Page 3 - 173 it support tech jobs found

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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

job summary: We are seeking a Regulatory Submission Manager to support global regulatory initiatives and ensure compliance with regulatory requirements for investigational and marketed products. Role involves working closely with cross-functional teams and regulatory leads to support submission activities, labeling development, and strategic regulatory guidance. The ideal candidate has a strong background in regulatory submissions and document review, as

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. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowle

job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco

a. Review global engineering work processes request from network workshops and create controlled documentation for overall process flow. b. Assist with the development and/or revision of global design standards (consult regional experts for local variances) c. Provide support to manage engineering systems, digital tools and application to our engineering community.salary: $28 - $31 per hourshift: Firstwork hours: 8 AM - 4 PMeducation: BachelorsRe

Self-motivated individual with innovative ideas to address technical issues in TFR and IC packaging projects. Team player with good communication and collaboration ability with senior chemists, managers and technicians. Ability to discuss and present results in a logical manner and propose next steps. • Pursuing a degree MS or PhD degree in organic, polymer chemistry or related materials science fields, working experience in polymer synthesis and char

job summary: We are seeking an experienced Regulatory Writer with a strong background in writing protocols, clinical study reports (CSRs), briefing books, informed consent forms (ICFs), and CTD Module 2 documents. This expertise is critical to the role. The successful candidate will play a key role in preparing high-quality regulatory documentation to support clinical and regulatory submissions, ensuring compliance with global regulatory requirements. Thi

job summary: Project Manager - Clinical Trial Process Optimization Exciting opportunity to drive innovation in clinical trial processes! 4 Openings: (3) Traditional PMs (1) Change Management PM Salaried Contract - 12 Months w/Full Benefits | Remote Join a high-impact team within a large pharmaceutical company, supporting continuous improvement and change management initiatives across the end-to-end clinical trial process. This role offers visibility and

job summary: Manufacturing Science is a partner of biologics manufacturing operations and is the custodian of manufacturing processes. Manufacturing Science ensures manufacturing processes are capable, compliant, in control, cost effective, and continuously improved. location: Framingham, Massachusetts job type: Contract salary: $85 - 88 per hour work hours: 9 to 5 education: Bachelors responsibilities: Provide collocated technical lea

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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines

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. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their bus

job summary: As a global leader in staffing and recruitment, we are dedicated to connecting you with opportunities that foster growth and advancement in the life sciences sector. Working with a recruiter gives you exclusive access to a vast network of top employers and valuable insights into a wide range of roles. One of our premier partnerships is with a world-renowned leader in eye care, committed to advancing vision health through innovative surgical a

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. Our dedicated teams are at the forefront of pioneering beauty tech innovations, meeting individual needs a

job summary: The LBA Operations Bioanalytical team at ABC QTAS conducts quantitative bioanalysis assays of large molecule therapeutics like mAb, ADC, fusion protein and bi-specifics for Pharmacokinetic (PK), Pharmacodynamic (PD) and Toxicokinetic (TK) studies using ligand binding assays to support drug discovery and early development efforts. location: Worcester, Massachusetts job type: Contract salary: $35 - 40 per hour work hours: 9 to 5 ed

job summary: Analytical Chemistry role is a 100% onsite, lab-based position, supporting the oligonucleotide (oligo) program with a focus on synthetic small molecules. The ideal candidate holds a Master's degree in Analytical Chemistry (preferred) or a Bachelor's with 2-3 years of relevant experience, with hands-on expertise in LC, GC, KF, and proficiency in Empower software. location: Newbury Park, California job type: Contract salary: $25.37 -

Exciting Career Opportunity: Biomanufacturing Associate II – Downstream/Purification Randstad has partnered with a leading RTP Biotech Company to create career opportunities for driven individuals ready to make an impact. This is a temp-to-perm contract role with incredible potential to transform a 6–18-month contract into a full-time career in the biotech industry!. What You’ll Do: As a Biomanufacturing Associate II in Downstream/Purific

job summary: Role is responsible for designing, planning, and executing large scale data analysis, and algorithm development to identify gaps in the care continuum and to measure impact using RWD. This work highlights the value of utilizing real world data to inform or address strategic questions in the disease areas of interest. The role involves the application of statistical theories, analytical methods, and technical programming skills to analyze clin

