Specialist QA 1

At Amgen if you feel like youre part of something bigger its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980 weve helped pioneer the world of biotech in our fight against the worlds 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 youll 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 youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Lets do this. Lets change the this vital role you will serve as Quality Assurance Specialist responsible for Plant Quality Assurance (PQA). This position provides the opportunity to work directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. This is a unique opportunity to foster a strong partnership and learning environment between Manufacturing and Quality staff. Amgens Quality Assurance Specialist provides coaching guidance and direction to Manufacturing Quality Control Supply Chain and Facilities & Engineering staff in regard to compliance and quality systems. Responsibilities include the following:

• Responsible for providing Quality oversight to ensure that Operations products are manufactured tested stored and distributed according to current Good Manufacturing Practices (cGMP) Good Distribution 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.
• Performs review and approval of cGMP processes procedures documents and records including but not limited to Batch Production Records Deviations work-orders Change Controls and Corrective Action/Preventative Actions (CAPA)
• Author/review/approve quality documents such as SOPs user requirements risk assessments training materials engineering documents automation documents environmental qualification protocols/reports validation protocols/reports.
• Oversee and provide guidance during on-the-floor analytical testing.
• Ensure that production records and testing results are complete accurate and documented according to written procedures and cGMP requirements.
• 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.

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

Basic Qualifications:

• High school diploma / GED and 10 years of Quality Manufacturing Process Development or Process Engineering experience OR
• Associates degree and 8 years of Quality Manufacturing Process Development or Process Engineering experience OR
• Bachelors degree and 4 years of Quality Manufacturing Process Development or Process Engineering experience OR
• Masters degree and 2 years of Quality Manufacturing Process Development or Process Engineering experience OR
• Doctorate degree

Preferred Qualifications:

• Educational background in Life Science or Engineering.
• Understanding of regulations standards and guidelines that apply to cGMP biotech manufacturing in a multi-product environment including familiarity of cell banking cell culture and protein purification operations.
• Experience with Quality Management Systems including Exceptions Change Control Risk Management and Disposition
• Familiarity with Computer / Automation systems (MES Delta-V PI data historian)
• Capability to build strong and collaborative partnerships with client groups and influence changes in practices to ensure compliant operations.
• Demonstrated ability in problem solving and experience in managing Root Cause Analysis / Deviation investigations.
• Experience participating in managing and responding to health authority inspections partner and corporate audits.
• Strong organizational skills including ability to follow assignments through to completion.
• Excellent written and verbal communication skills.

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 well support your journey every step of the way.

The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $xxxxxx.00 to $xxxxxx.00. 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.

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