Manufacturing Production Supervisor (2nd Shift)

Manufacturing Production Supervisor (2nd Shift)
Cresilon, Inc., United States

Experience
1 Year
Salary
0 - 0
Job Type
Job Shift
Job Category
Traveling
No
Career Level
Telecommute
No
Qualification
Bachelor's Degree
Total Vacancies
1 Job
Posted on
Apr 27, 2021
Last Date
May 27, 2021
Location(s)

Job Description

Cresilon, Inc is a medical device company based out of Brooklyn, NY that focuses on bringing new technologies to the animal health industry that aim to solve problems associated with wound healing. We have created a hemostatic device that can instantly stop traumatic bleeding.

Please refer to these associated links to learn more about Cresilon:

1. http://www.bloomberg.com/video/vetigel-the-band-aid-of-the-future-stops-bleeding-instantly-PaIvLxjcS66F5IWO1SsKtA.html

2. http://www.ted.com/talks/joe_landolina_this_gel_can_make_you_stop_bleeding_instantly?language=en


Position Description:

The Production Supervisor leads a sound, efficient, safe, and effective production environment and implements our vision for this business-critical function at Cresilon. The production operations must comply with local, State and Federal regulations, including current Good Manufacturing Practices (cGMP). This role also organizes and deploys optimal and cost-effective aseptic manufacturing practices in a fast-paced environment through collaboration with Cresilon suppliers, stakeholders, production engineers and technicians to meet challenging customer demands. The Production Supervisor should have a strong operational, quality, compliance, and technical background, with proven team building, project management, continuous improvement, and supplier management abilities. This is often a hands-on role working closely with production team or other functions, to identify improvements, troubleshoot processes and equipment challenges. This is a second shift position, although for training purposes only work hours will be during first shift (7am-4:30pm) for the first few months.

Responsibilities:

  • Plans, organizes, and leads batch production operations and associated production activities to maintain quality, cost, and customer service expectations within a safe working environment.
  • Manages a team of production technicians, in execution of daily work. Ensures technicians comply with established process parameters and standard operating procedures, cGMP regulations and safety requirements. Provides operators with constructive feedback.
  • Performs tasks associated to manufacturing operations in accordance to cGMP/SOP and batch records requirements.
  • Manage operations to assure all products are visually inspected, labeled and packed into their finished containers as per applicable standard operating procedure and specifications including documentation such as batch records, protocols, and logs to assure accurate recording of processes in conformance to policies and procedures and in compliance with Good Documentation Practices
  • Supervises the assembly, disassembly, cleaning, and storage of manufacturing equipment.
  • Supervises the cleaning of the sterile room facility.
  • Ensures target production numbers are met and cGMP documents are completed in a timely manner.
  • Acts as a subject matter expert on Manufacturing Practices, including in aseptic behaviors and practices.
  • Implements continuous improvement, leveraging expertise in Six Sigma, Lean or Toyota Production System (TPS) approaches.
  • Adheres to all workplace safety laws, regulations, standards and practices and actively advances a culture of safety within their team and organization.
  • Resolves or escalates any problem occurring in the area that affects product quality, safety, and other aspects of production line performance.
  • Demonstrates the ability to properly operate equipment, perform equipment set-up/change-over/cleanups, assist in preventative maintenance and troubleshoot equipment problems to achieve optimum production targets.
  • Establishes a working environment that fosters participation within and between teams.
  • Hires, trains, develops, disciplines and discharge production operators and engineers.
  • Develops, mentors, and supports production operators in driving continuous improvement efforts, improving employee engagement, and supporting business growth.
  • Represents manufacturing on launch teams focused on design and process transfer.
  • Ensures compliance with Quality Assurance and Quality Control requirements and participates in timely investigations and implementation of corrective and preventative action.
  • Ensures records of critical process parameters and documentation are maintained.
  • Generates production batch procedural documentation, manages change assessments, risk assessment reports, process validation protocols and standard operating procedures (SOPs).
  • Creates, updates, reviews, and maintains production-related SOPs.
  • Reviews and approves documents, including standard operating procedures, batch records, material specifications and validation protocols and reports.
  • Leads the execution of the validation master plan for

Job Specification

Job Rewards and Benefits

Cresilon, Inc.

Information Technology and Services - Brooklyn, United States
© Copyright 2004-2024 Mustakbil.com All Right Reserved.