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PCI Pharma Services

Quality Coordinator

Posted 15 Days Ago
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In-Office
Rockford, IL
18-20 Hourly
Junior
In-Office
Rockford, IL
18-20 Hourly
Junior
Coordinate and review batch documentation and records to ensure cGMP/GCP and customer compliance. Prepare/distribute production paperwork, update batch records and specifications, submit accountability and release documentation, track and resolve document issues, support customer queries, provide quality metrics, and assist management with quality matters. May require overtime/weekend work.
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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 Coordinator

Location: :Linden Road, 2 South, Rockford, IL 61109

Shift: 1st Shift

The Quality Coordinator assists with coordinating quality activities of a designated Customer Focused Team to ensure that goals and objectives of the team are accomplished within prescribed time frames and in budget. Helps drive project success to provide PCI a competitive advantage in long-term quality customer management.

Essential Duties and Responsibilities:

  • Prepares and distributes required documentation for requested production work orders.

  • Perform documentation and records review of completed orders to ensure compliance with cGMP's and customer requirements.

  • Creating and updating batch records, forms and material specifications as well as organizing internal and customer approval of batch records and specifications.

  • Performs and submits batch records, accountability reports and necessary documentation to customers to facilitate product release.

  • Help identify, communicate, track and resolve document related issues with other departments and customers.

  • Function as one of the customer points for comments or questions pertaining to batch documentation.

  • Assist with providing quality related metrics.

  • Performs finished product batch release of approved production lots.

  • Meet with management to address issues or concerns with the batch documentation.

  • 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.

  • This position may require overtime and/or weekend work.

  • Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.

  • Attendance to work is an essential function of this position

  • Performs other duties as assigned by Manager/Supervisor.

  • Required Qualifications:

  • TABE testing requirements met at approved grade level for position.

  • Basic Mathematical Skills

  • Intermediate Computer Skills: Ability to perform more complex computer tasks and has knowledge of various computer programs.

  • Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.

  • Very High Reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions.

  • Be able to interpret an extensive variety of technical instructions in math or diagram form and deal with several abstract/concrete variables.

  • Preferred Qualifications:

  • Ability to follow instructions and respond to management direction.

  • Ability to identify and resolve problems in a timely manner.

  • Ability to hold oneself in a professional manner.

  • Ability to demonstrate attention to detail.

  • High School Diploma or GED

  • 2 years of experience in Operations/Quality and/or providing support in an office or manufacturing environment. .

The hiring rate for this position is $18.15 - $20.42 per 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).

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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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