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Offer: April 30 2021:Neopharm Labs Blainville,

Job description:

Specialist validation IT

View other Neopharm Labs offers

April 30 2021

Categories Pharma, Biotech, Sciences, R&D, Quality assurance and control, Validation

Blainville, QC

Do you aspire to
make significant contributions to the life sciences industry and the global
community that improves the lives of patients? Do you want to join a company
that is a trusted partner of the largest life science organizations? If you
answered yes to either, we would like to hear from you! We have a job opening
for a specialist validation IT.

The function of the prosperous
is to ensure software verification for consistency, completeness and
correctness of the IT systems in place and their supporting documentation
through development and support following implementation of systems. AS the
validation of computerized systems (including LIMS) are defined by project /
user needs and intended uses, this function will act as the IT liaison and support
for through creating and implementing standard protocols and blueprints for
system uses and applications consistent over time and across multiple
projects. This person will be
interacting with all department of Neopharm Labs.

Neopharm Labs has supported leading organizations in the pharmaceutical and life sciences industry for more than 30 years. Our success is the result of our integrity, quality, problem-solving capability and superior customer practice. We offer a full range of chemistry, microbiology and stcapability tests in the vision of Good Manufacturing Practices. We can process large volumes to meet all the testing needs of our customers. Driven by excellence and our desire to acquire new technologies, we are continually looking for sustainable ways to improve our services to our customers around the world.

Our corporate culture is rooted in positivity, innovation and collaboration. We are a growing company offering essential services to our long-standing clients. We have a customer-focused approach located on transparency, flexibility and
relicapability. We are proud to play a vital function in our
clients' mission to improve the lives of the global community through new
medical discoveries.


   » You have capability
to build and maintain respectful and trusting relationships with all internal
and external stakeholders at all levels;
   » You have an
excellent written and oral communication expertise, in both French and English;
   » You have capability
to work effectively independently and as a team;
   » You have a strong
reporting skill to various user levels;
   » You have capability
to prioritize work and switch between different tasks and projects seamlessly;
   » You have a strong
attention to detail, and capability for problem solving and root cause
   » You can negotiate
with internal staff, subcontractors, consultants and suppliers to ensure that
GxP-sensitive systems are implemented and remain in a validated state;
   » You have a bachelor's
degree required, preferably in health or computer sciences;
   » You have a
minimum 5 years of practice directly in or in a function affiliated to the life
sciences industry, with a minimum of 3 years of practice in computer system validation;
   » You have a proven
expertise of the validation processes of computer systems using the guidelines
ISPE GAMP5 and other international guidelines (PIC / S, ICH);
   » You must be
familiar with a GMP environment;
   » You have an
practice/expertise of business systems such as LIMS LabWare is an asset;
   » You have a
strong expertise of Health Canada, FDA regulations.

   » Flexible schedule;
   » Possibility of remote
   » Great employee perks;
   » A diverse, warm and
friendly work environment;
   » A rapidly changing
environment that keeps you up to date with new industry development;
   » Opportunity for personal and professional development;
   » A safe workplace when on
site, as we are rated an exemplary employer by the INSPQ in adhering to Covid's avoidance guidelines;

   » Plan the work to be done
and ensure that deadlines are met in collaboration with Write IT validation,
including hardware and software, to support enterprise systems that impact GxP;
   » Write computer
validation plans and protocols;
   » Review of deliverable
validation products, including URS, FRS, IQ/QO, QP, etc.;
   » Correct discrepancies
connected with computer system validation for impact and resolution;
   » Write reports to
summarize the results of computer validation activities;
   » Assess system changes
using a risk-located approach and assign the appropriate level of validation
   » Manage data integrity in
conformity with various regulations in force (BPF, FDA, 21CFR Part 11, etc.);
   » Ensure compliance is
established and maintained at all times;
   » Write and maintain
operating procedures and/or computer validation policies as required;
   » Keep abreast of industry
guidelines and regulations.

Are you interested in this opportunity and want more information? Don't
be embarrassed! Send us your CV and we'll get in touch with you.

Neopharm Labs needs people like you to shine!

Apply now!


Job Category: Health Services [ View All Health Services Jobs ]
Language requirements:
Employment type:
Salary: Unspecified
Degree: Unspecified
Experience (year): Unspecified
Job Location: Blainville, QC Other
Address: Blainville, QC
Company Type Employer
Post Date: 05/04/2021 / Viewed 23 times
Contact Information
Company: Neopharm Labs Blainville,

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