend equipment manuals and translate operational limits into protocols acceptance criteria; able to readily identify/report deviations to management in a timely manner.
  
  

California residents should review our Notice for California Employees and Applicants before applying.

Equal Opportunity Employer

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

Apply Now

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

Referrals increase your chances of interviewing at Kindeva Drug Delivery by 2x

Get notified about new Validation Engineer jobs in St Louis, MO.

St Louis, MO $85,000.00-$100,000.00 7 hours ago

St Louis, MO $140,000.00-$150,000.00 4 hours ago

St Louis, MO $84,000.00-$100,000.00 10 hours ago

St Louis, MO $85,000.00-$100,000.00 10 hours ago

St Louis, MO $85,000.00-$100,000.00 9 hours ago

St Louis, MO $80,000.00-$130,000.00 1 week ago

St Louis, MO $84,000.00-$100,000.00 10 hours ago

Flight Test Engineer (Entry-Level, Associate or Mid-Level)

Country Life Acres, MO $27.00-$30.00 5 days ago

Digital Platform Senior Validation Engineer

High Voltage Test Engineer (Connecticut)

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.