Lab Information Systems Specialist
Company: Sun Pharmaceutical Industries
Location: New Brunswick
Posted on: March 17, 2023
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Job Description:
COME WORK FOR US - INVESTING IN YOU AS A SUN PHARMA
EMPLOYEE!
* Medical, Dental, Vision Benefits
* Health Savings Account (HSA), Flexible Spending Account (FSA)
* Prescription Drug Coverage
* Telehealth and Behavior Health Services
* Income Protection - Short Term and Long Term Disability
Benefits
* Retirement Benefits - 401k Company Match on Day One (100% vesting
immediately)
* Group Life Insurance
* Wellness Programs
* Corporate Discounts on personal services: Cellular phones,
Entertainment, and Consumer Goods!
Sun Pharma Vision: Reaching People And Touching Lives Globally As A
Leading Provider Of Valued Medicines
Sun Pharmaceutical Industries Ltd. (Sun Pharma) is the fourth
largest specialty generic pharmaceutical company in the world with
global revenues of over $ 4.5 billion US Dollars. Supported by more
than 40 manufacturing facilities, we provide high-quality,
affordable medicines, trusted by healthcare professionals and
patients, to more than 100 countries across the globe including the
United States. Sunology is a combination of Sun Values and Ideology
and is the way of life at Sun Pharma. Sunology is
Humility.Integrity.Passion.Innovation. It represents our promise to
all stakeholders including patients, physicians, and employees.
Our Code of Conduct
Our Global Code of Conduct governs every aspect of our operations.
Sun Pharma is a family of thousands of people, working across many
countries, speaking multiple languages, and all united, with one
common purpose: to make good health accessible and affordable to
local communities and society at large. Through active fieldwork,
dedicated research teams, and in recognition of the efforts who
work behind the scenes to combat illness and disease, the Sun
Pharmaceutical Group helps as many people as possible, to secure
their right to good health. The way we work every day is important
to us.
DOWNLOAD OUR CODE OF CONDUCT
The Laboratory Information Systems Specialist is person with
pharmaceutical chemist experience, will act as SME, and will play a
key role in the implementation of LIMS other laboratory system.
This position will also responsible to create specifications
masters in SAP system and creating specifications and methods in
LIMS.
* Lead implementation of laboratory Information Management System
(LIMS) and other laboratory systems in QC Laboratory.
* Act as LIMS Subject Matter Expert and provide training to
users.
* Optimize laboratory systems to align with LIMS practices and
create/modify Laboratory SOP's accordingly.
* Transfer laboratory specifications and methods from DCM system to
LIMS.
* Ensures that the integrity and accuracy of all laboratory
documents are maintained; must assess overall document compliance
with protocols, SOPs, company policies, and applicable
regulations.
* Crate new and update current method and specifications in the
LIMS.
* Create specification maters in SAP system and create different
quality views.
* Act as Writes of technical documents such as methods,
specifications and department SOP's
* Generates change requests required for analytical documents, and
routes documents for review and approval. Maintains hard copies and
electronic file of technical documents.
* Timely provide the QC documents required for CBE, PAS and ANDA
submission to RA.
* Collaborates with colleagues and external partners to achieve
individual and department goals.
* Ensure continuous laboratory compliance by adopting best industry
practice and complying with procedure requirements.
Qualifications
* Minimum BS or equivalent degree in Chemistry or related
discipline.
* Minimum of four (8) years of experience in the pharmaceutical
industry.
* Degree in computer software is preferred.
* Experience as a chemist with hands on experience with HPLC, GC,
UV-VIS, dissolution etc
* Advance computer skills, and competence with Microsoft Office
(Word, Excel, PowerPoint) and Access.
* Must have an understanding of FDA guidelines, ICH guidance and
DEA regulations. Ensures compliance with cGMPs, DEA regulations,
safety and site operating procedures under the direction of
Management.
* Must be familiar with proper cGMP practices for analytical
laboratories and working knowledge of basic laboratory instrumental
analysis and wet chemistry skills.
* Collaborates with colleagues and external partners to achieve
primary Department goals.
* Works in coordination with project plans and goals as assigned by
Management.
* Demonstrated strong communication: verbal, written and
presentation skills.
* A self-starter with a hands-on approach and a can-do
attitude.
* Excellent project management and problem solving skills.
* The requirement for English language proficiency for this job
role is Intermediate-B1+ (comparable to Global CEFR Independent B1)
level based on the Common European Framework of Reference for
Languages (CEFR).
Keywords: Sun Pharmaceutical Industries, New Brunswick , Lab Information Systems Specialist, Other , New Brunswick, New Jersey
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