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Chemence Jobs (NOW HIRING)

Material Handler

Alpharetta, GA · On-site

$16.25 - $19.50/hr

They will also be responsible for performing material transactions within the Chemence electronic inventory control system. Key Duties and Responsibilities: * Receives, distributes, and stores ...

Material Handler

Alpharetta, GA · On-site

$16.25 - $19.75/hr

They will also be responsible for performing material transactions within the Chemence electronic inventory control system. Key Duties and Responsibilities: * Receives, distributes, and stores ...

The primary function for this position is to ensure that CHEMENCE, Inc. complies with all applicable environmental, health and safety regulations. Key Duties and Responsibilities: Reasonable ...

Director of Regulatory Affairs - PRRC

Alpharetta, GA · On-site

$144K - $191K/yr

CHEMENCE ® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age ...

CHEMENCE ® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age ...

CHEMENCE ® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age ...

Chemence information

What is Chemence and what do they do?

Chemence is a global specialty chemical company that manufactures adhesives, sealants, resins, and other polymer-based products. They serve various industries, including medical, industrial, printing, and consumer goods. Chemence is known for its innovative solutions in cyanoacrylate adhesives (super glues), anaerobic adhesives, and UV-curable products. With a strong focus on research and development, the company provides custom formulations and private labeling for clients worldwide.

What are some common challenges faced by employees working at Chemence, especially in technical or production roles?

Employees in technical or production roles at Chemence often encounter challenges such as maintaining strict quality standards, adapting to evolving manufacturing technologies, and ensuring safety compliance in a fast-paced environment. Collaboration with cross-functional teams—such as R&D, quality assurance, and logistics—is essential to meet production targets and resolve issues quickly. New hires should be prepared for hands-on problem-solving and continuous learning, as the company emphasizes innovation and process improvement.

What is the difference between Chemence vs Chemist?

AspectChemenceChemist
Required CredentialsTypically technical certifications or industry-specific trainingBachelor's degree or higher in chemistry or related field
Work EnvironmentManufacturing, laboratory, or industrial settingsLaboratories, research facilities, or industrial labs
Employer & Industry UsageManufacturers, chemical companies, industrial firmsResearch institutions, pharmaceutical companies, chemical industries
Common Search & ComparisonOften compared for technical roles in chemical productionCompared for scientific research and development roles

While Chemence refers to a technical role involving chemical processes and production, a Chemist typically holds a degree in chemistry and focuses on scientific research, analysis, and development. Both roles are integral to the chemical industry but differ in education requirements and work focus.

What are the key skills and qualifications needed to thrive as a Chemist, and why are they important?

To thrive as a Chemist, you need a solid background in chemistry principles, laboratory techniques, and typically a bachelor's or advanced degree in chemistry or a related field. Familiarity with laboratory equipment, analytical instruments such as HPLC and GC, and safety protocols is essential, and certifications like OSHA or hazardous materials handling can be beneficial. Strong attention to detail, problem-solving abilities, and effective communication skills help chemists excel in research and collaborative environments. These skills ensure accurate experimentation, data integrity, and the safe development of chemical products or processes.
More about Chemence jobs
What cities are hiring for Chemence jobs? Cities with the most Chemence job openings:
What states have the most Chemence jobs? States with the most job openings for Chemence jobs include:
Infographic showing various Chemence job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Physical job distribution.
Senior Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

Chemence

Alpharetta, GA • On-site

Full-time

Posted 5 days ago


Key responsibilities

  • Implement new projects or programs to comply with newly implemented or changed regulations.

  • Assist with managing global registrations and Economic Operators.

  • Perform scientific and technical analyses on medical devices during early product development to assess compliance requirements.


Job description

Summary:

Under general supervision, the Senior Regulatory Affairs Specialist is an expert in specific field of study responsible for liaising with other departments to lead efforts to update systems and processes in compliance with guidelines or regulations that govern Chemence Medical products.

The Senior Regulatory Affairs Specialist will also assist the organization in training, implementation and preparation for new or updated standards, guidance and regulations (e.g. 21 CFR 820, ISO 13485, EU MDR and MDSAP).

The Senior Regulatory Affairs Specialist will serve as the project lead for successful implementation of systems, processes and training programs.

Key Duties and Responsibilities:

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

  • Implement new projects or programs at Chemence Medical to comply with newly implemented or changes to existing regulations.
  • Assists with managing Global registrations and Economic Operators.
  • Perform scientific and technical analyses on medical devices during early product development to assess compliance requirements.
  • Updates PMS, GSPRs, PMCF and Essential Principal documents as needed.
  • Assess changes to marketed devices, determine effects on regulatory global regulatory status, and perform resulting regulatory activities.
  • Research regulatory and industry changes that may impact global regulatory operations and reports to teams for evaluation
  • Prepare adverse event reports in accordance with applicable regulations
  • Provides audit support during FDA, ISO and Notified Body Audits and Corporate
  • May perform other duties as required

Qualifications, Education and/or Experience Required:

  • Bachelor’s degree (or higher) in scientific or engineering discipline
  • 8+ years of related industry experience
  • Expert in specific guidance, standard or area (e.g. Auditing, EU MDR, Clinical Studies)
  • Excellent English verbal and written communication skills
  • Strong analytical and organizational skills with the ability to multi-task and prioritize competing demands
  • Computer skills with proficiency in Microsoft Office (Word, Excel) and Adobe Acrobat

Language Skills:

  • English required, bilingual (Spanish) a plus.

Physical Demands:

  • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms.

Work Environment:

  • This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines.

Other Duties:

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

AAP/EEO Statement:

CHEMENCE® provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.