- Accept and perform production or project role while working in a contracted position within customer’s work environment utilizing clients tools and systems to complete daily assignments
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Utilize client tools and systems as required to provide transactional support or personal compliance:
- Training requirements
- Mailbox management
- Document/Report management
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Log all billable time against correct program codes and cost centers in time tracking spreadsheet
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Provide management with job specific Key Performance Indicators (KPIs), as need
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Attend group meetings as a contractor and participate with constructive feedback to processes ed
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Contribute to SOP revisions, efficiency projects or client initiatives, as needed
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Packaging Operations: Execute primary (bottle filling) and secondary (labeling) packaging activities, including setup of packaging rooms and coordination with QA for checks.
- Documentation & Compliance: Follow batch records, maintain logbooks, and ensure timely corrections; Create job-related binders and upload completed labeling documentation in Global Document Management System (GDMS).
- Label Management: Print clinical and other labels, perform second label checks, and upload label artwork internally and externally.
- Quality Assurance: conduct visual inspections and verification of labeling accuracy; support occasional review of label proofs.
- Inventory & Housekeeping: Maintain inventory, perform equipment and room cleaning, and ensure compliance with GMP and SOP standards.
- System Updates: Post packaging job data in system and create document folders as required.
- Training & Meetings: Attend weekly meetings, maintain required training certifications, and support team knowledge sharing
- High School Diploma/GED with 3+ years work experience
- Minimum two years work experience
- Bachelor's Degree in Science or business-related field preferred
- Experience working as a Grade 1 or Grade 2 Production Coordinator
- Pharmaceutical or similar GMP environment
- Team Lead or Group Lead experience (not required to be in Pharmaceutical)
- Project management experience within a manufacturing environment
- Strong attention to detail and adherence to GMP guidelines.
- Ability to work in temperature-controlled environments (e.g., 2–8°C).
- Familiarity with clinical packaging processes and documentation systems.
- Good organizational and communication skills.
- Medical, Vision & Dental benefits from the 1st of the month following start date
- 20 days PTO per year, accrued monthly following start date
- 12 holidays per year
- Company paid Long and Short-term disability along with Life Insurance
- 401k company contribution
- Professional development programs/ continuous learning opportunities