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Temporary Sop Writing Jobs in California (NOW HIRING)

... SOP writing, Clinical Samples, 21 CFR Part 111, ISO-78512, Dietary Supplement, Gummy Formulation ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Unload and break down freight onto good wood pallets, in compliance with the SOP and at a pace that ... Should accomidations be required, please request them in writing to Human Resources. While ...

Role Overview This is a 60-day temporary position supporting data collection efforts. You'll be ... Perform data collection tasks by following written SOPs and project guidelines. * Set up ...

Role Overview This is a 60-day temporary position supporting data collection efforts. You'll be ... Perform data collection tasks by following written SOPs and project guidelines. * Set up ...

... written department SOPs. o Generates an appropriate audit trail for all activities. Provides ... May perform pipette calibrations and document according to SOP. Minimum Qualifications * High ...

... written department SOPs. o Generates an appropriate audit trail for all activities. Provides ... May perform pipette calibrations and document according to SOP. Minimum Qualifications * High ...

Compliance to SOP's, GMPs, Housekeeping, Safety, and all other FE policies.Obtains empty barrels ... Must be able to follow oral and written instruction.Must be able to read and write.Must pass ...

Compliance to SOP's, GMPs, Housekeeping, Safety, and all other FE policies.Obtains empty barrels ... Must be able to follow oral and written instruction.Must be able to read and write.Must pass ...

Compliance to SOP's, GMPs, Housekeeping, Safety, and all other FE policies. * Obtains empty barrels ... Must be able to read and write. * Must pass physical strength test that measures physical strength ...

Compliance to SOP's, GMPs, Housekeeping, Safety, and all other FE policies. * Obtains empty barrels ... Must be able to read and write. * Must pass physical strength test that measures physical strength ...

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Temporary Sop Writing information

What is temporary SOP writing?

Temporary SOP (Standard Operating Procedure) writing involves creating detailed, step-by-step instructions for processes that are only needed for a limited time or specific projects. This can include procedures for short-term initiatives, pilot programs, or unique operational needs. Temporary SOP writers ensure that teams follow consistent methods, even for tasks that aren’t part of regular workflows. Their documents help maintain quality and compliance during the lifespan of a temporary process.

What are the key skills and qualifications needed to thrive as a temporary SOP writer?

To excel as a Temporary SOP Writer, you need strong technical writing skills, attention to detail, and familiarity with industry regulations or standards relevant to the organization. Proficiency with document management systems, word processing software, and possibly tools like SharePoint or Adobe Acrobat is often required. Exceptional communication, adaptability, and the ability to quickly learn new processes are valuable soft skills in this role. These skills ensure the creation of clear, accurate, and compliant standard operating procedures that support organizational efficiency and compliance.

What are some common challenges faced when writing SOPs in a temporary role, and how can they be effectively managed?

In a temporary SOP writing position, common challenges include quickly adapting to company-specific processes, understanding technical language, and meeting tight deadlines. To manage these challenges, it's important to proactively communicate with subject matter experts, utilize any available templates or reference documents, and prioritize clarity and compliance with regulatory standards. Building strong relationships with team members and asking targeted questions can also help ensure that the SOPs meet organizational needs while maintaining accuracy and consistency.

What is the difference between Temporary Sop Writing vs Technical Writer?

AspectTemporary Sop WritingTechnical Writer
CredentialsBasic writing skills, industry-specific knowledgeOften requires a degree in technical communication, engineering, or related fields
Work EnvironmentProject-based, often on-site or remote, within industries like manufacturing or healthcareOffice or remote, across various industries including technology, engineering, and science
Employer & Industry UsageUsed by organizations needing quick, specific SOPs for compliance or safetyUsed by companies creating manuals, guides, and documentation for products or processes

Temporary SOP Writing focuses on creating specific Standard Operating Procedures for immediate needs, often short-term and industry-specific. Technical Writers develop comprehensive documentation, manuals, and guides, usually with formal training. While both roles involve technical writing, Temporary SOP Writers are typically hired for quick, targeted tasks, whereas Technical Writers handle broader, ongoing documentation projects.

