Production Coordinator - Deputy Head of Manufacturing

About the job

Production Coordinator - Deputy Head of Manufacturing

for the Bad Aibling site, Germany

Would you like to make a valuable contribution to the health of patients? And take responsibility to achieve something truly meaningful? Then we look forward to hearing from you! Excellence beyond manufacturing – that is what we stand for at Aenova, one of the world’s leading contract manufacturers and developers for the pharmaceutical industry with 4,000 employees at 15 locations. Our site in Bad Aibling is a competence centre for blister packaging and effervescent tablets.

Your area of responsibility

Supporting the Head of Operations as Deputy Head of Manufacturing in planning, scheduling and monitoring production activities to ensure products are manufactured within the specified time, cost and quality limits, with particular focus on ensuring compliance with GMP, AMG, AMWHV and HACCP-/IFS guidelines

Documentation:

Approval of manufacturing instructions, bills of materials, packaging and labelling documents

Review and approval of all relevant production documents

Processing deviations and complaints as well as developing and implementing corrective and preventive actions (CAPAs).

Supporting the assurance of SOP compliance through regular monitoring and training of employees.

Quality assurance:

Supporting the assurance that all production processes comply with established quality standards.

Implementing immediate measures in case of deviations, including staff training if necessary

Timely implementation of CAPA and CR measures.

Communication:

Active participation in internal and external audits as well as self-inspections

Providing information to authorities and customers

Process optimisation:

Identifying and implementing improvements in production processes

Creating changes

Implementing SOP changes

Development: Supporting the introduction of new production technologies or processes.

Your profile

Successfully completed studies in pharmacy, process engineering, chemistry or comparable fields

Initial professional experience in the pharmaceutical environment, ideally experience in manufacturing

Comprehensive knowledge of Good Manufacturing Practice (GMP) and relevant legal regulations, such as the Medicinal Products and Active Substances Manufacturing Ordinance (AMWHV)

Commercial knowledge for evaluating production processes

Proactive, independent and solution-oriented working style

High quality standards, absolute reliability and resilience, as well as confident appearance

Strong team spirit and excellent communication skills adapted to hierarchical levels

Proficient with Office functionalities and database systems

Good command of English, both spoken and written

Your motivation

Are you looking for new challenges in a competitive environment? And do you want to tackle them creatively and independently? Do you prefer a "get-it-done" culture and think more in solutions than problems? What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!

If you have any questions, I - Franziska Schlüter / Human Resources - am happy to assist you: +49 8061 931 104