Manufacturing Technician B2
Manufacturing Technician B2
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Job Description
People. Passion. Possibilities.
We are now recruiting for Manufacturing Technicians to join our diverse Biologics (B2) team in Westport on a fixedterm contract basis. As our newest technician you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding filling and capping of an aseptic product preparing autoclave loads testing filters preparing components documenting batch related activities housekeeping and environmental monitoring.
PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern covering days nights weekdays and weekends.
So are you ready to join the AbbVie team in Westport as our new Manufacturing Technician Then read on
Your Key Activities will include but are not limited to:
- Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system
- Perform activities associated with the compounding filling and capping of an aseptic process.
- Prepare components and equipment for processing into a Grade A environment.
- Accurately completing documentation on time accurately and legibly.
- Keeping the Manufacturing area tidy and clean.
- Review and update documentation as requested by the Production Manager
- Participating in root cause analysis and problemsolving.
- Completing compliant investigations and environmental excursions.
- Adhering to all company standards in the area of safety housekeeping and quality notifying management of any discrepancies.
- Follow gowning procedures on entry to areas
- Report any machine issues to the Production Manager and the maintenance department.
- Setup clean and maintain equipment
- Transfer of waste material out of the cleanroom areas
- Perform environmental monitoring
- Participate in media runs
- Adhere to and support all EHS & E standards procedures and policies.
Qualifications :
Qualifications
Education and Experience:
- Leaving cert or equivalent qualification required
- 3rd level qualification in a Science/Engineering or related discipline is preferred but not requied
- 23 years GMP experience preferably Aseptic/Sterile Manufacturing in a cleanroom environment
- Experience working with SAP within a similar industry is preferable.
- Strong communication documentation and IT skills.
- Ability to multitask and adapt in a fastpaced environment.
- Outstanding organization flexibility and time management skills
- High attention to detail and methodical in approach
- Ability to build strong relationships and work within crossfunctional teams.
- Adaptability to work in a fast dynamic environment whilst adjusting readily to meet unexpected constraints.
- Drive high energy maturity and ability to work under pressure deliver results and overcome obstacles.
- Team player who can collaborate with others to achieve organizational targets and goals.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives serving our community and embracing diversity and inclusion. It is AbbVies policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race color religion national origin age sex (including pregnancy) physical or mental disability medical condition genetic information gender identity or expression sexual orientation marital status status as a protected veteran or any other legally protected group status.
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US & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
