Formulation Associate Job at 360 Resourcing Solutions

Group Leader, Formulation Development & Manufacturing

This role is pivotal for delivering high-quality formulation and manufacturing s...

Location

Belgium

Salary:

Not provided

Mantell Associates

Expiration Date

Until further notice

Requirements

MSc or PhD in Pharmaceutical Sciences, Chemical Engineering, or a related discipline
significant hands-on experience in formulation development and GMP manufacturing
At least 8-10 years in the pharmaceutical industry, including experience working with oral and/or injectable dosage forms in GMP production settings
Proven leadership experience managing and mentoring scientific teams in both R&D and GMP production environments
In-depth knowledge of GMP regulations, drug product formulation, process optimization, tech transfer and regulatory documentation practices
Strong organizational, communication, and scientific reporting skills
capable of driving technical excellence in a growing team
Fluent in English

Job Responsibility

Lead, plan and oversee GMP production projects from formulation development through clinical batch manufacturing – ensuring deliverables are on time, within budget, and compliant with GMP standards
Translate project specs from Project Managers into actionable tasks for Development & GMP teams
supervise Associate Scientists in formulating and manufacturing oral and injectable dosage forms
Develop and refine formulation strategies, select excipients and delivery formats, and guide tech transfers from R&D to GMP production
Ensure documentation quality: master batch records, batch records, technical reports, GMP manufacturing reports
coach the team to maintain standards in non-conformance management and quality assurance alignment
Coordinate with QA / QP and supply chain to ensure availability of starting materials, manage deviations, and resolve GMP / compliance issues swiftly and effectively
Act as scientific & technical problem-solver: troubleshoot formulation, process, equipment, and compliance challenges when they arise
Represent the Formulation & GMP Manufacturing team in project core meetings
provide scientific input to clients and internal cross-functional teams

Fulltime

New

Formulation Associate

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

United Kingdom

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Degree qualification in a field of science-related or pharmacy subject is highly desired
Experience developing formulations for veterinary pharmaceutical products is highly desirable
Good numerical and writing skill
Ability to follow instruction
Detail oriented, and excellent memorization skill
Eager to learn and adaptive to any changes
Good IT skills and good administrative skills such as email writing, filing and presentation skill
Good initiative, introspective skill with ‘can do’ attitude
Positive mindset and ability to resolve problems
Team player with ability to work with multi-cultural environment

Job Responsibility

Support maintenance of formulation for daily order requirements and assist with formulation related enquiries
Support product development formulation related tasks
To approve product request and create formulations to meet the requirements of the daily orders
To create and review Formulation Reports and Product Data Sheets
To assist in formulation related enquiries from the Customer Services Department and the Production Department
To approve licensed medicine specifications and unlicensed medicines specifications as required
To support appropriate QMS activities relevant to formulation
To gather information to support product development and product optimisation
To organise trials and create trial protocols
To maintain up-to-date knowledge of GMP and MHRA guidelines with regards to supplying of specials

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

Fulltime

New

Senior Formulation Associate

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

United Kingdom

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Degree qualification in a field of science-related or pharmacy subject is highly desired
Experience developing formulations for veterinary pharmaceutical products is highly desirable
Minimum of 3 yrs Good Manufacturing Practice experience
Good numerical and writing skill
Ability to follow instruction
Detail oriented, and excellent memorization skill
Eager to learn and adaptive to any changes
Good IT skills and good administrative skills such as email writing, filing and presentation skill
Good initiative, introspective skill with ‘can do’ attitude
Positive mindset and ability to resolve problems

Job Responsibility

Manage formulations for daily order requirements and formulation related enquiries and documentation
Lead and support product development and formulation related tasks, with ownership and accountability for delivery
To approve product request, create and approve formulation to meet the requirements of the daily orders
To support and lead appropriate QMS activities relevant to formulation
To create, review, and maintain Formulation Reports, Product Data Sheets, and formulation related documents
To assist in formulation related enquiries from the Customer Services Department and the Production Department
To gather information to support and lead product development and product optimisation
To train, support, and mentor junior team members
To approve licensed medicine specifications and unlicensed medicines specifications as required
To organise trials and create trial protocols

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

Fulltime

New

Senior Formulation Associate

At Target Healthcare Group, we are pioneers in the pharmaceutical industry, comm...

