Our client is a specialized player in the life science sector and a leader in their field. The company is characterized by its fast-paced environment, innovative approach, and strong team spirit.
This business-critical role provides the opportunity to take on diverse responsibilities within a pharmaceutical manufacturing environment while growing through collaboration with senior colleagues. The position is available for immediate start.
External Manufacturing Manager (f/m/x)
Location: Vienna
YOUR FUTURE ROLE
* Assist as a technical contact for assigned external partners and internal departments across downstream and upstream manufacturing sites
* Support senior team members in daily technical activities for commercial manufacturing, such as reviewing process change requests and deviation reports
* Assist in managing projects related to vaccine production, including process improvements, capacity expansion, and product introductions
* Conduct technical evaluations, such as Deviations and CAPAs
* Contribute to the development and implementation of technical plans aligned with product strategies
* Support risk management activities and product lifecycle processes, including tech transfers and product launches
* Participate in troubleshooting and problem-solving initiatives under the guidance of senior colleagues
* Provide support for Change Control processes and prepare technical impact assessments
* Assist in reviewing technical documents like Master Batch Records, risk assessments, and qualification protocols
* Collaborate with senior team members to drive process improvements and maintain efficient communication with external partners and internal departments at manufacturing sites
JOB REQUIREMENTS
* A few years of experience in a cGMP manufacturing environment, ideally in technical operations or large-scale commercial pharmaceutical manufacturing
* Knowledge of pharmaceutical manufacturing processes, particularly sterile injectable products, with hands-on experience in a plant setting
* Experience working with external suppliers or within a cross-functional, matrix organization
* Eager to learn and grow under the guidance of experienced team members
* Hands-on, results-oriented, and dynamic team player with extensive project management skills
* Understanding of cGMP, post-approval changes, ICH guidelines, and regulatory validation
* Fluent in English; German is a plus
* Willingness to travel from time to time
OUR CLIENT OFFERS
* Successful and growing company with an attractive product portfolio and a promising pipeline
* Diverse range of tasks in a newly created position
* Possibility to actively shape the company's success
The compensation for this position consists of a gross annual salary of EUR 70.000 (excluding bonus). Overpayment is possible and depends on your qualifications and work experience.
ARE YOU INTERESTED?
We are looking forward to receiving your application (English CV & cover letter incl. salary expectations) over the application-dashboard. Our responsible consultant will contact you immediately after receipt.
We kindly ask you to support us in handling your application according to the GDPR regulation more effectively and refrain from applying via e-mail.
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