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Production Support Admin position at a Medical Devices Company in San Diego, CA. This is a 12-month contract role for US Citizens or GC Holders only, working a 1st Shift (Monday - Friday 6:00Am - 2:30Pm) for 40 hours per week.
Job Responsibility:
Learn and Understand: Basic product characteristics for Batch Record and Label printing including templates, specifications, and formatting
Use of thermal printer (Zebra) for descriptive and barcode label output generation
Monitoring output as it comes off of the printer for legibility, alignment, and content
Proficient in changeover tasks related to the thermal printer: ribbon replacement, label stock changeover as necessary, and general machine troubleshooting
Use of SAP and Filemaker Pro for the purposes of label and batch record printing
Understand the label specifications for label template, Bill of Material requirements for label stock, and acceptable output
Understand the batch record specifications related to batch record ID specification and careful review of specification comments for unique handling or Quality Notification adherence
Documentation: Propose revisions to packaging Work Instructions and Standard Operating Procedures
Generate packaging process documentation, such as label and batch record output using the specified templates, and other documentation required for production
Log, maintain, and generate data capture for daily/weekly/monthly/quarterly metrics compilation related to batch record and label printing tasks
Administer and maintain Product Insert/Technical Data Sheet/Technical Manual printing program
Maintain packaging supplies inventory pertinent to production documentation support and re-order, as necessary
Input data, as required, in the SAP and/or other Production Planning/ Manufacturing Resource database system(s)
Interface with Quality Assurance and other departments as needed on packaging documentation related issues
Support and lead daily shift start up meetings
Ability to lift 10-15 pounds in a safe manner
requesting assistance when appropriate
Support and lead Continuous Improvement and Process Improvement initiatives
Follow all departmental guidelines and procedures
Follow Client Biosciences Environmental, Health and Safety (EH&S) policies and procedures: Take responsibility for safety in immediate work area
Participate in EH&S programs
Notify supervisor of all observed hazardous conditions or unsafe work practices
May provide recommendations on maintaining the safety of the work environment
Other duties as assigned by Supervisor
Requirements:
Excellent computer skills
Proficiency in MS Word, Excel, and Outlook
Adobe Acrobat and SAP knowledge are beneficial
Ability to effectively prioritize tasks
Proactive self-starter
Ability to interface independently with internal customers
Fast learner with strong written and verbal communication skills
High School diploma, some college experience preferred
Must be able to work independently and with minimal supervision
Ability to read, write, and speak English effectively
Detail-Oriented, team player
Stable employment and/or education within the last 3-5 years
General office, computer data entry, zero to three years related experience
For many roles at this client, assignment is contingent upon the Employer of Record’s receipt of sufficient proof that you are fully vaccinated against COVID-19 (meaning two weeks have passed after the last injection of Pfizer/Moderna or two weeks after receipt of the J&J). In some locations, weekly testing for COVID-19 may be available instead of vaccination.
Nice to have:
Lab and/or pharmaceutical/biotech manufacturing experience a plus
Some laboratory and/or pharmaceutical/biotech manufacturing and/or bottling/packaging experience preferred.