Boehringer Ingelheim Posted October 16, 2026

Scientist III, Manufacturing Science & Technology (Gainesville, GA, United States, Georgia)

Gainesville, Georgia, United States Type not listed
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About this opportunity

Description

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 an opportunity for all employees to collaborate internationally, offering visibility and the opportunity to directly contribute to the company's success. We realize that our strength and competitive advantage lie with our people. We support our employees in several 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.

The Scientist III, Manufacturing Science & Technology will support BIAH products, processes and test methods with specialized technical analysis and recommendation throughout product / process life cycle. This role will explore and research new technologies to support future definition of innovative manufacturing platforms. The incumbent will support development and maintenance of technical body of knowledge for BIAH products and processes. This role will execute independent technical deliverables and appropriately sized technical projects as Project Leader or Project Contributor.

Duties & Responsibilities

Supports BIAH products and processes with specialized technical analysis and recommendation throughout product / process lifecycle:

Evaluates & approves minor/moderate change requests autonomously; assesses major change requests and provide recommendation for expert approval.

Analyzes process / product data and prepares reports in support of Technical Expert.

Provides troubleshooting, root cause analysis and scientific guidance in support of other scientists and experts for technical transfer, manufacturing deviations, validations, analytical tests, etc.

Provides technical input and support for questions received from Regulatory Authorities in various regulatory processes, e.g. geographical expansion of existing products, post approval changes on existing registrations.

Develops technical solutions for process optimization/ improvement of analytical test methods with possible impact on cost of goods.

Explores and researches new technologies to support future definition of innovative manufacturing platforms:

Researches and analyzes existing BIAH technologies to support definition of Technology Standards.

Researches, assesses, and trends internal / external data sources to support Expert Position Papers.

Investigates and assesses new technologies for potential use in existing or new manufacturing processes or quality control test methods; execute process/materials/methods improvements.

Assists other scientists and experts in developing future-oriented Technology Platforms.

Supports development and maintenance of technical body of knowledge for BIAH products, processes and test methods:

Continually develops and maintains an appropriate individual level of theoretical and practical expertise to respond to the needs of BIAH.

Facilitates exchange of Technology expertise across global, network and local MSAT teams.

Captures and maintains ongoing product / process knowledge within global, network and local MSAT teams.

Guides lower-level scientists during project execution, if applicable.

Executes independent technical deliverables and appropriately sized technical projects as Project Leader or Project Contributor:

Provides ad hoc support to Global Supply Lead in New Product Development CMC Development sub-team; if applicable, represents Global Supply/MSAT function in cross-functional teams such as development teams or project teams by actively participating, escalating concerns and inform MSAT management about progress and challenges.

Responsible for technical assessment of user requirements, product or process changes.

Develops, structures, and leads cross-functional streams / projects aligned with project management methodology.

Proposes and manages scope, budget, schedule, and associated risks to deliver fully functional deliverables / projects meeting Customer requirements.

Ensures compliance to regulatory requirements and BI / external standards (EHS, VICH, Corporate procedures, GxP etc.)

Establishes & maintains communication tools (e.g. project charter, monthly reports) to effectively communicate with all relevant stakeholders.

Ensures and measures customer satisfaction along the project lifecycle.

Requirements

Master’s degree required in scientific discipline (Pharmacy, Chemistry, Biochemistry, Biological sciences preferred) with a minimum of three (3) years direct industry experience.

OR

Bachelor's degree required in scientific discipline (Pharmacy, Chemistry, Biochemistry, Biological sciences preferred) with a minimum of six (6) years direct industry experience.

Additional qualification in Business (Supply Chain, Economics) preferred.

Professional Certification in Scientific field or Project Management preferred.

Expertise in novel technologies or sciences is an advantage.

Intense willingness to develop technical expertise at bench and production scale.

Fluency in English required – additional language skills are an asset.

Willingness to travel domestically and internationally.

Strong interest for international/intercultural collaboration.

Training and experience in Agile Management preferred.

Ability to adapt communications and truly engage with diverse audience.

Proven specialized/depth of knowledge in identified discipline.

Eligibility Requirements :

Must be legally authorized to work in the United States without restriction.

Must be willing to take a drug test and post-offer physical (if required).

Must be 18 years of age or older.

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Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Gainesville, Georgia, United States
Employment type
Not listed

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.

3753Comparable roles tracked
3373Currently active
173Companies hiring similar roles
64Countries represented

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.

This roleSubject Not listed on this posting
Lowest disclosed · Biologics Support Operator I (3rd Shift) · AbbVie $14/hr – $26/hr (≈ $29,099–$54,122/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $41,610 – $381,150 (median $125,550)

Where these roles are based

Top locations among the 3753 comparable roles

United States1738
Germany251
India166
France146
Ireland137
China123

+ 58 more countries

Seniority mix

1670 of 3753 peers have a known seniority level

Senior431
Manager381
Intern/Fellow/Postdoc259
Associate162
Principal138
Associate Director119
Director115
Senior Director57
Executive/VP8

Therapeutic area mix

24 of 3753 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease15
Rare Disease3
Oncology3
Respiratory1
Dermatology & Aesthetics1
Immunology1

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

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.

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