quality specialist
- nacka, stockholm
- contingent
Är du en problemlösare som vågar ta beslut och vill bidra till kvalitetssäkringen av läkemedel som gör skillnad i människors liv? Då kan detta vara nästa steg i din karriär!Randstad Life Sciences söker nu en Senior Quality Specialist för ett spännande konsultuppdrag hos AstraZeneca i Södertälje. Här får du möjlighet att arbeta på en av Sveriges största produktionsanläggningar för läkemedel, där kvalitet och innovation står i fokus.Om rollen:Som Senior
14 may 2025
Är du en problemlösare som vågar ta beslut och vill bidra till kvalitetssäkringen av läkemedel som gör skillnad i människors liv? Då kan detta vara nästa steg i din karriär!Randstad Life Sciences söker nu en Senior Quality Specialist för ett spännande konsultuppdrag hos AstraZeneca i Södertälje. Här får du möjlighet att arbeta på en av Sveriges största produktionsanläggningar för läkemedel, där kvalitet och innovation står i fokus.Om rollen:Som Senior
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erfaren qa
- in demand job
- solna, stockholm
- contingent
Har du erfarenhet av kvalitetsarbete inom Life Science och är redo för ditt nästa steg i karriären? Drivs du av att arbeta med kvalitetsfrågor och ständiga förbättringar? Då har du hittat rätt!Vi på Randstad Life Sciences vänder sig nu till dig som vill bli en del av vårt konsultteam och jobba med brett kvalitetsarbete inom läkemedel, livsmedel eller medicinteknik. Vi söker dig med erfarenhet av kvalitetsfrågor från GxP verksamhet och som vill arbeta med
2 june 2025
Har du erfarenhet av kvalitetsarbete inom Life Science och är redo för ditt nästa steg i karriären? Drivs du av att arbeta med kvalitetsfrågor och ständiga förbättringar? Då har du hittat rätt!Vi på Randstad Life Sciences vänder sig nu till dig som vill bli en del av vårt konsultteam och jobba med brett kvalitetsarbete inom läkemedel, livsmedel eller medicinteknik. Vi söker dig med erfarenhet av kvalitetsfrågor från GxP verksamhet och som vill arbeta med
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job details

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summary

nacka, stockholm
contingent
full-time
bachelors or equivalent

posted 3 june 2025

number of offers

reference number
JN -062025-503802

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job details

Are you ready to contribute to life-changing medicines and be part of a company that makes a real difference in patients' lives? Randstad Life Sciences is now looking for a Quality Release Manager for an exciting consultancy assignment at AstraZeneca in Gärtuna.

At AstraZeneca, you’ll join a global organization where scientific innovation, collaboration, and a shared purpose drive everything we do. Within External Quality (EQ) – a dynamic global quality organization – you will experience an inclusive and development-focused culture.

...

About the Assignment:

This is a full-time consultancy role via Randstad Life Sciences, based at AstraZeneca’s Gärtuna site. A hybrid setup is possible, but you are expected to be onsite at least 3 days per week.

Role Responsibilities:

As a Quality Release Manager, you will be responsible for product release from external contract manufacturers and quality process oversight. Your key tasks will include:

Managing product release, change control, SOPs, and quality risk processes
Maintaining quality data and documentation in relevant systems
Driving process and system improvements
Supporting audits and inspections
Leading deviation investigations and quality issue resolution
Collaborating cross-functionally with supply chain, technical, regulatory, and project teams

Requirements:

Master’s degree in a scientific or technical discipline (Pharmacy, Biology, Chemistry, Engineering)
Minimum 1 year of experience in pharmaceutical operations or Quality Assurance
At least 1 year of experience with release processes, deviation handling, and change control
Strong knowledge of cGMP, Quality Systems, and pharmaceutical supply chain
Excellent communication skills in English (spoken and written)
Independent, proactive work style
Strong problem-solving and influencing skills

Desirable:

Experience working in a PCO/PET organization
Lean/Six Sigma training or certification
Experience in multi-site or cross-functional roles

Why apply through Randstad Life Sciences?

As a consultant with Randstad Life Sciences, you get a secure employment contract, dedicated support from your consultant manager, and access to a wide professional network within the life sciences sector.

If you’re eager to bring new ideas and fresh thinking to the table – this is your chance! We are hiring continuously, so don’t wait to submit your application.

About the Assignment:

This is a full-time consultancy role via Randstad Life Sciences, based at AstraZeneca’s Gärtuna site. A hybrid setup is possible, but you are expected to be onsite at least 3 days per week.

...

Role Responsibilities:

As a Quality Release Manager, you will be responsible for product release from external contract manufacturers and quality process oversight. Your key tasks will include:

Managing product release, change control, SOPs, and quality risk processes
Maintaining quality data and documentation in relevant systems
Driving process and system improvements
Supporting audits and inspections
Leading deviation investigations and quality issue resolution
Collaborating cross-functionally with supply chain, technical, regulatory, and project teams

Requirements:

Master’s degree in a scientific or technical discipline (Pharmacy, Biology, Chemistry, Engineering)
Minimum 1 year of experience in pharmaceutical operations or Quality Assurance
At least 1 year of experience with release processes, deviation handling, and change control
Strong knowledge of cGMP, Quality Systems, and pharmaceutical supply chain
Excellent communication skills in English (spoken and written)
Independent, proactive work style
Strong problem-solving and influencing skills

Desirable:

Experience working in a PCO/PET organization
Lean/Six Sigma training or certification
Experience in multi-site or cross-functional roles

Why apply through Randstad Life Sciences?

If you’re eager to bring new ideas and fresh thinking to the table – this is your chance! We are hiring continuously, so don’t wait to submit your application.

experience
qualification
Essentials for the role.

• Masters degree in a science / technical field such as Pharmacy, Biology, Chemistry or Engineering.
• Minimum 1 yrs experience in either the pharmaceutical operations environment or pharmaceutical Quality Assurance role
• Minimum 1 yrs demonstrated experience of release processes, the quality event process, change control process
• Strong demonstrated knowledge of cGMPs, Quality Systems and the pharmaceutical supply chain environment.
• Excellent oral and written communication skills [English and local language(s)]
• Strong problem solving skills
• Strong negotiating/influencing skills
• Ability to work independently under their own initiative
• Ability to be in the office in Gärtuna, minimum 3 days/week

Desirable for the role

• Experience working in a PCO/PET organization or Lean/Six Sigma training
• Multi-site / multi-functional experience
key responsibilities
Key Responsibilities:
- Manage product release from external contract manufacturers
- Oversee quality system elements including change control, SOP management, and quality risk management
- Maintain quality data and documentation in relevant Quality Management Systems (QMS)
- Drive continuous improvement of processes and systems
- Support internal and external audits and regulatory inspections
- Lead and document deviation investigations and manage quality issues
- Collaborate with cross-functional teams including supply chain, technical, regulatory, and project management
- Ensure compliance with current Good Manufacturing Practices (cGMP) and AstraZeneca quality standards
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