Production & manufacturing jobs with the salary shown at employers that can sponsor a visa

Only postings that publish a salary or range. Useful for checking a role against the highly skilled migrant salary threshold before you apply.

open jobs
22 open jobs
employers
14 employers
state a salary
17 state a salary
mention relocation
0 mention relocation
Language
Experience level
Field
More filters

Newest production & manufacturing jobs with the salary shown

Filters open the full board with your choice applied.

NovartisPosted 4 days ago

Quality Control Officer

Baarle Nassau · Hybrid · Full-time

What we know about this job

  • Novartis is on the IND register of recognised sponsors
  • The posting is in English
  • The posting states a salary
Apply on Novartis' site Opens the employer's own site.
Sponsor register
On the IND register
Language
English
Experience
Entry level
Salary
€44,000 – €82,000/year
Relocation
Not stated
Job type
Full-time

About the role

What they look for

  • 1+ years of experience as radiopharmaceutical QC laboratory or company equivalent in a strongly regulated environment.
  • Excellent knowledge of good laboratory practices and cGMP.
  • Analytical mind-set and eye for detail.
  • Open to new technologies and continuous improvement behaviour.
  • Open and clear collaboration and communication with third parties.
  • Shows the appropriate sense of urgency around given tasks.
  • Fluent English, written and spoken.

What you get

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen.

Expected Annual Base Salary Range for role: €44,100 to €81,900.

The base salary offered is determined based on gender-neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically.

In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.

The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.

Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics.

Read our brochure to learn more about our global total rewards offering: https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf

Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Salary Range

€44,100.00 - €81,900.00


 

Job Description Summary

#LI-Onsite
Location: Baarle Nassau, Netherlands

Relocation Support: This role is based in Baarle Nassau, Netherlands. Novartis is unable to offer relocation support: please only apply if accessible.

The QC Officer contributes to the quality control processes of the medicinal products of Novartis RLT according to the Standard Operating Procedures, Work Instructions, Specifications and Methods of Analysis as laid down in the quality system.

The QC Officer has a deep knowledge in the analytical processes and systems in a strong GMP environment and acts as Subject Matter Expert.

The QC Officer contributes to writing of investigations (deviations, Out-of-Specifications, etc), quality risk/impact assessments and qualification documentation, and execution of investigational/qualification activities for laboratory systems and processes, including laboratory equipment, computerized systems and analytical methods.


 

Job Description

Deadline for applications: 18th of September 2026.

Major Accountabilities

  • The accurate execution of the quality control as defined in the specification of the respective medicinal product, intermediate or raw material.
  • Awareness for any uncommon or unexpected incident, condition or detail during these controls and immediate notification of such deviation to the Qualified Person.
  • Execution of the routine quality control testing conform analytical procedures and methods.
  • Sampling, review and documentation of environmental monitoring according to the environmental control program effective on site. Reviewing the data and perform trend analysis.
  • Manage and maintains the progress on document generation, qualification execution, document review and approval. Escalate the issue/delay to management team.
  • Collaboration with AS&T in project management, validation, revalidation and/or technology transfer related to analytical equipment.Coordinate and manage deviation and out-of-specification/out-of-expectation (OOX) investigations to be initiated, assessed, and closed out in timely manner
  • Responsible for all other activities related to qualification activities but not limited to change control, tag out, PM/Calibration program, equipment configuration, SOP generation.
  • Communicate needs and opportunities for improvement of devices / software / methods conform GMP requirements and needs of customer.
  • Ensuring the QC Laboratory is maintained in an orderly and clean state.
  • Adherence to radiation and conventional regulations, and preventing oneself to a state that could expose her/him or colleagues to any hazardous situation.

Commitment to Diversity and Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.


 

Read the rest on the job page

About these jobs

17 open production & manufacturing jobs with the salary shown (in English, no Dutch needed) at employers that can sponsor: 17 state a salary (most stated salaries are between €2,700 and €6,000 a month gross), and none mention relocation or visa support. The most openings are at Enza Zaden (3), Philips (2) and Anteryon (1); there are also 161 postings in Dutch or asking for Dutch for the same search, not counted here. Related pages: software engineering jobs with the salary shown (98), research & science jobs with the salary shown (89) and sales jobs with the salary shown (64).

Being listed means the employer can sponsor, not that every role includes it; the relocation badge marks postings that say so. Every job links straight to the employer.

Questions about production & manufacturing jobs with the salary shown

How many production & manufacturing jobs with the salary shown are open right now?

22 at the moment, every one from an employer on the IND Public Register of Recognised Sponsors. A job leaves this page when the employer takes the posting down.

Can these employers sponsor my visa?

Being on the register means an employer is allowed to sponsor a highly skilled migrant visa. Whether it does for a specific role is the employer's decision.

What salary do I need for a highly skilled migrant visa in 2026?

From 1 January 2026 the IND requires a gross monthly salary of €5,942 if you are 30 or older, €4,357 if you are under 30, and €3,122 for recent graduates of Dutch universities and orientation-year holders. Holiday allowance is not counted in these amounts.

More in the guides to visa sponsorship in the Netherlands.