Thousand Oaks
Biotech Jobs in Thousand Oaks, California
47 Thousand Oaks, CA Biotech jobs found on Monster.
Description Seeking a qualified individual to provide scientific support for development, qualification, transfer and oversight of clinical flow cytometry based biomarker assays. Experience: Minimum of a Bachelors degree (or equivalent) in Biological Sciences with specialization in Immunology, Molecular Biology, Biochemistry or another relevant area. Basic flow cytometry experience, preferably wit...
Description Seeking a motivated individual to function as a member of a commercial drug product team. The position will focus on evaluating the impact of drug product formulation and fill/finish manufacturing process on product quality attributes of the protein, antibody or peptides. The successful candidate will conceive, design, implement and execute specific scientific experiments, which contri...
Yoh has a long term contract opportunity for an Associate Scientist II to join our client, the world leader in the pharmaceutical industry, located in Thousand Oaks, CA. Job Responsibilities: - Monitors or follows established experimental design and protocols and performs routine tasks and studies to obtain reproducible and reliable results with limited supervision - Plans, monitors or conducts, a...
Yoh has a long term contract opportunity for a Senior Associate Scientist to join our client, the world leader in the pharmaceutical industry, located in Thousand Oaks, CA. Job Responsibilities: - Evaluate the impact of drug product formulation and fill/finish manufacturing process on product quality attributes of the protein, antibody or peptides. - Conceive, design, implement and execute specifi...
Description Job Posting Title Senior Associate Career Category Quality (Quality Assurance) Provide swing shift (1:30-10:30 PM or later) Quality Assurance oversight for bulk manufacturing operations for clinical biopharmaceutical products. Shift may change based upon need. Ensure compliance to GMP regulations for area operations and associated processes. Typical tasks include: Support investigation...
Job_Other_Compensation: Up to $50.00 Job Description: Top Biotech Company in Thousand Oaks is hiring a Clinical Data Manager III Several Month long contract! The position is responsible for leading clinical data management (CDM) operational activities in one or more therapeutic areas. Responsibilities: 1) Manage the creation, execution and maintenance of Data Management Plans in support of clinica...
This is a leadership position within Amgen’s Process & Product Development organization. This Principal Scientist will be responsible for leading a group of scientists that develop early and late phase recovery and purification processes for Amgen’s large molecule pipeline. Responsibilities include purification process development that utilizes harvest, clarification, chromatography, and/or filtra...
To support the regulatory, safety and product development needs of the Amgen Biosimilars Operating Unit through detailed development and implementation of global regulatory strategies, submissions, and plans. - Coordination of global regulatory CMC activities relevant to the successful execution and implementation of biosimilar CMC regulatory strategies and plans - Development of CMC and analytica...
The position's primary responsibilities may include oversight of the development and qualification of analytical methods for proteins and leading state-of-the-art characterization of protein therapeutic candidates. Other responsibilities include communicating project updates as appropriate, and generation of regulatory submissions, publications or patents. The candidate will actively chart the cou...
Amgen is investing in creating a new start-to-finish drug product facility. This facility will encompass operations from UF/DF to fill/finish and house high, throughput, state-of-the art analytical technologies to add new capability and higher capacity to perform drug product development. This Principal Scientist position is to lead the technical operations in the drug product workstation, part of...
The purpose of this group is to provide strategic direction for product and disease communications and activities by interpreting current FDA regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public. This position is primarily responsible to formulate and communicate the regulatory promotional position for approved products Key A...
This position can be located at either of our Thousand Oaks, CA or Rockville, MD locations. The Senior Manager will provide strategic direction for product and disease communications and activities by interpreting current FDA regulatory environment to ensure truthful and non-misleading communication to health care community, patients, and the public. This position is primarily responsible to formu...
Amgen, Thousand Oaks, CA is seeking a highly motivated and team-oriented candidate for the position of Senior Scientist in the Biosimilar Business Unit Process Development group in Analytical Sciences. The Senior Scientist will support the development of several biosimilar projects including the planning and execution of analytical similarity strategy. The individual will effectively interface wit...
This position is responsible for conducting internal compliance investigations globally within Amgen’s Worldwide Compliance & Business Ethics function. This includes: • Preparing written investigation plans; • Reviewing relevant documents and evidence; • Conducting witness interviews; • Analyzing facts and reaching conclusions as to whether or not compliance violations occurred and, if so, conduct...
The GCP Compliance Strategy Lead is a global role based in Thousand Oaks, US. The GCP Compliance Strategy Lead reports to the GCP Compliance Strategy Director in Global R&D Compliance and Audit (GRDCA); The role of the GCP Compliance Strategy Lead is to provide proactive GCP compliance oversight and guidance to assigned functional areas and stakeholder groups within the R&D organization. This incl...
Infosphere Clinical Research, Inc. (ICR) is currently seeking an experienced clinical research coordinator for our fast growing company. The primary focus of this role will be to coordinate and manage clinical pharmaceutical research studies conducted at ICR while following applicable federal regulations/ICH guidelines, medical ethics, HIPAA rules, GCPs, IRB requirements, ICRs SOPs, and Sponsor/Co...
There's quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, it's a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we seek a Positive Certigying Scientist. Tuesday-Saturday - hours are TBD Main Job Duties: Revi...
There's quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, it's a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we seek a Clinical Laboratory Scientist Level 1 in our Serology Department. Basic Purpose: Repo...
There's quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, it's a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we seek a Clinical Laboratory Scientist Level 1 in our Hematology Department. Basic Purpose: Re...
There's quite a distance between wondering and knowing. And for patients waiting for answers to important health questions, it's a road they want to travel as quickly as possible. At Quest Diagnostics Incorporated, we understand urgency. But more than speed, we focus our energies on accuracy. Currently, we seek a Clinical Laboratory Scientist Level 1 in our Hematology Department. Basic Purpose: Re...
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©2013 Monster - All Rights Reserved U.S. Patents No. 5,832,497; 7,599,930 B1; 7,827,125 and 7,836,060 MWW - Looking for Monster Cable? - V: 2013.1.5.22-202