Biotech Manufacturing Supervisor — Process Leader

RoslinCT US; Hopkinton (MA); On-site; USD 110,000 - 165,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) program

Educational assistance

Job summary

RoslinCT is seeking a Supervisor of Manufacturing to lead the cell processing team and oversee documentation, quality systems, and regulatory compliance. You will drive process improvements, manage cross-functional interactions, and develop staff to ensure safe and efficient manufacturing operations.

Responsibilities include enforcing SOPs, completing batch records, and minimizing waste while maintaining cGMP standards and quality.

Qualifications

• HS Diploma/GED equivalent; some college preferred.
• 4-8 years' experience in a bio-pharma environment.
• Extensive experience in a cGMP environment relevant to pharma.
• Strong business acumen and process improvement knowledge.
• Excellent communication and cross-functional collaboration.
• Hands-on problem solver with contingency planning.

Responsibilities

• Ensure SOPs, batch records and documentation are accurate and up to date.
• Investigation and troubleshooting of equipment and the process.
• Coordinate with support departments for scheduling services.
• Identify and implement process improvements.
• Develop processes to support staff and growth.
• Maintain CFRs, cGMPs, SOPs and company policies.
• Ensure cGMP compliance and quality standards.
• Minimize manufacturing costs through efficient use of resources.
• Supervise manufacturing activities and assign projects.
• Improve safety and housekeeping; ensure staff training and development.
• Other duties as assigned.

Skills

Organizational skills

Attention to detail

Problem solving

Communication skills

Time management

Team collaboration

Education

HS Diploma/GED

Some college

Tools

Microsoft Office Suite

Excel

Word

PowerPoint

Job description

RoslinCT is seeking a Supervisor of Manufacturing to lead the cell processing team and oversee documentation, quality systems, and regulatory compliance. You will drive process improvements, manage cross-functional interactions, and develop staff to ensure safe and efficient manufacturing operations.

Responsibilities include enforcing SOPs, completing batch records, and minimizing waste while maintaining cGMP standards and quality.