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Pciservices

QA Specialist I - ACM 2nd Shift

  • Seen live on Pciservices' site yesterday
  • New grad
Pay
Not stated
Location
Madison, WI, USA
Open for
12+ days
First seen
Oct 23, 2026
Apply on Pciservices' site (opens in a new tab)

Posting record

No flags

Open 12+ days

The posting's record, oldest first
  1. Pciservices' site dates the posting
  2. Ghostless first sees this listing
  3. Last checked: still up
How we know

It hasn't been reposted, listed twice, or left up unusually long, and the posting doesn't say it's a talent pool.

Ghostless records the day it first sees a posting, so a repost can't reset its age. This one was already up when Ghostless started tracking Pciservices, so its true age is longer.

Last checked Nov 3, 2026.

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What it asks of you

1–3 years of experience
“1-3 years of experience in Quality Assurance, aseptic processing, or cleanroom functions within a cGMP‑regulated environment; equivalent combination of education a” (quoted from the posting)

What the posting discloses

Not stated: Pay, real vacancy, AI screening.

Why these three

Ontario requires postings from employers with 25 or more staff to state the pay, whether the vacancy exists, and whether AI screens applicants.

Some employers add pay only on their own site. Check the original posting before you rule it out.

About the role

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

Position Title : Quality Specialist I – ACM

Location: Madison, Wisconsin

Department: Quality Assurance

Reporting To: Supervisor, Quality Assurance Internal Operations

Responsible For (Staff): No

The Quality Specialist I - ACM provides real-time monitoring of aseptic behaviors during sterile manufacturing, including gowning, interventions, environmental monitoring, and material handling in ISO 5/ISO 6 environments. This role supports PCI’s mission of maintaining a high standard of aseptic integrity, product quality, and patient safety.

ESSENTIAL DUTIES AND RESPONSIBILITIES

  • Review operator aseptic behavior within the ISO 5 core and adjacent classified areas, and escalate any concerns to the operator or their supervisor.
  • Observe and document real-time activities during manufacturing operations, including setup, filling, environmental monitoring, sanitization and routine/corrective interventions.
  • Ensure compliance with PCI aseptic technique expectations, gowning standards, and cleanroom behavior as outlined in SOPs and training.
  • Identify and escalate deviations from aseptic practices, personnel behaviors, or environmental controls that pose potential contamination risks.
  • Capture detailed and objective records of events, interventions, and nonconformances using PCI-approved documentation tools or checklists.
  • Support media fill (aseptic process simulation) operations by providing visual monitoring and feedback throughout the process.
  • Collaborate with Quality Assurance, Operations, Microbiology, and Training to identify opportunities for coaching, retraining, and continuous improvement.
  • Participate in contamination control and environmental monitoring trending to drive site-level improvements and reduce contamination risk.
  • Assist with investigations and root cause analysis for contamination events, EM excursions, and aseptic technique deviations.

QUALIFICATIONS

Required

  • High school Diploma, GED, or equivalent credential required, AS degree or BS degree in Life Sciences or related field preferred.
  • 1-3 years of experience in Quality Assurance, aseptic processing, or cleanroom functions within a cGMP‑regulated environment; equivalent combination of education and experience will be considered
  • Ability to learn aseptic techniques, contamination control, and cGMP regulations (21 CFR Parts 210/211, EU Annex 1).
  • Demonstrated ability to observe critically and document behaviors accurately and objectively.
  • Excellent verbal and written communication skills; must be comfortable providing real time coaching.
  • Ability to gown for entry into ISO 5, 6 and 7 cleanroom environments and remain in those areas for extended periods.

Preferred

  • ​ Proficient in Microsoft Office and electronic quality systems (preferred).
  • Prior experience in a QA or manufacturing oversight role at PCI or a similar aseptic operation is strongly preferred.

#LI-RS1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement

PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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