This Job Offer is no longer active.

SIRE Life Sciences®

Operations Specialist (Process Development)

Leiden, Other countries Full time

SIRE Life Sciences®

Operations Specialist (Process Development)

Location: Leiden
Operations Specialist 

The company  
Our client is the leader in the field of biomedicines. They continuously seeking innovative ways to treat cancer, infectious diseases, cardiovascular and metabolic diseases, and immune-mediated inflammatory disorders.

The role 
You will be responsible for representing operations on tech and manufacturing teams, supporting first line trouble-shooting of the day to day activities within Operations.

Responsibilities 
-Performing troubleshooting. 
-Ensuring the process performance using statistical process control. 
-Updating the Batch Records, procedures, and work instructions. 
-Support the production of quality medicines with regard to cGMP and EHS requirements. 


Requirements 
- Master in Microbiology, Biochemistry, Pharmacy, Biotechnology, or Engineering. 
- Working experience either with cell culture or purification processes. 
- Downstream experience.  
- Excellent oral and written communication in English. 


Other information 
Are you interested and want to apply for role, feel free to contact me.


 
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
SIRE Life Sciences®

Job Description

Operations Specialist 

The company  
Our client is the leader in the field of biomedicines. They continuously seeking innovative ways to treat cancer, infectious diseases, cardiovascular and metabolic diseases, and immune-mediated inflammatory disorders.

The role 
You will be responsible for representing operations on tech and manufacturing teams, supporting first line trouble-shooting of the day to day activities within Operations.

Responsibilities 
-Performing troubleshooting. 
-Ensuring the process performance using statistical process control. 
-Updating the Batch Records, procedures, and work instructions. 
-Support the production of quality medicines with regard to cGMP and EHS requirements. 


Requirements 
- Master in Microbiology, Biochemistry, Pharmacy, Biotechnology, or Engineering. 
- Working experience either with cell culture or purification processes. 
- Downstream experience.  
- Excellent oral and written communication in English. 


Other information 
Are you interested and want to apply for role, feel free to contact me.


 

Additional Information

Last updated
Employment type
Full time
Contract type
Permanent
Number of vacancies
1
Min. experience
One year
Min. education
High School
Industry / category
Jobs in Research and Development (R&D), Jobs in Science / Education / Training