CrawlJobs Logo

Chemical Regulatory Specialist

vrs-regulatory.net Logo

VRS Regulatory

Location Icon

Location:
United Kingdom , Cheshire

Category Icon
Category:

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

Not provided

Job Description:

A chemical raw materials company is looking to recruit a chemical regulatory specialist to join their regulatory function. This is a flexible hybrid role. The company provides a wide range of chemical ingredients/raw materials to sectors including coatings, adhesives, plastics and life sciences to global markets. This is a desk based regulatory role providing a vital compliance service to internal stakeholders; it could be suited to a chemist who splits time between the lab and SDS authoring/compliance checks or for an existing regulatory officer looking for a new challenge. This is an ambitious and growing company with a growth mindset and dynamic approach.

Job Responsibility:

  • Ensuring products are compliant with chemical regulations (CLP, GHS, REACH, DG etc)
  • Learn about application regulations (regs impacting customers’ final products)
  • Compliance check new raw materials
  • Manage chemical / regulatory data
  • Author SDSs and labels
  • Answer customer regulatory enquiries
  • Complete customer questionnaires
  • Liaise with suppliers
  • Keep abreast of regulatory developments that may impact any products
  • Contribute to project work eg accreditations, sustainability
  • Be a regulatory subject matter expert

Requirements:

  • Some existing chemical regulatory experience (SDS authoring, classifications, labelling etc)
  • CLP, GHS, REACH compliance, labelling, compliance checks, supplier liaison, DG, customer enquiries, questionnaires, regulatory support, advice, data management, regulatory research

Additional Information:

Job Posted:
January 21, 2026

Work Type:
Hybrid work
Job Link Share:

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Chemical Regulatory Specialist

Regulatory Specialist

Regulatory Specialist (East Windsor, NJ) (Multiple Openings).
Location
Location
United States , East Windsor
Salary
Salary:
Not provided
novitiumpharma.com Logo
Novitium Pharma
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Must have bachelors in Pharmaceutical sciences / biology / microbiology / chemistry / chemical / Regulatory Affairs / Related + 1 year exp. as Regulatory Specialist /Quality Control Analyst / Chemist / Analyst / Scientist/ Research Associate / Related
Job Responsibility
Job Responsibility
  • Review, manage and write regulatory submissions electronically which include New ANDA filings, Complete Response letters, Information requests, Amendments to the ANDA’s (Labeling, Chemistry & Bioequivalence) of different dosage forms (Tablet, Capsule, Liquid & Solutions)
  • responsible for filing the Post Approval Supplements like CBE-0, CBE-30 (Changes being effective in 30 days) and Prior Approval Supplements (PAS)
  • submitting dossiers electronically after the approval of initial product submissions (ANDA)
  • review of the leachable and extractable reports generated for the oral Liquid & Solution drug products
Read More
Arrow Right

Senior REACH Regulatory Specialist

An exciting opportunity for a Chemicals Regulatory professional who is looking f...
Location
Location
United Kingdom
Salary
Salary:
Not provided
vrs-regulatory.net Logo
VRS Regulatory
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Chemical regulatory professional with experience and strong knowledge of chemical regulations (REACH – EU and UK)
  • Understanding of the procedures to compliantly market chemical substances and products
  • Strong technical knowledge
  • Confident communication and interpersonal skills
  • Looking for an opportunity to use a broad skill set – regulatory, project management and strategic commercial development
  • Degree/higher degree qualified
  • Proven track record in industry, consultancy or competent authority managing the deliver of industrial chemical regulatory projects
Job Responsibility
Job Responsibility
  • Management of regulatory projects for industrial chemical (REACH)
  • Strategic and commercial activities to develop company processes, systems and online/social media presence
  • Technical aspects: regulatory advice, regulatory strategies, data reviews, study placement and monitoring, study summaries, management of experts, dossier preparation and submission
  • Work with a REACH and CLP focus, likely covering other regulations
  • Strategic and commercial aspects: development of technical marketing content and the company’s online profile including website, blogs, social media
  • Develop strategy and specify work to IT consultants
Read More
Arrow Right
New

