Job Description
Job description
Our purpose is to bring hope to life by enabling life-changing 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 GMP bioprocess operations in Manufacturing for a team; evaluates and monitors ongoing compliance with established processes and standards
Essential Job Duties/Responsibilities
• Monitor and improve compliance with company quality systems, safety procedures, and other company policies
• Determine production activities, staffing requirements, and shift schedules to ensure on-time delivery of a quality product
• Prioritize work and resources for team across all shifts
• Monitor operations team based on SOP and batch records
• Correct and prevent errors during manufacturing operations
• Train, coach, and mentor manufacturing associates on manufacturing functions
• Review and approve required documentation
• Develop team members and supervisors (i.e. set goals, assign development activities, review performance, etc.)
• Manages daily team operations
• Prioritizes and assigns technical resources internally and externally; ensures tasks are completed and work area/project goals and objectives are met
• Coordinates and collaborates with other teams to meet organizational goals and work requirements
• May coach and develop team members on skill proficiency and performance with general direction on tasks and regular feedback
Leadership Skills
• Begins to play a hand in professional development of others; may mentor less experienced employees on job duties and general departmental operations
• Provides direct supervision to professional individual contributors and/or skilled, support individual contributors
Required
QUALIFICATIONS
• BS/BA degree with 8+ years of industry experience, or Master’s degree with 6+ years of industry experience.
• Equivalent education and experience may substitute for stated requirements.
Compensation Range
$108,080-148,610
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 side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based 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 cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. 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, ****** orientation, or any other characteristic protected by applicable laws, regulations and ordinances.
Our purpose is to bring hope to life by enabling life-changing 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 GMP bioprocess operations in Manufacturing for a team; evaluates and monitors ongoing compliance with established processes and standards
Essential Job Duties/Responsibilities
• Monitor and improve compliance with company quality systems, safety procedures, and other company policies
• Determine production activities, staffing requirements, and shift schedules to ensure on-time delivery of a quality product
• Prioritize work and resources for team across all shifts
• Monitor operations team based on SOP and batch records
• Correct and prevent errors during manufacturing operations
• Train, coach, and mentor manufacturing associates on manufacturing functions
• Review and approve required documentation
• Develop team members and supervisors (i.e. set goals, assign development activities, review performance, etc.)
• Manages daily team operations
• Prioritizes and assigns technical resources internally and externally; ensures tasks are completed and work area/project goals and objectives are met
• Coordinates and collaborates with other teams to meet organizational goals and work requirements
• May coach and develop team members on skill proficiency and performance with general direction on tasks and regular feedback
Leadership Skills
• Begins to play a hand in professional development of others; may mentor less experienced employees on job duties and general departmental operations
• Provides direct supervision to professional individual contributors and/or skilled, support individual contributors
Required
QUALIFICATIONS
• BS/BA degree with 8+ years of industry experience, or Master’s degree with 6+ years of industry experience.
• Equivalent education and experience may substitute for stated requirements.
Compensation Range
$108,080-148,610
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 side-by-side with our clients and partners, every step of the way. We provide world-class development and manufacture of mammalian and microbial-based 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 cGMP-compliant facilities in Seattle, Washington; Boulder and Longmont, Colorado; Copenhagen, Denmark; Heidelberg, Germany; Milan, Italy; and Chiba, Japan. We currently employ more than 2,500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients’ most complex challenges, including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more, visit www.agcbio.com. 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, ****** orientation, or any other characteristic protected by applicable laws, regulations and ordinances.
💡 Quick Summary
Seeking a career-building opportunity? The Manager| Manufacturing position is now open for candidates interested in the Manufacturing Jobs sector. This role in Bothell offers a professional environment and growth potential.
Requirement Snapshot: Candidates should possess basic communication skills, a proactive attitude, and the ability to work in a team. Experience in Manufacturing Jobs is a plus.
