QA Specialist - 1st Shift

Job Title:

QA Specialist - 1st Shift

Job Description

This role provides real-time Quality oversight during the Flu Mist/Fluenz Packaging operation. The Quality Specialist is responsible for QA On the Floor support to the Packaging Operation, ensuring operations are executed in accordance with cGMPs. They make real-time decisions on GDP, GMP, and quality compliance issues, partnering with production to ensure processes are carried out in compliance with approved standards. Primary responsibilities include AQL Sampling, inspection, line monitoring, and cleaning confirmations.

Responsibilities

+ Conduct AQL Sampling and inspection of final product containers and packaging.

+ Provide oversight of Packaging Operations through line monitoring.

+ Perform line clearance inspections during the changeover process.

+ Adhere to PPE gowning guidelines.

+ Review documents for Good Documentation Practices.

+ Maintain a high level of understanding of relevant production processes and quality systems.

+ Collaborate with Packaging personnel and other Quality professionals to ensure consistent application and execution of key quality systems.

+ Execute QA processes to maintain the flow of products and documents to meet site objectives.

+ Ensure that training is up to date and all tasks are completed per SOP or other defined standard.

+ Use lean principles to make suggestions on opportunities to reduce waste and improve processes in Quality Operations.

+ Report potential issues of non-compliance.

+ Conduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to your role.

+ Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time.

+ Other tasks and responsibilities may be assigned as needed.

Essential Skills

+ Experience in pharmaceutical industry in roles covered by GMP oversight.

+ Excellent oral and written communication skills.

+ Ability to perform mathematical calculations to determine sample size and acceptance criteria.

+ Strong interpersonal skills.

Additional

Skills & Qualifications

+ Bachelor's degree in a Science/technical field such as Pharmacy, Biology, Chemistry, or Engineering.

+

Experience with aseptic techniques.

+ Prefer at least a year or two of GMP experience in a QA inspection or documentation within a cGMP role such as manufacturing or lab.

+ Professional manner and excellent verbal communication skills.

+ Good judgment skills.

+ Knowledge of packaging operations (could be from Operations/Production or QA background).

+ Ability to work alone for majority of shift.

+ Able to stand/walk around packaging area for 90% of shift.

Work Environment

1st shift Tuesday-Friday 5:45AM-4:15PM. The work environment is fun and welcoming, providing PPE including lab glasses and boots. This is a large international pharmaceutical company offering an opportunity for recent college graduates to gain GMP experience. The company provides a 2-week notice before the end of the season to assist in finding the next opportunity. Many seasonal workers return annually, receiving pay increases each year.

Several hiring managers started as seasonal workers and transitioned to full-time roles.

Job Type & Location

This is a Contract position based out of PHILADELPHIA, PA.

Pay and Benefits

The pay range for this position is $35.38 - $39.81/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

- Medical, dental & vision - Critical Illness, Accident, and Hospital - 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available - Life Insurance (Voluntary Life & AD&D for the employee and dependents) - Short and long-term disability - Health Spending Account (HSA) - Transportation benefits - Employee Assistance Program - Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in PHILADELPHIA,PA.

Final date to receive applications

This position is anticipated to close on Mar 13, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or…