job summary: As a Second Shift Laboratory Technician working onsite in our production support QC Labs in Delaware, OH, you will be responsible for a variety of laboratory operations in quality assurance and research settings. In the QC team, you will validate raw material and finished good samples, identify result abnormalities, work to mitigate risk of defective material, and aid in the support of our continuous improvement and project initiatives. Labor
job summary: As a Second Shift Laboratory Technician working onsite in our production support QC Labs in Delaware, OH, you will be responsible for a variety of laboratory operations in quality assurance and research settings. In the QC team, you will validate raw material and finished good samples, identify result abnormalities, work to mitigate risk of defective material, and aid in the support of our continuous improvement and project initiatives. Labor
job summary: The Associate Quality Systems Specialist will be part of the Quality team and responsible for providing quality support for the site quality management system. This position ensures compliance of the quality system with regulations relevant to the business, including but not limited to, ISO13485, MDSAP, IVDD/IVDR, CFR 21, GxP, and the quality manual. This position is multi-disciplinary with opportunities to work on future products and current
job summary: The Associate Quality Systems Specialist will be part of the Quality team and responsible for providing quality support for the site quality management system. This position ensures compliance of the quality system with regulations relevant to the business, including but not limited to, ISO13485, MDSAP, IVDD/IVDR, CFR 21, GxP, and the quality manual. This position is multi-disciplinary with opportunities to work on future products and current
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. As the world's leading provider of diagnostic information services, our client is committed to sharing our
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. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: Sr. Manager, Clinical Supplies (Oral Solid Dose) 6 Month Contract (may extend or convert) Remote (75%) + 1 week / month in South SF Looking for West Coast Based Candidates (travel reimbursed) Must Have: Experience with oral tablet dosage form Phase 1 & Small Biotech experience APAC logistics experience is a plus Strong MS Excel skills Seeking a talented, independent, and highly motivated Senior Manager, Clinical Supplies Planning
job summary: Sr. Manager, Clinical Supplies (Oral Solid Dose) 6 Month Contract (may extend or convert) Remote (75%) + 1 week / month in South SF Looking for West Coast Based Candidates (travel reimbursed) Must Have: Experience with oral tablet dosage form Phase 1 & Small Biotech experience APAC logistics experience is a plus Strong MS Excel skills Seeking a talented, independent, and highly motivated Senior Manager, Clinical Supplies Planning
job summary: Shift: 2 week 12-hour shift cycle on either a day or night shift assignment. The Quality Control Scientist is responsible for performing multi-discipline analytical test methods for a variety of product lines to help achieve overall business objectives. This role is also responsible for maintaining the Product Stability, Product Retention, and Reverse Osmosis Water Quality Programs in accordance with the current regulatory guidelines. Ad
job summary: Shift: 2 week 12-hour shift cycle on either a day or night shift assignment. The Quality Control Scientist is responsible for performing multi-discipline analytical test methods for a variety of product lines to help achieve overall business objectives. This role is also responsible for maintaining the Product Stability, Product Retention, and Reverse Osmosis Water Quality Programs in accordance with the current regulatory guidelines. Ad
job summary: A top biopharma company in North Chicago, IL is looking for a Chemist II to join their analytical research team. In this hands-on lab role, you'll work Monday through Friday (8:00 AM - 5:00 PM), conducting experiments using advanced instrumentation like HPLC, GC, UV/VIS, and MS. You'll play a key part in supporting regulated research through precise data generation, method development, and clear documentation in a GMP/GLP environment. Ideal c
job summary: A top biopharma company in North Chicago, IL is looking for a Chemist II to join their analytical research team. In this hands-on lab role, you'll work Monday through Friday (8:00 AM - 5:00 PM), conducting experiments using advanced instrumentation like HPLC, GC, UV/VIS, and MS. You'll play a key part in supporting regulated research through precise data generation, method development, and clear documentation in a GMP/GLP environment. Ideal c
job summary: We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, supporting batch disposition of drug substance, ensuring that our products meet both Local and Global quality standards. location: Cambridge, Massachusetts job type: Contract salary: $59.00 - 61.63 per hour work hours: 9 to 5 education: Bachelors resp
job summary: We are seeking a highly skilled and experienced Senior QA Specialist to join our dynamic team. In this role, you will be responsible for overseeing the quality assurance process, supporting batch disposition of drug substance, ensuring that our products meet both Local and Global quality standards. location: Cambridge, Massachusetts job type: Contract salary: $59.00 - 61.63 per hour work hours: 9 to 5 education: Bachelors resp
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: 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: The Analytical Development team is seeking a highly creative and self-motivated candidate to join us for a 6-month contract. This role will support the development of small molecule and oligonucleotide drug substance and drug product by developing innovative analytical technologies and establishing control strategies. This role will be responsible for chromatographic method development guided by analytical quality by design (AQbD) principles
job summary: The Analytical Development team is seeking a highly creative and self-motivated candidate to join us for a 6-month contract. This role will support the development of small molecule and oligonucleotide drug substance and drug product by developing innovative analytical technologies and establishing control strategies. This role will be responsible for chromatographic method development guided by analytical quality by design (AQbD) principles
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: 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: The Analytical Development team is seeking a highly creative and self-motivated candidate to join us for a 6-month contract. This role will support the development of small molecule and oligonucleotide drug substance and drug product by developing innovative analytical technologies and establishing control strategies. This role will be responsible for chromatographic method development guided by analytical quality by design (AQbD) principles
job summary: The Analytical Development team is seeking a highly creative and self-motivated candidate to join us for a 6-month contract. This role will support the development of small molecule and oligonucleotide drug substance and drug product by developing innovative analytical technologies and establishing control strategies. This role will be responsible for chromatographic method development guided by analytical quality by design (AQbD) principles
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: 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: **Must have a PHD** **Must be familiar with mouse models** **Bilingual in Mandarin/English is Preferred** Randstad Life Sciences is working with a fast-growing biotech company with broad cutting-edge technologies. You will have the best opportunity to learn and utilize the science and business in the fields of immunooncology, animal model gene engineering, preclinical pharmacology, therapeutic antibody discovery, etc. The biggest advantage of
job summary: **Must have a PHD** **Must be familiar with mouse models** **Bilingual in Mandarin/English is Preferred** Randstad Life Sciences is working with a fast-growing biotech company with broad cutting-edge technologies. You will have the best opportunity to learn and utilize the science and business in the fields of immunooncology, animal model gene engineering, preclinical pharmacology, therapeutic antibody discovery, etc. The biggest advantage of
job summary: The Manager, Health Economics and Outcomes Research (HEOR) Oncology will join a high caliber team to execute HEOR strategies and tactics for Oncology and early pipeline assets in Oncology. The individual will support Oncology HEOR Strategy Lead/TA Head to ensure project plans integrate and align with the product strategic plans from matrix teams to maintain Company's leadership in Oncology. He/she helps to provide updates on execution of plan
job summary: The Manager, Health Economics and Outcomes Research (HEOR) Oncology will join a high caliber team to execute HEOR strategies and tactics for Oncology and early pipeline assets in Oncology. The individual will support Oncology HEOR Strategy Lead/TA Head to ensure project plans integrate and align with the product strategic plans from matrix teams to maintain Company's leadership in Oncology. He/she helps to provide updates on execution of plan
Must be able to work 4 AM-12:30 PM EST. We are seeking an experienced and proactive Customer Experience Specialist to join our team in a remote role that blends Customer Service and Customer Experience responsibilities. This position is critical to bridging operational support and long-term relationship management, primarily for our international customers, especially during early morning hours—but also extending support to other customer segments
Must be able to work 4 AM-12:30 PM EST. We are seeking an experienced and proactive Customer Experience Specialist to join our team in a remote role that blends Customer Service and Customer Experience responsibilities. This position is critical to bridging operational support and long-term relationship management, primarily for our international customers, especially during early morning hours—but also extending support to other customer segments
job summary: The Pivotal Drug Substance Technologies organization at Company develops, characterizes and supports clinical drug substance manufacturing processes for all late-stage programs in the Company portfolio. This lab-based position is located at our Cambridge, MA site. The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advanceme
job summary: The Pivotal Drug Substance Technologies organization at Company develops, characterizes and supports clinical drug substance manufacturing processes for all late-stage programs in the Company portfolio. This lab-based position is located at our Cambridge, MA site. The successful candidate will be responsible for support of the development, characterization, scale-up and support of upstream and downstream processes to enable clinical advanceme
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. Located in 100 countries, our longtime partner is known for being the world's largest producer of vaccines
job summary: This position is for a major Pharmaceutical company whose purpose is to transform the practice of medicine through breakthrough science and make a positive impact on our people and the communities we serve. Chasing the miracles of science to improve people's lives, Join us to make a positive impact in health care!! KEY SKILLS: Upstream group - cell culture development experienceBio reactor operations - Ambr15, ambr250 etc.Bench-scale experi
job summary: This position is for a major Pharmaceutical company whose purpose is to transform the practice of medicine through breakthrough science and make a positive impact on our people and the communities we serve. Chasing the miracles of science to improve people's lives, Join us to make a positive impact in health care!! KEY SKILLS: Upstream group - cell culture development experienceBio reactor operations - Ambr15, ambr250 etc.Bench-scale experi
job summary: The Senior Manager/Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with product label. Functions as the lead medical reviewer and sign-off for all promotional materials in designated area(s) of responsibility. Provides proactive guidance as needed for brand concepts and
job summary: The Senior Manager/Associate Director, Medical Communications Ad Promo, represents the Medical function in the Material Review Process to guarantee medical, clinical, and scientific data accuracy, relevance, objectivity, balance and alignment with product label. Functions as the lead medical reviewer and sign-off for all promotional materials in designated area(s) of responsibility. Provides proactive guidance as needed for brand concepts and
job summary: Immunology R&D organization is expanding its early discovery team at the Cambridge Research Center (CRC) in Cambridge, MA. We are seeking a highly motivated contractor/Scientist III to join the Tissue Homeostasis team. Immune mediated inflammatory diseases (IMIDs) pose a high burden on the healthcare system worldwide. Long term remission from IMIDs represents an unmet need. Current therapeutic options that target the stromal compartments are
job summary: Immunology R&D organization is expanding its early discovery team at the Cambridge Research Center (CRC) in Cambridge, MA. We are seeking a highly motivated contractor/Scientist III to join the Tissue Homeostasis team. Immune mediated inflammatory diseases (IMIDs) pose a high burden on the healthcare system worldwide. Long term remission from IMIDs represents an unmet need. Current therapeutic options that target the stromal compartments are
job summary: Immediate opening for a QA Frontline Associate (Night Shift) to support the Technical Operations team at a leading, global pharmaceutical company specializing in rare diseases. The Technical Operations group is responsible for creating drugs for use in clinical trials and for scaling production of those drugs for the commercial market. The QA Frontline team is committed to providing real time QA support to the manufacturing facilities by perf
job summary: Immediate opening for a QA Frontline Associate (Night Shift) to support the Technical Operations team at a leading, global pharmaceutical company specializing in rare diseases. The Technical Operations group is responsible for creating drugs for use in clinical trials and for scaling production of those drugs for the commercial market. The QA Frontline team is committed to providing real time QA support to the manufacturing facilities by perf
job summary: The Real World Evidence Leads are part of the Medical Evidence Generation function comprised of subject matter experts in evidence planning, study design and data interpretation. The function works to drive excellence in evidence planning and implement novel study design approaches to generate robust evidence to enhance understanding of unmet medical need; support patient and endpoint selection for Clinical studies; and inform clinical practi
job summary: The Real World Evidence Leads are part of the Medical Evidence Generation function comprised of subject matter experts in evidence planning, study design and data interpretation. The function works to drive excellence in evidence planning and implement novel study design approaches to generate robust evidence to enhance understanding of unmet medical need; support patient and endpoint selection for Clinical studies; and inform clinical practi
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. As the world's leading provider of diagnostic information services, our client is committed to sharing our
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. As the world's leading provider of diagnostic information services, our client is committed to sharing our
job summary: A research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Telecommute job type: Contract salary: $38 - 40 per hour work hour
job summary: A research-driven biopharmaceutical powerhouse focused on developing treatments for complex, hard-to-cure diseases. This esteemed company has brought 32 groundbreaking products to market, making a significant global impact. If you're ready to make your mark in the field and contribute to the future of innovative therapies, this is the opportunity for you! location: Telecommute job type: Contract salary: $38 - 40 per hour work hour
job summary: Join a leading team in Life Cycle Management (LCM) for Vision Care! Seeking a clinical expert with experience in EUMDR, medical / clinical writing, and ophthalmology / eye care to support regulatory documentation and post-production risk reviews. Location: Fort Worth, TX (Onsite preferred; candidates will be considered for remote work within CST or EST time zones). location: Fort Worth, Texas job type: Contract salary: $50.00 - 65.
job summary: Join a leading team in Life Cycle Management (LCM) for Vision Care! Seeking a clinical expert with experience in EUMDR, medical / clinical writing, and ophthalmology / eye care to support regulatory documentation and post-production risk reviews. Location: Fort Worth, TX (Onsite preferred; candidates will be considered for remote work within CST or EST time zones). location: Fort Worth, Texas job type: Contract salary: $50.00 - 65.
job summary: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 90% lab work including sample isolation, drying, and testing location: New
job summary: Perform experiments, organize data and analyze results under minimal supervision. With minimal supervision, plans, conducts or monitors experiments, records and organizes data, analyses results, generates robust and reliable data and/or Ensures that contracted studies are conducted in compliance with the respective protocol and applicable guidelines and regulations. 90% lab work including sample isolation, drying, and testing location: New
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 Scientist will work closely with a team of analytical chemists, organic chemists, engineers and formulators responsible for the technical aspects of developing the analytical to
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 Scientist will work closely with a team of analytical chemists, organic chemists, engineers and formulators responsible for the technical aspects of developing the analytical to
job summary: Regulatory Systems Manager (RIM / eCTD) Join a leading biopharma company driving critical initiatives in Regulatory Systems and Global Submission Management. We're seeking a detail-oriented consultant with hands-on expertise in RIM tools, eCTD submission oversight, and regulatory process optimization. This role sits at the intersection of Reg Ops, Tech Systems, and Process Excellence, supporting global teams through system implementation, doc
job summary: Regulatory Systems Manager (RIM / eCTD) Join a leading biopharma company driving critical initiatives in Regulatory Systems and Global Submission Management. We're seeking a detail-oriented consultant with hands-on expertise in RIM tools, eCTD submission oversight, and regulatory process optimization. This role sits at the intersection of Reg Ops, Tech Systems, and Process Excellence, supporting global teams through system implementation, doc
job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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 thei
job summary: As the world's largest staffing and recruitment agency in the world, we can commit to find 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 thei
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: 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