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Lead Validation Eng at Keenova Therapeutics and Par Health - ApplyBlast

Lead Validation Eng

Keenova Therapeutics and Par Health

6 months ago

3.4 on Glassdoor

St. Louis, MO

Onsite

Full Time

Senior

0 applicants

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About this role

The Lead Validation Engineer ensures product quality and regulatory compliance by managing validation activities for equipment, processes, and software systems. They collaborate across departments to develop and review validation protocols and ensure data integrity across manufacturing and laboratory environments.

Skills

Qualifications

Bachelor’s degree in science/engineering10 years' experience in pharmaceutical validationKnowledge of GxP, GAMP5, Part 11, Data IntegrityUnderstanding of ICH Q7, Q9, Q11

About Keenova Therapeutics and Par Health

mallinckrodt.com

Headquarters

Dublin, Dublin, Ireland

Company Size

1001-5000 employees

Founded

1867

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Keenova Therapeutics and Par Health are the successor entities formed after Mallinckrodt's merger with Endo; Keenova Therapeutics focuses on specialty therapeutics across rare and unaddressed conditions (immunology, urology, hepatology, ophthalmology, orthopedics, critical care), while Par Health develops high-quality generics, sterile injectables, and active pharmaceutical ingredients (APIs) with a robust U.S.-advantaged manufacturing network.