Qc & Formulation Assistant Job at SRG (Brighouse)

Production Associate-Reagent

10x Genomics is looking for an outstanding individual to join its consumable man...

Location

United States , Pleasanton

Salary:

30.00 - 36.00 USD / Hour

10x Genomics

Expiration Date

Until further notice

Requirements

B.S./M.S. in one of the following disciplines – Molecular Biology, Analytical Chemistry, Chemical Engineering, or equivalent
3+ years of relevant laboratory experience in manufacturing or QC of Life Science products
Basic understanding of DNA sequencing, PCR or other nucleic acid based technologies required
Ability to multi-task and prioritize work load to meet strict deadlines under supervision
Good documentation skills and ability to write procedures and reports
Desire to be part of a rapidly evolving organization and taking products and processes to the next level

Job Responsibility

Execute production operations according to defined procedures and ensure the integrity and quality of products
Perform formulation and dispensing of reagent consumables and assemble into final kit configurations
Operate liquid handling robotic system and complex manufacturing equipment for production biochemistry under supervision
Operate and maintain laboratory to clean room standards required in the production of Life Science products
Process work orders accurately using an ERP system in a timely manner
Maintenance of production batch records and good documentation under ISO requirement
Initiate Non-Conformance Material or Deviation report and follow up on progress and action items
Accurate tracking of production data, test data and inventory
Disposition material based on QC and production data
Assist in writing and revising work instructions and production batch records

What we offer

Equity grants
Comprehensive health and retirement benefit programs
Annual bonus program or sales incentive program
Generous time off
Competitive and comprehensive health benefits package
Family friendly policies like parental leave

Fulltime

Customer Formulation Chemist

Join PPG, a global leader in paints, coatings, and specialty materials, as a Cus...

Location

United States of America , Oak Creek

Salary:

Not provided

PPG Industries

Expiration Date

Until further notice

Requirements

Bachelor's degree in Chemistry, Chemical Engineering, or a related discipline
Strong mathematical skills, particularly in scale-up calculations to support formulation and production processes
Proficiency in computer skills, including ERP systems (e.g., Oracle) for data entry and formula management
Quick learner with the ability to adapt to a fast-paced, varied work environment
Well-developed oral and written communication skills to interact effectively with technical and non-technical personnel, including direct customer engagement
Strong problem-solving ability and attention to detail to ensure high-quality work and accurate documentation
Good interpersonal skills to foster collaboration within a small team and build relationships with customers
Self-motivated with independent project management skills to drive tasks to completion
Commitment to safety as the top priority in all work activities

Job Responsibility

Adhere to all PPG safety protocols and promote a strong safety culture in a laboratory and customer-facing work environment
Support manufacturing processes by assisting with formulation, troubleshooting, and resolving production-related issues
Work directly with customers to understand their needs, reformulate coatings based on customer specifications, and build strong customer relationships
File and manage formulas accurately, ensuring compliance with quality standards and customer requirements
Provide support to Quality Control (QC) teams to ensure product consistency and adherence to specifications
Communicate results, observations, and customer feedback effectively to direct supervisor and relevant stakeholders
Maintain an accurate, neat laboratory notebook, documenting all observations, including unusual results, with meticulous attention to detail
Demonstrate initiative by accomplishing tasks, meeting mutually agreed-upon deadlines, and effectively incorporating feedback
Act consistently with The PPG Way in all daily activities

Fulltime

Scientist, Product Transfer II

This position is responsible for Product Transfer activities including creation ...

