Job Location : Pearl River,NY, USA
Job Title: Manager, Quality Control Microbiology
Location: Pearl River, NY
About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. Your job, as [Job Title] within our [Team Name], will be to [summary of opportunity].
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
Demonstrate expertise in performance of activities in the Microbiology group by strictly adhering to site procedures, Federal Regulations, and cGMP guidance.
Ensure the laboratory is maintained in an audit ready state at all times and represent the department during audits/inspections as a subject matter expert.
Facilitate team compliance via quality systems such as change control, CAPA and deviation investigations. Support daily laboratory operations, including resolution of test schedule conflicts, review of data, assisting analysts in troubleshooting activities and incident investigations.
Assist with maintaining safety of the laboratory work area.
Provide microbiological testing and support to the Microbiology and Manufacturing departments.
Ensure individual training requirements are maintained as well as participate in cross-training activities. Ensure the level of cross-training within the team is sufficient to meet the business needs. Serve as a coach and mentor to team members.
Effective interaction with other departments (internal and external). In particular, close contact maintained with the Microbiology, Production, Validation, Manufacturing and Planning Departments, & QA
Actively contribute to continuous improvement initiatives in the lab
Identifies areas of opportunity and leads continuous improvement projects. Directly supports manufacturing operations in sampling and testing as well as serves as technical expertise in making decisions.
QC Micro representation at cross functional meetings
Conduct duties in a safe manner and report all safety issues or concerns
About You
Education/ Experience:
Bachelor's degree in Microbiology, Biological Sciences, Biochemistry, Biotechnology, Chemistry, or a related scientific field with 8+ years of relevant work experience in a cGMP or Quality environment, or extensive industry experience OR 12+ years in lieu of a degree required.
Excellent communication skills, natural influencer, and ability to work effectively in cross -functional teams
Knowledge of microbiological techniques including sterility, bioburden, microbial identification, environmental monitoring, culturing of both bacterial and viral isolates or tissue culture preferred. Previous Quality Control experience desired.
Exceptional attention to detail and strong writing skills are crucial.
Candidate should be familiar with cGMP guidelines must be able to work off shift and in a team environment.
Preferred Qualifications:
Degree in Microbiology
An understanding of routine QC operations, including testing and documentation practices.
Professional writing capability.
Experience with laboratory electronic systems
Audit/Inspection Experience
Method validation experience
Proficient using Microsoft Office
Proven logic and decision-making abilities and critical thinking skills.
Knowledge of continuous improvement techniques and problem-solving skills
Proven leadership, verbal and written communication, organizational, critical thinking, and action oriented.
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to gain experience and drive your career, whether it's through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take diligent care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
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