Development Engineer II
Lexington, MA · On-site
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Additional responsibilities will include performing drug product process development studies in ...
Lexington, MA · On-site
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Additional responsibilities will include performing drug product process development studies in ...
Lexington, MA · On-site
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Additional responsibilities will include performing drug product process development studies in ...
$105K - $136K/yr
... to support integrated development strategies. The role provides subject matter expertise ... Design, execute, and/or oversee process development studies to improve productivity, product ...
$105K - $136K/yr
... to support integrated development strategies. The role provides subject matter expertise ... Design, execute, and/or oversee process development studies to improve productivity, product ...
Rahway, NJ · On-site
$105K - $136K/yr
... to support integrated development strategies. The role provides subject matter expertise ... Design, execute, and/or oversee process development studies to improve productivity, product ...
Rahway, NJ · On-site
$105K - $136K/yr
... to support integrated development strategies. The role provides subject matter expertise ... Design, execute, and/or oversee process development studies to improve productivity, product ...
Rahway, NJ · On-site
$105K - $136K/yr
... to support integrated development strategies. The role provides subject matter expertise ... Design, execute, and/or oversee process development studies to improve productivity, product ...
Rahway, NJ · On-site
$105K - $136K/yr
... to support integrated development strategies. The role provides subject matter expertise ... Design, execute, and/or oversee process development studies to improve productivity, product ...
Lexington, MA · On-site
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Additional responsibilities will include performing drug product process development studies in ...
Lexington, MA · On-site
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Additional responsibilities will include performing drug product process development studies in ...
You think in integrated development plans - pairing nonclinical pharmacology, DMPK, biomarkers ... Research Operations • Oversee nonclinical and translational study execution and vendor management ...
You think in integrated development plans - pairing nonclinical pharmacology, DMPK, biomarkers ... Research Operations • Oversee nonclinical and translational study execution and vendor management ...
Palo Alto, CA · On-site
You think in integrated development plans -- pairing nonclinical pharmacology, DMPK, biomarkers ... Research Operations • Oversee nonclinical and translational study execution and vendor management ...
Quick apply
Palo Alto, CA · On-site
You think in integrated development plans -- pairing nonclinical pharmacology, DMPK, biomarkers ... Research Operations • Oversee nonclinical and translational study execution and vendor management ...
Lexington, MA · On-site
$27 - $36.25/hr
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... validation/or development studies. Testing may include but not limited to samples from drug ...
Lexington, MA · On-site
$27 - $36.25/hr
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... validation/or development studies. Testing may include but not limited to samples from drug ...
Boston, MA · On-site
$288.06 - $432.09/hr
... study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ). You will be ... to integrated development plan * Development of medical content for regulatory document, and ...
Boston, MA · On-site
$288.06 - $432.09/hr
... study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ). You will be ... to integrated development plan * Development of medical content for regulatory document, and ...
... study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ). You will be ... to integrated development plan * Development of medical content for regulatory document, and ...
... study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ). You will be ... to integrated development plan * Development of medical content for regulatory document, and ...
... study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ). You will be ... to integrated development plan * Development of medical content for regulatory document, and ...
... study stage to Proof of Concept /Phase2 stage, Phase 3 and regulatory approval ). You will be ... to integrated development plan * Development of medical content for regulatory document, and ...
Execute comprehensive feasibility studies and experiments to characterize processes throughout the development lifecycle, ensuring robust and reliable integration * Utilize big data analytics ...
Execute comprehensive feasibility studies and experiments to characterize processes throughout the development lifecycle, ensuring robust and reliable integration * Utilize big data analytics ...
Execute comprehensive feasibility studies and experiments to characterize processes throughout the development lifecycle, ensuring robust and reliable integration * Utilize big data analytics ...
Execute comprehensive feasibility studies and experiments to characterize processes throughout the development lifecycle, ensuring robust and reliable integration * Utilize big data analytics ...
Execute comprehensive feasibility studies and experiments to characterize processes throughout the development lifecycle, ensuring robust and reliable integration * Utilize big data analytics ...
Execute comprehensive feasibility studies and experiments to characterize processes throughout the development lifecycle, ensuring robust and reliable integration * Utilize big data analytics ...
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Contribute to the planning and timely execution of Clinical Development studies, within appropriate ...
Company Description A Few Words About Us Integrated Resources, Inc is a premier staffing firm ... Contribute to the planning and timely execution of Clinical Development studies, within appropriate ...