Location

United States , Stillwater, Minnesota

Salary:

70000.00 - 86000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor’s or Master's degree in Chemistry, Biology, Medical Technology OR related science field or a 2 year degree (i.e. MLT) with equivalent experience
5+ Years of related laboratory experience or demonstrated competence within the in-vitro diagnostic industry
Comprehensive understanding of immunology and immunoassay technology and systems
Ability to work in a regulated industry
Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
Knowledge of good manufacturing practices (GMP)
Knowledge of statistical analysis and reporting methods
Ability to train and mentor team members on basic group procedures and tasks
Ability to train and mentor team members in higher level skills
Proven ability to work with minimal supervision

Job Responsibility

Work in conjunction with Product Development in creation of all documentation for LIAISON® Reagent Manufacturing and Quality Control for new products. Create part numbers for new products in the design cycle
Create routings for new part numbers created in design cycle
Aid in creation of part numbers and routings for newer team members
Manufacture new Internal Controls for product in the design cycle
Serve on Core Teams for assigned development projects
Perform material processing and reagent formulation for bulk intermediates and components
Determine reprocessing need for calibrator, controls and conjugates, with assistance
Maintain clean work space in QC and Reagent Prep labs, consistent with Good Laboratory Practices (GMP)
Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
Utilize basic SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting and flow through facility

What we offer

comprehensive plan of health benefits
retirement and financial wellbeing
time off programs
wellbeing support and perks
may be eligible to participate in an annual incentive program

Fulltime

New

Process Scientist I

This position is responsible for material processing, reagent formulation, techn...

Location

United States , Stillwater, Minnesota

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates degree in Chemistry, Biology or Medical Technology required
1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry
Basic understanding of immunology and immunoassay techniques
Ability to work in a regulated environment
Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
Working knowledge of MS Excel
familiarity with Google Suite
Basic understanding of statistical analysis
Advanced skills in: Math and calculations
Writing and documentation

Job Responsibility

Perform material processing and reagent for formulation bulk intermediates and components
Determine reprocessing need for calibrator, controls, and conjugates with assistance
Perform Good laboratory practices - maintain clean workspace in QC and Reagent Prep labs. Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility
Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family
Assign calibrator values to optimize kit performance
Assign kit control ranges per established procedures
Monitor internal control supplies and manufacture new controls as needed
Perform second-checking to ensure accurate records

What we offer

comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks
may be eligible to participate in an annual incentive program

Fulltime

Process Scientist I

This position is responsible for material processing, reagent formulation, techn...

Location

United States , Stillwater

Salary:

61000.00 - 70000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates degree in Chemistry, Biology or Medical Technology required
Bachelor's or Master's degree preferred in Chemistry, Biology, Medical Technology or related science field or a 2 year degree (i.e. MLT) with equivalent experience
1+ years of related laboratory experience and/or demonstrated competence within the in-vitro diagnostic industry
Basic understanding of immunology and immunoassay techniques
Ability to work in a regulated environment
Working knowledge of general lab equipment (e.g. pH meter, balances, mixers, etc.)
Working knowledge of MS Excel
familiarity with Google Suite
Basic understanding of statistical analysis
Advanced skills in: Math and calculations

Job Responsibility

Perform material processing and reagent for formulation bulk intermediates and components
Determine reprocessing need for calibrator, controls, and conjugates with assistance
Perform Good laboratory practices - maintain clean workspace in QC and Reagent Prep labs. Contribute to group Reagent Prep and QC duties, including lab and equipment maintenance
Utilize SAP (kitting, ordering to Cost Center, assign expiration dates, etc.) to ensure correct dating, accounting, and flow through facility
Participate in inventory accountability - PSA count, cycle counts, accurate kitting, etc.
Perform in-process testing and final Quality Control for LIAISON products per established procedures using the LIAISON analyzer family
Assign calibrator values to optimize kit performance
Assign kit control ranges per established procedures
Monitor internal control supplies and manufacture new controls as needed
Perform second-checking to ensure accurate records

What we offer

comprehensive plan of health benefits
retirement and financial wellbeing
time off programs
wellbeing support and perks
may be eligible to participate in an annual incentive program

Fulltime

Process Validation Engineer

Reporting to the Senior Manager process Validation, the Process Validation Engin...

