Jobs and Careers
MS

3rd Shift QA, Associate Specialist

MSD
United StatesRemotefull_timeVerifiedPosted 5 Mar 2026
💰 $113,200/yr($71,900/yr$113,200/yr)

About the role

Job Description

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!

Under the general direction of the Director, Wilson Quality Operations, the Associate Specialist is responsible for the following (but not limited to): 

  • Qualification, routine and per process monitoring of the facilities, utilities and personnel

  • Trending for Utility Systems and Classified Areas including evaluating data for adverse trends

  • Collection and submission of samples in GLIMS

  • Authoring of investigations and implementation of appropriate corrective/preventative actions

  • Assist with protocol development and execution of the Process Simulation program

  • Adherence to departmental Quality metrics

  • Provide Shopfloor support and review of batch generated documentation

  • Performs other duties as assigned

Primary Activities include, but are not limited to:

Specific to Environmental and Utility Monitoring, this position will be responsible for maintaining the EM program to include the following:

  • Directly support performance qualification activities

  • Collection of utility systems samples including water, clean steam, and clean dry air

  • Execute environmental sampling of classified areas including active viable air, non-viable air, and surface sampling

  • Compile and author annual reviews

  • Provide data entry, review, and approval as required in GLIMS

  • Provide summaries of test results to appropriate personnel as necessary

  • Compile and evaluate environmental monitoring data for adverse trends

  • Conduct investigations for deviations and Out of Specification results Interprets our company's Quality policies, GMPs and other agency regulations for application to Wilson Operations

Specific to Quality Operations, this position will be responsible for, but not limited to the following:

  • Identifies and implements continuous improvement activities

  • Batch documentation review and/or approval

  • Provide shopfloor support, through aseptic observations or other observations, during operations

  • Demonstrates leadership by maintaining a safe workplace and identifying actions to prevent safety incidents 

Schedule: 11:00 pm to 7:00 am Mon -Fri

Education Minimum Requirement:

  • Must possess at a minimum an associate degree or equivalent experience in the pharmaceutical industry

Required Experience and Skills:

  • Must possess a minimum of one (1) year of GMP pharmaceutical industry experience.

  • Working knowledge of cGMPs and of regulatory requirements as they apply to the vaccine/pharmaceutical industry.

  • Ability to perform routine assignments and develop competence by performing structured work assignments.

  • Ability to use existing procedures to solve routine and standard problems.

  • Promotes the team’s effectiveness through actions that demonstrate respect and appreciation for diverse perspectives.

  • Readily accepts performance feedback and incorporates this feedback into future performance.

  • Ability to interpret our company's Quality Policies, Procedures and Guidelines for daily application.

  • Ability to independently respond to basic requests for data and trending of data.

  • Willing to work irregular hours to support multi-shift operation on an as needed basis

Preferred Experience and Skills:

  • GLIMS experience preferred

  • Experience with aseptic filling, environmental monitoring and process simulations.

  • Ability to learn new processes and computerized systems with limited support.

  • Experience in continuous improvement, LEAN manufacturing, problem solving, and/or Right First Time methodologies.

  • Strong written and verbal communication skills including technical writing experience with investigations, change requests, standard operating procedures, protocols, etc.

VETJOBS

MSJR

Required Skills:

Aseptic Filling, cGMP Compliance, Deviation Management, Good Manufacturing Practices (GMP), Quality Assurance (QA), Quality Auditing, Quality Management Systems (QMS), Quality Standards, Root Cause Analysis (RCA), Technical Writing, Test and Evaluation (T&E)

Preferred Skills:

Current Employees apply HERE

<

Apply for this role

Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.

Apply Now →Generate Application Kit

Free account required — sign up in 30s

Company

MSD

View company profile →