AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
The primary function is to provide the plant with effective and that are performed according to requirements with review/verification of laboratory investigations, problems or audit if required.
- Develops and maintains Environmental and Utilities monitoring program
- Write/revises procedures as necessary and make recommendations for process improvement
- Lead and responsible for EM track and trend discussion/report
- Ensure that all test equipment is used and maintained correctly
- Acts as an SME for simple to complex instruments and techniques where needed
- Lead and perform any method transfer or method validation protocols or equipment qualifications and support the transfer of new products
- Understands, implements and maintains cGMP and 6S concept
- Able to present clearly and lead confidently during audits and site leadership inquiries
- Trains new analysts and technicians on all instruments/techniques, as well as routinely reviewing that all lab personnel are adhering to proper GMP standards
- Responsible for assisting the lab supervisor in following up with corrective actions
- Responsible for ownership of laboratory investigation - Able to lead the whole laboratory investigation and work alongside with QA for success closure of investigation
- Effectively perform a multitude of laboratory techniques for which they are trained on with minimal error
- Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements by driving all EHS standards, procedures and policies
- Bachelor of Science majoring in Microbiology or related scientific degree or diploma
- At least 5 years of experience in a QC Microbiological Lab
- At least 1-3 years of experience in a pharmaceutical manufacturing environment
- Strong GMP background and proficient with using laboratory equipment
- Excellent knowledge in aseptic working techniques
- Highly motivated, independent and able to work under pressure
- Possess good interpersonal and communication skills
- Strong analytical, problem solving and writing skills
- Team motivator – able to motivate and be role model for less experienced peers
- Total commitment to quality and maintaining a high standard of work at all times