Quality Coordinator

Posted 10 Hours Ago
Be an Early Applicant
America, AL
1-3 Years Experience
Pharmaceutical
The Role
The Quality Coordinator role entails preparing production documentation, reviewing completed orders for compliance, updating batch records, facilitating product release, and addressing customer queries regarding batch documentation. This position involves ensuring adherence to cGMP policies and may require overtime.
Summary Generated by Built In

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.

1. Prepares and distributes required documentation for requested production work orders.
2. Perform documentation and records review of completed orders to ensure compliance with cGMP’s and
customer requirements.
3. Creating and updating batch records, forms and material specifications as well as organizing internal and
customer approval of batch records and specifications.
4. Performs and submits batch records, accountability reports and necessary documentation to customers to
facilitate product release.
5. Help identify, communicate, track and resolve document related issues with other departments and
customers.
6. Function as one of the customer points for comments or questions pertaining to batch documentation.
7. Assist with providing quality related metrics.
8. Performs finished product batch release of approved production lots.
9. Meet with management to address issues or concerns with the batch documentation.
10. Reviews and interprets customer standards, procedures and specifications for dissemination relative to
batch records, forms and material specifications. Organize internal and customer approval of batch records
and specifications.
11. This position may require overtime and/or weekend work.
12. Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.
13. Attendance to work is an essential function of this position
14. Performs other duties as assigned by Manager/Supervisor

#LI-DT1

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, Diversity, Equity, and Inclusion (DEI) 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.

The Company
HQ: Philadelphia, PA
2,259 Employees
On-site Workplace

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.

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