Qc Supervisor Job at PPG Industries (Tianjin)

Supervisor, QC Chemistry Lab

The Supervisor, QC Chemistry Lab leads the Chemistry lab to develop, meet, and r...

Location

Canada , Coquitlam

Salary:

75500.00 - 90000.00 CAD / Year

Natural Factors

Expiration Date

Until further notice

Requirements

Completion of a Bachelor of Science degree in Chemistry or related discipline
Experience in GMP analytical lab, with similar responsibility for KPI and personnel management (5+ years)
Analytical instrumentation experience (i.e.: HPLC, ICP) (an asset)
Strong computer skills (including MS Word, Excel, PowerPoint, and SharePoint)
Strong understanding of laboratory information management systems (LIMS)
Six Sigma yellow belt (required)
Six Sigma green belt or higher (an asset)
Strong communication skills (verbal & written) in English, with the ability to communicate effectively with a variety of internal and external stakeholders
Effective leadership skills to influence, support and develop a team of high performers

Job Responsibility

Provide training, particularly in terms of HPLC operations/methods and development and maintenance of a standardized HPLC training regime
Continuous improvement to HPLC efficiency and method accuracy
Support any LIR, NC, CAPA efforts related to HPLC methodologies
Support growth and development of direct reports
Work with other supervisors to enhance lab operations, safety culture, and regulatory compliance
Other duties as assigned

What we offer

Great benefits (healthcare, health & personal spending accounts, wellness days, Employee & Family Assistance Program)
Company provided RRSP
Bonus eligible
$200.00 safety boot voucher & company provided PPE
$300.00 per year to spend on company products
Employee discount pricing
Employee appreciation events & rewards
Free onsite parking
Bus pass reimbursement
Exclusive discounts with various vendors

Fulltime

Pharma QC Supervisor

A manufacturer of specialist pharmaceuticals are currently seeking a QC Supervis...

Location

United Kingdom , Guildford

Salary:

35000.00 - 45000.00 GBP / Year

Network Scientific Recruitment

Expiration Date

Until further notice

Requirements

Prior experience with HPLC and GC in an industrial setting is essential
Ideally within pharmaceutical/aseptic manufacturing
Prior experience with environmental monitoring highly beneficial
Educated to Degree level or equivalent in relevant Analytical Chemistry related discipline is essential
Must be able to work shifts that include nights
Must be able to work occasional Saturday work (overtime)

Job Responsibility

Routine Analysis of pharmaceutical products in line with cGMP and company standards
Utilise a range of analytical techniques and equipment including HPLC, GC, RTLC, LAL and Gamma Spectrometer
Environmental monitoring
Take part in maintenance and calibration of analytical equipment
Take part in deviations, change controls and other quality processes, working closely with QPs
Supervise the QC department

What we offer

Clear progression and development opportunities

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

Supervisor, QC Microbiology, Second Shift

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

Master’s degree in Microbiology, Biology, or related life science (preferred)
Bachelor’s degree with 5+ years of progressive GMP QC Microbiology experience
1–3+ years in a leadership role within a QC Microbiology lab
Hands-on experience with aseptic processing, environmental monitoring, and USP microbiological testing required
Skilled in data analysis and report writing
Must be able to work across NH PCI sites, including remote locations
Ability to gown for ISO-classified cleanroom work
Ability to lift up to 20 lbs
Occasional off-shift support may be required

Job Responsibility

Lead daily lab operations—including oversight of environmental monitoring, microbial testing of utilities (USP <61>, <62>, <85>), and in-process/final product testing
Supervise, mentor, and develop a high-performing team of microbiologists and lab personnel
Manage scheduling, workloads, and ensure timely testing and release of all microbiological samples
Perform risk assessments and investigations (EM excursions, aseptic incidents) and implement effective CAPAs
Perform data trending and statistical analysis
author quarterly reports on environmental and utility data
Oversee testing for endotoxins, bioburden, growth promotion, EM sampling, and clean utility sampling
Collaborate cross-functionally with Operations and Facilities to protect aseptic integrity
Support and coordinate equipment validation, calibration, and maintenance
Drive compliance with cGMP, FDA, EU, and international microbiology regulations

What we offer

Opportunities for growth and advancement within a science-driven, patient-focused organization
A collaborative, team-oriented environment with cross-functional exposure
The chance to make an impact on public health by ensuring the safety of every batch
Ongoing training and development to keep your skills sharp in a fast-evolving industry

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

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

New

Quality Lab Senior Supervisor

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

Location

United States , Marion

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. Degree in Life Science Field (e.g. Biology, Microbiology, related)
Minimum of 5 years of experience or Master’s Degree in biological science with applied experience, preferably in the pharmaceutical or medical device industry
Knowledge of aseptic technique and microbiological testing according to FDA, cGMP, GLPs, and USP testing methodology
Computer skills including knowledge of Microsoft office applications (Word, Excel)
Able to manage multiple tasks/priorities in a timely manner
Able to work independently and manage time to complete assigned tasks
Ability to create an environment that values people, encourages trust, and open communication through feedback and recognition
Applicants must be authorized to work for any employer in the U.S.

Job Responsibility

Coordinate all activities required to occur for assigned shift responsibilities relative to the QC Laboratory including but not limited to: Personnel management
Conducting non-conformance investigations within TrackWise 8 for procedural non-compliances and non-conforming results
Assign tasks, set priorities, and ensure effective performance and development of team members
Conduct regular training for staff
Conduct ACE Check-ins with staff and additional communications as needed
Ensure testing is performed accurately and efficiently, following established protocols and standards
Oversee the accurate recording and analysis of test results, review results, and address documentation errors in accordance with procedural requirements
Ensure results are provided to document control within specified timeframes for release
Cross train in all areas of the QC Microbiology Laboratory which has staffing represented on night shift to enable troubleshooting of issues and/or guidance as necessary
Perform documentation review of all areas of QC Microbiology Laboratory as assigned by the Quality Manager

What we offer

Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off

Fulltime

New

Quality Lab Senior Supervisor

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

Location

United States , Marion

Salary:

96000.00 - 132000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

B.S. Degree in Life Science Field (e.g. Biology, Microbiology, related)
Minimum of 5 years of experience or Master's Degree in biological science with applied experience, preferably in the pharmaceutical or medical device industry
Knowledge of aseptic technique and microbiological testing according to FDA, cGMP, GLPs, and USP testing methodology
Computer skills including knowledge of Microsoft office applications (Word, Excel)
Able to manage multiple tasks/priorities in a timely manner
Able to work independently and manage time to complete assigned tasks
Ability to create an environment that values people, encourages trust, and open communication through feedback and recognition

Job Responsibility

Coordinate all activities required to occur for assigned shift responsibilities relative to the QC Laboratory including but not limited to: Personnel management
Conducting non-conformance investigations within TrackWise 8 for procedural non-compliances and non-conforming results
Assign tasks, set priorities, and ensure effective performance and development of team members
Conduct regular training for staff
Conduct ACE Check-ins with staff and additional communications as needed
Ensure testing is performed accurately and efficiently, following established protocols and standards
Oversee the accurate recording and analysis of test results, review results, and address documentation errors in accordance with procedural requirements
Ensure results are provided to document control within specified timeframes for release
Cross train in all areas of the QC Microbiology Laboratory which has staffing represented on night shift to enable troubleshooting of issues and/or guidance as necessary
Perform documentation review of all areas of QC Microbiology Laboratory as assigned by the Quality Manager

What we offer

Shift flexibility to trade shifts and leverage overtime opportunities
Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits

Fulltime

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Qc Supervisor

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