Job summary
Job post source
This job is directly from LFB USA
Job overview
The Validation Lead at LFB USA provides expert technical support in validation and engineering, ensuring compliance with FDA and EU regulations and managing lifecycle validation activities.
Responsibilities and impact
The role involves analyzing instrument and software performance data, authoring and approving reports related to corrective actions, investigations, and validation activities, and designing engineering solutions within LFB's lifecycle program.
Experience and skills
Requires a Master's Degree in Industrial Engineering, Systems Engineering, or related field, with at least two years of validation engineering experience in pharmaceutical or biopharmaceutical industries.
Company information
LFB USA is a company involved in pharmaceutical or biopharmaceutical engineering and validation, complying with regulatory standards.
Team overview
The role is within the Engineering and Validation department, providing subject matter expertise and technical support.
Job location and travel
The position is located at 175 Crossing Boulevard, Suite 420, Framingham, MA 01702 and 87 New Spencer Road, Charlton, MA 01507.
Application process
Applicants must apply through the company's career page at https://lfb.wd3.myworkdayjobs.com/LFB_External_Careers.
Company overview
LFB USA is a biopharmaceutical company that specializes in the development, manufacturing, and commercialization of therapeutic proteins for the treatment of serious and rare diseases. They generate revenue by producing plasma-derived medicinal products and recombinant proteins, which are essential in treating conditions like immunodeficiencies, bleeding disorders, and other critical health issues. The company is a subsidiary of the LFB Group, a French biopharmaceutical firm with a long history of innovation in the healthcare sector. LFB USA is committed to advancing medical research and delivering high-quality treatments to improve patient outcomes.
How to land this job
Position your resume to highlight your expertise in validation and engineering within pharmaceutical or biopharmaceutical settings, emphasizing your knowledge of FDA and EU regulations.
Focus on showcasing your experience with lifecycle management of commissioning, qualification, and validation, especially related to computerized systems, equipment, and laboratory instrumentation.
Apply through multiple channels including LFB USA's official career page and LinkedIn to maximize your application visibility.
Connect with professionals in LFB USA's Engineering and Validation department on LinkedIn; start conversations by asking about recent validation projects or their approach to compliance challenges.
Optimize your resume for ATS by incorporating keywords such as 'validation engineer,' 'FDA compliance,' 'equipment qualification,' 'computerized systems,' and 'engineering lifecycle management' to pass initial screenings.
Use Jennie Johnson's Power Apply feature to automate applying through various platforms, tailor your resume for ATS, and identify relevant LinkedIn contacts, freeing up your time to prepare for interviews and networking.
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