Quality control supervisor Jobs in Indianapolis, IN

Job details

Spherion is hiring Pharmaceutical Production Technicians in Indianapolis, IN!


This is a mid-level position in the aseptic filling group within the Manufacturing department. It utilizes those with experience and the training needed to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through a number of job functions and be required to demonstrate increasing skill levels while demonstrating leadership capabilities ...

Responsibilities:
-Become certified for entry into the GMP cleanroom space to be able to perform sanitization, stock/replenish supplies, equipment setup, and all related aseptic filling operations.
-Execute aseptic fill processes using batch records and SOPs.
-Responsible for verifying the calibration of all related equipment and sanitization of supplies to support production
-Increasing level of competency in the manufacturing area procedures. Assigned job duties will include Aseptic and clean room areas, Component Preparation, Filling and Capping
-Learn the functions necessary to work in the Fill suite. This will include the operation of the associated equipment.
-Ability to perform tasks with minimal supervisor direction.
-Provide training for new team members.
-Able to understand the manufacturing schedule and coordinate tasks to achieve the schedule.
-Provide floor leadership in the absence of a supervisor or PT3 technicians.
-Transport and/or dispose of hazardous chemicals.
-Perform all other duties as assigned.
-Must immediately notify supervisor if affected by an infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist.

Working hours: 7:00 AM - 3:30 PM

Skills:
-B.S. degree in chemistry/biology/life sciences is a plus.
-Extensive knowledge of and experience in bulk formulation along with equipment cleaning, preparation, and assembly are preferred.
-Computer skills in Microsoft Office such as Word and Excel are a plus.
-College coursework preferred
-Experience in stopper prep, capping, and packaging preferred.

Education:
High School

Experience:
1-4 years

Qualifications:
-Isolator experience
-Minimum 3-5 years, including relevant aseptic filling experience in a cGMP pharmaceutical
manufacturing facility.
-Must possess working knowledge and understanding of GMP compliance regulations.
-Must possess knowledge and experience in the aseptic filling process, along with equipment cleaning,
preparation, and assembly.
- Must be able to comprehend and follow detailed procedural instructions in written and verbal form.
-Must possess adequate working knowledge of arithmetic functions to accurately perform or check calculations required in the product documentation.


Apply today or email your resume to !Show lessShow more

Spherion is hiring Pharmaceutical Production Technicians in Indianapolis, IN!


This is a mid-level position in the aseptic filling group within the Manufacturing department. It utilizes those with experience and the training needed to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through a number of job functions and be required to demonstrate increasing skill levels while demonstrating leadership capabilities

Responsibilities:
-Become certified for entry into the GMP cleanroom space to be able to perform sanitization, stock/replenish supplies, equipment setup, and all related aseptic filling operations.
-Execute aseptic fill processes using batch records and SOPs.
-Responsible for verifying the calibration of all related equipment and sanitization of supplies to support production
-Increasing level of competency in the manufacturing area procedures. Assigned job duties will include Aseptic and clean room areas, Component Preparation, Filling and Capping
-Learn the functions necessary to work in the Fill suite. This will include the operation of the associated equipment. ...

-Ability to perform tasks with minimal supervisor direction.
-Provide training for new team members.
-Able to understand the manufacturing schedule and coordinate tasks to achieve the schedule.
-Provide floor leadership in the absence of a supervisor or PT3 technicians.
-Transport and/or dispose of hazardous chemicals.
-Perform all other duties as assigned.
-Must immediately notify supervisor if affected by an infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist.

Working hours: 7:00 AM - 3:30 PM

Skills:
-B.S. degree in chemistry/biology/life sciences is a plus.
-Extensive knowledge of and experience in bulk formulation along with equipment cleaning, preparation, and assembly are preferred.
-Computer skills in Microsoft Office such as Word and Excel are a plus.
-College coursework preferred
-Experience in stopper prep, capping, and packaging preferred.

Education:
High School

Experience:
1-4 years

Qualifications:
-Isolator experience
-Minimum 3-5 years, including relevant aseptic filling experience in a cGMP pharmaceutical
manufacturing facility.
-Must possess working knowledge and understanding of GMP compliance regulations.
-Must possess knowledge and experience in the aseptic filling process, along with equipment cleaning,
preparation, and assembly.
- Must be able to comprehend and follow detailed procedural instructions in written and verbal form.
-Must possess adequate working knowledge of arithmetic functions to accurately perform or check calculations required in the product documentation.


Apply today or email your resume to !Show lessShow more

• key responsibilities

  -Become certified for entry into the GMP cleanroom space to be able to perform sanitization, stock/replenish supplies, equipment setup, and all related aseptic filling operations.-Execute aseptic fill processes using batch records and SOPs.-Responsible for verifying the calibration of all related equipment and sanitization of supplies to support production-Increasing level of competency in the manufacturing area procedures. Assigned job duties will include Aseptic and clean room areas, Component Preparation, Filling and Capping-Learn the functions necessary to work in the Fill suite. This will include the operation of the associated equipment.-Ability to perform tasks with minimal supervisor direction.-Provide training for new team members.-Able to understand the manufacturing schedule and coordinate tasks to achieve the schedule.-Provide floor leadership in the absence of a supervisor or PT3 technicians.-Transport and/or dispose of hazardous chemicals.-Perform all other duties as assigned.-Must immediately notify supervisor if affected by an infectious disease or open lesions on the body, as individuals are not permitted to enter manufacturing areas or handle products if these conditions exist.

• experience

  1-4 years

• skills

  -B.S. degree in chemistry/biology/life sciences is a plus.-Extensive knowledge of and experience in bulk formulation along with equipment cleaning, preparation, and assembly are preferred.-Computer skills in Microsoft Office such as Word and Excel are a plus.-College coursework preferred-Experience in stopper prep, capping, and packaging preferred.

• qualifications

  -Isolator experience-Minimum 3-5 years, including relevant aseptic filling experience in a cGMP pharmaceuticalmanufacturing facility.-Must possess working knowledge and understanding of GMP compliance regulations.-Must possess knowledge and experience in the aseptic filling process, along with equipment cleaning,preparation, and assembly. - Must be able to comprehend and follow detailed procedural instructions in written and verbal form.-Must possess adequate working knowledge of arithmetic functions to accurately perform or check calculations required in the product documentation.

• education

  High School

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