179 sales agent jobs found

job summary: This role will initially be a part-time consultancy with the potential to evolve into a full-time operating position. The consultant will be responsible for identifying industry trends, tracking competitive players, discovering business opportunities, screening potential deals, and developing negotiation strategies within the Preclinical and Clinical CRO spaces. A key aspect of this role will be providing operational and strategic leadership

Onsite in Bedford, MA 3 days per week. Must have Order Management Systems experience. The Business Analyst for the Commercial Order Management Systems (OMS) plays a pivotal role in bridging the gap between business needs and technology solutions. This role involves gathering, analyzing, and documenting business requirements for the OMS, ensuring the system effectively supports the order management process for radio pharmaceutical products. The Business A

job summary: The Senior Clinical Development Scientist for the Ultrasound group will be responsible for developing, generating, and disseminating clinical and economic evidence ensuring innovation, and transformation with best-in-class clinical evidence. Your role: Contribute strategic guidance for clinical and economic evidence related to the end to end (E2E) development process from ideation through post-market for products in the Ultrasound business.

We’re looking for an enthusiastic and customer-focused Customer Service Representative to join our dynamic team! If you have 2 years or more of customer service experience and a passion for helping others, this is the perfect opportunity for you. In this hybrid role, you’ll enjoy the flexibility of working from home two days a week, while collaborating in the office three days a week. With a Monday to Friday schedule from 10:30 AM to 7:00 PM ES

Are you passionate about providing top-tier customer support in a dynamic and fast-paced environment? We are seeking a Customer Service Representative to join our team! This role offers an exciting opportunity to work with a leading company in the radiopharmaceutical industry, where your contributions will directly impact healthcare professionals and patients.salary: $24 - $26 per hourshift: Firstwork hours: 10:30 AM - 7 PMeducation: High SchoolR

We’re looking for an enthusiastic and customer-focused Customer Service Representative to join our dynamic team! If you have 2 years or more of customer service experience and a passion for helping others, this is the perfect opportunity for you. In this hybrid role, you’ll enjoy the flexibility of working from home two days a week, while collaborating in the office three days a week. With a Monday to Friday schedule from 10:30 AM to 7:00 PM ES

job summary: Responsible for performing the accurate and detailed medical review of complex advertising and promotional materials and non-promotional materials. Provides timely and accurate reviews of promotional materials in accordance with established policies and practice standards, including regulatory guidelines to meet customer needs. Ensures deliverables convey a clear and appropriate medical message. location: Telecommute job type: Contract s

job summary: We are seeking a highly skilled Senior Manager - CMC Regulatory to lead the planning, preparation, and submission of global regulatory CMC-related content for clinical trial applications, marketing applications, and periodic reports. This role involves ensuring compliance with US and international regulatory requirements, collaborating with cross-functional teams, and providing strategic guidance on manufacturing changes to optimize regulator

A Global Biotech/Pharma located in Round Lake, IL is seeking a Production Associate to join their Team! Support manufacturing operations in Inspection and/or Packaging Inspect manufactured product for irregularities or defects Supplies components, small parts, glassware, tubing, etc. to cell culture and purification areas Operate general production equipment (such as labelers, parts washers, autoclave, stir plates, etc.) Complete relevant paperwork follow

job summary: A major pharmaceutical company who work to benefit patients wherever they live by uniting worldwide talent and resources with their vision. KEY SKILLS: PharmacovigilanceDrug safetyPhase 1-3 clinical study experienceProtocol, IB, ICF developmentSMC, DMCSAE and aggregate data review and analysisSignal detection and signal evaluationDSUR authoring location: Telecommute job type: Contract salary: $85 - 100 per hour work hours: 9 t

job summary: The US Global Regulatory Policy and Innovation Lead is partnering across Global Regulatory Affairs and the broader R&D organization to advance regulatory policy priorities. location: Telecommute job type: Contract salary: $180.00 - 188.76 per hour work hours: 9 to 5 education: Doctorate responsibilities: This role includes leadership on policy integration with product development teams to ensure teams have the regulatory inte

job summary: This is an 18-month onsite contract role based in Thousand Oaks, CA, with potential for extension. The position supports Drug Product Quality Assurance by providing daily compliance oversight on the manufacturing floor. Key responsibilities include batch record review, SOP approvals, MES and Maximo system updates, and minor deviation/CAPA record approvals. The role requires a detail-oriented team player with quality experience and the ability

job summary: To clean the production, lab, and warehouse areas according to site procedures and complying to safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. Off-shift hours (including night work) may be required. location: King Of Prussia, Pennsylvania job type: Contract salary: $20.00 - 22.50 per hour work hours: 9 to 5 education: High School responsibilities: Safe

job summary: To clean the production, lab, and warehouse areas according to site procedures and complying to safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. Off-shift hours (including night work) may be required. location: King Of Prussia, Pennsylvania job type: Contract work hours: 9 to 5 education: High School responsibilities: Safety Follow all EHS procedures, stand

job summary: To clean the production, lab, and warehouse areas according to site procedures and complying to safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. Off-shift hours (including night work) may be required. location: King Of Prussia, Pennsylvania job type: Contract work hours: 9 to 5 education: High School responsibilities: Safety Follow all EHS procedures, stand

