Senior Validation Engineer

Who We Are

Since 1990, weve grown into a global leader in personalized medicine.

Today, our +5,000 energetic employees are based in +80 locations in Europe, North America, South America, Africa and Asia-Pacificand are working together to support over 200,000 customers worldwide.

From compounding and natural products to software, equipment, and genomics we deliver smart, ready-to-use solutions that make healthcare better.

We're passionate, science-driven, and always looking for new ways to improve lives.

The successful candidate will have experience validating manufacturing equipment and PLC and Computer-Based control systems.

Perform and document instrument calibration and validation activities on a variety of pharmaceutical manufacturing equipment and troubleshooting and repair and, process validation i.e., media fills and stability studies.

• [Prepare, execute and summarize validation protocols and reports.
• [Proficiency with the Kaye AVS Validator (Programming, Operating, Setup etc.).
• [Able to read and understand equipment PI&Ds, Electrical, Pneumatic and arrangement drawings.]
• [Working knowledge of PC and PLC base control systems software and hardware.]
• [Working knowledge of FDA and cGMP guidelines as related to CVQ.]
• [Experience validating and qualifying, but not limited to Utilities, Distillate Systems, Syringe, Vial and Eye Dropper Filling Machines, Autoclaves, Glassware and Vial Washers, Stability Chambers Drug Product Storage and Clean rooms.]
• [Experience with PV and Stability studies.]
• [Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.]
• [Uses rigorous and logic and methods to solve difficult problems with effective solutions.]
• [Maintains a conscious balance between work and personal life as to not allow one to dominate the other.]

• [BS degree in Mechanical, Industrial, Automation, or Chemical Engineering. and/or equivalent experience in pharmaceutical related discipline.]
• [3 to 5 years experiences in metrology and validation of pharmaceutical manufacturing equipment.]
• [Experience participating in regulatory inspections and explaining/defending work.]
• [General knowledge of the injectable pharmaceutical industry, sterile compounding preferred.]
• [Experience working in cGMP environments meeting FDA, EMA, ICH guidelines, local regulations, and industry best practices.]
• [Working knowledge of applicable GMP regulations, particularly 21 CFR Part 11, Eudralex Volume 4 Annex 11, and current FDA/MHRA guidance on Data Integrity.]
• [Experience with aspects of pharmaceutical GMP regulations (e.g. quality systems, root cause analysis).]
• [Knowledge of GMP including international regulations.]
• [Knowledge of applicable parts of 21 CFR Part 210, and 211 regulations and guidance.]
• [Ability to handle multiple and changing priorities and tight deadlines while remaining detail-oriented.]
• [Good verbal and written communication skills.]