• Amgen
  • Shannock , RI
  • Information Technology
  • Full-Time
  • 70C N Rd

The Quality Assurance Specialist will be responsible for Quality Validation, PQA On the Floor and Off the Floor activities, and may include Raw Materials and Drug Substance Disposition for Quality Assurance 1st Shift/administrative shift. 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. The focus of this role will be to support Quality Validation activities but may include PQA On the Floor and Off the Floor, Raw Materials and Drug Substance Disposition activities as required by the needs of the department. Amgen's Quality Assurance Shift 1/Administrative shift provides coaching, guidance and direction to Manufacturing, Quality Control, Process Development, Supply Chain and Facilities & Engineering staff regarding compliance and quality systems.

Responsibilities include the following:

Provide 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, procedures and products comply with cGMP practices and other applicable regulations.

Quality review and approve Validation Documents including: DT, CRSIQ/OQ, RTM, FT/FTF, protocols, and reports.

Perform ownership, QA review, and QA approval of cGMP processes, procedures, documents and records, including but not limited to Nonconformance, Corrective Action/Preventative Actions (CAPA), Change Control records, validations, and Raw Materials and Drug Substance documentation.

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.

Establish and enable LEAN practices.

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.

Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements.

Alert senior management of quality, compliance, supply and safety risks.

Complete required assigned training to permit execution of required tasks.

Drive operational improvement initiatives, programs and projects.

Basic Qualifications

Doctorate degree

OR

Master's degree and 3 years of Quality, Manufacturing, Process Development or Process Engineering experience

OR

Bachelor's degree and 5 years of Quality, Manufacturing, Process Development or Process Engineering experience

OR

Associate's degree and 10 years of Quality, Manufacturing, Process Development or Process Engineering experience

OR

High school diploma / GED and 12 years of Quality, Manufacturing, Process Development or Process Engineering experience

Preferred Qualifications

Scientific degree in Life Sciences or Physical Sciences or Applied Engineering or Manufacturing Technologies

Previous QA oversight of manufacturing, analytical and engineering activities

Experience in investigations, change controls, and CAPAs processes system knowledge

Direct Validation experience with pharmaceutical or biopharmaceutical processes

Ability to evaluate compliance issues and interact with regulatory inspectors

Experience and training in EDMQ, Trackwise, Maximo, LIMS

Experience in managing multiple, competing priorities in a fast-paced environment

Experience leading and/or managing teams

Direct bulk drug substance and drug product experience

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.

Ability to solve complex problems and make scientific risk-based decisions

Experience representing Amgen while interacting with representatives of regulatory agencies

Experience of trending analysis

Demonstrated proficiency using Excel, Word and Power Point

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 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.

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, or disability status.
Associated topics: automation, performance test, qa, quality, quality assurance, quality assurance lead, software quality, software quality engineer, test engineer, tester

* The salary listed in the header is an estimate based on salary data for similar jobs in the same area. Salary or compensation data found in the job description is accurate.

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