Sr Associate QA - PQA - 1st Shift

Amgen Inc.; Holly Springs (NC); On-site; USD 82,000 - 111,000; Full time

Benefits offered by this job

Retirement plan

Medical insurance

Vision and dental coverage

Disability insurance

Bonus program

Stock-based incentives

Flexible work options

Job summary

Amgen Inc. is seeking a Sr Associate Quality Assurance for the PQA team to ensure real-time quality oversight across manufacturing and new product introduction activities.

The role focuses on coaching, compliance, and collaboration between Manufacturing and Quality groups to uphold cGMP standards. The position requires shift flexibility, including late afternoons and nights, and offers opportunities within a leading biotechnology environment with a strong focus on patient impact.

Qualifications

• Experience in quality, manufacturing and regulated environments is required.
• Knowledge of cGMP and GDP behaviors is preferred.
• Experience supporting GMP testing laboratories is advantageous.
• Strong organizational skills with the ability to manage multiple tasks and meet deadlines.

Responsibilities

• Staff for the PQA team on-site.
• Support 24/7 operations and shift transitions (including late afternoons and nights).
• Provide quality oversight for new product introduction, deviations, CAPA, change control, and validations.
• Collaborate with Manufacturing and Quality to ensure compliance and timely task completion.

Education

High school/GED + 4 years of Quality, manufacturing and/or other regulated environment work experience

Associate’s + 2 years of Quality, manufacturing and/or other regulated environment work experience

Bachelor’s + 6 months of Quality, manufacturing and/or other regulated environment work experience

Master’s

Tools

Microsoft Office

EBR/MES

Delta V

Electronic Quality Systems

Job description

Career Category Quality 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 QUALITY ASSURANCE – PQA - 1ST SHIFT

What you will do

Let’s do this. Let’s change the world. In this vital role you will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction‑including development, clinical, and commercial operations. The Sr Associate PQA position will facilitate real-time decision making to ensure adherence to GMP quality requirements. This is a unique opportunity to maintain and further build a strong partnership and learning environment between Manufacturing and Quality staff providing coaching, guidance and direction for manufacturing events, deviations, quality systems and compliance.

• Staff for the PQA team are on-site workers.

The Plant Quality Assurance team will work different shift structures to provide ongoing support to our functional teams and 24/7 operations. There are several openings for this position. The successful incumbent will be expected to transition to a shift working schedule, to include late afternoons and nights. Support ANC facility commissioning and qualification and manufacturing Analytical Equipment Qualification and Validation activities, perform quality review and approval of documents according to project timelines. Quality oversight of new product introduction activities covering facilities, utilities, equipment, systems and process with alignment into the Amgen Quality Systems. May include support on commissioning and qualification and validation activities in addition to new document support. Provide on‑going Quality oversight to ensure products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP) and other applicable regulations. Ensure that facilities, equipment, materials, organization, processes, and procedures comply with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other controls. Drive closure/completion (including review and approve) of cGMP processes, procedures, documents and records, including but not limited to deviations, investigations, corrective action/preventative actions (CAPA), change control records and validations. Ensure production and testing records/results are complete, accurate, and documented according to procedures, GDP and cGMP requirements. Oversee and provide guidance during on‑the‑floor analytical testing. Ensure that changes that could potentially impact product quality are assessed according to procedures. Ensure that deviations from established procedures are investigated and documented per procedures. Alert senior management of quality, compliance, supply and safety risks. Provide project management support, leading efforts to drive timely achievement of tasks and develop strategies for system implementation. Identification and implementation of continuous improvement opportunities within our processes and systems. Support and represent PQA during audits and inspections; may directly interact with regulatory agencies during on‑site inspections.

What we expect of you

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

• High school/GED + 4 years of Quality, manufacturing and/or other regulated environment work experience
• Associate’s + 2 years of Quality, manufacturing and/or other regulated environment work experience
• Bachelor’s + 6 months of Quality, manufacturing and/or other regulated environment work experience
• Master’s

Preferred Qualifications

• Strong cGMP and GDP behaviors
• Experience in biotechnology or pharmaceutical plant start up
• Knowledge and process experience within a cGMP manufacturing facility or other highly regulated environment
• Technical understanding of upstream and/or downstream manufacturing within a biotechnology production operation
• Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems
• Demonstrated experience with deviations records
• Experience supporting GMP testing laboratories.
• Strong organizational skills and ability to manage multiple tasks at one time, ability to follow assignments through to completion and meet timelines
• Strong communication skills, both written and oral
• Demonstrated ability to work as a team player and independently

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.

… 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.

Salary Range 82,081.95USD -111,052.05 USD

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 82,081.95USD -111,052.05 USD Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its biologics manufacturing expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

For more information, visit www.amgen.com and follow us on www.twitter.com/amgen