Senior QC Laboratory Analyst Job at Pfizer

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 Ii

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...

Location

United States , Orangeburg

Salary:

24.00 - 29.00 USD / Hour

werfen

Expiration Date

Until further notice

Requirements

B.S./B.A. Degree in Science or Medical Technology or equivalent required
2 years clinical laboratory experience with a basic knowledge of quality control principles

Job Responsibility

Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product
Interprets test results against specifications and decides if assays pass or fail
Maintains documentation of all work performed in accordance with GMP requirements
Evaluates product complaints upon Team Leader or Team Champion's request
Performs product stability, proficiency, environmental testing and water system testing
Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of Lab equipment
Updates departmental SOP's and QC Monographs as directed by Team Leader or Senior QC Analyst
Performs microbial testing per SOP's and QC Monographs
Orders required laboratory supplies, reagents and other consumables
Monitors proper storage conditions and expiration dates

Fulltime

QC Analyst II

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...

Location

United States , Orangeburg

Salary:

24.00 - 29.00 USD / Hour

werfen

Expiration Date

Until further notice

Requirements

B.S./B.A. Degree in Science or Medical Technology or equivalent required
2 years clinical laboratory experience with a basic knowledge of quality control principles
Ability to lift and move materials per current OSHA standards

Job Responsibility

Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product
Interprets test results against specifications and decides if assays pass or fail
Maintains documentation of all work performed in accordance with GMP requirements
Evaluates product complaints upon Team Leader or Team Champion's request
Performs product stability, proficiency, environmental testing and water system testing
Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of Lab equipment
Updates departmental SOP's and QC Monographs as directed by Team Leader or Senior QC Analyst
Performs microbial testing per SOP's and QC Monographs
Orders required laboratory supplies, reagents and other consumables
Monitors proper storage conditions and expiration dates

Fulltime

QC Analyst II

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...

Location

United States , Orangeburg

Salary:

24.00 - 29.00 USD / Hour

werfen

Expiration Date

Until further notice

Requirements

B.S./B.A. Degree in Science or Medical Technology or equivalent required
2 years clinical laboratory experience with a basic knowledge of quality control principles
ability to lift and move materials per current OSHA standards

Job Responsibility

Performs automated and manual assays as detailed in departmental/plant SOPs and QC Monographs including raw material, in-process and finished product
Interprets test results against specifications and decides if assays pass or fail
Maintains documentation of all work performed in accordance with GMP requirements
Evaluates product complaints upon Team Leader or Team Champion's request
Performs product stability, proficiency, environmental testing and water system testing
Responsible for routine preventive maintenance, general trouble shooting, general cleanliness and calibration of Lab equipment
Updates departmental SOP's and QC Monographs as directed by Team Leader or Senior QC Analyst
Performs microbial testing per SOP's and QC Monographs
Orders required laboratory supplies, reagents and other consumables
Monitors proper storage conditions and expiration dates

Fulltime

Senior Analyst, QC Chemistry

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United Kingdom , Thetford

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Science based degree (preferably in Chemistry, BioChemistry Biology OR Microbiology)
Experience working in a laboratory essential
Demonstrates strong leadership skills
Excellent understanding of Microsoft Office Packages
Previous experience in a GMP environment/ pharmaceutical QC laboratory

Job Responsibility

Manage and develop direct reports through performance reviews (ACE Check-In) and identify training or development needs
Conduct testing, stability studies, reporting, and checking/reviewing of results in accordance with relevant local and global procedures, testing methods, protocols, and/or pharmacopeial requirements
Ensure direct reports meet safety, quality, and performance standards, and escalate any issues to the QC Manager
Initiate, conduct, and manage quality records, such as deviations, CAPAs, effectiveness checks, and laboratory investigations
Initiate and coordinate document updates, change controls, and successfully manage timelines for implementation of changes
Perform the batch release activities
Participate in internal, customer, and regulatory audits
complete any assigned action items in a timely manner
Perform if required and coordinate general laboratory support activities including housekeeping, equipment maintenance, and inventory of supplies and reagents/ standards
Perform and coordinate calibration checks in accordance with written procedures

What we offer

25 days annual leave + bank holidays
Employee discount scheme
Blue light card
Progression opportunities
Subsided canteen
Westfield healthcare
Up to 8% pension contribution
Employee assistance programme
Support for Parents
Continuing Education/ Professional Development

Fulltime

Senior Analyst, QC Chemistry

This is where you make a difference in our patients’ safety. As a member of the ...

