Manufacturing Visual Inspection

Mindlance

  • Fremont, CA
  • 30+ days ago
  • $25–$26 Per Hour
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Skills

  • Biotech and Pharmaceuticalunmatched
  • Color Vision Deficiencyunmatched
  • Communication Skillsunmatched
  • Corrective Actionunmatched
  • Current Good Manufacturing Practice (cGMP)unmatched
  • Detail Orientedunmatched
  • Drug Manufacturingunmatched
  • Drug Productsunmatched
  • GMP (Good Manufacturing Practices)unmatched
  • High School Diplomaunmatched
  • Logisticsunmatched
  • Manufacturingunmatched
  • Manufacturing Execution Systems (MES)unmatched
  • Manufacturing Systemsunmatched
  • Pallet Jackunmatched
  • Presentation/Verbal Skillsunmatched
  • Regulationsunmatched
  • Safety Standardsunmatched
  • Standard Operating Procedures (SOP)unmatched
  • Team Playerunmatched
  • Time Managementunmatched
  • Training/Teachingunmatched
  • Writing Skillsunmatched

Description

  • Executes routine unit operations in Visual Inspection as assigned related to the manufacturing of drug product in a multi-product facility.
  • Performs duties under limited supervision and according to standard operating and manufacturing procedures.
  • Executes independently with adequate training, complex fundamental operations as visual inspection, advance visual inspection, palletizing, cleaning, inspection hood prep for operations, BioMES Operations and Exceptions.
  • Performs internal support duties including assisting drug product filling and packaging.
  • Executes independently with adequate training fundamental operations:

-Logistics Coordination

-Batch record executions

-Equipment use logs

-Work order initiation and tracking

-Support Projects

-Support Creation/Maintain Training Kits Documents work according to cGMP and cGDP.

-Adheres to established regulations and follows cGMP established by site.

-Reports abnormalities and deviations in a timely and accurate manner.

-Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.

-Maintains production areas according to predefined standards (5s).

-Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.

-Contributes to Quality activities such as supporting investigations, corrective actions and area walk throughs.

Skills:

-1 or more years of experience in cGMP regulated industry.

-Ability to concentrate on detail-oriented work in a complex technical setup with a Quality and Right the first-time mindset.

-Strong written and verbal communication skills.

-Ability to work with computer-based systems and manufacturing execution systems (MES).

-Ability to read and understand SOPs and instructions and document work in a written format applying cGMP standards.

-Ability to work as part of a high performing team and collaborate effectively with staff.

-Must be able to read and see clearly.

PHYSICAL DEMANDS:

- Duties of this position may require the incumbent to exert some physical effort.

-Lifting requirements may vary dependent on the drug product manufacturing visual inspection area activity. Weight is typically no more than 25 pounds.

- Employees required to participate and have acceptable result from vision testing including color blindness.

Education:
  • High school degree + minimum 1 year work experience in GMP regulated industry
  • Associates/Bachelor s degree or biotechnology vocational training preferred

EEO:

Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

Numbers & Facts

LocationFremont, CA
Salary$25–$26 Per Hour

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