Qc Officer - Analytical Chemistry Job at SRG (Stirling)

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 Specialist Ii, Analytical Investigations

Life changing therapies. Global impact. Bridge to thousands of biopharma compani...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or related field
2–5 years of QC Analytical Chemistry experience (pharma experience preferred)
Hands-on experience with UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer, and Osmometer
Solid understanding of cGMP, ICH, USP, and global compendia guidelines, especially in analytical method validation and stability studies
Strong organizational and documentation skills, technical writing ability, and excellent communication skills (written and verbal)
Ability to thrive in a fast-paced, dynamic environment, juggling multiple priorities while maintaining a sharp eye for detail
Proficiency in MS Office
experience with lab-based data management systems a plus

Job Responsibility

Lead investigations into QC Analytical deviations, OOS/OOT/OOE results, and other quality issues
Serve as a key point of contact during audits and inspections, ensuring timely and compliant responses
Draft and revise change controls, technical reports, cGMP documents, and protocols
Perform QC analytical testing, review data, and identify trends to proactively address risks
Assist in managing analytical equipment to maintain compliance and efficiency
Collaborate cross-functionally to close out quality events and audit findings on time
Help shape and refine QC processes that support continuous improvement

What we offer

Be part of a collaborative team where your expertise directly impacts patient safety and product quality
Gain exposure to diverse analytical techniques and regulatory processes
Opportunity to work in a GMP environment supporting both clinical and commercial product lifecycles
Professional growth through hands-on problem solving, cross-functional collaboration, and continuous learning

Fulltime

Qc Team Leader

As QC Team Leader you will play an important role within your team, developing y...

Location

United Kingdom , Dundee

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Bachelor's degree in Science (Chemistry
Pharmacy
Biology) or equivalent experience
Proven track record of leading and developing a team of QC analysts
Strong knowledge of GMP and Global Pharmaceutical Regulations
Expertise in chemistry, laboratory techniques, and chromatography systems/software
Proficiency in analytical method development, transfer, and technical documentation (e.g., SOPs, reports)
Excellent communication, conflict resolution, and resource management skills
Strong Microsoft Office skills, particularly in Excel
A collaborative, solution-oriented mindset with a focus on continuous improvement

Job Responsibility

Champion Health and Safety by adhering to policies, reporting incidents, identifying risks, and promoting a strong safety culture
Support the Head of QC in cultivating a culture of quality, compliance, and continuous improvement (GMP, GLP, Data Integrity, Housekeeping)
Provide leadership and technical guidance to analysts, including training, coaching, development, mentorship, and ongoing performance management
Oversees the QC analysts' day-to-day operations
Ensure timely review and approval of QC testing across raw materials, in-process, finished products, stability, and validation samples
Oversee the closure of CAPAs, incidents, change controls, audits, SOPs, and method updates
Manage laboratory systems and processes to maintain efficiency and regulatory compliance
Participate in client and project meetings, ensuring seamless process management and timely invoicing
Maintain accurate planning and scheduling, including 12-week visibility and timely completion of PQRs
Ensure effective stability sample management and documentation

Fulltime

Medical Laboratory Scientist Group Lead

Medical Laboratory Scientist Group Lead - Mount Kisco, NY, Monday to Friday, 8:0...

Location

United States , Mount Kisco

Salary:

35.59 - 58.75 USD / Hour

Quest Diagnostics

Expiration Date

Until further notice

Requirements

Three (3) to five (5) years of clinical experience as a Medical Technologist within the designated discipline
Foreign educated candidates must provide a detailed credential evaluation from IERF (International Education Research Foundation)
United States educated candidates must provide a detailed original transcript
Bachelor's Degree Medical Technology, Chemistry or Biology or Previously qualified as a Technologist under 42 CFR 493. 1433 published in March 14, 1990
Comprehensive theoretical and operational job knowledge in designated specialty required
Knowledge of organizational/departmental policies and procedures
Proven leadership and problem-solving skills
Must be detail-oriented, have the ability to work independently, establish work priorities for self and others and to handle several tasks simultaneously for maximum department efficiency
Ability to schedule and manage resources to meet department goals
Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients

Job Responsibility

Demonstrate proficiency in all duties of a Medical Technologist I and II
Perform and report on assigned analytical tests in accordance with applicable Standard Operating Procedures (SOP) ensuring that applicable quality control requirements are met
Actively support and comply with laboratory policies and procedures for specimen handling and processing, test analysis, reporting and maintaining records of patient test results
Adhere to analytical schedules to maintain turnaround time of results including STATS or critical results to clients
Perform, review and document QC analysis to ensure accuracy of clinical data and proper instrument function
Make quality control decisions regarding the disposition of an assay or test
Review requests for validity checks and recommend an appropriate course of action taking into account the limitations of specimen requirements and the effects of time and the quality of additional and/or repeat testing
Serve as a technical resource for the department by investigating and resolving analytical testing problems, recommending a course of action in instances identified as beyond acceptable limits, and responding to non-routine/complex inquiries and/or requests from clients and sales representatives
Assist Lab Supervisor by monitoring workflow to meet testing schedules
distributing and reviewing work assignments

What we offer

Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
Best-in-class well-being programs
Annual, no-cost health assessment program Blueprint for Wellness
healthyMINDS mental health program
Vacation and Health/Flex Time
6 Holidays plus 1 'MyDay' off
FinFit financial coaching and services
401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
Employee stock purchase plan
Life and disability insurance, plus buy-up option

Fulltime

Quality Control Analyst

We are supporting a growing and forward-thinking API manufacturer within the med...

