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AstraZeneca

Senior Team Lead Visual Inspection and Packaging

AstraZeneca is hiring a Senior Team Lead Visual Inspection and Packaging. Level rates it ; you can apply on AstraZeneca.

Level's read on this job

  • Little AI ●○○○ is how Level rates this role: aI is not part of the work.
  • Tools and skills the posting cites include SAP, visual inspection and packaging.
  • Level classifies it as a senior role.
  • Level lists 1,200+ other open roles at AstraZeneca.
  • The role was posted within the past two weeks.

AI in this role

Senior team lead overseeing hands-on visual inspection and packaging of biological medicines in a regulated GMP environment.

sap
visual-inspectionpackaginggmp-complianceshift-leadershipquality-assurance

Precision on the floor. Leadership in the room.

 

Team Lead Visual Inspection & Packaging

Nijmegen, full time

Shifts: 7.00 - 15.30 or 13.30 - 18.00 (Mo – Fri)

 

Our Visual Inspection and Packaging team in Nijmegen inspects and packages biological medicines that reach patients worldwide. It is a highly regulated, GMP driven environment where precision, documentation and safety aren’t optional and where the people on the floor are the last line of quality assurance before a product goes out.


Due to growth and expansion, we are looking for a team lead who leads by working alongside the team. This is a hands-on operational role split between performing Visual Inspection and Packaging work yourself and coaching, coordinating and supporting your team. You will be the “go to” person for the team’s day to day questions on inspection and pack matters. Over time we see this role as an opportunity to take on more responsibility within the department.


This Is not a people management position. Formal line manager responsibility falls under our Manager Supply Chain Operations, who you will work closely with.

 

What will you be doing?

On the floor:

  • Perform hands-on Visual Inspection and Packaging tasks, including high-complexity work
  • Operate equipment per SOPs and complete activities per Batch Records, with full cGMP adherence
  • Model excellent cleanroom behavior, gowning, sanitation and compliance standards
  • Act as Subject Matter Expert (SME) and administrator for key inspection and packaging equipment, including passwords and recipes
  • Ensure cleaning, environmental checks, logbooks, worksheets and checklists are completed and reviewed on time
  • Maintain the Lot Data file and carry out SAP tasks including POs and TRs

Leading & Coaching

  • Organise the day-to-day operation during your shift and translate the production schedule into daily work allocation and shift planning
  • Direct and coordinate the team on the floor, confirming staffing, skills and qualification coverage before assigning work
  • Monitor progress against schedule and adjust resources or priorities as needed
  • Run and own shift handovers and escalate unresolved constraints
  • Be the first point of contact for safety, quality, equipment, material, staffing and schedule issues
  • Take immediate containment action within your authority, and make clear stop / continue / escalate decisions where safety, quality or GMP compliance could be affected
  • Record and communicate downtime, deviations, missed targets and recovery actions

Quality, improvement and support

  • Coach and train colleagues, including onboarding newly hired Visual Inspection Technicians through training, skills verification and qualification
  • Perform first-line review of batch records, pre-reviews and logbook checks on the floor, and support deviation investigations and root-cause analysis
  • Lead and support problem solving, kaizens and practical departmental improvements; apply Lean practices including Gemba walks, Layered Audits, Tier and 5S, and lead Tier 1
  • Drive procedural updates through DCR, AZDoc and Just Do It, and flag outdated procedures for revision
  • Coordinate support from QA, Engineering, Facilities and Supply Chain
  • Support operational, validation and new product introduction projects with ME and MS&T
  • When qualified and formally delegated in writing, act as operational back-up to the Manager SCO

 

What do you bring?

You bring a naturally calm presence, you are decisive, you have a hands-on mentality, and you are reliable. You are a genuine coach and motivator, and it gives you energy to develop the people around you instead of fixing their problems for them. You are a great planner, and you have excellent organisational skills, with a keen eye for where improvements are needed. You set high standards when it comes to quality and you are comfortable and experienced with working within strict procedures and documentation requirements. You are action driven and proactive.

