Sr Associate Project Manager - Remote

Socket.dev; United States; Hybrid; USD 89,000 - 121,000; Full time

Benefits offered by this job

Remote/hybrid work options

Total rewards plan

Job summary

Amgen is seeking a Sr Associate Project Manager to join the Biosimilars Business Unit PD/Operations. You will manage analytical similarity sample management from development through regulatory submission and support cross-functional teams to keep biosimilar programs on track.

The role requires strong organizational and communication skills, experience in project management, and familiarity with ELN/LIMS systems; remote and hybrid work options are available, and the company offers a comprehensive

Qualifications

• Master’s degree ORBachelor’s degree with 2 years of Project Management experience ORAssociate’s degree with 6 years of Project Management experience ORHigh school diploma/GED with 8 years of Project Management experience
• Experience coordinating scientific or regulatory documents throughout the document lifecycle
• Strong organizational and multitasking abilities in a fast paced environment

Responsibilities

• Provide project management to technical teams developing biosimilar candidates through to regulatory approval
• Manage biosimilar business unit analytical similarity sample management
• Collaborate with cross functional teams including Similarity Team, CRG, Data Management and scientific staff to plan and maintain inventory
• Coordinate logistics for distribution of samples for testing and communicate incoming data
• Create ELN entries for sample submission and generate lot numbers and data retrievals in LIMS
• Assist staff with ELN updates, database queries, data review and verification with Data Management
• Assist in data verification for internal documents and regulatory filings
• Format documents to Amgen style guidelines and standards

Job description

Career Category

Project Management

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.

Sr Associate Project Manager

Live

What you will do

Let’s do this. Let’s change the world. The Project Manager will work in the Biosimilars Business Unit PD/Operation group, responsible for analytical similarity sample management of biosimilar programs to commercialization.

Manages/optimizes routine workflows to support technical teams responsible for developing biosimilar candidates through to regulatory approval. Regularly interacts with management and cross‑functional contacts. Skills: strong analytical skills; strong MS Word and MS Excel skills; knowledge of good data practices/data verification, understanding of systems for sharing and collaboration; excellent communication skills.

Responsibilities

• Provide project management to technical teams responsible for developing biosimilar candidates through to regulatory approval
• Provide project management of biosimilar business unit (BBU) analytical similarity sample management.
• Collaborate closely with cross‑functional team including Similarity Team, Critical Regents Group (CRG), Data Management, and scientific staff to plan and maintain inventory.
• Manage logistics for distribution of samples for testing and communicate incoming data for biosimilar projects.
• Create electronic laboratory notebooks (ELN) for sample submission.
• Generate lot number, sample ID, and retrieving data in QC LIMS.
• Assist BBU staff with navigating ELN software and placing work orders for ELN updates. Database queries of LIMS, ELN and other databases including the compiling and organizing data to review, verify independently or in coordination with Data Management.
• Retrieve and organize data for review with Data Management
• Document archival in controlled document repository
• Provide data verification as needed for internal documents and regulatory filings in controlled document system.
• Utilize a strong foundation in scientific principles to thoroughly review regulatory documents and accurately determine the data elements that require verification in accordance with established protocols.
• Collaborate with cross‑functional teams to ensure the completion and accuracy of the data verification processes.
• Assist in formatting documents in compliance with Amgen's internal style guidelines and standards.

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The Sr Associate Project Manager we seek is a motivated professional with these qualifications.

Basic Qualifications:

• Master’s degree OR

• Bachelor’s degree and 2 years of Project Management experience OR

• Associate’s degree and 6 years of Project Management experience OR

• High school diploma / GED and 8 years of Project Management experience

Preferred Qualifications:

• Experience supporting pharmaceutical research and development or nonclinical drug development programs within the biotechnology, pharmaceutical, or life sciences industry.

• Experience working with document management systems, collaboration platforms, and project management tools.

• Experience coordinating scientific or regulatory documents throughout the document lifecycle.

• Strong organizational skills with the ability to manage multiple priorities in a dynamic, fast‑paced environment.

• Bachelor's or advanced degree in a life science discipline, regulatory affairs, business, or a related field.

Thrive

What you can expect from 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 and bi‑annual company‑wide shutdowns
• Flexible work models, including remote and hybrid work arrangements, where possible

.

Salary Range

89,168.40USD -120,639.60 USD