Associate Manufacturing
Breda, Noord-Brabant, Netherlands
€ 40.000 - 60.000
A driven and knowledgeable, learnable, coachable, and self-reflective person. A person who is competent and willing to work on a pharmaceutical production line. He/she has preferable experience with principles of GMP, standard work and production environment. He/she has constant focus on work during the day, needs to work in a defined speed to deliver planned routing. He/she likes working in a challenging environment, is a team-player by heart and flexible. Can easily and readily switch between production lines and assigned tasks. Showing ownership and maturity by following procedure and escalating when necessary is standard for him/her. Looking for opportunities and challenges are natural for this person.
Context:
Employee is working in ABR manufacturing department in the central flex force, potentially working on all production lines of either fully automated, semi-automated or manual nature. Staff is working in a 3 shift, 5-day schedule. According to standard work principles team/individuals is/are taking care that defined performance on Safety, Quality, delivery, inventory and performance are executed. Respect and working together in a professional and mature manner is key. Diversity of culture and native makes that a good knowledge (verbal, reading, writing) of English language is necessary. Escalation and reporting out on Tier 1 level he/she needs to do towards the Line Lead of the assigned line in a clear and factual manner.
Working experience:
• 1 – 2 years experienced in manufacturing environment (preferable Pharmacy, GMP/GDP environment)
• Working with Standard Operating Processes
• Working with colleagues from different countries
• Has inside in what Continuous improvement means regarding own role.
Education:
• General MBO (level 2)
• MBO level knowledge of English language
Competences:
• Flexible, can readily adjust to assigned work
• Team player
• Efficient and accurate
• Structured/discipline
• Clear in communication
• Accountability/Responsibility
• Trustworthy
• Knowledgeable on production processes
Personal characteristics:
• Learning attitude (wants to learn constantly)
• Self-reflection
• Good in working with teams and people with various backgrounds and cultures
• Pro-active working attitude
• Willing to work in different shift patterns
• Open for change and challenges
Functional tasks:
• Running a production line according to operating procedures
• Working together/communicate with other operators and line lead in order to deliver defined goals
• Looking for improvement and efficiency in and around working processes
• Taking care of escalation when necessary
• Taking ownership for all tasks and results
• Taking active part on Shift hand over process in the line
• Taking care, all training has been followed according to deadlines
Telefoonnummer *
Emailadres *
Land *
CV * Toegestane bestandstypen: doc, docx, pdf, jpg, jpeg, gif, png, Max. bestandsgrootte: 4 MB.
Responsibilities Perform QA assessments in support of complaint investigations by means of product inspections. (e.g. Reserve sample inspection, Return sample inspection and Safety Features verification) Perform triage on received product complaint units and if required support process for shipment of the return units to external sites Partner with...
AccountabilitiesEnsure product batches are ready for release by the QP and all procedural requirements for release have been met.Execute sampling, inspection, review and release of incoming materials.Execute sampling and/or inspection of LDP/ IDP/ FDP/ NAMP.Perform GMP compliance checks in Warehouse area.Approve minor deviations related to IQA and ...
Responsibilities Perform QA assessments in support of complaint investigations by means of product inspections. (e.g. Reserve sample inspection, Return sample inspection and Safety Features verification) Perform triage on received product complaint units and if required support process for shipment of the return units to external sites Partner with...
AccountabilitiesEnsure product batches are ready for release by the QP and all procedural requirements for release have been met.Execute sampling, inspection, review and release of incoming materials.Execute sampling and/or inspection of LDP/ IDP/ FDP/ NAMP.Perform GMP compliance checks in Warehouse area.Approve minor deviations related to IQA and ...
#J-18808-Ljbffr