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Temporary Contract Regulatory Affairs Jobs (NOW HIRING)

PrideStaff

Regulatory Affairs Associate

Tustin, CA · On-site

$32 - $36/hr

Regulatory Affairs Associate for a biotechnology company located in Tustin ... Temporary to Hire opportunity. Paying $32-36/hr, depending on qualifications. Hours are 9:00 AM - 5 ...

New

Corning Inc.

$71 - $98/hr

Partner with Quality, Regulatory Affairs, Legal, Supply Chain, and Commercial teams to ensure agreements reflect business needs and compliance requirements. * Coordinate contract review with internal ...

edrone

NY · On-site

$75 - $95/hr

Permanent contract* Private healthcare and life insurance* Training and development opportunities ... regulatory affairs### Znajomość języków#### Angielski: B2### Lokalizacja biura*

MWI Animal Health

NY · On-site

$68.51 - $102.76/hr

Temps Pleinposted on: Publié aujourd'huijob requisition id: R2612110Cherchez-vous à faire une ... Regulatory Affairs Manager - Poland** to support regulatory strategy, submissions, lifecycle ...

Just Energy

Manager Regulatory Affairs

Austin, TX · On-site

Job Title: Regulatory Affairs Manager - Mass Markets South Location: Remote (Austin, Houston ... Review customer-facing materials, contracts, marketing collateral, and operational procedures to ...

Merck & Co.

Regulatory Affairs Specialist

Warsaw, IN · On-site

$70 - $90/hr

Regulatory Affairs Specialist 1 Year Contract Warsaw, IN (100% Onsite) Duties * Assist with assembly, distribution, storage and tracking and retrieval of information pertinent to the regulatory ...

New

Aequor

Regulatory Affairs Specialist 1 Year Contract Warsaw, IN (100% Onsite) Duties Responsible for assisting the team with regulatory filings as necessary to market our client's products. This position ...

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How much do temporary contract regulatory affairs jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for temporary contract regulatory affairs in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What is the difference between Temporary Contract Regulatory Affairs vs Permanent Regulatory Affairs?

AspectTemporary Contract Regulatory AffairsPermanent Regulatory Affairs
DurationFixed-term, project-basedOngoing, indefinite
CertificationsTypically requiredTypically required
Work EnvironmentContract roles, often in multiple companiesIn-house, stable environment
Employer UsageUsed for specific projects or peak workloadsLong-term employment

Temporary Contract Regulatory Affairs roles are short-term positions focused on specific projects or regulatory submissions, offering flexibility but less job security. Permanent Regulatory Affairs roles provide ongoing employment with broader responsibilities. Both roles require similar certifications and industry knowledge, but differ mainly in duration and employment stability.

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Temporary Contract Regulatory Affairs jobs near you
Infographic showing various Temporary Contract Regulatory Affairs job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 9% Part Time, and 2% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Senior Manager, Regulatory Affairs

West Pharmaceutical Services

Exton, PA • Hybrid

Full-time

Re-posted 21 days ago

Key responsibilities

  • Design, optimize, and oversee end-to-end business processes supporting contract regulatory services.

  • Interface with clients to understand requirements, define scope, and ensure processes meet contractual obligations.

  • Map and manage workflows, monitor KPIs, and implement improvements to ensure efficiency, scalability, and compliance.

West Pharmaceutical Services rating

8.5

Company rating: 8.5 out of 10

Based on 32 frontline employees who took The Breakroom Quiz

13th of 122 rated packaging manufacturers

Job description

This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week

Who We Are:

At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?  

There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.  

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.  

Job Summary

In this role, you will be responsible for designing, optimizing, and overseeing the endtoend business processes that support the delivery of contract regulatory services. You will ensure that regulatory service operations are efficient, scalable, compliant, and aligned with evolving global regulatory expectations and customer needs. This role serves as a key bridge between regulatory experts, quality, commercial teams, and external clients to enable consistent, highquality execution of contracted regulatory deliverables. You must proactively maintain an understanding of health authority guidelines, regulations, and best practice to establish regulatory strategy.

Essential Duties and Responsibilities
  • Lead the development, standardization, and continuous improvement of business processes supporting contract regulatory services (e.g. submission support, technical documentation, advisory services). Ensure those processes support highquality regulatory outputs.
  • Interface with clients to understand requirements, define scope, and ensure processes deliver against contractual obligations.
  • Map and manage endtoend workflows, ensuring efficiency, scalability, and alignment with regulatory requirements.
  • Support onboarding of new services, customers, and regulatory requirements into operational workflows.
  • Establish and monitor KPIs (e.g. cycle time, quality metrics, client satisfaction) to identify process gaps, risks, and inefficiencies; implement improvements using datadriven and riskbased approaches.
  • Partner with subject matter experts to translate regulatory requirements into standardized and repeatable service offerings.
  • Work closely with Regulatory Affairs, Quality Assurance, Commercial, Legal, and IT teams to ensure seamless execution of services in line with business strategy and objectives.
  • Identify and qualify vendors, tools, templates and systems to build efficiency.
  • Maintain effectiveness when experiencing major changes in work responsibilities or environment; adjusting effectively to work within new work structures, processes, requirements, or cultures.
  • Other duties as assigned.
Work Experience

  • Bachelor's degree  in science, math, engineering, or related discipline required with a minimum 10 years of experience OR

  • PhD / Master's degree in  science, math, engineering, or related discipline required with a minimum 5 years of regulatory/pharmaceutical experience 

Preferred Knowledge, Skills and Abilities
  • Excellent interpersonal, communication and listening skills.
  • Experience in medical device regulatory affairs and/or design control process, direct interactions with regulatory agencies and management of regulatory support systems.
  • Regulatory compliance competency including Quality Systems
  • International regulatory competency
  • Advanced degree 
  • Regulatory Affairs Certification (R.A.C)
  • Able to comply with the company's safety and quality policies at all times
Additional Requirements
  • Strong collaborator and communicator, experienced engaging with and presenting to crossfunctional teams, customers, and industry stakeholders.
  • Demonstrated technical leadership with broad understanding of pharmaceutical/biologic operations, device development, and combination products.
  • Skilled in negotiation, decisionmaking, and managing multiple projects with competing priorities and timelines.
  • Able to analyze and synthesize complex scientific, technical, and regulatory information to drive sound conclusions and actions.
  • Selfmotivated, adaptable, and effective in fastpaced environments, with solid organizational, problemsolving, and documentation skills.
License and Certifications
  • Pharmaceutical and Medicine\Regulatory Affairs Certifications (RAC)-RAPS Regulatory Affairs Certification (R.A.C) Upon Hire preferred
Travel Requirements
20%: Up to 52 business days per year
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
What We Offer
Community Involvement: West encourages volunteerism through its West without Borders initiative and other charitable programs that make a difference in local communities.
Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion-where all voices are heard and respected in a supportive environment.
Recognition & Rewards: Performance-based bonuses, service recognition, and employee appreciation initiatives celebrate dedication and impact.
This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week

#LI-DJ1 #LI-HYBRID

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.  If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com.  Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.

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