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USP/DSP Manufacturing Technician

CV MARKET´S CLIENT

Darbo skelbimas negalioja

Darbo skelbimo numeris 342409

Darbo skelbimo numeris

342409

Job Description

The successful candidate will join 3P Biopharmaceuticals, in Navarra, Spain, as an downstream/upstream manufacturing technician in Industrial Scale up and Manufacturing Department.
The candidate will be expected to provide development oversight, know-how and technical input in specific tasks and in the group in general. In addition, the candidate will be involved in the downstream/upstream manufacturing to obtain products (biomass or recombinant proteins) with the specifications required by our clients, in the execution of the tech transfer processes; as well as, contribution to routine laboratory activities.
Proficiency and capability in managing multiple projects in a fast paced environment with client interaction is expected.
Responsibilities will include (but not limited to):
• Creation of operating procedures & other relevant documentation for large scale manufacturing.
• Execution of commercial manufacturing processes according to established work instructions.
• Adheres to Good Manufacturing Practices and Standard Operating Procedures.
• Takes part in investigations and optimizations of processes using scientific, engineering and lean principles.
• Operates all USP/DSP production equipment within the assigned functional area.
• Assists with reviewing batch and manufacturing reports in conjunction with Quality representative and provide input to related investigations and QA audit activities. Engages in and supports culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment and safe work environment.


Requirements

• From two to three years’ experience in either R&D or manufacturing departments in upstream/downstream processes, within the biopharmaceutical industry or the academic field.
• Knowledge of microbiology and/or cell culture.
• Knowledge of biochemistry and metabolic pathways is essential.
• Experience in working with bioreactor and filtration systems is desirable.
• Experience in working on downstream/upstream processes with yeast, bacterial and mammalian cells would also be highly valued.
• Experience in GMP environment is an advantage.
• Experience in the preparation and review of documentation (SOPs, Development Reports, Validation Reports, protocol) in English to regulatory standards is essential.
• Proven initiative and independent thinking to deliver tasks on time, whilst working in a team environment.
• Capable to identify technical and scientific problems and propose solutions.
• Experience in managing studies and/or small-teams are expected.
• Proficient verbal and written communicator.
• Proficiency to work within regulatory guidelines.


Company offers

• Attractive remuneration according to the proven experience.
• Attractive salary between 22.000 € gross salary – 26.000 € gross salary.
• The company will support with relocation issues to Spain (accommodation and ect.)
• First interview will take in place through Skype
.
Province: Navarra
Country: España
Institution: Noain (Navarra)


Please send you CV to


Location:
Spain
Job type:
full-time, employee
Expiration date:
2018 m. liepos 28 d.
Published:
2018 m. birželio 29 d.
Gross salary:
From 1833 up to 2166 EUR monthly

CV MARKET´S CLIENT

3P Biopharmaceuticals is a leading European CDMO specialized in the process development and GMP manufacturing of biologics and cell therapy products. 3P offers its customers solutions at all stages of bio drug development: from initial research, preclinical and clinical phases to commercial phases. Its extensive experience in projects covering all stages of the process development and manufacturing in three different expression systems (mammalian, bacterial and yeasts), its flexibility and adaptation with its innovative technology and its vast human capital have made it a reference for the European market.

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