Visual Inspection Operator
Visual Inspection Operator
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
More than a job Its a chance to make a real difference
Working at AbbVie is more than a job. Its a career with meaning. A chance to make a difference in the world and in your life.
We are now recruiting Visual Inspection Operator join our diverse Packaging team in Westport on a fixed term contract. As our newest operator you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our packaging area. This role would suit career changers or anyone wishing to gain valuable experience within the pharmaceutical industry. You will operate highspeed equipment for the manual and/or automated assembly and packaging of pharmaceutical products ensuring adherence to specifications.
Is this a team you want to be part of Then read on
Key Responsibilities:
Core duties include:
- Perform all assigned duties in accordance with SOPs and cGMPs.
- Operate Core lines which includes coding and inspection.
- Operate Inspection and vacuum equipment.
- Complete in process check.
- Ensure all samples are handled as per procedure.
- Ensure line clearances are completed diligently and in accordance with department procedures and cGMP every time.
- Complete batch documentation associated with activity in compliance with cGMP
- Maintain a clean and organized workstation with good housekeeping.
- Complete all assigned duties according to departmental SOPs and cGMP.
- Remain current on effective procedures relating to the job through eLMS and on the job training.
- Complete and remain current with all required cGMP and safety training.
- Engage and be proactive in departmental incentives for safety quality and BBI program.
- Perform other duties as assigned.
Qualifications :
What you will need:
- Leaving cert or equivalent qualification required.
- Previous experience in Pharma OR GMP regulated industry
- Ability to build strong relationships and work within crossfunctional teams.
- Strong communication and presentations skills both written and oral. Articulate the quality requirements in a clear concise and persuasive manner.
- Aptitude to Plan & Organise work schedules with an analytical mindset.
- Good decision making to identify and understand issues problems and opportunities whilst providing a viable solution.
- 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.
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.
US & Puerto Rico only to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
No
Employment Type :
Fulltime
Employment Type
Full-time