Product Compliance Specialist

Avantor is seeking a Product Compliance Specialist (f/m/d) to ensure that the or...
Location
Location
Romania
Salary
Salary:
Not provided
avantorsciences.com Logo
Avantor
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Chemistry, Chemical Engineering, Environmental Science, Toxicology, or a related scientific discipline
  • Several years of experience in product stewardship, regulatory affairs, or chemical compliance, ideally within manufacturing, life sciences, distribution, or specialty chemicals
  • Hands-on experience with SAP Product Compliance is required (e.g., PC Basic, Dangerous Goods, Safety Data Sheet Management, Marketability, Environmental Compliance, Global Label Management)
  • Strong understanding of global chemical regulations and product compliance frameworks (e.g., REACH, RoHS, WHMIS, Prop 65, GHS/CLP, TSCA, K-REACH, food contact, etc.)
  • Ability to analyze product composition and regulatory data to determine compliance status
  • Familiarity with SDS authoring, hazard classification, and chemical labeling requirements
  • Business fluency in English (C1 level)
  • Innovation: Curiosity and a continuous-improvement mindset
  • Customer Centricity: Partner effectively with internal and external customers
  • Accountability & Excellence: Take ownership for the accuracy and completeness of product regulatory data
Job Responsibility
Job Responsibility
  • Regulatory Compliance & Risk Management: Assess and interpret global chemical and product regulations to determine applicability and compliance obligations
  • SAP Product Compliance & Data Management: Ensure accurate chemical classifications, composition data, and regulatory attributes within SAP Product Compliance
  • Documentation & Labelling: Oversee generation and review of Safety Data Sheets (SDS), labels, and compliance declarations
  • Cross-Functional Collaboration: Provide regulatory and product stewardship guidance to R&D, sourcing, quality, commercial, and operations teams
  • Monitoring & Continuous Improvement: Track evolving global regulations and assess potential impact on product portfolios
What we offer
What we offer
  • Flexible working hours
  • Option to work remotely
  • Meal vouchers
  • Gift vouchers
  • Benefit Online Platform
  • Private medical insurance
  • Employee Assistance Program
  • Learning and development opportunities
  • In-house trainings
  • Language learning
  • Fulltime
Read More
Arrow Right

Lead Regulatory Specialist / Manager

An opportunity to become the Lead Regulatory Specialist / Regulatory Manager at ...
Location
Location
United Kingdom , South Manchester
Salary
Salary:
Not provided
vrs-regulatory.net Logo
VRS Regulatory
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Good, practical knowledge of REACH and CLP
  • Ability to research and implement new regulations
  • Desire to provide an efficient regulatory service to internal and external stakeholders
  • Must be confident of your abilities and have personable communication skills
  • A background in fine chemicals eg pigments, additives would be ideal
  • Any experience of inks, coatings or plastics would also be beneficial
Job Responsibility
Job Responsibility
  • Managing REACH registrations
  • Implementation of global REACH like schemes
  • Participation in SIEFs and consortia
  • Management of test data
  • Oversight of hazard communication (all SDSs and labels)
  • Completion of customer questionnaires
  • Support to internal departments – sales, R&D etc
  • Develop knowledge of customer application regulations and directions eg food contact, packaging, plastics
Read More
Arrow Right

Global Substance Registration Specialist

An opportunity to join the Substance Registration Team at a global speciality ch...
Location
Location
United Kingdom
Salary
Salary:
Not provided
vrs-regulatory.net Logo
VRS Regulatory
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Regulatory officer/specialist with hands-on EU REACH registration experience
  • Degree qualified (chemistry etc)
  • Proven track record registering chemical substances
  • Proficient with IUCLID
  • Good understanding of the complexities of registration projects
  • Good communicator
  • Organised planner with ability to influence and negotiate
Job Responsibility
Job Responsibility
  • Support NPD projects, maintenance of existing registrations and new registrations in new geographies
  • Manage registrations from start to finish: regulation requirements, strategy, data review, gap analysis, working with consortia/SIEFs, placing/monitoring studies at CROs, working with internal and external technical experts, writing robust study summaries, working with IUCLID to build/submit dossiers
What we offer
What we offer
  • comprehensive benefits
Read More
Arrow Right
New

