Top 56 Eli program representative Jobs

Associate Director, Analytical Development – Small Molecule
Centessa Pharmaceuticals —Boston, MA
- $190,000 - $210,000 a year
- Full-time
- Analysis skills
- Doctor of Philosophy
- Travel
- Wellness program
- Health insurance
Executive Director, Head of Toxicology
Centessa Pharmaceuticals —Boston, MA
- $320,000 - $350,000 a year
- Full-time
- 11+ years
- Doctor of Philosophy
- Travel
- Wellness program
- Health insurance
Senior Associate - LP1 QA
Eli Lilly —Lebanon, IN
- $65,250 - $169,400 a year
- 8 hour shift
- Bachelor of Science
- Engineering
- Mid-level
- Health insurance
- Dental insurance
QA Representative - Warehouse
Eli Lilly —Durham, NC
- $65,250 - $169,400 a year
- 8 hour shift
- Mid-level
- Travel
- Mentoring
- Health insurance
- Dental insurance
6d
Climate Change: Greenhouse Gas Emissions – Fuel Sector Planner (Environmental Planner 4)
State of Washington —Lacey, WA
- $6,384 - $8,583 a month
- Full-time
- Hybrid work
- System design
- Mid-level
- Office
- Paid holidays
- Disability insurance
Associate/Sr. Associate/Manager - Global CMC Regulatory, Regulatory Delivery and Excellence
Eli Lilly —Indianapolis, IN
- $63,000 - $149,600 a year
- Full-time
- Bachelor's degree
- Travel
- US work authorization
- Health insurance
- Dental insurance
9d
Senior Advisor, Manufacturing Science and Technology
Eli Lilly —Watertown, MA
- $141,000 - $228,800 a year
- Full-time
- 7 years
- Office
- Analysis skills
- Health insurance
- Dental insurance
Principal Scientist, Large Molecules Mass Spectrometry
Eli Lilly —Indianapolis, IN
- $65,250 - $193,600 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Mentoring
- Health insurance
- Dental insurance
Post-Doctoral Scientist – Delivery, Devices & Connected Solutions (DDCS) Inhaled Drug Formulation & Aerosol Science
Eli Lilly —Boston, MA
- $58,000 - $123,200 a year
- Full-time
- Doctor of Philosophy
- Mentoring
- US work authorization
- Health insurance
- Dental insurance
9d
Scientist Quality Assurance
Eli Lilly —Durham, NC
- $65,250 - $148,500 a year
- Full-time
- 3 years
- Continuous improvement
- Mentoring
- Health insurance
- Dental insurance
8d
Principal Scientist - Molecular Biology, Cell Culture Upstream Process Development
Eli Lilly —Indianapolis, IN
- $65,250 - $169,400 a year
- Full-time
- Bachelor of Science
- 3 years
- Bachelor's degree
- Health insurance
- Dental insurance
Associate Director - Global Regulatory Affairs - Product Communications
Eli Lilly —Indianapolis, IN
- $132,000 - $193,600 a year
- Full-time
- 3 years
- Bachelor's degree
- US work authorization
- Health insurance
- Dental insurance
12d
Pharmaceutical Sales Representative - Associate Territory Manager, Caridometabolic Health
Eli Lilly —Fargo, ND
- $63,000 - $151,800 a year
- Full-time
- Bilingual
- Clean driving record
- Mid-level
- Health insurance
- Dental insurance
12d
Pharmaceutical Sales Representative - Territory Manager - Dermatology Specialty
Eli Lilly —Spokane, WA
- $87,000 - $159,500 a year
- Full-time
- Clean driving record
- Driver's License
- Bachelor's degree
- Health insurance
- Dental insurance
11d
Associate Director - Computer Systems Validation
Celltrion Branchburg, LLC —Branchburg, NJ
- $135,000 - $180,000 a year
- On call
- 5 years
- Engineering
- Analysis skills
- Paid holidays
- Disability insurance
Quick Apply
10d
Director/Sr. Director/Exec. Director Computational Biophysics, Advanced Molecular Design (AMD)
Eli Lilly —Louisville, CO
- $193,500 - $338,800 a year
- Full-time
- Computer Science
- Office
- Doctor of Philosophy
- Health insurance
- Dental insurance
Climate Change: Greenhouse Gas Emissions – Fuel Sector Planner (Environmental Planner 4)
State of Washington Dept. of Ecology —Lacey, WA
- $76,608 - $102,996 a year
- Full-time
- Hybrid work
- Background check
- Mid-level
- Office
- Paid holidays
- Disability insurance
Senior/Principal Scientist, Bioprocess Purification Development
Eli Lilly —Indianapolis, IN
- $79,500 - $116,600 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- US work authorization
- Health insurance
- Dental insurance
Scientist, Reference Standard Manufacturing - BRD Corporate Reference Standards Organization (CRSO)
Eli Lilly —Indianapolis, IN
- $65,250 - $169,400 a year
- Full-time
- 3 years
- Master's degree
- Analysis skills
- Health insurance
- Dental insurance
Post-Doctoral Scientist, Bioconjugation Process Innovation
Eli Lilly —Indianapolis, IN
- $58,000 - $123,200 a year
- Full-time
- Doctor of Philosophy
- In-person
- Senior level
- Health insurance
- Dental insurance
11d

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Associate Director, Analytical Development – Small Molecule

Centessa Pharmaceuticals
Boston, MA

Apply Now

Job Details

Full-time
$190,000 - $210,000 a year

Benefits

Wellness program
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Vendor relationship building
Dissolution testing
Biotechnology
USP standards
Stability testing
Stability studies in drug product development
High-performance liquid chromatographs
ICH guidelines
Pharmaceutical company experience
Pharmaceutical analysis
Vendor relationship management
Vendor communication
GMP for research safety and compliance
Cross-functional collaboration
Chemical testing
Pharmaceutical research
Cross-functional communication
Moisture analysis for quality control

Full Job Description

Centessa Pharmaceuticals, a wholly subsidiary of Eli Lilly and Company is advancing a portfolio of high conviction programs with strong biological validation. Our asset-centric model offers a unique R&D logic that has been applied by single asset companies to improve productivity. This operating model has minimal centralized infrastructure, reduced hierarchy, and exclusive focus on data driven capital allocation. Our teams are uniquely incentivized to expeditiously interrogate key scientific hypotheses. We believe the asset-centric model can lead to improved success rates for programs with greater speed and modest costs.

