Search Results: 476 vacancies
...objectives are delivered to a high standard and on time.
As a Manager Biotech Production (Downstream Operations) a typical day may include,... ...in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities...
...site expectations.
This is a Limerick based role within a leading Biotech Multinational.
Duties and Responsibilities:
* Responsible for... ...documents relating to quality systems to ensure compliance with company policy and local and international regulatory requirements.
*...
Limerick
5 days ago
£ 38.85 - 51.79 per hour
A global medical device company are urgently looking for a Senior Project Manager to join their Research and Development team on a contract... ...medical device R&D project.
Essential skills:
Medical device, biotech or pharmaceutical project management experience
Degree in...
Limerick
7 days ago
...Qualified Person
Our client, a global biotech,are seeking a highly motivated and detail-oriented Qualified Person to join the quality... ...quality-related documents. An approval signature confirms that the company, GMP and relevant regulatory requirements have been met
~Review...
...foster and implement on daily basis a quality culture and any other company manufacturing standards, policies and procedures.
Coach and... ...experience as SME in highly regulated environment (e.g. pharma, biotech, medical devices) in both internal and external regulatory...
...Associate Director Quality Assurance
Our client, a global biotech, are currently recruiting for anAssociate Director Quality Assurance... ...systems and processed needed to run the site, leveraging existing company knowledge and practices where necessary, but also incorporating...
...years of relevant experience, preferably in the pharmaceutical or biotech industries or related field or equivalent combination of... ...characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known...
...inspections
This role might be for you if:
Knowledgeable in Biotech/ Pharmaceutical Quality systems inclusive of cGMP, FDA... ...characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities...
...required by Careerwise recruitment to work with our Limerick based biotech client…12-month contract position.
Role of this position... ...and regulatory groups, as well as other departments across the company, with respect to all quality instances and compliance support....
...client in their search for a Principal Microbiologist – Technical Services / Manufacturing Sciences for their state-of-the-art start up biotech manufacturing campus in Limerick.
ABOUT THE ROLE:
The Principal Microbiologist Technical Services / Manufacturing Sciences...
...Sr. Associate - Quality - Biotechnology Operations
Our client, a global biotech company, are seeking a highly motivated and detail-oriented Biotechnology QA Sr. Associates to join our quality assurance team and ensure the highest standards of product quality and compliance...
...needed.
Education and Work Experience:
~ Bachelor degree REQUIRED.
~4 Plus years of prior experience in a pharmaceutical, biotech and clinical supply logistics environment preferred
~ Supply Planning experience Highly desired.
~ Drug Forecasting or Demand...
...~8-10+ years of managing employees and budgets
~7-10+ years of experience in a GMP manufacturing environment and experience in a biotech/pharma environment
~ Experience with IT Compliance guidelines as per GAMP 5.
#JOBSIEST #IRELIM #LI-Onsite
Does this sound like...
A Validation Executor is required by Careerwise recruitment to work with our Limerick based biotech client. 12 month contract position.
Role of this position
Execution of Cleaning Validation protocols.
Generate/Review/Approval of Cleaning Validation protocols.
Generate...
...systems and applications
You are familiar with regulatory and quality policies, procedures and documentation methods, ideally in cGMP biotech/pharma operations
You enjoy helping application end-users solve problems
You possess stellar organizational skills
To be...
...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...
...Chromatography software
You are familiar with regulatory and quality policies, procedures and documentation methods, ideally in cGMP biotech/pharma operations
You have familiarity with general laboratory operations and GLP (Good Laboratory Practice)
You enjoy working...
...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...
...systems and applications
You are familiar with regulatory and quality policies, procedures and documentation methods, ideally in cGMP biotech/pharma operations
You enjoy helping application end-users solve problems
You possess stellar organizational skills
To be...
A QA Validation Technical Writer is required by Careerwise recruitment to work with our Limerick based biotech client on a 12-month contract position.
Role of this position
Execution of SIP/ cleaning and continuing validation protocols.
Writing and approving Deviations...
