Specialist, Quality Control

Posted 10 Days Ago
Be an Early Applicant
Tustin, CA, USA
In-Office
32-40 Hourly
Junior
Healthtech • Pharmaceutical
Transforming the CDMO experience: Unrivaled expertise. Worldclass facilities. Exceptional quality. Personalized process.
The Role
Performs biopharmaceutical QC sample receipt, logging, aliquoting, storage, shipment, documentation, inventory management, and disposal. Coordinates outside contract-laboratory testing, stability sample pulls, storage-unit monitoring, and liquid nitrogen fills. Compiles test reports and protocols while supporting continuous-improvement initiatives. Requires an associate degree with one year of QC experience or a relevant bachelor’s degree, plus familiarity with analytical testing, equipment, reports, procedures, GMP, and GxP inspections.
Summary Generated by Built In

Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
Your Role:
The Specialist, Quality Control will perform sample receipt for lot release, manage sample storage, coordinate outside testing, and assist with stability sample pulls.  Analyst will support QC continuous improvement initiatives.
Key Responsibilities:

  • Picking up, logging in, aliquoting, sample storage, and preparing associated documentation (STWs and QC test forms) for the associated Avid QC laboratories
  • Shipping samples to contract laboratories, including aliquoting, packaging, and preparation of associated sample submission forms, shipping documentation and associated purchase requisitions
  • Filing/copying test reports and protocols, compiling report binders, documenting and labeling samples and completing submission forms/cover letters/purchase orders for contract testing
  • Organizing and monitoring of storage units, LN2 fills of Dewer, Defrosting.
  • Contribute to QCA Continuous Improvements projects.
  • File/copy test reports and protocols, compile reports, document and label samples, complete submission forms/cover letters/purchase orders for contract testing labs.
  • Inventory management and disposal.
  • Other duties as assigned.

Minimum Qualifications:

  • Associate’s degree with 1 year experience in QC environment.
  • BS in Chem/Bio or Science related field or equivalent combination of education/experience. 
  • Experience with analytical testing and equipment, writing reports, procedures, GMP and GxP inspections will be favorable.

 

Position Type/Expected Hours of Work: 

This role is a full-time onsite position. Days and hours of work are Monday through Friday 8:00 a.m. to 5:00 p.m. unless otherwise stated by Supervisor. The employee must also have the ability to work overtime and/or weekends when necessary.

Compensation:  

We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off. 

The compensation range for this role is $32.30 - $40.38 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment. 

Who you are:  

  • You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
  • Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
  • You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
  • You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.

Physical Demands & Work Environment:  

In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 25 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.

Skills Required

  • Associate degree and one year of experience in a quality control environment
  • Bachelor’s degree in chemistry, biology, or a related science field, or equivalent combination of education and experience
  • Experience with analytical testing and equipment
  • Experience writing reports and procedures
  • Familiarity with GMP and GxP inspections
  • Ability to work full-time onsite Monday through Friday, with overtime or weekends when necessary

Avid Bioservices Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Avid Bioservices and has not been reviewed or approved by Avid Bioservices.

  • Healthcare Strength Health coverage includes medical, dental, and vision alongside life and disability insurance. Plan breadth is presented as solid, with health benefits frequently highlighted as a strong element of the package.
  • Equity Value & Accessibility An Employee Stock Purchase Plan with a discounted purchase feature and the availability of stock grants provide accessible ownership opportunities. These components add long-term value beyond base pay.
  • Fair & Transparent Compensation Pay ranges are posted for some roles, offering upfront clarity on expected compensation. This transparency supports clearer expectations during hiring.

Avid Bioservices Insights

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The Company
HQ: Tustin, California
343 Employees
Year Founded: 2002

What We Do

Avid Bioservices is transforming the CDMO experience, with more than 30 years of unrivaled experience manufacturing biologics, and world-class mammalian protein facilities. We’ve produced more than 250 commercial batches, and 5 commercial products marketed in 90+ countries. For more than 10 years, we’ve maintained a flawless quality track record which we’re committed to uphold. We do it right the first time, which saves money and time. From early-stage to late-stage, concept to market, every part of our process is personalized. We’re your advocates, your trusted experts, your true partners.

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