Location

United Kingdom , Thetford

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Science based degree (preferably in Chemistry, BioChemistry Biology OR Microbiology)
Experience working in a laboratory essential
Demonstrates strong leadership skills
Able to work as part of a team as well as independently
Excellent understanding of Microsoft Office Packages
Is dedicated to meeting the expectations and requirements of internal and external customers
Strong work ethic
Excellent communication skills
Previous experience in a GMP environment/ pharmaceutical QC laboratory

Job Responsibility

Manage and develop direct reports through performance reviews (ACE Check-In) and identify training or development needs
Conduct testing, stability studies, reporting, and checking/reviewing of results in accordance with relevant local and global procedures, testing methods, protocols, and/or pharmacopeial requirements
Ensure direct reports meet safety, quality, and performance standards, and escalate any issues to the QC Manager
Initiate, conduct, and manage quality records, such as deviations, CAPAs, effectiveness checks, and laboratory investigations
Initiate and coordinate document updates, change controls, and successfully manage timelines for implementation of changes
Perform the batch release activities
Participate in internal, customer, and regulatory audits
complete any assigned action items in a timely manner
Perform if required and coordinate general laboratory support activities including housekeeping, equipment maintenance, and inventory of supplies and reagents/ standards
Perform and coordinate calibration checks in accordance with written procedures

What we offer

25 days annual leave + bank holidays
Employee discount scheme
Blue light card
Progression opportunities
Subsided canteen
Westfield healthcare
Up to 8% pension contribution
Employee assistance programme
Support for Parents
Continuing Education/ Professional Development

Fulltime

Senior Scientist I, Quality Control

This position is within the Quality Control structure, under the Quality Organiz...

Location

United States , Verona

Salary:

90000.00 - 108000.00 USD / Year

Arrowhead Pharmaceuticals, Inc

Expiration Date

Until further notice

Requirements

M.S. in Chemistry (or related field) with 7+ years relevant laboratory experience
B.S. in Chemistry (or related field) with 9+ years of relevant laboratory experience
Fully knowledgeable of cGMP and ICH laboratory requirements and operations
Proficient and demonstrated experience with analytical instrumentation, test methodology/validations/transfers, data acquisition systems, and typical cGMP policies/practices

Job Responsibility

Fully knowledgeable of cGMP requirements and ICH guidelines
Works independently to meet project timelines and deliverables with minimal supervision to no supervision
Collaborates routinely with Analytical Development on procedural method transfers and may participate in the execution of method validation protocols
Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and stability samples using established test methods and procedures
Proficient with various analytical instrumentation theory and practice
Executes training requirements for assigned SOPs and participates in department specific training modules
Independently completes complex instrumentation for testing according to written test methods and procedural documents to analyze samples
Demonstrates proficiency with a variety of instrumentation (e.g., HPLC, GC, LC-MS, KF, FTIR, Endotoxin plate readers, and/or Raman spectroscopy) and will assist in training on instrumentation
Is a subject matter expert in technical aspects of both instrumentation and workflow management and prioritization
Performs analyses in a timely and efficient manner to support ongoing prioritized studies

What we offer

competitive salaries and an excellent benefit package

Fulltime

New

Teaching assistant (sen ta)

A life changing and inspiring specialist setting local to you is looking for a 1...

Location

United Kingdom , Hassocks, West Sussex

Salary:

19342.00 - 24089.00 GBP / Year

Randstad

Expiration Date

April 14, 2026

Requirements

Any experience level will be considered, ideal candidates will be flexible, resilient and have a positive approach to supporting learners with SEN (direct SEN experience is not essential)
Relevant experience/Knowledge of working with children or young people
Maths and English GCSE or equivalent
Eligibility to work in the UK

Job Responsibility

Supporting KS1- KS5 SEN learners on a 1:1, small group and classroom basis
Communicating with parents and carers over pupils' progress and participating in departmental meetings, parents' evenings and whole school training events

What we offer

Excellent rates of pay/ 6 month pay reviews
Fully funded training and qualifications
Access to onsite facilities/ free hot meals and games room
Staff rewards - staff team building days
There is lots of room for progression in the roles, from senior teaching assistant to skill development and other areas to branch into (therapies, inclusion support etc.)

!

Senior QC Laboratory Analyst

Pfizer

Location:
Singapore

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

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Location:Singapore

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Contract Type:Not provided

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Job Description:

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Requirements:

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Additional Information:

Job Posted:February 20, 2026

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