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Summary of Primary Responsibilities:
This position is responsible for managing the Bedford Site’s Validation program that includes start-up, commissioning, qualification, validation and revalidation projects for facility, equipment, critical utility, automation/computer system, cleaning, sterilization, and medical device/drug product manufacturing processes according to current Good Manufacturing Practices (cGMP), ISO requirements, and ICH guidelines. Reporting to the Director of Engineering, this position works internally across the Anika organization to define, administer, and continuously improve the site’s validation programs.
Responsibilities:
Job Complexity:
The job requires the ability to act on problems of diverse and highly technical scope, requiring critical thinking and interaction with internal and external technical professionals.
Implements strategic policies and adheres to budgets, schedules, work plans, and performance requirements. The position exercises broad judgment within generally defined practices and policies and exercises analytical decision-making abilities.
Supervisory Responsibilities:
Manage validation engineering direct reports and vendors, contractors and consultants as required.
Experience, Knowledge, and Skills Required:
Desired Experience, Knowledge, and Skills:
Full Time
$99k-114k (estimate)
05/04/2024
05/20/2024
ATLANTA, GA
<25
2013
FAHMIDA NORRALI
<$5M
Retail
The following is the career advancement route for Validation Manager positions, which can be used as a reference in future career path planning. As a Validation Manager, it can be promoted into senior positions as a Validation Engineer III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Validation Manager. You can explore the career advancement for a Validation Manager below and select your interested title to get hiring information.