**HOW MIGHT YOU DEFY IMAGINATION?**

You’ve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge you’ve worked hard to acquire and the passion you already have. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

Senior Associate Quality Assurance

**Live**

**What you will do**

Let’s do this. Let’s change the world. The AR30 Plant Quality Assurance (PQA) on-the-floor position will work directly with plant manufacturing and support groups for on-going bulk drug substance manufacturing and new product introduction-including development, clinical, launch and commercial operations. The 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 in regard to deviations, quality systems and compliance.

The Plant Quality Assurance team shift structure aligns with Manufacturing, which is a 12-hr rotating shift work schedule. For this specific day shift role, the shift pattern will be a 7AM – 7PM structure with a rotation that offers an average of 14 days on shift per month with every other weekend off.

+ 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.

+ 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.

+ Ensure facilities, equipment, materials, organization, processes and procedures align with cGMP practices and other applicable regulations.

+ Lead all aspects of and provide guidance during on-the-floor analytical testing.

+ Audit and inspection support.

+ Assess changes that could potentially impact product quality.

+ Support management updates (via various reporting tools) on metric performance to goals and alert senior management of quality, compliance, supply and safety risks.

+ Complete required assigned training for self to permit delivery of required tasks.

+ Perform training activities, as needed.

+ Support operational improvement initiatives, programs and projects.

**Win**

**What we expect of you**

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

**Basic Qualifications** **:**

+ Master’s Degree

+ OR

+ Bachelor’s Degree and 2 years of Quality experience

+ OR

+ Associate’s degree and 6 years of Quality experience

+ OR

+ High school diploma/GED and 8 years of Quality experience

**Preferred Qualifications** **:**

+ Strong cGMP and GDP behaviors

+ Demonstrated experience with deviations and CAPA records

+ Previous experience supporting GMP testing laboratories.

+ Knowledge of electronic systems including LIMS, Trackwise, and Maximo

+ Strong word processing, presentation, database and spreadsheet application skills

+ Strong organizational skills and ability to manage multiple tasks at one time

+ Ability to follow assignments through to completion and meet timelines

+ Exposure to regulatory agency inspectors or participation in regulatory agency audits.

+ Strong technical communication skills, both written and oral

+ Demonstrated ability to work as a great teammate and independently

**Thrive**

**Some of the vast rewards of working here**

As we work to develop treatments that take care of others, so we work to care for our teammates’ professional and personal growth and well-being.

+ Full support and career-development resources to expand your skills, enhance your expertise, and improve your potential along your career journey

+ A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act

+ Generous Total Rewards Plan—comprising health, finance and wealth, work/life balance, and career benefits—with compensation and benefits rated above 4 stars (out of 5) on Glassdoor

**Apply now**

**for a career that defies imagination**

Objects in your future are closer than they appear. Join us.

**careers.amgen.com**

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 uses its 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.

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