QA Chemist Job at Randstad (Dahej)

Manufacturing QA Chemist

The Manufacturing QC Chemist is responsible for supporting Quality Control and Q...

Location

United States , Brownsburg

Salary:

24.00 USD / Hour

Antech Diagnostics

Expiration Date

Until further notice

Requirements

Associates degree required/ bachelor’s degree in science related discipline preferred
Experience with general laboratory and IVD manufacturing equipment
Knowledge of GMP, GLP, & GDP standards
Experience handling hazardous chemicals
Experience in general reagent compounding or buffer preparation
Proficiency in laboratory techniques, including precision filling and pipetting
Familiarity with molecular assays (PCR, ELISA, radioactive, fluorescent)
Strong statistical analysis skills
High attention to detail and commitment to work quality
Effective problem-solving abilities

Job Responsibility

Perform visual inspections and laboratory analyses to verify product quality and compliance
Perform laboratory assays (e.g., PCR, ELISA, radioactive/fluorescent assay) and support validation of new & existing products and processes
Document, report, and investigate non-conformance issues
perform root cause analysis and recommend corrective actions
Monitor QC parameters using statistical tools (e.g., Levy-Jennings charts) and maintain accurate records in QA databases
Calibrate, maintain, and troubleshoot laboratory equipment and instrumentation
Handle hazardous chemicals and small quantities of radioactive materials in accordance with safety and regulatory guidelines (e.g., NRC regulations)
Assist with sample collection, validation studies, and initial data review for new & existing products
Support method and assay validation, including analytical testing and documentation
Participate in internal audits and continuous improvement initiatives within manufacturing and Biobank facilities

What we offer

Paid Time Off & Holidays
Medical, Dental, Vision (Multiple Plans Available)
Basic Life (Company Paid) & Supplemental Life
Short and Long Term Disability (Company Paid)
Flexible Spending Accounts/Health Savings Accounts
Paid Parental Leave
401(k) with company match
Tuition/Continuing Education Reimbursement
Life Assistance Program
Pet Care Discounts

Fulltime

Production Chemist II

Production Chemist II role for a Medical Device Company. Duration: 12+ Months Co...

Location

United States , San Diego

Salary:

25.00 - 29.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

M.S. degree in Chemistry with a minimum of 2 years of experience in an industry synthetic chemistry lab or a B.S. in Chemistry with 3+ years of relevant work experience
Industry laboratory experience (prefer chemistry over biochemistry/bio)
Experience working in an ISO, GMP, or GLP environment
Organization skills
Solid MS Office Knowledge, Intermediate to Advanced Excel usage
Ability to follow standard operating procedures
Must possess strong organizational skills, attention to detail, and the ability to adapt to changing priorities in a fast-paced environment
Be a self-starter, quick learner with the ability to work independently and efficiently
Hands-on team player with the ability to be proactive and work independently
Ability to influence others without direct reporting ties

Job Responsibility

Support the production of commercial dyes using established technical SOPs
Perform variety of chemical reactions and subsequent processing, purification, and characterization steps
Support inventory management of raw materials, intermediate products, finished goods, analytical samples, and QA Retains through cycle counts, database management, etc.
Work collaboratively with Research, Sustaining Engineering, Process Development, Quality Control, Quality Assurance, and other Production Chemists/Supervisor to ensure successful transfer of new products into Production and to improve processes within the production department
Documentation in lab notebooks, batch records, and basic databases
Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices
Other responsibilities or projects as assigned by reporting manager

Fulltime

Production Chemist I

The Production Chemist I supports the manufacture, analysis, and processing of p...

Location

United States , San Diego

Salary:

25.00 - 31.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

B.S. Degree in Chemistry, Engineering, or Life Science
Minimum of 1 year relevant industry experience preferred
Industry laboratory experience (synthetic organic chemistry preferred over biochemistry/bio)
Experience working in an ISO, GMP, or GLP environment
Organization skills
Ability to follow standard operating procedures
Strong organizational skills, attention to detail, and the ability to multi-task/adapt to changing priorities in a fast-paced environment
Experience with operation of rotary evaporator preferred
Familiarity with operation of routine laboratory instruments and applicable software
Familiarity with glovebox, lyophilization

Job Responsibility

Perform a variety of polymer processing, purification, and characterization steps to support the production of commercial dyes
May perform synthesis of polymers using established procedures
Perform small scale reactions according to established standard processes
Support inventory management of raw materials, intermediate products, finished goods, analytical samples, and QA Retains through cycle counts, database management, etc
Documentation in lab notebooks, batch records, and basic databases
Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices
Other responsibilities or projects as assigned by reporting manager

Fulltime

Production Chemist I

The Production Chemist I supports the manufacture, analysis, and processing of p...

