Biotech Jobs in North Carolina

1000+ jobs

Sr. Regulatory Associate, CMC Our client is a successful specialty pharmaceutical company focused on commercializing products for the hospital and adjacent specialty markets. They are currently seeking to fill a Senior Regulatory Affairs position. The focus of this position is to provide regulatory expertise with a concentration on Chemistry, Manufacturing and Controls (CMC) related issues includ...

Clinical Research Careers for Health Care Research Professionals at an Innovative Site Specific Research Organization (SSRO) CTMG Inc. is seeking RNs, LPNs, CMAs, or others possessing U.S. medical licensure who have always wanted the opportunity to achieve greatness, by helping us change how clinical trials are managed, and building a lasting new paradigm to bring Speed and Certainty to clinic...

ARGOS IS GROWING! Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases based on its Arcelis™ technology platform. We are currently seeking a well-qualified Quality Control Analyst. SCOPE: The individual will conduct routine and non-routine analysis of raw mater...

ARGOS IS GROWING! Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases based on its Arcelis™ technology platform. We are currently seeking a well-qualified Senior Validation Engineer. SCOPE: Prepare, execute, and summarize validation protocols and other validat...

ARGOS IS GROWING! Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases based on its Arcelis™ technology platform. We are currently seeking a well-qualified Senior Quality Assurance Auditor. SCOPE: This position will plan and conduct quality audits. The person i...

ARGOS IS GROWING! Argos Therapeutics is a biopharmaceutical company focused on the development and commercialization of fully personalized immunotherapies for the treatment of cancer and infectious diseases based on its Arcelis™ technology platform. We are currently seeking a well-qualified Process Development Associate. SCOPE: Assist in the design, testing and implementation of processes, instr...

Momentum Research, Inc. IT Manager Job Description Reports to: Vice President, Business Operations Job summary Responsible for all IT operations and procedures to ensure organizational effectiveness, efficiency and ability to use all necessary IT products and applications Summary of essential job functions · Provide maintenance of laptops, smartphones and other products as needed · Provide...

Bench Scientist Chemist IIneeded for acontractopportunity with Yoh's client located inZebulon, NC. The Big Picture - Top Skills You Should Possess: - HPLC - Dissolution - cGMP What You'll Be Doing: - Conduct routine analytical testing of raw materials, packaging materials, finished products and environmental samples using approved methods and various instrumentation (e.g., HPLC, Vitek, GC, U...

Job Title: Bench Scientist Chemist - L2 Position Description Conduct routine analytical testing of raw materials, packaging materials, finished products and environmental samples using approved methods and various instrumentation (e.g., HPLC, GC, UV, microscope, robotics). Generate valid data at expected levels of productivity while adhering to cGMP. Interpret validity of own test data and gen...

Our client a global leader in the pharmaceutical industry is looking for a Regulatory Manager to join the Holly Sprins, NC, location. DUTIES : Develop global Chemistry, Manufacturing and Control (CMC) regulatory strategy for development and licensed products and Manage preparation of dossiers. Coordinate and prepare CMC (Quality) documentation for new Clinical Trial Applications, IND submissions...

Job Title: Regulatory Manager Location: Holly Springs, NC Job Description Develop global Chemistry, Manufacturing and Control (CMC) regulatory strategy for development and licensed products and Manage preparation of dossiers. Coordinate and prepare CMC (Quality) documentation for new Clinical Trial Applications, IND submissions and amendments, CTD submissions and subsequent variations - Respons...

Kelly Scientific Resources has a client in the Raleigh, NC area with an opening for a Director, Regulatory Affairs. Reporting to the VP of Regulatory Affairs, the Director collaborates in the development and implementation of regulatory affairs programs to assure the most efficient and timely submission of regulatory filings and to maintain IND and NDA registrations. Must be able to integrate and ...

I. Overview The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. II. Department Summary The Site Services de...

Regulatory Manager You're precision-oriented and a stickler for doing it right. You have deep expertise in pharmaceutical compliance and regulatory affairs. Your critical thinking prowess makes you a problem solver extraordinaire. You generate powerful ideas and know how to get them implemented. If this describes you, this opportunity from Experis is just right for you. As a Regulatory Manager, ...

Large device company is seeking 3 Senior Clinical Research Associates for a 3 month contract supporting an orthopedic device trial. This is a remediation study for a newly acquired device supporting a post market study with 2 protocols. The ideal candidate will be able to review hospital charts, QC source documents, and have the following experience: 5+ years of experience monitoring clinical mon...

A top tier automotive manufacturer is looking for a sharp Senior Level Controls Engineer. The controls engineer is a key member of the industrial team. In this role, you will assist in requirements gathering, technical proposals, design and development of complex equipment controls projects. The position is located in the greater Asheville NC, York SC or Laurensburg NC area (multiple plants). This...

Leading pharmaceutical services company has immediate positions for “Drug Safety Associate”. If you are interested then please email your updated resume to ***** or please call 732-788-3483. JOB DESCRIPTION : Position Title : Safety Specialist / Drug Safety Associate Location : Morrisville, NC Duration : 6-12 Months The Safety Specialist performs day-to-day adverse event report...

I Overview The laboratory groups at Catalent RTP are responsible for the support of pharmaceutical product development in a range of dosage forms both directly with customers and in collaboration with other Catalent facilities. This includes formulation development, structural chemistry, analytical support, and clinical trials material manufacturing. II. Department Summary As a member of the NM...

Job ID: 5309 Position Description: A full-time Representative is needed to exemplify the values of our client which include personal commitment, integrity and teamwork. The representative will be responsible to meet or exceed established program sales and market share targets within a given geographical territory targeting primary care physicians.  Consistently meet and exceed established prog...

PURPOSE Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretat...