Page 3 - 167 contingency recruiter jobs found

job summary: As the world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment

job summary: We are seeking a highly motivated and detail-oriented Cell Culture Manufacturing Technician to join our cGMP commercial manufacturing facility. In this role, you will be responsible for the execution of standard operating procedures (SOPs) and batch records in the production of Flublok Drug Substance within the dedicated Cell Culture area, focusing on cell maintenance and virus stock generation. location: Pearl River, New York job type: C

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: We are seeking a highly motivated and detail-oriented Cell Culture Manufacturing Technician to join our cGMP commercial manufacturing facility. In this role, you will be responsible for the execution of standard operating procedures (SOPs) and batch records in the production of Flublok Drug Substance within the dedicated Cell Culture area, focusing on cell maintenance and virus stock generation. location: Pearl River, New York job type: C

job summary: We are seeking a highly motivated and detail-oriented Cell Culture Manufacturing Technician to join our cGMP commercial manufacturing facility. In this role, you will be responsible for the execution of standard operating procedures (SOPs) and batch records in the production of Flublok Drug Substance within the dedicated Cell Culture area, focusing on cell maintenance and virus stock generation. location: Pearl River, New York job type: C

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 world's largest staffing and recruitment agency, we are dedicated to helping you find the ideal role that offers growth and development opportunities within the life sciences sector. By working with a recruiter, you gain access to a vast network of leading employers and detailed insights into a wide range of positions. One of our premier partnerships is with a research-driven biopharmaceutical powerhouse focused on developing treatment

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: The Associate of Manufacturing will work in a dynamic production environment at the Company Thousand Oaks Site supporting development, clinical, and launch activities.Under general supervision, employee will perform operations in the Manufacturing area.Operations will be performed according to Standard Operating Procedures (SOPs). location: Newbury Park, California job type: Contract salary: $28.00 - 30.36 per hour work hours: 7

job summary: The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-process, final product testing and stability studies when needed. Applies job skills and company's policies and procedures to complete a variety of tasks of increased scope. Works on assignme

We are seeking a Distribution Specialist to oversee and coordinate distribution processes with third-party logistics (3PL) partners. This role ensures efficient order processing, accurate inventory management, and timely product delivery. The ideal candidate will work closely with warehouse teams, logistics providers, and internal departments to optimize operations and maintain compliance with industry standards.salary: $30 - $35 per hourshift: F

job summary: As a trusted staffing and recruitment partner, we are committed to connecting you with the perfect opportunity at a leading beverage company known for its diverse portfolio of iconic brands. Leveraging our extensive network, we provide access to top-tier roles that allow you to grow and make a meaningful impact in the food and beverage industry. This company is dedicated to innovation, sustainability, and quality, delivering refreshing and be

job summary: A great opportunity with a base salary ($47,000), commission and shift differential-potential, and full benefits to be a part of something that can make a real impact on peoples lives. Consider joining us as we work to provide living tissue donations to leaders in the wound care products industry. location: Hickory, North Carolina job type: Permanent work hours: 9 to 5 education: High School responsibilities: In this role you

job summary: Under general supervision, this position will perform routine procedures to support drug substance and drug product testing within Quality Control. Tasks may include but are not limited to performing sample collection, sample handling, testing equipment/laboratory support. location: West Greenwich, Rhode Island job type: Contract salary: $20 - 24 per hour work hours: 9 to 5 education: Bachelors responsibilities: Performing

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: 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: 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: **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: One of our premier partnerships is with 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: North Chicago, Illinois job type:

job summary: Job Description Intern, Global Patient and Site Engagement, will be a member of the GPSE team under GCDO. The Intern will work cross functionally across the portfolio supporting the vision to bring the patient and site voice into the clinical design and clinical trial working group teams, as well as study feasibility and global monitoring with activities related to site relationship management, strategic planning for new and ongoing studies,

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: We are seeking a Quality Control Associate to work in GMP Pharmaceutical Manufacturing, in support of the Microbiology and Environmental Monitoring groups, with our Global Pharmaceutical Client in Holly Springs, NC. Day to day responsibilities will include daily sampling of clean utilities water systems, routine sampling of compressed gas systems, and routine environmental monitoring of the classified areas in the manufacturing building. This

job summary: Shift: Monday - Friday 4:00pm -2:30am (Friday shift would be Overtime pay) Responsible 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 manuf

job summary: Join a Leading Biologics & Cell/Gene Therapy Company! We are seeking several QC Analysts to join a top-tier, biologics and cell & gene therapy company in a dynamic, fast-paced environment. The Quality Control Technical Transfer Analyst 3 will act as a team member of the Quality Control department to support production by contributing to the completion of the technical transfer activities. Also participate in quality testing for customer in-p

job summary: Immediate opportunity for a Process Development Associate with one of the world's leading biotechnology companies located in Thousand Oaks, CA. The ideal candidate is a recent Bachelor's or Master's graduate in a life sciences field with hands-on lab experience, particularly in protein purification techniques such as filtration, chromatography, and UF/DF. While mammalian cell culture experience is beneficial, a strong foundation in protein p

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: 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

Maintain cleanliness in manufacturing clean rooms, ensuring compliance with cGMP standards. Perform daily cleaning, waste removal, and PPE inventory management. Follow safety protocols, report issues, and assist in maintaining a hygienic production environment. Support clean room readiness for audits and operations.salary: $21.18 - $24.35 per hourshift: Firstwork hours: 6 AM - 2:30 PMeducation: High SchoolResponsibilitiesKey Responsibilities: P

job summary: This individual will support the PK/PD aspects of clinical studies (from protocol to CSR) and related regulatory submission activities. This role requires a strong pharmacokinetics/pharmacodynamics/pharmacometrics knowledge. #LI-KH1 location: Telecommute job type: Contract salary: $175 - 208 per hour work hours: 9 to 5 education: Doctorate responsibilities: Support PK/PD aspects of clinical studies, including synopsis/prot