Manufacturing Process Specialist

Manufacturing Process Specialist - Eye Care

Location: Beerse

Duration: Until November 2025 

Hours: Full time, 40 hours per week on-site

Imagine your next project as a Manufacturing Process Specialist, working at the forefront of cutting edge work and technology with one of the leading Pharmaceutical companies in the world!

roles and responsibilities

• Supports the operational teams of filling & packaging.

• Represents operations in project teams in his area.

• Acts as a driving force in achieving the lean goals & objectives of the

• department.

• Investigating incidents/discrepancies in collaboration with Quality Assurance for

• quality and compliance issues and taking appropriate corrective actions to

• prevent them from reoccurring.

• Identifying and implementing improvements in areas of quality, compliance,

• costs, stocks, yields, competencies and customer service.

• Ensuring that the yearly budgeted volume is produced in accordance with priorities and updates set by the planning department.

• Identifying and implementing improvements in terms of safety, quality and cost.

• Leading quality / complaint investigations executed by a multidisciplinary team

• Focus on root cause analysis (5 Why’s, fishbone diagram), impact assessments, risk analysis

• Contributing to the documentation of Quality Investigations.

• Writing and assessing change controls for Operations.

• Delivering input to Master Data department when changes in batch documentation are applicable.

• Updating procedures

• GMP responsibilities:

  • Actively deploys the company's compliance strategy.

  • Acts as a role model and performs risk analyses, check rounds, incidents, investigation, ...

  • o Provides the appropriate instructions and training and adequate supervision.

  • Involves and consults operational staff for all aspects of cGMP, provides information and feedback.

  • Measures and evaluates the cGMP performance and ensures appropriate

  • behavior.

  • Monitors compliance with cGMP

how to succeed

• Fluency in Dutch AND English

• 2-3 years of relevant experience in Pharma and / or Production

• Experience leading investigations 

• Insight in microbiology and hygiene

• Insight in technical aspects of production.

• Experience in aseptic manufacturing.

• Clear understanding of cGMP regulations.

• Clear understanding of prevention regulations.

• Project management skills.

• Insight in various problem-solving methods (e.g. RCPS, RATIO, FMEA).

• Process thinking / analytical skills.

• Strong passion for innovation, out-of-the box mindset

• Strong partnership with Quality, Tech Ops, MAM departments.

• Experience in using Truvault - TrakSYS - Comet - SAP (general) or similar beneficial. Microsoft Office - Checklist Manager

details

• Contract until November 2025

• Full time hours (40), on-site

you are welcome here

Johnson & Johnson Innovative Medicine is working to create an inclusive environment where diverse backgrounds, perspectives, and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are.

about Johnson & Johnson Innovative Medicine

Patients inform and inspire our science-based innovations, which continue to change and save lives. Applying rigorous science and compassion, we confidently address some of the most complex diseases of our time and unlock the potential medicines of tomorrow.

Our diverse portfolio spans multiple therapeutic areas — Oncology, Immunology, Neuroscience, Cardiovascular, Pulmonary Hypertension, and Retina.

We are continuously working to develop treatments, aspiring to find cures, pioneering the path from lab to life, and championing patients every step of the way.

Janssen UK: https://www.janssen.com/uk/

Janssen Ireland: https://www.janssen.com/ireland/

application process

We are looking to process the first round of applications within the next 2 working days.

We do not accept applications via email.

questions

If you would like some additional information about the role please contact: simone.strong@randstadsourceright.co.uk

Diversity, Equity & Inclusion

For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo.

We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each one of our people feels that they belong and can reach their potential. No matter who they are. Diversity, Equity & Inclusion at Johnson & Johnson means “You Belong”.