Referso Jobs

Surgical Technician

Buffalo Surgery Center · Posted Nov 12, 2026

Open

Amherst, New York, United States
On-site
Full-time · Associate

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Surgical Technician

Buffalo Surgery Center · Posted Nov 12, 2026

Open

Amherst, New York, United States
On-site
Full-time · Associate

Apply with Referso

Sterile Pharmacist 503B

Empower Pharmacy · Posted Nov 10, 2026

Open

Houston, Texas, United States
On-site
Full-time · Staff

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The Sterile Pharmacist supports safe, accurate, and timely preparation and dispensing of sterile medications within Empower Pharmacy's fast growing, highly regulated 503A and 503B environment.

Responsibilities

Verify sterile compounding activities against approved formulations, procedures, and applicable standards to support consistent product quality and patient safety.
Evaluate medication orders, ingredient suitability, calculations, and relevant clinical considerations to identify discrepancies before preparation or dispensing.
Prioritize assigned pharmacy activities, coordinate with operational partners, and maintain accurate processing to meet quality and turnaround expectations.
Follow applicable pharmacy regulations, sterile compounding standards, and established procedures while maintaining required documentation and operational controls.
Examine compounding records, labeling, and relevant documentation for completeness and accuracy, addressing discrepancies before applicable release or dispensing decisions.

Requirements

Doctor of Pharmacy (PharmD) or Bachelor of Science in Pharmacy degree from an accredited pharmacy program, with appropriate pharmacist licensure.
Nice to have: Sterile compounding
Nice to have: Aseptic processing
Nice to have: Pharmacy production operations

Skills

Sterile compounding principles

Manager - Product Development Quality

Zoetis · Posted Nov 3, 2026

Open

Lincoln, Nebraska, United States
Full-time · Manager
15+ years

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Lead quality assurance and compliance for Veterinary Medicine Research & Development, ensuring product and process compliance with USDA, EU, FDA, and Zoetis standards.

Responsibilities

Ensure VMRD production facilities and product transfers comply with applicable regulations
Work with DST colleagues on scale-up, technical transfers and regulatory coordination
Serve as QA consultant for development, clinical, and VICH batches
Review and approve validation protocols and reports
Conduct deviation investigations and oversee CAPAs

Requirements

Bachelor's degree in biological or pharmaceutical sciences, engineering, or related discipline
Nice to have: Master's or PhD in biological science or chemical/bioprocess engineering
Nice to have: validation of processes, equipment, cleaning procedures, software, and computerized systems
Nice to have: knowledge of Zoetis biological and biopharmaceutical products

Skills

Quality Assurance auditing cGMP quality systems aseptic practices

Microbiology Analyst

QRC Group · Posted Nov 11, 2026

Open

Cayey, Puerto Rico, Puerto Rico
Entry
2+ years

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The Microbiology Analyst I is responsible for performing routine microbiological testing and laboratory activities in support of quality control, manufacturing, and compliance requirements.

Responsibilities

Perform routine microbiological testing, including Bioburden, Endotoxin (LAL), Sterility Testing, and Growth Promotion Testing.
Conduct Environmental Monitoring activities in controlled manufacturing and laboratory areas.
Prepare culture media, reagents, and laboratory solutions according to approved procedures.
Operate laboratory equipment and maintain accurate test records and documentation.
Record and review laboratory data in compliance with Good Documentation Practices (GDP).

Requirements

Bachelor Degree in Microbiology or Biology
Nice to have: Bilingual (English and Spanish)

Skills

Microbiological techniques Aseptic practices Laboratory documentation Microsoft Office

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Scientist - Product Development Quality

Zoetis · Posted Nov 3, 2026

Open

Lincoln, United States
On-site
Full-time · Staff
5+ years
Visa sponsorship

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Provide quality assurance and compliance expertise for Veterinary Medicine Research & Development (VMRD), including the design, execution, and transfer of new biological/biopharmaceutical products to ensure department and site objectives are achieved.

