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Quality Assurance Release Coordinator

Blistex Inc -
Oak Brook, IL

Quick Apply

Job Details

Full-time
$62,500 - $66,000 a year

Qualifications

Statistics
Customer communication
Confidential information handling
Production data analysis
Laboratory document review
Document control experience within pharmaceutical industry
Quality control statistical data analysis
Technical writing experience within manufacturing
Production deviation management
Compliance audits & assessments
Internal investigations
Quality reports
High school diploma or GED
Manufacturing standard operating procedures
Bachelor's degree
Quality assurance experience within pharmaceutical industry
Compliance documentation
Data interpretation
Relationship management
Internal compliance assessments
Regulatory/legal compliance standards in production
Investigative reports
Quality audits
Investigating compliance violations
Production batch record review
Data collection
Quality control communication
Cross-functional collaboration
Standard operating procedures (SOPs)
Quality control records management

Full Job Description

JOB SUMMARY

The Coordinator is responsible for performing duties and assisting the Manager, Quality Assurance with product disposition functions, encompassing the review of production batch records and the associated documentation required to release a production lot. He/she ensures compliance to product specification, good documentation practices, data entry, completeness of COAs, Company SOPs and cGMPs reviewing all documents from Production, Quality Control Laboratory, Quality Assurance and/or other related documents to a batch. The completed production batch (finished product) does not release from the building without the incumbent’s approval to prevent distribution of non-conforming products to customers. A similar release process is followed with the review of the raw materials sampling, testing, approve and/or reject activities.

ESSENTIAL JOB FUNCTIONS

Coordinates the assembly of batch information generated by Quality Assurance, Production, Manufacturing and Quality Control Departments.
Reviews and audits batch records. Collects data for trending performance measurements.
Makes final decision on product release, in absence of discrepancies.
Coordinate correction of documentation errors with appropriate department(s); and notifies management of batch record errors.
Notifies management of discrepancies and documentation errors with batch records.
Verifies counts of finished products prior to release. Notifies production of count discrepancies.
Prepares release or quarantine notices/stickers for in-process batches and finished products.
Maintains the quarantine hold area.
Performs transactions in Adage system.
Troubleshoots quality issues and initiates non-conformance investigations and deviations, as needed.
Collects information for investigations of quality issues.
Maintains the deviation files and deviation log.
Maintains all in process batch files. Archives all completed batch records.
Provides customers with Certificates of Compliance and Certificates of Analysis when necessary.
Proficient at reading, reviewing, and auditing documents and follow procedures.
Mastered the understating of Batch documentation requirements and all associated production and compliance steps.
Proficient at understanding, reviewing, and auditing all compliance steps associated with the production of OTC drugs (i.e., line clearances, filling/packaging labeling, production sampling requirements, batch records, deviations, non-conformances etc.)

ADDITIONAL RESPONSIBILITIES

Participates in cGMP compliance audits and other committees, as required by the Manager, Quality Assurance.
Performs and assumes other duties and responsibilities, as may be required by the Manager, Quality Assurance (e.g. serves as back-up to Inspector, Quality Assurance and Inspector, Receipt).
Supports the Winner’s Circle and Blistex Quality processes.

REQUIRED EDUCATION, EXPERIENCE AND SKILLS

High School Diploma or GED with 4-6 years of applicable Quality Assurance environment preferable in the pharmaceutical OTC industry.
Bachelor's degree in Chemistry, Biology, or related scientific discipline with 2-3 years of applicable Quality Assurance environment preferable in the pharmaceutical OTC industry.
Must demonstrate effective communication skills for interactions with Quality colleagues, and colleagues from numerous functional areas.
Must listen actively and readily assumes responsibility for actions. Capable of managing tactical steps to push tasks forward.
Proficient at reading, reviewing, and auditing documents and follow procedures.
Mastered the understating of Batch documentation requirements and all associated production and compliance steps.
Proficient at understanding, reviewing, and auditing all compliance steps associated with the production of OTC drugs (i.e., line clearances, filling/packaging labeling, production sampling requirements, batch records, deviations, non-conformances etc.)
Firm understanding of the organization QMS for retrieval requirements, retrieve essential records, following record keeping procedures.
Solid ability to detect errors in production documents reviews, deviations files, all quality documents support product release.
Master the understanding of "deals" associated with various markets and the cGMP requirements associated with the production and Quality life-cycle of a OTC drug.
Solid understanding of technical requirements for all quality documentation supporting batch production documents and their lifecycle.
Firm understanding of the Stability program/schedule and the compliance requirements associated with them.
Firm understanding of the departmental compliance role and responsibilities.
Master the ability to plan, organize and complete concurrent tactical tasks independently.
Ability to plan, organize and complete strategic Departmental tasks independently.
Firm understanding of the calculations as required in Production and Quality Assurance SOPs and in performing basic statistical calculations related to % Difference, Average, Standard Deviation, % RSD.
Understanding of how to review data for calculation errors and how to interpret data under supervision. Assist in writing deviations, non-conformances, and investigational reports.
Firm understanding of the company nonconformance SOPs and assist with performing the investigations.
Firm understanding of Quality and Compliance requirements while mastering the ability to identify deficiencies in Quality and Production documentation.
Ability to understand the requirements of a good investigation and/or deviation.
Considerable interpersonal skills are required to interact with various levels of internal and external customers.
Must possess the ability to prepare detailed and accurate documentation.
Good organizational ability and detail minded.
Must possess ability to work independently on a multitude of concurrent tasks.
Must be discreet with confidential information of which he/she has access.
Must possess high degree of familiarity with and ability to use office machines.
Willingness to accept other duties, as assigned.
Must possess the ability to develop and maintain an effective working relationship with internal and external customers, function as a team player, accept constructive criticism from management and comply with Company policies.

1st Shift:
7 AM - 3:30 PM

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