drjobs
Cleaning Support Specialist
drjobs
Cleaning Support Spe....
drjobs Cleaning Support Specialist العربية

Cleaning Support Specialist

Employer Active

1 Vacancy
drjobs

Job Alert

You will be updated with latest job alerts via email
Valid email field required
Send jobs
drjobs

Job Alert

You will be updated with latest job alerts via email

Valid email field required
Send jobs

Jobs by Experience

drjobs

1-3years

Job Location

drjobs

Tipperary - Ireland

Monthly Salary

drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2669876

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.




A fantastic career opportunity has arisen for a Cleaning Support Specialist.






Requirements


Bring energy knowledge innovation to carry out the following:

  • Responsible for issuing and management of cleaning changes and documentation.
  • Responsible for reviewing and incorporating relevant updates as communicated via the Technical Team Lead.
  • Responsible for management and tracking of Cleaning validation parameters and commitments.
  • Support for Cleaning Investigations
  • Compilation of CPV reports CAR and APRs
  • Ownership and management of changes.
  • Generation and tracking of cleaning campaign documentation.
  • Stewardship of validated campaign data.
  • Liaising with product teams to align turnaround targets.
  • Investigation support for Cleaning QNs.
  • Assessments of OOTs.
  • Support project assignments as required.
  • Completion of validation reports.



What skills you will need:

In order to excel in this role you will more than likely have:

  • Degree qualification in a science or engineeringrelated discipline.
  • Knowledge of GMP standards.
  • Good communication skills both written and verbal.
  • Strong technical writing skills.
  • Previous experience in API or Drug Product manufacturing is desirable.
  • To maintain accurate records in compliance with GMP expectations.
  • To understand and internalise procedures relevant to GMP operations.
  • To communicate clearly and concisely on technical issues.
  • To deliver project goals on time.
  • Demonstrated ability to work as part of a diverse team in an inclusive manner.
  • High personal integrity credibility and energy.
  • Must be motivated and focused with a demonstrated ability to be selfdriven.
  • Communication written oral


#LIKV1


Bring energy, knowledge, innovation to carry out the following: Responsible for issuing and management of cleaning changes and documentation. Responsible for reviewing and incorporating relevant updates as communicated via the Technical Team Lead. Responsible for management and tracking of Cleaning validation parameters and commitments. Support for Cleaning Investigations Compilation of CPV reports, CAR, and APRs Ownership and management of changes. Generation and tracking of cleaning campaign documentation. Stewardship of validated campaign data. Liaising with product teams to align turnaround targets. Investigation support for Cleaning QNs. Assessments of OOTs. Support project assignments as required. Completion of validation reports. What skills you will need: In order to excel in this role, you will more than likely have: Degree qualification in a science or engineering-related discipline. Knowledge of GMP standards. Good communication skills, both written and verbal. Strong technical writing skills. Previous experience in API or Drug Product manufacturing is desirable. To maintain accurate records in compliance with GMP expectations. To understand and internalise procedures relevant to GMP operations. To communicate clearly and concisely on technical issues. To deliver project goals on time. Demonstrated ability to work as part of a diverse team in an inclusive manner. High personal integrity, credibility and energy. Must be motivated and focused, with a demonstrated ability to be self-driven. Communication - written, oral

Employment Type

Full Time

Company Industry

Pharma / Biotech / Clinical Research

About Company

Report This Job
Disclaimer: Drjobpro.com is only a platform that connects job seekers and employers. Applicants are advised to conduct their own independent research into the credentials of the prospective employer.We always make certain that our clients do not endorse any request for money payments, thus we advise against sharing any personal or bank-related information with any third party. If you suspect fraud or malpractice, please contact us via contact us page.