Lab Technical Specialist
| Branche | Zie onder |
| Dienstverband | Zie onder |
| Uren | Zie onder |
| Locatie | |
| Salarisindicaties | 50.000-60.000 |
| Opleidingsniveau | Zie onder |
| Organisatie | J&J |
| Contactpersoon | Zie onder |
Informatie
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.
Functieomschrijving
As a Technical Specialist, you'll be a key player in ensuring the highest quality and compliance standards at our lab. You'll independently handle complex quality and compliance issues, act as a Subject Matter Expert (SME) during cGMP inspections, and serve as the Single Point of Contact (SPOC) for new product introductions and investigations. Your work will directly support our mission of developing and producing pharmaceutical products and vaccines that help patients worldwide.
- Lead investigations for non-conformances and manage deviation cases.
- Coordinate corrective and preventive actions to resolve quality issues.
- Create and review lab documentation, including supporting documents for new product introductions.
- Provide technical support to the lab and collaborate with local and global customers.
- Serve as a technical system owner for analytical equipment.
- Lead continuous improvement projects to enhance efficiency and reliability.
- Act as an SME during audits and inspections, demonstrating our commitment to quality.
- Maintain and promote a culture of safety, compliance, and reliability.
- Communicate effectively with team members and build strong, trusted relationships with colleagues and customers.
Functie-eisen
- Bachelor’s degree (HLO) or higher in Life Sciences, molecular biology, or a related field.
- Excellent written and oral communication skills in English.
- Ability to work both independently and collaboratively within cross-functional teams.
- Proven experience with microbiological techniques like bioburden, endotoxin, and sterility is highly preferred.
- Strong analytical and technical problem-solving skills.
- Experience with Good Manufacturing Practices (GMP) is a significant plus.
Arbeidsvoorwaarden
At Janssen Biologics, you'll be part of a global market leader and a highly motivated team that is passionate about its work. We are committed to fostering your personal and professional growth with opportunities to work on exciting projects and assignments.
- Flexible working hours.
- Excellent benefits and competitive compensation (Salary scale B23-24).
- A dynamic and inspiring work environment.
- Continuous professional development and educational opportunities.
- The chance to make a real impact on the lives of patients.
- Duration: 12-month contract
- Hours: 40 hours per week
- Work Model: Hybrid (3 days on-site)
Omschrijving
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 130 years. As a skilled contractor, you’ll play a key part in the thinking, strategy, dynamism - and impact - of this iconic global healthcare company as they touch the lives of nearly a billion people every day. Contribute to the next healthcare breakthrough with your next project at Johnson & Johnson.
Functieomschrijving
As a Technical Specialist, you'll be a key player in ensuring the highest quality and compliance standards at our lab. You'll independently handle complex quality and compliance issues, act as a Subject Matter Expert (SME) during cGMP inspections, and serve as the Single Point of Contact (SPOC) for new product introductions and investigations. Your work will directly support our mission of developing and producing pharmaceutical products and vaccines that help patients worldwide.
- Lead investigations for non-conformances and manage deviation cases.
- Coordinate corrective and preventive actions to resolve quality issues.
- Create and review lab documentation, including supporting documents for new product introductions.
- Provide technical support to the lab and collaborate with local and global customers.
- Serve as a technical system owner for analytical equipment.
- Lead continuous improvement projects to enhance efficiency and reliability.
- Act as an SME during audits and inspections, demonstrating our commitment to quality.
- Maintain and promote a culture of safety, compliance, and reliability.
- Communicate effectively with team members and build strong, trusted relationships with colleagues and customers.
Functie-eisen
- Bachelor’s degree (HLO) or higher in Life Sciences, molecular biology, or a related field.
- Excellent written and oral communication skills in English.
- Ability to work both independently and collaboratively within cross-functional teams.
- Proven experience with microbiological techniques like bioburden, endotoxin, and sterility is highly preferred.
- Strong analytical and technical problem-solving skills.
- Experience with Good Manufacturing Practices (GMP) is a significant plus.
Arbeidsvoorwaarden
At Janssen Biologics, you'll be part of a global market leader and a highly motivated team that is passionate about its work. We are committed to fostering your personal and professional growth with opportunities to work on exciting projects and assignments.
- Flexible working hours.
- Excellent benefits and competitive compensation (Salary scale B23-24).
- A dynamic and inspiring work environment.
- Continuous professional development and educational opportunities.
- The chance to make a real impact on the lives of patients.
- Duration: 12-month contract
- Hours: 40 hours per week
- Work Model: Hybrid (3 days on-site)
