1

Ngo Contract Jobs (NOW HIRING)

Build and maintain trusted relationships with NRO, NGO and other stakeholders to gain insight ... Expertise in engineering and SETA type contracts in the Intel Space environment. * An advanced ...

Audit contracts, orders, and vouchers for accuracy * Maintain fixed asset records * Develop and ... How to Apply Apply online at: www.actionpathways.ngo This position will remain open until filled.

Lead Project Forester

Golden, CO · On-site

$60K - $65K/yr

Manage budgets, grants, and contracts; track deliverables, timelines, and compliance; maintain ... Develop and sustain partnerships with landowners, local governments, and federal/state/tribal/NGO ...

... contracts and key provisions; legal awareness in deal structuring * Experience in multi-year sales, to several stakeholders * Experience supporting ecological restoration projects via CWA, NGO, and ...

Washington, DC, or remote Duration: 12 months contract (Limited Term) Minimum Requirements ... to partners, NGO networks, and donors. The position will provide programmatic and fiduciary ...

Showing results 21-40

Ngo Contract information

See salary details

$10

$28

$65

How much do ngo contract jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for ngo contract in the United States is $28.66, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.97 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Ngo Contract position, and why are they important?

To thrive in an NGO Contract role, you need a solid understanding of contract management, compliance regulations, and project oversight, usually supported by a degree in business, law, or public administration. Familiarity with contract management software, donor reporting platforms, and knowledge of procurement guidelines are key technical requirements. Excellent negotiation, attention to detail, and the ability to communicate across multicultural teams are crucial soft skills in this position. These competencies are vital for ensuring transparent, compliant, and successful partnerships that support the NGO’s mission.

What are the typical daily responsibilities of someone working in an NGO Contract position?

In an NGO Contract position, you can expect to draft, review, and manage agreements with donors, partners, and vendors, ensuring all terms comply with organizational and legal requirements. Daily tasks often involve coordinating with program managers, finance teams, and external stakeholders to monitor contract deliverables and address any issues or modifications. You may also be responsible for maintaining accurate records, preparing compliance reports, and supporting audits. This role requires strong organizational skills and close collaboration with various departments to ensure all contractual obligations are successfully met.

What is an NGO Contract job?

An NGO Contract job refers to a temporary or fixed-term position within a non-governmental organization (NGO), typically governed by a contractual agreement. These roles can vary in duration and scope, covering areas such as project management, fundraising, program coordination, and field work. Employees under contract may have specific deliverables and timelines, differing from permanent staff roles. Such contracts are often funded by grants or donor contributions, influencing their terms and renewal possibilities.

More about Ngo Contract jobs
What cities are hiring for Ngo Contract jobs? Cities with the most Ngo Contract job openings:
What are the most commonly searched types of Ngo jobs? The most popular types of Ngo jobs are:
What states have the most Ngo Contract jobs? States with the most job openings for Ngo Contract jobs include:
Infographic showing various Ngo Contract job openings in the United States as of July 2026, with employment types broken down into 57% Full Time, 22% Part Time, 1% Temporary, and 20% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $59,612 per year, or $28.7 per hour.
Regulatory Affairs Specialist, Cosmetics and OTC Personal Care, Growing Contract Manufacturer

Regulatory Affairs Specialist, Cosmetics and OTC Personal Care, Growing Contract Manufacturer

Pave Talent

Ottawa, IL • On-site

$70K - $100K/yr

Full-time

This job post has expired today. Applications are no longer accepted.


Job description

???????????????? ???????????????????????????????????????? ???????????????????????????????????? ???????? ???????????? ???????????????????????? ???????????????????????????????????????? ???????????????????????????????? ???????????????????? ????????????????????????????. ????????????????'???? ???? ???????????????? ???????????????????? ????????????'???????? ???????????? ???? ???????????????????????????? ????????????????????????????????: ????????????'???????? ???? ???????????????????????????????? ???????????????????????????? ???????????????????????????? ???? ???????????????????????????? ???????????????????????????? ???????????? ????????????????????????????????.


