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Job Requirements of Biotechnician:
-
Employment Type:
Contractor
-
Location:
San Diego, CA (Onsite)
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Biotechnician
Careers Integrated Resources Inc
San Diego, CA (Onsite)
Contractor
Pay: $21.61 hourly
Duration: 6 months, possibility of extension
Job Description:
The GMP Biotechnician will work closely with several departments such as QA and Inventory Control to understand and streamline manufacturing production processes. This position is responsible for filling, capping, labeling, completing detailed batch records, putting away finished good inventory (FGI), data entry, equipment maintenance, and supply inspections and storage.
This role requires verification and sign-off on records, as well as label creation and inspections. Data entry responsibilities include scanning and attaching records into the system, CoA creation, and processing work orders through the Enterprise Resource Planning (ERP) system.
BioLegend’s regulated products are produced in a US FDA-registered Good Manufacturing Practices (cGMP) manufacturing facility.
Additional duties include vialing products according to standard operating procedures, preparing product/project-related documentation, and maintaining device history records for all regulated products.
Essential Functions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Perform vialing and labeling of regulated products
Maintain batch records and other documentation to ensure compliance with ISO13485:2016 and MDSAP regulations
Maintain laboratory equipment and manage laboratory supplies
Receive materials (inspection, organizing/labeling, and updating logs)
Print labels for final product production
Perform general buffer formulation
Wash lab glassware
Perform data entry responsibilities
Other projects or responsibilities as required
Education
Minimum Qualifications – Education and Experience
Associate's Degree in Biology, Biochemistry, Chemistry, or other related area
0–6 months of relevant experience in a laboratory and/or biotech manufacturing and/or filling/bottling/packaging work environment
Demonstrated ability to be detail-oriented, organized, work well in small work groups, and adhere to timelines
Knowledge of Good Documentation Practices
Knowledge of aseptic techniques in a biosafety cabinet
Ability to pipette small volumes
Ability to perform simple math calculations
Ability to communicate effectively both orally and in writing
Preferred Qualifications – Education and Experience
2 years of relevant experience in a laboratory and/or biotech manufacturing and/or filling/bottling/packaging work environment
Working experience in the biotechnology industry with quality system knowledge including ISO 13485 or cGMP regulations
Advanced pipetting skills
Familiarity with raw material supply receiving and inspection processes
Duration: 6 months, possibility of extension
Job Description:
The GMP Biotechnician will work closely with several departments such as QA and Inventory Control to understand and streamline manufacturing production processes. This position is responsible for filling, capping, labeling, completing detailed batch records, putting away finished good inventory (FGI), data entry, equipment maintenance, and supply inspections and storage.
This role requires verification and sign-off on records, as well as label creation and inspections. Data entry responsibilities include scanning and attaching records into the system, CoA creation, and processing work orders through the Enterprise Resource Planning (ERP) system.
BioLegend’s regulated products are produced in a US FDA-registered Good Manufacturing Practices (cGMP) manufacturing facility.
Additional duties include vialing products according to standard operating procedures, preparing product/project-related documentation, and maintaining device history records for all regulated products.
Essential Functions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Perform vialing and labeling of regulated products
Maintain batch records and other documentation to ensure compliance with ISO13485:2016 and MDSAP regulations
Maintain laboratory equipment and manage laboratory supplies
Receive materials (inspection, organizing/labeling, and updating logs)
Print labels for final product production
Perform general buffer formulation
Wash lab glassware
Perform data entry responsibilities
Other projects or responsibilities as required
Education
Minimum Qualifications – Education and Experience
Associate's Degree in Biology, Biochemistry, Chemistry, or other related area
0–6 months of relevant experience in a laboratory and/or biotech manufacturing and/or filling/bottling/packaging work environment
Demonstrated ability to be detail-oriented, organized, work well in small work groups, and adhere to timelines
Knowledge of Good Documentation Practices
Knowledge of aseptic techniques in a biosafety cabinet
Ability to pipette small volumes
Ability to perform simple math calculations
Ability to communicate effectively both orally and in writing
Preferred Qualifications – Education and Experience
2 years of relevant experience in a laboratory and/or biotech manufacturing and/or filling/bottling/packaging work environment
Working experience in the biotechnology industry with quality system knowledge including ISO 13485 or cGMP regulations
Advanced pipetting skills
Familiarity with raw material supply receiving and inspection processes
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