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Supervisor, Quality Operations

PCI Pharma Services

Rockford, ILOnsitePosted 10 days ago$62,960 - $70,830/year
Full TimeMid LevelQuality (QA / QC)CDMO
Original posting ↗

Summary

Determines and maintains quality standards developed in compliance with current Good Manufacturing Practices, the Company's own Standard Operating Procedures and customer requirements. Provides resolution to quality deviations/issues. Recommends solutions based on SOP / cGMP requirements.

Job description

Summary of Objective

Determines and maintains quality standards developed in compliance with current Good Manufacturing Practices, the Company's own Standard Operating Procedures and customer requirements. Provides resolution to quality deviations/issues. Recommends solutions based on SOP / cGMP requirements.

Essential Duties and Responsibilities

  • Coordinates the daily activities of the QA Auditors.
  • Assists with the daily activities of Production Inspection personnel for packaging.
  • Implements inspection criteria and testing Study and standardizes departmental work practices to improve quality and efficiencies of subordinates.
  • Helps resolve quality related issues with other departments and customers.
  • Motivates, develops and provides continuous training either through the use of departmental work instructions, examination of cGMP's and SOP's, specific customer requirements or by personal instruction.
  • Review records for accuracy of information, compliance with established procedures.
  • Reviews daily paperwork to assure all customer requirements and quality standards have been met and maintained.
  • Promotes continuity of shifts through cooperation and communication within as well as with other departments.
  • Assist in the performance of monthly internal audits and any necessary corrective action to follow-up. Oversees Pest Control and Environmental (humidity, temperature, MKT) Monitoring Programs. May disposition NMR's.
  • Recommend and participate in disciplinary activities of subordinates. Maintain testing equipment and supplies needed for the department.
  • May assist in performing investigations, may write reports, memos, or letters. This position may require overtime and/or weekend work.
  • Carries out essential functions of the Quality Operations Manager in his/her absence.
  • Knowledge of and adherence to all PCI, cGMP, and GCP policies, procedures, rules.
  • Attendance to work is an essential function of this position.
  • Perform Quality Health Check assessments to identify if processes and day to day activities are performed according to procedures.
  • Performs other duties as assigned by Manager/Supervisor.

Qualifications

The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position.

Required

  • Bachelor's Degree in a related field and/or 1-5 years related experience and/or training.
  • College Level 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.
  • High Reasoning: Ability to solve practical problems and deal with a variety of concrete variables in situations where there is only limited standardization. Ability to interpret a variety of instructions that may be provided in various forms.
  • High Standard of Report Writing

Preferred

  • Ability to effectively present information to various people as the job requires.
  • Ability to work independently and/or part of a team.
  • Ability to display a willingness to make decisions.
  • Ability to display excellent time management skills.

Requirements

  • Bachelor's Degree in a related field and/or 1-5 years related experience and/or training
  • College Level Mathematical Skills
  • Intermediate Computer Skills
  • Full Professional Proficiency in English
  • High Reasoning ability
  • High Standard of Report Writing
  • Knowledge of cGMP and SOP requirements

Benefits

  • Paid Time Off
  • Health Insurance
  • Dental Insurance
  • Vision Insurance
  • Flexible Spending Account
  • 401(k)
  • Annual Performance Bonus

Company overview

PCI Pharma Services is a global contract development and manufacturing organization (CDMO) that provides comprehensive pharmaceutical supply chain solutions to pharmaceutical and biopharmaceutical companies worldwide. Founded in 1991 and headquartered in Philadelphia, Pennsylvania, the company has established itself as a trusted partner in the healthcare industry, offering integrated services that span the entire drug development lifecycle. PCI specializes in drug development support, clinical trial supply management, contract drug manufacturing, sterile and non-sterile drug product packaging, and global pharmaceutical logistics. With a global footprint encompassing 30 GMP-compliant facilities across multiple continents, the company serves as a strategic partner that follows the molecule from early development through commercial launch. PCI's expertise enables clients to accelerate time-to-market while ensuring regulatory compliance and quality standards. The company's comprehensive service portfolio includes analytical services, formulation development, commercial manufacturing, packaging, supply chain management, and distribution, making it a one-stop solution for pharmaceutical companies seeking to outsource their development and manufacturing needs.

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