at Amgen
Location
US - Massachusetts - Cambridge
Compensation
$108k USD
Posted
6 days ago
Market range · company + function + seniority
p25 · target · p75 · n=133
Posted $108k · well below market
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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 Sr Associate
Let’s do this. Let’s change the world. In this vital role you will be responsible for the invention, development, and implementation of drug substance manufacturing processes and technologies to advance Amgen's exciting portfolio of synthetic and hybrid assets. Process chemistry senior associates in our team collaborate with chemists, process engineers, and attribute scientists to support drug substance manufacturing from early to late-stage development. The successful candidate will be a highly motivated and team-oriented individual with prior lab-based research experience in organic chemistry or biochemistry/chemical biology.
Work within a drug substance team comprised of chemists, engineers, and attribute scientists to solve technical problems
Contribute to the invention of synthetic routes and development of safe, robust, and cost-effective processes to manufacture synthetic and hybrid drug substances
Support cGMP manufacturing and technology transfer to our internal manufacturing facilities and external contract manufacturers
Support process characterization activities, including process understanding and modeling
Contribute to drug substance development teams by providing experimental results, technical updates, documentation, data interpretation, recommendations, etc.
Works regularly with a supervisor to advance projects within required deadlines.
Work cross-functionally to deliver regulatory documents and support regulatory filings
Follows good laboratory documentation practices and standard operating procedures
We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a leader with these qualifications.
Basic Qualifications:
Master’s degree
OR
Bachelor’s degree and 2 years of Process Development experience
OR
Associate’s degree and 4 years of Process Development experience
OR
High school diploma / GED and 6 years of Process Development experience
Preferred Qualifications:
M.S. in organic chemistry or biochemistry/chemical biology with a specialization in synthetic methodology, total synthesis, peptide/protein chemistry, oligonucleotide chemistry, or synthetic/conjugation chemistry
Prior research experience in the biopharmaceutical or pharmaceutical industry
Demonstrated ability to work in a chemistry laboratory with minimal supervision
Ability to independently collect and interpret analytical results (NMR, HPLC, MS, IR, Raman, etc)
Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on projects
A research summary included with CV is strongly encouraged
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:
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.
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 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
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