Biologics Manufacturing Technical Shift Lead
Biologics Manufacturing Technical Shift Lead
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Job Description
Our pipeline holds the promise of medicines and solutions that could treat 1.6 billion people. Learn more about bringing this promise to life.
Welcome to AbbVie!
AbbVie employees work every single day to discover and address many of the worlds most pressing health challenges. Our work helps people live better lives. When you have patients depending on your solutions you look for the best people and when we find them we make it our business to treat them well.
Our Westport team invites technical experts to join our NPI Biopharma operations team as our new Technical Shift Leader. In the role you will have the opportunity to lead an established team developing and guiding its members technically and professionally.
This is a shift based role you will be required to work 12hour shifts between days and nights on a monthly rotation.
Delivering high levels of customer service in this role you will ensure the quality of the product comply with all regulatory requirements achieve desired financial performance including cost reductions and build a highperformance culture for the team.
If great benefits a defined career path and worklife balance are important in your next career move then read on to find out more:
Key activities:
- Act as your teams key point of contact and technical expert.
- Lead and support your team to deliver compounding filling lyophilization equipment preparation formulation buffer preparation and processing activities in the biologics fillfinish facility to meet clearly stated operating objectives
- Coach & mentor your manufacturing team to maximize its effectiveness through clear and effective communication
- Promote and develop a culture of contamination control and compliance with aseptic best practices
- Communicate departmental goals to provide costeffective quality compliant products in a safe effective manner
- Collaborate 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 with team members project customers and others as appropriate.
- Drive operations excellence and key operations targets including OEE where applicable
- Provide direct interface as a subject matter expert with the QA department to interact with HPRA FDA and applicable health authorities and internal audits.
Qualifications :
So what will you need to be successful in this role
Education and preferred experience:
- Minimum of 5 years experience in batch processing automation commissioning and/or validation in an FDA/HHPRAregulated industry.
- Bachelors degree in chemistry pharmacy engineering or a related scientific field is required; an advanced degree is preferred.
- Detailed knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry is required for this role.
- Comprehensive understanding of contamination control principles and regulatory expectations for aseptic processing.
- Technical background in pharmaceutical biologics or similar industries.
- A minimum of 1 year of direct supervisory experience in a team environment is preferred
- Possess 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 the appropriate actions
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
