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You will be updated with latest job alerts via email$ 94000 - 129250
1 Vacancy
Our purpose is to bring hope to life by enabling lifechanging therapies for patients around the globe creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.
JOB SUMMARY
Oversees daytoday staff in of production processes for GMP bioprocess operations in Manufacturing; monitors compliance with established processes and standards.
ESSENTIAL JOB DUTIES & RESPONSIBILITIES
Ensures compliance with company quality systems safety procedures and other company policies
Plan daily activities priorities and workflow for team to adhere to overall schedule
Perform and monitor staff during unit operations based on SOP and batch records in compliance with requirements in Quality System
Review and ensure errors are corrected during manufacturing operations
Train coach and mentor manufacturing technicians/associates on manufacturing functions
Complete required documentation; review and approve executed manufacturing MBRs
Develop staff i.e. set goals assign development activities review performance etc.
Supervises daily operations for a project/team comprised of support and/or professional employees
Provides technical leadership in a specific work area
Prioritizes and assigns project goals; ensures tasks are completed and work area goals are met
Coordinates with other supervisors and teams to meet the business need and output requirements
May coach team members on task and skill proficiency and performance with managers guidance
TECHNICAL & LEADERSHIP SKILLS
Applies understanding of how the team relates to other related areas to improve efficiency of own team
Recognizes performance improvements and conveys feedback constructively
Works across teams effectively
EDUCATION & EXPERIENCE
BS/BA degree with 5 years of industry experience orMasters degree with 3 years of industry experience. Equivalent education and experience may substitute for stated requirements
COMPENSATION
$94000 $129250
Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work sidebyside with our clients and partners every step of the way. We provide worldclass development and manufacture of mammalian and microbialbased therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMPcompliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fasttrack projects and rare diseases. AGC Biologics is the partner of choice. To learn more visitwww.agcbio.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!
AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.
Required Experience:
Manager
Full-Time