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Recipharm Höganäs AB is looking for an experienced QP/QA Specialist
Recipharm Höganäs AB is looking for an experienced QP/QA Specialist
Do you want to join the quality department at Recipharm AB during its ongoing expansion?
In collaboration with Recipharm Höganäs AB, we are now recruiting an experienced QP/QA specialist.
This position entails responsibility as an expert (QP) according to the company's manufacturing permit. You find it exciting to take on different types of tasks depending on the need and to collaborate with manufacturing personnel on site in production and gain knowledge about technical solutions and manufacturing processes. We offer a workplace with stimulating tasks and good development opportunities.
Main tasks are:
• Release finished goods
• Participate in the development of the company's quality system as a process owner for quality processes
• Participate in various product or equipment projects as a QA representative
• Participate in inspections from customers and authorities
• Approve change requests, deviations and CAPA
The position means that you will have contact with all departments within the company and receive a stimulating mix of tasks with great opportunity for personal responsibility and development in the work. You have the ability to make decisions independently. You have an easy time collaborating and the ability to create and further develop good relationships, as well as to create commitment and participation. Communication with customers, suppliers and partners from all over the world means that it is a prerequisite that you are fluent in both Swedish and English in speech and writing.
We are looking for someone who has a pharmaceutical education or other chemical engineering education of at least 4 years and experience of similar tasks in the pharmaceutical industry. You need to meet the expert (QP) profile according to the requirements of the Swedish Medicines Agency. You have worked for several years in the pharmaceutical industry or in the life science area, preferably in the quality organization. As a person, you are meticulous, structured, service-oriented and a good communicator.
The position is a permanent position. The working hours are daytime with flexitime.
If you would like to know more and/or have questions, please contact Charlotte Curman, Senior Recruitment Manager for a confidential conversation. Tel: 070/165 22 62.
Mail: charlotte.curman@pharmarelations.se
Recipharm is a leading CDMO (Contract Development and Manufacturing Organization) company in the pharmaceutical industry.
Recipharm offers manufacturing services for pharmaceuticals in various forms, production of materials for clinical trials and APIs, pharmaceutical product development and development and manufacturing of means for drug administration. Recipharm manufactures several hundred different products for both large pharmaceutical companies and smaller development companies.
Blue Wolf Capital Partners has acquired 7 former Recipharm sites, of which the site in Strängnäs is one, as well as Synerlab with 6 facilities in France and Spain. These organizations will be combined into a world-class CDMO organization where the company name has not yet been launched but is expected to be announced shortly. Recipharm Höganäs AB primarily manufactures and packages powdered pharmaceuticals in various types of sachet packaging and currently has approximately 100 employees. Blue Wolf Capital Partners has development and manufacturing facilities in France, Spain and Sweden with its headquarters in London, UK.
Recipharm Höganäs AB is looking for an experienced QP/QA Specialist
Do you want to join the quality department at Recipharm AB during its ongoing expansion?
In collaboration with Recipharm Höganäs AB, we are now recruiting an experienced QP/QA specialist.
This position entails responsibility as an expert (QP) according to the company's manufacturing permit. You find it exciting to take on different types of tasks depending on the need and to collaborate with manufacturing personnel on site in production and gain knowledge about technical solutions and manufacturing processes. We offer a workplace with stimulating tasks and good development opportunities.
Main tasks are:
• Release finished goods
• Participate in the development of the company's quality system as a process owner for quality processes
• Participate in various product or equipment projects as a QA representative
• Participate in inspections from customers and authorities
• Approve change requests, deviations and CAPA
The position means that you will have contact with all departments within the company and receive a stimulating mix of tasks with great opportunity for personal responsibility and development in the work. You have the ability to make decisions independently. You have an easy time collaborating and the ability to create and further develop good relationships, as well as to create commitment and participation. Communication with customers, suppliers and partners from all over the world means that it is a prerequisite that you are fluent in both Swedish and English in speech and writing.
We are looking for someone who has a pharmaceutical education or other chemical engineering education of at least 4 years and experience of similar tasks in the pharmaceutical industry. You need to meet the expert (QP) profile according to the requirements of the Swedish Medicines Agency. You have worked for several years in the pharmaceutical industry or in the life science area, preferably in the quality organization. As a person, you are meticulous, structured, service-oriented and a good communicator.
The position is a permanent position. The working hours are daytime with flexitime.
If you would like to know more and/or have questions, please contact Charlotte Curman, Senior Recruitment Manager for a confidential conversation. Tel: 070/165 22 62.
Mail: charlotte.curman@pharmarelations.se
Recipharm is a leading CDMO (Contract Development and Manufacturing Organization) company in the pharmaceutical industry.
Recipharm offers manufacturing services for pharmaceuticals in various forms, production of materials for clinical trials and APIs, pharmaceutical product development and development and manufacturing of means for drug administration. Recipharm manufactures several hundred different products for both large pharmaceutical companies and smaller development companies.
Blue Wolf Capital Partners has acquired 7 former Recipharm sites, of which the site in Strängnäs is one, as well as Synerlab with 6 facilities in France and Spain. These organizations will be combined into a world-class CDMO organization where the company name has not yet been launched but is expected to be announced shortly. Recipharm Höganäs AB primarily manufactures and packages powdered pharmaceuticals in various types of sachet packaging and currently has approximately 100 employees. Blue Wolf Capital Partners has development and manufacturing facilities in France, Spain and Sweden with its headquarters in London, UK.
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