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At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
for a Validation Engineer I involve validation equipment operation, protocol development, protocol execution and associated activities.
This position will support a wide range of validation activities, including laboratory and manufacturing equipment of all types, laboratory and manufacturing technical support services, facilities/utilities, computerized systems, and data integrity assessment/remediation.
The Validation Engineer I works with supervision to gain experience with more experienced staff.
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The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee will regularly stand, walk, and use hands, frequently reach, stoop, kneel, crouch or crawl and talk or hear, and occasionally sit and climb or balance.
In this role, you will frequently work in an office, lab or at customer sites and be exposed to extreme cold (non-weather).
You will occasionally be exposed to wet or humid conditions, work near moving mechanical parts, work in high places, near toxic or caustic chemicals, in outdoor weather conditions and exposure to vibration.
The noise level that is typical for this position is loud.
US-based CDMO serving pharmaceutical and biotechnology companies with laboratory, drug manufacturing, packaging, and cGMP storage services.
Visit company websiteJobs and hiring trendsUSD 32-38 hourly
Full-time
Entry
Onsite
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