Biotech Associate - 23 Month Fixed Term Contract
Tralee, County Kerry, Ireland · Vertrag
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- Erfahrung
- Beliebig
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- Stellenangebote
- 1
- Veröffentlicht
- vor 21 Stunden
- Work mode
- Im Büro
- Ausbildung
- Level 6 qualification in Engineering/Science or equivalent
- Eligibility
- Applicants with a Level 6 qualification in Engineering, Science, or an equivalent area, and preferably experience in cGMP, aseptic fill-finish, audits, or Lean/Six Sigma environments, are suitable for this position. The role is intended for candidates able to work onsite in Tralee and contribute in…
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Where you'll work
Stellenbeschreibung
Role Overview
Astellas is a global life sciences organization focused on creating meaningful value for patients through innovative science. Its work spans areas such as oncology, ophthalmology, urology, immunology, and women’s health, with an emphasis on addressing diseases that have significant unmet medical needs.
This opportunity is for people who want to contribute to patient outcomes, work in fast-moving settings, and bring fresh ideas to a purpose-driven team.
Location and Work Setting
This role is fully based onsite in Tralee, County Kerry, Ireland.
Role Purpose
The Biotech Associate will help manufacture pharmaceutical drug products in a cleanroom environment. The work includes aseptic filling and lyophilisation activities, with responsibility for meeting regulatory, quality, and site-specific standards.
The position also supports day-to-day manufacturing efficiency, offers input into improvement activities, and contributes value across production operations.
Key Duties
- Carry out cleanroom manufacturing tasks while meeting requirements for safety, quality, and productivity.
- Follow cGMP, ISO 14001, health and safety rules, and all relevant site procedures.
- Enter and retrieve information from computerized systems accurately while protecting data integrity.
- Identify and resolve equipment or material-related issues and take part in investigations when needed.
- Complete mandatory training and help maintain a strong culture of teamwork and safety.
- Assist with operational projects, validation work, and introductions of new products.
Required Education
A minimum Level 6 qualification in Engineering, Science, or an equivalent discipline is required.
Preferred Background
Experience working in cGMP settings, aseptic fill-finish operations, and audit environments would be an advantage. Familiarity with Lean or Six Sigma methods, especially Yellow Belt level or above, is also beneficial.
The role calls for someone with strong analytical ability, clear communication, solid interpersonal skills, and good organization. You should be comfortable working both independently and collaboratively, and be able to adapt as priorities change.
Values and Culture
Astellas highlights a culture built around impact, innovation, integrity, accountability, courage, urgency, outcome focus, and a shared approach known as One Astellas.
Benefits and Employer Highlights
- Opportunity to collaborate globally with leaders in the life sciences sector.
- Chance to contribute to therapies that have real-world patient impact.
- Exposure to innovation at the cutting edge of scientific development.
- A supportive environment that encourages growth, development, and ambition.
Equal Opportunity Statement
The employer considers all qualified applicants fairly, regardless of race, colour, religion, sex, national origin, disability, protected veteran status, or any other legally protected characteristic.
Recruitment Safety Notice
Applicants should be cautious of impersonation or fraudulent recruitment activity. Genuine communication will come from an official company LinkedIn profile or a verified company email address. Suspicious profiles or messages should be reported through LinkedIn Help.