Asks for

The ad says“Support cGMP manufacturing and technology transfer to external contract manufacturers”
The ad says“Let’s do this. Let’s change the world. In this vital role you will join our Drug Substance Technologies - Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, the individual will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre-IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. The individual will be highly motivated and team-oriented with a proven track record of scientific innovation and achievement.”
The ad says“Let’s do this. Let’s change the world. In this vital role you will join our Drug Substance Technologies - Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, the individual will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre-IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. The individual will be highly motivated and team-oriented with a proven track record of scientific innovation and achievement.”
The ad says“Let’s do this. Let’s change the world. In this vital role you will join our Drug Substance Technologies - Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, the individual will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre-IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. The individual will be highly motivated and team-oriented with a proven track record of scientific innovation and achievement.”
The ad says“Let’s do this. Let’s change the world. In this vital role you will join our Drug Substance Technologies - Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, the individual will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre-IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. The individual will be highly motivated and team-oriented with a proven track record of scientific innovation and achievement.”

Career Category

Process Development

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career

Process Development Senior Scientist.

What you will do

Let’s do this. Let’s change the world. In this vital role you will join our Drug Substance Technologies - Synthetics (DSTS) group at either our Thousand Oaks, California or Cambridge, Massachusetts campus. In this dynamic role, the individual will drive innovative solutions to support manufacturing of therapeutic peptides at various stages of development; pre-IND through commercial production. The successful candidate will have a strong background and experience in industrialization of solid phase peptide synthesis, ideally complemented with experience in peptide purification, isolation, and characterization techniques. The individual will be highly motivated and team-oriented with a proven track record of scientific innovation and achievement.

Responsibilities:

Work effectively with a diverse team of synthetic chemists, chemical engineers and analytical chemists to develop scalable synthetic processes utilizing solid phase peptide synthesis
Drive technology innovation in solid-phase synthesis, purification, and characterization of synthetic peptides
Support cGMP manufacturing and technology transfer to external contract manufacturers
Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency
Ensure process performance through process understanding, modeling and characterization
Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
Work cross-functionally to deliver regulatory documents and support regulatory filings
Serve as a technical expert and keep current in the field of solid phase peptide synthesis
Work independently in advancing projects and studies within required deadlines.

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is an individual with these qualifications.

Basic Qualifications:

Doctorate degree PhD OR PharmD OR MD [and relevant post-doc where applicable]
OR
Master’s degree and 3 years of scientific experience
OR
Bachelor’s degree and 5 years of scientific experience

Preferred Qualifications:

Ph.D. in organic chemistry, biochemistry, or chemical engineering with expertise in synthetic peptide process development
Extensive hands-on expertise in the synthesis and purification of synthetic peptides produced by solid phase synthesis
Experience within the pharmaceutical/biotech industry developing solid phase peptide synthesis processes and scaling/transferring the process into GMP manufacturing
Proficiency in analytical characterization techniques such as Hydrophobic Interaction Chromatography (HIC)-HPLC, Size Exclusion Chromatography (SEC), Liquid Chromatography–Mass Spectrometry (LC-MS), Ion-Exchange (IEX), and Reversed Phase (RP)-HPLC.
Familiarity with laboratory automation, data analysis and visualization techniques and tools
Track record of peer-reviewed publications and research presentations
Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results
Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on complex projects
A research summary included with CV is strongly encouraged

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

Apply now and make a lasting impact with the Amgen team.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

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 and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

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, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided 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 accommodation.

Salary Range

126,066.05USD -170,559.95 USD