35 sr java developer jobs found

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:

job summary: The Sr. Associate Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction-including development, clinical, and commercial operations. The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. location: Holly Springs, North Carolina job type: Co

job summary: The Sr. Associate Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction-including development, clinical, and commercial operations. The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. location: Holly Springs, North Carolina job type: Co

job summary: The Sr. Associate Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction-including development, clinical, and commercial operations. The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. location: Holly Springs, North Carolina job type: Co

job summary: Seeking a self-motivated and detail-oriented Quality Complaints Sr Associate to join a fast-paced team. Ideal candidates will have a Bachelor's degree, a keen eye for GDP / GMP compliance, and strong organizational and communication skills. This role involves handling returned product samples, performing evaluations and documentation, and ensuring compliance with quality standards. location: Newbury Park, California job type: Contract

job summary: Sr. Medical Editor - Medical Communications REMOTE / Part-Time 20 hrs/wk | EST Hours ELS Certification Required (Editor in the Life Sciences) via Board of Editors in Life Sciences (BELS) Randstad is hiring a Senior Editor for Scientific Services to join an award-winning, best-in-class in-house agency at a leading pharmaceutical company. This full-service agency develops cutting-edge digital, video, AR/VR, and print assets, consistently outper

job summary: We are seeking a Clinical Site Contracts Specialist to manage end-to-end processes for clinical site contracts and consulting agreements, ensuring smooth study start-up and trial operations. If you're detail-oriented, proactive, and passionate about negotiation and collaboration, this is your chance to contribute to critical clinical research initiatives. Apply today to take the next step in your career-let's start the conversation! locati

job summary: We are seeking a Senior Engineer - Equipment and Utilities to support GMP manufacturing operations by ensuring the proper maintenance and functionality of building systems, utilities, and manufacturing equipment. This role involves 70% desk-based responsibilities and 30% vendor management, requiring a strong technical background and the ability to oversee third-party maintenance activities effectively. This is a 6-month contract 100% on-site

job summary: Our Commercial Attribute Sciences department is responsible for commercial analytical support, including method validation, method transfer, method remediation, method investigation support, process and product development as well as manufacturing and QC support.The Senior Scientist will work closely with a team of analytical & bioanalytical chemists, organic chemists, engineers and formulators responsible for the technical aspects of devel

job summary: The Cell Culture Manufacturing Senior Technician position will directly enable the initial start-up phase of the Hopewell manufacturing facility and then shift focus to hands-on execution and support of cGMP manufacturing operations. location: Pennington, New Jersey job type: Contract salary: $45.13 - 53.10 per hour work hours: 9 to 5 education: High School responsibilities: Hands-On cGMP Operations: Focused on execution of c

job summary: Randstad Life Sciences is working with a global leader in the manufacture of cGMP-produced, high purity, injectable grade excipients and bioprocessing solutions. We are looking for someone to join their program and further their career! This candidates needs to possess the following API HPLC ICP-MS EMPOWER ANALAYTICAL METHOD DEVELOPMENT ANALAYTICAL METHOD VALIDATION QC Individual will perform testing of raw materials, in process samples, fini

job summary: True Title: Clinical Pharmacologist (Director, Clinical Pharmacology) 6-Month Initial Contract Remote | EST hours This role will play a pivotal part in supporting the late-stage clinical development of biologics in the fields of immunology, neurology, and hematology. The ideal candidate will bring deep expertise in pharmacokinetics (PK) and pharmacodynamics (PD) to contribute to regulatory submissions (IND, BLA), clinical study reports (CSR)

job summary: Design and implement experiments to screen for drug candidates, and to address mechanisms-of-action of therapeutic molecules. Perform complex cell-based functional experiments independently. Act as a subject matter expert (SME) for drug discovery in the Cell therapy pillar. location: Cambridge, Massachusetts job type: Contract salary: $40 - 48 per hour work hours: 9 to 5 education: Bachelors responsibilities: Design and im

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 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

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: This Sr Associate position is a laboratory-based position, responsible for analysis of process development samples, multiple instrument operation, analytical method development, sample management, data analysis and reporting. Candidate will work in a cross-function laboratory with following GMP and safety compliance. location: Newbury Park, California job type: Contract salary: $25.37 - 29.98 per hour work hours: 9 to 5 education:

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: 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 Drug Metabolism and Disposition group in QTAS has an open position for a Senior /Research Associate Scientist to perform drug metabolism/metabolite identification studies supporting a series of small molecule drug discovery projects. The selected candidate will be responsible for designing and conducting in vitro metID studies, processing the data, and interpreting MS/MS results. It is a fully drug metabolism laboratory-based role. It wou

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: 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.

job summary: This research scientist's primary responsibility is to perform the characterization of raw materials and hydrogel polymers using chemical and physical characterization techniques. In addition, this scientist is also going to assist senior scientists to develop new analytical methods. location: Duluth, Georgia job type: Contract salary: $40.00 - 43.48 per hour work hours: 9 to 5 education: Bachelors responsibilities: Perform

job summary: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours Join a mission-driven team committed to ensuring the safe and effective use of pharmaceutical products worldwide. We're seeking a Global Labeling Manager with a passion for regulatory excellence, precision, and cross-functional collaboration. About the Role: As a Global Labeling Manager, you will drive global labeling strategy and ensure high-quality, compliant labeling documents

job summary: A current top partnership with a research-driven biopharmaceutical company is known as a powerhouse that aims to develop treatments for difficult-to-cure diseases. This renowned employer has created 32 products, that have highly impacted lives across the globe. If you're looking to stand out in your field and lead the way to innovative therapies, this position is for you! location: North Chicago, Illinois job type: Contract salary: &#x

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

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

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: 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

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 knowled