Amgen Inc.

Director Process Development: Pivotal Drug Substance

Posted on: 12 Feb 2021

Cambridge, MA

Job Description

HOW MIGHT YOU DEFY IMAGINATION?

If you feel like youre part of something bigger, its because you are. At Amgen our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. Its time for a career you can be proud of. Join us.

Director, Process Development: Pivotal Drug Substance

Cambridge, MA

Live

What you will do

Lets do this. Lets change the world. In this vital role, you will lead with an entrepreneurial approach and ambition to drive innovation and develop efficiency through exploration of process, technology and capacity improvement opportunities. The Director confirms the groups outputs are safe, compliant, and aligned with Pivotal drug substance goals.

This leader develops a team within Pivotal Drug Substance who are responsible for the late stage development of biologics programs as well as advancing technology development. The programs represent a wide range of biologics molecules including mAbs, BiTEs, biosimilars, bispecifics, and other novel modalities. As the primary process development point of contact with key leadership partners in Manufacturing and Quality, you will ensure that drug substance process development deliverables including: commercial process development and process characterization; development and implementation of new technologies; process control strategy for Process Performance Qualification (PPQ); regulatory filing and response to questions are managed and executed.

Responsibilities

* Lead diverse high performing multi-functional drug substance team that is comprised of an integrated cell culture and purification disciplines located in both Cambridge, MA and Thousand Oaks, CA.

* Develop staff and manage portfolio resourcing.

* Advance integrated holistic drug substance processes for Amgens multi-modal portfolio (mAbs, BiTEs, bispecifics, and biosimilars) for late stage clinical and commercial implementation. This includes commercial process development, process characterization, lifecycle management, development of control strategies as well as supporting transfer of process to internal and external manufacturing network.

* Author global filings including IND/INDa/MA and responding to Regulatory questions.

* Ideation, development, and deployment of differentiating technologies and establishing a culture of innovation.

* Contribute to Amgens external eminence at scientific and regulatory conferences and other industry forums.

* Serve as member of Drug Substance Technology extended leadership team and advancing the process development function. Work in partnership with management to develop plans that support the directions of the business, plans implementation of major change efforts and contributes to organization thought leadership.

Win

What we expect of you

Basic Qualifications:

Doctorate degree and 4 years of Scientific, Process Development and/or Technical Services experience

OR

Masters degree and 8 years of Scientific, Process Development and/or Technical Services experience

OR

Bachelors degree and 10 years of Scientific, Process Development and/or Technical Services experience

AND

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

We are all different, yet we all use our unique contributions to serve patients. The top tier Project Controls professional we seek is experienced with these qualifications:

* PhD degree in Biochemistry, Biochemical or Chemical Engineering

* 10+ years of experience in biopharmaceutical process development and global regulatory expectations

* Demonstrated ability in providing scientific and engineering expertise to multi-functional teams in Process Development, Manufacturing, Quality and Supply Chain to advance complex projects to completion and to interface on technical problem resolution

* Ability to compile and statistically analyze data, draw appropriate conclusions and make presentations to cross-functional audience and senior management

* Detailed understanding of all stages of Late Stage process development for biologics: commercial process development, process characterization, process design, Process Performance Qualification (PPQ), regulatory filing and response

* Experience in authoring marketing authorization applications

* Strong technical communication skills, both written and verbal, to interact effectively with all stakeholders

* Practical knowledge of the technologies related to mammalian cell culture, purification, automation, and validation

* Active participation in the scientific community through a record of peer-reviewed publications and/or patents, as well as active participation in industry forums and/or conferences

* Established success developing staff, including effective feedback and coaching or mentoring

* Exemplify collaborative experience and ability to effectively work through others

Thrive

What you can expect of us

As we work to develop treatments that take care of others, so we work to care for our teammates professional and personal growth and well-being.

* Vast opportunities to learn and move up and across our global organization

* Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

* Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Apply now

for a career that defies imagination

In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.

careers.amgen.com

Equal Opportunity Statement

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

We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.

Amgen Inc.

Oakland, CA

Amgen Inc. discovers, develops, manufactures, and delivers human therapeutics worldwide. It offers products for the treatment of oncology/hematology, cardiovascular, inflammation, bone health, and neuroscience. The company’s products include Enbrel to treat plaque psoriasis, rheumatoid arthritis, and psoriatic arthritis; Neulasta, a pegylated protein to treat cancer patients; Prolia to treat postmenopausal women with osteoporosis; Aranesp to treat anemia; Xgeva for skeletal-related events prevention; Sensipar/Mimpara products to treat sHPT in chronic kidney disease; and EPOGEN to treat a lower-than-normal number of red blood cells.

It also markets other products in various markets, including Kyprolis, Nplate, Vectibix, Repatha, NEUPOGEN, Parsabiv, Blincyto, Aimovig, Imlygic, Corlanor, Kanjintitm, and Amgevitatm. Amgen Inc. serves healthcare providers, including physicians or their clinics, dialysis centers, hospitals, and pharmacies. It distributes its products through pharmaceutical wholesale distributors, as well as direct-to-consumer channels. The company has collaborative agreements with Novartis; UCB; Bayer HealthCare Pharmaceuticals Inc.; and DaVita Inc. Amgen Inc. was founded in 1980 and is headquartered in Thousand Oaks, California.

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