Quality Control Head

AR000 Argentina LE
A tiempo completo
En el sitio

Job Description:

At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.

In Buenos Aires (Argentina) we are looking for a Quality Control Head.


You will be in charge of the management of quality control activities. The QC Head is responsible for the delivery of analytical results on time. All documented results are in compliance with GMP, DI, Regulatory and customer requirements. The QC Head is responsible for the QC staff and the safety, health and environment of the laboratories. All equipment and facilities used must be qualified and maintained.

Ensure the validation of analytical methods for finished product and the stability program. Execute sector activities in order to optimize internal processes to meet the standards established by the policies of the Organization, health authorities and current law.

Your day at Ferring

- Ensure analytical results are performed, approved, reviewed and delivered on time. The delivery and sales plans of all batches to be analyzed are translated into operational QC plans for the respective samples.

- Coordination of the analysis schedule for local finished products, raw materials and packaging materials.

- Verify analysts' notebooks by double checking the results included in the certificate of analysis of raw materials and packaging materials.

- Planning, execution, implementation and documentation of validations of methods and qualifications of instruments. Prepare URS, Protocols and reports. Support QC's part in the stability testing program. Write APR reports and be responsible for trending of data.

- Control of solids and liquids stocks. Control of stock and validity of QC standards.

- Training plan for QC staff and carry out training of QC staff, both for GMP and improving technical skills and know-how. Support that compliance and GMP level of staff is high. Supplying the technical guidance to the staff in the laboratory.

- Coordination and follow-up of analyses conducted by third parties.

- Ensure Data Integrity Compliance during raw materials, packaging materials and finished products analysis.

Behind our Innovation… There’s you

- Studies: Bachelor’s degree in pharmacy, biochemistry or or related technical discipline

- Experience: 5 years in a similar position within the pharmaceutical industry.

- Additional knowledge: computer systems and GMP rules.

- Languages: English.

People come first at Ferring

  • Get inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love
  • Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role
  • Parental leave for both birthing and non-birthing parents
  • Extended support on family building journey

Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member’s contributions. Imagine the power of your career when it’s Ferring + You.

Behind our purpose… There’s you

If our mission and your vision are aligned, please apply!


Ferring Argentina Production

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