Job details
Spherion is hiring Production Technicians in Indianapolis, IN!
This is a senior-level position in the bulk processing area. The employee will utilize experience and training to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through several job functions and be required to demonstrate increasing skill levels. ...
Responsibilities :
- Learn, understand, and comply with all Company and GMP compliance policies / procedures.
- Learn and perform area sanitization procedures in a GMP Manufacturing facility (Formulation Rooms,
Staging Areas, Raw Material Dispensing Room, and Airlocks).
Learn and become competent in performing filter integrity testing.Learn and become competent in cleaning miscellaneous pieces of manufacturing equipment andvessels.
Learn and perform raw material weighing (dispensing) and bulk formulation.Perform system maintenance PM?s / procedures.Become and maintain qualification for entry into the Aseptic Core in order to perform sterile filtrations,unload the autoclave, and complete Steam-in-Place operations as deemed necessary by area
management.
Perform other duties supporting the production schedule as assigned by area supervision.Execute tasks / operations with minimal supervision.Provide training / guidance / leadership for Production Technician I and II personnel.Supervise the activities of other members of the manufacturing team, taking full responsibility forresults.
Coordinate manufacturing activities with other support groups to receive components, batch records,QC results, etc.
Conduct QTS nonconforming product investigations, identify corrective actions, and implementchanges as needed.
Place purchase orders and monitor supplies.Perform final batch record reviews before QA review.Attend mandatory annual hazardous waste training meeting(s) and demonstrate competency in thattraining by passing test(s) administered by the company or consultant providing such training.
Performs special projects and other duties as assigned.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.Education : High School
Experience : 1-4 years
Qualifications :
High school diploma or the equivalent.Minimum of five years of experience using current Good Manufacturing Practices (GMP) in a regulated manufacturing facility pharmaceutical / biotech / diagnostic industry) with Processing experience.Adequate communication skills to read, comprehend, and discuss detailed GMP documentation (batch record instructions, Standard Operating Procedures, etc.).Strong attention to detail.Ability to perform arithmetic functions to accurately perform or check calculations required in manufacturing instructions.Leadership experience in training / directing others.Strong mechanical aptitude.Ability to troubleshoot, identify problems, and propose solutions.While performing the duties of this job, the employee is regularly required to use their hands and arms. The employee is frequently required to stand.The employee must regularly lift and / or move up to 10 pounds, and frequently lift and / or move up to 25 pounds.Isolator experienceApply today or email your resume to !Show lessShow more
Spherion is hiring Production Technicians in Indianapolis, IN!
This is a senior-level position in the bulk processing area. The employee will utilize experience and training to manufacture pharmaceuticals in a strictly controlled GMP environment. The employee will progress through several job functions and be required to demonstrate increasing skill levels.
Responsibilities :
Learn, understand, and comply with all Company and GMP compliance policies / procedures.Learn and perform area sanitization procedures in a GMP Manufacturing facility (Formulation Rooms,Staging Areas, Raw Material Dispensing Room, and Airlocks).
Learn and become competent in performing filter integrity testing.Learn and become competent in cleaning miscellaneous pieces of manufacturing equipment andvessels.
Learn and perform raw material weighing (dispensing) and bulk formulation.Perform system maintenance PM?s / procedures.Become and maintain qualification for entry into the Aseptic Core in order to perform sterile filtrations,unload the autoclave, and complete Steam-in-Place operations as deemed necessary by area
management. ...
Perform other duties supporting the production schedule as assigned by area supervision.Execute tasks / operations with minimal supervision.Provide training / guidance / leadership for Production Technician I and II personnel.Supervise the activities of other members of the manufacturing team, taking full responsibility forresults.
Coordinate manufacturing activities with other support groups to receive components, batch records,QC results, etc.
Conduct QTS nonconforming product investigations, identify corrective actions, and implementchanges as needed.
Place purchase orders and monitor supplies.Perform final batch record reviews before QA review.Attend mandatory annual hazardous waste training meeting(s) and demonstrate competency in thattraining by passing test(s) administered by the company or consultant providing such training.
Performs special projects and other duties as assigned.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.Education : High School
Experience : 1-4 years
Qualifications :
High school diploma or the equivalent.Minimum of five years of experience using current Good Manufacturing Practices (GMP) in a regulated manufacturing facility pharmaceutical / biotech / diagnostic industry) with Processing experience.Adequate communication skills to read, comprehend, and discuss detailed GMP documentation (batch record instructions, Standard Operating Procedures, etc.).Strong attention to detail.Ability to perform arithmetic functions to accurately perform or check calculations required in manufacturing instructions.Leadership experience in training / directing others.Strong mechanical aptitude.Ability to troubleshoot, identify problems, and propose solutions.While performing the duties of this job, the employee is regularly required to use their hands and arms. The employee is frequently required to stand.The employee must regularly lift and / or move up to 10 pounds, and frequently lift and / or move up to 25 pounds.Isolator experienceApply today or email your resume to !Show lessShow more
key responsibilities
Learn, understand, and comply with all Company and GMP compliance policies / procedures.-Learn and perform area sanitization procedures in a GMP Manufacturing facility (Formulation Rooms,Staging Areas, Raw Material Dispensing Room, and Airlocks).-Learn and become competent in performing filter integrity testing.-Learn and become competent in cleaning miscellaneous pieces of manufacturing equipment andvessels.-Learn and perform raw material weighing (dispensing) and bulk formulation.-Perform system maintenance PM?s / procedures.-Become and maintain qualification for entry into the Aseptic Core in order to perform sterile filtrations,unload the autoclave, and complete Steam-in-Place operations as deemed necessary by areamanagement.-Perform other duties supporting the production schedule as assigned by area supervision.-Execute tasks / operations with minimal supervision.-Provide training / guidance / leadership for Production Technician I and II personnel.-Supervise the activities of other members of the manufacturing team, taking full responsibility forresults.-Coordinate manufacturing activities with other support groups to receive components, batch records,QC results, etc.-Conduct QTS nonconforming product investigations, identify corrective actions, and implementchanges as needed.-Place purchase orders and monitor supplies.-Perform final batch record reviews before QA review.-Attend mandatory annual hazardous waste training meeting(s) and demonstrate competency in thattraining by passing test(s) administered by the company or consultant providing such training.-Performs special projects and other duties as assigned.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.qualifications
High school diploma or the equivalent. -Minimum of five years of experience using current Good Manufacturing Practices (GMP) in a regulated manufacturing facility pharmaceutical / biotech / diagnostic industry) with Processing experience.-Adequate communication skills to read, comprehend, and discuss detailed GMP documentation (batch record instructions, Standard Operating Procedures, etc.).-Strong attention to detail.-Ability to perform arithmetic functions to accurately perform or check calculations required in manufacturing instructions.-Leadership experience in training / directing others.-Strong mechanical aptitude.-Ability to troubleshoot, identify problems, and propose solutions.-While performing the duties of this job, the employee is regularly required to use their hands and arms. The employee is frequently required to stand. -The employee must regularly lift and / or move up to 10 pounds, and frequently lift and / or move up to 25 pounds.-Isolator experienceeducation
High School
share this job.