Sysco

Sysco

64 jobs near Columbus, OH

37506390 QC Associate Fremont, CA 6 Months Sigma Inc is currently looking for a QC Associate to work in with our client in Fremont, CA 1st Shift: Mon- Fri 8.00 AM - 5.00 PM Responsibilities: * As ...

37506390 QC Associate Fremont, CA 6 Months Sigma Inc is currently looking for a QC Associate to work in with our client in Fremont, CA 1st Shift: Mon- Fri 8.00 AM - 5.00 PM Responsibilities: * As ...

Quality Control Associate

Richmond, VA · On-site

$63K - $90K/yr

Quality Control Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the HITT quality control plan. This includes working ...

QC Associate - GMP Laboratory | HPLC | Biotechnology | Fremont, CA | 6-Month Contract Job ID: 37506390 Location: Fremont, CA (Onsite) Job Type: 6-Month Contract Shift: Monday-Friday | 8:00 AM - 5:00 ...

Quality Control Associate Location: Research Triangle Park, NC Duration: 12+ months (possibility of extension) ROLES & RESPOSNISBILTIES: * The Quality Control Raw Materials Associate I is responsible ...

Be Seen First

The Quality Control Associate plays a critical role within the Quality Team, focusing on routine quality checks to ensure products meet established standards. This standalone position involves ...

QC Associate

Manhattan, NY · On-site

$17 - $24/hr

Quality Control Associate R2Net Inc. is an innovative technology company that provides e-commerce and supply chain platforms to connect the entire span of the diamond industry ecosystem, including ...

QC Associate

Manhattan, NY · On-site

$17 - $24/hr

Quality Control Associate R2Net Inc. is an innovative technology company that provides e-commerce and supply chain platforms to connect the entire span of the diamond industry ecosystem, including ...

Be Seen First

The Quality Control Associate plays a critical role within the Quality Team, focusing on routine quality checks to ensure products meet established standards. This standalone position involves ...

QC Associate Onsite role at the Devens site This position will perform routine testing including testing In support of Manufacturing. Primary responsibilities include testing of Northern Blot ...

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all ...

Quality Control Associate

Manhattan, NY · On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all ...

Job title: QC Associate Duration: 12 months Location: Tucson, AZ The Quality Control Associate - Reagent Manufacturing will be an integral part of a team that performs raw material and finished goods ...

Quality Control Associate

Manhattan, NY · On-site

$22.50 - $24/hr

Blue Nile is seeking a detail-oriented and highly organized QC Associate (Quality Control Associate) to join our manufacturing team. In this role, they will be responsible for ensuring that all ...

Showing results 21-40

QC Associate

Sigma Systems, Inc.

Fremont, CA • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

37506390 QC Associate Fremont, CA 6 Months
Sigma Inc is currently looking for a QC Associate to work in with our client in Fremont, CA
1st Shift: Mon- Fri 8.00 AM - 5.00 PM
Responsibilities:

  • As part of the QC In-Process Testing (IPC) team, execute and coordinate routine and non-routine testing of bulk drug substance and intermediates within a multi-product facility.
  • Perform laboratory operations independently following appropriate training, including but not limited to: HPLC titer, UV-Vis absorbance, endotoxin testing, pH, osmolality, total organic carbon (TOC), conductivity, and sample aliquotation.
  • Perform essential laboratory support activities such as maintaining inventory of consumables and materials, properly disposing of expired reagents, and identifying and reporting process or equipment anomalies.
  • Deliver high-quality analytical results within established timelines, ensuring accuracy "right first time. Accurately document all work in compliance with cGMP and cGDP requirements.
  • Adhere to all site-specific procedures, regulatory standards, and quality systems.
  • Promptly and accurately report deviations, abnormalities, or out-of-specification results. Maintain strict adherence to safety standards by recognizing and escalating unsafe conditions or behaviors.
  • Maintain laboratory workspaces in accordance with established 5S and cleanliness standards. Ensure personal training is current and compliant with all regulatory and organizational requirements.

Requirements:

  • Bachelor's degree in biology or Life Sciences required
  • 3-5 years of industry experience GMP experience is preferred.
  • Technical skills preferred: HPLC (titer), aseptic technique, osmolality, total organic carbon (TOC), conductivity

The ideal candidate can demonstrate:

  • Strong interpersonal and communication skills (both written and oral), a strong customer focus, and an ability to interact with various departments and levels.
  • Ability to work independently and as part of a team, to meet departmental/facility goals; is also able to work across functions to achieve common goals
  • Strong attention to detail, and an ability to focus on details of execution.