Quality control chemist job description

The Quality Control Chemist is responsible for daily lab testing with the purpose of accepting or rejecting test samples based on pre-determined specifications. The successful candidate will be able to work quickly and safely and will assist the Quality Control Manager with other tasks, as needed.
ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.
• Performs laboratory tests including pH, fluoride, viscosity, specific gravity, color, and appearance.
• Tests raw materials, bulk intermediates, finished products and stability samples for specific quality attributes.
• Uses and maintains HPLC, GC, FTIR, and other instruments.
• Assists in performing method validations.
• Performs a variety of wet lab techniques including but not limited to: titrations, pH, ISE, etc.
• Writes and revises SOPs and tests methods as needed.
• Follows documented procedures: SOPs, test methods, transfer protocols.
• Prepares reports and reviews data.
• Follows lab safety procedures.
• Performs other tasks, as assigned.
SUPERVISORY RESPONSIBILITIES None
Competencies
QUALIFICATIONS to perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION and/or EXPERIENCE Bachelors of Science in Chemistry.
LANGUAGE SKILLS Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
MATHEMATICAL SKILLS Able to calculate figures and amounts such as proportions, percentages, area, circumference and volume. Able to apply concepts of basic algebra and geometry.
REASONING ABILITY Able to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Able to deal with problems involving several concrete variables in standardized situations.
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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Specific vision abilities required by this job include close vision and depth perception.
WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Company DescriptionDental Technologies, Inc. is a company specializing in the research, formulation, compounding and packaging of dental, orthodontic and oral pharmaceutical products. Some products include dental restoratives, core build-ups, bonding agents, orthodontic adhesives, prophylaxis paste, fluoride treatments, toothpaste and varnishes. Dental Technologies maintains the ISO 13485:2016 quality system and employs more than 70 people, with research at the focus of our strategy. Dental Technologies, Inc. is dedicated to excellence in research & development, manufacturing, in-depth testing, efficient packaging, and personalized service. With process control experts committed to the highest level of integrity, quality, and service, Dental Technologies, Inc. ensures risk free product manufacturing - See more at: www.dentaltech.com/

Come Be Part of a Mission that Matters!
The Animal Safety Division is currently seeking a candidate for a QC Chemist II position. The ideal candidate will possess a knowledge of instrumentation such as FTIR, HPLC, UV/VIS, and KF to be used in the routine analytical testing of samples supporting incoming raw materials, in-process production, finished product, and validation. Microbiology experience a plus.The selected candidate will be responsible for performing instrument/method troubleshooting as well as validation, qualification, calibration, and preventative maintenance, and performing investigations on out-of-specification results, method transfer and method qualifications of new and existing products. The selected candidate will be responsible for training other chemists on analytical methods, instruments, SOPs, and documentation and will participate in QA functions of the QCU including document review, room and equipment log review, room cleaning approvals, and other quality functions as assigned by the Sr. Quality Manager.

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

Completes routine analytical testing of samples supporting incoming raw materials, in-process production, finished product, and validation. Use analytical instrumentation such as FTIR, HPLC, UV/VIS, Karl Fischer, viscometer, and dissolution apparatus Performs instrument/method troubleshooting within analytical method parameters and management guidance Performs investigations on out-of-specification and out-of-trend results Performs instrument validation, qualification, calibration and preventative maintenance Participates in method transfer and method qualifications of new and existing products Participates in cleaning method validations and analytical method qualifications for cleaning and other validation projects Maintains the data archives and samples Trains technicians and other chemists on analytical methods, instruments, SOP's and documentation Logs and tracks samples Documents/reviews laboratory work using laboratory notebooks/worksheets that is detailed, timely and in compliance with GLP/cGMP requirements Writes, reviews and updates standard operating procedures Compiles data to support trending program Orders chemicals and laboratory supplies as needed Possesses the ability to identify, analyze, and work towards correcting potential hazards Maintains strictest standards of hygiene in laboratory area
Performs/facilitates quality audits on procedures, as well as on documents being used to perform these procedures

EDUCATION and/or EXPERIENCE: Bachelor's degree (B.S.) from four-year college or university and two to three years related experience and/or training; or equivalent combination of education and experience

WHO IS NEOGEN:

From farm to fork, we offer solutions to enhance the quality, quantity and safety of the global food supply. Our animal safety solutions are used on farms, veterinary practices and manufacturers around the world to provide the best animal care possible. Whether food or pharmaceuticals, Neogen's provides a one-stop shop for the health and safety to our animals and our customers operations.

Neogen's culture combines stability with a deep belief in providing professional and personal growth. Our Pillars of Trust - the principles that guide our everyday decision-making, include Openness, Honesty, Credibility, Respect, and Service. It's our belief in these characteristics that provides a consistent, happy and healthy work environment for our employees.

Job Title: QC Laboratory Chemist (Licensed)
Job Function: Performs Quality Control Data Audit in an FDA Regulated environment.
Job Type: Full Time Contract
Location: Caguas, PR

About RCM:
RCM IT & Life Sciences is a leading provider of IT Business Solutions and Engineering Services to over 1,000 clients in the commercial and government sectors. RCM partners with clients to define implement and manage a broad range of technologies across multiple platforms, systems, and networks. Our broad geographic presence ensures that a proven and reliable tactical and strategic capability is available and deployable virtually everywhere in North America.

Scope of Job RCM is looking for QC Laboratory Chemist to perform Data Auditing in an FDA regulated environment for our client located in Caguas, PR.

Primary Responsibilities & Qualifications Audit Data to support the methods transfer, development and validation data testing of experimental, confirmation and registration lots, stabilities, new products manufactured at the site and transfer of analytical technology to the commercial laboratories.
Knowledge in FDA, USP and ICH guidelines for method transfer and validation is required
Work with minimum supervisin.
Must be computer literate, bilingual (Spanish / English)
Support EHS program to assure compliance with safety policies.
Interpret results obtained during method transfer
Experience performing analytical test within the pharmaceutical industry.
Manage multiple tasks
Able to work independently
Strong knowledge of cGMPs regulations.
Good skills writing general documentation in English and using MS Office applications.
Bilingual (both English/Spanish)

Education & Certifications BS in Chemistry or related discipline and five years of related experience within the life sciences industry. Chemist license is a must.

Equal Opportunity Statement

RCM is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Disclaimer

This job description is intended to describe the general nature and the level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. RCM reserves the right to amend and change responsibilities to meet business and organizational needs as necessary.