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

Qa senior analyst

We are currently looking for a QA Senior Analyst for a leading player in the Foo...

Location

Malaysia , Selangor

Salary:

4000.00 - 9000.00 MYR / Year

Randstad

Expiration Date

February 26, 2026

Requirements

Bachelor’s degree in Food Science, Food Technology, Food Engineering, or a related field
3–5 years of progressive experience in QC/QA within food manufacturing, covering laboratory testing, in-process control, and finished product release
Strong knowledge of GLP, GMP, HACCP, FSSC 22000, and ISO standards, with experience in analytical method standardization, calibration, and test validation

Job Responsibility

Lead all QC testing activities across Incoming, In-Process, Finished Goods, and Sensory laboratories, ensuring accuracy and reliability of results
Ensure strict adherence to GLP, calibration schedules, standardized analytical methods, and reporting practices in compliance with company and regulatory standards
Serve as subject matter expert (SME) for analytical methods, supporting product release decisions with integrity and evidence-based evaluations
Oversee timely inspection and testing of raw materials, packaging, in-process checks, finished products, and sensory evaluations, providing informed disposition recommendations (release/on-hold/rejection) based on results and risk assessments
Collaborate with cross-functional teams to support NPD, shelf-life studies, and special batch trials through robust analytical evaluations
Manage supplier quality, including review and validation of COAs, investigation and closure of supplier non-conformances, and providing trend analyses to support risk mitigation
Drive operational discipline in in-process quality control through coaching, proactive engagement with production teams, and continuous process improvement
Maintain compliant laboratory documentation, SOPs, and test records per FSSC 22000, ISO, HACCP, and GMP standards, track KPIs, monitor non-conformances, and ensure perpetual audit readiness

!

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

QC Stability Coordinator

The stability and sample coordinator reports directly to the QC Manager and is r...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

February 20, 2026

Requirements

Bachelor of Sciences degree, or higher, in a technical discipline (physical, engineering, IT, chemical or biological sciences) is required
Minimum 3-5 years relevant industry experience
Good project management skills
Experience in presenting to senior management
Lead from front attitude
Knowledge of regulatory guidelines and directives
Data orientated with good risk management understanding

Job Responsibility

Contribute to selection of intermediate and product lots produced at BioMarin for stability studies
Coordinate and contribute to the scheduling of stability testing in QC
Trend stability data and report on same
Prepare stability related protocols, summaries, and reports - often for direct submission to pharmaceutical regulatory agencies
Coordinate movement and storage of samples for testing within QC, within Biomarin and to and from contract laboratories
Manage the retention and reserve sample program
Act as technical resource (SME) and train other analysts in areas of expertise
Review and approve documents such as standard operating procedures, protocols, reports and track-wise documents
Develop and demonstrate an active approach to safety, industrial hygiene, environmental and regulatory compliance
Interact indirectly with regulatory agency inspectors during audits

New

Social Care Worker

TTM Healthcare Solutions (TTM) is recruiting dedicated Social Care Workers for t...

Location

Ireland , Delvin, Westmeath

Salary:

17.41 - 25.24 EUR / Hour

TTM Healthcare

Expiration Date

Until further notice

Requirements

Minimum of a level 7 or 8 degree in Social Care
Previous Social Care experience
Resident in Ireland and hold one of the following: EU passport or GNIB card with Stamp 1G, Stamp 2, Stamp 4, Stamp 4D, Stamp 5, or 4 EUFam
Willing to undergo Garda Vetting
International Police Clearance (if lived outside of Ireland for more than 6 months after the age of 16)

Job Responsibility

24 hour cover required
sleepover shift patterns
1:1 home support required within intellectual disabilities, challenging behavior, and dementia

What we offer

Competitive pay rates ( €17.41 to €25.24 )
Weekly payroll
Access rewarding opportunities in top services
Extended booking in a single service
Dedicated support from an experienced consultant
Exclusive discounts with TTM Perks at Work
Confidential wellbeing support programme
Refer a Friend bonus

Fulltime

New

Driver

The Driver II has a valid Driver License and may drive a bus, shuttle van, or st...

Location

United States , Oakland

Salary:

23.00 USD / Hour

Aramark

Expiration Date

Until further notice

Requirements

Must be age 21 years or older
1 year + professional driving experience and vehicle mechanical experience is preferred as well as customer service experience
Must be able to communicate effectively in written and spoken English
Must have a valid Driver License with a clean driving record showing 5 years of prior safe driving
Must pass a DOT physical examination and obtain a medical card
Must pass a pre-employment drug/alcohol test and participate in the random drug/alcohol testing pool
Must complete and pass Defensive Driving Course prior to driving a company vehicle
Experience driving in all weather conditions including winter weather and tire chain installation

Job Responsibility

Must complete a daily vehicle inspection form prior to driving and after finishing their route
Ensure a pleasant and clean atmosphere is always maintained in and out of the vehicle
Apply all safety equipment available, always wear seat belt when driving
Operate company vehicle weighing under 26,000 lb (GVW) transporting passengers or transporting supplies and equipment to and from designated locations
Drivers are required to drive defensively, safely, and cautiously in all situations
Exceptional customer service skills are needed when encountering guests
Picking up and dropping off guests at designated locations
Drivers transporting passengers should be highly knowledgeable about the property and the surrounding areas, acting as a concierge resource for all guests
May have to lift guest luggage weighing up to 80 lb into the vehicle
Fuel, clean, and inspect vehicle when required

What we offer

medical
dental
vision
work/life resources
retirement savings plans like 401(k)
paid days off such as parental leave and disability coverage

Fulltime

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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