Analytical chemist Job at Argenta (Auckland)

Chemist

Performs chemical testing to Raw Material, Initials, In-Process Analysis, Water ...

Location

Puerto Rico , Aibonito

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor Degree in Chemistry or Related Natural Science
Licensed Chemist is preferable
Bilingual English & Spanish
Knowledge of GLP’s/ QSR and Good Documentation Practices
Computer knowledge
Must be related with all principles of chemical testing
Knowledge on GC, UV/ VIS, pH, IR, TOC Analyzer, Polarimeter and others
Knowledge in analysis of Ethylene Oxide Residue
Excellent gravimetric, volumetric, and analytical techniques
Willing to work extra hours, at any shift, weekends and holidays when its required

Job Responsibility

Analyze finished product samples versus specified parameters using specifications and chemical procedures
Analyze purchase raw materials against established procedures assuring compliance with all regulations and specifications
Audit chemical test procedures, retests, additional testing, and SOP's in the laboratory
Request and order all materials required in the laboratory on a timely basis to assure an efficient performance
Initiate and implement changes or new chemical procedures including data gathering
Fill out monthly, quarterly, and annual reports for the chemical laboratory as required
Perform specialized tests and chemical tests to raw materials and finished products
Prepare general material and solutions needed for laboratory tests
Collect and enter data for statistical and trend evaluation
Perform calibration and preventive maintenance as required

What we offer

Vacation and Paid Holidays
Medical, Dental, Disability and Life Insurance coverage
Vision and Voluntary Benefits
Paid Parental Leave
Retirement Savings Plan
Employee Stock Purchase Program
Educational Assistance Plan.

Fulltime

Analytical Chemist

Analytical Chemist / Lab Technician Scientist to join a global pharmaceutical or...

Location

Switzerland

Salary:

Not provided

CK Group

Expiration Date

Until further notice

Requirements

Hands-on experience with biochemical analytical techniques
Experience with antibodies, binding assays, cell-based assays, or PCR
Experience with HPLC / UPLC, capillary electrophoresis, or other large molecule analytical techniques
Previous experience working in a GMP laboratory
Laboratory technician qualification or Bachelor’s degree in Chemistry, Biochemistry, Biotechnology, or related discipline
Experience working in a regulated laboratory environment
Fluent English required
Strong team player with good communication skills

Job Responsibility

Perform analytical testing of biologics for release, stability, and characterization in accordance with GMP / GDP requirements
Support analytical method validation, transfer, and qualification activities
Troubleshoot analytical methods and laboratory procedures
Prepare technical protocols, reports, and GMP documentation
Maintain accurate records using electronic laboratory notebooks
Support equipment maintenance, calibration, and qualification activities
Perform raw material, in-process, and finished product testing
Ensure compliance with internal safety, quality, and environmental procedures
Contribute to continuous improvement of laboratory methods and processes

Fulltime

Analytical Chemist

Location

United States , Vernon Hills

Salary:

30.00 - 36.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

BS in Chemistry/Pharmaceuticals with related science experience
Experience: 2-4 years of experience in pharmaceutical analytical chemistry
Experience with GMP documentation requirements
Hands-on experience with wet-chemistry testing techniques (i.e. pH, GC, HPLC)
Working in an FDA regulated environment
Defining problems, collecting and interpreting data, establishing facts, drawing valid scientific conclusions, and proposing solutions or corrective actions
Previous experience with writing scientific protocols and reports
Troubleshooting equipment and experimental problems
Maintaining laboratory equipment and optimizing laboratory operations for efficient use of time and resources
Demonstrates a specific set of in-depth skills and knowledge in the related area of expertise

Job Responsibility

This position provides analytical chemistry support and/or remediation to all chemistry-related projects

Fulltime

Analytical Chemist I

The Analytical Chemist I is responsible for completing physical tests on raw mat...

Location

United States , Hodges

Salary:

20.00 - 21.00 USD / Hour

Bureau Veritas Certification CZ, s.r.o.

Expiration Date

Until further notice

Requirements

Bachelor’s Degree in Chemistry or closely-related field
Knowledge of GMP regulations, preferred
Written and verbal communication skills including the ability to communicate effectively in a group setting, with colleagues and clients
Organizational and time management skills
Ability to organize and prioritize workload to meet or exceed deadlines
Individual and Team work ethic
Proficiency with Windows, Word & Excel
Attention to detail
Positive attitude, self-motivated, high level of engagement
Ability to present both facts and recommendations effectively

Job Responsibility

Perform physical testing of raw materials using prescribed testing methods, following testing standards / specifications appropriate to the sample
Maintain and calibrate lab equipment as required
Maintain lab cleanliness and restock reagents and consumables
Support Quality and continuous improvement projects for facility
Understand and adhere to standards for appropriate test methods and SOP’s
Prepare a variety of samples for testing using prescribed testing methods, following testing standards / specifications
Perform any required quality and safety checks on samples submitted prior to testing
Performs testing in coordination with clients, coworkers, and supervision from management
Escalates troubleshooting to client as soon as possible
Accurately report and record test data in electronic notebook or handwritten notebooks as needed in a timely manner

Fulltime

Qc Chemist I

This position will have responsibility to support various activities in the Qual...

