Page 2 - 46 employee relations director jobs found in california

job summary: The QC Critical Reagents Analyst is responsible for maintaining the Critical Reagents program for commercial products in the global network, including but not limited to reagent preparation, maintaining material inventory, generating technical documentation, and supplying materials to the global testing network. Materials in the Critical Reagents program include qualified reagents, reference standards, custom reagents, analytical cell banks a

job summary: Are you passionate about small molecule drug development and eager to apply your expertise in synthetic drugs? We're seeking a highly motivated Associate Scientist to join the Pivotal Synthetic Drug Product Team at one of the world's leading biotechnnology companies located in Thousand Oaks, CA. We're looking for candidates with a strong academic foundation in Chemical Engineering, Pharmaceutical Engineering, Organic Chemistry, or related fi

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: Immediate openings for 15-20+ Bioprocess / Biomanufacturing Associates with a leading, global company focused on gene therapy innovation, located in the North Bay region of the Bay area. Shifts: All shifts/days available: Manufacturing operations are 24/7 5 x 8 hour shift4 x 10 hour shift3 x 12 and 4x12 hour shifts Shift pay rates are as follows: 1st shift: 7am-3pm2nd shift: 3pm-11pm (10% shift differential added to the pay rate)3rd s

job summary: Immediate opportunity for four (4) MCS Manufacturing Manufacturing Associates to perform visual inspection at one of the world's leading biotechnology companies located in Thousand Oaks, CA. This MCS Manufacturing Associate position will be focused on manual visual inspection. If candidate excels in inspection there may be opportunities to expand training to analytical testing. This role is supporting the Drug Product Supply, Manufacturing

job summary: Immediate opportunity for four (4) MCS Manufacturing Manufacturing Associates to perform visual inspection at one of the world's leading biotechnology companies located in Thousand Oaks, CA. This MCS Manufacturing Associate position will be focused on manual visual inspection. If candidate excels in inspection there may be opportunities to expand training to analytical testing. This role is supporting the Drug Product Supply, Manufacturing

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 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: 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: One of the world's leading companies in the fields of health and nutrition, delivering breakthrough innovations in healthcare and agriculture. Contribute to a world in which diseases are not only treated but effectively prevented or cured, in which people can take better care of their own health needs, Join this team which is Guided by the purpose "Science for a better life" This role requires employees to be fully vaccinated against COVID-19

job summary: Regulatory Medical Writer - Protocols/Immunology We are seeking an experienced Regulatory Medical Writer to support a small biotech on a part-time contract basis. This role will focus on developing and revising protocols and amendments for three Phase III immunology studies. Contract: Through 12/31/25 Hours: PT~10-20 hours per week Rate: $110-120 per hour w2 only Therapeutic Area: Immunology Focus: Phase III protocols & amendments loc

job summary: Our purpose is to solve the toughest problems in life science by collaborating with the global scientific community - and through that, we aim to accelerate access to better health for people everywhere. We provide scientists and engineers with best-in-class lab materials, technologies and services. We now have a broad portfolio of 300,000 products, an expanded global footprint and an industry-leading eCommerce platform. We are dedicated to m

job summary: The 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 product a

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: Immediate opportunity for an experienced, Specialist Product Quality, to manage change control, deviations, and compliance records for biologics and synthetic chemical manufacturing. The Specialist Product Quality will collaborate cross-functionally with Supply Chain, Manufacturing, Quality Control, Regulatory, and other teams to ensure quality and compliance. Key Responsibilities include: Own and review change control, deviation records, a