Responsibilities

Ensure VMRD production facilities and product transfers comply with USDA, EU, FDA, and Zoetis quality standards.
Work with VMRD Development Science & Technology on scale-up and technical transfers.
Serve as QA consultant for development, clinical, and VICH batches/serials.
Review new product master batch records, manufacturing documents, and analytical documents for compliance.
Review and approve validation protocols and reports.

Requirements

Bachelor's degree in biological or pharmaceutical sciences, engineering, or related discipline (minimum 5 years experience)
Master's degree in biological or pharmaceutical sciences, engineering, or related discipline (minimum 3 years experience)
Nice to have: Master's or PhD degree in a biological science or chemical/bioprocess engineering
Nice to have: Expert-level competency in validation of processes, equipment, cleaning procedures, software, and computerized systems
Nice to have: Solid knowledge of Zoetis biological and biopharmaceutical products

Skills

Quality Assurance auditing

Manufacturing Technician II

Mindlance · Posted Nov 9, 2026

Open

North Chicago, Illinois, United States

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Responsible for maintaining fibroblast cell cultures and supporting manufacturing operations in a GMP-regulated biologics production facility.

Responsibilities

Maintain human fibroblast cell culture in a clean room environment
Assist in the manufacture of solutions used in production and processing of raw materials
Sample by-products using standard methodologies
Complete all relevant documentation compliant with cGMP and GDP guidelines
Maintain the cell culture complex and surrounding environment

Requirements

Bachelor’s degree preferably in a Natural Science, Cell Biology, Biology, Biochemistry, Chemical Engineering or a related field
Associate degree from an accredited two-year program with relevant work experience will be considered
Nice to have: mechanical skills
Nice to have: clean room work experience

Skills

cGMP manufacturing operations GMP regulated environment cleanroom environment LIMS SAP automated control systems sampling of in process and raw materials glass washer autoclave buffer/media preparation equipment preparation (CIP/SIP)aseptic practices column chromatography tangential flow filtration

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Certified Surgical Technologist in Operating Room

St. Charles Health System · Posted Oct 30, 2026

Open

Bend, Oregon, United States
On-site
Full-time · Associate
$43–$64 per hour
1+ years

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The Certified Surgical Tech (CST) functions as a member of the Surgical Services Perioperative Team, performing duties as a Scrub Technologist or Second Assisting Technologist while maintaining a safe and sterile environment.

Compensation

Pay Range: $42.87 - $63.89. Shift differentials under the OFNHP: Evening: $2.50/hr. Weekend: $4/hr. Night: Starts at $10/hr.

Responsibilities

Functions duties to ensure patient care is accomplished in a safe, efficient, and cost-effective manner.
Ensures the perioperative regime for each patient is implemented as prescribed by the physician.
Prepares the operating room and obtains necessary equipment.
Drapes and covers operating and instrument tables; lays out supplies and equipment.
Assists and procures appropriate equipment that will be used during surgery, checks for any malfunctions.

Requirements

Graduate of a CAAHEP (Commission on Accreditation of Allied Health Education Programs) accredited program
ABHES (Accrediting Bureau of Health Education Schools) accredited program
military surgical technologist program

Skills

Surgical Technology Aseptic practices Scrub Technologist

Quality Control Technician II

Teva Pharmaceuticals · Posted Nov 6, 2026

Open

Full-time · Mid

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Perform routine and non-routine microbiological analyses, inspections, and testing on presented samples in a GMP-regulated environment.

Responsibilities

Independently perform routine and non-routine microbiological analyses according to established procedures.
Conduct bioburden, endotoxin, sterility, and microorganism testing using approved microbiological methods.
Perform microbial identification using Gram staining and/or MALDI-TOF.
Carry out release testing of growth media and work within safety cabinets and isolators.
Record and report test results in LIMS.

Requirements

MLO Level 4 or higher with a specialization in Microbiology, or an equivalent scientific qualification.

Skills

Microbiological analysis techniques GMP and/or GLP-regulated environment LIMS or other digital laboratory systems Aseptic practices Laboratory safety principles LIMS

Benefits

Generous annual leave
Reward plans
Flexible working schedules (dependent on role)
Access to tailored health support
Meaningful ways to give back to the community

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