Manufacturing Supervisor (Pharmaceutical Packaging) - Sterling Engineering
Chicago, IL
About the Job
Job Title: Manufacturing Supervisor (Pharmaceutical Packaging)
Location: Chicago, IL
Hire Type: Direct-hire, Onsite
Shift: 1st shift (8:30am - 5:00pm) with occasional OT on weekends
Target salary: $80K - $100K/year
Position Summary:
The Manufacturing Supervisor is the shift leader for the manufacturing operation of Fill finish packaging or visual inspection and finished product and is responsible for producing high quality products in accordance with regulatory requirements to achieve the operations production plan. This employee must maintain effective employee relationships, compliance to cGMP and other regulatory and SOP requirements, as well as environmental, health and safety obligations and company policies.
Essential Duties & Responsibilities:
- 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 for ISO6, ISO7, ISO8 manufacturing area as well as Visual inspection and finished product area.
- 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 daily.
- Responsible for training personnel on equipment, processes and Standard Operating Procedures (SOPs).
- Trains and develops personnel, develops and maintains packaging schedules, and manages within the department budget.
- Ensures that projects are completed on schedule per established procedures.
- Participate in execution of qualification and validation activities.
- Participate in process related investigation(s) and implement CAPA derived from investigation outcome in timely manner.
- 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.
- 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.
Position Requirements and Qualifications:
Education:
- Bachelor’s degree, in engineering, pharmaceutical, related life science and at least 5 years of experience;
- Master’s degree, in engineering, pharmaceutical, related life science and at least 2 years of experience.
Experience:
- Aseptic Processing experience preferred
- PFS manual visual inspection experience
- Finished Product packaging experience with Serialization preferred
Special Skills:
- Prior aseptic process execution and supervisory experience is strongly preferred
- Previous biotechnology experience in a pharmaceutical environment is preferred
- Knowledge of FDA cGMPs
- Strong communication and leadership skills
- Strong problem-solving skills
- Strong technical writing skills with ability to author SOPs and deviations
- Proven ability to lead operational teams
- Ability to lead/participate in cross-functional teams
- Competent with MS Office Applications
- Leadership and professional development of others
- Knowledge of current Code of the Federal Regulations (CFRs) and current Good Manufacturing Practices (cGMPs)
- Problem solving
- Planning and documentation
Qualified applicants will receive consideration for employment without regard to race, color, age, religion, sex, sexual orientation, gender identify, national origin, disability, protected veteran status, or genetic information.
Source : Sterling Engineering