Pave Talent is recruiting on behalf of a well-established personal care contract manufacturer in Ottawa, IL. This company produces hair care, skin care, and over-the-counter (OTC) drug products for major consumer brands, and it is in an extraordinary growth phase. Business did not slow during the pandemic, shifts are expanding, and the OTC division is scaling aggressively. They need a full-fledged Regulatory Affairs Specialist to sit alongside the Global Regulatory Manager and own a meaningful piece of the compliance work.


This is not a coordinator or clerk position. The hiring manager put it plainly: "I need an experienced regulatory person that can hit the ground running."


???????????? ???????????????????????????? ????????????????

- You come from beauty, cosmetics, or OTC manufacturing — not pharma-only, not food

- You have hands-on Modernization of Cosmetics Regulation Act (MoCRA) experience and know what it means in practice

- You are comfortable talking to government agencies and writing the documentation that makes those conversations go well

- You move fast and do not need hand-holding to figure out what has to happen next

- You want to own work, not just assist with it


???????????? ????????????????????????????????????????????

You will report to the Global Manager of Regulatory Affairs and serve as that person's key specialist, supporting compliance across a broad portfolio of cosmetic, personal care, and OTC drug products. The company is ramping its OTC line substantially, which means the regulatory workload is real, growing, and consequential. No one is doing this job now at this level, which means you will set the standard.


You will work cross-functionally with R&D, Quality, Operations, and Marketing teams across U.S. and international markets.


???????????????? ????????????'???????? ????????????

- Provide regulatory guidance for new product development, reformulations, and market expansions

- Prepare and maintain regulatory documentation including ingredient listings, quantitative formulas, cosmetic compliance files, product registrations, claims support packages, and safety documentation

- Conduct label and claims reviews for compliance with Food and Drug Administration (FDA) regulations, Health Canada, European Union (EU) Cosmetic Regulation, and key state requirements including California Proposition 65

- Support MoCRA compliance and cosmetic facility and product registration

- Manage OTC Drug Facts labeling, monograph compliance, and product information file (PIF) preparation

- Monitor emerging regulations and assess business impact, recommending practical compliance strategies

- Partner with R&D to establish formulation and ingredient guidelines for global market access

- Support compliance with retailer standards including Target Clean, Walmart Clean, Sephora Clean, Ulta Clean, and Amazon ingredient programs

- Maintain regulatory files supporting audits, inspections, customer inquiries, and legal matters

- Provide regulatory training and guidance to internal stakeholders


????????????????????????????????

- Bachelor's degree in Chemistry, Biology, Regulatory Science, Pharmaceutical Sciences, or a related scientific discipline

- 2 to 4 years of Regulatory Affairs experience within cosmetics, personal care, or OTC manufacturing — beauty industry backgrounds strongly preferred; pharma-only or food backgrounds will not be considered

- Hands-on MoCRA compliance experience

- Working knowledge of FDA cosmetic and OTC drug regulations, current Good Manufacturing Practices (cGMP), and EU Cosmetic Regulation

- Experience with OTC Drug Facts labeling and monograph requirements

- Experience conducting label reviews and claims substantiation assessments

- Government agency interface experience

- Strong technical writing, documentation, and organizational skills


???????????????????? ????????????????????????

- Experience with PIF preparation, Cosmetic Products Notification Portal (CPNP) notifications, and EU Responsible Person requirements

- Familiarity with International Fragrance Association (IFRA) standards, allergen disclosures, Volatile Organic Compound (VOC) regulations, and sustainability certifications

- Experience supporting NGO and certification programs such as Non-GMO Project, vegan, and clean beauty initiatives

- Knowledge of state-level requirements beyond Prop 65


???????????????????????????????????????????????? ???????????? ????????????????????????????????

???????????????? ????????????????????????: $70,000 to $100,000 annually, depending on experience

????????????????????: None

????????????????????????????????: Monday through Friday, first shift, on-site in Ottawa, IL

????????????????????????????????: Details to be confirmed; relocation considered for exceptional candidates


Interested? Apply and we'll be in touch. Confidential search; your application is fully private.


???????????????? ???????????????????????? | ???????????????????????? ????????????????????????????????????????