Randstad Controlled Environment Manufacturing Supervisor in Jacksonville, Florida

Controlled Environment Manufacturing Supervisor

job details:

  • location:Jacksonville, FL

  • salary:$20 - $24 per hour

  • date posted:Thursday, January 3, 2019

  • experience:Experienced

  • job type:Permanent

  • industry:Mesr/Anlyz/Cntrl Instrmnts

  • reference:S_718503

  • questions:lauren.livengood@randstadusa.com904-730-9760

job description

Controlled Environment Manufacturing Supervisor

Randstad Southside Manufacturing and Logistics is currently recruiting for a Controlled Environment Manufacturing Supervisor.

This is a direct hire position and they pay is $20 to $24 per hour.

The hours for this position are Monday - Friday from 7:00am - 5:00pm.

Responsibilities:

What You Will Be Doing

You will be working as part of a team of operators in the Clean Room. You will with operations and management. You will ensure that operators in the Clean Room follow the Clean Room procedures to ensure that we can make sterile product that is safe for our customers. Although you will be supervising other staff, this is an hourly position i.e. you will be paid overtime if that is required.

You will report to the Manager of Operations. Initial activities will be focused on setting up and validating the new Clean Room as part of the validation team. Initial operations in the Clean Room will be conducted as a single day time shift. As we grow, you will lead growth in the team membership to support a two shift operation.

Working hours: 7:00 AM - 5:00 PM

Skills:

You must be able to stand on your own two feet as part of a cross-functional team. If you don't know how do something; let us know and we will show you how. If you have ideas on how to improve what we do, we will want to hear about it. You have to have a sense of humor and to show respect to everyone in the team.

We do not expect people coming into this position to be experts in medical device regulations. We work in a regulated industry. If you come here, you must be willing to learn about and comply with the regulatory requirements of ISO 13485: 2016 and the regulations of the FDA (21 CFR 820). The things we make go into people and help make their lives better. Understanding the significance of what we do is very important.

Primary Duties and Responsibilities:

--Lead the operators working in the Clean Room so that all procedures for gowning and clean processing are followed.

--You will work with the Operations Manager to make sure that shift work is properly supervised within the Clean Room.

--Support testing and maintenance of the room at the instruction of Management.

--Perform bench-type processes to complete assemblies and sub-assemblies using hand and inspection tools.

--Utilizes assembly equipment, such as bag/tray sealers, and, other equipment in the assembly area.

--Utilizes GMP techniques and completes all device history sheets in accordance with instructions.

Education:

No Degree Required

Experience:

Experienced

Qualifications:

Secondary Duties and Responsibilities:

? Performs manufacturing, shipping & inventory control, or office related tasks as requested by Anjon management.

Education and Experience:

? Minimum high school graduate or equivalent.

? At least 3 years experience working in a Clean Room; preferably with medical device product.

Job Knowledge, Skills, and abilities:

Following established procedures must be able to read and understand bills-of-materials, routers, and job instructions. Must be familiar with assembly and measuring tools, must be able to interpret drawings, and must be able to complete inspection procedures.

Training Requirements:

This position requires training in general safety, GMPs, Quality System Regulations, ISO regulations, Material Safety Data Sheets, Departmental Work Instructions, and Device History Sheets.

Physical Demands:

? Light to moderate lifting is required, as well as using various assembly and shop equipment.

? Regularly required to sit or stand.

? Will be working in air-conditioned environments

If you meet the qualifications listed for this position, please apply directly to this position with your most updated resume. Thank you!

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