Location

United States , Bedford

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

Experience in pharmaceutical or biopharmaceutical environment in operations/engineering/manufacturing/quality environments
Proficient in the development and execution of PPQs
Review commissioning, qualification and validation related system lifecycle documentation
Combination of equipment qualification, process validation, or cleaning validation is acceptable
QA pharmaceutical experience also preferred
Validation experience with the following is highly preferred: Vacuum physics, Heat and mass transfer, Formulation, Aseptic Filling and Lyophilization, Steam Sterilization, data analysis and statistics
Engagement and knowhow with regulatory inspections and knowledgeable in current industry standards and regulatory trends as they pertain to Validation of pharmaceutical or biopharmaceutical processes
Bachelor of Science degree in Chemical Engineering, Biochemistry, Biology or related scientific discipline required with a minimum of 7 – 10 years of Pharmaceutical industry experience or combination of work experience in Validation, QA, MFG, MTS, Process Development or Engineering
Highly organized professional who is accustomed to working in a result oriented-focused, dynamic CMO environment
Professional and collaborative team player must have excellent interpersonal skills

Job Responsibility

Develop and support the detailed project plans and timelines for the execution of process validation activities
Prepare validation & change control documentation, including protocols, summary reports, etc.
Author Process Performance Qualification/ verification validation plans
Author and perform the technical review of deviations and planned deviations, change controls, perform process monitoring, perform activities for lot release
Participate in client and Regulatory Audits
Work on CAPA and QS with minimal oversight to achieve timely results
Assist with determining impact of change control on qualified process and aseptic operations
Work closely with other validation department personnel and cross-functionally with MTS, Manufacturing, Engineering, QC, Quality Assurance, and project management to achieve all project deliverables
Assist management with mentoring and training of colleagues on policies and procedures including the requirements for validation
Perform all functions associated with process validation support

Fulltime

New

Assistant QAQC Manager

To establish the quality assurance system in accordance with the requirements of...

Location

Singapore , Singapore

Salary:

Not provided

Airswift Sweden

Expiration Date

Until further notice

Requirements

Establish quality assurance system in accordance with ISO 9001
Formulate Project Quality Plan
Develop, review and revise Inspection & Test Plan
Attend QA/QC meetings
Advise on quality control issues
Ensure quality of works in accordance with Quality Management Plan
Develop Method Statements, Inspection & Testing Plans and Checklists
Know process of handling, storage and handover process of materials
Monitor implementation of Project Quality and Environmental Plan
Prepare and conduct site inspections and close reports

Fulltime

Post Extraction Technician

Post-Extraction Technician (Cannabis Lab). The Post-Extraction Technician is a m...

Location

United States , Tempe

Salary:

19.00 - 23.00 USD / Hour

Green Dot Labs

Expiration Date

Until further notice

Requirements

High school diploma or GED required
College experience preferred
Strong desire to work in a lab with extraction equipment and a strong understanding of safety requirements
Prior experience with extraction methods, equipment and/or purging techniques is desirable
Previous experience working in a licensed extraction lab desirable
Must maintain current FA card
Must have a reliable form of transportation
Able to work in a fast-paced environment under deadlines with competing priorities
Continually exhibit honesty and integrity
Punctual and reliable

Job Responsibility

Adhere to all SOPs and Post-Extraction protocols
Whip badder
Ensure a wet texture
Formulate vape cartridge concentrate
Release pressure from concentrate vessels and flip shatter slabs
Observe and record the reaction/activity of the concentrates
Confirm and record weight of production runs
Rate batches of concentrate based on internal quality control standards
Notify Management of QC concerns
Ensure concentrates meet internal residual solvent standard prior to submittal for contaminant testing

What we offer

Company sponsored and partially paid Health, Dental and Vision insurance
401k
Life insurance
Paid time off
401(k) matching

Fulltime

Qc & Formulation Assistant

SRG

Location:
United Kingdom , Brighouse

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 25, 2025

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