• Follow all cGMP’s and SOPs as written.
• Sign off to initiate production run (includes verification that equipment is clean and ready for use.
• Check/review any changes made during the filling/packaging process for compliance to written procedures.
• Perform all in-process (hourly) line checks on bottle/jar/tube filling lines/Jones Cartoner, etc.
• Observe area for cleanliness; report any/all deviations to supervisors for immediate correction,
• Make sure that no production begins until packaging work order is signed by QAI.
• Ensure all paperwork is completed and accurate at the end of each shift.
• Collect all paperwork, cleaning slips, etc. when the filling/packaging run is complete.
• Performance/documentation of production line clearance inspections.
• Ensure compliance with cGMPs and written procedures for all activities.
• Ensure FP samples are labeled correctly and delivers them to the QC lab, STAB & Micro.
• Assists in process validation procedures.

Schedule:

• 1st Shift M-F 5:30 a.m. -1:30 p.m.

Education/Experience:

• High School Diploma, Associate’s Degree
• 2+ years related work experience or similar combination of education and experience; experience in a pharmaceutical environment
• Interfaces with all departments at all levels on an as needed basis.
• Must be able to read, write and speak English

Benefits

• Competitive Salary
• Health Care Plan (Medical, Dental & Vision)
• 401(k) with company match
• Life Insurance (Basic, Voluntary & AD&D)
• Paid Time Off (Vacation, Sick & Public Holidays)
• Short Term & Long-Term Disability
• Training & Development

*Candidate must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.