Manufacturing Supervisor

Quotient Sciences•Boothwyn, PA

1d•Onsite

About The Position

Quotient Sciences is seeking a Manufacturing Supervisor to join our team at our Philadelphia sites (Boothwyn and Garnet Valley). This role is critical in ensuring the successful daily execution of GMP manufacturing operations, equipment cleaning/sanitization, and compliance with cGMP standards. If you are passionate about operational excellence, team leadership, and high-quality pharmaceutical production, we would love to hear from you.

Requirements

BS preferred or 3-5 years’ experience or equivalent combination of education and relevant work experience with previous supervisory/people leader responsibilities in a manufacturing environment.
Pharmaceutical manufacturing experience highly preferred in a Clinical/Commercial processing,
Read and interpret documents such as safety rules, equipment operating and maintenance instructions, and standard operating procedures and material safety data sheets.
Ability to apply concepts such as fractions, percentages, ratios, rounding and proportions to practical solutions.
Proficient in the use of a calculator, ability to work independently in a diverse and fast paced environment.
Good decision-making skills and ability to multi-task.
Spatial management - Organization skills
Ability to interpret and carry-out instructions, Maintains a Professional appearance, demeanour.

Nice To Haves

Continuous improvement experience beneficial
Other duties as assigned.

Responsibilities

Support day to day operations with an “on the shop floor” presence.
Monitor’s operators and equipment throughout shift to ensure all SOPs are properly followed and executed.
Coaches’ operators on proper operation and addresses violations with proper documentation.
Directs machine operators and service personnel in details of daily schedule, standard operating procedures, and requirements.
Ensures production schedule is maintained by making necessary corrections and adjustments to equipment to maintain maximum performance. Reports issues that may result in schedule not being maintained to management immediately.
Adjust process parameters and makes changes by setting up assigned equipment for change in material, size, and product. Tests equipment for quality of operation when changeover is completed.
Routinely checks product for defects and imperfections.
Examines finished product for conformity with quality specifications and records.
Trains and supervises machine operators in their essential duties and safety precautions required when working on the equipment.
Ensures accurate and timely completion of all equipment logs and documentation.
Ensures proper cleanliness and assembly of all manufacturing equipment per the approved SOP.
Responsible for maintaining a neat, clean, and safe working environment always.
Understands and adheres to all cGMP and FDA regulations.
Identifies and reports any quality issues to management or quality department.
Understands and adheres to all Company policies, procedures, SOPs, and Safety regulations.
Mentor and lead teams of diverse memberships to successful results
Comprehend, educate others, and enforce relevant policies/procedures pertinent to safety, quality, sanitation, security, and operations
Communicate with all levels of personnel and elevate issues when necessary
Schedule finite resources effectively so continuous improvement is not sacrifice for day-to-day results
Develop systems for standardization of work functions
Represent departmental interests while participating on cross functional teams
Demonstrated ability to utilize a personal computer effectively in a LAN environment.
Proven skill in analytical thinking, understanding, technical concepts, and problem solving
Must be able to work overtime when required.