The Laboratory Supervisor – Microbiology supervises the Riverside microbiology laboratory and serves as its technical lead for cosmetic and over-the-counter products, managing personnel, daily testing priorities, laboratory controls, investigations, and audit readiness.
Compensation
The base pay for this position ranges from $75,000 in our lowest geographic market up to $110,000 in our highest geographic market.
Responsibilities
Oversee and perform microbiological testing of raw materials, bulk and finished products, purified water, environmental samples, and other assigned samples
Ensure microbial enumeration, specified-organism testing, microbial identification, and assessment of objectionable organisms are performed appropriately
Perform or coordinate preservative effectiveness testing, method suitability studies, and microbiological method validation or verification
Oversee purified water testing and environmental monitoring
Control media, reagents, cultures, and test materials
Requirements
Bachelor’s degree in microbiology, biology, biochemistry, or a related scientific discipline preferred
Nice to have: Bilingual English and Spanish
Nice to have: SAP
Nice to have: Previous laboratory leadership, supervisory, or lead experience
Supports research, design and development projects including creating tooling and fixtures to meet product and process development needs.
Responsibilities
Supports research, design and development projects including creating tooling and fixtures to meet product and process development needs.
Assume technical role on a cross-functional team on new products, design changes, process changes, design for manufacturability, and product enhancements including related testing, tooling and fixtures.
Propose solutions to design, process, and quality issues through the application of engineering principles, analysis, and empirical methods.
Act a liaison between R&D New Product and Manufacturing Engineering.
Create and maintain accurate documentation of prototype concepts, tooling, drawings and shop orders in coordination with the Quality Assurance and manufacturing functions.
Utilise safe systems of working and risk assessment of plant and processes, support site compliance to FSSC 22000, ISO 45001 and FEMAS certifications, and undertake routine daily physical-chemical and microbiological analysis of in-process beer and water samples.
Responsibilities
Utilise safe systems of working and risk assessment of plant and processes
Maintain a clean, orderly, safe work environment using 5S Standards
Ensure Good Safe Laboratory Practices are adhered to
Support the development and implementation of the Quality & Food Safety Strategy on site
Undertake routine daily physical-chemical analysis of in-process beer and water samples
Requirements
Relevant science degree or equivalent
Bachelor/Masters of Science (analytical or microbiology preferred)
Nice to have: Laboratory setting experience (regulatory sector preferred)
Nice to have: LIMS system operation (e.g. Harford)
The Analytical Quality Assurance (AQA) associate I position is a team contributor role responsible for reviewing and confirming compliance related to raw materials, in-process and finished product analytical documents.
Compensation
$66,300 - $86,000
Responsibilities
Reviewing and confirming the compliance related to raw materials, in-process and finished product analytical documents
Monitoring and ensuring of current Good Laboratory Practices (cGLP) followed by laboratory personnel during routine operation
Verifying the laboratory chemicals/reagents, standards for completeness of the labels against standard operating procedures (SOPs)
Review of laboratory audit trials during data review against standard operating procedures (SOPs)
Coordinating with the Analytical Laboratory Teams to arrange required documents to cross functional teams
Requirements
Bachelor's degree in chemistry, Pharmaceutical Sciences, or related field of study
Master’s degree in chemistry, Pharmaceutical Sciences, or related fields of study (preferred)
Nice to have: Master’s degree in chemistry or Pharmaceutical Sciences
Nice to have: Experience in Inhalation products (MDI)
Nice to have: Knowledge of good manufacturing practices and good documentation practices
Perform routine microbiological testing of environmental samples, raw materials, in-process samples, and finished products to ensure compliance with company and regulatory standards.
Responsibilities
Perform routine microbiological testing of environmental samples, raw materials, in-process samples, and finished products
Accurately document, review, and report test results in accordance with Good Laboratory Practices (GLP) and company standard operating procedures (SOPs)
Maintain, calibrate, and troubleshoot laboratory equipment and instruments to support accurate and reliable testing
Assist with investigations involving microbiological issues, product quality concerns, and potential contamination, including recommending corrective actions
Maintain and update laboratory records, SOPs, work instructions, and other required documentation
Requirements
Bachelor of Science degree in Microbiology, Biology, or a related scientific field
Manufacturing Associate I/II (Nights) responsible for execution of upstream or downstream production activities for early and late-phase cell culture programs within a GMP environment.
Responsibilities
Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR).
Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.
Requirements
Bachelor’s degree in a related scientific or engineering discipline
The primary role of the EHS Specialist is to implement all policies and procedures that comprise the EHS program including, but not limited to, evaluation and control of safety and health hazards in the workplace, routine hazard recognition, environmental management, and performs routine tasks associated with inspection of necessary equipment.
Locations (2)
Green Bay, Wisconsin, United States
Freeman, South Dakota, United States
Compensation
Starting Salary: $25 - $26
Responsibilities
Implement EHS policies and procedures
Evaluate and control safety and health hazards
Perform routine hazard recognition
Manage environmental monitoring
Inspect equipment and perform finished product inspections
Requirements
Bachelor’s degree in safety management, industrial health and safety, a discipline of safety engineering or related field
Certified Safety Professional with OSHA 511 course completion
Process Engineer responsible for design, qualification, and optimization of process equipment and systems for cell culture and cryopreservation in a clinical-stage biotechnology company.
Responsibilities
Plan and execute small-scale process development experiments
Develop viable cGMP manufacturing processes for cell culture and cryopreservation
Participate in technology transfer activities
Contribute to development, optimization, and characterization of processes to manufacture and process human neural cell therapeutics
Assist with maintaining laboratories and equipment
Requirements
Bachelor’s or master’s degree in chemistry, biology or biochemistry
Nice to have: industrial research experience
Nice to have: upstream or downstream cell culture process development
Nice to have: Immunocytochemistry
Nice to have: confocal or fluorescent microscopic image analysis
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