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DeltaPharma Jobs & Careers

15 jobs

Randstad Life Sciences
Summary Provides medical support with emphasis on the intake of medical product experiences and processing standard communication requests. Acts as a liaison with Quality Assurance for product quality problems where an adverse event is involved. Works with Customer Service to provide standard information and product replacement as necessary. Provides assistance to the medical and lay community wi...
Randstad Life Sciences
Positions may be 5 x 8 hour shift, 4 x 10 hour shift, or 3 x 12 hour shift. Operations are 24/7, so position may be for any one of several shift schedules. Shifts will be discussed at interviews. Please note candidates will receive weighted overtime for the 2nd shift (10% extra) and the 3rd shift (15% extra). Manufacturing Associates must have a degree or 1-2 years of manufacturing experience and ...
Randstad Life Sciences
Job Title: Sr. Medical Writer Requirements: Education: • Requires an advanced degree in a scientific discipline or a bachelor’s degree with equivalent work experience. MS or PhD in biological science preferred. Experience: • 6 + years experience writing high-quality clinical regulatory documents including clinical study reports across multiple therapeutic areas. Experience writing CSRs for pi...
Randstad Life Sciences
MUST BE BILINGUAL ENGLISH/SPANISH - FOOD PRODUCTION EXPERIENCE REQUIRED. Provide assistance to quality assurance manager in the implementation of food safety and quality procedures. Also, provide guidance and direction to quality assurance technicians in order to ensure regulatory and customer specifications compliance. Able to fill in and assume role of quality assurance manager. Duties: Monit...
Randstad Life Sciences
Seeking a Quality Assurance Associate responsible for assisting with the development, implementation and maintenance of a quality system to support bioanalytical lab operations. Assist with the development and execution of regulatory training for all employees and for training on quality assurance policies, programs, and initiatives. Ensure that documents are reviewed and processes conducted and c...
Randstad Life Sciences
SUMMARY OF POSITION Primary responsibilities include support of NCQA accreditation, auditing and monitoring compliance with NCQA standards and regulatory standards. This requires familiarity with the clinical regulatory requirements of DOH, State, HCR and CMS and associated agencies that monitor health plans. The majority of responsibilities will be focused on auditing/monitoring of compliance w...
Randstad Life Sciences
MSL training (does not have to be a trainer) a. Assist with delivery of data training (live and webex) to MSLs, internal medical affairs personnel, partner companies – mostly all planned, just needs to be delivered b. Assist with content development, as needed c. We are currently onboarding 2 x waves of new hire MSLs through an intensive 6-week program, which is due to complete at the end of Au...
Randstad Life Sciences
HPLC Analytical Specialist Job Description: • Perform specialized non-routine and routine HPLC analysis for R&D and QC purposes. • Perform analytical methods development and validation for HPLC test methods. • Provide analytical summary, analytical project and/or validation reports. • Adherence to SOPs and maintain good documentation: data management and maintenance to ensure compliance for a...
Randstad Life Sciences
Formulation Scientist Talented Formulation Scientists needed in Illinois, New Jersey, and New York area who will be responsible for developing the final product formulation, process procedures and packaging of sterile injectable and ophthalmic products. Duties & Responsibilities: Literature searching and review, patent searching and interpretation, performing risk assessment for formulation/proc...
Randstad Life Sciences
The Analytical Chemist will work within a dedicated Technical Service Laboratory. The scope of work will include direct laboratory testing but will also include product troubleshooting strategy/test plan development, analytical method remediation activities, and impurity isolation for a broad range of materials and product types. The Analytical Chemist works under the direction of the Director, A...
Randstad Life Sciences
New Position- Clinical Studies Specialist Responsibilities Member of the clinical team responsible for conducting Phase I-IV studies according to Federal Regulations and ICH guidelines. Support clinical team, primarily in tracking, organizing and filing Phase I-IV study documents according to Federal Regulations and ICH guidelines . Assist Clinical Team members in handling data queries, drug i...
Randstad Life Sciences
Executive Director, Quality Control/Quality Assurance Job Description This position is responsible for the organizational and programmatic elements of Quality Assurance, Quality Control, Microbiology, and Validation. This responsibility includes, but is not limited to, the effective planning and organization of personnel and workflow utilization in order to implement the timely submission, appro...
Randstad Life Sciences
CAN BE REMOTE - WOULD PREFER A CANDIDATE THAT CAN COME IN PERIODICALLY - LOCAL WOULD BE GREAT Publication manager - Will not be doing writing, will be working with the Publications Planning vendor to keep the project moving. a. General assistance with executing the publication plan for 2 products b. Oversee manuscripts, abstracts, posters and oral presentations that are being delivered by our v...
Randstad Life Sciences
Investigator sponsored trial (IST) manager (Project Management Experience Required) a. Oversee all aspects of the IST program for 2 products (total 30 studies in various stages of start-up, conduct and reporting) b. Receiving and reviewing IST concepts; chairing review committee meetings of new concepts c. Ensuring all elements are in place to get a study from concept approved to open d. Prima...
Randstad Life Sciences
Experienced Regulatory Submissions Publishing Expert Needed In NJ Responsible for global regulatory submissions/dossiesr Performs day-to-day activities and deliverables as it relates to publishing of submission-related documents for agency submissions Performs review and validation of submissions documents to ensure compliance with FDA and ICH guidelines and internal standards for submission th...