Job summary
Job post source
This job is directly from Amneal Pharmaceuticals
Job overview
The Associate Validation Engineer at Amneal Pharmaceuticals supports equipment, facility, and utility qualification to ensure compliance with cGMP and quality standards, impacting the company's manufacturing quality assurance.
Responsibilities and impact
The role involves preparing and executing qualification protocols (IQ/OQ/PQ), performing re-qualifications, identifying and mitigating deviations, drafting SOPs, supporting process and cleaning validations, collaborating with vendors and maintenance teams, and assisting with engineering projects.
Compensation and benefits
The position offers a base salary range of $65,000 to $90,000 annually, a short-term incentive bonus within the first year, comprehensive health and insurance benefits, and a significant 401(k) matching contribution.
Experience and skills
Candidates must have a Bachelor's degree in Pharmaceutical manufacturing, Engineering, Science, or a related field, with at least 1 year of experience in Engineering or the Pharmaceutical Industry in a cGMP environment, proficiency in MS Office, and strong technical writing and communication skills.
Work environment and culture
Amneal Pharmaceuticals promotes equal opportunity employment and supports employee well-being with flexible benefits and programs balancing career and life commitments.
Company information
Amneal Pharmaceuticals is a company committed to quality and compliance in pharmaceutical manufacturing, emphasizing equal opportunity and employee well-being.
Company overview
Amneal Pharmaceuticals is a global pharmaceutical company that develops, manufactures, and distributes generic and specialty pharmaceutical products. They generate revenue primarily through the sale of generic medications, which are bioequivalent to branded drugs but offered at lower prices, as well as through their specialty products that address niche therapeutic areas. Founded in 2002 by Chirag and Chintu Patel, the company has grown significantly through strategic acquisitions and partnerships, including the merger with Impax Laboratories in 2018, which expanded their product portfolio and market reach.
How to land this job
Position your resume to highlight your experience in equipment, facility, and utility qualification activities, emphasizing familiarity with IQ/OQ/PQ protocols and cGMP compliance relevant to Amneal Pharmaceuticals.
Focus on showcasing your technical writing skills by including examples of SOP drafting and report generation, as well as your ability to identify and resolve deviations during qualification processes.
Apply through multiple platforms including Amneal Pharmaceuticals' corporate careers page and LinkedIn to maximize your application reach and visibility.
Connect on LinkedIn with current Validation Engineers or team members in the engineering or quality divisions at Amneal Pharmaceuticals; open your message with an interest in their recent projects or ask about their experience working on equipment qualification or cGMP compliance.
Optimize your resume for ATS by incorporating keywords from the job description such as 'Installation Qualification,' 'Operational Qualification,' 'Performance Qualification,' 'cGMP,' 'SOP,' and 'equipment re-qualification' to ensure it passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify the best job posting platforms, and pinpoint relevant LinkedIn contacts, allowing you to focus more on preparing for interviews and networking.
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