In addition:

  • (Technical) education at a minimum of MBO level 4 (a bachelor’s degree is an advantage)
  • 3–5 years' experience in a similar role in the pharmaceutical or related industry, ncluding cGMP and technical skills
  • Experience in a heavily regulated environment — we're happy to consider backgrounds from pharmaceutical, food, medical devices, or semiconductor industries
  • Strong verbal and written skills in English, it is an advantage if you bring some understanding of Dutch.
  • Ability to work within operational timeframes and deadlines

 

What we offer

At AstraZeneca we support continuous learning and provide room to grow, both professionally and personally. In addition, we offer: 27 vacation days + option to buy 10 additional days, 1 paid volunteering day, €230 annual sports allowance, 8% holiday allowance, 9% target bonus.


Please note:

  • A VOG (Certificate of Conduct) will be required as part of the hiring process for the successful candidate.
  • A colour vision test will be required as part of the hiring process for the successful candidate (you can not be colour blind to carry out this role)
  • The successful candidate will already be living and working in the Netherlands. We are unable to offer relocation support or sponsorship at this site.

 

About AstraZeneca

AstraZeneca works to improve quality of life for patients with serious diseases. We develop medicines in oncology, cardiovascular, renal and metabolic diseases, respiratory and immune disorders, and vaccines.


Globally, 75,000 colleagues work across six continents. In Nijmegen, around 100 colleagues produce, test, and package biologics for early clinical development. Our site plays a crucial role in bringing new medicines into first-in-human and early-phase studies.


We follow science, put patients first, and strive to do the right thing. We value curiosity, collaboration, and continuous improvement - creating an environment where people can grow and thrive.

A great opportunity to help shape the future of our site and contribute to meaningful work.


Apply today

Ready to lead, improve and build what comes next? We'd like to hear from you. This is a role where your leadership will be visible day to day.


You'll work with skilled, knowledgeable people in an environment that is evolving and full of opportunity. If you want to join a company in change, lead a capable team and build something stronger for the future, this could be the right next step. Apply by clicking on the apply button at the bottom of this page.


Questions?

Our Recruitment Team, Karin Raadschelders or Caroline van Oppen, is available at info@werkenbijastrazeneca.nl or +31 (0)85 - 047 0244.


We don’t work with a fixed closing date; we will commence our screening process immediately - the vacancy will close as soon as we’ve found the right candidate.

 

 

 

 

 

Date Posted

15-Oct-2026

Closing Date

03-Nov-2026

AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills.  We believe that the more inclusive we are, the better our work will be.  We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics.  We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

How we rate this

Senior Team Lead Visual Inspection and Packaging at AstraZeneca rates 0 out of 100 for how much of the daily work is AI. That makes it Little AI (AI Level 1 of 4). The level is about AI in the job, not seniority.

Classification

Little AI. AI is not part of the work.

  1. ●●●● Builds AI80 to 100
  2. ●●●○ Works on AI60 to 79
  3. ●●○○ Uses AI40 to 59
  4. ●○○○ Little AI0 to 39

Levels come from how often the tools, models and workflows of the role are named in the posting itself. Read the description and count the AI tools, models and workflows it names.

Prepare for this job

Built from this posting and from similar jobs on Level.

Skills and AI tools this role asks for

Visual InspectionPackagingGmp ComplianceShift LeadershipQuality AssuranceSAP

Questions you could be asked

  1. Tell me about a project where visual inspection was part of your work. What did you do?
  2. Tell me about a project where packaging was part of your work. What did you do?
  3. Tell me about a project where gmp compliance was part of your work. What did you do?
  4. Tell me about a project where shift leadership was part of your work. What did you do?
  5. Tell me about a project where quality assurance was part of your work. What did you do?

Adapt your resume

  • List these exact terms on your resume: Visual Inspection, Packaging, Gmp Compliance, Shift Leadership, and Quality Assurance. An applicant tracking system matches the wording, not the idea.
  • Attach one line of real, concrete experience to at least one of them. A tool named with nothing behind it rarely survives a human read.

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