eTeam
Overview
Job Title: Quality Control Analyst Location: 100% onsite at client site in Holly Springs, NC Hourly Pay Rate: $25 - 28/an hr. Employer : eTeam (Pharmaceutical Talent Acquisition SME) Responsibilities
Primary responsibilities include performing tasks associated with critical testing on raw materials, environment, utilities, validation samples, and manufactured materials. Ensure CSL Seqirus samples are tested and reviewed according to quality requirements; ensure results are valid, accurate, and documented per applicable regulatory and corporate requirements. If QC Support work is required, ensure QC samples are delivered and transported in a timely manner; operate autoclave and parts washer; assist with coordinating QC sample shipments as necessary. Maintain GMP documentation for all activities and follow applicable SOPs. Lifecycle responsibilities may include shift work to support operations. QC Microbiology Accountabilities
Performs testing and related tasks without errors per applicable SOPs and protocols. Complies with policies and procedures to maintain compliance with legal regulations, health and safety, and regulatory requirements. Develops and maintains SOPs. Develops expertise in assigned assays/techniques. Authors lab investigations and invalid assay assessments. May be required to perform shift work as needed to support operations. QC Support Accountabilities
Responsible for Lab services including running a Parts Washer, operating an Autoclave, and delivering samples through the Bulk process by reviewing sample plans before delivery. Responsible for aliquoting production material in a BSC. Responsible for processing incoming and outgoing shipments. Perform GMP documentation activities and follow schedules; demonstrate excellent communication skills. Work within clearly defined SOPs and/or scientific methods; adhere to quality guidelines. Demonstrate teamwork and willingness to assist others. Qualifications
Minimum Required Qualifications: Bachelor's degree in a Scientific discipline required. Recent college graduates (entry level / no experience) acceptable. Must be willing to have a current flu shot. Preferred / Nice to Have Qualifications: Degree in Biology or Microbiology is highly preferred. Experience with environmental monitoring in a pharmaceutical manufacturing environment is beneficial. Experience in an analytical testing lab (academic or industry) is beneficial. Experience in a cGMP Pharmaceutical Laboratory is beneficial. Experience with Laboratory Information Management Systems (LIMS) is beneficial. Experience performing Bioburden, Endotoxin, Sterility testing is beneficial. Intermediate knowledge of GMPs, safety regulations and data integrity is a plus. Intermediate knowledge of analytical methods and related instrumentation is a plus. Please note, a current flu vaccine is required for this role.
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Job Title: Quality Control Analyst Location: 100% onsite at client site in Holly Springs, NC Hourly Pay Rate: $25 - 28/an hr. Employer : eTeam (Pharmaceutical Talent Acquisition SME) Responsibilities
Primary responsibilities include performing tasks associated with critical testing on raw materials, environment, utilities, validation samples, and manufactured materials. Ensure CSL Seqirus samples are tested and reviewed according to quality requirements; ensure results are valid, accurate, and documented per applicable regulatory and corporate requirements. If QC Support work is required, ensure QC samples are delivered and transported in a timely manner; operate autoclave and parts washer; assist with coordinating QC sample shipments as necessary. Maintain GMP documentation for all activities and follow applicable SOPs. Lifecycle responsibilities may include shift work to support operations. QC Microbiology Accountabilities
Performs testing and related tasks without errors per applicable SOPs and protocols. Complies with policies and procedures to maintain compliance with legal regulations, health and safety, and regulatory requirements. Develops and maintains SOPs. Develops expertise in assigned assays/techniques. Authors lab investigations and invalid assay assessments. May be required to perform shift work as needed to support operations. QC Support Accountabilities
Responsible for Lab services including running a Parts Washer, operating an Autoclave, and delivering samples through the Bulk process by reviewing sample plans before delivery. Responsible for aliquoting production material in a BSC. Responsible for processing incoming and outgoing shipments. Perform GMP documentation activities and follow schedules; demonstrate excellent communication skills. Work within clearly defined SOPs and/or scientific methods; adhere to quality guidelines. Demonstrate teamwork and willingness to assist others. Qualifications
Minimum Required Qualifications: Bachelor's degree in a Scientific discipline required. Recent college graduates (entry level / no experience) acceptable. Must be willing to have a current flu shot. Preferred / Nice to Have Qualifications: Degree in Biology or Microbiology is highly preferred. Experience with environmental monitoring in a pharmaceutical manufacturing environment is beneficial. Experience in an analytical testing lab (academic or industry) is beneficial. Experience in a cGMP Pharmaceutical Laboratory is beneficial. Experience with Laboratory Information Management Systems (LIMS) is beneficial. Experience performing Bioburden, Endotoxin, Sterility testing is beneficial. Intermediate knowledge of GMPs, safety regulations and data integrity is a plus. Intermediate knowledge of analytical methods and related instrumentation is a plus. Please note, a current flu vaccine is required for this role.
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