What are the most commonly searched types of Sop Writing jobs in California?

The most popular types of Sop Writing jobs in California are:

What job categories do people searching Temporary Sop Writing jobs in California look for?

The top searched job categories for Temporary Sop Writing jobs in California are:

What cities in California are hiring for Temporary Sop Writing jobs?

Cities in California with the most Temporary Sop Writing job openings:

Infographic showing various Temporary Sop Writing job openings in California as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution.

Senior Formulator

Santa Clarita, CA

Actalent
Business Management Consulting • 5 - 10K employees

$40 - $62/hr

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

Description

We are seeking a Sr. Formulator to support the development and commercialization of innovative dietary supplement products. This individual will lead formulation activities from concept through launch, including benchtop development, scale-up, stability testing, pilot batches, and manufacturing support. The role works closely with cross-functional teams including R&D, Quality, Regulatory, Operations, and Marketing.

Responsibilities

Develop and optimize formulations for a variety of dosage forms including tablets, capsules, powders, gummies, and other delivery systems

Lead product development activities from pre-formulation through commercialization

Design and execute benchtop, pilot, scale-up, and verification batch studies

Develop stability protocols and evaluate stability testing results

Support technology transfer and manufacturing implementation activities

Evaluate raw materials, excipients, and ingredient compatibility

Prepare technical documentation including SOPs, batch records, specifications, reports, and development records

Troubleshoot formulation and process-related issues during development and production

Collaborate with Quality, Regulatory, Manufacturing, Marketing, and Supply Chain teams to meet project objectives

Mentor junior formulators and laboratory personnel

Skills

Formulation, Chemistry, nutraceutical, Formulation Development, Product Development, R&d, Research & development, Dietary Supplements, Gmp, Scale-Up, Technology Transfer, Stability Testing, Design of Experiments (DOE), Tablets, Capsules, Powders, Gummies, Softgels, Food Science, ingredient, Raw material, Benchtop Formulation, SOP writing, Clinical Samples, 21 CFR Part 111, ISO-78512, Dietary Supplement, Gummy Formulation, Softgel Formulation, Flavor Development, Sensory testing, Sensory evaluation

Top Skills Details

Formulation,Chemistry,nutraceutical,Formulation Development,Product Development,R&d,Research & development,Dietary Supplements,Gmp

Additional Skills & Qualifications

Bachelor's degree in Food Science, Chemistry, Chemical Engineering, Pharmacy, or related scientific discipline

4+ years of formulation or product development experience within nutraceuticals, dietary supplements, food, cosmetics, or related industries

Experience developing products from concept through commercialization

Strong understanding of formulation science, processing technologies, and GMP environments

Experience with stability studies, scale-up activities, and technical transfers

Ability to analyze experimental data and solve complex technical challenges

Experience working in a cross-functional product development environment

DOE (Design of Experiments) experience is preferred

Preferred Background

Nutraceuticals

Dietary Supplements

Functional Foods

Vitamins & Minerals

Botanicals

Consumer Health Products

Key Skills

Formulation Development

Product Development

Nutraceuticals

Dietary Supplements

GMP

Stability Testing

Scale-Up

Technology Transfer

DOE

Raw Material Evaluation

Excipient Selection

Commercialization

Process Development

Cross-Functional Collaboration

Technical Documentation

Experience Level

Expert Level

Job Type & Location

This is a Contract position based out of Santa Clarita, CA.

Pay and Benefits

The pay range for this position is $40.00 - $62.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Santa Clarita,CA.

Application Deadline

This position is anticipated to close on Aug 28, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance:Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in thecity and county of San Francisco, we will consider for employment qualified applicantswith arrest and conviction records.

Massachusetts Lie Detector:It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI):We may use Artificial Intelligence (AI) to support parts of our hiring process,including sourcing, screening, and evaluating candidates. AI helps assess applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Industry

Business management consulting

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

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