Operations Test Associate

SGS_JOB_2450

Scientific
 California
Lab Experience
GMP/GLP
ERP
LIMS
or QSR

Contract - 06 Months

Location : San Diego CA The Operations Test Associate candidate will be responsible for performing QC release testing and analysis of raw materials, in-process, and finished goods for the Molecular Diagnostics Division. The candidate will be responsible for understanding and executing testing on multiple assay platforms in a cGMP environment to ensure timely release of products.

Job Responsibilities:

  • The incumbent may be asked to perform other function-related activities in addition to the responsibilities mentioned below as reasonably required by business needs.
  • Performs routine testing using GMP/GLP practices.
  • The incumbent may be asked to perform other function-related activities in addition to the responsibilities mentioned below as reasonably required by business needs.
  • Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
  • May perform microbiology testing and activities for the QC Micro team.
  • May perform pH and/or HPLC testing for the QC Analytical team.
  • Responsible for maintaining product and QC material inventories.
  • Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
  • Responsible for the maintenance and cleanliness of equipment, calibrating, or submitting items for calibration as needed.
  • Responsible for completing training in a timely manner and maintaining the records.
  • Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
  • Prepares documents for storage in our document management system and manages original data files.
  • Performs routine testing using GMP/GLP practices.
  • Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
  • May perform microbiology testing and activities for the QC Micro team.
  • May perform pH and/or HPLC testing for the QC Analytical team.
  • Responsible for maintaining product and QC material inventories.
  • Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
  • Responsible for the maintenance and cleanliness of equipment, calibrating, or submitting items for calibration as needed.
  • Responsible for completing training in a timely manner and maintaining the records.
  • Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
  • Prepares documents for storage in our document management system and manages original data files.
  • The incumbent may be asked to perform other function-related activities in addition to the responsibilities mentioned below as reasonably required by business needs.
  • Performs routine testing using GMP/GLP practices.
  • Performs data analysis and results interpretations comparing to protocol-defined specifications, validity criteria, and alert limits.
  • May perform microbiology testing and activities for the QC Micro team.
  • May perform pH and/or HPLC testing for the QC Analytical team.
  • Responsible for maintaining product and QC material inventories.
  • Responsible for the maintenance and cleanliness of the laboratory, stocking shelves/drawers with testing materials.
  • Responsible for the maintenance and cleanliness of equipment, calibrating, or submitting items for calibration as needed.
  • Responsible for completing training in a timely manner and maintaining the records.
  • Participates in Laboratory Investigations for Invalid assays and Out-of-Specifications results.
  • Prepares documents for storage in our document management system and manages original data files.

Skills:

  • Intermediate computer skills (i.e., Microsoft programs)
  • Working knowledge of industry/regulatory standards and GMP/GLP requirements
  • Preferred working knowledge of Enterprise Resource Planning (ERP), LIMS, and/or QSR
  • Intermediate computer skills (i.e., Microsoft programs)
  • Intermediate computer skills (i.e., Microsoft programs)
  • Working knowledge of industry/regulatory standards and GMP/GLP requirements
  • Working knowledge of industry/regulatory standards and GMP/GLP requirements
  • Preferred working knowledge of Enterprise Resource Planning (ERP), LIMS, and/or QSR
  • Preferred working knowledge of Enterprise Resource Planning (ERP), LIMS, and/or QSR

Education/Experience:

  • Bachelor’s degree in a science-related field
  • Bachelor’s degree in a science-related field
  • Bachelor’s degree in a science-related field
  • 1 to 2 years of industrial lab experience (preferably QC)
  • 1 to 2 years of industrial lab experience (preferably QC)
  • 1 to 2 years of industrial lab experience (preferably QC)

Related Jobs

Compliance Specialist CMC, Quality Assurance

Scientific
 Massachusetts
6 Months

Location : Westborough MA USA The Compliance Specialist will perform critical QA tasks in support of GMP and non-GMP manufacturing programs and Regulatory Submissions at AIRM. The successful candidate will foster data integrity, quality, and compliance across a broad range of Quality Assurance areas and will work closely with talented counterparts at Astellas to help ensure high quality standards and value delivery for our patients. This position is based in Westborough, MA and will require on-site work.

Quality Assurance
Data review
QA review
GMP

The Compliance Specialist CMC, Quality Assurance

Scientific
 Massachusetts
6 Months

Location (mandatory): Westborough MA USA The Research Associate role will provide a supporting role for ongoing research activities.

