2nd Shift Manufacturing Operations Lead

RXinsider LTD.; New Jersey; On-site; USD 99,000 - 136,000; Full time

Benefits offered by this job

Health benefits

401k with match

Paid time off

Shift differential

Annual incentive bonus

Career advancement opportunities

Job summary

Quva seeks a Manager of Manufacturing Operations to lead sterile pharmaceutical production on 2nd shift in Bloomsbury, NJ. You will oversee staff, ensure adherence to validated parameters and cGMP, and drive continuous improvement in quality and safety.

The role emphasizes staff development, cross-functional collaboration, and a strong focus on delivering compliant, high-quality products. Requires a Life Science degree and 5+ years of supervision, with US work authorization.

Qualifications

• Bachelor’s Degree in Life Science or related field.
• 5 years of supervisory or management experience.
• Hands-on direct shop floor involvement: Troubleshooting.
• U.S. work authorization; no sponsorship available.

Responsibilities

• Manage staff in daily operations and ensure compliance with validated parameters, cGMP, and safety requirements.
• Operate to meet or exceed delivery performance objectives for products/projects.
• Counsel, train, and develop Supervisors for efficient performance and teamwork.
• Prepare weekly/monthly reports; track metrics and trends for continuous improvement.
• Maintain cooperative cross-functional relationships with Quality and other manufacturing colleagues.
• Lead in maintaining a safe manufacturing environment; participate in safety meetings and corrective actions.

Skills

Staff supervision

Regulatory knowledge

Quality focus

Leadership

Communication skills

Education

Bachelor's degree in Life Science

Tools

Computerized tracking tools

Job description

Quva seeks a Manager of Manufacturing Operations to lead sterile pharmaceutical production on 2nd shift in Bloomsbury, NJ. You will oversee staff, ensure adherence to validated parameters and cGMP, and drive continuous improvement in quality and safety.

The role emphasizes staff development, cross-functional collaboration, and a strong focus on delivering compliant, high-quality products. Requires a Life Science degree and 5+ years of supervision, with US work authorization.