Specialist, Technical Production M-F 8:00pm -4:30am (Athens, GA, United States, Georgia)
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Description
To perform support/process duties associated with the continuous manufacture of Boehringer Ingelheim vaccines, will perform and coordinate with other groups and lead the activities associated with the preparation of active ingredient vaccine and components(cells and medias)requirements.
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Duties & Responsibilities
Plans, executes and evaluate outcomes of Production protocols/experiments for new product transfers and productivity improvements. Full participation of direct and indirect tasks as required.
Oversee and ensure training and qualification of team members.
Review in process documentation for accuracy and compliance in a timely manner; maintenance of technical data sheets and support documentation.
Initiate and facilitate root cause analysis and implement corrective and preventative actions to address problems; escalation of production flow disturbances to Team or Group Leader.
Demonstrate a visible and tangible commitment to EHS (Environment, Health, and Safety) programs and initiatives.
Provide feedback of individual and team performance in Production.
Participate and provide support to site projects and initiatives.
Requirements
High School Diploma or equivalent plus minimum three-five (3-5) years in related field.
Preferred Biology Degree or Science Degree or in a related field from an accredited institution, plus three-four (3-4) years of experience in related field.
Basic math skills.
Technical writing and equipment/automation trouble shooting skills.
Proficient with Microsoft Office and other database software systems.
Excellent oral and written communication skills.
Demonstrated, strong organizational and time management skills with exceptional attention to detail.
Clean room and aseptic technique knowledge.
Working knowledge of GMP and USDA requirements for Vaccine Manufacturing.
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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 3753 comparable Manufacturing & CMC roles across 173 biopharma companies.
Salary context
921 of 3753 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 3753 comparable roles
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Seniority mix
1670 of 3753 peers have a known seniority level
Therapeutic area mix
24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.