Location

United States , Madison

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

0-3 years relevant Analytical Chemistry experience, preferably in Quality Control
Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study
General knowledge of analytical techniques using instruments such as: UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer and Osmometer is preferred
Excellent organizational skills and ability to document technical data
Excellent interpersonal skills and the ability to communicate well orally and in writing to all levels of the organization
Ability to multi-task in a dynamic environment with changing priorities
Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment.

Job Responsibility

Perform routine analytical testing of samples supporting incoming raw materials, in-process production, finished product release, long term stability and validation samples
Assist in deviation investigation, out-of-specification or aberrant results and process changes
Assist in authoring and/or review of GMP documentation including test methods, protocols, reports and raw data
Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals with support
Logging and tracking of samples and chemicals
Order chemicals and laboratory supplies as needed
Documents/peer reviews laboratory work using laboratory notebooks/worksheets
May participate in communication between PCI, clients, and analytical testing vendors to support activities including release testing, analytical methods transfer, qualification, validation and implementation
Performs routine data generation and problem solving
Other duties, as assigned.

Fulltime

Qc Chemist I

This position will have responsibility to support various activities in the Qual...

Location

United States , Madison

Salary:

Not provided

PCI Pharma Services

Expiration Date

Until further notice

Requirements

0-3 years relevant Analytical Chemistry experience, preferably in Quality Control
Bachelor of Science in Analytical Chemistry, Chemistry, Pharmaceutical Sciences or a closely related area of study
General knowledge of analytical techniques using instruments such as: UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer and Osmometer is preferred
Excellent organizational skills and ability to document technical data
Excellent interpersonal skills and the ability to communicate well orally and in writing to all levels of the organization
Ability to multi-task in a dynamic environment with changing priorities
Must have strong attention to detail, strong problem-solving skills, as well as the ability to work in a cross-functional team environment.

Job Responsibility

Perform routine analytical testing of samples supporting incoming raw materials, in-process production, finished product release, long term stability and validation samples
Assist in deviation investigation, out-of-specification or aberrant results and process changes
Assist in authoring and/or review of GMP documentation including test methods, protocols, reports and raw data
Perform analytical equipment validation, and ensure routine calibration and preventive maintenance is performed at the required intervals with support
Logging and tracking of samples and chemicals
Order chemicals and laboratory supplies as needed
Documents/peer reviews laboratory work using laboratory notebooks/worksheets
May participate in communication between PCI, clients, and analytical testing vendors to support activities including release testing, analytical methods transfer, qualification, validation and implementation
Performs routine data generation and problem solving
Other duties, as assigned.

Fulltime

Scientist - Small Molecule Technology

Develop safe, robust, scalable, and efficient manufacturing processes for interm...

Location

India , Chennai

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Ph.D in the field of Organic Chemistry
Demonstrated capabilities and experience in performing chemical reactions, structure characterizations, basic understanding of chromatography, Crystallizations, Basic safety principles, Basic quality principles, basic understanding of analytical techniques
Experience and demonstrated competencies in working with teams in a matrixed organization, building and nurturing relationships and effective engagement resulting in successful outcomes
Candidate should have skill in preparing the technical reports and adherence to compliance.

Job Responsibility

Develop safe, robust, scalable, and efficient manufacturing processes for intermediate and Active Pharmaceutical Ingredients (APIs) suitable for both pilot plant and commercial scale production
Performing literature search and identifying various synthetic routes for process development
Promotes the use of novel experimental approaches within sub-function
routinely investigates/creates innovative processes, hypotheses and methodologies
Knowledge of interpretation of structures using spectral techniques like NMR, IR & Mass spectra
Planning and Performing experiments as per process governance (Lab feasibility, Optimization, Pre-validation, CPP and Validation)
Performing What if studies, stress studies, holding time studies, Mass balance, recovery studies and scale up studies
Encountering the process challenges on time and supporting production teams for scale up activities
Handling of business critical / supply chain critical related investigational projects on fast track
Participate in brainstorming activity for the project in identifying scope of improvement

Fulltime

Principal Product Development Chemist

Full time permanent role for a Principal Product Development Chemist at a global...

Location

New Zealand , Auckland

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Previous experience in the Pharmaceutical Industry in Analytical Method Development [minimum 15 yrs experience]
Experience in a GMP / GLP compliant environment
Expert in using and troubleshooting key Analytical Instruments and software
Knowledge of the pharmaceutical regulatory approval processes and requirements for submission of Drug Substance and Drug Product
Providing technical expertise and direction to a team of Chemists
Strong understanding of health and safety requirements
The ability to manage resources to meet changing priorities
Strong computer literacy with the ability to pick up new packages and processes easily
Strong numeracy skills and the ability to analyse and interpret data
Excellent written and verbal English language communication skills

Job Responsibility

Lead the development and optimisation of analytical methods for drug substances and products
Troubleshoot complex technical challenges
Provide scientific expertise to drive product development and method validation excellence
Comply with pharmaceutical good manufacturing practices (GMP), principles and protocols
Follow the standard operating procedures (SOPs), and quality standards in a safe and timely manner

What we offer

Comprehensive insurance cover
Access to EAP support
Fresh fruit every week
Regular on-site events

Fulltime

Analytical chemist

Argenta

Location:
New Zealand , Auckland

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 04, 2026

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