Array ( [id] => 1322 [azienda_id] => 174 [lauree] => {59}{60}{67}{68} [settore] => [ruolo] => [inserimento] => [time_c] => 0 [last_mod] => 1729686200 [title] => Sterile Operator Stage [body] =>

Per candidarti alla Job incontra dal vivo i selezionatori di BSP Pharmaceuticals a ROMA, il 29 ottobre.

We are currently looking for a Sterile Operator Stage - that will mainly ensure:

Main Activities:

• Perform dissolution and filtration of pharmaceuticals according to the directions on Batch Records;
• Complete Batch Record and departmental documentation related to duties performed;
• Perform the washing and sterilization of the tanks present within the Sterile Department following the indications described on the current SOPs;
• Provide preparation of disinfectants for periodic cleaning of the Sterile and Pre-sterile Area as described on current SOPs;
• Perform the periodic checks of proper functionality of the machines and equipment in the preparation room as described on the current SOPs;
• Take care of the machinery, materials and work environment, reporting any anomalies to the supervisor in a timely manner;
• Perform the cleaning of the Sterile area at the end of Production activities in accordance with current SOPs

Requirements:

• Master's Degree in Chemistry, Chemistry and Pharmaceutical Technology, Biology, Pharmacy…
• Professional knowledge of English
• Great can-do attitude

At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity , the different backgrounds and experiences and provide equal opportunity for all.

We are BSP.

 

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Array ( [id] => 1321 [azienda_id] => 174 [lauree] => {59}{68} [settore] => [ruolo] => [inserimento] => [time_c] => 0 [last_mod] => 1729686217 [title] => Technology Transfer Stage [body] =>

Per candidarti alla Job incontra dal vivo i selezionatori di BSP Pharmaceuticals a ROMA, il 29 ottobre.

We are currently looking for a Technology Transfer Stage - that will mainly ensure:

Main Activities:

• Define the product transfer team, the transfer times, the assignment of responsibilities between the client and the internal company functions, the coordination of activities and management of the budget assigned to the project;
• Ensure the transfer within the site and of the project technical information acquired by the client;
• Be the main interface with the client during the execution of the project activities;
• Ensure the execution of the transfer protocol, the review and approval of the manufacturing instructions of the batches involved in the transfer, the definition and management of the materials involved in the project based on client needs and company needs;
• Supervise the manufacturing of the batches involved in the transfer;
• Support the TT Manager in acquiring the necessary informations for the preparation of contracts with client and in the revisioning after possible changes requested;
• Support the finalization of the new business opportunities definition process, by supporting Business Development during meetings with client.

Requirements:

• Master's Degree in Chemistry, Chemistry and Pharmaceutical Technology, Engineering
• Professional knowledge of English
• Strong analytical skills, business-oriented, client-oriented
• Great can-do attitude

At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity , the different backgrounds and experiences and provide equal opportunity for all.

We are BSP.

 

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Per candidarti alla Job incontra dal vivo i selezionatori di BSP Pharmaceuticals a ROMA, il 29 ottobre.

Posizione
We are currently looking for a QA Stage - that will mainly ensure:

Main Activities:

• Batch record review
  Ensure compliance and completeness of the Batch record, through collection and analysis of all necessary documentation, documentary verification of material approval status, check list and current SOPs, in compliance with applicable regulations (laws, GMP regulations, FDA, etc.) and company quality standards.
• Investigation Management
  Support the supervisor in managing investigation of deviations and complaints, preparation of appropriate reporting, complete with corrective and preventive actions in compliance with company procedures.
• Planning GMP Training
  Ensure, through the coordination and control of the employee structure, efficient planning of training required by GMP standards towards all personnel, through analysis of training needs and coordination of the organizational needs of different functions, in compliance with GMP standards.
• Quality
  Ensure compliance with company quality standards, through the implementation of procedures related to areas of responsibility, in accordance with company quality policies and procedures.

Requirements:

• MA degree (CTF/Chemistry, Pharmacy, Biology…)
• Knowledge of GMP
• English working knowledge
• Great can-do attitude

At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity , the different backgrounds and experiences and provide equal opportunity for all.

We are BSP

 

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Array ( [id] => 1319 [azienda_id] => 174 [lauree] => {59}{67}{83}{68} [settore] => [ruolo] => [inserimento] => [time_c] => 0 [last_mod] => 1729684443 [title] => QC Analyst Stage [body] =>

Per candidarti alla Job incontra dal vivo i selezionatori di BSP Pharmaceuticals a ROMA, il 29 ottobre.

Posizione
We are currently looking for a QC Analyst Stage- that will mainly ensure:

Main Activities - QC Microbiology Analyst:
· Daily use and control of the main laboratory equipment (chromogenic kinetic, isolator, biolog);
· Microbiological analysis of raw materials, semi-finished and finished products according to current analytical methods;
· Sterility testing within the isolator system;
· Microbiological validation activities;
· Issuance and review of laboratory documentation;
· Preparation and sterilization of culture medium;

Main Activities - QC Chemical Analyst:
· Chemical analysis of raw materials, semi-finished and finished products according to current analytical methods or Pharmacopoeias;
· Daily use and control of the main laboratory equipment (HPLC, UPLC, UV, SoloVPE, KF, IR);
· Evaluation of analytical results obtained;
· Drafting of GMP documentation;
· Proper handling and use of reagents and laboratory standards;
· Use of major data processing and management software (Empower, Totalchrom, UV WinLab ES, Excel, LIMS).

Main Requirements:
· MA degree (CTF/Chemistry/Biology/Biotechnology)
· Available on working on shifts
· English working knowledge
· Great can-do attitude

At BSP we believe in an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. We respect the diversity , the different backgrounds and experiences and provide equal opportunity for all.

We are BSP.

 

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