Dir Product Quality

Amgen Inc. Thousand Oaks , CA 91360

Posted 2 weeks ago

Career CategoryQualityJob Description

The Product Quality Director is the champion for a product team as the Product Quality Leader (referred to as PQL), providing technical expertise, strategic and project leadership to the Product Quality (PQ) organization. The PQL has responsibility for working with PQ staff and executive leadership, International Quality, Quality Control, Contract Manufacturing Quality, Regulatory, Process Development, Quality Assurance, and other functional areas on the resolution of issues associated with process/manufacturing, in process controls, analytical methods, specifications, reference standards, importation testing, investigations, change control, regulatory submissions and inspections. The PQL has responsibility for driving change to implement operationally efficient processes and corporate alignment across international sites. As a leader in Product Quality, the successful candidate is expected to have experience, knowledge and understanding of large and/or small molecule development and commercial lifecycle maintenance, product stability programs, regulatory filings, risk assessment, and Amgen Quality Management Systems.

Amgen offers the opportunity to be at the interface between research, global development and manufacturing to ensure that our molecules become medicines. Many of the technologies we're employing are not only new to Amgen but are new to the industry as a whole. Help us to pave new roads for helping patients.

This role is directly responsible for the product quality and related activities (e.g., comparability, specifications, stability, annual product review) in support of the Product Development Team (PDT). The PQL provides scientific oversight for the product quality of pivotal and/or commercial product(s) including timely product data review, ownership of GMP documents and regulatory filing sections, execution of transactions in relevant GMP system (EDMQ, change control, etc), and support for regulatory audits and responses to questions. The individual is directly responsible to lead a Product Quality Team (PQT), including oversight of the product stability programs, providing indirect staff management and guidance to members of the PQT.

Key Responsibilities include:

  • Provide effective, cross-functional quality leadership, and manage multiple, complex long-term PDT deliverables for late phase and commercial programs, including actions required for the PQT/APR; specification, comparability, and stability programs; site and method transfers; product quality impact statements for NCs; and PQ owned regulatory filing sections and RTQs

  • Provide expertise in science and risk-based evaluation of complex process and product quality data, including ability to develop patient-oriented strategies that account for business needs and/or provide novel solutions to complex issues

  • Demonstrate proficiency in oral and written communication of complex information to Amgen leadership, peers and regulatory agencies including communications associated with inspectional activities

  • Demonstrate proficiency in knowledge of cGMP and international regulatory expectations

  • Understand and respond to the impact of emerging scientific/technical trends and their implications for Amgen

  • Actively mentor new and existing team members to develop Product Quality core skills

Basic Qualifications:

Doctorate Degree & 4 years of directly related experience

OR

Master's Degree & 8 years of Quality, Operations, Scientific, or Manufacturing experience

OR

Bachelor's Degree & 10 years of Quality, Operations, Scientific, or Manufacturing experience

AND
4 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources

Preferred Qualifications:

  • Advanced degree in chemistry, biochemistry, biology, or a related biotechnology sciences field

  • Expertise in the areas of protein and small molecule analysis and industry regulations

  • 8+ years of pharmaceutical experience with increasing responsibility in a quality, analytical development, process development, pharmaceutics, regulatory, or manufacturing environment experience

  • 6+ years working in a regulated environment (direct GMP)

  • 5+ years managing staff with increasing responsibilities and larger groups

  • 2+ years experience as a PQL, technical expert or product champion

  • 1+ years of experience with authoring or review of regulatory filing or similar regulatory documentation.

  • 1+ years of experience supporting non-conformance investigations, authoring, reviewing and defending critical product impacting non-conformances

  • Experience in Project Management in support of product development

  • Knowledge of protein and small molecule quality, compliance and regulatory requirements

  • Knowledge of analytical techniques used for protein molecule product quality control

  • Understanding of drug substance and drug product development and manufacturing

  • Strong leadership and management skills

  • General knowledge of cGMP and filing regulations, practices, and trends pertaining to the manufacture and testing of pharmaceuticals

  • Previous experience working on a cross-functional team in a matrix environment

  • Excellent written and verbal communication skills, including facilitation and presentation skills

Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

We understand that to successfully sustain and grow as a global enterprise and deliver for patients we must ensure a diverse and inclusive work environment.

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.

Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

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.

.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Sr Quality Associate Product Complaints Lab

Amgen Inc.

Posted 3 days ago

VIEW JOBS 3/21/2019 12:00:00 AM 2019-06-19T00:00 Career CategoryQualityJob Description Job Summary The Sr. Quality Associate Product Complaints Lab executes day to day operations in the product complaint laboratory and ensures the daily workload is executed (e.g. PMs, calibrations, and general servicing). Responsibilities include: * Applies analytical skills to evaluate product complaint return samples using multiple sources of information * Interprets SOP requirements * Identifies product quality and safety risk with product complaint return samples * Provides technical advice on complaint investigations * Provides subject matter experts assessments (Return Unit Inspections) * Partners with FPT on return sample evaluations, establishing inspection criteria and inspection method. * Perform return inspection for complaints and product security inspections Basic Qualifications: * Master's degree OR * Bachelor's degree and 2 years of directly related experience OR * Associate's degree and 6 years of directly related experience OR * High school diploma / GED and 8 years of directly related experience Preferred Qualifications: * Quality and manufacturing experience in biotech or pharmaceutical industry * Bachelor's Degree in a Science Field * Ability to successfully manage workload to timelines * Familiarity with basic project management tools * Demonstrated ability to consistently deliver on-time, and high-quality results * Ability to operate in a matrix or team environment * Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes) Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. 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. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. 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. . Amgen Inc. Thousand Oaks CA

Dir Product Quality

Amgen Inc.