Qc Supervisor Job at PPG Industries (Tianjin)

Clinical Laboratory QC Specialist

The Clinical Laboratory Quality Control (QC) Specialist I performs and functions...

Location

United States , Madison

Salary:

76000.00 - 125000.00 USD / Year

Exact Sciences

Expiration Date

Until further notice

Requirements

Bachelor’s degree in chemical, biological, or clinical laboratory sciences or medical technology from an accredited institution
For a degree not one of those listed above: 90 semester hours which must include 16 semester hours in chemistry (6 of which must be in inorganic chemistry)
16 semester hours in biology courses and 3 semester hours of math
2+ years of experience in a laboratory setting
1+ years of experience performing, reviewing and understanding quality control on a routine basis
Demonstrated ability to perform the Essential Duties of the position with or without accommodation
Authorization to work in the United States without sponsorship

Job Responsibility

All assigned job duties are performed following laboratory policies and procedures
Responsible for running daily QC scripts using statistical software and reviewing generated daily QC data
Responsible for identifying quality control issues, errors, and trends and promptly informing QC Specialist II and/or other QC team members of issues identified
May be requested to assist QC Specialist II and/or other QC team members in investigation of quality control issues, errors, and trends
May be requested to assist QC Specialist II and/or other QC team members in preparation of monthly quality control reports
Responsible for performing validations, verifications, and studies under the guidance of the QC Specialist II and/or other QC team members
Responsible for obtaining validation, verification, and study data for review
May be requested to assist in review of validation, verification, and study data
Assists QC Supervisor, QC Lead, and other QC team members in ensuring that all section turn-around times are maintained
Assists the QC Supervisor, QC Lead, and other QC team members by escalating concerns and answering technical questions from laboratory staff and others in Exact Sciences labs, as appropriate

What we offer

paid time off (including days for vacation, holidays, volunteering, and personal time)
paid leave for parents and caregivers
a retirement savings plan
wellness support
health benefits including medical, prescription drug, dental, and vision coverage
bonus eligible

Fulltime

Quality Control Intern

Welcome to Golden Owl Solutions - an environment full of youthful, dynamic and c...

Location

Vietnam , Ho Chi Minh City

Salary:

Not provided

Golden Owl Solutions

Expiration Date

Until further notice

Requirements

Fresh graduated or 4th-year students, can join full-time
Major in IT or related faculty
Bold passion for IT software development and testing
Good IT background, critical and logical thinking skills
Commitment to excellence and self-improvement
Good command in English

Job Responsibility

Study SRS, acceptance criteria, design document to design tests
Design, review, and update test cases
Execute tests based on test cases/test scripts and report test results
Log, report, and track defects
Ensure that all bugs are recorded in an efficient, complete and informative manner, either on the Scrum board or bug tracking tools
Evaluate test execution results and report them to the QC Lead
Respond to the development team’s request in line with the project e.g. providing more information for bugs, balancing, build installation, validating bugs, etc
Self-improve domain knowledge: EDI, CRM, Supply chain management, Inventory, Human resource management, Accountancy, Logistics…etc
Report to Supervisor/ QC Lead
Work effectively in completing assigned QC tasks by supervisor

What we offer

Allowance: 3.000.000 VND / month
Team-building, tea-break party
Opportunity to become a official staff after internship period
On-job training program provided by Supervisor/ QC Lead
Possibility to join a practical project
Improve English skills by working with foreign clients
Improve communications skills

Fulltime

Office Manager

This role operates within the manufacturing industry, providing critical back-of...

Location

United States , Grand Blanc

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Applicant must have a minimum of 10 years of experience in an office management role
Proficiency in budget processes and budgeting is essential
Experience with financial statement preparation is required
Knowledge of ADP - Payroll is a must
Familiarity with credit terms and job cost is required
Capability to handle month-end close activities is needed
Experience in human resources (HR) administration is necessary
Knowledge of MIOSHA standards is desirable
Experience as an investment advisor would be beneficial
Proficiency in balance sheet account reconciliation is necessary

