New · posted Nov 8
Amgen · Biotechnology
Manager Quality Assurance - PQA
- Holly Springs, NC
- On-site
- Full-time
- Manager
What you need
4 ways to qualify
High school
+ 12 years of experience
High school diploma / GED and 12 years of Quality experience OR
- or
Associate
+ 10 years of experience
Associate’s degree and 10 years of Quality experience OR
- or
Bachelor’s
+ 5 years of experience
Bachelor’s degree and 5 years of Quality experience OR
- or
Master’s
+ 3 years of experience
Master’s degree and 3 years of Quality experience OR
Basic Qualifications
- Doctorate degree
In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above
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.
Preferred Qualificationsnice to have
- Scientific degree in Life Sciences or Physical Sciences or Applied Engineering or Manufacturing Technologies
- Experience and training in CDOCS, Trackwise, Maximo, LIMS, MES Werum and other systems and applications
- Experience in managing multiple, competing priorities in a fast-paced environment
- Experience leading and/or managing teams
- Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff.
- Quality assurance or combination of quality and manufacturing experience in the biotechnology/pharmaceutical industry
- Experience and systems knowledge in areas of manufacturing investigations, Corrective Actions/Preventative Actions (CAPA), product release, validation and/or change control
- Experience in regulations, standards and guidelines that apply to biotech manufacturing in a multi-product environment
- Ability to develop meaningful team and staff goals, manage performance and coach and develop staff
- Ability to manage timelines and deliver results to meet or exceed department and company goals and objectives
- Ability to communicate clearly, facilitate discussions and present to audiences at all levels of a site organization
- Ability to solve complex problems and evaluate scientific data. Decisive and independent risk-based decision-making ability on the floor to support manufacturing needs.
Skills named in this posting
What you'll do
Let’s do this. Let’s change the world. In this vital role you will be the Manager Quality Assurance for the PQA team and will work directly with plant manufacturing and engineering staff during the Amgen North Carolina (ANC) facility startup and transition to on-going bulk drug substance manufacturing, including development, clinical, launch and commercial operations.
The Manager Quality Assurance will hire, train, develop, and manage Quality Assurance professionals to successfully deliver on role to support (Good Manufacturing Practices) GMP Manufacturing and to oversee and manage change in an effective, efficient and compliant manner. This includes partnership with Manufacturing, Facilities & Engineering and other support functions providing coaching, guidance and direction in regards to deviations, quality systems and compliance aspects.
The initial focus of this role will be on the ANC startup to prepare the new facility for Operational Readiness.
* 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. After the facility startup phase, the successful incumbent will be expected to transition to a shift working schedule, including weekends, and is intended to serve 1st shift hours (very early morning through mid-afternoon). Specific hours will be determined based on operational needs.
- Oversee ANC startup activities for facilities, utilities, equipment, systems and processes
- with alignment and integration into the Amgen Quality Systems, including: Interview
- candidates to build the ANC PQA team, Author/review/approve quality documents, related
- to: Standard Operating Procedures (SOPs), user requirements, risk assessments, training
- materials, engineering documents, automation documents, commissioning test
- protocols/reports, environmental & utility qualification protocols/reports, validation
- protocols/reports, Oversee execution of, and change management related to, the following:
- factory acceptance, commissioning tests, facility qualifications and validation
- activities.
- Manage a team of PQA staff and their daily operations (verify training, schedules, ongoing tasks, prioritization and support needed)
- Oversee staff/team performance
- Prioritize and support staff development
- 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
- Participate in Inspection Readiness program activities to ensure facilities, equipment, materials, organization, processes and procedures comply with cGMP practices and other applicable regulations
- Develop or contribute to the development of procedures and standards by which others will
- operate
- Develop and communicate goals and objectives to staff and key partners
- Monitor goal performance and coordinate action for improvement of team and overall Plant
- Quality Assurance (PQA) performance by championing department operational excellence and Lean efforts.
- Assist project teams in establishing priorities, project timelines and in securing resources
- Actively represent Quality Assurance on incident triage teams or support efforts by providing
- guidance and/or technical leadership
- Partner with internal personnel at various management levels to resolve issues, establish
- direction, obtain resources, and drive change
- Review and approve operational and product manufacturing procedures, process validation
- protocols and reports for manufacturing processes, environmental characterization reports
- and change control documents.
- Support site audits and inspections.
Pay and benefits
$118,000 – $160,000 a year
Employer provided118,235.00USD -159,965.00 USD
What you can expect of us
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.
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:
Where you'll work
Holly Springs, NCOn-siteOpen in Maps (opens in a new tab)
More jobs in Holly Springs, NCWorking conditions
Career Category
Quality
careers.amgen.com
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.
From the posting
About Amgen
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. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. 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.
Equal opportunity, accessibility and legal noticesAmgen's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 8, 2026
Salary intelligence
How the pay compares
This role's midpoint is 2% below the US median for Quality Assurance roles at this level.
This roleEmployer provided
Manager roles in the US57 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $118,000 | — | $160,000 |
| All US (middle half) | $116,000 | $142,000 | $162,500 |
This role: Amgen's own published range. Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, November 8, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Quality Assurance
The general path across 345 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Amgen's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 53 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership18
- Documentation and SOPs12
- GMP and compliance6
- Validation and qualification5
- Quality systems and risk5
- Clinical trial conduct3
- Lab testing and methods2
- Investigations and CAPA2
- Data and digital systems1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Quality Assurance work in biotechnology, led by the three this posting names, each linked to the agency or standards body that publishes it.
- FDA21 CFR Parts 210 and 211(official source, opens in a new tab)FDA current good manufacturing practice for finished pharmaceuticalsNamed in the posting
- FDAFDA process validation guidance(official source, opens in a new tab)Process Validation: General Principles and PracticesNamed in the posting
- EUEU Good Distribution Practice(official source, opens in a new tab)Guidelines on good distribution practice of medicinal products for human useNamed in the posting
- ICHICH Q10(official source, opens in a new tab)The pharmaceutical quality system across the product lifecycle
- ICHICH Q9(R1)(official source, opens in a new tab)Quality risk management
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- ICHICH Q7(official source, opens in a new tab)Good manufacturing practice for active pharmaceutical ingredients
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- FDA21 CFR 314.70(official source, opens in a new tab)Supplements and other changes to an approved application (post-approval CMC changes)
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- ISPEISPE GAMP 5(official source, opens in a new tab)A risk-based approach to compliant GxP computerized systems
- FDAFDA data integrity guidance(official source, opens in a new tab)Data Integrity and Compliance With Drug CGMP: Questions and Answers
- EUEU GMP (EudraLex Volume 4)(official source, opens in a new tab)The EU's good manufacturing practice rules, including Annex 1 sterile and Annex 15 validation
- FDAFDA quality agreements guidance(official source, opens in a new tab)Contract Manufacturing Arrangements for Drugs: Quality Agreements
- FDA21 CFR Part 7(official source, opens in a new tab)FDA enforcement policy, including product recalls
- FDA21 CFR Parts 600 to 680(official source, opens in a new tab)FDA standards for biological products, from licensing to lot release
Company hiring pulse
Amgen on Regulatory Jobs
- 55
- Open roles
- 55
- Distinct roles
- 5
- Locations
By discipline
- Quality31 55%
- Regulatory13 23%
- Clinical12 21%
By level
- Manager20 36%
- Senior & Principal17 30%
- Director13 23%
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Manager Quality Assurance - PQA at Amgen
Applications close November 20. $118K–$160K a year, employer provided.