What are the responsibilities and job description for the Process Optimization Technician position at R&D Partners?
Job Overview:
R&D Partners is committed to providing high-quality products and services to our clients. As a Process Optimization Technician, you will play a critical role in identifying areas for improvement and implementing changes to enhance efficiency and productivity.
About the Role:
This is a 12-month contract position, working 6AM-7PM or 6PM-7AM shifts. The ideal candidate will have a strong background in biopharmaceutical manufacturing, excellent analytical and problem-solving skills, and the ability to work effectively in a fast-paced environment.
Key Responsibilities:
* Identify areas for process improvement and implement changes to enhance efficiency and productivity.
* Analyze data and develop recommendations for process improvements, working closely with cross-functional teams to implement changes.
* Collaborate with the manufacturing team to ensure seamless execution of production schedules and maintenance of high-quality standards.
Requirements:
* Bachelor's degree in science-related area or engineering, and 1 year of experience, or Associate's degree in science-related area or Biotech certificate with 2 years of experience in a biotech manufacturing environment or other regulated industry.
* Strong analytical and problem-solving skills, with the ability to think critically and make sound decisions.
* Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
Benefits:
* Comprehensive benefits package including medical insurance, dental & vision insurance, 401k plan, Employee Assistance Program, Long-term disability, weekly payroll, expense reimbursement, online timecard approval, and more.
R&D Partners is committed to providing high-quality products and services to our clients. As a Process Optimization Technician, you will play a critical role in identifying areas for improvement and implementing changes to enhance efficiency and productivity.
About the Role:
This is a 12-month contract position, working 6AM-7PM or 6PM-7AM shifts. The ideal candidate will have a strong background in biopharmaceutical manufacturing, excellent analytical and problem-solving skills, and the ability to work effectively in a fast-paced environment.
Key Responsibilities:
* Identify areas for process improvement and implement changes to enhance efficiency and productivity.
* Analyze data and develop recommendations for process improvements, working closely with cross-functional teams to implement changes.
* Collaborate with the manufacturing team to ensure seamless execution of production schedules and maintenance of high-quality standards.
Requirements:
* Bachelor's degree in science-related area or engineering, and 1 year of experience, or Associate's degree in science-related area or Biotech certificate with 2 years of experience in a biotech manufacturing environment or other regulated industry.
* Strong analytical and problem-solving skills, with the ability to think critically and make sound decisions.
* Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams.
Benefits:
* Comprehensive benefits package including medical insurance, dental & vision insurance, 401k plan, Employee Assistance Program, Long-term disability, weekly payroll, expense reimbursement, online timecard approval, and more.
