QC Analyst Job at SRG (Falkirk)

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

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

New

Qc Analyst Ii, Microbiology

We are looking for an enthusiastic Microbiology Analyst to support the cGMP Qual...

Location

Canada , Vancouver

Salary:

78200.00 - 92000.00 CAD / Year

AbCellera Biologics

Expiration Date

Until further notice

Requirements

5+ years of QC experience in addition to a Bachelor’s degree
Master’s degree in a relevant scientific discipline and 3+ years of QC experience
Strong knowledge and experience in Good Manufacturing Practices (GMPs), QC microbiological testing and method qualification requirements
Experience with using Milliflex Oasis, Charles River Endosafe nexgen-MCS, LIMS, as well as basic benchtop techniques such as Gram staining, plate reading, vacuum filtration and LAL gel-clot
Excellent interpersonal skills, ability to work independently and in a team environment, detail oriented, organized and methodical in execution of tasks
Ability to problem solve with sound analytical thinking

Job Responsibility

Providing microbial support for aseptic product manufacturing in a cGMP regulated environment
Performing site support activities such as environmental monitoring, compressed gas and water system sampling within the graded manufacturing area
Planning, scheduling, and coordinating microbiological sampling and testing activities to support manufacturing operations, including routine monitoring, batch-related testing, and time-critical samples, ensuring alignment with production schedules and testing timelines
Carrying out a variety of routine microbiological techniques on utilities including but not limited to bioburden, endotoxin, TOC, conductivity and growth promotion testing on incoming microbial media
Responsible for micro release testing on raw materials, in-process drug substance and final product samples
Evaluating and reviewing test results for conformance to appropriate specifications and highlighting any suspect results to the QC Lab Manager
Participating in identification, investigation (deviations/out of specifications) and resolution of problems in the microbiology lab
Authoring method verification protocols, SOPs, WIs and TMs based on industry standard compendial methods

What we offer

Equity
Annual bonus dependent on team and company performance
6% (non-match) RRSP contribution
CAD $1,500 annual Active Lifestyle Allowance
Annual vacation
Professional development opportunities
Comprehensive health benefits
Scientific and technical mentorship
Teams and social groups to build community and connections

Fulltime

New

Qc analyst - 4 cycle shift

BioMarin is a global biotechnology company that relentlessly pursues bold scienc...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

2-4 years of experience working in a GMP environment
BS/BA in Life Sciences or equivalent experience
Some experience in quality control practices, current Good Manufacturing Practices or Good Laboratory Practices
Understanding of GxP guidelines
Must have excellent record keeping, written and verbal skills
Ability to perform most tasks with minimal supervision
Computer literacy is required
Experience with Microsoft Excel and Word is required

Job Responsibility

Coordinate the calibration, maintenance and repair of analytical laboratory instruments and support equipment using the BioMarin’s Enterprise Computerized Maintenance Management System (CMMS)
Responsible for the completion of QC equipment related documentations
Perform change request using the BioMarin’s Enterprise Quality Management System (Trackwise)
Maintain vendor service contracts using BioMarin’s SpringCM system
Maintain good working relationships with vendors to ensure vendor meets BioMarin’s current and future needs
Work with vendors to troubleshoot equipment
Maintain the laboratory equipment inventory for tracking equipment assets and vendor contacts
Maintain the electronic and paper inventory for equipment qualification packages
Perform equipment inventory reconciliation with physical assets in each laboratory
assessing the current and future suitability

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

Sr. Credit Analyst

Robert Half Finance & Accounting has partnered with a highly successful financia...

Location

United States , Tiffin

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Bachelor’s in business, finance, accounting, ideally (open to Associates with requisite experience)
5+ years’ experience analyzing commercial, consumer, ag & mortgage loans
Strong analytical, communication, and problem-solving skills
Experience leading more junior level credit analysts

Job Responsibility

Take the lead on analyzing new and complex commercial loan requests
Identifying and managing credit risk
Ensuring all credits align with bank policy and regulatory guidelines
Partner closely with loan officers
Structure sound credit solutions
Present findings to leadership
Deep financial analysis
Independent industry research
Managing loan presentations
Overseeing the commercial appraisal and secondary market QC programs

What we offer

strong benefits
bonus potential
ESOP
medical, vision, dental, and life and disability insurance
401(k) plan

Fulltime

Supervisor, QC Analytical

The QC Analytical Supervisor will have responsibility for supporting all activit...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

5+ years relevant Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
Experience working in a cGMP laboratory required
Experience working in a CMO (contact manufacturing/development organization) preferred
Prior leadership experience is preferred
Bachelor of Science in a scientific area of study
Master of Science in a scientific area of study and 3+ years Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company
Ability to prioritize tasks for staff
Ability to make informed decisions
Detail oriented
Strong oral and written communication skills

Job Responsibility

Prioritize and distribute work to the analysts working in the QC Analytical laboratory
Conduct OOS and customer complaint investigations
Complete peer review of work executed within the analytical laboratory
Train new Employees
Routine Analytical testing of samples supporting incoming raw materials, in-process production and finished product testing
Performs analytical testing using HPLC, Karl Fischer, Particle Size Analyzer, UV Vis, Densitometer, Osmometer and other instrumentation as required
Perform instrument calibrations and preventative maintenance as needed
Documents laboratory work using laboratory worksheets/notebooks. Documentation must be detailed and meet CGMP requirements
Write, review and revise SOPs as required
Other duties as assigned or required

Fulltime

QC Analyst

SRG

Location:
United Kingdom , Falkirk

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 19, 2026

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Job Description:

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Requirements:

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