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QA Specialist - 100%

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QA Specialist - 100%

Are you a good team player? Able to work in a team as well as independently? Are you an organized person with a proactive mindset and decision-making ability based on risk management? 

Do you have a solid experience in quality assurance within biotechnology environment?

In this case, you should take a look at this opportunity!
 

Biotech Operations QA Specialist (full time) - temporary until end of 2021
 

Our client, a global biopharmaceutical company is looking for their future Biotech Operations QA Specialist .


As the successful candidate for this key role, you will be part of the Quality Assurance operational team in charge of biotechnology manufacturing support (Drug Substance). 
Your proven Biotech-Quality Assurance expertise makes you a key player to support biotech manufacturing activities.

Major Accountabilities:
  • Maintain, develop, and collaborate with the Organization "QA Biotech" within the Quality Assurance department in alignment with the Site Vision, Mission, Long Term Plan, and company Values.
  • Responsible for compliance activities and quality strategies for projects with regards to technical operations related to manufacturing of biological actives Drug Substances (DS) in compliance with national and/or international regulations, guidelines (GMP), and relevant company Quality Policies.
  • Manage and approve routine manufacturing operations (upstream/downstream & Utilities): Deviations, CAPAs, Change Control, audits Inspections support, and batch record review.
  • Responsible to proactively support operations (on the floor) in order to identify, develop, and implement quality and operational excellence improvements in response to business requirements and/or technical changes and/or regulatory requirements to drive and enhance site competitiveness in alignment with Quality Standards.
  • Maintain, develop a high-quality culture in close cooperation within QA, internal and external partners.

Your Profile:
  • Qualification: Pharmacist or Master degree level in life science (biology or chemical).
  • Proven QA work experience in biotech manufacturing environment.
  • Experience in operational production and ability to work closely with operational teams in the manufacturing area.
  • Agile, Independent worker under tight and shifting priorities.
  • Demonstrated understanding of the GxP environment and technical competence in core areas of Biotech product manufacturing.
  • Ambassador for quality, continuous improvement & EHS culture implementation at shop floors level.
  • Languages: French & English (written and spoken).
  • Soft skills: communicative, able to work in a team as well as independently, organized with pro-active mindset, decision- making ability based on risk management.

Are you a good team player? Able to work in a team as well as independently? Are you an organized person with a proactive mindset and decision-making ability based on risk management? 

Do you have a solid experience in quality assurance within biotechnology environment?

In this case, you should take a look at this opportunity!
 

Biotech Operations QA Specialist - temporary until end of 201
50% part time

 

Our client, a global biopharmaceutical company is looking for their future Biotech Operations QA Specialist .


As the successful candidate for this key role, you will be part of the Quality Assurance operational team in charge of biotechnology manufacturing support (Drug Substance). 
Your proven Biotech-Quality Assurance expertise makes you a key player to support biotech manufacturing activities.

Major Accountabilities:
  • Maintain, develop, and collaborate with the Organization "QA Biotech" within the Quality Assurance department in alignment with the Site Vision, Mission, Long Term Plan, and company Values.
  • Responsible for compliance activities and quality strategies for projects with regards to technical operations related to manufacturing of biological actives Drug Substances (DS) in compliance with national and/or international regulations, guidelines (GMP), and relevant company Quality Policies.
  • Manage and approve routine manufacturing operations (upstream/downstream & Utilities): Deviations, CAPAs, Change Control, audits Inspections support, and batch record review.
  • Responsible to proactively support operations (on the floor) in order to identify, develop, and implement quality and operational excellence improvements in response to business requirements and/or technical changes and/or regulatory requirements to drive and enhance site competitiveness in alignment with Quality Standards.
  • Maintain, develop a high-quality culture in close cooperation within QA, internal and external partners.

Your Profile:
  • Qualification: Pharmacist or Master degree level in life science (biology or chemical).
  • Proven QA work experience in biotech manufacturing environment.
  • Experience in operational production and ability to work closely with operational teams in the manufacturing area.
  • Agile, Independent worker under tight and shifting priorities.
  • Demonstrated understanding of the GxP environment and technical competence in core areas of Biotech product manufacturing.
  • Ambassador for quality, continuous improvement & EHS culture implementation at shop floors level.
  • Languages: French & English (written and spoken).
  • Soft skills: communicative, able to work in a team as well as independently, organized with pro-active mindset, decision- making ability based on risk management.
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Overall rating

3,8

Based on 57 reviews

2,3 Career / Further education
3,2 Salary / Social benefits
3,8 Work-life balance
2,3 Management

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