Únete a nuestro equipo

Creemos que nuestro equipo es esencial para nuestro éxito actual y futuro. Nuestro departamento de recursos humanos siempre está buscando nuevos candidatos para cubrir puestos en una variedad de áreas. Si estás interesado en trabajar con nosotros, por favor envía una carta de presentación junto con tu CV a:

cv@sagmanufacturing.com

POLÍTICA DE PRIVACIDAD

SAG Manufacturing, S.L.U. le garantiza que trataremos sus datos con total confidencialidad. Para más información, consulte nuestra política de privacidad.

INFORMACIÓN BÁSICA SOBRE PROTECCIÓN DE DATOS

Responsable:

SAG Manufacturing, S.L.U.

Delegado de Protección de Datos:

protecciondedatos@sagmanufacturing.com

Finalidad:

Gestionar la relación con los candidatos a un empleo en la empresa.

Legitimación:

Consentimiento.

Destinatarios:

Sus datos no serán cedidos a terceros, salvo obligación legal.

Derechos de los titulares de los datos:

De acceso, rectificación, supresión, portabilidad, limitación del tratamiento, y de oposición al tratamiento, dirigiéndose al correo electrónico: protecciondedatos@sagmanufacturing.com.

Ofertas de trabajo

QA Manager

QA Manager

September 13, 2017

Position in organization:

  • Department: Quality Assurance  
  • Reporting to: QA Head
  • Staff in charge: 9
  • Location: Esplugues de Llobregat

Education / experience:

  • Degree in Pharmacy
  • Status as a European Qualified Person
  • Excellent level of English and Spanish, spoken and written.

Previous experience required:

  • Minimum of 2 years working in the pharmaceutical industry in a quality management position.
  • Experienced in implementing quality systems in a GMP environment, and direct experience with health authority inspections.
  • Operational GMP experience would be a distinct advantage
  • Preferibly, with previous experience as Qualified Person (Pharmaceutical). QP/Responsible Person should meet the qualification and all conditions provided for by the EU regulation.
  • Extensive knowledge of EU GMP requirements, compliance regulations and pharmaceutical industry practices.
  • Experience MS Office 

Roles and responsibilities:

  • Ensure that all aspects of the handling and distribution of pharmaceuticals products comply with the requirements of the EU Good Manufacturing Practices/ Good Distribution Practices and relevant local regulatory and legislative requirements.
  • Ensure the implementation, maintenance and upgrading of the local Quality System in order  to drive compliance with local/International GDP regulatory requirements and Galenicum global standard operating procedures.
  • Provide quality oversight to GMP/GDP CMO/ vendors particularly such as API suppliers, FP Manufacturers, warehouse/distribution service providers in compliance with Galenicum Quality Standards (qualification, quality agreements, vendor management).
  • Act as a Qualified Person/ Responsible Person
  • Represent QA at senior management and board
  • Budgetary and managerial responsibility for Quality Assurance
  • Work with other departments to ensure a strong QA culture throughout the business and  provide quality guidance to product development projects and programs.
  • Monitoring performance and directing objectives to maximize profitability
  • Acting as a catalyst for change a

Personal Profile:

  • Self-sufficient, influencing, leadership and management skills.
  • Strong analytical and critical skills to troubleshoot complex problems.
  • Highly responsible and capable to work under pressure to meet deadlines.
  • Ability to prioritize multiple tasks
  • Good team player and collaborative working style with the ability to build partnerships with key stakeholders
  • Excellent organizational, planning and time management skills
  • Detail oriented professional with strong written and oral communication skills.
  • Motivated, proactive, dynamic, methodical, organized and decisive.
  • Ability to absorb, digest and relate detailed scientific, quality, and regulatory information.

Launch Senior Technician (Madrid)

Launch Senior Technician (Madrid)

September 13, 2017

Position in organization:

  • Department: Supply Chain
  • Reporting to: Launch Manager, Supply Chain department
  • Staff in charge: -
  • Location: Madrid office

Education / experience:

  • University degree valuable
  • International Commerce knowledge it is necessary
  • Additional courses in Logistics / Customs dispatch are highly valued
  • Excellent in English and Spanish
  • ERP user friendly – production / procurement / logistic / purchasing / customer service modules, preferable advance excel, knowledge on CRM environment.
  • Basic knowledge in Regulatory, Quality and Legal areas in Pharmaceutical companies.

Previous experience required:

  • At least 6 years working experience in Logistic/Planning/Customer management in Pharmaceutical companies
  • Experience in product launches areas on an international level in a Pharmaceutical company

Roles and responsibilities:

  • To gather all the information necessary for new product launches and their transfer to planning in time and form, of the B2B and B2C business lines of Galenicum.
  • Coordinate the product deliveries on time with clients, production plants, clients and all the departments involved in Galenicum - Sales, Regulatory Affairs, QA, Legal, among others -.
  • Collaborate with the Customer Service and with the Procurements departments, AW’s, Regulatory departments, etc.
  • Attention to customers and Contract Manufacturers.
  • Attention to visits, preparing necessary information.
  • Program all reporting; launch status reports, etc

Personal Profile:

  • Excellent communication and interpersonal skills
  • Self-motivated and work independently under pressure
  • Good team player
  • Highly responsible, proactive, dynamic and resolutive individual
  • Strong organizational and time management skills
  • Analytical capabilities to understand, follow SC processes to promote new improvements

Validation and Transfer Internship

Validation and Transfer Internship

July 24, 2017

Position in organization:

  • Department: R&D
  • Reporting to: Laboratory Manager
  • Staff in charge: -
  • Location: Esplugues de Ll.

Education / experience:

  • Degree in Chemistry
  • Preferably Master’s degree in Analytical Chemistry or Pharmaceutical Industry.
  • Excellent level of scientific and business English, spoken, reading and written.

Roles and responsibilities:

  • Writing Protocols & Reports of analytical validation of new analytical methods for active pharmaceutical ingredient and finished dosage forms.
  • Writing Protocols & Reports of transfers analytical methods between different Sites for active pharmaceutical ingredient and finished dosage forms.
  • Management and review of the documentation provide by CRO’s and CMO’s in reference to the analytical validations & transfers activities.
  • Management of all the material (such standards, samples of finish product, HPLC Columns,etc) needed to complete the activities. (Validations or Transfers)
  • Follow-up of all the tasks that are carrying out.
  • Collect external product methods of analysis current version and edit Galenicum MoA’s.
  • Act as an interlocutor between the transferring laboratory and receiving laboratory.
  • Writing of technical reports and SOP’s (Standards Operating Procedures).
  • Propose improvement flows for the department.
  • Technically guide the staff of whom in charge and provide answers and support to allow them to generate valuable results.
  • Responsibility to replies to deficiency letters.
  • Motivational skills to allow your team to achieve better results with time.
  • Be focused on accomplishing the company goals.

Personal Profile:

  • Self-sufficient, critical, disciplined, confident, hard working, creative, motivated, proactive, dynamic, methodical, organized and decisive.
  • Highly responsible and capable to work under pressure to meet deadlines.
  • Excellent organizational, planning and time management skills, to achieve project timelines.
  • Detail oriented professional with good communication skills.
  • Ability to absorb, digest and related detailed scientific, quality and regulatory information.
  • Supportive and able to build effective working relationships throughout the organization.
  • Ability to prioritize multiple tasks and execute projects on time in a fast-paced environment.
  • Ability to use and generate documentation in English.
  • Ability to increase technical knowledge and apply new skills.
  • Availability to travel
  • Strong analytical skills and problem solving.