Supervisor, Quality Control Microbiology (Flex)

Posted 9 Hours Ago
Be an Early Applicant
Tustin, CA, USA
In-Office
67K-84K Annually
Senior level
Healthtech • Pharmaceutical
Transforming the CDMO experience: Unrivaled expertise. Worldclass facilities. Exceptional quality. Personalized process.
The Role
Supervises QC microbiology testing in a GMP biopharmaceutical manufacturing environment. Leads investigations, root-cause analysis, CAPAs, microbiological studies, environmental monitoring reviews, trending reports, continuous improvement, SOP updates, employee training, and compliance activities. Oversees testing such as bioburden, growth promotion, gram staining, and sterility testing while ensuring adherence to cGMP, USP, EP, Annex 1, aseptic practices, and internal procedures.
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:
Oversees microbiological testing in support of Avid manufacturing processes within a GMP biopharmaceutical manufacturing organization. Writes and/or approves protocols and reports to support various microbiological studies.  Leads microbiological/environmental monitoring investigations to determine root cause and corrective action.  Assists in the preparation of environmental monitoring trending reports.  Identifies and leads continuous improvement opportunities in the QC Microbiology group.  Promotes awareness of aseptic techniques and procedures used in the microbiology lab.  Ensures compliance to the internal policies and procedures, applicable regulatory guidelines, and cGMPs.
Key Responsibilities:

  • Perform DRs/OOLs/OOSs investigations and determine root cause and implementation of CAPAs
  • Lead continuous improvement projects including reviewing SOPs/Test Methods/Forms to update existing procedures and ensure compliance
  • Lead various microbiological studies and write and/or approve protocol and reports for the study 
  • Perform data review of environmental monitoring and prepare environmental monitoring data trending reports
  • Oversees a variety of microbiological tests such as bioburden, growth promotion, and gram stain for samples submitted to the QCM lab
  • Train employees on microbiological test methods and Global SOPs
  • Assist in various other functions as deemed necessary to maintain a state of compliance
  • Directs activities of functional areas through direct reports.  Represent QCM in interdepartmental meetings
  • Perform other duties as assigned

Minimum Qualifications:

  • B.S. in Microbiology or related field with a minimum of 5 years of experience in a GMP facility working in a Microbiology lab.
  • Experience in performing the following tasks on a routine basis: Protocol and report writing; Investigations to determine root cause and corrective action; Growth promotion testing; Bioburden testing of water systems, raw materials, in-process materials/components, and finished product; Gram Staining and experience with colony morphology; Basic microbiological techniques used in the microbiology lab to prevent contamination and cross contamination; Enumeration and sterility testing of spore strips/discs; Knowledge of aseptic techniques and behavior
  • Must have knowledge of cGMP and should have necessary skills working in controlled environments
  • Working knowledge of USP, EP, and Annex 1

 

Position Type/Expected Hours of Work: 

This role is a full-time onsite position. Days and hours of work are Monday through Friday, 3:00 PM - 12:00 AM 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 $67,200 - $84,000 annually 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

  • Bachelor of Science degree in Microbiology or a related field
  • Minimum 5 years of experience working in a Microbiology laboratory within a GMP facility
  • Experience writing protocols and reports
  • Experience conducting investigations, determining root cause, and implementing corrective actions
  • Experience with growth promotion testing
  • Experience with bioburden testing of water systems, raw materials, in-process materials or components, and finished products
  • Experience with gram staining and colony morphology
  • Knowledge of basic microbiological techniques to prevent contamination and cross-contamination
  • Experience with enumeration and sterility testing of spore strips or discs
  • Knowledge of aseptic techniques and behavior
  • Knowledge of cGMP and ability to work in controlled environments
  • Working knowledge of USP, EP, and Annex 1
  • Ability to work full-time onsite, Monday through Friday, 3:00 PM to 12:00 AM
  • Ability to work overtime and 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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