Description of Role

Centessa continues to expand its CMC group and currently seeks an Associate Director of Analytical R&D within the CMC group. The successful candidate will have hands-on experience leading the execution of small molecule analytical activities across early to late-stage development. This position will oversee work with various vendors and oversee analytical functions across programs. Comprehensive working knowledge of cGMP and regulatory guidance as they relate to development, testing, characterization, and shelf-life management of biologics is paramount. This position will be accountable for design, execution, and reporting of analytical data at external CDMOs to meet company deliverables and timelines. Travel to vendors both domestically and internationally will be required.

Key Responsibilities

Support analytical development activities related to method development and qualification/validation, product characterization, and comparability assessment for multiple programs
Work in a team environment to manage drug substance and drug product analytical development activities primarily at third-party vendors including analytical method implementation, qualification/validation, and transfer for drug substance and drug product projects
Review method validation protocols, reports, and transfer activities
Review test data for release, stability, and characterization plans for projects
Save and store documentation, generate stability result tables, file stability data and results data
Monitor stability due dates and coordinate data transfer from vendors
Review analytical documents including but not limited to protocols, reports, and procedures
Act as the CMC team analytical representative member in cross functional developmental teams
Contribute to CMC analytical aspects of regulatory filings; review and assemble information for analytical sections in regulatory submission documents (e.g. IND, IMPD, NDA, etc)
Coordinate and execute domestic and international shipments
Serve as a technical expert and aid in analytical investigations and troubleshooting
Assist with batch record review and deviation investigations

Qualifications

PhD in Chemistry, Pharmaceutical Sciences, or a related discipline or MS with extensive relevant biotech/pharmaceutical industry experience
10+ years of experience in biotech/pharmaceutical industry in small molecules, working in early to late-development (pre-clinical to phase 3)
Strong analytical planning and resource management skills in a dynamic environment located across multiple geographies
In depth knowledge of assay and related substances development, forced degradation, HPLC/UPLC, GC, KF, XRPD, residual solvents, elemental impurities, microbial testing, dissolution, compendial methods.
Hands-on experience in carrying out stability studies for drug substance and drug product in development and/or QC settings
Experience managing DS/DP stability, and knowledge of ICH stability guidelines
Knowledge of compendial (USP, EP, etc) requirements and standards
Detailed knowledge and understanding of current Good Manufacturing Practices (cGMP) related to the QC laboratory and ability to identify/remediate gaps in processes or systems
Strong organizational skills and attention to detail
Good interpersonal and communication skills to collaborate effectively with internal and external business partners
Requires a good understanding of managing groups, CMOs, CDMOs and other vendors

Work Location

The Associate Director, Analytical Development role is based in the US, with occasional travel.

Compensation

The annual base salary range for this position is $190,000.00 to $210,000.00. Individual compensation within this range will be determined based on a variety of factors, including qualifications, skills, relevant experience, and job knowledge.

In addition to base pay, this role is eligible for a discretionary annual bonus. Centessa also offers a comprehensive benefits package, which includes a 401(k) plan, company-sponsored medical, dental, vision, and life insurance, generous paid time off, and a health and wellness program.

POSITION: Full-Time, Exempt

EEOC Statement: Centessa Pharmaceuticals a wholly owned subdisary of Eli Lilly and Company believes in a diverse environment and is committed to equal employment opportunity for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion, or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. We will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Please note: We will not assign referral rights for any unsolicited resumes from recruitment agencies.

Apply Now

Refine Your Search

eli program representative jobs

Associate Director, Analytical Development – Small Molecule

Executive Director, Head of Toxicology

Senior Associate - LP1 QA

QA Representative - Warehouse

Climate Change: Greenhouse Gas Emissions – Fuel Sector Planner (Environmental Planner 4)

Associate/Sr. Associate/Manager - Global CMC Regulatory, Regulatory Delivery and Excellence

Senior Advisor, Manufacturing Science and Technology

Principal Scientist, Large Molecules Mass Spectrometry

Post-Doctoral Scientist – Delivery, Devices & Connected Solutions (DDCS) Inhaled Drug Formulation & Aerosol Science

Scientist Quality Assurance

Principal Scientist - Molecular Biology, Cell Culture Upstream Process Development

Associate Director - Global Regulatory Affairs - Product Communications

Pharmaceutical Sales Representative - Associate Territory Manager, Caridometabolic Health

Pharmaceutical Sales Representative - Territory Manager - Dermatology Specialty

Associate Director - Computer Systems Validation

Director/Sr. Director/Exec. Director Computational Biophysics, Advanced Molecular Design (AMD)

Climate Change: Greenhouse Gas Emissions – Fuel Sector Planner (Environmental Planner 4)

Senior/Principal Scientist, Bioprocess Purification Development

Scientist, Reference Standard Manufacturing - BRD Corporate Reference Standards Organization (CRSO)

Post-Doctoral Scientist, Bioconjugation Process Innovation

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