Manufacturing Shift Manager - Biologics
Manufacturing Shift Manager - Biologics
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Job Description
Do your best work at AbbVieas part of a brilliant curious team
We are currently sourcing an experienced Manufacturing Shift Manager to join our Biologics Manufacturing team in AbbVie Westport on a permanent basis. In this role you will lead and facilitate the safe operations of the 24/7 Biologics manufacturing team in a biopharmaceutical processing facility in line with all safety regulatory and operational requirements.
This is a shift based role you will be required to work 12hour shifts between days and nights on a monthly rotation.
As part of your new and exciting role you will assure the longterm effectiveness of the team: deliver high levels of customer service ensure quality of product and services comply with all regulatory requirements achieve desired financial performance including cost reductions and build a culture of high performance for the team
Does this interest to you then read on....
Heres a snapshot of your key responsibilities for this role:
- Act as key point of technical contact for aseptic fill finish activities.
- Supervision and of compounding filling lyophilization equipment preparation formulation buffer preparation and support processing activities in the biologics fill finish facility to meet clearly stated operating objectives
- You will lead coach & mentor your manufacturing team across a 12hour rotating shift to maximize the effectiveness through clear and effective communication of task details and goals to their team members to allow the biologics technicians to work effectively
- As part of this diverse and inclusive team you will conduct on the floor promotion of a culture of contamination control and compliance with aseptic best practice.
- Communicate the departmental goals to provide cost effective quality compliant products in a safe effective manner
- We believe in collaboration so in this role you will liaise with program management supply chain technical operations quality and engineering groups to ensure effective planning scheduling and of commercial and NPI clinical manufacturing
- Resolve operations/project issues by working with team members project customers and others as appropriate.
- Responsible for driving operations excellences and Key operations targets including OEE where applicable
- Provides direct interface as a subject matter expert with QA department to interaction with HPRA FDA and applicable health authority and internal audits
Qualifications :
So what do you need to do this role
- Minimum of 3 years experience in batch processing automation commissioning and validation in an FDA/HPRA regulated industry.
- A minimum of 1 year team direct supervisory experience in a team environment
- 3rd level qualification in a Science Engineering or related scientific field advanced degree is preferred
- Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
- Comprehensive understanding of the principles of contamination control and regulatory expectations for aseptic processing.
- Has a technical background in pharmaceutical biologics or similar industries
- Flexibility with working 12hour shift rotating between days and nights on a monthly rotation
- Possess a strong technical knowledge and application of concepts practices and procedures. Works on problems of complex scope where analysis of situations or data involves multiple competing factors. Exercises judgment and advises management as to the appropriate actions
So are you ready now lead this ambitious and diverse Manufacturing team Apply today!
Its important to remember AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
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
