HPLC Analyst Job at Pfizer (Zagreb)

QC Analyst

Are you a QC Analyst/Analytical Chemist based in Central Belt of Scotland lookin...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

Degree or equivalent in a relevant scientific discipline
Experience in QC Analytical techniques such as UV, HPLC, FTIR
Previous effective experience in a similar environment is essential
Prior experience working in a regulated GxP environment

Job Responsibility

Use a range of analytical chemistry techniques- predominantly HPLC
Ensuring all analysis and documentation are conducted and recorded in compliance with GMP standards
Working to set protocols within a busy environment
Preparation and update of SOPs, instructions and protocols and other Quality Control documentation
Checking and reviewing of data in compliance with Data Integrity requirements
Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner
Perform stability study programme activities, storage of in process, and final products samples and retention sample management
Supporting the team leader where required

What we offer

bonus scheme
healthcare
flexi-time
shift bonus

Fulltime

Sr. Quality Control Analyst

Sr. Quality Control Analyst (East Windsor, NJ) (Multiple Openings) Conduct resea...

Location

United States , East Windsor

Salary:

Not provided

Novitium Pharma

Expiration Date

Until further notice

Requirements

Must have masters in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related
In lieu of Masters, we will accept bachelors in Pharmaceutical Sciences / Biology / Chemistry / Microbiology / Chemical / Related besides five years of alternative experience

Job Responsibility

Conduct research, analysis, synthesis, and experimentation on substances, for such purposes as product and process development & application, quantitative and qualitative analysis, & improvement of analytical methodologies
conduct testing & analysis of pharmaceutical raw materials like drug substance, excipients & packaging materials to analyze various parameters like assay, dissolution, impurities, related substances, residual solvents using various technical instruments like HPLC, GC, UV spectrometry
Conduct testing & analysis of finished product for different dosage forms like capsules, tablets, powder for oral suspension and solutions

QC Analyst

Are you a QC Analyst/Analytical Chemist based in Central Belt of Scotland lookin...

Location

United Kingdom , Falkirk

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

Degree or equivalent in a relevant scientific discipline
Experience in QC Analytical techniques such as UV, HPLC, FTIR
Previous effective experience in a similar environment is essential
Prior experience working in a regulated GxP environment

Job Responsibility

Use a range of analytical chemistry techniques- predominantly HPLC
Ensuring all analysis and documentation are conducted and recorded in compliance with GMP standards
Working to set protocols within a busy environment
Preparation and update of SOPs, instructions and protocols and other Quality Control documentation
Checking and reviewing of data in compliance with Data Integrity requirements
Assist in investigation of quality incidents and other problem solving forums and complete QMS documentation in a timely manner
Perform stability study programme activities, storage of in process, and final products samples and retention sample management
Supporting the team leader where required

What we offer

bonus scheme
healthcare
flexi-time
additional shift bonus

Fulltime

Senior QC Analyst

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field
Minimum 5–8 years of QC laboratory experience in the pharmaceutical or biopharmaceutical industry
Strong working knowledge of analytical techniques such as HPLC, GC, UV-Vis, FTIR, TOC and dissolution
Proven experience in method validation, instrument troubleshooting, and data integrity compliance
Excellent understanding of cGMP, GLP, and regulatory requirements
Strong attention to detail and analytical thinking
Proficiency in laboratory software including Chromeleon
Strong communication, leadership, and mentoring skills
Ability to work independently and manage multiple priorities under tight timelines

Job Responsibility

Perform qualitative and quantitative chemical and microbiological analyses of raw materials, in-process samples, finished products, and stability samples using validated methods (e.g., HPLC, GC, UV, FTIR, Dissolution)
Review and verify analytical data, ensuring accuracy, completeness, and compliance with cGMP and SOPs
Lead out-of-specification (OOS), out-of-trend (OOT), and deviation investigations, including root cause analysis and CAPA development
Support release testing and timely completion of batch records to ensure uninterrupted product supply
Participate in method validation, method transfer, and equipment qualification activities
Develop and optimise analytical methods as required to support new product development or process changes
Troubleshoot complex analytical and instrumentation issues independently and provide guidance to peers
Ensure all activities comply with cGMP and ICH, and other applicable regulatory guidelines
Prepare, review, and maintain laboratory documentation including test records, logbooks, and SOPs
Support internal and external audits and respond to audit findings

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

QC Analyst

QC Analyst required on a temporary 6-month contract, based in Cheshire. Requirin...

