HPLC Analyst Job at Pfizer (Zagreb)

Qc Analyst

Location

United Kingdom , Worthing

Salary:

15.92 - 16.92 GBP / Hour

SRG

Expiration Date

Until further notice

Requirements

Relevant scientific qualification (eg
HNC or equivalent level in scientific discipline)
Understanding of laboratory analysis
Experience of working in a laboratory environment
Keen attention to detail
Strong quality and continuous improvement mind-set
Strong communication skills

Job Responsibility

To test routine production and stability samples supplied from the site Value Streams and meet testing lead-time targets
Calibrate and maintain analytical equipment
Carry out qualitative and quantitative analysis of antibiotic powders and solid dose forms using a wide range of analytical techniques (eg: HPLC, Karl Fischer, dissolutions etc)
To carry out OOS investigations and discuss the outcome with Team Leader, or relevant production Dept, QA manager or a Qualified Person, as required
To check and verify analytical testing and data generated by other analysts
To adhere to and help maintain the highest levels of safety and GLP within the section and ensure training records are kept up to date
Daily liaison with both other analysts and team leader regarding testing and test results
May be required to take a lead role within a small team of analysts working together on a common analytical technique e.g. HPLC
Supplying data / reports to Value Stream as requested
May be required to communicate with the relevant Value Steam to progress OOS investigations

Scientist I, Quality Control (2nd Shift)

Carex is partnering with a Pharmaceutical industry partner to identify a Scienti...

Location

United States , Madison

Salary:

Not provided

Carex Consulting Group

Expiration Date

Until further notice

Requirements

M.S. in Chemistry or a related scientific field with 7+ years of relevant laboratory experience
or B.S. in Chemistry or a related scientific field with 9+ years of relevant laboratory experience
Extensive knowledge of cGMP requirements, ICH guidelines, and pharmaceutical quality control laboratory operations
Demonstrated experience with analytical method validation, method transfers, and routine testing in a regulated environment
Strong proficiency with analytical instrumentation, data acquisition systems, and laboratory software platforms
Ability to independently execute complex analytical testing and make scientifically sound decisions
Experience reviewing technical data and supporting quality investigations and corrective actions
Strong troubleshooting skills related to instrumentation, analytical methods, and laboratory processes
Excellent written and verbal communication skills
Strong organizational skills and attention to detail

Job Responsibility

Perform analytical method validation, method transfer, and routine testing of pharmaceutical raw materials, in-process samples, finished products, and stability samples
Execute laboratory testing using established analytical methods, procedures, and instrumentation
Collaborate with Analytical Development and Manufacturing teams to support validation activities and project timelines
Operate, calibrate, maintain, and troubleshoot analytical instrumentation with minimal oversight
Demonstrate expertise with analytical technologies including HPLC, GC, LC-MS, Karl Fischer, FTIR, endotoxin plate readers, Raman spectroscopy, and related systems
Analyze and interpret data, including tracking and trending stability results and identifying degradation patterns
Utilize stability tracking software for data entry, review, approval, and record management
Lead technical discussions, scientific problem-solving sessions, and laboratory investigations
Identify, troubleshoot, and resolve analytical method, instrumentation, and sample-related issues
Review analytical data generated by other QC analysts to ensure accuracy and compliance

Fulltime

New

Qc Analyst

Randstad Inhouse, Specialty Pharma, for a multinational company in consumer heal...

Location

Italy , Pomezia

Salary:

28000.00 - 34000.00 EUR / Year

Randstad

Expiration Date

August 14, 2026

Requirements

Bachelor's or Master's degree
Good knowledge of English
Knowledge of HPLC
Knowledge of GC
Knowledge of Ion Chromatography (IC)
Knowledge of UV Spectrophotometry
Knowledge of Atomic Absorption
Knowledge of Robotic Titrator
Knowledge of pH meter
Knowledge of Viscometer

Job Responsibility

Perform analytical and chemical-physical testing on finished products in compliance with GMP standards and internal procedures
Execute stability studies and analytical validation activities on cosmetic products and medical devices
Perform routine and non-routine analyses on finished products and raw materials
Support complaint management activities and related investigations
Conduct investigations on finished products (e.g. deviations, OOS/OOT results)
Ensure proper use, maintenance, and calibration of laboratory equipment
Collaborate with cross-functional teams (QA, Production, Regulatory Affairs)

Quality Control Validation Analyst

Join our team as QC Validation Analyst and start a new adventure in an internati...