Location

United Kingdom

Salary:

Not provided

360 Resourcing Solutions

Expiration Date

Until further notice

Requirements

Degree qualification in a field of science-related or pharmacy subject is highly desired
Experience developing formulations for veterinary pharmaceutical products is highly desirable
Minimum of 3 yrs Good Manufacturing Practice experience
Good numerical and writing skill
Ability to follow instruction
Detail oriented, and excellent memorization skill
Eager to learn and adaptive to any changes
Good IT skills and good administrative skills such as email writing, filing and presentation skill
Good initiative, introspective skill with ‘can do’ attitude
Positive mindset and ability to resolve problems

Job Responsibility

Manage formulations for daily order requirements and formulation related enquiries and documentation
Lead and support product development and formulation related tasks, with ownership and accountability for delivery
To approve product request, create and approve formulation to meet the requirements of the daily orders
To support and lead appropriate QMS activities relevant to formulation
To create, review, and maintain Formulation Reports, Product Data Sheets, and formulation related documents
To assist in formulation related enquiries from the Customer Services Department and the Production Department
To gather information to support and lead product development and product optimisation
To train, support, and mentor junior team members
To approve licensed medicine specifications and unlicensed medicines specifications as required
To organise trials and create trial protocols

What we offer

Active Social and charity committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

Fulltime

Research Associate, Injectable Formulation Development

Be the backbone of innovation and join a leading pharmaceutical company to help ...

Location

United States , Lexington

Salary:

30.00 - 37.00 USD / Hour

Proclinical

Expiration Date

Until further notice

Requirements

Degree in biological, biochemical, pharmacological sciences, or a related field
Knowledge and expertise in biophysical characterization and injectable formulation development
Familiarity with spectroscopy, calorimetry, light scattering, and other biophysical methods is advantageous
Proficiency in data analysis and interpretation to draw conclusions and make recommendations
Strong attention to detail and ability to document experimental work using electronic laboratory notebooks (ELN)
General knowledge of cGMP, GLP, and regulatory requirements for the pharmaceutical industry is a plus

Job Responsibility

Prepare peptide and protein injectable formulations, including buffer, excipient, and surfactant selection
Conduct biophysical characterization and stability studies for formulations
Collaborate with cross-functional teams to ensure dosage forms meet desired biophysical and biochemical profiles
Contribute to early screening strategies and execution
Operate, maintain, and troubleshoot laboratory instruments for biophysical and analytical characterization
Perform laboratory work safely and efficiently, ensuring a secure working environment for colleagues

New

Associate Principal Scientist - Formulation (Complex Meds)

Exciting Opportunity: Associate Principal Scientist - Formulation - Complex Meds...

Location

United Kingdom , Cheadle

Salary:

Not provided

SRG

Expiration Date

Until further notice

Requirements

PhD with 3+ years' of recent experience or a Bachelor's degree with 6+ years' recent experience in formulation development
Expertise in oral and parenteral formulation development, including modified-release, nano-particulate, or liposomal systems - Specifically Complex Drug Products
Strong knowledge of material properties, drug delivery systems, and global CMC regulatory requirements
Recent experience progressing complex drug products from discovery through to launch
Recent formulation experience with Peptides, Proteins, Lipids is essential
A valid UK driving licence

Job Responsibility

Leading formulation and process design for oral and parenteral drug products across clinical phases in the Complex Meds space
Applying scientific and pragmatic thinking to deliver innovative product and technology solutions
Providing hands-on troubleshooting and laboratory support when needed
Collaborating with analytical scientists to ensure robust testing of formulations
Acting as project leader for pharmaceutical development programmes
Managing CRO activities and client communications
Supporting regulatory strategy and authoring CMC documentation
Introducing new formulation technologies and contributing to continuous improvement
Coaching and mentoring junior staff and contributing to team development
Representing the company at conferences and industry events

Fulltime

New

Journeyman Program Manager

Astrion has an exciting opportunity for a Journeyman Program Manager to directly...

