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.
This position performs a range of routine and semi-routine QA Raw Materials activities to ensure compliance with Quality Assurance and regulatory requirements. Responsibilities include supporting audits, training programs, and documentation review for GMP operations. The role promotes a compliant cGMP environment by following SOPs and provides quality support for investigations related to GMP manufacturing events. It also generates and reviews documentation for batch disposition and batch record assembly. The individual can work independently, within guidelines, and as part of a team. Additional duties include leading projects and training junior staff.
ESSENTIAL JOB FUNCTIONS-OTHER DUTIES MAY BE ASSIGNED:
Assists in regular follow ups with end users to ensure timely completion of open investigations and investigation activities.
Assist in ensuring the adequacy of investigations performed in relation to manufactured drug product and drug substance to support the batch release process.
Provides quality support in the review and approval of quality reports including deviations, OOSs, complaints, OOTIs, SCARs, and corrective and preventive actions (CAPAs)
Generates and compiles lot file review documentation for batch disposition.
Updates lot status in ERP system.
Responsible for equipment inductions, revisions and record maintenance within the electronic database.
Performs Technical Quality review of validation protocols and reports.
Performs logbook documentation audits for cGMP regulated logs and SOPs.
Creates, revises and approves procedures.
Performs the review of equipment and facility related Change Control documentation.
Assists with internal, client and regulatory audits.
Assists with the generation of department metrics.
Assists with developing recommendations for continuous improvement projects.
Assists in the review and approval of production batch records and associated data for product disposition.
Assists in the review and approval of controlled documents including standard operating procedures, protocols, and reports.
Regular and reliable attendance on a full-time basis [or in accordance with posted schedule].
Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices.
Fosters a safe and environmentally sustainable workplace by following all PCI EHS policies and procedures.
Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture.
EDUCATION AND EXPERIENCE:
High School Diploma or equivalent. Bachelor’s degree strongly preferred in a Life Sciences discipline or equivalent.
Minimum of three to five (3-5) years of relevant GMP experience in documentation, QA on the floor, manufacturing, or equivalent.
Knowledge of cGMP regulations and good documentation practices preferred.
Strong organizational and analytical skills.
Must be familiar with Microsoft Office applications.
The hiring rate for this position is $29.65 - $33.36/hour plus eligibility for an annual performance bonus. Final offer amounts are determined by multiple factors including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), flexible spending account, and 401(k).
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.
Skills Required
- High School Diploma or equivalent
- Bachelor's degree in a Life Sciences discipline
- Minimum 3-5 years relevant GMP experience (documentation, QA on the floor, manufacturing)
- Familiarity with Microsoft Office applications
- Experience updating lot status and working with ERP systems
- Knowledge of cGMP regulations and good documentation practices
- Experience performing audits, supporting investigations, and reviewing batch records and controlled documents
- Strong organizational and analytical skills
- Ability to lead projects and train junior staff
PCI Pharma Services Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about PCI Pharma Services and has not been reviewed or approved by PCI Pharma Services.
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Retirement Support — Feedback suggests the company provides a 401(k) with an employer match in the mid‑single‑digit range, with immediate vesting noted in certain cases. This is viewed as a solid component of the overall package.
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Leave & Time Off Breadth — PTO and paid holidays are commonly available, and some roles indicate vacation is accessible from early tenure. Availability of time off is frequently described as a positive element of the package.
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Affordable Benefits — Health insurance is sometimes described as reasonably priced depending on plan tier. Feedback suggests core medical, dental, and vision coverage is part of a standard offering.
PCI Pharma Services Insights
What We Do
PCI is a leading provider of integrated pharmaceutical development services to the global healthcare market. With facilities in North America and Europe, PCI supports pharmaceutical and biotech companies with products destined for more than 100 countries around the world. PCI provides services for each stage of the product lifecycle – from early Phase I through commercial launch and long-term supply – and partners with customers to provide key insight and expertise in enabling successful commercialization and bringing lifesaving medications to patients. For more information, go to www.pci.com.
