Specialist QA @ Amgen | Jobright.ai
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Amgen · 1 day ago

Specialist QA

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BiotechnologyHealth Care
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Comp. & Benefits
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H1B Sponsor Likelynote

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Responsibilities

Review and approve controlled documents, including Standard Operating Procedures, Validation Protocols, Validation Reports, Electronic Master Batch Records etc.
Provide quality oversight for quality records including deviations/CAPAs, technical change controls and work orders assuring adherence to procedural requirements and confirming assessments and evaluations of different partners are complete and accurate
Ensure that all activities & related documentation for facilities, equipment, materials and processes align with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and Controls.
Own quality related Standard Operating Procedures, Work Instructions, Forms and Methods
Provide quality oversight for manufacturing and be responsible for batch disposition.
Provide quality and compliance expertise & guidance and agrees on strategies related to the design, installation, commissioning & qualification and process qualification of the new facility, equipment and information systems.
Support and represent Quality during audits and inspections; may directly interact with regulatory agencies during on-site inspections.
Support Lean Transformation and Operational Excellence initiatives

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

GMP regulationsQuality OperationsQuality oversightRoot Cause AnalysisValidation documentationLeadership capabilitiesDigital innovationQuality engineering

Required

Doctorate degree
Or
Master’s degree and 2 years of Quality and/or Manufacturing experience
Or
Bachelor’s degree and 4 years of Quality and/or Manufacturing experience
Or
Associate’s degree and 8 years of Quality and/or Manufacturing experience
Or
High school diploma / GED and 10 years of Quality and/or Manufacturing experience

Preferred

Master's or Bachelor’s Degree in Science
Educated in a science field with 5 years of experience in GMP/GCP operations or similarly regulated industry
Affinity with digital innovation, data sciences and Quality engineering
Experience in review/approval validation documentation
Ability to complete tasks autonomously, providing updates to senior management, and identifying potential issues
Ability in problem solving and experience in managing Root Cause Analysis / Deviation investigations
Experience working with dynamic cross-functional teams and abilities in decision making
Strong organizational skills, including ability to follow assignments through to completion
Strong leadership capabilities and experience applying GMP requirements in an operational setting
Ability to independently interact with various levels, drives tasks to completion, and is a self-starter.

Benefits

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, including remote and hybrid work arrangements, where possible

Company

Amgen is a biotechnology company that develops and manufactures human therapeutics for various illnesses and diseases.

H1B Sponsorship

Amgen has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (349)
2022 (523)

Funding

Current Stage
Public Company
Total Funding
$28.5B
2022-12-12Post Ipo Debt· $28.5B
1983-06-17IPO

Leadership Team

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Robert Bradway
Chairman and Chief Executive Officer
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Howard Chang
SVP of Research
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Company data provided by crunchbase
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