Supervisor, Production - 2nd Shift - Baltimore

Bora Pharmaceuticals; Baltimore (MD); On-site; USD 75,000 - 114,000; Full time

Job summary

An established industry player in pharmaceutical manufacturing is seeking a Production Supervisor for the 2nd shift in Baltimore. This role involves overseeing production fill activities, ensuring compliance with safety standards, and developing operational procedures. The ideal candidate will possess strong leadership and communication skills, along with a solid background in cGMP environments. You will be instrumental in training operators and supporting qualification activities, making a significant impact in a dynamic production setting. If you are a motivated individual with a passion for excellence in manufacturing, this opportunity is perfect for you.

Qualifications

• 5+ years in a cGMP or regulated environment.
• 3 years supervisory experience preferred.

Responsibilities

• Monitor compliance with cGMP regulations and company policies.
• Develop procedures and train operators for filling operations.

Skills

Communication Skills

Leadership Ability

Problem-Solving Skills

Decision-Making

Flexibility

Multitasking

Time Management

Education

BA/BS in Science or Technical Field

High School/AA with Experience

Tools

RABS Technology

Aseptic Drug Manufacturing

cGMP Compliance

Job description

Supervisor, Production - 2nd Shift - Baltimore

Join to apply for the Supervisor, Production - 2nd Shift - Baltimore role at Bora Pharmaceuticals

Job Summary

The Production Supervisor will be responsible for executing production fill activities associated with a RABS (Restricted Access Barriers System) fill line. This includes developing procedures, training operators, supporting qualification activities, and ensuring compliance with safety standards and policies. The role requires strong communication skills, leadership ability, problem-solving skills, decision-making, flexibility, multitasking, and good time management.

This position supports the 2nd shift operations, working 2pm-10:30pm, Monday to Friday.

Essential Functions

• Monitor and ensure compliance with cGMP regulations, company policies, SOPs, and batch records. Maintain visibility and access to employees throughout the shift.
• Develop procedures and batch records for filling operations and train operators.
• Provide technical support for qualification activities.
• Review documentation for compliance with Good Documentation Practices.
• Coordinate equipment preparation activities.
• Interface with various departments to resolve production, supply, and equipment issues, documenting deviations and assisting investigations.
• Operate vial and syringe fill machines, capping, sterilization, lyophilization, and manual cleaning in a pharmaceutical environment.

The above describes typical duties and is not exhaustive. Management may assign additional duties as needed.

Minimum Education, Experience, Skills

• BA/BS in science or technical field with at least 5 years’ experience in a cGMP or regulated environment.
• Or High School/AA with at least 10 years’ experience in a cGMP environment.
• Preferred: 3 years supervisory experience in cGMP, RABs/Isolator technology, aseptic drug manufacturing.

Compensation Range

$75,789.00 - $113,684.00

Bora Pharmaceuticals is committed to equal employment opportunity and prohibits discrimination based on race, color, religion, sex, national origin, age, disability, and other protected categories.

Additional Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job functions: Management and Manufacturing
• Industry: Pharmaceutical Manufacturing