Location

Italy , Latina

Salary:

26000.00 - 50000.00 EUR / Year

Amaris Consulting

Expiration Date

Until further notice

Requirements

2-3 years of experience with HPLC analysis using Empower3 software
Knowledge of cGMP and QC laboratory procedures in the pharmaceutical industry
Academic background: Degree in Chemistry, Pharmaceutical Chemistry and Technology or related field
Experience in analytical method validation in a GMP-regulated chemistry laboratory
Fluent Italian and good command of English
You have an ability to work precisely and efficiently in a regulated environment

Job Responsibility

Perform chemical analysis using HPLC with Empower3 software
Execute and document QC testing activities in compliance with GMP guidelines
Design and execute validation protocols for analytical methods (e.g., HPLC, GC, UV-Vis) in compliance with ICH and GMP guidelines
Perform validation experiments to assess accuracy, precision, specificity, linearity, range, detection and quantitation limits, robustness, and system suitability
Prepare and review validation documentation, including protocols, reports, and risk assessments
Support method transfer and verification activities between laboratories or from R&D to QC
Collaborate with cross-functional teams to ensure product quality compliance

What we offer

An international community bringing together 110+ different nationalities
An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
A robust training system with our internal Academy and 250+ available modules
A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)
Strong commitments to CSR, notably through participation in our WeCare Together program

Fulltime

Process Development Principal Scientist

Location

United States , Thousand Oaks

Salary:

148363.00 - 171657.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

PHD degree or (foreign equivalent) in analytical chemistry, chemistry, or related field & 3 years of experience in the job offered or in a process development-related occupation. Position requires 3 years of experience in the following: 1. Mass spectrometry knowledge in mechanism of different ionization techniques, configuration of mass spectrometry platforms by different vendors including Waters, Thermo Fisher, or Agilent, and gas-phase ion chemistry for structural elucidation
2. Sample preparation including liquid-liquid extraction and solid phase microextraction for qualitative and quantitative analysis of both small molecules and large molecules
3. Analytical techniques including FT-IR (Fourier-transform infrared spectroscopy), NMR (nuclear magnetic resonance), and UV (ultraviolet–visible spectroscopy)
4. Chromatography and related separation techniques including RP-HPLC (reversed phase high-performance liquid chromatography) and GC (gas chromatography)
5. High-throughput analysis in processing multidimensional mass spectrometry-based data and implementing statistical analysis and interpreting statistical results
and 6. Software applications including ChemDraw, Xcalibur, or ChemStation and programming language for data processing including Python or Matlab.

Job Responsibility

Lead analytical method development, validation and trouble-shooting for drug substances and drug products and in-process testing for synthetic small molecules and/or synthetic peptide testing and characterization
Define analytical control strategies and implement methodologies for development of late phase clinical programs
Collaborate closely with drug substance and drug product process development colleagues to achieve project objectives
Lead and mentor a group of analysts in supporting process development
Provide career development guidance to the team members
Provide concise summary to cross-functional leadership for endorsement of key decisions
Oversee activities at contract manufacturing and testing sites
Author technical reports and analytical Chemistry, Manufacturing and Controls (CMC) sections in regulatory documents
Address analytical and product quality inquiries from health authorities
Supervises direct reports

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program

Fulltime

Stability Analyst

Synergy is a leading scientific services provider supporting clients across the ...

