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Quality Control Senior Analyst

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1 Vacancy
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Jobs by Experience drjobs

4-5years

Job Location drjobs

Dunboyne - Ireland

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description


About PSC Biotech


Who we are


PSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloudbased software solutions for Quality Management and Regulatory Inspections pharmaceuticals contract manufacturing professionals and metrology services to our clients.


Take your Career to a new Level


PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling points which includes the opportunity to work with the most talented cohort of likeminded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diversecultural work setting.


Employee Value Proposition


Employees are the heartbeat of PSC Biotech we provide unparalleled empowering career development though Learning & Development inhouse training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client s expectations with regards to quality of all scalable and business unit deliverables staying under budget and ensuring timelines for our deliverables are being met.




Quality Control Senior Analyst in the Biochemistry & Cell Biology Laboratory. This role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and Cell Biology methods in client site.




Requirements


What you will do:


Perform a variety of routine Biochemistry and Cell Biology analytical testing techniques and associated documentation; including but not limited to ELISA PCR Bioassays and Cell Culture WFI testing and compendial methods in compliance with GMP requirements.

Review and approve Analytical Testing data.

Support activities including general lab readiness audit readiness laboratory equipment qualification and analytical method technical transfer verification and validation.

Be part of a motivated and high performing team.

Contribute to a continuous improvement environment and bring problem solving and troubleshooting capabilities.

Demonstrate a commitment to learning and personal development.

Consistently deliver on specific area Key Performance Indicators.

Operate to the highest standards of Safety Quality and Compliance.




What skills you will need:


Degree qualification (Science/Quality/Technical).

Minimum of 4 years experience in the biotechnology and/or pharmaceutical industry preferably in relation to ELISA PCR or Bioassay Analytical Testing.

Preferably Lean Six Sigma experience.

Ability to think logically and be proactive under pressure.

Ability to work as part of a team and on own initiative in a constructive manner.

Flexible and selfmotivated.





#LIPM3

What you will do: Perform a variety of routine Biochemistry and Cell Biology analytical testing techniques and associated documentation; including but not limited to ELISA, PCR, Bioassays and Cell Culture, WFI testing and compendial methods in compliance with GMP requirements. Review and approve Analytical Testing data. Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation. Be part of a motivated and high performing team. Contribute to a continuous improvement environment and bring problem solving and troubleshooting capabilities. Demonstrate a commitment to learning and personal development. Consistently deliver on specific area Key Performance Indicators. Operate to the highest standards of Safety, Quality and Compliance. What skills you will need: Degree qualification (Science/Quality/Technical). Minimum of 4 years experience in the biotechnology and/or pharmaceutical industry, preferably in relation to ELISA, PCR or Bioassay Analytical Testing. Preferably Lean Six Sigma experience. Ability to think logically and be proactive under pressure. Ability to work as part of a team and on own initiative in a constructive manner. Flexible and self-motivated.

Employment Type

Full Time

Company Industry

Pharma / Biotech / Clinical Research

About Company

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