Job Responsibility

Oversee the operations of the office and inside sales, ensuring efficiency and accuracy
Manage accounts payable and receivable, ensuring timely transactions and accurate record keeping
Generate monthly financial and management reports, providing detailed insights into business performance
Establish customer credit terms and address payment issues, balancing business needs with customer relationships
Handle Human Resources administration, including MIOSHA reporting and forms, and collaborate with payroll companies
Participate in profit sharing committee, reviewing the work of advisors and administrators
Account for a small private foundation, handling financial transactions, and liaising with various charities
Ensure cross-training within the team, promoting flexibility, and covering for absences
Collaborate with various stakeholders, including profit sharing and investment advisors, outside accounting firm, Engineering and QC Supervisor, Plant Supervisor, and GM/Owner
Utilize Microsoft Excel for data analysis, financial reporting, and record keeping

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Fulltime

QC/QA Chemical Technician

This person is responsible for ensuring the company’s products meet quality and ...

Location

United States , Perrysburg

Salary:

Not provided

Formlabs GmbH

Expiration Date

Until further notice

Requirements

Bachelor degree in Chemistry
Familiar with ISO Standards
Strong training abilities
Attention to detail, accuracy, and concise
Strong organizational and time management skills

Job Responsibility

Performs QC testing on all finished goods and incoming materials and components (including ISO 13485 materials)
Performs in-process inspections for conformance to quality standards
Responsible for performing all calibration on QC equipment and vendor equipment
Establish QC procedures for all new products with supervisor
Supports QC scale-up activities for new products
Ordering supplies and materials for R&D, QC, and Chemists
Training R&D employees and QC technicians when necessary
Periodically review ISO 13485 departmental operational procedures for QC
Maintaining and improving procedures for quality
Conduct quality issue investigations

What we offer

Medical/dental/vision insurance
3% 401k match
Lunch 3 days a week
Unlimited access to 3d printing

Fulltime

Quality Control Specialist

The QC Associate I is responsible for conducting routine, accurate, and timely t...

Location

United States , San Diego

Salary:

Not provided

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

BA/BS degree in a related scientific discipline OR some related college coursework with a minimum of 2 years of experience in a biotech lab environment
Industrial or research laboratory experience preferred
Flow Cytometry experience required
Tissue Culture experience highly preferred
Basic computer skills, including MS Excel & Word
Knowledge of general laboratory safety procedures
Effective interpersonal, written, and oral communication skills
Strong analytical and problem-solving skills
Ability to follow established policies and procedures
Attention to detail with the ability to maintain neat, accurate, and complete records

Job Responsibility

Train and become proficient in required techniques, equipment operation, and software related to testing, data analysis, and reporting
Perform routine QC tests accurately and timely under supervision, prioritizing workload to develop independent working skills
Analyze data, report results, and complete necessary documentation and database entries as per QC protocols
Calibrate and maintain equipment, report issues to the QC Supervisor or Manager, and maintain required logs
Prepare supplies and reagents while assisting with laboratory maintenance
Ensure a safe work environment by identifying and addressing hazards, participating in Environmental, Health & Safety programs, and adhering to safety compliance requirements
Participate in group projects, cross-training, and intra-departmental teams as required
Perform additional duties and assignments as needed

Fulltime

Qc temp

The QC Temp is responsible for routine, accurate and timely testing of QC sample...

Location

United States , San Diego

Salary:

20.00 - 25.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

BA/BS degree in Biology/Microbiology or in a related scientific discipline or some related college coursework
Experience in a biotech lab environment preferred
Flow cytometry knowledge and/or experience
Basic computer skills: MS Excel & Word
Knowledge of general laboratory safety
Effective interpersonal skills
Effective written and oral communication skills
Demonstrated ability to follow established policies and procedures
Demonstrated ability to keep neat, accurate, and complete records and logs
Effective analytical and problem solving skills

Job Responsibility

Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting
Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures
Prioritize daily workload and develop skills to work independently
Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures
Calibrate and maintain equipment
Report problems to QC Supervisor or Manager
Maintain logs and required documentation as necessary
Prepare supplies and reagents, and assist with laboratory maintenance as needed
Promote a safe work environment
May provide recommendations on maintaining the safety of the work environment

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

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

Qc Supervisor

PPG Industries

Location:
China , Tianjin

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 20, 2026

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