Are you looking for an opportunity to contribute to groundbreaking advancements in biotechnology? We are committed to transforming medicine and improving lives. As an Associate, Document Control and Records Management, you will play a crucial role in ensuring compliance and accuracy in our document management processes. If you are detail-oriented, thrive in a regulated environment, and are eager to be part of a high-impact team, we encourage you to apply!s

job summary: The QC Associate I is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology. Responsibilities include, but are not limited to, training, water and environmental sampling, support for testing. A fundamental understanding of the company's Quality Systems and able to apply it in their daily support functions. Adherence to all GMP requirements, effective interactions/ communication with Quality Contro

job summary: To clean the production, lab, and warehouse areas according to site procedures and complying to safety and quality requirements. Conduct GMP Cleaning operations in accordance with Biopharm Safety Procedures and cGMPs. Off-shift hours (including night work) may be required. location: King Of Prussia, Pennsylvania job type: Contract work hours: 9 to 5 education: High School responsibilities: Safety Follow all EHS procedures, stand

Join a global leader in agricultural innovation! We are seeking a Lab Technician to support high-throughput Seed Quality Testing in our Row Crop Production Organization. If you have a passion for scientific research and hands-on laboratory work, this is your opportunity to contribute to cutting-edge agricultural advancements.salary: $24 - $24.5 per hourshift: Firstwork hours: 9 AM - 5:30 PMeducation: AssociateResponsibilitiesWhy You Should Apply:

job summary: Sr. Pharmacovigilance (PV) Operations Manager | Remote | West Coast This critical role is responsible for managing and overseeing PV operations across clinical development programs, ensuring seamless collaboration with PV vendors. You will play a key role in preparing for the initiation of two global Phase 3 trials, ensuring all PV activities are in place. Your expertise in global trial management, study document review, and vendor oversight

job summary: A large, multinational medical device company is seeking Medical Device Toxicologists to review product documentation and determine compliance status per ISO 10993 series of standards. location: Telecommute job type: Contract salary: $30.00 - 33.33 per hour work hours: 9 to 5 education: No Degree Required responsibilities: Solely focused on reviewing documentation and confirming evidence.Prior experience conducting biocompa

job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With therapeutic areas that include Oncology, Vaccines, and Rare Diseases, our partner aims to make treatm

job summary: Performs very basic functions to assist in the preparation of histopathology samples. location: Canoga Park, California job type: Contract salary: $17.20 - 22.37 per hour work hours: 7 to 3 education: High School responsibilities: Perform routine activities involved in the preparation of histopathology slides under general supervision and according to policies and procedures. Receive/collect, label and prepare tissue s

job summary: Responsible for collection and testing of routine environmental monitoring samples within aseptic processing fill lines, Isolator fill line, compounding, sterility suite, and component preparation areas for aseptic lines (Building A) and clean rooms areas in new expansion Building B. Collect and test utility samples such as WFI, clean steam and compressed gases. Monitors environmental conditions in laboratory areas during test sessions. Repor

1st Shift, Monday- Thursday, 6:00 AM - 4:30 PMResponsible for the labeling and packaging of pharmaceuticals for world wide distribution. The kit packaging operation is largely a manual operation, with some labeling operations performed by the use of automated labeling machines. Kit Packaging personnel primarily perform a manual visual inspection of filled vials. Must follow SOP’s and the ability to follow manufacturing batch records and understand

Randstad has an exciting opportunity for Biologist with a background in horticulture or plant science. As the successful candidate, you will have the opportunity to put your skills to work with a global leader in agricultural research. This is an on-site position in St. Louis, MO. Local candidates are preferred as relocation cost reimbursement is not available for this position. salary: $24 - $30 per hourshift: Firstwork hours: 8 AM - 5 PMeduc

job summary: Seeking a skilled Epidemiologist to execute data analyses, contribute to regulatory deliverables, and design epidemiological studies. Proficiency in SAS / R, real-world datasets, and excellent communication skills are essential. We're looking for a motivated professional with an MPH degree and 2+ years of experience, ready to grow in a dynamic pharmaceutical environment. Flexible, Part time hours (20 hours/week) Fully Remote, any time zone in

job summary: The Associate, Quality Assurance Documentation, will assist in maintaining and administering all aspects of the GMP document control system compliant with international cGMP expectations and Company policies and procedures. location: Marlborough, Massachusetts job type: Contract salary: $24 - 29 per hour work hours: 9 to 5 education: Bachelors responsibilities: Document Issuance Support: Assist with the issuance of GxP doc

job summary: Under general supervision, this position will perform routine procedures and testing in support of the lab. location: Newbury Park, California job type: Contract salary: $24.00 - 27.32 per hour work hours: 9 to 5 education: High School responsibilities: Performing routine laboratory proceduresRoutine analytical testingDocumenting, computing, compiling, interpreting, and entering dataMaintaining and operating specialized equ

job summary: The Sr. Associate Quality Assurance position supports Company's Quality Assurance program under the Plant QA organization providing daily oversight of the Drug Product manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities and Engineering staff in the execution of their processes, procedures, and use of quality systems. location: Newbury Park, California job type: