153 call center jobs found

We’re looking for an enthusiastic and customer-focused Customer Service Representative to join our dynamic team! If you have 3 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: This is a high level contract role, requiring Direct Global Regulatory Labeling Operations Project Management experience in the Pharma/Biotech industry, as deep knowledge of pharmaceutical labeling regulations, compliance, and processes are critical for this role. The Labeling Project Manager is responsible for all activities associated with the development, creation and execution of labeling for assigned product lines for domestic and/or i

Onsite in Billerica, MA 9:00 AM-6:30 PM, with some weekend work. Provide oversight and technical guidance for daily Outbound Shipment operations ensuring the safe, legal tender of products to our carriers. Responsible to ensure compliance with all relevant distribution laws and regulations. Accountable for the accuracy and traceability for the products in preparation for the shipment process to the transportation carrier network. salary: $25 - &#

job summary: As a QA Analyst I, supporting the QC, analysis and test services team, you will be responsible for the in-process and final product quality analyses/inspection in compliance with standards and regulatory requirements within the manufacturing facility at Fort Worth, Texas. location: Fort Worth, Texas job type: Contract salary: $20.00 - 22.88 per hour work hours: 7 to 3 education: Bachelors responsibilities: Interprets and ev

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: Global Labeling Manager - Regulatory Affairs REMOTE | EST Hours | RATE (TBD awaiting confirmation) 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-qu

job summary: The Biologics Drug Product Development team develops antibody drug conjugates (ADC) and other biologics by state-of-the-art formulation and analytical technologies. We create valuable intellectual property through new formulation compositions, cost effective manufacturing processes and prepare and defend CMC (Chemistry, Manufacturing and Control) regulatory content. We are looking for a highly motivated person to support Developability and Fo

job summary: The Analytical Development-Early Stage group within Biologics ARD is responsible for support of programs that are preparing for FIH clinical studies. The team leads Stage 1 method development, optimization, and validation. In collaboration with cross-functional partners, the team supports early phase formulation and process development studies. Key deliverables include product control strategies informed by analytical data and method understa

job summary: The Facilities Mechanical Technician is primarily responsible for maintaining all building, utility and operations equipment for our Pharmaceutical Diagnostics client. This position is responsible for assisting in the development and coordination of mechanical, controls, and maintenance services to assure equipment reliability. This position will require the use of technical manuals, on-line resources, and OEM representatives to maintain equi

A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician 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 fo

job summary: A precision medicine company using innovative science to improve patient care and solve serious and costly problems. We are working to narrow the gap between scientific innovation and clinical decision- If you're passionate about having an impact on medicine, we'd love to hear from you. location: Telecommute job type: Permanent salary: $130,000 - 140,000 per year work hours: 9 to 5 education: Bachelors responsibilities: This

job summary: Discovery Biotherapeutics and Genetic Medicine at Company is seeking a highly motivated research scientist to join the Cell and Functional Biology group. In this role, you will be responsible for the execution of cell- and protein- based functional characterization assays for lead antibody identification/optimization and collaborating to generate stage-gate appropriate in vitro / cellular / in vivo data packages supporting PoC. The ideal cand

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

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: 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: 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: We are seeking a bilingual (Mandarin and English) Content Marketing Scientist who is a recent graduate that has Postdoctoral fellow experience in Immunology/Pharmacology. Qualified applicants should be familiar with writing for the web, email marketing, and blog strategy and execution. This role will produce high-quality content to increase brand awareness, execute marketing campaigns, drive engagement, and support inbound lead generation. Th

A Global Biotech/Pharma located in Round Lake, IL is seeking a Manufacturing Technician 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 fo

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

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 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 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: 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: 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: 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: Medical Writer (Medical Communications - Oncology) Contract ~20-30 hrs/wk | EST core business hours Are you a seasoned Medical Writer with deep Oncology expertise looking to make a meaningful impact in a dynamic, fast-paced, and collaborative startup environment? We're supporting an award-winning, in-house agency at a global pharmaceutical company-recognized for its innovation and execution-and we're looking for flexible, detail-obsessed med

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

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