Manufacturing Associate
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We are looking for Manufacturing Associate for our client in Pearl River, NY
Job Title: Manufacturing Associate
Job Type: Contract
Job Description:
Job Description:
Pay Range: $21.56hr- $26.56hr
Responsibilities:
- In depth understanding of techniques and processes being executed on a routine basis.
- Responsible for all aspects of large-scale bioreactor cell expansion and protein production including equipment preparation (CIP and SIP), appropriate use of raw materials and components (FIFO), material sampling for applicable analytical testing, filter integrity testing, etc.
- Perform cell analysis and data interpretation of cell culture samples with the use of the cell counter, including operation of microscope for contamination checks.
- Responsible for the operation and maintenance of ancillary equipment such as floor scales, turbidity meters, tube welder, tube sealer, peristaltic pumps, etc.
- Interacts with other departmental personnel to assist in resolving manufacturing quality issues.
- Technicians should have the ability to manage and analyze manufacturing data.
- Ability to take initiative to identify issues, troubleshoot, propose solutions, and keep management informed.
- Ability to present and explain techniques and results of manufacturing processes with outside departmental personnel.
- Ensure good documentation practices (GDP) in execution and reviews of production records.
- Responsible for all required cGMP training including additional training assigned by their manager.
- Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.
- Follows established SOPs for the flow of materials, personnel, and equipment in and out of the cGMP facility.
- Work a flexible work schedule, weekends and holidays as required, and as needed by the department.
- Work with Compliance regarding notification of deviations and CAPAs as they occur and provide information during investigations.
- Other duties as they are required.
- High School degree with at least 2 years of work experience, or training within a cGMP manufacturing environment.
- General knowledge of cGMP, GDP, SOP s.
- Good communication and social skills Basic understanding of the Baculovirus Expression Vector System (BEVS) manufacturing process is desired but not required.
- The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job and include the ability to stand over intervals of several hours at a time, ability to bend, squat, and reach, and Due to the nature of the job the candidate should be able to lift 50 pounds with assistance.
- The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- May involve work with hazardous materials.
- Based on production schedules, different start time scenarios may occur, requiring a flexible work schedule for the candidate.
- This role requires frequent work on weekends depending on production demands.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job We are looking for Manufacturing Associate for our client in Pearl River, NY
Job Title: Manufacturing Associate
Job Type: Contract
Job Description:
Job Description:
Pay Range: $21.56hr- $26.56hr
Responsibilities:
- In depth understanding of techniques and processes being executed on a routine basis.
- Responsible for all aspects of large-scale bioreactor cell expansion and protein production including equipment preparation (CIP and SIP), appropriate use of raw materials and components (FIFO), material sampling for applicable analytical testing, filter integrity testing, etc.
- Perform cell analysis and data interpretation of cell culture samples with the use of the cell counter, including operation of microscope for contamination checks.
- Responsible for the operation and maintenance of ancillary equipment such as floor scales, turbidity meters, tube welder, tube sealer, peristaltic pumps, etc.
- Interacts with other departmental personnel to assist in resolving manufacturing quality issues.
- Technicians should have the ability to manage and analyze manufacturing data.
- Ability to take initiative to identify issues, troubleshoot, propose solutions, and keep management informed.
- Ability to present and explain techniques and results of manufacturing processes with outside departmental personnel.
- Ensure good documentation practices (GDP) in execution and reviews of production records.
- Responsible for all required cGMP training including additional training assigned by their manager.
- Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.
- Follows established SOPs for the flow of materials, personnel, and equipment in and out of the cGMP facility.
- Work a flexible work schedule, weekends and holidays as required, and as needed by the department.
- Work with Compliance regarding notification of deviations and CAPAs as they occur and provide information during investigations.
- Other duties as they are required.
- High School degree with at least 2 years of work experience, or training within a cGMP manufacturing environment.
- General knowledge of cGMP, GDP, SOP s.
- Good communication and social skills Basic understanding of the Baculovirus Expression Vector System (BEVS) manufacturing process is desired but not required.
- The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job and include the ability to stand over intervals of several hours at a time, ability to bend, squat, and reach, and Due to the nature of the job the candidate should be able to lift 50 pounds with assistance.
- The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- May involve work with hazardous materials.
- Based on production schedules, different start time scenarios may occur, requiring a flexible work schedule for the candidate.
- This role requires frequent work on weekends depending on production demands.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
Report this job