Salary
$83k – $113k per year
Location
Remote/Hybrid (Dublin, Ireland)
Seniority
Staff · 10+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Amgen is an American biotechnology company founded in Thousand Oaks in 1980 that became one of the first firms to turn recombinant protein research into large commercial medicines. Its history rests on Epogen and Neupogen, and its current portfolio spans bone health with Prolia and Evenity, inflammation with Otezla and Tezspire, cardiovascular disease with Repatha, oncology including the bispecific antibody Blincyto, and a biosimilars business built on its own manufacturing capacity. The company is listed on Nasdaq, is a component of the Dow Jones Industrial Average, and expanded further into rare disease through its acquisition of Horizon Therapeutics.
Career Category
ManufacturingJob Description
Specialist Manufacturing
Overview: Reporting to the Sr Manager Deviations Manufacturing Support, this position will manage the manufacturing deviations for Amgen Dun Laoghaire (ADL).
The Manufacturing Specialist (Investigation Lead) will be primarily responsible for leading investigations for fill/finish/inspection and packaging deviations. Specialists will also be involved in applying process, quality, compliance, and analytical knowledge to complete the following:
- Manage deviation investigations, including establishing investigation teams, leading root cause analysis, development of CAPAs, completing product impact assessments and writing compliant documentation of all findings.
- Clear and concise technical writing of complex investigations
- Drive improvements to the investigation process
- Present investigations to regulatory inspectors and internal auditors
- Clearly communicate investigation progress to impacted areas and leadership
- Coordinate and lead cross-functional teams through complex investigations, and complete tasks on-schedule.
- Project management of the investigations end to end
- Present complex topics to large and small groups at various levels and quickly understand and clearly communicate complex issues.
- Build effective relationships across functions.
- Navigate through ambiguity and provide a structured problem-solving approach.
- Able to apply inductive and deductive reasoning in the investigation process
Qualifications:
- Bachelor's Degree in Science or Engineering and 5+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (ie process development, engineering, quality) OR * Associate's Degree in Science or Engineering and 8+ years of directly related experience in a biotech/pharma manufacturing or manufacturing support role (ie process development, engineering, quality) * 10+ years directly related experience in a biotech/pharma manufacturing or manufacturing environment.
- Detailed technical understanding of fill/finish operations.
- Experience with compliance, problem-solving, root cause analysis, critical thinking, project management, and quality systems.
- Experience leading complex investigations.
- Experience participating in and leading cross-functional teams.
- Experience in managing multiple, competing priorities in a fast-paced environment.
- Experience presenting to inspectors during regulatory inspections and internal audits.
- Excellent technical writing.
- Excellent presentation and communication skills, ability to communicate and collaborate with technical and management staff.
- Ability to be flexible and manage change.
Personal Attributes
- Detail-oriented with a strong focus on quality and compliance.
- Ability to work under pressure and manage multiple priorities effectively.
- Proactive and self-motivated with a continuous improvement mindset.
- Flexible and adaptable, with the ability to lead a team through change.
Salary Range
71,721.30 EUR - 97,034.70 EURFree account
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