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Aseptic Production Supervisor

2 months ago

Chicago Illinois, United States Global Life Science Hub Full time

Our client, a prominent entity in the pharmaceutical sector, is experiencing significant expansion and is in search of a skilled Manufacturing Supervisor (DP) to become a vital part of their innovative team.

As a Manufacturing Supervisor (DP), you will assume a pivotal role as a shift leader within their production environment.

Your duties will encompass ensuring the generation of superior quality products while adhering to regulatory standards, operational strategies, and corporate policies.

Make a meaningful contribution to the success of our client’s operations.

Key Responsibilities:


Oversee and direct production floor staff to guarantee the effective utilization of equipment and materials, resulting in high-quality product outputs in line with cGMP and production objectives.

Provide mentorship, guidance, and development opportunities to direct reports, including conducting annual performance evaluations.

Ensure alignment with departmental goals and objectives.

Encourage safe working practices and adherence to policies, as well as environmental, health, and safety regulations.

Educate personnel on equipment, processes, and standard operating procedures (SOPs).

Develop and manage packaging timelines within budgetary constraints.

Guarantee timely project execution and engage in qualification and validation processes.

Identify and resolve issues, suggest process enhancements, and promote teamwork.

Monitor operational processes, create reports, and provide strategic direction.

Review documentation for compliance and establish project timelines.

Participate in cross-functional project teams and undertake additional responsibilities as necessary.

Qualifications:
A Bachelor's degree in engineering, pharmaceuticals, related life sciences, or a comparable field with a minimum of 4 years of relevant experience.

A Master's degree in engineering, pharmaceuticals, related life sciences, or a comparable field with at least 2 years of relevant experience.

Preferred background in aseptic processing, manual visual inspection, and finished product packaging with serialization.

Excellent communication, leadership, and problem-solving abilities.

Proficient in technical documentation, MS Office software, and leading operational teams.

Familiarity with FDA cGMPs and regulations.

Capability to operate in both office and biotechnology manufacturing settings.

Willingness to accommodate various shifts, overtime, and travel.