Job added in hotlist
Applied job
Contract job
90-day-old-job
part-time-job
Recruiter job
Employer job
Expanded search
Apply online not available
View more jobs in Thousand Oaks, CA
View more jobs in California

Job Details

Sr. Associate Regulatory Affairs CMC

Company name
Amgen, Inc.

Location
Thousand Oaks, CA

Apply for this job






3 hit(s)  

Profile

Amgen

Sr. Associate Regulatory Affairs CMC

in

Thousand Oaks

California

Amgen is a leading human therapeutics company in the biotechnology industry. For more than 35 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine.

As a Fortune 500 company serving millions of patients. Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness.

Amgen is searching for a Regulatory Affairs, Chemistry, Manufacturing and Controls Senior Associate (RA CMC) to work in their main corporate campus in Thousand Oaks, CA.

Regulatory Affairs, Chemistry, Manufacturing and Controls facilitates product development and global registration by developing and executing regulatory strategies and managing effective

regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle.

The RA CMC team generates the regulatory CMC strategy of the product/variation and provides feedback to the technical teams, including plans for execution of the strategy. The RA CMC Senior Associate will interface with the Amgen RA CMC leads, product teams, regional offices, and site teams for specific strategies or activities that impact a product.

The RA CMC Senior Associate will be responsible for varying levels of product support, including leading projects, based upon their experience level.

Additional responsibilities of the RA CMC Senior Associate include:

Contribute to the organization and preparation of CMC investigational product amendments and post-market supplements, organization and preparation CMC sections of IND annual reports and annual reports of minor changes for specific products to meet the strategy defined by the global CMC team.

Document CMC submissions and related communications in InSight Manager for Registrations.

Utilize InSight Manager for Registrations (IMR); archiving documents in document management systems.

Initiate and maintain CMC product timelines at the direction of product lead.

Process regulatory assessments of change control requests.

Train staff on select CMC procedures and systems.

Interface with regulatory operations staff.

Contribute to CMC product teams: interacts with authors/reviewers with respect to delivery of documents required for regulatory submissions.

Provide report status of activities and projects to teams and department.

Participate in cross-functional special project teams.

Contribute to the design and content development of department training programs.

Basic Qualifications:

Master's degree

OR

Bachelor's degree and 2 years of experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry

OR

Associate's degree and 6 years of experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry

OR

High school diploma / GED and 8 years of experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry

Preferred Qualifications:

BS degree in Life Science

Regulatory CMC experience

Process Development experience

Quality Assurance, or Analytical development experience

CMC-specific regulatory knowledge & experience

Strong & effective oral and written communication skills

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.

Company info

Amgen, Inc.
Website : http://www.amgen.com

Company Profile
Amgen discovers, develops, manufactures, and delivers innovative human therapeutics. A leader in biotechnology since 1980, Amgen was one of the first companies to realize the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics have changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses.

Similar Jobs:
Amgen Sr Manager EHSS - Product Stewardship Toxicology in Thousand Oaks California We are seeking an experienced toxicologist in the Product Stewardship group within our Environment, Health, Safety and Sustainability (EHSS) organi...
Sr Associate Research Operations
Location : Thousand Oaks, CA
The Discovery Research Operations Team within Discovery Research is responsible for business operations, budget management, portfolio and project management of Discovery pipeline projects, and continuous improvement initiatives. R...
Project Mgr
Location : Thousand Oaks, CA
Amgen Project Mgr in Thousand Oaks California Reporting into the Program Management Office within the Process Development Late-Stage and Life Cycle Management (LCM) organization, this role will support cross-functional teams from ...
EmploymentCrossing is great because it brings all of the jobs to one site. You don't have to go all over the place to find jobs.
Kim Bennett - Iowa,
  • All we do is research jobs.
  • Our team of researchers, programmers, and analysts find you jobs from over 1,000 career pages and other sources
  • Our members get more interviews and jobs than people who use "public job boards"
Shoot for the moon. Even if you miss it, you will land among the stars.
BiotechCrossing - #1 Job Aggregation and Private Job-Opening Research Service — The Most Quality Jobs Anywhere
BiotechCrossing is the first job consolidation service in the employment industry to seek to include every job that exists in the world.
Copyright © 2018 BiotechCrossing - All rights reserved. 168