Chemical Regulatory Specialist Job at VRS Regulatory (Cheshire)

EHS&S Specialist – Chemical Safety, Industrial Hygiene, and Emergency Response

This role will lead the day-to-day implementation and maintenance of Environment...

Location

United States , Marietta

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in environmental science, safety, industrial hygiene, engineering, occupational health or related field
2+ years of experience in the EHS&S field with progressive roles and responsibilities, including managing and executing EHS programs
Experience must include time in a facility EHS role as well as specific work experience related to chemical safety/industrial hygiene and emergency response
Professional certification (either a CSP or CIH) is highly preferred. If not currently certified, the candidate must have the ability to become certified within 2 years of date of hire
Member of relevant professional EHS institution in order to stay current in the field such as ASSP or ACGIH
Experience with Chemical, laboratory, oil & gas, pharmaceutical, or similar regulatory manufacturing environment
Availability to support occasional extended hours, shift/weekend coverage and 24/7/365 emergency response
willingness to travel occasionally (< 5% travel)

Job Responsibility

Assess chemical and biological hazard risks from new and existing materials and processes, evaluate the effectiveness of existing exposure controls, and advise on different control methodologies
Conduct Industrial Hygiene monitoring, analyze results, issue reports, and manage site plans, including exposure monitoring/modeling and the chemical safety program
Integrate Industrial Hygiene considerations into capital and minor works projects and effectively identify and manage risks through technical innovation and support
Evaluate compliance with federal, state, and local legislation and GSK requirements related to EHS&S, interpret requirements, and provide recommendations for compliance
Perform program audits, facility inspections, and generate recommended corrective actions
Manage key health and safety risks to GSK personnel, contractors, visitors, and the company’s reputation with regulators and the public
Implement EHS&S programs at the Marietta site, verify their effectiveness, and ensure proper identification and mitigation of hazards and risks
Ensure GSK standards are embedded into the project and operations to mitigate key risks for the site
Implement EHS&S Management Systems for health, safety, environment, and security regulations and requirements
Oversee the formation and management of the Emergency Response Team (ERT), including team member selection, equipment procurement and maintenance, and targeted training for efficient emergency handling

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

Senior Regulatory Specialist - Biocides

A trusted partner at nearly three million customer locations, Ecolab (ECL) is th...

Location

Poland , Kraków

Salary:

Not provided

Edgerton Dental Clinic

Expiration Date

Until further notice

Requirements

PhD or MSc degree in Natural Science or Life Science (Chemistry, Toxicology, Ecotoxicology or similar)
At least five years of professional experience in Biocides Regulation (EU) 528/2012 or other European chemical regulations, such as REACH, is required.
Proven project management, communication and problem-solving skills in a regulated environment
Ability to prioritize tasks effectively and excellent time management skills
Demonstrated success coordinating activities with internal businesses and external customers or business partners
Excellent English skills (written and spoken)

Job Responsibility

Develop regulatory strategies to safeguard assigned biocidal active substance portfolio in Europe
Facilitate business growth by obtaining active substance approvals and driving innovation initiatives in accordance with the Biocidal Product Regulation (BPR)
Organize and lead cross-functional authorization projects addressing key business needs with assigned resources
Liaise with notified bodies and competent authorities with tasks related to the BPR and lead with quick response on short-term requests.
Review and document budget, internal data, contracts and data sharing agreements to ensure Regulatory and Legal compliance
Monitor, communicate and implement changing EU and biocide guidance
Provide regulatory surveillance (i.e. intelligence) and business impact assessment of emerging regulations

What we offer

Attractive salary (Base pay & Variable Plan) and benefits package (private medical care, life insurance, stock purchase, lunch subsidy, sport cards)
Flexible working arrangements with hybrid model of work (approx. 60% from the office and 40% from home)
Thrive in our matrix organization, working across Europe with various teams and cultural backgrounds
Strong teamwork and diverse interactions
Personalized plans with rapid progression
Professional growth supported by active committee for different career levels
High employee satisfaction and responsive feedback
Continuous learning and technical training incl. subject matter experts’ trainings, soft skills and management trainings and LinkedIn learning
Assistance for international candidates and candidates living outside of Krakow
Social events such as family events and charity auctions

Fulltime

Regulatory Specialist

Regulatory Specialist (East Windsor, NJ) (Multiple Openings).

Location

United States , East Windsor

Salary:

Not provided

Novitium Pharma

Expiration Date

Until further notice

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

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

Lead Regulatory Specialist / Manager

An opportunity to become the Lead Regulatory Specialist / Regulatory Manager at ...

Location

United Kingdom , South Manchester

Salary:

Not provided

VRS Regulatory

Expiration Date

Until further notice

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

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

Senior REACH Regulatory Specialist

An exciting opportunity for a Chemicals Regulatory professional who is looking f...

