CrawlJobs Logo

Senior QC Laboratory Analyst

pfizer.de Logo

Pfizer

Location Icon

Location:
Singapore

Category Icon
Category:
Quality Control

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided
Save Job
Save Icon
Apply Position

Job Description:

The Senior QC Laboratory Analyst is to support the operation of Reference Standards Program. The incumbent is accountable for: Meeting Key Performance Indices for Reference Standard program; Completing certification/recertification of reference standards in a timely manner; Complying to safety and cGMP policies, procedures and guidelines.

Job Responsibility:

  • Conduct analytical testing
  • Conduct equipment training
  • Troubleshoot and rectify technical issues pertaining to equipment and tests
  • Calibrate/maintain equipment assigned
  • Maintain good house-keeping and safe working environment
  • Maintain/manage general lab inventories (e.g. reference standards, chemicals or consumables)
  • Detect and report deviations, questionable/out of specification results and safety concerns
  • Participate in laboratory/safety investigations
  • Participate/lead in equipment qualification
  • Write/revise procedures, user guide, etc.
  • Guide junior analyst
  • Participate in assigned committees (e.g. safety committee, team building committee, etc.)
  • Participate/lead improvement projects
  • Participate in internal/external audits
  • Perform peer review for laboratory tasks
  • Any other tasks as assigned by supervisor based on business needs

Requirements:

  • Diploma/Degree in Chemistry, Pharmacy or related fields
  • Minimum 1 year relevant laboratory working experience
  • Familiar with cGMP and ALCOA
  • Knowledge in Microsoft office (such as Excel, Word, Teams)
  • Adaptable to dynamic work environment
  • Independent & self-motivated/driven
  • Good communications skills
  • Effective team player

Nice to have:

  • Experience in similar field will be an added advantage
  • Knowledge in analytical instrument and Empower 3 will be an added advantage

Additional Information:

Job Posted:
February 20, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
Pfizer - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon
PREMIUM
More languages and countries
+ Unlock 31694 hidden job offers
Languages
English Čeština Deutsch Ελληνικά Español Français +15
Countries
United States United Kingdom India Canada Australia +
See plans
Plans from $2.99 / month

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Senior QC Laboratory Analyst

Senior QC Analyst

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...
Location
Location
Salary
Salary:
Not provided
jobs.360resourcing.co.uk Logo
360 Resourcing Solutions
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
What we offer
  • Active Social and charity committee
  • Cycle to Work Scheme
  • Electric Vehicle Scheme
  • Eye Care Vouchers
Read More
Arrow Right

Qc Analyst Ii

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...
Location
Location
United States , Orangeburg
Salary
Salary:
24.00 - 29.00 USD / Hour
werfen.com Logo
werfen
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
Read More
Arrow Right

QC Analyst II

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...
Location
Location
United States , Orangeburg
Salary
Salary:
24.00 - 29.00 USD / Hour
werfen.com Logo
werfen
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
Read More
Arrow Right

QC Analyst II

Performs analyses of Clinical Chemistry, Critical Care, Coagulation and/or Micro...
Location
Location
United States , Orangeburg
Salary
Salary:
24.00 - 29.00 USD / Hour
werfen.com Logo
werfen
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
Read More
Arrow Right

Senior Analyst, QC Chemistry

This is where you make a difference in our patients’ safety. As a member of the ...
Location
Location
United Kingdom , Thetford
Salary
Salary:
Not provided
https://www.baxter.com/ Logo
Baxter
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Senior Scientist I, Quality Control

This position is within the Quality Control structure, under the Quality Organiz...
Location
Location
United States , Verona
Salary
Salary:
90000.00 - 108000.00 USD / Year
arrowheadpharma.com Logo
Arrowhead Pharmaceuticals, Inc
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
What we offer
  • competitive salaries and an excellent benefit package
  • Fulltime
Read More
Arrow Right

Software Development Senior Specialist

We are currently seeking a Software Development Senior Specialist to join our te...
Location
Location
India , Noida
Salary
Salary:
Not provided
nttdata.com Logo
NTT DATA
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Strong hands-on experience with LabVantage LIMS (v7.x / v8.x preferred)
  • In-depth knowledge of laboratory operations (QC, stability, sample management, batch release)
  • Experience with LIMS integrations (ERP, instruments, CDS, MES)
  • Fluent or professional-level German (spoken and written) – mandatory
  • Excellent English and German communication and documentation skills
  • Strong presentation skills with the ability to confidently interact with senior client stakeholders
  • Proven experience in client-facing roles or consulting engagements
  • Ability to manage multiple stakeholders and align business and technical teams
  • Strong analytical, problem-solving, and decision-making skills
Job Responsibility
Job Responsibility
  • Act as the primary client-facing Business Analyst for LabVantage LIMS engagements
  • Lead and facilitate requirements workshops, solution discussions, and stakeholder meetings in German and English
  • Build strong relationships with customer stakeholders across QC, QA, IT, and business teams
  • Clearly articulate solution designs, impacts, and benefits to non-technical audiences
  • Gather, analyze, and document business and functional requirements (URS, FRS, user stories)
  • Translate laboratory processes into LabVantage LIMS functional designs and workflows
  • Perform gap analysis and recommend best-practice solutions aligned with LabVantage capabilities
  • Support LIMS configuration including workflows, master data, and role-based access
  • Ensure all solutions comply with GMP, GxP, and data integrity principles
  • Support Computer System Validation (CSV) activities including URS, FS, IQ/OQ/PQ, and traceability matrices
  • Fulltime
Read More
Arrow Right
New

Senior Lecturer/Associate Professor in Literacy

As a Senior Lecturer / Associate Professor in Literacy, you will play a key role...
Location
Location
Australia , Albury-Wodonga, Bathurst, Port Macquarie, Wagga Wagga
Salary
Salary:
Not provided
csu.edu.au Logo
Charles Sturt University
Expiration Date
June 08, 2026
Flip Icon
Requirements
Requirements
  • A doctoral qualification relevant to literacy or education, with a recognised teaching qualification
  • A strong record of high-quality teaching and student-centred learning
  • An established or emerging research profile aligned to literacy, curriculum or pedagogy
  • The ability to build productive partnerships and contribute to academic leadership
Job Responsibility
Job Responsibility
  • Lead impactful literacy teaching and research
  • Teach across online and on-campus environments
  • Shape future teachers and education practice
  • Contribute to curriculum innovation
  • Build strong relationships with students and partners
  • Provide academic leadership in literacy education
  • Contribute to the School's research profile
  • Supervise higher degree research students
  • Actively engage with professional, community and government stakeholders
  • At Associate Professor level: significant academic leadership, research impact, and contribution to the broader discipline at national/international level
What we offer
What we offer
  • 17% superannuation
  • Fulltime
Read More
Arrow Right