Production Process Technician

SIRE LIFE SCIENCES; Breda; On-site; EUR 32,000 - 42,000; Full time

Job summary

SIRE LIFE SCIENCES in Breda seeks an Associate Manufacturing Process Technician to support pharmaceutical production across multiple lines, ensuring GMP compliance and quality. The role covers automated, semi-automated and manual lines with a focus on safety and continuous improvement.

You will join a fast-paced, team-oriented environment, participate in shift handovers, document production records, and contribute to efficiency gains while maintaining strict regulatory standards.

Qualifications

• Experience operating pharmaceutical production lines and following SOPs.
• Familiarity with GMP/GDP and documentation practices.
• Ability to work in a multicultural production team.
• Strong attention to detail and accuracy in records.

Responsibilities

• Operate production lines per approved procedures.
• Follow GMP and SOPs at all times.
• Support targets for safety, quality, delivery and inventory.
• Collaborate with operators, technicians and line leaders.
• Participate in shift handovers and daily reporting.
• Escalate issues promptly to line leadership.
• Complete required trainings within deadlines.
• Identify opportunities for process improvements.
• Maintain accurate production records and documentation.
• Adapt to different lines and tasks quickly.

Skills

GMP experience

SOP adherence

Attention to detail

Teamwork

English communication

Shift flexibility

Education

General MBO Level 2

Job description

The Company
A global leader in the pharmaceutical and life sciences industry focused on delivering high quality healthcare products through advanced manufacturing operations. The organization operates in a highly regulated environment with a strong emphasis on safety, quality, continuous improvement, and teamwork.

About the Role
We are looking for an Associate Manufacturing Process Technician to support pharmaceutical production operations across multiple manufacturing lines. This role is ideal for someone with manufacturing experience who enjoys working in a fast paced production environment, follows procedures accurately, and is committed to quality and safety standards.
The successful candidate will work across automated, semi automated, and manual production lines while contributing to operational excellence, continuous improvement initiatives, and team performance goals.

Responsibilities

• Operate pharmaceutical production lines according to approved procedures
• Follow GMP and standard operating procedures at all times
• Support production targets related to safety, quality, delivery, inventory, and performance
• Work collaboratively with operators, technicians, and line leaders
• Participate actively in shift handovers and daily reporting
• Escalate issues promptly and communicate clearly with line leadership
• Ensure assigned training is completed within required deadlines
• Identify opportunities for process improvements and efficiency gains
• Maintain accurate documentation and production records
• Adapt quickly to different production lines and assigned tasks

Requirements

• 1 to 2 years of experience in a manufacturing environment
• Pharmaceutical, GMP, or GDP experience preferred
• Experience following standard operating procedures
• Experience working with multicultural teams
• General MBO Level 2 education or equivalent
• Good English communication skills, both written and verbal
• Understanding of continuous improvement principles
• Strong attention to detail and accuracy
• Ability to work in a structured and disciplined manner
• Flexible and willing to work different shift patterns
• Strong sense of ownership and accountability
• Team oriented mindset

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