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Laboratory Analyst with expertise in LCMS
Shields Pharma Inc. —Markham, ON
Minimum M.Sc. or B.Sc. degree in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 4 years direct hands…
De 60 000 $ à 65 000 $ par an
Postuler rapidement
il y a 14 jours
Bioanalytical Laboratory Analyst
Nucro-Technics —Scarborough, ON
The LC/MS Bioanalyst performs quantitative LC‑MS/MS analysis of drug candidates and biomarkers in biological matrices to support nonclinical and clinical…
À partir de 60 000 $ par an
Postuler rapidement
il y a 8 jours

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Laboratory Analyst with expertise in LCMS

Shields Pharma Inc.
Markham, ON

Postuler rapidement

Détails du poste

Permanent | Temps plein
Il y a 14 jours

Avantages

Assurance Dentaire
Assurance Vision
Assurance Vie
Stationnement sur place

Compétences

Microsoft Powerpoint
Microsoft Word
Microsoft Excel
Expérience en laboratoire
Microsoft Office
Maîtrise
Esprit d'analyse
Baccalauréat
Chimie
Compétences en informatique
Compétences en communication

Description complète du poste

ABOUT SHIELDS PHARMA INC.

Shields Pharma Inc. is a Health Canada approved GMP organization located in Markham, Ontario.

We offer Laboratory R&D and QC testing services as well as production and formulation of certain psychedelic therapeutics for treatment of certain mental health disorders such as anxiety, depression, obsessive-compulsive disorder, PTSD, and problematic substance.

Shields Pharma Inc. is an equal opportunity employer committed to diversity and inclusion for everyone. We are continuously looking for smart-minded, skilled, qualified, experienced, independent, reliable, and detail-oriented candidates to join our successful team.

Our people are at the heart of everything we do.

You can count on;

Safety as our first core value,
Integrity,
Accountability, and
Continuous Training and skill development

POSITION TITLE: Laboratory Analyst with expertise in LCMS

REPORTS TO: Director of Laboratory Operation

POSITION SUMMARY:

Shields Pharma is seeking a Laboratory Analyst with proven expertise in LC-MS/MS particularly in the analysis of nitrosamine impurities.

The main responsibility of this position is to generate accurate results while following GMP requirements. Responsible for analyzing laboratory raw material, in-process, and finished products samples using various chemical and instrumental techniques, in accordance with compendial; USP, BP, EP, and JP methods and specifications and established in-house testing methods, while under minimum supervision.

The Laboratory Analyst is responsible to operating, maintaining, performing and basic troubleshooting of analytical instruments, including; Dissolution, HPLC, UPLC, LC/MS, GC, GC/MS, ICP-MS, etc.

ESSENTIAL FUNCTIONS

Perform raw material, in-process, finished product, and stability sample testing using instrumental analytical, wet chemicals, and physical analytical methods and techniques following the written procedure or compendial methods.
Prepare analytical equipment for experiments; Including reagents, standards, test solutions, and mobile phase as required by the test procedure.
Perform analytical method Transfer, Verification, Validation and Stability testing.
Maintain accurate documentation including lab reports, records of procedures, results, and data analysis in accordance with Good Documentation Practices (GDP) guidelines
Ordering general lab supplies (chemicals/non-chemicals) when required.
Document analytical test results in lab notebooks; Ensure the data generated is accurate and meets the specifications, report results on the testing worksheets (finished products and raw materials) according to standard operating procedures in a timely manner, meeting specified deadlines.
Maintain laboratory lab-books, equipment logbooks, and trackers on daily basis in accordance with department policies and procedures.
Demonstrate sound knowledge of Pharmaceutical Compendial (i.e., USP, BP, EP, JP, etc.) General Chapters’ methods
Effectively manage the prioritization to meet multiple goals and timelines.
Demonstrate a strong understanding of cGMP, cGLP, Health Canada, FDA, ICH, and other regulatory guidelines
Be able train new or existing personnel as identified by QC management.
Notify any aberrant/OOS/OOT results to QC management and participate to investigate results following the SOP.
Conduct laboratory instruments qualification, calibration, and preventive maintenance when requested
Be able to work in a collaborative, fast-paced environment.

POSITION REQUIREMENTS : (Work Status, Qualification, Knowledge, and Experience)

Must possess Permanent Canadian residency with work permit and/or Canadian citizenship.
Must be living in Canada, preferably in Toronto area
Minimum M.Sc. or B.Sc. degree in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 4 years direct hands-on experience working in pharmaceutical disciplines.
Solid knowledge and expertise (including operation, Qualification, trouble-shooting, and maintenance) working with laboratory instrumentation such as Dissolution, HPLC, GC, ICP-MS, UV-VIS, FT-IR, TOC, TLC, KF, etc.
Experience with LC-MS/MS instrumentation and nitrosamine impurity analysis would be considered a strong asset
Possess extensive experience and in-depth technical knowledge in the method validation, and application of analytical methods used to support pharmaceutical product development and quality control. This includes a strong focus on assay determination, related substances (impurities) analysis, and residual solvents (organic volatile impurities) testing, aligned with ICH, USP, EP, and regulatory expectations.
Well versed in understanding USP, BP, EP, and JP, methods and specifications.
In-depth knowledge and competency in cGMP/GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), GXP, FDA CFR 211, ICH, and ALCOLA+ regulation and quality system guidelines.
Strong attention to detail
Strong problem solving and analytical skills including decision analysis and implementation
Computer Proficiency with MS office (Excel, Word, PowerPoint), Spreadsheets, etc.
Strong ability to function as a team member; ability to communicate effectively with team members and other plant personnel, both verbally and in writing
Track record of multi-tasking, being detail-oriented, trouble-shooting/problem solving abilities, working in a fast-paced environment with minimal instruction on routine work and moderate instruction on new assignments.
Be punctual, team player, fast learner, and have strong Interpersonal and communication skills.

HOW TO APPLY

Please reference “Laboratory Analyst with expertise in LCMS” in subject line and submit resume with cover letter to [email protected]

We welcome and encourage applications from all qualified applicants. We are committed to adhering to our company objectives and requirements outlined above. Kindly refrain from applying if you are not qualified.

We thank all applicants for their interest, however, only those qualified and selected shall be contacted for an interview.

No phone calls please.

Pay: $60,000.00-$65,000.00 per year

Benefits:

Dental care
Life insurance
On-site parking
Vision care

Application question(s):

Minimum M.Sc. or B.Sc. degree in Chemistry, Pharmaceutical, Analytical Chemistry or similar applied scientific disciplines with at least of 4 years direct hands-on experience working in pharmaceutical disciplines.
Solid knowledge and expertise (including operation, Qualification, trouble-shooting, and maintenance) working with laboratory instrumentation such as Dissolution, HPLC, GC, ICP-MS, UV-VIS, FT-IR, TOC, TLC, KF, etc.
Possess extensive experience and in-depth technical knowledge in the method validation, and application of analytical methods used to support pharmaceutical product development and quality control. This includes a strong focus on assay determination, related substances (impurities) analysis, and residual solvents (organic volatile impurities) testing, aligned with ICH, USP, EP, and regulatory expectations.
Well versed in understanding USP, BP, EP, and JP, methods and specifications
Experience with LC-MS/MS instrumentation and nitrosamine impurity analysis would be considered a strong asset
In-depth knowledge and competency in cGMP/GMP (Good Manufacturing Practices), GDP (Good Documentation Practices), GXP, FDA CFR 211, ICH, and ALCOLA+ regulation and quality system guidelines

Work Location: In person

Postuler rapidement

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