Location

United States , San Diego

Salary:

28.00 - 31.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

B.S. Degree in Chemistry, Engineering, or Life Science
Minimum of 1 year relevant industry experience preferred
Industry laboratory experience (synthetic organic chemistry preferred over biochemistry/bio)
Experience working in an ISO, GMP, or GLP environment
Organization skills
Ability to follow standard operating procedures
Must possess strong organizational skills, attention to detail, and the ability to multi-task/adapt to changing priorities in a fast-paced environment
Works well in a team-based environment
Strong MS Office Knowledge, Intermediate to Advanced Excel usage preferred

Job Responsibility

Perform a variety of polymer processing, purification, and characterization steps to support the production of commercial dyes
May perform synthesis of polymers using established procedures
Perform small scale reactions according to established standard processes
Support inventory management of raw materials, intermediate products, finished goods, analytical samples, and QA Retains through cycle counts, database management, etc
Documentation in lab notebooks, batch records, and basic databases
Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment. Participates in Environmental Health and Safety programs. Addresses corrective actions whenever a hazard is identified. Notifies supervisor of all observed hazardous conditions or unsafe work practices
Other responsibilities or projects as assigned by reporting manager

Fulltime

New

Retail and Gallery Manager

We are seeking a Retail and Gallery Manager to join our Barraga Retail & Art Gal...

Location

Australia , Mossman Gorge, Queensland

Salary:

Not provided

Voyages Indigenous Tourism

Expiration Date

March 29, 2026

Requirements

Retail management experience with strong commercial accountability
Proven ability to manage stock, shrinkage and financial controls
Sales experience with a strong focus on performance outcomes
Experience leading and developing teams
Cash handling and POS compliance experience
A National Criminal History Check is a mandatory step in the recruitment process

Job Responsibility

Lead retail and gallery operations, ensuring service excellence and cultural integrity
Own financial performance including P&L, stock control and shrinkage management
Drive sales growth through merchandising, product strategy and seasonal planning
Develop and coach the retail leadership team to maximise performance
Ensure compliance with financial controls, cash handling and operational standards
Own retail and gallery P&L, stock integrity and commercial performance
Lead and develop the Barraga team to deliver culturally rich guest experiences
Drive sales strategy, merchandising and shrinkage control initiatives

What we offer

Competitive pay and benefits
Resort Discounts at Accor Hotels & Ayers Rock Resort
Internal Growth and movement within the resort and our company

Fulltime

New

Ima legal internship

International Markets (IMa) brings together AXA markets in Latin America, Africa...

Location

Spain , Madrid

Salary:

Not provided

Axa

Expiration Date

Until further notice

Requirements

Law degree or a Double Bachelor’s Degree in Business Administration and Law
A specialization in Corporate Law is preferable
Spanish, English (Proficiency level, C1-C2)
French is an additional asset
Advanced proficiency in Microsoft Office (Excel, Word, PowerPoint)
Strong communications skills
Ability to multitask effectively and adapt to fast-paced environments
Professional, proactive and detail-oriented work style

Job Responsibility

Take care of the corporate documentation and deal with the Notary and Commercial Registry
Discuss and review all type of services agreements
Take care of the internal administrative work
Participate in some M&A files depending on the needs
Reviewing all types of agreements (e.g., Service Level Agreements, Share Purchase Agreements, Shareholder Agreements)
Preparing and reviewing documentation needed for internal committees (presentations, memos, summaries, etc.)
Drafting the documentation related with corporate law matters (powers of attorney, proxies, minutes, certificates, etc.)
Handle the documentation and day-to-day relation required with notaries, registries and embassies
Updating the Corporate Information in the Group Database

What we offer

Multicultural and diverse environment
Multiple international career development opportunities
Possession of a disability certificate will be positively valued

Fulltime

New

Community Meals Driver

Community-focused organisation delivering nutritious meals directly to homes and...

Location

United Kingdom , Blackburn

Salary:

12.21 GBP / Hour

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Full UK Driving License
Own vehicle
Customer service experience preferred
Positive attitude
Excellent communication skills
Willingness to collaborate
Flexibility
Diligence
Valid driver’s license and reliable vehicle
Work related car insurance

Job Responsibility

Deliver nutritious meals safely and punctually
Conduct wellbeing calls to check on clients
Provide friendly service
Ensure compliance with company policies
Contribute to continuous improvement

What we offer

Blue Light Card discounts reimbursed
Employee Assistance Programme
Mileage allowance
Comprehensive training
Growth opportunities
Supportive environment
Make a real difference
Champion sustainability
Flexibility of zero-hour contract

New

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...

Location

United States

Salary:

142100.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
Experience writing, reviewing, or editing protocols and clinical study reports required
Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
Experience writing, reviewing, or editing regulatory briefing books preferred
Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
Ability to interpret and create complex tabular and graphical clinical data presentations
Advanced applied knowledge of basic clinical laboratory tests
Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection

Job Responsibility

Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives (eligibility may vary based on role)
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

QA Chemist

Randstad

Location:
India , Dahej

Category:
Quality Control

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 21, 2026

Expiration:
March 22, 2026

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Randstad

Location:India , Dahej

Category:Quality Control

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:February 21, 2026

Expiration:March 22, 2026

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