Product Quality Associate Director

Amgen; United States; On-site; USD 180,000 - 230,000; Full time

Job summary

Amgen's Product Quality team is seeking an enthusiastic, highly motivated, and team-oriented leader for the position of Product Quality Associate Director. You will provide technical leadership within the Product Quality Team and partner with Quality Assurance, Regulatory, Process Development and Manufacturing to advance programs.

The role covers product filings, investigations, and in-process controls, with emphasis on strategy, risk assessment, and cross-functional collaboration.

Qualifications

• Demonstrated ability to communicate complex information orally and in writing to leadership, peers and regulatory agencies.
• Strong knowledge of cGMP and international regulatory expectations.
• Robust data management and organization skills with attention to detail.

Responsibilities

• Define and deliver Product Quality milestones within timelines for the Product Delivery Team.
• Lead cross-functional discussions for strategies within the Product Quality Team and related functions.
• Coordinate activities to ensure program deliverables across QA, Stability, Process Development and Manufacturing.
• Author regulatory filing sections and support inspections and regulatory submissions.

Skills

Communication

cGMP knowledge

Data management

Education

Doctorate degree

Master's degree

Bachelor's degree

Associate's degree

High school diploma

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.

Product Quality Associate Director

What You Will Do

Let’s do this. Let’s change the world. Amgen’s corporate Product Quality team is seeking an enthusiastic, highly motivated, and team-oriented leader for the position of Product Quality Associate Director. As Product Quality Associate Director, you will provide technical expertise and leadership within a Product Quality Team. You will engage with Product Quality, International Distribution Quality, Quality Control, Regulatory, Process Development, Quality Assurance and other departments on a variety of activities. Such activities include product filings, program improvements, and investigations associated with product manufacturing, in-process controls, analytical methods, specifications, stability, reference standards, importation testing, change control, regulatory submissions and inspections.

Primary Responsibilities include the following

• Ensures Product Quality deliverables are appropriately defined within timelines across the Product Delivery Team. Deliverables are clear with priorities set based on program guidance.
• Coordinates discussion and leads decision making for strategies and activities supported within the Product Quality Team (Quality Assurance, Stability, Process Development, and other functions as needed) for programs they support.
• Accomplishes results by leading activities across the product quality team and with cross-functional SMEs for programs they support.
• Provide effective, cross-functional Quality leadership, and influence and support program deliverables for late phase and commercial programs, including actions required for the annual product reviews, specifications, comparability, and stability programs; site and method transfers; product quality impact assessments; and author PQ-owned regulatory filing sections and RTQs
• Provide subject matter expertise and strategic influence for 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

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.

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 and 3 years of Quality, Operations, Scientific, or Manufacturing experience OR
• Master’s degree and 5 years of Quality, Operations, Scientific, or Manufacturing experience OR
• Bachelor’s degree and 7 years of Quality, Operations, Scientific, or Manufacturing experience OR
• Associate’s degree and 12 years of Quality, Operations, Scientific, or Manufacturing experience OR
• High school diploma / GED and 14 years of Quality, Operations, Scientific, or Manufacturing experience

Preferred Qualifications

• B.S. or advanced degree in chemistry, biochemistry, biology, or a related pharmaceutical sciences field and experience with increasing responsibility in a quality, analytical development, process development, pharmaceutics, regulatory, or manufacturing environment
• 6+ years working in a regulated environment (either direct GMP or technical support) with experience working with biologic products
• 1+ year experience with authoring or review of market applications, IND, supplements or similar regulatory documentation

Functional Skills

Must-Have Skills

• Demonstrate proficiency in oral and written communication of complex information to Product Quality leadership, peers and regulatory agencies
• Demonstrate proficiency in knowledge of cGMP and international regulatory expectations
• Strong scientific data management and organization skills with attention to detail

Soft Skills

• Analytical and problem-solving skills
• Ability to work effectively with global, virtual teams
• High degree of initiative and self-motivation
• Ability to manage multiple priorities successfully, react quickly to address urgent requests and meet challenging timelines
• Team-oriented, with a focus on achieving team goals

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.

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.