Location

United Kingdom , Cheshire

Salary:

27000.00 - 33000.00 GBP / Year

SRG

Expiration Date

Until further notice

Requirements

Recent Degree in Chemistry (or similar)
Knowledge and/or recent, proven industrial experience of wet chemistry analysis, HPLC and/or GC
Willingness to learn and develop
Work well within a small team with good time management and organisational skills

Job Responsibility

Performing wet chemistry techniques to analyse raw materials and finished products (including titrations, pH testing, density testing and others)
Using analytical instrumentation for analysis including HPLC, GC and IC through following methodology provided
Recording and reporting data within the quality system- completing documents and spreadsheets accurately
Reporting results in a timely fashion under direction and priority
Performing analytical investigations and tests to meet research and customer needs
Having responsibility for maintenance and upkeep of analytical equipment
Approving and rejecting raw materials

What we offer

An opportunity to gain great experience within a highly respected, multi-national company, with significant intellectual property potential and commercial impact
37.5 hours, Mon-Fri, 8:30-4:30 (with flexibility)
Full training can be provided

Fulltime

Qc analytical analyst

The QC Analytical Analyst, under minimal supervision, is responsible for the tim...

Location

United States , Novato

Salary:

31.00 - 50.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

1-2+ years of experience in a cGMP/GLP laboratory
1-2+ years hands-on experience in separation sciences (HPLC, UPLC, CE)
Ability to follow written instructions and to perform tasks with direct or minimal supervision
Strong leadership skills demonstrated through past work history
Proficient in Windows, Microsoft Word, Excel
Good written and verbal communication skills
Attention to detail and strong documentation skills
Ability to contribute effectively in team environments and independently
B.S./B.A. in Science (Major in Chemistry, Biology, Biochemistry)

Job Responsibility

Performs biochemical/physical/chemical analyses of test samples under cGMP to meet specified timelines
Works independently on assays they have mastered
Develops and maintains proficiency in a broad range of test methods
Develops a technical understanding of each assay and assists with trouble shooting and laboratory investigations
Evaluates data against defined criteria/specifications
Actively applies knowledge in non-routine situations using a thorough understanding of the work processes and practices
Identifies key issues in complex situations, analyzes problems, and makes sound decisions
Assists in the revision of written procedures, method/equipment validation, and/or method transfers as assigned
Mentors and trains other analysts, including new hires and more junior analysts, in areas of expertise
Holds self and others accountable for adherence to department and company policies and practices

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Laboratory Analyst- Chemistry

We offer commercial analytical lab chemistry testing for food and drink, includi...

Location

United Kingdom , Chipping Campden, Gloucestershire

Salary:

27000.00 GBP / Year

Campden BRI

Expiration Date

Until further notice

Requirements

Degree in Chemistry
Experience working in a laboratory environment
Experience working with chromatography techniques desirable, particularly LC/MS/MS and HPLC
Ability to undertake routine analysis with minimal supervision
Good organisational skill for managing workload and complex projects
Computer literate
Well-developed communication skills

Job Responsibility

Undertake administration and analysis of samples in the Chromatography Section together with all associated activities
Booking in of samples, preparation of samples and reporting of results to clients
Routine analysis of food stuffs and associated materials using instrumental methods e.g. HPLC and LC/MS/MS
Produce accurate laboratory record, calculate results, collate data for inclusion in scientific reports and produce reports for bespoke and routine analysis
Ensure all aspects of quality are managed according to the Campden BRI standards, including maintaining QC records for UKAS accredited methods
Responding to client enquires relating to testing within the section
Training and supervision of junior staff as required
Basic maintenance and calibration of equipment, including GC/MS/MS, LC/MS/MS and HPLC systems

What we offer

Reward platform with employee discounts and rewards
25 days holiday + 8 bank holidays
Buy and sell holiday scheme
A generous work save pension scheme, with employee contributions matched by the company up to 10%
Culture focus around work/life balance (early finish Fridays)
Subsidised onsite restaurant

Fulltime

New

Lab technician 分析实验员

Location

China , 苏州市

Salary:

96000.00 - 120000.00 CNY / Year

Randstad

Expiration Date

March 21, 2026

Requirements

Bachelor with minimal 2 years related working experience, or Master
Experience in analytical technologies, e.g. HPLC, GC, LCMS, NMR, titration etc.
Capability in written English
Passion of work in lab

Job Responsibility

Performing analytical experiments in lab according to Health Safety & Environment standards and cGMP regulations (if applicable)
Generating exact testing data and documents lab work in appropriate form (GMP/non-GMP)
Supporting responsible analytical expert and analyst by developing and validating method, testing according to analytical procedure, etc.
Reporting abnormal experiment results and HSE incidents/observations timely and effectively
Supporting lab investigations
Taking instrument/equipment responsibilities of e.g. operation, maintenance, calibration and qualification

Fulltime

HPLC Analyst

Pfizer

Location:
Croatia , Zagreb

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

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