Microbiologist II

Job Description Purpose: The primary role is to ensure smooth QC operational activities support to routine or new product introduction per cGMP/EHS/Regulatory expectations with global/site standards. Enables QC functional operational readiness, infrastructure/instrumentation support and compliance readiness. Major Responsibilities: Team Support Responsible for supporting QC micro-operations by timely conduct of test/release of routine or new product introduction activities. Develops technical competency and jointly creates a great place to work in. Financial Support Supports financial spending are within the latest best estimates. Compliance (Quality and Safety) SME for QC Micro - Operational readiness (Eg: Environment, Utilities and Product test), infrastructure/instrumentation needs and compliance readiness (Eg: Track & Trend) against cGMP/EHS/Regulatory compliance expectations to global/site procedures. Authors/Reviews lab documentation per cGMP or EHS expectations of the global/local site procedural needs. Support in resolution of manufacturing/laboratories investigation or exceptions for timely closure or issue resolution. Support in internal/external audits and enables audit response for a successful outcome in sustaining licenses to operate. Infrastructure & Instrumentation Supports QC function infrastructure/instrumentation needs through supporting PM/CAL or Technological refresh needs. New Product Introduction, Projects & Continuous Improvement Support in New Product Introduction (Small molecule or Biologic product) are conducted (TMT, Eqmt qualification) and delivered to enable a successful / timely program launch. Any other task/projects assigned by line manager. Qualifications Bachelors in Sciences (i.e. Biologicals, Biomedical, Chemistry, Life Sciences, Pharmaceutical), Pharmacy, or Engineering (i.e. Biomedical, Chemical, Pharmaceutical), or equivalent. Essential Skills, Experience, and Competencies (includes Licenses, Credentials) Analytical thinking with problem-solving skills and technical writing skills. Independent and motivated. Good GMP knowledge/Experience in laboratory Good Collaborator with cross functional teams. Able to work towards timeline. Minimum 4 years for Bachelor graduate with relevant work experience in Biotechnology / Pharmaceutical industry is preferred. Additional Information 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 https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html Company Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.