Qa Associate I - Ops

PCI Pharma Services; Alabama; On-site; USD 42,000 - 64,000; Full time

Job summary

PCI Pharma Services is hiring a QA Associate I - Operations in Madison, WI. The role provides real-time QA support on GMP manufacturing floors, ensuring compliant documentation and product quality.

You will review batch records, support deviations and CAPA processes, and participate in on-floor audits to uphold QA standards across manufacturing operations.

Qualifications

• Bachelor’s degree in a relevant scientific discipline with 0–2 years of pharmaceutical or biotech QA Ops experience preferred

Responsibilities

• Perform on-the-floor QA activities including room release, audit critical processes, and real-time documentation review
• Audit manufacturing and support areas; review batch records for compliance
• Review manufacturing batch records and related docs for completeness and correctness
• Assist in deviations, CAPA issuance, and quick corrective actions on the floor

Skills

QA Operations

GMP knowledge

Documentation review

Root cause analysis

Education

Bachelor’s Degree in a scientific field

Tools

AQL inspection

CAPA process

Job description

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.

SECOND SHIFT

Position Title : QA Associate I - Operations

Location: Madison, Wisconsin

Department: Quality Assurance

Reporting To: Quality Assurance Operations Supervisor

Responsible For (Staff): No

The Quality Associate I - Operations is the first of two levels within the QA Associate jobfamily Theassociate I provides real-time QA support on the floor for GMP Manufacturing of drug product. The work scope includes floor oversight of manufacturing includingobservingcritical processes and performing AQL visual inspection,executedGMP documentation review and supporting other QA functions as needed.Real timecontinuous monitoring of manufacturing related systems and processes to ensure compliance with applicable regulatory and industry standards, needed quality improvements, and safety/efficacy for phaseappropriate GMPmanufacture of drug products

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Perform QA On-the-Floor activities supporting client projects, including room release, auditing critical processes, reviewing documentation in real time, and resolving issues that occur during manufacturing
• Perform audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and Good Documentation Practices
• Review executed Manufacturing Batch Records and supporting documentation for completeness,accuracyand compliance
• Support the evaluation and lot disposition of intermediates, finish bulk drugsubstanceand drug product
• Act as first responder for on the floor quality issuesin a timely manner, documentation of all events/investigations andrequiredimmediate corrective actions
• Mayparticipatein root cause analysis using methodologies,such as:fishbone, 5 whys, etc.
• Act as QA reviewer for deviations and CAPA issuance; with limited approval authority asdesignatedby QA Management
• Perform Acceptable Quality Limit (AQL) visual inspection of drug product
• Participate in SOP revision as it pertains to process improvements
• Participate in site quality and process improvement initiatives. Represent QA on project teams and represent QA perspective as necessary
• Guide personnel indirectly and directly involved in GMP operationspertaining tocGMP compliance, internal procedures, regulatoryrequirementsand industry best practices

QUALIFICATIONS:

Required:

• Bachelor’s Degree in a relevant scientific discipline preferred with a minimum of 0-2 years of pharmaceutical or biotech industry experience with 1+ years of experience in a QA Operations role supportinglate stageclinical and/or commercial production preferred
• Exposure to RCA, technical writing, and working with quality related investigations
• Exposure to lean operation excellence highly desirable
• Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as ICH
• Knowledge and ability to apply basic scientific principles to solve operational, as well as routine quality tasks
• Knowledge and exposure to using Risk Management Tools (FMEA, HACCP, PHA, etc.) and familiarity with ICH Q9 preferred
• ASQ certification preferred

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.