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Telecommute Pharmaceutical Inspector Jobs (NOW HIRING)

kindeva

Senior Quality Assurance Specialist

Brentwood, MO

$77K - $106K/yr

... inspection readiness walk-throughs, line clearance, in-process checks, deviation and laboratory ... Pharmaceutical or related industry * Experience in Batch Record Review/Audit/Disposition * The ...

kindeva

Senior Quality Assurance Specialist

Brentwood, MO · On-site

$77K - $106K/yr

... inspection readiness walk-throughs, line clearance, in-process checks, deviation and laboratory ... Pharmaceutical or related industry * Experience in Batch Record Review/Audit/Disposition * The ...

kindeva

Senior Quality Assurance Specialist

Brentwood, MO

$77K - $106K/yr

... inspection readiness walk-throughs, line clearance, in-process checks, deviation and laboratory ... Pharmaceutical or related industry * Experience in Batch Record Review/Audit/Disposition * The ...

kindeva

Senior Quality Assurance Specialist

Brentwood, MO · On-site

$77K - $106K/yr

... inspection readiness walk-throughs, line clearance, in-process checks, deviation and laboratory ... Pharmaceutical or related industry * Experience in Batch Record Review/Audit/Disposition * The ...

Atos

SD · On-site

... adheres to GxP pharmaceutical compliance. Author and maintain accurate and timely system ... ROVING/TELECOMMUTING EMPLOYEE: Reports to company headquarters in Irving, TX. Will work at various ...

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How much do telecommute pharmaceutical inspector jobs pay per hour?

As of Jul 29, 2026, the average hourly pay for telecommute pharmaceutical inspector in the United States is $27.36, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.49 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Pharmaceutical Inspector jobs? The most popular types of Pharmaceutical Inspector jobs are:
Telecommute Pharmaceutical Inspector jobs near you

Supervisor, Quality Assurance (2nd Shift)

kindeva

Brentwood, MO • On-site

Other

Re-posted 14 days ago

Kindeva rating

6.7

Company rating: 6.7 out of 10

Based on 9 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. 

#LI-onsite #LI-BM1

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