Visual Inspection Operator in Drug Product Manufacturing (12-month temporary position)

FUJIFILM Diosynth Biotechnologies
Hillerod,
FUJIFILM Diosynth Biotechnologies logo

Jobdetaljer

Løn efter aftale
Fuldtid
37 timer/uge
Kun kontor
Hillerod

Jobbeskrivelse

Your New Role

You'll support the onboarding of new products in the visual inspection area, initially focusing on manual visual inspection and transitioning to automated visual inspection.

You'll have the unique opportunity to help establish all our processes, structures, and daily routines as our business area develops, working closely with your colleagues, including both operators and supporters.

Main Responsibilities:

  • Perform manual inspection activities related to on-boarding of new products.
  • Perform visual inspection related to on-going production (automated and manual visual inspection)
  • Documentation of tasks performed as per established Good Documentation Practices
  • Assist in the execution of equipment/process qualification, APS, validation, and studies as required
  • Participate in creation and development of departmental procedures to include but not limited to SOPs, OJTs, and work instructions.

Your New Team & Department

The Drug Product Manufacturing Department consist of more than 50 dedicated and enthusiastic employees organized in 3 teams covering Wash & Sterilization, Formulation, filling, and Inspection.

The department continuously strives to identify opportunities to improve systems and practices to optimize and streamline our operation.

We emphasize psychological safety, personal development, and a people-first culture. We are a multicultural, supportive, and flexible environment and strive to lead by example.

Your Talent & Skills

  • Certified per eye-sight requirements in our company
  • Able to read, write and talk in English (SOP/WI/MBR are in English).
  • Experience as an operator within Visual Inspection or from work within working under Aseptic conditions.
  • You are e.g. certified for visual Inspection, process technologists, process operators, industrial operators, or other related backgrounds.
  • A minimum 1-2 years of direct hands-on experience within GMP governed pharmaceutical manufacturing.
  • It is an advantage if you have experience with operating and running automated processes.
  • You have a strong quality mindset.

We hope you are

A positive and independent team player with a "can-do" attitude, eager to lean new skills and take ownership of tasks.

Application

If this temporary role excites you, please upload your CV and cover letter as soon as possible and latest by 31st of July. Please be aware that there can be a delay in response due to summer vacation.

Stillinger

Visual Inspection OperatorOperatorProcess TechnologistProcess OperatorIndustrial Operator

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