Medasource
Type:
6 month contract, possibility of extension or conversion
Schedule:
12 hour shifts, 2-2-3 schedule, Days(6am-6pm) or Nights(6pm-6am)
Position Description The Manufacturing Operator will work in the Device Assembly and Packaging area, where our client's autoinjector devices are assembled and packaged. Operators will be responsible for the safe operation of highly automated equipment producing products of the highest quality for our Client.
Responsibilities
Adhere to plant safety policies and procedures and contribute to a safe work environment.
Setup and operate highly automated equipment in the Device Assembly and Packaging area.
Adhere to standard operating procedures and current Good Manufacturing Practices (cGMP) to ensure product quality.
Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleaning Logs, etc.).
Attain and maintain qualification for the operation of assigned process equipment and duties in the area.
Identify opportunities for operational improvements.
Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision.
Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
Requirements (Education, Experience, Training)
Previous experience working in a GMP environment, preferably in the pharmaceutical industry.
Strong ability to multitask.
Ability to demonstrate attention to detail.
Education Requirements
High School Diploma or GED required.
Seniority level Not Applicable
Employment type Full-time
Job function Manufacturing and Quality Assurance
Industries Pharmaceutical Manufacturing
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6 month contract, possibility of extension or conversion
Schedule:
12 hour shifts, 2-2-3 schedule, Days(6am-6pm) or Nights(6pm-6am)
Position Description The Manufacturing Operator will work in the Device Assembly and Packaging area, where our client's autoinjector devices are assembled and packaged. Operators will be responsible for the safe operation of highly automated equipment producing products of the highest quality for our Client.
Responsibilities
Adhere to plant safety policies and procedures and contribute to a safe work environment.
Setup and operate highly automated equipment in the Device Assembly and Packaging area.
Adhere to standard operating procedures and current Good Manufacturing Practices (cGMP) to ensure product quality.
Document process steps on appropriate batch documentation (Electronic Ticket, SAP, Cleaning Logs, etc.).
Attain and maintain qualification for the operation of assigned process equipment and duties in the area.
Identify opportunities for operational improvements.
Proactively monitor documentation and product quality, properly documenting all activities and reporting issues to supervision.
Contribute to the achievement of key departmental objectives including improving safety performance, reducing deviations, improving productivity, and training compliance.
Requirements (Education, Experience, Training)
Previous experience working in a GMP environment, preferably in the pharmaceutical industry.
Strong ability to multitask.
Ability to demonstrate attention to detail.
Education Requirements
High School Diploma or GED required.
Seniority level Not Applicable
Employment type Full-time
Job function Manufacturing and Quality Assurance
Industries Pharmaceutical Manufacturing
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