Pharmaceutical Manufacturing Supervisor

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Job description

Kelly is actively recruiting for a Pharmaceutical Manufacturing Supervisor located in Chicago, IL.

Duties of the Pharmaceutical Manufacturing Supervisor includes:

• Provides daily supervision on the floor to personnel in the efficient use of equipment and materials to produce quality products under cGMP in accordance with the production plan.
• Provides coaching, counseling, development, discipline, and recognition of direct staff, including performing annual performance reviews.
• Responsible for maintaining alignment with department direction, goals and objectives.
• Promotes the use of safe work practices during all production and ensures all external and company policies and EHS standards are met on a daily basis.
• Responsible for performing and supervising Drug Substance manufacturing operation.
• Responsible for preparation, update, and training personnel on Standard Operating Procedures (SOPs) related to equipment operation and processes.
• Author and reviews SOPs and other documents to ensure integration of cGMPs and improve process efficiency.
• Works collaboratively to ensure flow of product, sharing of best practices and lean behaviors.
• Performs process monitoring, including use of databases, documents and/or spreadsheets to support business reporting requirements.
• Performs ongoing operational tasks of organization unit, actively assists, or provides direction to subordinates as required.
• Responsible for final review of completed documentation per compliance standards and establish timelines.
• Responsible for investigation and implementation of CAPAs related to discrepancies observed in department.
• Investigates and resolve problems, identifying root cause, and proposing process improvements through clear communication to senior management.
• Participation and/or leadership role in multi-functional project teams as necessary.
• Other tasks as requested by management.

Qualifications of the Pharmaceutical Manufacturing Supervisor includes:

• Minimum of a BA/BS degree in Scientific Discipline.
• 4-6 years of pharmaceutical manufacturing (GMP) experience in either upstream, downstream, packaging, etc.
• Ability to be trained and have flexibility to manage and learn all aspects of the manufacturing process.
• Experience with biosimilar, protein and drug products desired.

You should know: Your safety matters! Vaccination against COVID-19 may be a requirement for this job in compliance with current client and governmental policies. A Kelly recruiter will confirm and share more details with you during the interview process.

Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live (plus, did we mention we provide a ton of benefits ?). Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.

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