Manager, Manufacturing Science and Technology (NS)
Agilent (PEI & NS) is a contract developer and manufacturer of active pharmaceutical ingredients specializing in clinical-to-commercial scale production for microbial fermentation, synthetic small molecules including ADC, HPAPI, plasmid DNA, mRNA, LNP and sterile filling capabilities. They have an opening for a Manager, Manufacturing Science and Technology at their Windsor, Nova Scotia facility.
About the role
The Manager, Manufacturing Science and Technology will lead the development and implementation of manufacturing science and technology initiatives to support the company's strategic goals. This includes driving innovation in process development, quality control, and operational excellence, ensuring compliance with regulatory requirements and industry standards.
Responsibilities
- Develop and implement manufacturing science and technology strategies to enhance product quality and efficiency.
- Lead cross-functional teams to evaluate and implement new technologies and methodologies that improve manufacturing processes.
- Collaborate with R&D and engineering teams to ensure alignment on technical advancements and their integration into manufacturing operations.
- Oversee the validation and qualification of new manufacturing processes and equipment.
- Ensure compliance with all relevant regulations and industry standards, including FDA, EMA, and other global regulatory bodies.
- Provide technical guidance and support to manufacturing teams to maintain high levels of operational excellence.
- Conduct regular reviews of manufacturing performance metrics and identify areas for improvement.
- Develop and maintain strong relationships with external partners and suppliers to ensure timely delivery of materials and services.
Requirements
- Bachelor’s degree in Chemical Engineering, Biotechnology, Microbiology, or a related field.
- Minimum 10 years of experience in pharmaceutical manufacturing, with at least 5 years in a managerial role.
- Proven track record of successfully leading complex projects and managing cross-functional teams.
- Strong understanding of cGMP guidelines and regulatory requirements.
- Experience with process development, quality control, and operational excellence.
- Excellent communication and leadership skills.
Qualifications
- Ability to work independently and as part of a team.
- Strong analytical and problem-solving skills.
- Knowledge of statistical process control (SPC) and Six Sigma principles.
- Experience with data analysis tools and software.
Skills
- Expertise in process development and optimization.
- Understanding of bioprocesses and fermentation techniques.
- Experience with automation and robotics in manufacturing environments.
- Knowledge of sterile filling and packaging processes.
- Strong project management skills.
Benefits
- Competitive salary commensurate with experience.
- Health, dental, and vision insurance.
- Flexible work schedule.
- Professional development opportunities.
- Employee discount program.
Pay
Commensurate with experience.
Schedule
Full-time.