Supervisor, QC Analytical Job at PCI Pharma Services (Bedford)

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

Supervisor, QA Raw Materials

The Supervisor, QA Raw Materials is responsible for leading a team of QA Raw Mat...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in relevant scientific discipline with a minimum of 5+ years’ experience in related GMP industry working in Quality Assurance or Quality Control groups which support receipt, inspection, or release of materials
Equivalent combination of education and experience considered
Knowledge of USP and EP pharmacopoeias, and pharmaceutical raw material compendial testing
Knowledge of FDA regulations (i.e., 21CFR Part 210, 211 & 820) and some experience working with international regulations such as EU, ICH
Ability to apply basic scientific principles to solve operational and quality tasks
Experience with RCA, technical writing, and working with quality related investigations

Job Responsibility

Perform review of external documentation and internal GMP documentation associated with incoming raw materials, components, chemicals, excipients, and Active Pharmaceutical Ingredients (API)
Provide Quality Assurance oversight to Materials Management and Quality Control, ensuring that site SOP’s and raw material specifications are adhered to
Responsible for the review and analysis of test results
ability to interpret and comprehend scientific information and data related to QC Micro and QC Analytical testing
Initiation, review, and disposition or closure of raw material quality systems
Assist in the identification, isolation, and containment of potentially nonconforming materials
Assist in the identification and management of expired material
perform scrapping of materials with Materials Management
Assist Materials Management and Project Management with finished product shipments
Provide input, review, and approval of new and revised raw material specifications

Fulltime

Quality Control Supervisor

This is a senior-level position responsible for overseeing and supporting the wo...

Location

United States , Brookfield, Connecticut

Salary:

Not provided

Greenfield Global

Expiration Date

Until further notice

Requirements

Bachelor’s or master’s degree in chemistry, biochemistry, or a related field
Previous experience in a QC or quality role
3+ years of experience in supervisory or leading role
Strong supervisory, leadership, strategic thinking, and problem-solving skills
Excellent communication and organizational skills, with an ability to effectively communicate complex concepts to diverse stakeholders
Ability to manage multiple priorities under tight deadlines
Effective problem-solving and troubleshooting skills, with the ability to identify and address issues promptly
Excellent communication skills, both written and verbal, allowing for clear and concise reporting and collaboration with team members
Ability to work independently with minimal supervision while being a proactive and reliable team player

Job Responsibility

Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release
Utilize various analytical testing techniques such as Gas Chromatography (GC), UV-Visible spectroscopy, titrations, and other relevant methods
Provide guidance, support, and mentorship to foster professional growth and development within the team
Monitor compliance with established procedures, protocols, and regulatory requirements
Represent the QC department in cross-functional meetings and project teams
Review and revise quality control protocols and test plans to align with industry standards
Planning, scheduling, and coordinating analytical testing activities
Monitor the generation of analytical data by the QC team to ensure accuracy, integrity, and compliance
Assist the QC team in resolving technical problems related to instrumentation, method development, or other analytical issues
Interacts with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns

What we offer

Formal and informal training opportunities
Comprehensive health and dental benefits
Income protection: short- and long-term disability coverage, life insurance, paid personal sick time
Vacation time exceeding industry standards
Company funded retirement savings program with individual contribution opportunities
Meaningful and challenging work
Curated intentional culture focused on growth and development, engagement, and communication

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

New

Qa Specialist 2

Primary function is the timely and efficient advanced review ensuring accuracy, ...

Location

United States , Rockford

Salary:

22.15 - 24.92 USD / Hour

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Bachelor's Degree in a related field and/or 1-5 years of related experience and/or training
College-Level Mathematical Skills
Intermediate Computer Skills: Ability to perform more complex computer tasks and knowledge of various computer programs
Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs
Very High Reasoning: Ability to define problems, collect data, establish facts, and draw valid conclusions. Be able to interpret an extensive variety of technical instructions in math or diagram form and deal with several abstract/concrete variables
High Standard of Report Writing

Job Responsibility

Timely and efficient advanced review ensuring accuracy, completeness and compliance to in–house, customer and regulatory requirement, including data integrity
Record and maintain all related data and records in compliance with cGMP and ALCOA principles
Train other associates in data review for which expertise/competency has been demonstrated
On time completion of assigned training in ComplianceWire
Participate in internal Health and Safety audits including developing actions and follow up
Participates in internal, customer and regulatory audits
Maintains a high level of safety and highlights any potential unsafe act immediately
Participates in implementation and execution of continuous improvement activities
Play a role in creating and maintaining an atmosphere of teamwork throughout the laboratory
Knowledge of and adhere to all PCI, cGMP, and GCP policies, procedures, rules

What we offer

Eligibility for an annual performance bonus
Paid time off
Health insurance coverage (including dental and vision)
Flexible spending account
401(k)

Fulltime

QC Microbiologist

ABOUT THE JOB: Carry out sampling and biological testing of raw materials, in-pr...

Location

Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Experience in biological or microbiological testing within a laboratory environment
Understanding of GMP requirements and quality compliance
Experience with laboratory equipment operation, maintenance, and calibration
Experience with laboratory documentation systems and standard digital tools
Academic background in life sciences or a related scientific discipline
You demonstrate strong attention to detail and a quality mindset
You demonstrate problem-solving and analytical skills
You demonstrate clear and effective communication skills
You demonstrate a strong commitment to safety, quality, and regulatory standards

Job Responsibility

Carry out sampling and biological testing of raw materials, in-process materials, finished or intermediate products, and utilities (e.g. water systems and compressed gases) in accordance with GMP standards
Support manufacturing process validation activities through appropriate biological testing
Perform routine environmental monitoring within classified production areas
Provide laboratory support for new product introduction and transfer activities
Participate in laboratory investigations, contributing to root cause analysis and timely closure of deviations and CAPAs
Execute routine equipment upkeep, including maintenance and calibration activities
Support method transfer, verification, and validation processes as required
Assist with the preparation, review, and updating of quality documentation
Escalate any observed issues or non-conformities to the QC Supervisor in a timely manner
Apply 5S/6S principles to ensure proper inventory control, laboratory housekeeping, and continuous improvement

What we offer

Global Diversity: Be part of an international team of 110+ nationalities, celebrating diverse perspectives and collaboration
Trust and Growth: With 70% of our leaders starting at entry-level, we’re committed to nurturing talent and empowering you to reach new heights
Continuous Learning: Unlock your full potential with our internal Academy and over 250 training modules designed for your professional growth
Vibrant Culture: Enjoy a workplace where energy, fun, and camaraderie come together through afterworks, networking events, and more
Meaningful Impact: Join us in making a difference through our CSR initiatives, including the WeCare Together program, and be part of something bigger

Fulltime

Supervisor, QC Analytical

PCI Pharma Services

Location:
United States , Bedford

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 20, 2026

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