Manufacturing Process Specialist

6 months ago

Vancouver, Canada Cytiva Full time

Be part of something altogether life-changing

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us - working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity - so you can grow your career and expand your skills in the long term. Your health and wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

The **Manufacturing Process Specialist** at PNI in Vancouver is responsible for optimizing and improving the manufacturing processes within the Pharmaceutical clean room facility. The role ensures the efficient production of high-quality products while identifying and implementing process enhancements to increase productivity, reduce costs, and maintain safety standards You will get to collaborate with cross-functional teams (including production associates, process development engineers, and leadership) to achieve continuous improvement and sustainable manufacturing practices.

**What you'll do**
- Process Optimization: Analyze existing manufacturing processes to identify inefficiencies, bottlenecks, and areas for improvement. Develop and implement strategies to optimize production flows, reduce waste, and increase productivity.
- Continuous Improvement: Participate in Lean and Six Sigma initiatives to drive continuous improvement in manufacturing processes. Utilize data analysis and statistical methods to identify root causes of issues and implement corrective actions.
- New Process Development: Work closely with design and process development teams to provide manufacturing input during the product design phase. Support the design and development of new manufacturing processes that align with product requirements and cost objectives.
- Equipment Selection and Maintenance: Help evaluate and select appropriate manufacturing equipment, tools, and technologies. Ensure equipment maintenance to maximize uptime and efficiency.
- Quality Assurance: Help implement quality control measures and process monitoring techniques to ensure products meet established quality standards. Collaborate with Quality Assurance teams to resolve manufacturing-related quality issues as needed.
- Standard Operating Procedures (SOPs): Help develop and maintain comprehensive SOPs for manufacturing processes. Support training for production associates to ensure consistent and safe operations.
- Safety Compliance: Promote a culture of safety and adherence to safety regulations within the manufacturing environment. Identify and address potential safety hazards in manufacturing processes.
- Cost Analysis: Analyze manufacturing costs and identify opportunities for cost reduction without compromising quality and safety standards.
- Data Analysis and Reporting: Gather and analyze production data to track key performance indicators (KPIs) related to production efficiency, yield, and quality.
- Collaboration and Communication: Work closely with cross-functional teams, including production, engineering, supply chain, and management, to ensure effective communication and alignment on manufacturing process improvements.

**Who you are**
- You have a thorough understanding of cGMP regulations and requirements and ability to translate to operational details and communicate to work staff.
- A relevant Bachelor’s degree and/or diploma with demonstrated 3+ years experience.
- Experience in a sterile pharmaceutical manufacturing facility or similar environment is an asset.
- Ability to review, understand, and follow standard operating procedures (SOPs), protocols, work instructions, and other policies/procedures.
- Strong written and verbal communication skills.
- Ability to work in a group environment.
- Strong accuracy and attention to detail.
- Knowledge or ability to learn pharmaceutical regulatory requirements is needed.
- Proficiency in Microsoft Office Suite, comfortable with technology.
- Ability to adapt to and complete shift work in AM / PM.
- Ability to lift and move materials/equipment when needed.
- Reliable transportation to work on-site is needed.
- Demonstrated problem solving skills in identifying and resolving issues.
- Ability to execute tactical plans and maintain established timelines and budgets.
- Ability to develop and maintain strong working relationships with primary suppor

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