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Temp Aseptic Jobs (NOW HIRING)

PSC Manager - Pleasanton, CA - (Temp)

Pleasanton, CA · On-site

$19 - $23.75/hr

Temporary Position located in Pleasanton, CA A Phlebotomist serves patients by identifying the best ... Maintains specimen integrity by using aseptic technique, following Natera[KC1] procedures; observes ...

QC Technician

Fairfield, NJ · On-site

$23 - $24/hr

Aseptic Technician We are seeking an attentive and dedicated Aseptic Technician to join our team ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

... aseptic technique, aseptic processing, batch record, SOP, cGMP, GMP Top Skills Details ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Supply Technician

Loma Linda, CA · On-site

$43K - $52K/yr

Temporary Supply Technician Location: VA Loma Linda Health Care System (VALLHCS), Loma Linda, CAKey ... Stock specialty carts and clean storage areas per aseptic and Joint Commission standards. * Assist ...

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Temp Aseptic information

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$34.5K

$70.6K

$126K

How much do temp aseptic jobs pay per year?

As of Jun 10, 2026, the average yearly pay for temp aseptic in the United States is $70,647.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,500.00 and $83,000.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Aseptic jobs? The most popular types of Aseptic jobs are:

Supervisor, Quality Assurance (2nd Shift)

kindeva

Brentwood, MO • On-site

Other

Posted 25 days ago


Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz


Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

QA Supervisor – Aseptic, will be primarily based at the Sterile Product Manufacturing (SPM) building and will provide general oversight to Quality Inspector colleagues.  The ideal candidate will possess a working knowledge of aseptic processing principles including aseptic behaviors, good documentation practices (GDP), good manufacturing practices (GMP), facility controls and compliance / regulatory requirements relating to aseptic processing.  The incumbent will facilitate timely resolution and escalation of all manufacturing deviations and effectively communicate deviations to Production and QA Management.

Role Responsibilities

  • Proficiency of internal manufacturing and quality assurance procedures as well as compliance and regulatory requirements.
  • Proficiency in Batch Record reviews for conformance to established procedures and critical process parameters.
  • Provide leadership and guidance to quality inspectors and ensure adequate coverage through dynamic scheduling for APA and Grade D/CNC areas throughout the shift.
  • Ensure training is completed for direct reports 
  • Generate daily written shift reports for Quality and Production Management with clear and concise details of relevant issues.
  • Ability to solve problems and suggest solutions when escalating.
  • Ability to successfully don a sterile gown and complete gowning qualification requirements and maintain it to support critical aseptic processing areas (APA).
  • Participate in media fills as Quality Observer when needed.
  • Initiate incidents in QTS as applicable.
  • Train on performing line clearance / verification of critical areas.
  • Perform daily on-line auditing in the APA to ensure the area is maintained in an audit ready state.
  • Aid in Root Cause Analysis and identification of Preventive Actions to support manufacturing investigations.
  • Assists in identifying continuous improvements of Standard Operating Procedures (SOPs) and Master Batch Records.
  • Perform other Quality Assurance functions as needed.
  • Attend and participate in daily shift huddles/Gemba meetings

 

 Basic Qualifications

  • Education: BS in Chemistry, Biology, Microbiology, Pharmacy, Engineering, or other science related discipline. In lieu of a bachelor’s degree an associate’s degree with 2+ years of experience.
  • Experience: Minimum 3 years of pharmaceutical experience or equivalent combination of education and experience.
  • Experience at an aseptic manufacturing site preferred.  1 year of supervisory experience is preferred. 
  • Produces quality work with minimal guidance.  
  • Must be able to work in a team environment and across interdepartmental teams.

 NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

  • Position requires regular onsite attendance – this position cannot be performed on a remote or telecommute basis on a temporary, short, or long term basis.
  • Must have the ability to simultaneously multi-task across multiple capabilities, functions and manages competing priorities, including performing site and functional responsibilities, frequent e-mail and phone communications and attending multiple meetings and conference calls.  Note: these activities may not be time bound to core hours or presence at the site.
  • Must have the ability to work effectively under and manage to strict production, time, and performance deadlines. 
  • Must be willing and able to work beyond the hours typically defined as a “regular” workday, which may or may not include weekends and holidays.

This is a 2nd shift position, 2pm-10:30pm, Monday through Friday. 

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