Macleods Hiring Bioanalytical Analyst

MPharm MSc LCMS Analyst Jobs Pharma

M.Pharm/MSc LCMS Bioanalytical Analyst vacancies (3–6 yrs) at leading pharma company. Apply now for GLP lab role.

A leading pharmaceutical organization is hiring experienced professionals for its Bioanalytical Section (LCMS – Analyst). This role is designed for candidates with strong hands-on exposure to LC-MS/MS bioanalysis in a GLP-compliant laboratory environment. A total of three positions are open for skilled professionals with 3–6 years of relevant experience.

If you are searching for LCMS analyst jobs in pharma, bioanalytical research careers, GLP laboratory vacancies, drug metabolite analysis roles, or clinical bioanalysis opportunities, this position offers a technically advanced and compliance-driven work environment.

Company Overview

The hiring organization operates within the regulated pharmaceutical and bioanalytical research domain, supporting drug development, pharmacokinetic studies, and regulatory submissions. Bioanalytical laboratories play a critical role in evaluating drug concentration in biological matrices during preclinical and clinical studies.

Bioanalytical sections operating under GLP (Good Laboratory Practice) guidelines must maintain strict documentation, instrument calibration, and data integrity systems. These laboratories contribute directly to:

• Clinical trial data generation
• Pharmacokinetic and bioequivalence studies
• Regulatory submission support
• Drug safety and metabolite profiling
• Compliance with international regulatory authorities

Professionals working in LCMS-based bioanalysis gain highly specialized expertise that is in strong demand across pharmaceutical R&D, CROs, and regulatory-focused organizations.

Job Role & Responsibilities

Position: Bioanalytical Section – Analyst (LCMS)

Number of Positions: 3
Qualification: M.Pharm, M.Sc (Analytical Chemistry), M.Sc Chemistry, B.Pharm
Experience Required: 3–6 Years
Industry Type: Pharmaceutical / Bioanalytical Research

Role Profile

The selected candidate will assist the Project Leader in conducting bioanalysis and maintaining the bioanalytical laboratory in full compliance with GLP principles and internal SOPs.

Key Responsibilities

Bioanalytical Method Development & Validation:

• Develop and validate LC-MS/MS bioanalytical methods
• Optimize chromatographic conditions for drug and metabolite quantification
• Perform accuracy, precision, linearity, recovery, and stability assessments

Sample Processing & Analysis:

• Process biological samples (plasma, serum, urine, etc.)
• Quantify drug/metabolite concentrations using validated methods
• Review chromatograms and integration data for accuracy

Documentation & Compliance:

• Compile raw data in laboratory notebooks and data sheets
• Maintain equipment logbooks and calibration records
• Draft and revise Standard Operating Procedures (SOPs)
• Ensure strict adherence to GLP and data integrity (ALCOA principles)

Instrument Maintenance & Calibration:

• Maintain and troubleshoot LC-MS/MS systems
• Calibrate pipettes, dispensers, and laboratory instruments
• Ensure preventive maintenance documentation is audit-ready

Operational Support:

• Assist in internal and external audit preparations
• Support regulatory inspections if required
• Perform additional responsibilities assigned by the section head

This role demands strong analytical thinking, precision in documentation, and hands-on expertise in bioanalytical instrumentation.

Eligibility / Qualifications

Educational Qualifications (comma-separated):

M.Pharm (Pharmaceutical Analysis, Pharmaceutics), M.Sc Analytical Chemistry, M.Sc Chemistry, B.Pharm

Experience Requirements:

• 3–6 years of hands-on experience in LC-MS/MS bioanalysis
• Exposure to GLP-compliant laboratory systems
• Experience in bioanalytical method validation

Core Competencies:

• Strong knowledge of chromatographic techniques
• Expertise in LC-MS/MS operation and troubleshooting
• Understanding of pharmacokinetic sample analysis
• Excellent analytical writing and documentation skills
• Knowledge of regulatory expectations for bioanalytical data

Important Note: Freshers are not eligible for this role. Only experienced candidates will be considered.

Location & Work Environment

The position is based in a regulated pharmaceutical bioanalytical laboratory environment. Such facilities operate under stringent GLP, data integrity, and audit-readiness standards.

Bioanalytical laboratories contribute directly to drug approval pathways and regulatory filings. Analysts in this function work closely with R&D, clinical research, and regulatory affairs teams.

Compensation will be aligned with experience, technical proficiency in LCMS, and current CTC structure.

Application Process

Interested candidates should email their updated resume along with the following details:

• Total Experience
• Current CTC
• Expected CTC
• Notice Period
• Current Working Location

Email ID: adityab@macleodspharma.com

Application Tips:

1. Clearly highlight LC-MS/MS method development experience.
2. Mention GLP compliance exposure.
3. Specify types of biological matrices handled.
4. Include audit or regulatory inspection exposure if applicable.

Only shortlisted candidates will be contacted for further evaluation.

Why LCMS Bioanalytical Roles Are High-Value Careers

Bioanalytical LCMS expertise is among the most technically demanding specializations in pharmaceutical research. Regulatory authorities rely heavily on validated bioanalytical data for drug approval and bioequivalence studies.

Professionals in this domain gain advanced exposure to:

• Drug metabolism and pharmacokinetics
• Clinical research compliance standards
• GLP laboratory systems
• Advanced mass spectrometry instrumentation
• Regulatory submission data preparation

With increasing demand for clinical research and bioequivalence studies globally, experienced LCMS analysts enjoy strong career growth and salary progression.

Frequently Asked Questions (FAQs)

1. Are freshers eligible?

No. Only candidates with 3–6 years of relevant LCMS bioanalysis experience should apply.

2. What qualification is required?

M.Pharm, M.Sc (Analytical Chemistry), M.Sc Chemistry, or B.Pharm.

3. Is GLP experience mandatory?

Yes. GLP-compliant laboratory experience is strongly preferred.

4. How many vacancies are available?

Three positions are currently open.

5. How do I apply?

Send your resume with required details to adityab@macleodspharma.com.

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Job Summary

Company	Macleods Pharmaceuticals (Bioanalytical Section)
Vacancies	Bioanalytical Analyst – LCMS (3 Positions)
Required Education	M.Pharm, M.Sc (Analytical Chemistry), M.Sc Chemistry, B.Pharm
Experience	3–6 Years (LCMS & GLP Mandatory)