Join our team

SAG Manufacturing is a growing facility. We believe that our team is vital to our current and future success. Our HR department is always looking for new candidates to fill positions in a variety of areas. If you are interested in working with us, please send a cover letter along with your CV to:

cv@sagmanufacturing.com

PRIVACY POLICY

SAG Manufacturing, S.L.U guarantees that we will treat your data with complete confidentiality. For further information, see our Privacy policy.

BASIC INFORMATION CONCERNING DATA PROTECTION

Data controller:

SAG Manufacturing, S.L.U.

Data protection officer:

protecciondedatos@sagmanufacturing.com

Purpose:

Personnel selection: To manage the relationship with candidates for employment with the company.

Legitimation:

Consent.

Recipients:

Your data shall not be disclosed or communicated to third parties, unless required by legal provisions.

Rights of data subjects:

Of access, rectification, deletion, portability, limitation of processing and of opposition to processing, by sending an email to: protecciondedatos@sagmanufacturing.com.

Job Offers

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.