Exciting Career Opportunity: Biomanufacturing Associate II – Downstream/Purification Randstad has partnered with a leading RTP Biotech Company to create career opportunities for driven individuals ready to make an impact. This is a temp-to-perm contract role with incredible potential to transform a 6–18-month contract into a full-time career in the biotech industry!. What You’ll Do: As a Biomanufacturing Associate II in Downstream/Purific

The objective of this position is to provide supervision of operations associated with pharmaceutical product manufacturing on the Billerica Campus, while ensuring that all operations comply with all GMP, OSHA and other regulatory requirements. The Supervisor leads the execution of commercial pharmaceutical manufacturing according to standard operating procedures and production records in accordance with Current Good Manufacturing Practices (cGMP’s)

job summary: We are seeking a detail-oriented and motivated Analytical Chemist to join our Analysis Americas team for a 6-month contract. Our goal is to provide the best information within a short time to our customers in response to their characterization needs. The team operates regionally supporting all aspects of the business. The successful candidate will have expertise in a variety of wet chemistry techniques and ideally, experience with ICP-OES. Yo

job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco

job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a global leader in biotechnology. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the healthcare and life sciences industries. This company is dedicated to discovering and developing innovative therapies that address serious diseases, with a focus on onco

job summary: About the Company A global Pharmaceutical company that harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Our investment in research and development has yielded a robust pipeline that builds on our existing portfolio of medicines to treat cancer, heart disease, os

job summary: The Research Scientist will independently support analytical development, including method development, qualification/validation, sample testing, data analysis, and reporting. Working closely with Formulation Development, this role ensures compliance with OSHA, FDA regulations, and SOPs. This is a 6 month contract (some potential to extend) 100% onsite in Bridgewater, NJ location: Bridgewater, New Jersey job type: Contract salary: $

job summary: PRIMARY OBJECTIVE OF POSITION: Under minimal supervision, the Quality Specialist, Stability supports the stability program under regulatory requirements and ISO 13485 and runs stability studies from initial batch/lot selection to final report generation and study destruction; works closely with Quality, R&D, and Operations to assure appropriate batch/lot selection, initiation, and execution of Stability studies in a compliant and timely man

job summary: Seeking two (2) experienced QC Microbiology Environmental Monitoring (EM) Analysts II for a leading Contract Development and Manufacturing Organization (CDMO) specializing in cell and gene therapy, located in Houston, TX. This role supports the Quality Control, Environmental Monitoring team in maintaining the cleanrooms for commercial manufacturing and environmental monitoring performance qualifications. This role will also be central in all

job summary: Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objecti

job summary: The Global Regulatory Operations Publishing Intern prepares and delivers high quality, timely, and compliant regulatory submissions to global health authorities. The Publishing Intern represents Global Regulatory Publishing in cross-functional project teams, provides regulatory submission support for products and contributes to regulatory initiatives location: Telecommute job type: Contract salary: $25 - 30 per hour work hours: 9

job summary: Job Description The Medical Writing Intern (MWI) assists with medical writing activities in support of the GCDO - Medical Writing & Transparency department. The MWI works closely with MW personnel to develop regulatory documents in support of company products. This individual will work to assigned timelines, communicate effectively to the responsible medical writer, and ensure their deliverables are completed according to appropriate quality

job summary: Required: Must be currently enrolled in a Bachelor's degree program (Junior/Senior level)No industry experience requiredStrong verbal and written communication skillsBasic knowledge of Word, Excel, PowerPoint, and shared platforms (e.g., SharePoint, Box, Smartsheets) Preferred: Exposure to Good Clinical Practices (GCP) regulations and Standard Operating Procedures (SOPs)Understanding of clinical study phases and their role in clinical