Location

United Kingdom , Kingston Upon Hull

Salary:

27000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

Degree in a relevant scientific discipline (e.g. Chemistry, Pharmaceutical or Biological Science) or equivalent experience
Hands-on experience with analytical techniques such as HPLC (desirable)
Experience within healthcare, FMCG, or medical device environments is advantageous
Strong attention to detail with a quality-focused mindset
Self-motivated, proactive, and able to manage workload effectively
Excellent communication and interpersonal skills

Job Responsibility

Performing sample and batch analysis using HPLC, GC, and other analytical techniques
Preparing, labelling, and managing samples in line with SOPs
Generating, analysing, and reporting data in compliance with GMP/GLP standards
Monitoring trends and identifying any out-of-specification or unexpected results
Supporting stability study protocols and data interpretation
Contributing to method development, validation, and transfer activities
Participating in lab investigations, CAPA processes, and audit readiness
Ensuring compliance with health & safety, quality systems, and regulatory requirements
Driving continuous improvement initiatives across the laboratory

What we offer

Comprehensive technical and GMP training
Opportunities to gain exposure to method development, validation, and advanced lab processes
A strong focus on continuous improvement and professional development
The chance to work with a globally recognised client in a collaborative environment

Fulltime

Process Development Senior Associate

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , Cambridge

Salary:

85306.00 - 103484.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree or (foreign equivalent) in Chemical Engineering, Bioengineering, Analytical Chemistry, Biochemistry or a related field & completion of a university-level course, research project, internship, thesis, or one year of experience in the following: 1. Analytical chemistry experience for small molecules, and completion of project deliverables including: designing and conducting targeted metabolomics experiments, extracting and analyzing results via dedicated software: ChemStation, MassHunter, or MassAnalyzer
2. Analytical method development (chromatography and mass spectrometry), related technologies and instrumentation including: U/HPLC, GC, or LC-MS
3. Method qualification and transfer for analytical instruments, along with data analysis and statistical evaluation of experimental results
4. Application analytical instrument troubleshooting across different platforms: Waters, Agilent, or Sciex, and problem solving of such technologies
5. Implementing Standard Operating Procedures in a laboratory environment in accordance with GLP standards
and 6. Maintaining a laboratory notebook.

Job Responsibility

Conduct experiments, analyze results, and implement process improvements to enhance efficiency and product quality
Design, develop, and optimize manufacturing processes
Collaborate closely with a team of analysts and scientists
Responsible for the technical aspects of developing analytical tools to gain understanding of quality attributes in product and process for late phase synthetic small molecule, synthetic peptide, and siRNA programs
Utilize platform and in-depth product attribute knowledge to advance Amgen products and ensure success through pivotal clinical phases to marketing authorization application
Develop, optimize, and execute analytical methods for synthetic small molecules, synthetic peptide, and SiRNA release testing and process characterization
Collaborate closely with drug substance process development team to achieve project objectives and provide analytical data to support drug substance product development.

What we offer

stock
retirement
medical
life and disability insurance
eligibility for an annual bonus
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program

Fulltime

Qc Validation Specialist

We are looking for an experienced QC Validation Specialist to join a leading-edg...

Location

Singapore , Singapore

Salary:

9000.00 - 9500.00 SGD / Month

Randstad

Expiration Date

July 19, 2026

Requirements

Minimum of a Diploma or Bachelor's Degree in any Engineering field, Science, or a related technical discipline
Minimum of 5 years of hands-on experience in the qualification, requalification, relocation, or decommissioning of GMP laboratory equipment within the pharmaceutical or biopharmaceutical industry
Demonstrated, deep familiarity with analytical and laboratory instrumentation (e.g., Chromatography systems, spectrometers, counters, and controlled temperature units)
Robust understanding of GMP regulations, data integrity principles, and data lifecycle management

Job Responsibility

Execute end-to-end qualification (IQ/OQ/PQ), requalification, relocation, and decommissioning/retirement protocols for a wide range of QC laboratory analytical and micro equipment
Lead validation activities for systems including, but not limited to: HPLC, CE, UV-Vis Spectrometers, TOC Analyzers, Microplate Readers, Liquid Particle Counters, Analytical Balances, Incubators, and Particle Counters
Author, review, and execute validation master plans, protocols, deviations, and final summary reports in strict accordance with Good Manufacturing Practices (GMP)
Collaborate closely with QC Lab Analysts, Quality Assurance, and external vendors to minimize lab downtime during relocation and equipment retirement
Ensure instrument software, audit trails, and historical data are securely backed up and compliant with data integrity standards prior to equipment decommissioning

What we offer

SGD 250 Monthly Transport Allowance

Fulltime

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HPLC Analyst

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