27 vacancies
Job Description
Job Description Validation Lead
Location: Raleigh, NC
Working Situation: Hybrid
A global speciality pharmaceutical company is looking to bring on a Validation Lead to support the global quality organization. You will be supporting tech transfer...
Suggested
Job Description
Job Description Quality Control Manager
Location: Omaha, Nebraska
Working Situation: Onsite
Level: Mid-Senior Level
We are seeking a dedicate Quality Control Manager to oversee Quality Control projects within our manufacturing site. This...
Suggested
...whilst maintaining timelines along every stage from conception till delivery.
- Publications: Experience creating high-quality scientific content such as abstracts, posters, manuscripts, reviews etc., which meets international publication standards would be considered...
Scientific
Permanent employment
Work experience placement
Remote job
Job Description
Job Description Salary: $140-190K
Company Summary: Working with a clinical-stage biotech company that's looking for a Clinical Trial Manager or Sr. Clinical Trial Manager to come into their South SF office on a hybrid/full-time basis. Their mission...
Suggested
Full time
Flexible hours
Research Scientist
New York, New York
Starting at $70,000 | Commensurate with Experience | Full-time
Seeking an Immunologist with an unparalleled dedication for exploratory research along with a proven track record of valuable contributions that drive programs...
Suggested
Full time
Director of Formulation
Location: Illinois, USA
Salary: $200,000 - $230,000 + bonus + relocation
A Biopharmaceutical company is looking to hire a Director of Formulation to help lead a team focused on developing innovative dosages forms and delivery systems....
Suggested
Immediate start
Relocation
Job Description
Job Description Title: Senior Clinical Trial Project Manager in Los Angeles
Introductory Paragraph:
Our client, a small medical devices and diagnostics Contract Research Organization (CRO), is seeking an experienced Senior Clinical Trial Project...
Suggested
Contract work
Quality Control Chemist
5 days on-site
Support a well-established CDMO in Irvine, CA, while expanding on your analytical experience in a cGMP environment.
Day to day:
Analytical testing of raw materials, in-process samples, and final products
Predominately...
Suggested
I am partnered with a growing biotech company located in San Francisco who is looking for an Associate Director of DMPK to join their team! This company currently has 8 candidates in their preclinical pipeline and 2 clinical candidates across metabolic, neuro, ophthalmology...
Suggested
...Boston, MA (Hybrid)
$130,000 - $150,000
Job Description
EPM is partnered with a cutting-edge biotech that is dedicated to... ..., ensuring they adhere to regulatory standards and meet scientific objectives
Coordinate all aspects of clinical trial operations...
Scientific
Director, Clinical Operations (Hybrid in Boston, MA)
Salary: $220,000- $245,000
This company is a pioneering biotechnology company dedicated to advancing the field of gene therapy to address unmet medical needs and transform the lives of patients worldwide. Founded...
Suggested
Worldwide
Clinical Trial Manger (Hybrid in Boston, MA)
Salary: $150,000-$165,000
This company is a fast growing biotechnology company in Boston, MA dedicated to advancing research, development, and treatments for rare diseases. We are driven by a commitment to innovation and...
Suggested
Summary:
The Supplier Quality Manager is essential for overseeing supplier quality interactions and ensuring compliance with Supplier Controls. This involves translating regulations and standards into company policies and procedures, and taking ownership of continuously...
Suggested
...company is actively hiring a Principal Scientist for their analytical development team. You will be playing a pivotal role in leading scientific initiatives and collaborating with cross-functional teams. This position offers a unique opportunity to make an impact in the...
Scientific
Quality Assurance Manager
Location: Memphis, TN
Working situation: Onsite
Level: People Manager
Our client, a well-known CDMO that partners with innovative companies to produce healthcare products and devices, is looking for a new Quality Assurance ...
Suggested
Quality Systems Manager
As the Quality Systems Manager, you will play a pivotal role in championing daily activities for quality excellence. You will develop, implement, and enforce quality systems that meet the highest standards, including FDA Drug and Medical Device...
Senior Quality Process Engineer
Location
St. Louis, MO
Job Description
As a Senior Quality Process Engineer, you'll play a pivotal role in maintaining top-tier quality standards at our St. Louis, MO plant. Responsibilities include overseeing the Annual ...
We are currently working with a small to mid-sized biopharmaceutical company focused on Oncology. My client has 6+ clinical trials, with 4 clinical trials being in Phase 2 or further. With multiple sites in the United States and they're looking to add headcount to their...
Contract work
...Qualifications:
# Holds a Bachelor's degree (BA/BS) in Chemistry, Bioengineering, Chemical Engineering, or a closely related scientific field from an accredited four-year institution.
# Possesses a robust understanding of research methodologies, protocols, and techniques...
Scientific
Holiday work
Temporary work
Title: Senior Director, Clinical Regulatory Affairs
Salary : $250,000 to $285,000
Summary:
A clinical-stage biopharmaceutical client of ours is seeking a very experienced and motivated person to fill their Senior Director of Clinical Regulatory Affairs role...
