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Formulation Associate Jobs in Massachusetts (NOW HIRING)

CuriRx Inc

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Research & Development Assistant / Associate

Wilmington, MA · On-site

$65K - $75K/yr

CuriRx focuses on formulation and lyophilization development of biologics, small molecules ... The Research & Development Assistant / Associate is a hands-on laboratory position that will ...

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CuriRx Inc

Be Seen First

Research & Development Assistant / Associate

Wilmington, MA · On-site

$65K - $75K/yr

CuriRx focuses on formulation and lyophilization development of biologics, small molecules ... The Research & Development Assistant / Associate is a hands-on laboratory position that will ...

New

CuriRx Inc

Be Seen First

Research & Development Assistant / Associate

Wilmington, MA · On-site

$65K - $75K/yr

CuriRx focuses on formulation and lyophilization development of biologics, small molecules ... The Research & Development Assistant / Associate is a hands-on laboratory position that will ...

New

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Formulation Associate information

What is a formulation associate job?

A formulation associate is responsible for developing and preparing product formulations, often in the pharmaceutical, cosmetic, or food industries. They work with raw materials, follow strict safety and quality protocols, and may use laboratory equipment to ensure formulations meet specifications. Strong attention to detail and knowledge of chemistry or related sciences are essential for this role.

What cities in Massachusetts are hiring for Formulation Associate jobs?

Cities in Massachusetts with the most Formulation Associate job openings:

Formulation Associate jobs near you
Infographic showing various Formulation Associate job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Formulation Associate 2nd & 3rd

SHARP STERILE MANUFACTURING LLC

Lee, MA • On-site

$19.58 - $36.59/hr

Full-time

Re-posted 25 days ago

Job description

Shift Aviable:

1st: 6:30 am-3:00 pm

2nd: 2:30 pm - 11:00 pm: comes with 10% Shift differential 

3rd: 10:30 pm - 7:00 am: Comes with 15% shift differential 

Position Summary

Perform all formulation operations in the area of assignment and support start-up/changeovers/tech transfer activities. This position works under the immediate direction of the Formulation Supervisor and all work is conducted following a high standard of GMP compliance and written SOP and batch records.  

Duties and Responsibilities

  • Operate glass washers and autoclave, prepare buffers and medias and other solutions 
  • Operate process equipment such as tanks, filtration devices, autoclaves, glass washers, integrity testing and other small equipment
  • Daily completion of formulation activities ensuring all scheduled tasks/events are completed       
  • Formulation process steps including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or financial loss
  • Initiate the production of batch used for engineering and cGMP production and initiate thawing of the API as required
  • Execute Batch Records accurately and complete prior to submission for review 
  • Author process deviations when they occur within the department, participate in investigations and contribute to identifying corrective and preventative actions
  • Cross train to increase technical skills across the department  
  • Communicate, in a timely manner, to management and clients of issues, challenges as well as opportunities for process improvements
  • Other duties as assigned

Regulatory Responsibilities  

  • Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements        
  • Conduct all work in compliance with FDA, 21 CFR 820, 21 CFR 210 and 211, and other regulatory agency requirements sufficient to apply to quality operations and compliance

Supervisory Responsibilities

  • N/A

Experience

  • Formulation Associate I – Zero to two (0-2) years’ experience in a GMP environment performing and using formulation/compounding processes and equipment

Education

  • Formulation Associate I – Associates Degree in a science-related discipline or equivalent GMP experience

Degree in other discipline (or lack of degree) may be considered if sufficient technical depth has been achieved from professional experience

Knowledge, Skills & Abilities

  • Possess working knowledge of formulation/compounding processes and equipment
  • Attention to detail
  • cGMP and cGLP practices
  • Demonstrated ability to prioritize multiple projects and activities
  • Can perform routine work instructions and trouble shoot routine problems referring more complex issues to Formulation Supervisor
  • Experience with Microsoft Office and general computer proficiency
  • Effective communication and availability
  • Able to work effectively with others

Physical Requirements 

 

  • Ability to meet gowning requirements
  • Visual acuity
  • Fine and gross motor skills to manipulate tools and equipment
  • Ability to remain stationary for continuous prolonged periods of time
  • Able to lift 30lbs repeatedly
  • Able to wear PPE 
  • Medically qualified to participate in respirator program
  • Use of standard office equipment with or without reasonable accommodation


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