Location

United States , Bedford / Hanscom AFB, Massachusetts

Salary:

115000.00 - 125000.00 USD / Year

Astrion

Expiration Date

Until further notice

Requirements

Bachelor’s degree in a related field and at least three years of experience in the respective technical / professional discipline being performed, three of which must be in the DoD
OR seven years of directly related experience, five of which must be in the DoD
Must be a US Citizen

Job Responsibility

Possess comprehensive knowledge of principles, policies, and practices of systems acquisition and program management, as defined in DoDI 5000.02, AFI 63-101/20-101, as well as knowledge of roles and relationships within the DoD and the Air Force
Possess knowledge of qualitative and quantitative techniques for gathering, analyzing, and measuring the effectiveness, efficiency, and productivity of acquisition programs
Possess the knowledge of support activities that assist the program manager in assessing what programs are within schedule and cost baselines, be able to recommend viable solutions to problems, and the pursuit of alternative courses of action
Effectively communicate orally and in writing, providing quality acquisition and program documentation (briefings, documents, plans, etc.)
Plan, research, analyze, and assess system acquisition in terms of development, production, and deployment of weapons systems and associated equipment as well as formulate plans and recommend effective strategies in meeting cost, schedule and performance objectives
Support and develop acquisition reports, including statutory and regulatory reports (i.e., Defense Acquisition Executive Summary (DAES), Monthly Acquisition Report (MAR), etc.)
Support program management reviews, senior level meeting/reviews, and IMP/IMS reviews
Support and develop various briefings/schedules of program status and acquisition tasks to senior management

What we offer

Competitive salaries
Continuing education assistance
Professional development
Multiple healthcare benefits package options
401K with employer matching
Competitive time off policy along with a federally recognized holiday schedule

Product Manager, Data Collaboration

Take-Two Interactive is seeking a Product Manager (Data Collaboration) to join o...

Location

United States , New York

Salary:

85700.00 - 126860.00 USD / Year

Take-Two Interactive Software, Inc.

Expiration Date

Until further notice

Requirements

3-5+ years of practical experience developing and driving solutions powered by technology, with a strong emphasis on the partnership landscape
Practical experience with Data Clean Room platforms (e.g., Meta Advanced Analytics, Google Ads Data Hub, Snowflake, LiveRamp, or InfoSum)
Ability to speak to partners, pitch complex ideas, and build long term relationships
Solid understanding of digital advertising, marketing partnerships, and data architecture
Clear communicator with the ability to explain technical concepts and solutions to various audiences
Understanding of privacy-related regulations (e.g. COPPA, GDPR, CCPA, etc.) and experience managing sensitive data in a compliant manner
Strong background in digital innovation, preferably experience in the interactive entertainment industry
Ability to establish and navigate high-level relationships, prioritizing timely updates & risk management
Demonstrates strong creativity and scrappiness and can handle constraints with grace
Practical experience with budgeting, contract management, and compliance in a tech environment

Job Responsibility

Coordinate strategic data initiatives while managing relationships with a global network of technology vendors, advertising platforms, and data partners
Responsible for the end-to-end lifecycle of data collaboration solutions: identifying new market opportunities, pitching innovative partnership ideas, and operationalizing scalable technical workflows
Within 90 Days: Learn and Adapt
Understand the Roadmap
System Onboarding
Within 180 Days: Full Ownership
Proactive Growth
Operational Impact
Product strategy & development: Identify and prioritize opportunities
Formulate technical requirements and create associated documentation

What we offer

Medical (HSA & FSA), dental, vision, 401(k) with company match, employee stock purchase plan, commuter benefits, in-house wellness program, broad learning & development opportunities, a charitable giving platform with company match
Fitness allowance, employee discount programs, free games & events and stocked pantries

Fulltime

Formulation Associate

360 Resourcing Solutions

Location:
United Kingdom

Category:
Pharmacy

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 26, 2026

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