Quality System Specialist

ALLTECH CONSULTING SVC INC; Fort Wayne (IN); On-site; USD 60,000 - 80,000; Full time

Job summary

ALLTECH CONSULTING SVC INC is looking for a temporary Quality Management Systems Specialist for its Greendale, Indiana site. This role focuses on maintaining and improving quality systems, supporting compliance activities, and overseeing documentation.

The ideal candidate should have a minimum of 2 years experience in a GMP-regulated environment, knowledge of relevant regulations, and proficiency with TrackWise. Strong communication and organizational skills are essential for this role.

Qualifications

• 2+ years of experience in a GMP-regulated environment, preferably in pharmaceuticals or dietary supplements.
• Experience with 21 CFR 111, 21 CFR 211, or 21 CFR 11.
• Working knowledge of Quality Systems and Quality Assurance.

Responsibilities

• Support site-level quality systems including Change Control and Deviation processes.
• Ensure timely completion of documentation tasks.
• Support internal audits by preparing required documentation.

Skills

GMP knowledge

Quality Systems knowledge

Communication skills

Organizational skills

Time management

Tools

TrackWise

Microsoft Office Suite

Job description

I. Position Summary:
Our Company’sWellness is seeking a temporary Quality Management Systems Specialist to join our dynamic Quality Assurance team at our Greendale, Indiana site. This role is critical to the integrity and continuous improvement of our site’s Quality Systems and will be responsible for supporting key compliance and quality system activities such as entry of Change Controls, Deviations, Complaints, and CAPAs into TrackWise. The ideal candidate will bring an understanding of GMP principles, experience in pharmaceutical or dietary supplement manufacturing, and basic user knowledge of electronic quality systems (i.e. TrackWise or similar).

II. Specific Tasks, Duties and Responsibilities:
Responsibilities include, but are not limited to:Quality Systems Oversight
• Support site-level quality systems such as: Change Control and Deviation processes in accordance with internal procedures and regulatory expectations.
• Ensure timely and thorough completion of assigned documentation tasks.
• Support cross-functional teams quality system updates.Computerized System Compliance
• Support Data Integrity initiatives for electronic systems including TrackWise, EDMS, and other validated platforms.
• Participate in system upgrades, validation activities, and periodic reviews to ensure ongoing compliance.

Documentation & Audit Support

• Collaborate with Document Control and QA teams to ensure controlled documents are accurate, current, and compliant.
• Support internal, client, and regulatory audits by preparing documentation as assigned.
• Assist in batch record review/filing, complaint investigation initiation, and audit readiness activities as needed.

III. Essential Skills, Experience, Qualifications:
Required:
• 2+ years of experience in a GMP-regulated environment (pharmaceutical or dietary supplement preferred).
• Experience with 21 CFR 111, 21 CFR 211, or 21 CFR 11.
• Working knowledge of Quality Systems and Quality Assurance
• Experience with Microsoft Office Suite.
• Excellent written and verbal communication skills.
• Strong organizational and time management abilities.

Preferred:
• Experience with TrackWise and/or EDMS or equivalent
• Lean Six Sigma or similar continuous improvement training
• Project Management