Boston, MA · On-site
$288.06 - $432.09/hr
... to integrated development plan* Development of medical content for regulatory document, and ... History of leading cross-functional teams to define clinical strategy and clinical study design*
Boston, MA · On-site
$288.06 - $432.09/hr
... to integrated development plan* Development of medical content for regulatory document, and ... History of leading cross-functional teams to define clinical strategy and clinical study design*
Support integrated automation workflows and lab orchestration systems, including platforms such as ... Ability to support development studies demonstrating automated assay comparability, robustness, and ...
Support integrated automation workflows and lab orchestration systems, including platforms such as ... Ability to support development studies demonstrating automated assay comparability, robustness, and ...
Cambridge, MA · On-site
$87K - $119K/yr
Integrate scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP.
Cambridge, MA · On-site
$87K - $119K/yr
Integrate scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP.
Support integrated automation workflows and lab orchestration systems, including platforms such as ... Ability to support development studies demonstrating automated assay comparability, robustness, and ...
Quick apply
Support integrated automation workflows and lab orchestration systems, including platforms such as ... Ability to support development studies demonstrating automated assay comparability, robustness, and ...
Integrate scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP.
Integrate scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the Integrated Development Plan (IDP) and CDP.
$29K - $33.7K
7% of jobs
$33.7K - $38.5K
8% of jobs
$42.6K is the 25th percentile. Wages below this are outliers.
$38.5K - $43.2K
11% of jobs
$43.2K - $47.9K
14% of jobs
The median wage is $50.4K / yr.
$47.9K - $52.6K
19% of jobs
$52.6K - $57.4K
13% of jobs
$58.8K is the 75th percentile. Wages above this are outliers.
$57.4K - $62.1K
12% of jobs
$62.1K - $66.8K
8% of jobs
$66.8K - $71.5K
4% of jobs
$71.5K - $76.3K
3% of jobs
$76.3K - $81K
1% of jobs
$29K
$53.4K
$81K
| Aspect | Integrated Development Studies | Urban Planning |
|---|---|---|
| Required Credentials | Bachelor's or Master's in Development Studies, Social Sciences, or related fields | Bachelor's or Master's in Urban Planning, Geography, or Civil Engineering |
| Work Environment | Community development projects, NGOs, government agencies | Municipalities, government departments, consulting firms |
| Industry Usage | International development, social programs, policy analysis | City design, land use, infrastructure planning |
Integrated Development Studies focuses on holistic community and social development, often working with NGOs and international agencies. Urban Planning concentrates on designing and managing urban spaces and infrastructure. While both fields involve development, Integrated Development Studies emphasizes social and economic aspects, whereas Urban Planning centers on physical space and infrastructure design.

Contractor
Re-posted 2 days ago
A Few Words About Us
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
Development Engineer / Associate (Contract) - Clinical Drug Product Manufacturing Sciences (CDPMS)Â
The Development Engineer / Associate - CDPMS will assist drug product tech transfer teams with project management support. Project management support will include scheduling, resource planning, and project task tracking. A candidate with the right experience would have the opportunity to lead a drug product tech transfer team. The primary responsibility of the candidate will be to perform project management activities to manage the external manufacture of clinical trial materials. In addition, the candidate will coordinate external research projects such as compatibility and filter validation studies. Additional responsibilities will include performing drug product process development studies in collaboration with drug product manufacturing and formulation development teams. The Development Engineer / Associate will also analyze experimental data, document results and conclusions in technical reports, and assist Senior Staff with drug product tech transfer management projects.Â
This will be a visible and hands on role with opportunities to contribute to multiple clinical stage programs. In this role, the Development Engineer / Associate must be able to work independently and be self-motivated. The candidate must manage time efficiently to balance multiple projects and priorities. Excellent organization and communication (oral and written) skills are required.Â
QualificationsÂ
BS/MS in degree in chemical, biochemical, biomedical engineering, chemistry or related fieldÂ
3-6 years industry experience in formulation and/or drug product process developmentÂ
Experience in supporting tech transfer projects to contract research and/or manufacturing organizationsÂ
Project management experience including time and resource schedulingÂ
Experience in a GMP environment or GLP laboratory is preferredÂ
Experience with Microsoft Project, Vizio, and advanced Excel spreadsheets is preferredÂ
Experience managing outsourced research projects is a plusÂ
Knowledge of statistical design of experiments is a plus
Archana Melwani
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Inc. 5000 - 2007-2014 (8th Year)
Certified MBE I GSA - Schedule 66 I GSA - Schedule 621I I GSA - Schedule 70
Tel: 732-549-2030 x130
Direct: 732-429-1853
Fax: 732-549-5549
Gold Seal JCAHO Certified for Health Care Staffing
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th YearÂ
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996