Location

United Kingdom

Salary:

Not provided

VRS Regulatory

Expiration Date

Until further notice

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

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

Sap regulatory systems specialist

We are looking for a regulatory specialist with knowledge of SAP and experience ...

Location

United Kingdom

Salary:

Not provided

VRS Regulatory

Expiration Date

Until further notice

Requirements

Regulatory specialist with knowledge of SAP
Experience or interest in a systems and process development role
Analytical thinker
Systematic
High attention to detail
Ability to think commercially
Strong understanding of regulatory processes that support a global chemical manufacturing business

Job Responsibility

Develop and automate regulatory processes to support the wider product stewardship team
Ensure optimum use of the system and the data
Develop harmonised regulatory systems and processes across the global business
Lead the implementation of new functionality (eg substance volume tracking)
Ensure all regulatory developments are understood and implemented
Act as process subject matter expert
Provide user training to regulatory colleagues
Ensure all system data is robust and usable for analysis and assessment to support sound regulatory decision making

Senior Regulatory Affairs Specialist

Reporting to the Senior Manager, Regulatory Affairs within the RA Department, th...

Location

United States , St Louis

Salary:

74000.00 - 90000.00 USD / Year

STERIS

Expiration Date

Until further notice

Requirements

Bachelor's Degree
At least 5 years professional experience including regulatory affairs, quality systems, internal auditing, applicable scientific or technical functions
Self-starter with demonstrated organizational, project management, time management and problem-solving skills
Experience working effectively on cross-functional teams
Demonstrated ability to balance multiple high priority responsibilities on-time and effectively
Excellent PC skills, including Microsoft Office applications including Excel, Word and PowerPoint
Understanding of chemical / scientific industry
Experience with internal audit process and quality systems
Experience with Healthcare regulatory support for product assessments, Safety Data Sheet generation, and Customer inquiries

Job Responsibility

Identify regulatory requirements for new products or product enhancements early in the product development cycle
Assure that product registration and maintenance fees are tracked and paid
Gather information to support regulatory submissions. Use this information to prepare regulatory submissions in a complete, thorough format to support STERIS product claims
Review product revision requests to assure compliance with regulatory requirements
Work on product teams to develop regulatory strategy based on regulatory submission requirements
Review and approve labeling and marketing literature
Support Manager, Regulatory Affairs and other Regulatory Affairs staff with all regulatory matters
Provide Regulatory support for product assessments, Safety Data Sheet generation, and Customer inquiries to the Healthcare team
Work with direct Supervisor and senior internal stakeholders to identify key initiatives, which may be affect by present or emerging policies. As part of this, develop and recommend government affairs policy positions to upper management
Other duties as assigned

What we offer

Market Competitive Pay
Extensive Paid Time Off and (9) added Holidays
Excellent Healthcare, Dental and Vision Benefits
Long/Short Term Disability Coverage
401(k) with a company match
Maternity and Paternity Leave
Additional add-on benefits/discounts for programs such as Pet Insurance
Tuition Reimbursement and continued education programs
Excellent opportunities for advancement in a stable long-term care

Fulltime

Regulatory Affairs Data Specialist

Join LANXESS – Where Your Expertise Shapes Global Safety. LANXESS UK is looking ...

Location

United Kingdom , Manchester

Salary:

Not provided

LANXESS

Expiration Date

Until further notice

Requirements

Degree in Natural Sciences (Master’s/Diploma) OR extensive experience in global chemical regulations
Knowledge of Global chemical legislation and regulatory requirements
High level experience with SAP
Strong analytical and problem-solving skills to refine and improve regulatory processes
Excellent communication skills in English (bonus if you speak German, French, Portuguese, Chinese, or Spanish)
Project management experience to regulatory initiatives

Job Responsibility

Environmental, Health, and Safety Data Management
Update physical-chemical properties, safety information, toxicology, and regulatory data, while monitoring global regulatory sources
Assess the impact of data changes on the LANXESS product portfolio and support the Management of Change process to ensure smooth transitions
Regulatory Change Requests & Compliance
Process change requests from business units, ensuring data accuracy and compliance with global regulatory requirements
Maintain consistency within the Management of Change process
Data Quality & Process Improvement
Develop and refine maintenance standards and procedures, review existing environmental, health, and safety data, and drive data quality improvements within LANXESS systems
Cross-Functional Collaboration & Project Support
Work closely with Global Product Safety and other stakeholders, lead or support data management projects, and represent Global Data Management in cross-departmental initiatives

What we offer

Competitive compensation packages, inclusive of a global bonus program and an individual performance bonus program
Retirement plans, health programs, life insurance and medical care
Flexible working arrangements
Professional and personal development
Commitment to diversity and inclusion

Fulltime

Select Country

Chemical Regulatory Specialist

Job Description

Job Responsibility

Requirements

Looking for more opportunities?