Clinical Laboratory QC Specialist

The Clinical Laboratory Quality Control (QC) Specialist I performs and functions...
Location
Location
United States , Madison
Salary
Salary:
76000.00 - 125000.00 USD / Year
exactsciences.com Logo
Exact Sciences
Expiration Date
Until further notice
Flip Icon
Requirements
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
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
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
Read More
Arrow Right

Drug Substance Senior Specialist – Biologics

We are seeking a Drug Substance Senior Specialist with strong experience in biol...
Location
Location
Denmark , København og omegn
Salary
Salary:
Not provided
life-science-talent-solutions.dk Logo
Life Science Talent
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in biotechnology, chemical engineering, pharmaceutical sciences, or related field
  • 8+ years of industry experience in biologics process development and validation, including collaboration with CDMOs
  • Proven experience with PPQ and process characterization for antibody drug substances
  • Solid understanding of ICH Q8–Q11 and global validation expectations
  • Practical knowledge of commercial-scale GMP operations, tech transfer, and regulatory submissions
  • Experience in early-stage process development and scale-up
  • Strong project management and organizational abilities
  • Excellent communication and technical writing skills for regulatory documentation
  • Collaborative mindset and ability to work effectively with external partners
  • Flexible, proactive, and comfortable operating in a fast-paced biotech environment
Job Responsibility
Job Responsibility
  • Support early-stage antibody programs by applying phase-appropriate development strategies
  • Collaborate with Quality, Regulatory, and Analytical teams to align on validation approaches
  • Provide technical input to CDMOs on process design, scale-up, and risk assessments
  • Plan and manage process performance qualification (PPQ) and characterization studies in partnership with CDMOs
  • Define and document CPPs, CQAs, and control strategies based on risk and data-driven insights
  • Ensure validation documentation (protocols, reports, summaries) complies with ICH Q8–Q11, FDA, and EMA expectations
  • Support implementation of continuous process verification (CPV) and lifecycle validation strategies
  • Oversee technology transfer to external manufacturing partners for commercial readiness
  • Contribute to CMC regulatory submissions (BLA/MAA) focusing on validation and control strategy
  • Coordinate comparability studies and process optimization activities with CDMOs
  • Fulltime
Read More
Arrow Right
New

Environmental Specialist

This role exists to be part of an organization that values Safety, Health, and E...
Location
Location
Mexico , Nuevo León
Salary
Salary:
Not provided
unilever.com Logo
Unilever
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor's degree in Mechanical, Environmental, Chemical, Industrial Engineering or another engineering degree
  • Conversational English
  • Data management and analysis
  • ISO14001, LEED & Lighthouse certifications
  • Must be a team player able to work in a fast-paced environment with demonstrated ability to handle multiple competing tasks and demands
  • Strong communication skills
  • oral, written and presentation
  • Strong organization, planning and time management skills to achieve results
  • Strong personal and professional ethical values and integrity
  • Holds self-accountable to achieving goals and standards
Job Responsibility
Job Responsibility
  • Define & execute the strategy for the decarbonization of the site based on Unilever goals
  • Support the deployment of the global/cluster SHE strategy, policy and standards in the site to achieve excellent sustainable results
  • Responsible to deliver Environmental results E2E
  • Drive environmental risk assessment and assist in implementation of appropriate controls
  • Reduce the site’s environmental impact in the areas of COD, hazardous & non-hazardous waste, SOx & CO2 emissions and water & energy consumption
  • Influence line management and drive environmental leadership
  • Monitor site legal compliance and ensure the site meets all local/national regulatory requirements and Unilever standards
  • Conduct trend analysis from environmental incidents, near misses, safe behavior observations and deep compliance audits
  • Fulltime
Read More
Arrow Right