Location

United Kingdom , Sandwich, Kent

Salary:

28000.00 - 30000.00 GBP / Year

Cranleigh STEM

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensic Science, or related discipline (or equivalent experience)
Proven industrial or commercial laboratory experience using HPLC (assay and impurity analysis)
Experience in QC testing of APIs
Strong understanding of GMP environments
Good working knowledge of Microsoft Office (Word, Excel)
Excellent attention to detail and data accuracy
Ability to prioritise workload and adapt to changing priorities
Effective written and verbal communication skills
Right to work in the UK

Job Responsibility

Perform analytical and physical testing of Active Pharmaceutical Ingredients (API)
Conduct HPLC analysis (assay and impurities) within an industrial/commercial laboratory environment
Support production schedules through timely and accurate testing
Work collaboratively with Production and Quality Assurance teams to ensure GMP compliance
Accurately record, analyse, and report results in line with regulatory requirements
Contribute to maintaining controlled manufacturing processes aligned with international regulatory standards

Fulltime

Senior QC Laboratory Analyst

The Senior QC Laboratory Analyst is to support the operation of Reference Standa...

Location

Singapore

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

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

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.

Fulltime

QC Technician

The employee in this position will be responsible for the analysis of a wide ran...

Location

United States , Yazoo City

Salary:

Not provided

CF Industries

Expiration Date

Until further notice

Requirements

Bachelor’s degree in chemistry from an A.C.S. accredited chemistry program is preferred
Bachelor’s Degree in other physical science disciplines will be considered if strong evidence of laboratory analytical chemistry skill is demonstrated
Minimum of 1 year of Analytical Chemistry laboratory experience preferred
Experience with ICP, UV-VIS, GC, IC, and FT-IR, is valuable
Excellent written and verbal communication skills required
Presentation skills sufficient to communicate thoughts succinctly to Lab Supervisor and Operations managers
Proficient with Microsoft Office tools including Outlook, Word, Excel and PowerPoint
Excellent time management skills and be comfortable working in an environment where priorities change rapidly
Applicants considered for this position will be required to perform analytical skills or techniques to demonstrate proficiency (Examples: Spectroscopy, Chromatography, Qualitative Analysis etc.)

Job Responsibility

Receive and log samples into LIMS system
Perform Analytical Chemistry testing as required
Prepare Reports of Analytical Chemistry Results
Check, Calibrate, and Maintain Laboratory Equipment
Responsible for the analysis of a wide range of samples submitted by the Yazoo City Complex to ensure they meet quality specifications
Perform routine analysis on environmental samples, quality control and calibration of laboratory instrumentation, and data entry
Work closely with one or more quality control technicians
Certain samples will need to be collected by the lab

Fulltime

Operations Specialist II

The Operations Specialist II is a multi-functional role, responsible for invento...

Location

United States , San Diego

Salary:

28.00 - 30.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Bachelor degree in Chemistry/Biology
Prior experience in a chemistry laboratory (2+ years)
Prior experience with manual and automated pipetting
Ability to follow standard operating procedures
Experience with manual (pipette) and automated filling/dispensing
Prior experience in a chemistry lab
Proficiency in MS Office Skills (Word, Excel, and PowerPoint)
Must possess strong organizational skills, attention to detail, and the ability to adapt to changing priorities
Be a self-starter, quick learner with the ability to work independently and efficiently
Strong interpersonal communication skills, effective written and oral communications skills

Job Responsibility

Ensures security and accuracy of inventory of materials and finished goods through transaction documentation and by conducting physical cycle counts and reconciliation of any discrepancies
Manage physical inventory within a Glovebox for raw materials, intermediate products, finished goods, analytical samples, and QA Retains
Perform small scale chemical reactions (dye labeling) for Quality Control testing
Fulfill internal requests for samples from inventory and perform sample preparation for quality testing
Perform Aliquoting/Vialing of air and water sensitive finished goods using manual and automated processes and equipment
Perform lyophilization of finished good products
Perform Weight Checks and Packaging of air and water sensitive finished goods within a Glovebox
Prepare packaged products for QA inspection and shipments, including all required documentation
Coordinate with QC department to ensure timely testing and release of production materials
Accurately complete required documentation (batch records, data entry, etc.) on time

Fulltime

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Qc Officer - Analytical Chemistry

Job Description

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