Quality Assurance
Data review
QA review
GMP

Sourcing Manager, Diagnostics Direct Procurement

Scientific
 Arizona
12 Months (possible extension)

Location (mandatory): Tucson, AZ • Primary Location: Tucson, AZ (split time between Marana site and Oro Valley site) • Mandatory to be on-site at least 3 days per week (Tuesday and Thursdays at Oro Valley Campus. Wednesday at Marana campus). Experience: • Experience or demonstrated understanding in supporting cost reduction and value improvement programs. • Experience in operational excellence or continuous improvement methodologies as well as experience in Life Sciences are a plus. • Experience with enterprise systems and procure-to-pay tools and eSourcing tools is desired.

Procurement
Contracting
Business Enterprise Systems
Spot Buying
Cost Reduction ERP

Accounts Receivable Administrative

Scientific
 Florida
03+ Months Extendable

Location : Weston, FL 33331 (Hybrid). The Accounts Receivable Clerk will be a temporary position to aid and assist the Collections Department with general duties including, but not limited to, phone calls, data entry, and administrative tasks.

AR
Account Receivable
Collection
Past Due

Research Associate

Scientific
 Massachusetts
6 Months

Location (mandatory): Marlborough MA USA We are seeking a highly motivated Research Associate to support the analytical testing of cell therapy products to support development activities. The role requires hands-on laboratory work, including mammalian cell culture, flow cytometry, and PCR-based testing as well as data analysis. The Research Associate will work as part of a team under the guidance of Senior Project/Team Leads.

Tissue culture
Aseptic
Lab -based bioassay

Microbiologist

Scientific
 New York
$25 - $30 per Hour
06+ Months (possible extension)

Location : Rochester, NY 14606 Microbiologist responsible for performing routine quality control testing of raw materials, in-process samples, and finished products. Ensures compliance with GMP, HACCP, and ISO standards through accurate microbiological analysis, documentation, and product release in SAP. Skilled in aseptic techniques, microbial identification, and supporting operations with timely QC results. We are looking for a Microbiologist for our Quality Control team to be responsible for supporting the Rochester Laboratory in a manufacturing setting. This includes routine Microbiological lab testing with accurate, timely recording of test results into the business integrated module as well as utilizing lab reference materials for information regarding testing.

Microbiological Testing of Raw Materials
Aseptic Techniques & Good Laboratory Practices (GLP)
Quality Control Documentation & Compliance (ISO 22000
HACCP
GMP
FAMI-QS
NSF)
Microbial Identification
Serial Dilutions & Plating Techniques
Troubleshooting Non-Conforming Products & Corrective Action Support

Sensory Taste Panelist

Scientific
 New Jersey
$20.00
12+ Months (possible extension)

Location : Plainsboro, NJ 08536. Panelists will participate in sensory evaluations of food, beverages, and odorant samples, both individually and in groups, under the guidance of a panel leader. Responsibilities include following detailed instructions, completing evaluations using ballots or digital devices, and contributing to group discussions. Applicants must complete sensory screening tests prior to panel admission, with compensation provided for participation. Requirements: No experience required. Must be able to commit to at least 1 year of testing. Sensory evaluations will occur every Wednesday from 9:30am to 12:30pm. Please note: the panel runs during business hours. Must be free of major food allergies and dietary restrictions. Should have good communication skills, willingness to take direction from panel leaders and work well within a team of other sensory panelists. Applicants should have an excellent sense of smell and of taste, as well as the ability to accurately describe what they taste and smell. Applicants should be free of aversions to nearly all common foods and beverages.

Sensory evaluation
attention to detail
communication
critical thinking
teamwork
analytical skills
protocol adherence
objectivity
and computer proficiency.

Lab Technician

Scientific
 Ohio
03 months

Location: Cincinnati, OH (Onsite) The Lab Technician performs a variety of chemical, biological, and physical tests required for research, development or quality control. This position compiles data for reports and assists in special studies in the laboratory and in the field.

Chemical and biological tests for research
development and quality control.

QA Documentation Specialist I

Scientific
 California
$28.26
6 Months

Location : Vacaville CA We are seeking a highly motivated and experienced Quality Systems Support Specialist to join our team in Vacaville, CA. In this role, you will provide essential support to the Quality System Management process with document control and PQS integration, ensuring compliance with cGMP and global requirements.

Veeva
QMS
DMS
logo

At SGS Consulting, we go beyond resume-job matches, creating meaningful connections and pathways for individuals to thrive in defining careers.


2025. All right reserved.
logologologologo